1. Epidemiology and Global Health
  2. Microbiology and Infectious Disease

Mapping the zoonotic niche of Ebola virus disease in Africa

  1. David M Pigott
  2. Nick Golding
  3. Adrian Mylne
  4. Zhi Huang
  5. Andrew J Henry
  6. Daniel J Weiss
  7. Oliver J Brady
  8. Moritz UG Kraemer
  9. David L Smith
  10. Catherine L Moyes
  11. Samir Bhatt
  12. Peter W Gething
  13. Peter W Horby
  14. Isaac I Bogoch
  15. John S Brownstein
  16. Sumiko R Mekaru
  17. Andrew J Tatem
  18. Kamran Khan
  19. Simon I Hay  Is a corresponding author
  1. University of Oxford, United Kingdom
  2. Sanaria Institute for Global Health and Tropical Medicine, United States
  3. University of Toronto, Canada
  4. University Health Network, Toronto, Canada
  5. Harvard Medical School, United States
  6. Boston Children's Hospital, United States
  7. University of Southampton, United Kingdom
  8. National Institutes of Health, United States
  9. Flowminder Foundation, Sweden
  10. Li Ka Shing Knowledge Institute, St. Michael's Hospital, Canada
https://doi.org/10.7554/eLife.04395
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Cite this article
  1. David M Pigott
  2. Nick Golding
  3. Adrian Mylne
  4. Zhi Huang
  5. Andrew J Henry
  6. Daniel J Weiss
  7. Oliver J Brady
  8. Moritz UG Kraemer
  9. David L Smith
  10. Catherine L Moyes
  11. Samir Bhatt
  12. Peter W Gething
  13. Peter W Horby
  14. Isaac I Bogoch
  15. John S Brownstein
  16. Sumiko R Mekaru
  17. Andrew J Tatem
  18. Kamran Khan
  19. Simon I Hay
(2014)
Mapping the zoonotic niche of Ebola virus disease in Africa
eLife 3:e04395.
https://doi.org/10.7554/eLife.04395
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Abstract

Ebola virus disease (EVD) is a complex zoonosis that is highly virulent in humans. The largest recorded outbreak of EVD is ongoing in West Africa, outside of its previously reported and predicted niche. We assembled location data on all recorded zoonotic transmission to humans and Ebola virus infection in bats and primates (1976–2014). Using species distribution models, these occurrence data were paired with environmental covariates to predict a zoonotic transmission niche covering 22 countries across Central and West Africa. Vegetation, elevation, temperature, evapotranspiration, and suspected reservoir bat distributions define this relationship. At-risk areas are inhabited by 22 million people; however, the rarity of human outbreaks emphasises the very low probability of transmission to humans. Increasing population sizes and international connectivity by air since the first detection of EVD in 1976 suggest that the dynamics of human-to-human secondary transmission in contemporary outbreaks will be very different to those of the past.

https://doi.org/10.7554/eLife.04395.001

eLife digest

Since the first outbreaks of Ebola virus disease in 1976, there have been numerous other outbreaks in humans across Africa with fatality rates ranging from 50% to 90%. Humans can become infected with the Ebola virus after direct contact with blood or bodily fluids from an infected person or animal. The virus also infects and kills other primates—such as chimpanzees or gorillas—though Old World fruit bats are suspected to be the most likely carriers of the virus in the wild.

The largest recorded outbreak of Ebola virus disease is ongoing in West Africa: more people have been infected in this current outbreak than in all previous outbreaks combined. The current outbreak is also the first to occur in West Africa—which is outside the previously known range of the Ebola virus.

Pigott et al. have now updated predictions about where in Africa wild animals may harbour the virus and where the transmission of the virus from these animals to humans is possible. As such, the map identifies the regions that are most at risk of a future Ebola outbreak. The data behind these new maps include the locations of all recorded primary cases of Ebola in human populations—the ‘index’ cases—many of which have been linked to animal sources. The data also include the locations of recorded cases of Ebola virus infections in wild bats and primates from the last forty years. The maps, which were modelled using more flexible methods than previous predictions, also include new information—collected using satellites—about environmental factors and new predictions of the range of wild fruit bats.

Pigott et al. report that the transmission of Ebola virus from animals to humans is possible in 22 countries across Central and West Africa—and that 22 million people live in the areas at risk. However, outbreaks in human populations are rare and the likelihood of a human getting the disease from an infected animal still remains very low. The updated map does not include data about how infections spread from one person to another, so the next challenge is to use existing data on human-to-human transmission to better understand the likely size and extent of current and future outbreaks. As more people live in, and travel to and from, the at-risk regions than ever before, Pigott et al. note that new outbreaks of Ebola virus disease are likely to be very different to those of the past.

https://doi.org/10.7554/eLife.04395.002

Introduction

Ebola viruses have for the last forty years been responsible for a number of outbreaks of Ebola virus disease (EVD) in humans (Pattyn et al., 1977), with high case fatality rates typically around 60–70%, but potentially reaching as high as 90% (Feldmann and Geisbert, 2011). The most recent outbreak began in Guinea in December 2013 (Baize et al., 2014; Bausch and Schwarz, 2014) and has subsequently spread to Liberia, Sierra Leone and Nigeria (ECDC, 2014). The unprecedented size and scale of this ongoing outbreak has the potential to destabilise already fragile economies and healthcare systems (Fauci, 2014), and fears of international spread of a Category A Priority Pathogen (NIH, 2014) have made this a massive focus for international public health (Chan, 2014). This has led to the current outbreak being declared a Public Health Emergency of International Concern on the 8 August 2014 (Briand et al., 2014; Gostin et al., 2014; WHO, 2014d).

The Filoviridae, of which Ebolavirus is a constituent genus, belong to the order Mononegavirales. Two other genera complete the family: Marburgvirus, itself responsible for a number of outbreaks of haemorrhagic fever across Africa (Gear et al., 1975; Conrad et al., 1978; Smith et al., 1982; Towner et al., 2006) and Cuevavirus, recently isolated from bats in northern Spain (Negredo et al., 2011). Five species of Ebolavirus have been isolated to date (Kuhn et al., 2010; King et al., 2012); the earliest recognised outbreaks of EVD were reported in Zaire (now the Democratic Republic of the Congo [DRC]) and Sudan in 1976 (International Commission, 1978; WHO International Study Team, 1978). The causative viruses were isolated (Pattyn et al., 1977) and later identified to be distinct species, Zaire ebolavirus (EBOV) and Sudan ebolavirus (SUDV). A third species of Ebolavirus, Reston ebolavirus, was isolated from Cynomologus monkeys imported from the Philippines to a facility in the United States, where they experienced severe haemorrhaging (Jahrling et al., 1990). Whilst serological evidence of infection with this species has been reported in individuals in the Philippines (Miranda et al., 1991), no pathogenicity has been reported beyond primates and porcids (Barrette et al., 2009; Feldmann and Geisbert, 2011). In 1994 a fourth species, Tai Forest ebolavirus was isolated from a veterinarian who had autopsied a chimpanzee in Côte d’Ivoire (Le Guenno et al., 1995), though the virus has not been detected subsequently. The final species, Bundibugyo ebolavirus, was responsible for an outbreak of EVD in Uganda in 2007 (Towner et al., 2008), as well as a more recent outbreak in the DRC (WHO, 2012b).

Initial analysis suggested that the viruses isolated from the current outbreak, originating in Guinea, formed a separate clade within the five Ebolavirus species (Baize et al., 2014). Subsequent re-analysis of the same sequences however, indicated that these isolates instead nest within the Zaire ebolavirus lineage (Dudas and Rambaut, 2014), and diverged from Central Africa strains approximately ten years ago (Gire et al., 2014).

Which reservoir species are responsible for maintaining Ebola transmission between outbreaks is not well understood (Peterson et al., 2004b), but over the last decade significant progress has been made in narrowing down the list of likely hosts (Peterson et al., 2007) (Figure 1). Primates have long been known to harbour filoviral infections, with the first Marburg strains identified in African green monkeys in 1967 (Siegert et al., 1967; Beer et al., 1999). Significant mortality has also been reported in wild primate populations across Africa, most notably in gorilla (Gorilla gorilla) and chimpanzee (Pan troglodytes) populations (Formenty et al., 1999; Rouquet et al., 2005; Bermejo et al., 2006). The high case fatality rates recorded in the great apes combined with their declining populations and limited geographical range, indicate they are likely dead-end hosts for the virus and not reservoir species (Groseth et al., 2007). A large survey of small mammals in and around Gabon identified three species of bats which were infected with Ebola viruses—Hypsignathus monstrosus, Epomops franqueti and Myonycetris torquata (Leroy et al., 2005). Subsequent serological surveys (Pourrut et al., 2009; Hayman et al., 2010) and evidence linking the potential source of human outbreaks to bats (Leroy et al., 2009) lend support to the hypothesis of a bat reservoir. This, coupled with repeated detection of Marburgvirus in the fruit bat Rousettus aegypticus (Towner et al., 2009) and the only isolations of Cuevavirus also from bats (specifically Llovia virus [Negredo et al., 2011]), all support the suspicion that Chiroptera play an important role in the natural life-cycle of the filoviruses.

Figure 1
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The epidemiology of Ebola virus transmission in Africa.

Of the suspected reservoir species, 1, 2 and 3 represent the three bat species from which Ebola virus has been isolated (Hypsignathus monstrosus, Myonycteris torquata and Epomops franqueti) and n represents unknown reservoirs of the disease yet to be discovered. Of the susceptible species, A represents Pan troglodytes, B Gorilla gorilla and m represents other organisms susceptible to the disease, such as duikers. H represents humans. Blue arrows indicate unknown transmission cycles or infection routes and red arrow routes have been confirmed or are suspected. Adapted from Groseth et al. (2007).

https://doi.org/10.7554/eLife.04395.003

Humans represent a dead-end host for the virus, with only stuttering chains of transmission reported between humans in the majority of previous outbreaks (Chowell et al., 2004; Legrand et al., 2007) and no indication that humans can reintroduce the virus back into reservoir species (Karesh et al., 2012). The incubation period in humans ranges from two days to three weeks, after which a variety of clinical symptoms arise, affecting multiple organs of the body. At the peak of illness, haemorrhaging shock and widespread tissue damage can occur and can eventually lead to death within 6–16 days (Feldmann and Geisbert, 2011). Human-to-human transmission is mainly through direct unprotected contact with infected individuals and cadavers, with infectious particles detected in a number of different body fluids (Feldmann and Geisbert, 2011). The typical outbreak profile is defined by an index individual that has recently come into contact with the blood of another mammal through either hunting or the butchering of animal carcasses (Pourrut et al., 2005). Whilst it has been difficult to identify the zoonotic source for the index cases of some outbreaks, a recurring theme of hunting and handling bushmeat is suspected (Table 1; Boumandouki et al., 2005; Nkoghe et al., 2005, 2011; Leroy et al., 2009). For some outbreaks, including the most recent, the initial source of zoonotic transmission has not been identified. In subsequent human-to-human transmission, the highest risk activities are those that bring humans into close contact with infected individuals. These include medical settings where insufficient infection control precautions have been taken, as well as home care and funeral preparations carried out by families or close friends (Baron et al., 1983; Georges et al., 1999; Boumandouki et al., 2005). As the conditions required for transmission are culturally and contextually dependent, opportunities for sustained transmission are highly heterogeneously distributed. Typically, chains of infection do not exceed three or four sequential transmission events, although occasionally (and particularly in the early stages of infection) a single individual may be responsible for directly infecting a large number of others (Brady et al., 2014). In the outbreak in Gabon in 1996, a single person was responsible for infecting ten other individuals (Milleliri et al., 2004) whilst in the 1995 outbreak in the DRC, thirty five cases resulted from one individual (Khan et al., 1999). Secondary transmission can be restricted by effective case detection and isolation measures (Shoemaker et al., 2012; WHO, 2014c). Where this cannot be achieved, either due to a lack of infrastructure, poor understanding of the disease, or distrust of medical practices, secondary cases can continue to occur (Khan et al., 1999; Larkin, 2003; Hewlett et al., 2005). As the number of infections grows, the ability of healthcare systems to control the further spread diminishes and the risk of a large outbreak increases.

Table 1

Locations of outbreaks of Ebola virus disease in humans

https://doi.org/10.7554/eLife.04395.004
OutbreakCountriesDate rangeLocationSpeciesReference
1South SudanJun–Nov 1976NzaraSUDV(WHO International Study Team, 1978)
2DRCSep–Oct 1976YambukuEBOV(International Commission, 1978)
3DRCJun 1977BonduniEBOV(Heymann et al., 1980)
4South SudanJul–Oct 1979NzaraSUDV(Baron et al., 1983)
5Côte d’IvoireNov 1994Tai ForestTAFV(Le Guenno et al., 1995; Formenty et al., 1999)
6GabonNov 1994–Feb 1995Mekouka and Andock mining campsEBOV(Amblard et al., 1997; Georges et al., 1999; Milleliri et al., 2004)
7DRCJan–Jul 1995Mwembe ForestEBOV(Muyembe and Kipasa, 1995; Khan et al., 1999)
8GabonJan–Mar 1996Mayibout 2EBOV(Georges et al., 1999; Milleliri et al., 2004)
9GabonJul 1996–Jan 1997BooueEBOV(Georges et al., 1999; Milleliri et al., 2004)
10UgandaOct 2000–Feb 2001Rwot-ObilloSUDV(WHO, 2001; Okware et al., 2002; Lamunu et al., 2004)
11Gabon & ROCOct 2001–Mar 2002Memdemba Entsiami, Abolo and AmbomiEBOV(WHO, 2003; Milleliri et al., 2004; Nkoghe et al., 2005; Pourrut et al., 2005)
Ekata
Oloba
Etakangaye
Grand Etoumbi
12ROCDec 2002–Apr 2003YembelangoyeEBOV(WHO, 2003; Pourrut et al., 2005)
Nearby hunting camp
Mvoula
13ROCOct–Dec 2003MbandzaEBOV(Boumandouki et al., 2005)
14South SudanApr–Jun 2004Forests bordering YambioSUDV(WHO, 2005; Onyango et al., 2007)
15ROCApr–May 2005Odzala National ParkEBOV(Nkoghe et al., 2011)
16DRCMay–Nov 2007Mombo Mounene 2 marketEBOV(Leroy et al., 2009)
17UgandaAug–Dec 2007KabangoBDBV(Towner et al., 2008; MacNeil et al., 2010; Wamala et al., 2010)
18DRCNov 2008–Feb 2009LueboEBOV(Grard et al., 2011)
19UgandaMay 2011NakisamataSUDV(Shoemaker et al., 2012)
20DRCJuly–Nov 2012IsiroBDBV(CDC, 2014; WHO, 2012b)
21UgandaJuly–Oct 2012NyanswigaSUDV(CDC, 2014; WHO, 2012a)
22UgandaNov 2012–Jan 2013Luwero DistrictSUDV(WHO, 2012c; CDC, 2014)
23GuineaDec 2013 -MeliandouEBOV(Baize et al., 2014; Bausch and Schwarz, 2014)

  1. DRC = Democratic Republic of the Congo, ROC = Republic of Congo.

The recent outbreak in Guinea and surrounding countries indicate that the previous paradigm for Ebola outbreaks is shifting (Briand et al., 2014; Chan, 2014). The last 40 years of EVD outbreaks were accompanied by considerable changes in demographic patterns throughout Africa. There has been a large increase in population size coupled with increasing urbanisation (Cohen, 2004; Seto et al., 2012; Linard et al., 2013). African populations have also become better connected internally and internationally (Linard et al., 2012; Huang and Tatem, 2013). Only recently have we begun to understand the dynamic nature of these travel patterns (Garcia et al., 2014; Gonzalez et al., 2008; Simini et al., 2012; Wesolowski et al., 2013, 2012) which have been clearly demonstrated to influence disease transmission over different temporal and spatial scales (Hufnagel et al., 2004; Yang et al., 2008; Stoddard et al., 2009; Talbi et al., 2010; Brockmann and Helbing, 2013; Pindolia et al., 2014). Changes in land use and penetration into previously remote areas of rainforest bring humans into contact with potential new reservoirs (Daszak, 2000), while changes in human mobility and connectivity will likely have profound impacts on the dispersion of Ebola cases during outbreaks. These conditions are thought to have a major role in setting the stage for the current outbreak.

This paper aims to define the areas suitable for zoonotic transmission of Ebolavirus (i.e., those routes defined in Figure 1 excluding human-to-human transmission) through species distribution modelling techniques. The fundamental niche of a species can be conceptualised as the confluence of environmental conditions that support its presence in a particular location (Franklin, 2009). Species distribution models quantitatively describe this niche based on known occurrence records of the organism and their associated environmental conditions, enabling predictions of the likely geographic distribution of the species in other regions (Elith and Leathwick, 2009). The era of satellites and geographical information systems has made high resolution global data on environmental conditions increasingly available (Hay et al., 2006; Weiss et al., 2014b). Species distribution modelling using flexible machine learning approaches have been successfully applied to map the global distributions of disease vectors (Sinka et al., 2012) and pathogens such as dengue (Bhatt et al., 2013), influenza (Gilbert et al., 2014) and leishmaniasis (Pigott et al., 2014).

Previous studies applied the GARP (Genetic Algorithm for Rule-set Production) species distribution modelling approach (Stockwell and Peters, 1999) to the locations of 12 Ebola outbreaks in humans between 1976 and 2002 to map the likely distribution of Ebola viruses (Peterson et al., 2004a) and as a mechanism to identify potential reservoir hosts (Peterson et al., 2004b; Peterson et al., 2007). Here we update and improve the maps of the zoonotic transmission niche of EVD by: (i) incorporating more recent outbreak data from outside the formerly predicted niche of EVD; (ii) integrating for the first time data on outbreaks in primates and the occurrence of the virus in the suspected Old World fruit bat (OWFB) reservoirs; (iii) using new satellite-derived information on bespoke environmental covariates from Africa, including new distribution maps of the OWFB; and (iv) using new increasingly flexible niche mapping techniques in the modelling framework. To elucidate the relevance of these maps for transmission, we have also calculated the population at risk of primary spillover outbreaks from the zoonotic niche of EVD in Africa, and we investigated the changing nature of the populations within this niche.

Results

Reported EVD outbreaks

In total, 23 outbreaks of Ebola virus were identified in humans across Africa, consisting of a hypothesised 30 independent primary infection events (Table 1; Figure 2). These outbreaks span the last 40 years from the first outbreaks in 1976 to the five outbreaks that have occurred since 2010 (Table 1). The locations of the index cases span from West Africa, with the most westerly outbreak ongoing in Guinea, to Gabon, the Republic of Congo (ROC), the DRC, South Sudan and Uganda. Before December 2013, a total of 2322 cases had occurred from Ebolavirus infections, a number already overtaken by the likely underreported current case count of the ongoing outbreak >2250 (WHO, 2014a) (Figure 2A). Of the four viruses circulating in Africa, Zaire ebolavirus has been responsible for the most outbreaks (13), followed by Sudan ebolavirus (7) and Bundigbuyo ebolavirus with just two outbreaks in 2007/8 and 2012. Tai Forest has caused one confirmed infection in humans, from which the patient recovered (Le Guenno et al., 1995; Formenty et al., 1999). Although outbreaks have been reported since 1976, there was an absence of reported outbreaks in humans for 15 years between 1979 and 1994 (although antibodies in humans were identified over the period [Kuhn, 2008]) and the frequency of outbreaks has increased substantially post 2000 (Figure 2A).

Figure 2
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The locations of Ebola virus disease outbreaks in humans in Africa.

(A) Illustrates the 23 reported outbreaks of Ebola virus disease through time, with the area of each circle and its position along the y-axis representing the number of cases. The onset year is represented by the colour as per (B). (B) Shows a map of the index cases for each of these outbreaks. (C–H) Show these outbreaks over a series of time periods. Numbers refer to outbreaks as listed in Table 1. In (B–H) the species of Ebola virus responsible for the outbreak is illustrated by the symbol shape, the number of resulting cases and onset date by symbol colour. The most recent outbreak (#23) is indicated in orange. Countries in which zoonotic transmission to humans has been reported or is assumed to have occurred are coloured in blue. In each map the Democratic Republic of Congo is outlined for reference.

https://doi.org/10.7554/eLife.04395.005

Reported Ebola virus infections in animals

A total of 51 surveyed locations reporting infections in animals were identified in the literature since the discovery of the disease (Table 2; Figure 3). These comprised 17 infections in gorillas (Gorilla gorilla), nine infections in chimpanzees (Pan troglodytes), 18 in OWFB and 2 in duikers (Cephalophus spp.). A large proportion of the great ape cases originated from the ROC/Gabon border, coinciding with the main known distributions of both chimpanzees and gorillas (Petter and Desbordes, 2013) and representing a period of well-documented great ape Ebola outbreaks in and around the Lossi Animal Sanctuary (Rouquet et al., 2005; Bermejo et al., 2006; Walsh et al., 2009). All animal isolations of Ebola viruses have come from countries that have also reported index cases of human outbreaks, with the exception of several seropositive bats from a survey in southern Ghana.

Table 2

Locations of reported infections with Ebola virus in animals

https://doi.org/10.7554/eLife.04395.006
SiteCountryDate rangeLocationSpeciesDiagnosisReference
1Côte d’IvoireOct–Nov 1994Tai ForestChimpanzeeSerology(Formenty et al., 1999)
2GabonJan 1996Mayiboth 2ChimpanzeePCR(Lahm et al., 2007)
3GabonJul 1996Near BooueChimpanzeeSerology(Georges-Courbot et al., 1997)
4GabonSept 1996Lope National ParkChimpanzeePCR(Lahm et al., 2007)
5Gabon & ROCAug 2001Mendemba/Lossi Animal SanctuaryChimpanzeePCR(Lahm et al., 2007)
6Gabon & ROCAug 2001Mendemba/Lossi Animal SanctuaryGorillaPCR(Lahm et al., 2007)
7Gabon & ROCAug 2001Mendemba/Lossi Animal SanctuaryCephalophus dorsalisPCR(Lahm et al., 2007)
8GabonNov 2001ZadieGorillaPCR(Rouquet et al., 2005)
9GabonNov 2001EkataGorillaPCR(Wittmann et al., 2007)
10GabonDec 2001Medemba and neighbouring villagesChimpanzee and GorillaPCR(Leroy et al., 2002)
11GabonFeb 2002ZadieGorillaPCR(Rouquet et al., 2005)
12GabonFeb 2002EkataVarious bat speciesSerology(Leroy et al., 2005)
13GabonMar 2002ZadieGorillaPCR(Rouquet et al., 2005)
14GabonMar 2002Grand EtoumbiGorillaPCR(Wittmann et al., 2007)
15GabonApr 2002EkataGorillaPCR(Wittmann et al., 2007)
16ROCMay 2002OlobaChimpanzeePCR(Lahm et al., 2007)
17ROCDec 2002Lossi Animal SanctuaryGorillaPCR(Rouquet et al., 2005)
18ROCDec 2002Lossi Animal SanctuaryGorillaPCR(Rouquet et al., 2005)
19ROCDec 2002Lossi Animal SanctuaryChimpanzeeSerology(Rouquet et al., 2005)
20ROCDec 2002Lossi Animal SanctuaryGorillaPCR(Rouquet et al., 2005)
21ROCDec 2002Lossi Animal SanctuaryGorillaPCR(Rouquet et al., 2005)
22ROCDec 2002Lossi Animal SanctuaryCephalophus spp.PCR(Rouquet et al., 2005)
23GabonFeb 2003MbomoVarious bat speciesPCR(Leroy et al., 2005)
24ROCFeb 2003Lossi Animal SanctuaryGorillaSerology(Rouquet et al., 2005)
25GabonFeb 2003Lossi Animal SanctuaryChimpanzeePCR(Wittmann et al., 2007)
26GabonJun 2003MbomoVarious bat speciesPCR and serology(Leroy et al., 2005)
27ROCJun 2003Near Mbomo and Ozala National ParkEpomops franquetiSerology(Pourrut et al., 2009)
28ROCJun 2003Near Mbomo and Ozala National ParkHypsignathus monstrosusSerology(Pourrut et al., 2009)
29ROCJun 2003Near Mbomo and Ozala National ParkMyonycteris torquataSerology(Pourrut et al., 2009)
30ROCJun 2003MbanzaGorillaPCR(Rouquet et al., 2005)
31ROCJan–Jun 2004LokouéGorillaReported(Caillaud et al., 2006)
32ROCMay 2004LokouéGorillaPCR(Wittmann et al., 2007)
33GabonFeb 2005Near FrancevilleEpomops franquetiSerology(Pourrut et al., 2009)
34GabonFeb 2005Near FrancevilleMyonycteris torquataSerology(Pourrut et al., 2009)
35GabonApr 2005Near LambareneEpomops franqueti and Hypsignathus monstrosusSerology(Pourrut et al., 2007)
36ROCMay 2005Near Mbomo and Ozala National ParkEpomops franquetiSerology(Pourrut et al., 2009)
37ROCMay 2005Near Mbomo and Ozala National ParkHypsignathus monstrosusSerology(Pourrut et al., 2009)
38ROCMay 2005Near Mbomo and Ozala National ParkMyonycteris torquataSerology(Pourrut et al., 2009)
39ROCJun 2005Odzala National ParkGorillaPCR(Wittmann et al., 2007)
40GabonFeb 2006Near TchibangaVarious bat speciesSerology(Pourrut et al., 2009)
41ROCMay 2006Near Mbomo and Ozala National ParkEpomops franquetiSerology(Pourrut et al., 2009)
42ROCMay 2006Near Mbomo and Ozala National ParkHypsignathus monstrosusSerology(Pourrut et al., 2009)
43ROCMay 2006Near Mbomo and Ozala National ParkMyonycteris torquataSerology(Pourrut et al., 2009)
44GabonOct 2006Near FrancevilleEpomops franquetiSerology(Pourrut et al., 2009)
45GhanaMay 2007SagyimaseEpomops franquetiSerology(Hayman et al., 2012)
46GhanaMay 2007SagyimaseHypsignathus monstrosusSerology(Hayman et al., 2012)
47GhanaMay 2007AdoagyirEpomophorus gambianusSerology(Hayman et al., 2012)
48GhanaMay 2007AdoagyirEpomops franquetiSerology(Hayman et al., 2012)
49GhanaJun 2007OyibiEpomophorus gambianusSerology(Hayman et al., 2012)
50GhanaJan 2008AccraEidolon helvumSerology(Hayman et al., 2010)
51GabonMar 2008Near FrancevilleEpomops franquetiSerology(Pourrut et al., 2009)

  1. ROC = Republic of Congo.

Figure 3
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The locations of reported Ebola virus infection in animals in Africa.

(A) Shows the locations of reported Ebola virus infection in animals. (B–D) Show these records in animals over three different time periods. Numbers refer to records as listed in Table 2. In all panels, the species in which infection was detected is given by symbol shape and the year recorded by symbol colour. Blue countries represent locations where zoonotic transmission to humans has been reported or is assumed to have occurred. In each map the Democratic Republic of Congo is outlined for reference.

https://doi.org/10.7554/eLife.04395.007

Predicted distribution of suspected reservoir species of bats

Three species of bats, Hypsignathus monstrosus, Myonycteris torquata and Epomops franqueti, were identified as the most likely candidates to be reservoir species for Ebola viruses due to high seroprevalence and the isolation of RNA closely related to Zaire ebolavirus (Leroy et al., 2005; Olival and Hayman, 2014). In total, 239 locations were identified from the Global Biodiversity Information Facility (GBIF) (GBIF, 2014): 67 for H. monstrosus (Figure 4A), 52 for M. torquata (Figure 4B) and 120 for E. franqueti (Figure 4C). Distribution models for all three species demonstrated predictive skill (indicated by an area under the curve (AUC) greater than 0.5) as follows: H. monstrosus AUC 0.63 ± 0.04; M. torquata AUC = 0.59 ± 0.04; E. franqueti AUC = 0.58 ± 0.03, n = 50 submodels for all three species. In addition, each species was broadly predicted within its considered expert opinion range (Figure 4A–C) (Schipper et al., 2008). The marginal effect plots (not shown) were strongly influenced by land surface temperature (LST) and vegetation (as measured by the enhanced vegetation index [EVI]). The predicted combined distribution of these species (Figure 4D), covers West and Central Africa, specifically the moist forests of the northeastern, western and central Congo basin, and Guinea, as well as the Congolian coastal forest ecoregions (WWF, 2014).

Figure 4
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Predicted geographical distribution of the three species of Megachiroptera suspected to reservoir Ebola virus.

(A) Shows the distribution of the hammer-headed bat (Hypsignathus monstrosus), (B) The little collared fruit bat (Myonycteris torquata) and (C) Franquet's epauletted fruit bat (Epomops franqueti). In each map, the locations of reported observations of each species, extracted and curated from the Global Biodiversity Information Facility (GBIF, 2014) and used to train each model are given as grey points (H. monstrosus, n = 67; E. franqueti, n = 120 and M. torquata, n = 52). Expert opinion maps of the known range of each species, generated by the IUCN (Schipper et al., 2008), are outlined in grey. The colour legend represents a scale of the relative probability that the species occurs in that location from 0 (white, low) to 1 (green, high). Area under the curve statistics, calculated under a stringent ten-fold cross validation procedure, are 0.63 ± 0.04, 0.59 ± 0.04 and 0.58 ± 0.03 for H. monstrosus, M. torquata and E. franqueti respectively. (D) Is a composite distribution map giving the mean, relative probability of occurrence from (A–C).

https://doi.org/10.7554/eLife.04395.008

Predicted environmental suitability for zoonotic transmission of Ebola

The predicted environmental niche for zoonotic transmission of EVD is shown in Figure 5. All countries with observed index cases of EVD (n = 7, hereafter Set 1) have areas of the highest environmental suitability (see list in Table 1). In addition, areas of high environmental suitability for zoonotic transmission are predicted in a further 15 countries where, to date, index cases of the four African species of Ebolavirus have not been recorded. These are Nigeria, Cameroon, Central African Republic (CAR), Ghana, Liberia, Sierra Leone, Angola, Tanzania, Togo, Ethiopia, Mozambique, Burundi, Equatorial Guinea, Madagascar and Malawi (hereafter Set 2).

Figure 5 with 3 supplements see all
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Predicted geographical distribution of the zoonotic niche for Ebola virus.

(A) Shows the total populations living in areas of risk of zoonotic transmission for each at-risk country. The grey rectangle highlights countries in which index cases of Ebola virus disease have been reported (Set 1); the remainder are countries in which risk of zoonotic transmission is predicted, but in which index cases of Ebola have not been reported (Set 2). These countries are ranked by population at risk within each set. The population at risk Figure in 100,000 s is given above each bar. (B) Shows the predicted distribution of zoonotic Ebola virus. The scale reflects the relative probability that zoonotic transmission of Ebola virus could occur at these locations; areas closer to 1 (red) are more likely to harbour zoonotic transmission than those closer to 0 (blue). Countries with borders outlined are those which are predicted to contain at-risk areas for zoonotic transmission based on a thresholding approach (see ‘Materials and methods’). The area under the curve statistic, calculated under a stringent 10-fold cross-validation procedure is 0.85 ± 0.04. Solid lines represent Set 1 whilst dashed lines delimit Set 2. Areas covered by major lakes have been masked white.

https://doi.org/10.7554/eLife.04395.009

The AUC for the Ebola model was relatively high (AUC = 0.85 ± 0.04, n = 500 submodels) indicating that the model could strongly distinguish regions of environmental suitability for EVD. Enhanced vegetation index had the greatest impact on the distribution (relative contribution [RC] of 65.3%) followed by elevation (RC = 11.7%), night-time land surface temperature (LST) (RC = 7.7%), potential evapotranspiration (PET) (RC = 5.7%) and combined bat distribution (RC = 3.8%). Marginal effect plots are presented in Figure 5—figure supplement 2.

In total, 22.2 million people are predicted to live in areas suitable for zoonotic transmission of Ebola. The vast majority, 21.7 million (approximately 97%), live in rural areas, as opposed to urban or peri-urban areas (CIESIN/IFPRI/WB/CIAT, 2007; WorldPop, 2014). Of these, 15.2 million are in Set 1 and 7 million are in Set 2. In terms of ranked populations at risk, DRC, Guinea and Uganda are highest in Set 1 and Nigeria, Cameroon and CAR are top in Set 2. For a full listing of these populations living in areas of risk, see the stacked bar plot in Figure 5A.

National level demographic and mobility changes

Over the 40 year period since discovery of EVD, the total population living in those countries predicted to be within the zoonotic niche has nearly tripled (from 230 million to 639 million) and the proportion of the population in these countries living in an urban (rather than rural) setting has changed from 25.5% to 59.2% (Figure 6).

Figure 6
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Changes in national population for countries predicted to contain areas at-risk of zoonotic Ebola virus transmission.

For each country the population (in millions) is presented for three time periods (1976, 2000 and 2014) as three bars. Each stacked bar gives the rural (green) and urban (blue) populations of the country. The grey rectangle highlights countries in which index cases of Ebola virus diseases have been reported (Set 1); the remainder are countries in which risk of zoonotic transmission is predicted, but where index cases have not been reported (Set 2). The fractional change in population between 1976 and 2014 is given above each set of bars.

https://doi.org/10.7554/eLife.04395.013

Data on the connectivity of human populations over this period were not available. We can infer however, intuitively, empirically and theoretically (Zipf, 1946; Simini et al., 2012) that rates of population movement within a country will scale directly in proportion to population growth.

International connectivity by airline traffic

Records of passenger seat capacity are available since 2000 and show substantive increases over the period in Set 1 (from 2.96 to 4.77 million, a fractional change of 1.61) and Set 2 (from 5.6 to 15.6 million, a change of 2.8) (Figure 7A). More specific data on passenger volumes show almost universally similar increases since 2005 with Set 1 nations changing from 2 million to 2.5 million, a fractional change of 1.22 and Set 2 changing from 5 million to 7.9 million, a change of 1.57 (Figure 7B).

Figure 7
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Changes in international flight capacity and traveller volumes for countries predicted to contain areas at-risk of zoonotic Ebola virus transmission.

The grey rectangle highlights countries in which index cases of EVD have been reported (Set 1). The remainder are countries in which risk of zoonotic transmission is predicted, but where index cases have not been reported (Set 2). (A) Shows changes in annual outbound international seat capacity (between 2000 in red and 2013 in blue). (B) Depicts changes in annual outbound international passenger volume by country (between 2005 in red and 2012 in blue). For each country, the fractional change in volume is given above each set of bars. Note that only one bar is presented for South Sudan as data for this region prior to formation of the country in 2011 were unavailable.

https://doi.org/10.7554/eLife.04395.014

Global analysis of airline passenger volumes demonstrates that international connectivity has increased amongst all global regions and national income strata (Figure 8). Total passenger volumes have increased by a third from 9.5 to over 14 million during the eight year window (2005–2012) where records are available. The largest increases have occurred in WHO regions (WHO, 2014b) outside of the sub-Saharan African region (AFRO) (Figure 8A,B). In 2012, almost half of the final destinations of those travelling from these at-risk countries were to other AFRO nations (47%). Other frequent destinations were in Europe (EURO; 27%) and the Eastern Mediterranean (EMRO; 13%). Similarly, analysis of passenger volumes by World Bank national income groupings (WHO, 2014b) (Figure 8C,D) show that in 2012 40% of all passenger final destinations were to low or low-middle income countries.

Figure 8
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Numbers of airline passengers arriving from at-risk countries to other countries stratified by major geographic regions and national income groups.

(A) Shows the locations of WHO regions (AFRO–African Region; AMRO–Region of the Americas; EMRO–Eastern Mediterranean Region; EURO–European Region; SEARO–South-East Asian Region; WPRO–Western Pacific Region). (B) Displays the numbers of passengers arriving in each of these regions from countries predicted to contain areas at risk of zoonotic Ebola virus transmission (Sets 1 and 2) in 2005 and 2012. (C) Shows the income tiers of all countries as defined by the World Bank. (D) Displays the total numbers of passengers arriving in countries in each of these income strata from at-risk countries in 2005 and 2012. The number above each pair of bars indicates the fractional change in these numbers of incoming passengers between 2005 and 2012.

https://doi.org/10.7554/eLife.04395.015

Discussion

Summary of the main findings

We have re-evaluated the zoonotic niche for EVD in Africa. In doing so we have (i) used all existing outbreaks to assemble an inventory of index cases (n = 30); (ii) added to this all confirmed records of Ebola virus in animals (n = 51); (iii) assembled more accurate and contemporary environmental covariates including new maps of the distribution of confirmed OWFB reservoirs of the disease; and (iv) used the latest niche modelling techniques to predict the geographic distribution of potential zoonotic transmission of the disease. Using these predictions we have estimated the populations at risk of EVD both in countries which have confirmed index cases (Set 1, n = 7) and those for which we predict strong environmental suitability for outbreaks (Set 2, n = 15). In all countries at risk we show that since the discovery of EVD in 1976, urban and rural populations have increased and have become more interconnected both within and across national borders. During the last 40 years the increasing size and connectivity of these populations may have facilitated the subsequent spread of EVD outbreaks. These factors underline a change in the way in which EVD interacts with human populations.

Interpreting the zoonotic niche

The remote and isolated nature of Ebola zoonotic transmission events, paired with the relatively poor diagnostics and understanding of the disease transmission routes in early outbreaks, mean that under-reporting of previous outbreaks is probable. An increasing understanding and description of a broader range of symptoms used in case definitions of EVD (Leroy et al., 2000; Feldmann and Geisbert, 2011) also increase the possibility that past outbreaks may have been misattributed to different diseases (Tignor et al., 1993). This poor detectability of EVD also clearly limits capacity to accurately identify the locations and transmission routes of index cases (Heymann et al., 1980; Baize et al., 2014). We must assume, as has been done previously (Peterson et al., 2004a; Jones et al., 2008), that the first reported cases are representative of the true location of the index cases. Where possible we have represented this geographic uncertainty by attributing the index case to a wide-area polygon which then incorporated this uncertainty into the mapping process (see ‘Materials and methods’).

The relationship between the EVD niche and the environmental covariates (Figure 5—figure supplement 2), particularly the high relative contribution of the vegetation index, underscore that there are clear environmental limits to transmission of the virus from animals to humans, and that ecoregions dominated by rainforest are the primary home of such zoonotic cycles. Our analysis has shown that the zoonotic niche of the pathogen is more widespread than previously predicted or appreciated (Peterson et al., 2004a), most notably in West Africa.

This analysis used information from all human outbreaks and animal infections to delineate the likely zoonotic niche of the disease. Further analysis, excluding the existing outbreak focussed in Guinea from the dataset used to train the model (Figure 5—figure supplement 3), still resulted in prediction of high suitability in this region, with the presumed index village located within 5 km of an at-risk pixel. This implies that the eco-epidemiological situation in Guinea is very similar to that in past outbreaks, mirroring phylogenetic similarity in the causative viruses (Dudas and Rambaut, 2014; Gire et al., 2014). The ecological similarity between the past and current outbreaks also lends support to the notion that the scale of this outbreak is more heavily influenced by patterns of human-to-human transmission than any expansion of the zoonotic niche.

Interpreting population at risk

It is important to appreciate that this zoonotic niche map delineates areas in which populations are at-risk of zoonotic transmission of EVD (Figure 5B). It does not predict the likelihood of EVD spillover, the likelihood of an outbreak establishing, or its subsequent rate of spread within a population. Increasing human encroachment and certain cultural practices sometimes linked with poverty, such as bushmeat hunting, result in increasing exposure of humans to animals which may harbour diseases including Ebola (Daszak, 2000; Wolfe et al., 2005, 2007). Increasing human population may accelerate the degree of risk through these processes but spatially refined information on these factors is not available comprehensively. It is hoped that as the understanding of the risk factors for zoonotic transmission of Ebolavirus to humans increases, it will be possible to incorporate this information into future risk mapping assessments.

Previous considerations of the geographic distribution of EVD have used human outbreaks alone. We have updated this work to include the last decade of outbreaks, as well as disaggregated outbreaks where evidence suggests multiple independent zoonotic transmission events overlap in space and time. Furthermore, our modelling process accommodates uncertainty in geopositioning of these index cases by utilising both point and polygon data. In addition, we include occurrence of infection in wildlife, important to the wider scale of zoonotic transmission (Figure 1), which in total has increased the dataset used in the model to 81 occurrences. The rareness of EVD outbreaks and the prevalence of detectable Ebola virus in reservoir species suggests that there will always be a limited set of observation data when compared to mapping of more prevalent zoonoses (Pigott et al., 2014). The results demonstrate predictive skill using a stringent validation procedure, however, indicating strong model performance even with this relatively limited observation dataset.

A broad zoonotic niche is predicted across 22 countries in Central and West Africa. Whilst several of these countries have reported index cases of EVD, others have not, although serological evidence in some regions points to possible underreporting of small-scale outbreaks (Kuhn, 2008). With improved ecological understanding, particularly with improvements to our knowledge of specific reservoir species and their distributions, it may be possible to delineate areas not at risk due to the absence of these species.

Despite relatively a large population living in areas of risk and the widespread practice of bushmeat hunting in these predicted areas (Wolfe et al., 2005; Mfunda and Røskaft, 2010; Brashares et al., 2011; Kamins et al., 2011), Ebolavirus is rare both in suspected animal reservoirs (Leroy et al., 2005; Olival and Hayman, 2014) and in terms of human outbreaks (Table 1). There is some indication however, that the frequency of Ebola outbreaks has increased since 2000, as shown in Figure 2A. We have shown that the human population living within this niche is larger, more mobile and better internationally connected than when the pathogen was first observed. As a result, when spillover events do occur, the likelihood of continued spread amongst the human population is greater, particularly in areas with poor healthcare infrastructure (Briand et al., 2014; Fauci, 2014).

Whilst rare in comparison to other high burden diseases prevalent in this region, such as malaria (Gething et al., 2011; Murray et al., 2012), Ebola outbreaks can have a considerable economic and political impact, and the subsequent destabilisation of basic health care provisioning in affected regions increases the toll of unrecorded morbidity and mortality of more common infectious diseases (Murray et al., 2014; Wang et al., 2014), throughout and after the epidemic period. The number of concurrent infections during the present outbreak represents a significant strain on healthcare systems that are already poorly provisioned (Briand et al., 2014; Chan, 2014; Fauci, 2014) and many other Set 1 and Set 2 countries rank amongst the lowest per capita healthcare spenders. These considerations should be paramount when international organizations debate the financing requirements for the improvement of healthcare needed in the region and the urgency with which new therapeutics and vaccines can be brought into production (Brady et al., 2014; Goodman, 2014).

Together, these considerations necessitate prioritisation of efforts to reinforce and improve existing surveillance and control, and encourage the development of therapeutics and vaccines. The national population at risk estimates presented here would be a strong rationale for improving, prioritising and stratifying surveillance for EVD outbreaks and diagnostic capacity in these countries. We believe it would be prudent to test OWFB species in Set 2 countries for Ebola virus (Hayman et al., 2012), particularly during the bat breeding season to maximise chances of isolation in order to clarify the outbreak risk in these countries. In all Set 1 and Set 2 countries, raising awareness about the risk presented by reservoir bats and incidental primate hosts and the modes of transmission of this disease could be of value. Finally, increasing our capacity to rapidly map ever changing biological threats is also a core need (Hay et al., 2013b).

Interpreting International connectivity

The increasing connectedness of the Africa region means that EVD is now a problem of international concern. While most EVD secondary transmission occurs locally and is likely transported via ground transit (Francesconi et al., 2003), the potential for international spread of infection is possible, as demonstrated by the importation of the disease from Liberia to Nigeria, culminating in further secondary transmission in Lagos (WHO, 2014a). The aetiology of EVD infection and disease progression means that an international outbreak propagated by air travel remains unlikely, particularly in high-income countries better able to handle EVD cases (Fauci, 2014). Nevertheless, a non-negligible threat remains, particularly in the low and middle income destinations and the rapid increase in global connectivity of these at-risk regions indicates that international airports could see more imported cases (Chan, 2014).

Future work

We have focussed on reanalysing the zoonotic niche for EVD transmission and the characterisation of the populations at risk to improve the landscape in which future risk and impact of EVD outbreaks can be discussed. During the current emergency much of the work will concentrate on routes of secondary transmission in the human population—conceptually the red arrow of the H box in Figure 1. An important task is to stratify the risk of EVD spread both within and between countries and identify the most likely pathways of spread for characterisation and surveillance. Our next priority therefore is to investigate aspects of secondary human-to-human transmission by documenting the rate of geographic spread of EVD during the past and ongoing epidemics to help understand changes in these patterns in the historical record. Simulating these movements in a real landscape of population movement patterns, inferred from population movements assessed by mobile phones and other data (Garcia et al., 2014), as well as parametric movement models (Simini et al., 2013) is a logical next step, and can be used in future targeting of interventions and potential new treatments for both the current and future outbreaks (Brady et al., 2014; Goodman, 2014).

As previously discussed, whilst there is the risk of human travel during the latent phase of infection, and therefore potential for international spread, the high pathogenicity during infectiousness (immobilising infected persons) and the likely rapid and effective isolation measures implemented in regions with strong health care systems, limit the pandemic potential of EVD. Nevertheless, improvement of international containment plans and informed discussions of potential risks to airline carriers and populations of other regions will be supported by knowledge of local, regional and international population flows. Assessing these flows by air traffic volumes is an ongoing priority.

There are several other zoonotic viral haemorrhagic fevers (for example Marburgvirus, Lassa fever, hantaviral infections and arenaviruses) that are of similar public health and biosecurity concern (Bannister, 2010), due to their high virulence and mortality and their potential to cause outbreaks and spread internationally. Despite this their geographical distributions are poorly understood (Hay et al., 2013a). Many of the methods applied here can be adapted to these diseases and improve our geographical understanding of the risk presented by these pathogens.

We are in the midst of a public health emergency that will likely last for many more months (Chan, 2014) and which has brought EVD to global attention. We emphasise that the maps of zoonotic transmission presented here do not enable assessment of secondary transmission rates in human populations, but they do act as an evidenced-based indicator of locations with potential for future zoonotic transmission and thus outbreaks. Interestingly, early reports of another independent zoonotic outbreak in the DRC (MSF, 2014) are in predicted at-risk areas. An improved understanding of the spatial extent of the zoonotic niche can only help future efforts in biosurveillance.

Materials and methods

Methodological overview

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A boosted regression tree (BRT) modelling framework was used to generate predictive risk maps of the zoonotic Ebola virus niche in Africa. This methodology combines regression trees, where trees are built according to optimal decision rules based on how binary decisions best accommodate a given dataset (De'ath, 2007; Elith et al., 2008), and boosting, which selects the tree that minimises the loss function. In doing so, a parameter space is defined which captures the greatest amount of variation present in the dataset. In order to train the model, four component datasets were compiled: (i) a comprehensive dataset of the reported locations of Ebola virus transmission from a zoonotic reservoir to a human; (ii) a dataset of the locations of Ebola virus infections in suspected reservoir and (non-human) susceptible host species (iii) a suite of ecologically relevant environmental covariates for Africa, including predicted distribution maps of suspected reservoir bat species and (iv) background (or pseudo-absence) records representing locations where zoonotic Ebola virus has not been reported. This study was limited to the African continent since no natural outbreaks of EVD have occurred outside the continent (CDC, 2014). Only Reston ebolavirus has a distribution reported outside of Africa, focussed in the Philippines, but has never been reported as pathogenic in humans; as a result this species was not included in the analysis.

Identifying index cases and reconstructing zoonotic transmission events in space and time

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Tables detailing proven outbreaks of Ebola virus, initially sourced from the scientific literature (Kuhn, 2008) and from health reporting organisations (CDC, 2014), were used to coordinate searches of the formal scientific literature using Web of Science and PubMed for each specific outbreak. Relevant papers were abstracted and where possible outbreak-specific epidemiological surveys were sourced. The citations in these references were obtained in order to reconstruct the outbreak in detail and to identify the most probable index case. Index cases were defined as any human infection resulting from interaction with non-human sources of the disease. Some of these cases arose from presumed interactions with zoonotic reservoirs or hosts, such as primates and other mammals during hunting trips (Boumandouki et al., 2005; Nkoghe et al., 2005, 2011; WHO, 2003) or butchering of bats (Leroy et al., 2009). Any cases arising from existing human infections are considered as secondary infections rather than index cases. Similar to methodology employed elsewhere (Messina et al., 2014), the site, or supposed site, of this zoonotic transmission event was geopositioned using Google Earth. For locations where precise geographic information (e.g., geographic coordinates of a hunting camp) was provided by the authors, these were used. Where precise geographic information could not be accurately geopositioned, a geographic area (termed a polygon) was defined covering the reported region. In several cases only the first reported patient could be identified, with the source of infection unknown. With these outbreaks the location of the first patient was geopositioned under the assumption that an initial zoonotic spillover event occurred in the vicinity of this location. In two outbreaks multiple independent zoonotic transmission events were identified (WHO, 2003; Nkoghe et al., 2005; Pourrut et al., 2005), and each unique event was geopositioned and included in the model as separate entities. Table 1 catalogues the outbreaks used in this study.

Assembling a database of reported infections in animals

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A literature search was conducted in Web of Science using the search term “Ebola” that returned 8635 citations. The abstracts were examined and for those that contained possible data on animal Ebola infection, the full text was obtained. The sampling site or location of the animal in the study was identified and geopositioned using Google Maps. These locations were recorded either as precise locations or as polygons, as with human index cases. Records for which local transmission of Ebola virus was deemed unlikely (e.g., seropositive primates tested in containment facilities several years after their capture) were excluded from the study. The non-human Ebola virus occurrence data collected are detailed in Table 2, including the diagnostic methods used.

GenBank isolates

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The open access sequence database GenBank (NCBI, 2014) was searched using MESH Umbrella search terms for Ebola virus, returning 181 results. These were then manually cross-referenced with the existing human and animal Ebola information, collected above, and 30 duplicates were removed. For the remaining isolates, original references and GenBank information fields were examined, but as there was insufficient information to establish precise location of isolation and/or whether the isolate represented an index case for any of these data sources, they were excluded from subsequent analyses.

Covariates assembled and used in the analyses

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A suite of ecologically relevant gridded environmental covariates for Africa was compiled, each having a nominal resolution of 5 km × 5 km. The environmental covariates used in this analysis were: elevation (from the shuttle radar topography mission [ORNL DAAC, 2000]); the mean value, and a measure of spatial variation (range, described below) between 2000 and 2012 of Enhanced Vegetation Index (EVI), daytime Land Surface Temperature (LST) and night-time LST; and mean potential evapotranspiration from 1950–2000 (Trabucco and Zomer, 2009) (Figure 5—figure supplement 1).

The EVI and LST datasets were derived from satellite imagery collected by NASA's Moderate Resolution Imaging Spectroradiometer (MODIS) remote sensing platform (Tatem et al., 2004). EVI is a metric designed to characterise vegetation density and vigour based on the ratio of absorbed photosynthetically active radiation to near infrared radiation (Huete et al., 2002). LST is a modelled product derived from emissivity as measured by the MODIS thermal sensor (Wan and Li, 1997), which is correlated, though not synonymous with air temperature, and effective for differentiating landscapes based on a combination of thermal energy and properties of surface types. The MODIS datasets utilized in this research (EVI was derived from the MCD43B4 product and the MOD11A2 LST product was used directly) were acquired as composite datasets created using imagery collected over multiple days, a procedure that results in products with 8-day temporal resolutions. Despite compositing, the EVI and LST datasets contained gaps due to persistent cloud cover found in forested equatorial regions, and these gaps were filled using a previously described approach (Weiss et al., 2014a). The EVI and LST datasets were then aggregated from their native 1 km × 1 km spatial resolution to a final 5 km × 5 km resolution, calculating both the mean and the range of the values of the subpixels making up each larger pixel. These spatial summaries therefore characterise both the mean temperature in each location as well as the degree of spatial heterogeneity within that pixel. This is of interest as humans and susceptible species are more likely to come into contact in transitional areas (e.g., boundary areas between areas of highly suitable susceptible species habitat and areas heavily utilised by humans). The final covariate production step consisted of summarising temporally across the 13-year data archive to produce synoptic datasets devoid of annual or seasonal anomalies (Weiss et al., 2014a).

Implicated bat reservoir distributions

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Over recent years, significant research has been undertaken in investigating the role bats have to play in the transmission cycle of Ebola viruses (Olival and Hayman, 2014) and evidence of asymptomatic infection in fruit bats has been documented to varying extents (Leroy et al., 2005; Pourrut et al., 2007, 2009; Hayman et al., 2010; Hayman et al., 2012). In order to incorporate this potential driver of Ebola virus transmission into the model we developed predicted distribution maps for three species of fruit bat implicated as primary reservoirs of the disease: Hypsignathus monstrosus, Epomops franqueti and Myonycteris torquata. The evidence was strongest for these three species having a reservoir role as Ebola virus RNA (all nested within the Zaire ebolavirus phylogeny [Leroy et al., 2005]) has been detected in all three. Whilst a handful of other bat species have been found to be seropositive, no further viral isolations have been recorded (Olival and Hayman, 2014).

Whilst expert opinion range maps for these species exist (Schipper et al., 2008), there is some disagreement with independently-sourced occurrence data (all archived in the Global Biodiversity Information Facility). As a result, a predictive modelling approach was used to create a continuous surface of habitat suitability for these species which we then included as a predictor in the model. Occurrence data for all Megachiroptera in Africa was extracted from GBIF (GBIF, 2014) using the R packages dismo (Hijmans et al., 2014) and taxize (Chamberlain et al., 2014). To remove apparently erroneous records in the GBIF archive all occurrence records more than 100 km from the species known ranges, as determined by expert-opinion range maps (Schipper et al., 2008), were excluded, as were duplicate records and those located in the ocean. This resulted in a total dataset of 1341 unique occurrence records.

The occurrence database was then used to train separate boosted regression tree species distribution models (Elith et al., 2008) to predict the likely distribution of each of these suspected reservoir species. For each model, occurrence records for the target species (H. monstrosus, n = 67; E. franqueti, n = 120; and M. torquata, n = 52) were considered presence records and occurrence records of all other species were used as background records. This procedure is designed to account for the potentially biasing effect of spatial variation in recording of Megachiroptera occurrences (Phillips et al., 2009).

For each species we ran fifty submodels each trained to a randomly selected bootstrap of this dataset, subject to the constraint that each bootstrap contained a minimum of 10 occurrence and 10 background records. Each submodel was fitted using the gbm.step subroutine (Elith et al., 2008) in the dismo R package. In each submodel the background records were down weighted so that the weighted sum of presence records equalled the weighted sum of background records (Barbet-Massin et al., 2012) in order to maximise the discrimination capacity of the model. We generated a prediction map from each of these submodels and calculated both the mean prediction and 95% confidence interval around the prediction for each 5 km × 5 km pixel for each species.

Model accuracy was assessed by calculating the mean area under the curve (AUC) statistic for each submodel under a stringent 10-fold cross validation for each submodel and obtaining the mean and standard deviation across all 50 submodels. Under this procedure the dataset was split into ten subsets, each containing approximately equal numbers of presence and background points. The ability of a model trained on each subset to predict the distribution of the other 90% of records was assessed by AUC and the mean value taken. As so few presence records were used to train each fold model (i.e., around 5 presence records for M. torquata up to 12 for E. franqueti), this represents a very stringent test of the model's predictive capacity. Additionally, to prevent inflation of the accuracy statistics due to spatial sorting bias, these statistics were estimated using a pairwise distance sampling procedure (Hijmans, 2012). Consequently, the AUC statistics presented here are lower than would be returned by standard procedures but gives a more realistic quantification of the model's ability to extrapolate predictions to new regions (Wenger and Olden, 2012). We also generated marginal effect plots with associated uncertainty intervals and relative contribution statistics (how often each covariate was selected during the model fitting process) as quantification of the sensitivity of the model to the different covariates. These allow us to make inferences about the ecological relationship between each species and its environment as well as to identify where this relationship is most uncertain.

To generate a single surface describing the distribution of the bat reservoir species to be used as a covariate in the subsequent Ebola modelling, the three mean prediction distribution maps were merged by taking the average habitat suitability for each of the three bat species at each pixel.

Ebola distribution modelling

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The Ebola virus occurrence dataset was supplemented with a background record dataset generated by randomly sampling 10,000 locations across Africa, biased towards more populous areas as a proxy for reporting bias (Phillips et al., 2009). We fitted 500 submodels to bootstraps of this dataset. To account for uncertainty in the geographic location of those occurrences reported as polygons, for each submodel one point was randomly selected from each of these occurrence polygons. This Monte Carlo procedure enabled the model to efficiently integrate over the environmental uncertainty associated with imprecise geographic data. A bootstrap sample was then taken from each of these datasets and used to train the BRT model using the same procedure and weighting of background records as for the bat distribution models. Similarly, we generated a prediction map from each of these models and calculated both the mean prediction and corresponding 95% confidence intervals for each pixel and analysed prediction accuracy using the same stringent cross validation and sensitivity analysis procedure as for the bat distribution models (detailed above).

The predicted distribution map produced by this approach represents the environmental suitability of each pixel for zoonotic Ebola virus transmission. This may be interpreted as a relative probability of presence in the sense that more suitable pixels are more likely to contain zoonotic transmission than less suitable pixels, though not an absolute probability that transmission occurs in a given pixel. Similarly, the presence of zoonotic transmission increases the risk of transmission to a human, though this is also contingent on how humans interact with these zoonotic pools, through hunting or other activities.

Population living in areas of environmental suitability for zoonotic transmission

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In order to identify areas which are likely to be at risk of transmission of Ebolavirus from zoonotic reservoir hosts to humans, the continuous map of the predicted environmental suitability for zoonotic transmission (shown in Figure 5) was converted into a binary map classifying pixels as either at risk or not at risk. A pixel was assumed to be at risk if its predicted environmental suitability for zoonotic Ebola virus transmission was greater than 0.673, the lowest suitability value predicted at the locations of known transmission to humans (point records of human index cases). Countries containing at least one at-risk pixel are shown in Figure 5B—those countries that previously report an index case were defined as Set 1; countries with at least one at-risk pixel with no previous index cases of EVD were categorised as Set 2. The number of people living in at-risk areas in each of these countries was calculated by summing the estimated population of at-risk pixels using population density maps from the AfriPop project (Linard et al., 2012; WorldPop, 2014) and the proportion of those living in urban, periurban and rural areas was evaluated using the Global Rural Urban Mapping Project (CIESIN/IFPRI/WB/CIAT, 2007).

The R code used for all of the analysis has been made available on an open source basis (https://github.com/SEEG-Oxford/ebola_zoonotic).

National level demographic and mobility data

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For three separate years (1976, 2000 and 2014), total national populations were retrieved and the proportion of rural to urban populations noted from World Bank statistics (World Bank, 2014). To describe global air travel patterns from Set 1 and Set 2 countries, flight schedules data from the Official Airline Guide, reflecting an estimated 95% of all commercial flights worldwide, were analysed between 2000 and 2013 to calculate the annual volume of seats on direct flights that depart from each predicted country and which have an international destination. Complementing these seat capacity data, worldwide data on anonymised, individual passenger flight itineraries from the International Air Transport Association (2012) (IATA, 2014) were analysed between 2005 and 2012 to calculate the annual volume of international passenger departures out of each Set 1 and Set 2 country. The IATA dataset represents an estimated 93% of the world's commercial air traffic at the passenger level and includes points of departure and arrival and final destination information for travellers as well as their connecting flights.

References

    1. Baron RC
    2. McCormick JB
    3. Zubeir OA
    (1983)
    Ebola virus disease in southern Sudan: hospital dissemination and intrafamilial spread
    Bulletin of the World Health Organization 61:997–1003.
    1. Boumandouki P
    2. Formenty P
    3. Epelboin A
    4. Campbell P
    5. Atsangandoko C
    6. Allarangar Y
    7. Leroy EM
    8. Kone ML
    9. Molamou A
    10. Dinga-Longa O
    11. Salemo A
    12. Kounkou RY
    13. Mombouli V
    14. Ibara JR
    15. Gaturuku P
    16. Nkunku S
    17. Lucht A
    18. Feldmann H
    (2005)
    [Clinical management of patients and deceased during the Ebola outbreak from October to December 2003 in Republic of Congo]
    Bulletin de la Société de Pathologie Exotique 98:218–223.
    1. CDC
    (2014) Chronology of Ebola hemorrhagic fever outbreaks
    Accessed: August 2014. Available: http://www.cdc.gov/vhf/ebola/resources/outbreak-table.html.
    http://www.cdc.gov/vhf/ebola/resources/outbreak-table.html
    1. Chan M
    (2014)
    Ebola virus disease in West Africa - no early end to the outbreak
    The New England Journal of Medicine, online, 10.1056/NEJMp1409859.
    1. Conrad JL
    2. Isaacson M
    3. Smith EB
    4. Wulff H
    5. Crees M
    6. Geldenhuys P
    7. Johnston J
    (1978)
    Epidemiologic investigation of Marburg virus disease, Southern Africa, 1975
    The American Journal of Tropical Medicine and Hygiene 27:1210–1215.
    1. Dudas G
    2. Rambaut A
    (2014)
    Phylogenetic analysis of Guinea 2014 EBOV ebolavirus outbreak
    PLOS Currents, 6, ecurrents.outbreaks.84eefe85ce43ec89dc80bf0670f0677b0678b0417d, 10.1371/currents.outbreaks.84eefe5ce43ec9dc0bf0670f7b8b417d.
  27. Book
    1. ECDC
    (2014)
    Outbreak of Ebola virus disease in West Africa
    Stockholm: ECDC.
  34. Book
    1. Franklin J
    (2009)
    Mapping species distributions
    Cambridge: Cambridge University Press.
    1. GBIF
    (2014) Global biodiversity information facility
    Accessed: August 2014. Available: http://www.gbif.org/.
    http://www.gbif.org/
    1. Goodman JL
    (2014)
    Studying “secret serums” - toward safe, effective Ebola treatments
    The New England Journal of Medicine.
    1. Hay SI
    2. Battle KE
    3. Pigott DM
    4. Smith DL
    5. Moyes CL
    6. Bhatt S
    7. Brownstein JS
    8. Collier N
    9. Myers MF
    10. George DB
    11. Gething PW
    (2013a) Global mapping of infectious disease
    Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 368:20120250.
    https://doi.org/10.1098/rstb.2012.0250
    1. Hewlett BS
    2. Epelboin A
    3. Hewlett BL
    4. Formenty P
    (2005)
    Medical anthropology and Ebola in Congo: cultural models and humanistic care
    Bulletin de la Société de Pathologie Exotique 98:230–236.
    1. Hijmans RJ
    2. Phillips S
    3. Leathwick J
    4. Elith J
    (2014) dismo. R package
    Accessed: August 2014. Available: http://cran.r-project.org/web/packages/dismo/dismo.pdf.
    http://cran.r-project.org/web/packages/dismo/dismo.pdf
    1. IATA
    (2014) International Air Transport Association
    Accessed: August 2014. Available: http://www.iata.org/Pages/default.aspx.
    http://www.iata.org/Pages/default.aspx
    1. International Commission
    (1978)
    Ebola haemorrhagic fever in Zaire, 1976
    Bulletin of the World Health Organization 56:271–293.
  67. Book
    1. King AMQ
    2. Adams MJ
    3. Carstens EB
    4. Lefkowitz E
    (2012)
    Virus taxonomy: ninth report of the International Committee on Taxonomy of Viruses
    King AMQ, Adams MJ, Carstens EB, Lefkowitz E, editors. London: Elsevier.
    1. Kuhn JH
    (2008)
    Filoviruses: a compendium of 40 years of epidemiological, clinical, and laboratory studies
    413, Vienna, Springer-Verlag.
    1. Mfunda IM
    2. Røskaft E
    (2010)
    Bushmeat hunting in Serengeti, Tanzania: an important economic activity to local people
    International Journal of Biodiversity and Conservation 2:263–272.
    1. Milleliri JM
    2. Tevi-Benissan C
    3. Baize S
    4. Leroy E
    5. Georges-Courbot MC
    (2004)
    [Epidemics of Ebola haemorrhagic fever in Gabon (1994-2002). Epidemiologic aspects and considerations on control measures]
    Bulletin de la Société de Pathologie Exotique 97:199–205.
    1. MSF
    (2014) Ebola epidemic confirmed in Democratic Republic of Congo: MSF sends specialists and material to the epicentre
    Accessed: August 2014. Available: http://www.msf.org/article/ebola-epidemic-confirmed-democratic-republic-congo-msf-sends-specialists-and-material.
    http://www.msf.org/article/ebola-epidemic-confirmed-democratic-republic-congo-msf-sends-specialists-and-material
    1. Murray CJ
    2. Ortblad KF
    3. Guinovart C
    4. Lim SS
    5. Wolock TM
    6. Roberts DA
    7. Dansereau EA
    8. Graetz N
    9. Barber RM
    10. Brown JC
    11. Wang H
    12. Duber HC
    13. Naghavi M
    14. Dicker D
    15. Dandona L
    16. Salomon JA
    17. Heuton KR
    18. Foreman K
    19. Phillips DE
    20. Fleming TD
    21. Flaxman AD
    22. Phillips BK
    23. Johnson EK
    24. Coggeshall MS
    25. Abd-Allah F
    26. Abera SF
    27. Abraham JP
    28. Abubakar I
    29. Abu-Raddad LJ
    30. Abu-Rmeileh NM
    31. Achoki T
    32. Adeyemo AO
    33. Adou AK
    34. Adsuar JC
    35. Agardh EE
    36. Akena D
    37. Al Kahbouri MJ
    38. Alasfoor D
    39. Albittar MI
    40. Alcalá-Cerra G
    41. Alegretti MA
    42. Alemu ZA
    43. Alfonso-Cristancho R
    44. Alhabib S
    45. Ali R
    46. Alla F
    47. Allen PJ
    48. Alsharif U
    49. Alvarez E
    50. Alvis-Guzman N
    51. Amankwaa AA
    52. Amare AT
    53. Amini H
    54. Ammar W
    55. Anderson BO
    56. Antonio CA
    57. Anwari P
    58. Arnlöv J
    59. Arsenijevic VS
    60. Artaman A
    61. Asghar RJ
    62. Assadi R
    63. Atkins LS
    64. Badawi A
    65. Balakrishnan K
    66. Banerjee A
    67. Basu S
    68. Beardsley J
    69. Bekele T
    70. Bell ML
    71. Bernabe E
    72. Beyene TJ
    73. Bhala N
    74. Bhalla A
    75. Bhutta ZA
    76. Abdulhak AB
    77. Binagwaho A
    78. Blore JD
    79. Bose D
    80. Brainin M
    81. Breitborde N
    82. Castañeda-Orjuela CA
    83. Catalá-López F
    84. Chadha VK
    85. Chang JC
    86. Chiang PP
    87. Chuang TW
    88. Colomar M
    89. Cooper LT
    90. Cooper C
    91. Courville KJ
    92. Cowie BC
    93. Criqui MH
    94. Dandona R
    95. Dayama A
    96. De Leo D
    97. Degenhardt L
    98. Del Pozo-Cruz B
    99. Deribe K
    100. Des Jarlais DC
    101. Dessalegn M
    102. Dharmaratne SD
    103. Dilmen U
    104. Ding EL
    105. Driscoll TR
    106. Durrani AM
    107. Ellenbogen RG
    108. Ermakov SP
    109. Esteghamati A
    110. Faraon EJ
    111. Farzadfar F
    112. Fereshtehnejad SM
    113. Fijabi DO
    114. Forouzanfar MH
    115. Fra Paleo U
    116. Gaffikin L
    117. Gamkrelidze A
    118. Gankpé FG
    119. Geleijnse JM
    120. Gessner BD
    121. Gibney KB
    122. Ginawi IA
    123. Glaser EL
    124. Gona P
    125. Goto A
    126. Gouda HN
    127. Gugnani HC
    128. Gupta R
    129. Gupta R
    130. Hafezi-Nejad N
    131. Hamadeh RR
    132. Hammami M
    133. Hankey GJ
    134. Harb HL
    135. Haro JM
    136. Havmoeller R
    137. Hay SI
    138. Hedayati MT
    139. Pi IB
    140. Hoek HW
    141. Hornberger JC
    142. Hosgood HD
    143. Hotez PJ
    144. Hoy DG
    145. Huang JJ
    146. Iburg KM
    147. Idrisov BT
    148. Innos K
    149. Jacobsen KH
    150. Jeemon P
    151. Jensen PN
    152. Jha V
    153. Jiang G
    154. Jonas JB
    155. Juel K
    156. Kan H
    157. Kankindi I
    158. Karam NE
    159. Karch A
    160. Karema CK
    161. Kaul A
    162. Kawakami N
    163. Kazi DS
    164. Kemp AH
    165. Kengne AP
    166. Keren A
    167. Kereselidze M
    168. Khader YS
    169. Khalifa SE
    170. Khan EA
    171. Khang YH
    172. Khonelidze I
    173. Kinfu Y
    174. Kinge JM
    175. Knibbs L
    176. Kokubo Y
    177. Kosen S
    178. Defo BK
    179. Kulkarni VS
    180. Kulkarni C
    181. Kumar K
    182. Kumar RB
    183. Kumar GA
    184. Kwan GF
    185. Lai T
    186. Balaji AL
    187. Lam H
    188. Lan Q
    189. Lansingh VC
    190. Larson HJ
    191. Larsson A
    192. Lee JT
    193. Leigh J
    194. Leinsalu M
    195. Leung R
    196. Li Y
    197. Li Y
    198. De Lima GM
    199. Lin HH
    200. Lipshultz SE
    201. Liu S
    202. Liu Y
    203. Lloyd BK
    204. Lotufo PA
    205. Machado VM
    206. Maclachlan JH
    207. Magis-Rodriguez C
    208. Majdan M
    209. Mapoma CC
    210. Marcenes W
    211. Marzan MB
    212. Masci JR
    213. Mashal MT
    214. Mason-Jones AJ
    215. Mayosi BM
    216. Mazorodze TT
    217. Mckay AC
    218. Meaney PA
    219. Mehndiratta MM
    220. Mejia-Rodriguez F
    221. Melaku YA
    222. Memish ZA
    223. Mendoza W
    224. Miller TR
    225. Mills EJ
    226. Mohammad KA
    227. Mokdad AH
    228. Mola GL
    229. Monasta L
    230. Montico M
    231. Moore AR
    232. Mori R
    233. Moturi WN
    234. Mukaigawara M
    235. Murthy KS
    236. Naheed A
    237. Naidoo KS
    238. Naldi L
    239. Nangia V
    240. Narayan KM
    241. Nash D
    242. Nejjari C
    243. Nelson RG
    244. Neupane SP
    245. Newton CR
    246. Ng M
    247. Nisar MI
    248. Nolte S
    249. Norheim OF
    250. Nowaseb V
    251. Nyakarahuka L
    252. Oh IH
    253. Ohkubo T
    254. Olusanya BO
    255. Omer SB
    256. Opio JN
    257. Orisakwe OE
    258. Pandian JD
    259. Papachristou C
    260. Caicedo AJ
    261. Patten SB
    262. Paul VK
    263. Pavlin BI
    264. Pearce N
    265. Pereira DM
    266. Pervaiz A
    267. Pesudovs K
    268. Petzold M
    269. Pourmalek F
    270. Qato D
    271. Quezada AD
    272. Quistberg DA
    273. Rafay A
    274. Rahimi K
    275. Rahimi-Movaghar V
    276. Rahman SU
    277. Raju M
    278. Rana SM
    279. Razavi H
    280. Reilly RQ
    281. Remuzzi G
    282. Richardus JH
    283. Ronfani L
    284. Roy N
    285. Sabin N
    286. Saeedi MY
    287. Sahraian MA
    288. Samonte GM
    289. Sawhney M
    290. Schneider IJ
    291. Schwebel DC
    292. Seedat S
    293. Sepanlou SG
    294. Servan-Mori EE
    295. Sheikhbahaei S
    296. Shibuya K
    297. Shin HH
    298. Shiue I
    299. Shivakoti R
    300. Sigfusdottir ID
    301. Silberberg DH
    302. Silva AP
    303. Simard EP
    304. Singh JA
    305. Skirbekk V
    306. Sliwa K
    307. Soneji S
    308. Soshnikov SS
    309. Sreeramareddy CT
    310. Stathopoulou VK
    311. Stroumpoulis K
    312. Swaminathan S
    313. Sykes BL
    314. Tabb KM
    315. Talongwa RT
    316. Tenkorang EY
    317. Terkawi AS
    318. Thomson AJ
    319. Thorne-Lyman AL
    320. Towbin JA
    321. Traebert J
    322. Tran BX
    323. Dimbuene ZT
    324. Tsilimbaris M
    325. Uchendu US
    326. Ukwaja KN
    327. Vallely AJ
    328. Vasankari TJ
    329. Venketasubramanian N
    330. Violante FS
    331. Vlassov VV
    332. Waller S
    333. Wallin MT
    334. Wang L
    335. Wang SX
    336. Wang Y
    337. Weichenthal S
    338. Weiderpass E
    339. Weintraub RG
    340. Westerman R
    341. White RA
    342. Wilkinson JD
    343. Williams TN
    344. Woldeyohannes SM
    345. Wong JQ
    346. Xu G
    347. Yang YC
    348. Yano Y
    349. Yip P
    350. Yonemoto N
    351. Yoon SJ
    352. Younis M
    353. Yu C
    354. Jin KY
    355. El Sayed Zaki M
    356. Zhao Y
    357. Zheng Y
    358. Zhou M
    359. Zhu J
    360. Zou XN
    361. Lopez AD
    362. Vos T
    (2014) Global, regional, and national incidence and mortality for HIV, tuberculosis, and malaria during 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013
    Lancet.
    https://doi.org/10.1016/S0140-6736(14)60844-8
    1. Murray CJL
    2. Vos T
    3. Lozano R
    4. Naghavi M
    5. Flaxman AD
    6. Michaud C
    7. Ezzati M
    8. Shibuya K
    9. Salomon JA
    10. Abdalla S
    11. Aboyans V
    12. Abraham J
    13. Ackerman I
    14. Aggarwal R
    15. Ahn SY
    16. Ali MK
    17. Alvarado M
    18. Anderson HR
    19. Anderson LM
    20. Andrews KG
    21. Atkinson C
    22. Baddour LM
    23. Bahalim AN
    24. Barker-Collo S
    25. Barrero LH
    26. Bartels DH
    27. Basáñez MG
    28. Baxter A
    29. Bell ML
    30. Benjamin EJ
    31. Bennett D
    32. Bernabé E
    33. Bhalla K
    34. Bhandari B
    35. Bikbov B
    36. Bin Abdulhak A
    37. Birbeck G
    38. Black JA
    39. Blencowe H
    40. Blore JD
    41. Blyth F
    42. Bolliger I
    43. Bonaventure A
    44. Boufous S
    45. Bourne R
    46. Boussinesq M
    47. Braithwaite T
    48. Brayne C
    49. Bridgett L
    50. Brooker S
    51. Brooks P
    52. Brugha TS
    53. Bryan-Hancock C
    54. Bucello C
    55. Buchbinder R
    56. Buckle G
    57. Budke CM
    58. Burch M
    59. Burney P
    60. Burstein R
    61. Calabria B
    62. Campbell B
    63. Canter CE
    64. Carabin H
    65. Carapetis J
    66. Carmona L
    67. Cella C
    68. Charlson F
    69. Chen H
    70. Cheng AT
    71. Chou D
    72. Chugh SS
    73. Coffeng LE
    74. Colan SD
    75. Colquhoun S
    76. Colson KE
    77. Condon J
    78. Connor MD
    79. Cooper LT
    80. Corriere M
    81. Cortinovis M
    82. de Vaccaro KC
    83. Couser W
    84. Cowie BC
    85. Criqui MH
    86. Cross M
    87. Dabhadkar KC
    88. Dahiya M
    89. Dahodwala N
    90. Damsere-Derry J
    91. Danaei G
    92. Davis A
    93. De Leo D
    94. Degenhardt L
    95. Dellavalle R
    96. Delossantos A
    97. Denenberg J
    98. Derrett S
    99. Des Jarlais DC
    100. Dharmaratne SD
    101. Dherani M
    102. Diaz-Torne C
    103. Dolk H
    104. Dorsey ER
    105. Driscoll T
    106. Duber H
    107. Ebel B
    108. Edmond K
    109. Elbaz A
    110. Ali SE
    111. Erskine H
    112. Erwin PJ
    113. Espindola P
    114. Ewoigbokhan SE
    115. Farzadfar F
    116. Feigin V
    117. Felson DT
    118. Ferrari A
    119. Ferri CP
    120. Fèvre EM
    121. Finucane MM
    122. Flaxman S
    123. Flood L
    124. Foreman K
    125. Forouzanfar MH
    126. Fowkes FG
    127. Fransen M
    128. Freeman MK
    129. Gabbe BJ
    130. Gabriel SE
    131. Gakidou E
    132. Ganatra HA
    133. Garcia B
    134. Gaspari F
    135. Gillum RF
    136. Gmel G
    137. Gonzalez-Medina D
    138. Gosselin R
    139. Grainger R
    140. Grant B
    141. Groeger J
    142. Guillemin F
    143. Gunnell D
    144. Gupta R
    145. Haagsma J
    146. Hagan H
    147. Halasa YA
    148. Hall W
    149. Haring D
    150. Haro JM
    151. Harrison JE
    152. Havmoeller R
    153. Hay RJ
    154. Higashi H
    155. Hill C
    156. Hoen B
    157. Hoffman H
    158. Hotez PJ
    159. Hoy D
    160. Huang JJ
    161. Ibeanusi SE
    162. Jacobsen KH
    163. James SL
    164. Jarvis D
    165. Jasrasaria R
    166. Jayaraman S
    167. Johns N
    168. Jonas JB
    169. Karthikeyan G
    170. Kassebaum N
    171. Kawakami N
    172. Keren A
    173. Khoo JP
    174. King CH
    175. Knowlton LM
    176. Kobusingye O
    177. Koranteng A
    178. Krishnamurthi R
    179. Laden F
    180. Lalloo R
    181. Laslett LL
    182. Lathlean T
    183. Leasher JL
    184. Lee YY
    185. Leigh J
    186. Levinson D
    187. Lim SS
    188. Limb E
    189. Lin JK
    190. Lipnick M
    191. Lipshultz SE
    192. Liu W
    193. Loane M
    194. Ohno SL
    195. Lyons R
    196. Mabweijano J
    197. MacIntyre MF
    198. Malekzadeh R
    199. Mallinger L
    200. Manivannan S
    201. Marcenes W
    202. March L
    203. Margolis DJ
    204. Marks GB
    205. Marks R
    206. Matsumori A
    207. Matzopoulos R
    208. Mayosi BM
    209. McAnulty JH
    210. McDermott MM
    211. McGill N
    212. McGrath J
    213. Medina-Mora ME
    214. Meltzer M
    215. Mensah GA
    216. Merriman TR
    217. Meyer AC
    218. Miglioli V
    219. Miller M
    220. Miller TR
    221. Mitchell PB
    222. Mock C
    223. Mocumbi AO
    224. Moffitt TE
    225. Mokdad AA
    226. Monasta L
    227. Montico M
    228. Moradi-Lakeh M
    229. Moran A
    230. Morawska L
    231. Mori R
    232. Murdoch ME
    233. Mwaniki MK
    234. Naidoo K
    235. Nair MN
    236. Naldi L
    237. Narayan KM
    238. Nelson PK
    239. Nelson RG
    240. Nevitt MC
    241. Newton CR
    242. Nolte S
    243. Norman P
    244. Norman R
    245. O'Donnell M
    246. O'Hanlon S
    247. Olives C
    248. Omer SB
    249. Ortblad K
    250. Osborne R
    251. Ozgediz D
    252. Page A
    253. Pahari B
    254. Pandian JD
    255. Rivero AP
    256. Patten SB
    257. Pearce N
    258. Padilla RP
    259. Perez-Ruiz F
    260. Perico N
    261. Pesudovs K
    262. Phillips D
    263. Phillips MR
    264. Pierce K
    265. Pion S
    266. Polanczyk GV
    267. Polinder S
    268. Pope CA III
    269. Popova S
    270. Porrini E
    271. Pourmalek F
    272. Prince M
    273. Pullan RL
    274. Ramaiah KD
    275. Ranganathan D
    276. Razavi H
    277. Regan M
    278. Rehm JT
    279. Rein DB
    280. Remuzzi G
    281. Richardson K
    282. Rivara FP
    283. Roberts T
    284. Robinson C
    285. De Leòn FR
    286. Ronfani L
    287. Room R
    288. Rosenfeld LC
    289. Rushton L
    290. Sacco RL
    291. Saha S
    292. Sampson U
    293. Sanchez-Riera L
    294. Sanman E
    295. Schwebel DC
    296. Scott JG
    297. Segui-Gomez M
    298. Shahraz S
    299. Shepard DS
    300. Shin H
    301. Shivakoti R
    302. Singh D
    303. Singh GM
    304. Singh JA
    305. Singleton J
    306. Sleet DA
    307. Sliwa K
    308. Smith E
    309. Smith JL
    310. Stapelberg NJ
    311. Steer A
    312. Steiner T
    313. Stolk WA
    314. Stovner LJ
    315. Sudfeld C
    316. Syed S
    317. Tamburlini G
    318. Tavakkoli M
    319. Taylor HR
    320. Taylor JA
    321. Taylor WJ
    322. Thomas B
    323. Thomson WM
    324. Thurston GD
    325. Tleyjeh IM
    326. Tonelli M
    327. Towbin JA
    328. Truelsen T
    329. Tsilimbaris MK
    330. Ubeda C
    331. Undurraga EA
    332. van der Werf MJ
    333. van Os J
    334. Vavilala MS
    335. Venketasubramanian N
    336. Wang M
    337. Wang W
    338. Watt K
    339. Weatherall DJ
    340. Weinstock MA
    341. Weintraub R
    342. Weisskopf MG
    343. Weissman MM
    344. White RA
    345. Whiteford H
    346. Wiebe N
    347. Wiersma ST
    348. Wilkinson JD
    349. Williams HC
    350. Williams SR
    351. Witt E
    352. Wolfe F
    353. Woolf AD
    354. Wulf S
    355. Yeh PH
    356. Zaidi AK
    357. Zheng ZJ
    358. Zonies D
    359. Lopez AD
    360. AlMazroa MA
    361. Memish ZA
    (2012) Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010
    Lancet 380:2197–2223.
    https://doi.org/10.1016/S0140-6736(12)61689-4
    1. NCBI
    (2014) GenBank - ebola
    Accessed: August 2014. Available: http://www.ncbi.nlm.nih.gov/genbank/.
    http://www.ncbi.nlm.nih.gov/genbank/
    1. NIH
    (2014)
    NIAID emerging infectious diseases/pathogens
    Available: Accessed: August 2014.
    1. Nkoghe D
    2. Formenty P
    3. Leroy EM
    4. Nnegue S
    5. Edou SY
    6. Ba JI
    7. Allarangar Y
    8. Cabore J
    9. Bachy C
    10. Andraghetti R
    11. de Benoist AC
    12. Galanis E
    13. Rose A
    14. Bausch D
    15. Reynolds M
    16. Rollin P
    17. Choueibou C
    18. Shongo R
    19. Gergonne B
    20. Koné LM
    21. Yada A
    22. Roth C
    23. Mve MT
    (2005)
    [Multiple Ebola virus haemorrhagic fever outbreaks in Gabon, from October 2001 to April 2002]
    Bulletin de la Société de Pathologie Exotique 98:224–229.
    1. ORNL DAAC
    (2000) Shuttle radar topography mission near-global digital elevation models
    Accessed: August 2014. Available: http://webmap.ornl.gov/wcsdown/wcsdown.jsp?dg_id=10008_1.
    http://webmap.ornl.gov/wcsdown/wcsdown.jsp?dg_id=10008_1
  103. Book
    1. Petter JJ
    2. Desbordes F
    (2013)
    Primates of the world
    Princeton: Princeton University Press.
    1. Schipper J
    2. Chanson JS
    3. Chiozza F
    4. Cox NA
    5. Hoffmann M
    6. Katariya V
    7. Lamoreux J
    8. Rodrigues AS
    9. Stuart SN
    10. Temple HJ
    11. Baillie J
    12. Boitani L
    13. Lacher TE Jnr
    14. Mittermeier RA
    15. Smith AT
    16. Absolon D
    17. Aguiar JM
    18. Amori G
    19. Bakkour N
    20. Baldi R
    21. Berridge RJ
    22. Bielby J
    23. Black PA
    24. Blanc JJ
    25. Brooks TM
    26. Burton JA
    27. Butynski TM
    28. Catullo G
    29. Chapman R
    30. Cokeliss Z
    31. Collen B
    32. Conroy J
    33. Cooke JG
    34. da Fonseca GA
    35. Derocher AE
    36. Dublin HT
    37. Duckworth JW
    38. Emmons L
    39. Emslie RH
    40. Festa-Bianchet M
    41. Foster M
    42. Foster S
    43. Garshelis DL
    44. Gates C
    45. Gimenez-Dixon M
    46. Gonzalez S
    47. Gonzalez-Maya JF
    48. Good TC
    49. Hammerson G
    50. Hammond PS
    51. Happold D
    52. Happold M
    53. Hare J
    54. Harris RB
    55. Hawkins CE
    56. Haywood M
    57. Heaney LR
    58. Hedges S
    59. Helgen KM
    60. Hilton-Taylor C
    61. Hussain SA
    62. Ishii N
    63. Jefferson TA
    64. Jenkins RK
    65. Johnston CH
    66. Keith M
    67. Kingdon J
    68. Knox DH
    69. Kovacs KM
    70. Langhammer P
    71. Leus K
    72. Lewison R
    73. Lichtenstein G
    74. Lowry LF
    75. Macavoy Z
    76. Mace GM
    77. Mallon DP
    78. Masi M
    79. McKnight MW
    80. Medellín RA
    81. Medici P
    82. Mills G
    83. Moehlman PD
    84. Molur S
    85. Mora A
    86. Nowell K
    87. Oates JF
    88. Olech W
    89. Oliver WR
    90. Oprea M
    91. Patterson BD
    92. Perrin WF
    93. Polidoro BA
    94. Pollock C
    95. Powel A
    96. Protas Y
    97. Racey P
    98. Ragle J
    99. Ramani P
    100. Rathbun G
    101. Reeves RR
    102. Reilly SB
    103. Reynolds JE III
    104. Rondinini C
    105. Rosell-Ambal RG
    106. Rulli M
    107. Rylands AB
    108. Savini S
    109. Schank CJ
    110. Sechrest W
    111. Self-Sullivan C
    112. Shoemaker A
    113. Sillero-Zubiri C
    114. De Silva N
    115. Smith DE
    116. Srinivasulu C
    117. Stephenson PJ
    118. van Strien N
    119. Talukdar BK
    120. Taylor BL
    121. Timmins R
    122. Tirira DG
    123. Tognelli MF
    124. Tsytsulina K
    125. Veiga LM
    126. Vié JC
    127. Williamson EA
    128. Wyatt SA
    129. Xie Y
    130. Young BE
    (2008) The status of the world's land and marine mammals: diversity, threat, and knowledge
    Science 322:225–230.
    https://doi.org/10.1126/science.1165115
    1. Tatem AJ
    2. Goetz SJ
    3. Hay SI
    (2004) Terra and aqua: new data for epidemiology and public health
    International Journal of Applied Earth Observation and Geoinformation 6:33–46.
    https://doi.org/10.1016/j.jag.2004.07.001
  128. Book
    1. Walsh PD
    2. Bermejo M
    3. Rodriguez-Teijeiro JD
    (2009)
    Disease avoidance and the evolution of primate social connectivity: Ebola, bats, gorillas, and chimpanzees
    In: Huffman MA, Chapman CA, editors. Primate parasite ecology: the dynamics and study of host-parasite relationships. Cambridge: Cambridge University Press. pp. 183–197.
    1. Wang H
    2. Liddell CA
    3. Coates MM
    4. Mooney MD
    5. Levitz CE
    6. Schumacher AE
    7. Apfel H
    8. Iannarone M
    9. Phillips B
    10. Lofgren KT
    11. Sandar L
    12. Dorrington RE
    13. Rakovac I
    14. Jacobs TA
    15. Liang X
    16. Zhou M
    17. Zhu J
    18. Yang G
    19. Wang Y
    20. Liu S
    21. Li Y
    22. Ozgoren AA
    23. Abera SF
    24. Abubakar I
    25. Achoki T
    26. Adelekan A
    27. Ademi Z
    28. Alemu ZA
    29. Allen PJ
    30. Almazroa MA
    31. Alvarez E
    32. Amankwaa AA
    33. Amare AT
    34. Ammar W
    35. Anwari P
    36. Cunningham SA
    37. Asad MM
    38. Assadi R
    39. Banerjee A
    40. Basu S
    41. Bedi N
    42. Bekele T
    43. Bell ML
    44. Bhutta Z
    45. Blore J
    46. Basara BB
    47. Boufous S
    48. Breitborde N
    49. Bruce NG
    50. Bui LN
    51. Carapetis JR
    52. Cárdenas R
    53. Carpenter DO
    54. Caso V
    55. Castro RE
    56. Catalá-Lopéz F
    57. Cavlin A
    58. Che X
    59. Chiang PP
    60. Chowdhury R
    61. Christophi CA
    62. Chuang TW
    63. Cirillo M
    64. da Costa Leite I
    65. Courville KJ
    66. Dandona L
    67. Dandona R
    68. Davis A
    69. Dayama A
    70. Deribe K
    71. Dharmaratne SD
    72. Dherani MK
    73. Dilmen U
    74. Ding EL
    75. Edmond KM
    76. Ermakov SP
    77. Farzadfar F
    78. Fereshtehnejad SM
    79. Fijabi DO
    80. Foigt N
    81. Forouzanfar MH
    82. Garcia AC
    83. Geleijnse JM
    84. Gessner BD
    85. Goginashvili K
    86. Gona P
    87. Goto A
    88. Gouda HN
    89. Green MA
    90. Greenwell KF
    91. Gugnani HC
    92. Gupta R
    93. Hamadeh RR
    94. Hammami M
    95. Harb HL
    96. Hay S
    97. Hedayati MT
    98. Hosgood HD
    99. Hoy DG
    100. Idrisov BT
    101. Islami F
    102. Ismayilova S
    103. Jha V
    104. Jiang G
    105. Jonas JB
    106. Juel K
    107. Kabagambe EK
    108. Kazi DS
    109. Kengne AP
    110. Kereselidze M
    111. Khader YS
    112. Khalifa SE
    113. Khang YH
    114. Kim D
    115. Kinfu Y
    116. Kinge JM
    117. Kokubo Y
    118. Kosen S
    119. Defo BK
    120. Kumar GA
    121. Kumar K
    122. Kumar RB
    123. Lai T
    124. Lan Q
    125. Larsson A
    126. Lee JT
    127. Leinsalu M
    128. Lim SS
    129. Lipshultz SE
    130. Logroscino G
    131. Lotufo PA
    132. Lunevicius R
    133. Lyons RA
    134. Ma S
    135. Mahdi AA
    136. Marzan MB
    137. Mashal MT
    138. Mazorodze TT
    139. McGrath JJ
    140. Memish ZA
    141. Mendoza W
    142. Mensah GA
    143. Meretoja A
    144. Miller TR
    145. Mills EJ
    146. Mohammad KA
    147. Mokdad AH
    148. Monasta L
    149. Montico M
    150. Moore AR
    151. Moschandreas J
    152. Msemburi WT
    153. Mueller UO
    154. Muszynska MM
    155. Naghavi M
    156. Naidoo KS
    157. Narayan KV
    158. Nejjari C
    159. Ng M
    160. de Dieu Ngirabega J
    161. Nieuwenhuijsen MJ
    162. Nyakarahuka L
    163. Ohkubo T
    164. Omer SB
    165. Caicedo AJ
    166. Wyk VP
    167. Pope D
    168. Prabhakaran D
    169. Rahman SU
    170. Rana SM
    171. Reilly RQ
    172. Rojas-Rueda D
    173. Ronfani L
    174. Rushton L
    175. Saeedi MY
    176. Salomon J
    177. Sampson U
    178. Santos IS
    179. Sawhney M
    180. Schmidt JC
    181. Shakh-Nazarova M
    182. She J
    183. Sheikhbahaei S
    184. Shibuya K
    185. Shin HH
    186. Shishani K
    187. Shiue I
    188. Sigfusdottir ID
    189. Singh JA
    190. Skirbekk V
    191. Sliwa K
    192. Soshnikov SS
    193. Sposato LA
    194. Stathopoulou VK
    195. Stroumpoulis K
    196. Tabb KM
    197. Talongwa RT
    198. Teixeira CM
    199. Terkawi AS
    200. Thomson AJ
    201. Thorne-Lyman AL
    202. Toyoshima H
    203. Dimbuene ZT
    204. Uwaliraye P
    205. Uzun SB
    206. Vasankari TJ
    207. Vasconcelos AM
    208. Vlassov VV
    209. Vollset SE
    210. Vos T
    211. Waller S
    212. Wan X
    213. Weichenthal S
    214. Weiderpass E
    215. Weintraub RG
    216. Westerman R
    217. Wilkinson JD
    218. Williams HC
    219. Yang YC
    220. Yentur GK
    221. Yip P
    222. Yonemoto N
    223. Younis M
    224. Yu C
    225. Jin KY
    226. El Sayed Zaki M
    227. Zhu S
    228. Lopez AD
    229. Murray CJ
    (2014) Global, regional, and national levels of neonatal, infant, and under-5 mortality during 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013
    Lancet.
    https://doi.org/10.1016/S0140-6736(14)60497-9
    1. Weiss DJ
    2. Atkinson PM
    3. Bhatt S
    4. Mappin B
    5. Hay SI
    6. Gething PW
    (2014)
    An effective approach for gap-filling continental scale remotely sensed time-series
    ISPRS Journal of Photogrammetry and Remote Sensing, accepted manuscript.
    1. WHO
    (2001)
    Outbreak of Ebola haemorrhagic fever, Uganda, August 2000-January 2001
    Weekly Epidemiological Record 76:41–46.
    1. WHO
    (2003a)
    Outbreak(s) of Ebola haemorrhagic fever, Congo and Gabon, October 2001-July 2002
    Weekly Epidemiological Record 78:223–228.
    1. WHO
    (2003b)
    Outbreak(s) of Ebola haemorrhagic fever in the Republic of the Congo, January-April 2003
    Weekly Epidemiological Record 78:285–289.
    1. WHO
    (2005)
    Outbreak of Ebola haemorrhagic fever in Yambio, south Sudan, April - June 2004
    Weekly Epidemiological Record 80:370–375.
    1. WHO
    (2012) Ebola in Uganda - 29 July 2012
    Accessed: August 2014. Available: http://www.who.int/csr/don/2012_07_29/en/.
    http://www.who.int/csr/don/2012_07_29/en/
    1. WHO
    (2012) Ebola outbreak in democratic Republic of Congo - 17 August 2012
    Accessed: August 2014. Available: http://www.who.int/csr/don/2012_08_18/en/.
    http://www.who.int/csr/don/2012_08_18/en/
    1. WHO
    (2012) Ebola in Uganda - 17 November 2012
    Accessed: August 2014. Available: http://www.who.int/csr/don/2012_11_17/en/.
    http://www.who.int/csr/don/2012_11_17/en/
    1. WHO
    (2014) Ebola virus disease update - west Africa
    Accessed: August 2014. Available: http://www.who.int/csr/don/2014_08_15_ebola/en/.
    http://www.who.int/csr/don/2014_08_15_ebola/en/
    1. WHO
    (2014) Health statistics and information systems - definition of region groupings
    Accessed: August 2014. Available: http://www.who.int/healthinfo/global_burden_disease/definition_regions/en/.
    http://www.who.int/healthinfo/global_burden_disease/definition_regions/en/
  146. Book
    1. WHO
    (2014c)
    Interim manual - Ebola and Marburg virus disease epidemics: preparedness, alert, control, and evaluation
    Geneva: World Health Organization.
    1. WHO International Study Team
    (1978)
    Ebola haemorrhagic fever in Sudan, 1976
    Bulletin of the World Health Organization 56:247–270.
    1. World Bank
    (2014) World Bank open dataset
    Accessed: July 2014. Available: http://data.worldbank.org/.
    http://data.worldbank.org/
    1. WorldPop
    (2014) WorldPop project
    Accessed: August 2014. Available: http://www.worldpop.org.uk/.
    http://www.worldpop.org.uk/
    1. WWF
    (2014) List of terrestrial ecoregions
    Accessed: August 2014. Available: http://wwf.panda.org/about_our_earth/ecoregions/ecoregion_list/.
    http://wwf.panda.org/about_our_earth/ecoregions/ecoregion_list/

Article and author information

Author details

  1. David M Pigott

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    DMP, Advised and assembled the outbreak and animal infection data, Wrote the article
    Contributed equally with
    Nick Golding
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-6731-4034

  2. Nick Golding

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    NG, Extracted the bat data, Conducted all of the analysis, Drafting or revising the article
    Contributed equally with
    David M Pigott
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-8916-5570

  3. Adrian Mylne

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    AM, Assembled and geo-positioned the outbreak and animal infection data, Drafting or revising the article
    Competing interests
    No competing interests declared.

  4. Zhi Huang

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    ZH, Geo-positioned the outbreak and animal infection data, Provided all maps, Drafting or revising the article
    Competing interests
    No competing interests declared.

  5. Andrew J Henry

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    AJH, Analysed international flight data, Helped assemble maps, Drafting or revising the article
    Competing interests
    No competing interests declared.

  6. Daniel J Weiss

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    DJW, Assembled the covariate layers, Drafting or revising the article
    Competing interests
    No competing interests declared.

  7. Oliver J Brady

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    OJB, Screened GenBank data, Provided Figure 2A, Drafting or revising the article
    Competing interests
    No competing interests declared.

  8. Moritz UG Kraemer

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    MUGK, Analysis and interpretation of data, Drafting or revising the article
    Competing interests
    No competing interests declared.

  9. David L Smith

    1. Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    2. Sanaria Institute for Global Health and Tropical Medicine, Rockville, United States
    Contribution
    DLS, Analysis and interpretation of data, Drafting or revising the article
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-4367-3849

  10. Catherine L Moyes

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    CLM, Analysis and interpretation of data, Drafting or revising the article
    Competing interests
    No competing interests declared.

  11. Samir Bhatt

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    SB, Extracted Ebola information from GenBank, Drafting or revising the article
    Competing interests
    No competing interests declared.

  12. Peter W Gething

    Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    Contribution
    PWG, Assembled the covariate layers, Drafting or revising the article
    Competing interests
    No competing interests declared.

  13. Peter W Horby

    Epidemic Diseases Research Group, Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
    Contribution
    PWH, Advised on international public health context, Edited the final draft of the article
    Competing interests
    No competing interests declared.

  14. Isaac I Bogoch

    1. Department of Medicine, Division of Infectious Diseases, University of Toronto, Toronto, Canada
    2. Divisions of Internal Medicine and Infectious Diseases, University Health Network, Toronto, Toronto, Canada
    Contribution
    IIB, Assisted with international transportation analysis, Edited the final draft of the article
    Competing interests
    No competing interests declared.

  15. John S Brownstein

    1. Department of Pediatrics, Harvard Medical School, Boston, United States
    2. Children's Hospital Informatics Program, Boston Children's Hospital, Boston, United States
    Contribution
    JSB, Advised on international public health context, Edited the final draft of the article
    Competing interests
    No competing interests declared.

  16. Sumiko R Mekaru

    Children's Hospital Informatics Program, Boston Children's Hospital, Boston, United States
    Contribution
    SRM, Assisted in geopositioning, Drafting or revising the article
    Competing interests
    No competing interests declared.

  17. Andrew J Tatem

    1. Department of Geography and Environment, University of Southampton, Southampton, United Kingdom
    2. Fogarty International Center, National Institutes of Health, Bethesda, United States
    3. Flowminder Foundation, Stockholm, Sweden
    Contribution
    AJT, Provided information on urban change and migration data, Drafting or revising the article
    Competing interests
    No competing interests declared.

  18. Kamran Khan

    1. Department of Medicine, Division of Infectious Diseases, University of Toronto, Toronto, Canada
    2. Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Canada
    Contribution
    KK, Provided data, Conducted all analyses on international air traffic patterns, Drafting or revising the article
    Competing interests
    No competing interests declared.

  19. Simon I Hay

    1. Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom
    2. Fogarty International Center, National Institutes of Health, Bethseda, United States
    Contribution
    SIH, Conceived the work and analysis, Wrote content and edited the article at all stages of development, Acts as guarantor of the paper
    For correspondence
    simon.hay@zoo.ox.ac.uk
    Competing interests
    SIH: Reviewing editor, eLife.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-0611-7272

Funding

University Of Oxford (Sir Richard Southwood Graduate Scholarship)

  • David M Pigott

Bill and Melinda Gates Foundation (OPP1053338)

  • Nick Golding

Medical Research Council (K00669X)

  • Peter W Gething

Biotechnology and Biological Sciences Research Council (Studentship)

  • Oliver J Brady

German Academic Exchange Service (Graduate Scholarship)

  • Moritz UG Kraemer

U.S. National Library of Medicine (R01LM010812)

  • John S Brownstein
  • Sumiko R Mekaru

7th Framework Programme for Research and Technological Development (EU FP7) (602525)

  • Peter W Horby

Canadian Institutes of Health Research

  • Isaac I Bogoch
  • Kamran Khan

Wellcome Trust (095066)

  • Adrian Mylne
  • Simon I Hay

RAPIDD program of the Science & Technology Directorate

  • Andrew J Tatem
  • Simon I Hay

Fogarty International Center

  • Andrew J Tatem
  • Simon I Hay

Bill and Melinda Gates Foundation (OPP1106023)

  • Zhi Huang
  • Andrew J Henry
  • Catherine L Moyes

Bill and Melinda Gates Foundation (OPP1068048)

  • Daniel J Weiss
  • Samir Bhatt

Bill and Melinda Gates Foundation (OPP1093011)

  • Catherine L Moyes
  • John S Brownstein
  • Sumiko R Mekaru
  • Simon I Hay

National Institute of Allergy and Infectious Diseases (U19AI089674)

  • Andrew J Tatem

Bill and Melinda Gates Foundation (OPP1106427)

  • Andrew J Tatem

Bill and Melinda Gates Foundation (OPP1032350)

  • Andrew J Tatem

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We thank Katherine Battle, Maria Devine and Kirsten Duda for proof-reading and Jane Messina for creating Figure 1. We also thank Andrew Rambaut for his comments on the final draft.

Copyright

© 2014, Pigott et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

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  1. David M Pigott
  2. Nick Golding
  3. Adrian Mylne
  4. Zhi Huang
  5. Andrew J Henry
  6. Daniel J Weiss
  7. Oliver J Brady
  8. Moritz UG Kraemer
  9. David L Smith
  10. Catherine L Moyes
  11. Samir Bhatt
  12. Peter W Gething
  13. Peter W Horby
  14. Isaac I Bogoch
  15. John S Brownstein
  16. Sumiko R Mekaru
  17. Andrew J Tatem
  18. Kamran Khan
  19. Simon I Hay
(2014)
Mapping the zoonotic niche of Ebola virus disease in Africa
eLife 3:e04395.
https://doi.org/10.7554/eLife.04395

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