Spatio-temporal associations between deforestation and malaria incidence in Lao PDR

  1. Francois Rerolle  Is a corresponding author
  2. Emily Dantzer
  3. Andrew A Lover
  4. John M Marshall
  5. Bouasy Hongvanthong
  6. Hugh JW Sturrock
  7. Adam Bennett
  1. University of California, San Francisco, United States
  2. University of Massachusetts-Amherst, United States
  3. University of California, Berkeley, United States
  4. Ministry of Health, Lao PDR, Lao People's Democratic Republic

Abstract

As countries in the Greater Mekong Sub-region (GMS) increasingly focus their malaria control and elimination efforts on reducing forest-related transmission, greater understanding of the relationship between deforestation and malaria incidence will be essential for programs to assess and meet their 2030 elimination goals. Leveraging village-level health facility surveillance data and forest cover data in a spatio-temporal modeling framework, we found evidence that deforestation is associated with short-term increases, but long-term decreases in confirmed malaria case incidence in Lao People's Democratic Republic (Lao PDR). We identified strong associations with deforestation measured within 30 km of villages but not with deforestation in the near (10 km) and immediate (1 km) vicinity. Results appear driven by deforestation in densely forested areas and were more pronounced for infections with Plasmodium falciparum (P. falciparum) than for Plasmodium vivax (P. vivax). These findings highlight the influence of forest activities on malaria transmission in the GMS.

Data availability

All data generated or analysed during this study are included in the manuscript and supporting files. Source data files have been provided for Figures 2, 3, 4 and 5 and for Tables 1, 2 and 3.

The following previously published data sets were used

Article and author information

Author details

  1. Francois Rerolle

    Epidemiology & Biostatistics, University of California, San Francisco, San Francisco, United States
    For correspondence
    francois.rerolle@ucsf.edu
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-3837-5700
  2. Emily Dantzer

    Institute of Global Health Sciences, University of California, San Francisco, San Francisco, United States
    Competing interests
    The authors declare that no competing interests exist.
  3. Andrew A Lover

    Biostatistics and Epidemiology, School of Public Health and Health Sciences, University of Massachusetts-Amherst, Amherst, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-2181-3559
  4. John M Marshall

    Division of Epidemiology and Biostatistics, School of Public Health, University of California, Berkeley, Berkeley, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-0603-7341
  5. Bouasy Hongvanthong

    Center for Malariology, Parasitology and Entomology, Ministry of Health, Lao PDR, Vientiane, Lao People's Democratic Republic
    Competing interests
    The authors declare that no competing interests exist.
  6. Hugh JW Sturrock

    Institute of Global Health Sciences, University of California, San Francisco, San Francisco, United States
    Competing interests
    The authors declare that no competing interests exist.
  7. Adam Bennett

    Institute of Global Health Sciences, University of California, San Francisco, San Francisco, United States
    Competing interests
    The authors declare that no competing interests exist.

Funding

Bill and Melinda Gates Foundation (OPP1116450)

  • Francois Rerolle
  • Emily Dantzer
  • Andrew A Lover
  • Bouasy Hongvanthong
  • Hugh JW Sturrock
  • Adam Bennett

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

Reviewing Editor

  1. Ben S Cooper, Mahidol University, Thailand

Ethics

Human subjects: This study was approved by the National Ethics Committee for Health Research at the Lao Ministry of Health (Approval #2016-014; 8/22/2016) and by the UCSF ethical review board (Approvals #16-19649 and #17-22577). The informed consent process was consistent with local norms, and all study areas had a consultation meeting with, and approvals from, village elders. All participants provided informed written consent; caregivers provided consent for all children under 18, and all children aged 10 and above also provided consent directly. The study was conducted according to the ethical principles of the Declaration of Helsinki of October 2002.

Version history

  1. Received: March 16, 2020
  2. Accepted: February 19, 2021
  3. Accepted Manuscript published: March 9, 2021 (version 1)
  4. Version of Record published: April 6, 2021 (version 2)

Copyright

© 2021, Rerolle et al.

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

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  1. Francois Rerolle
  2. Emily Dantzer
  3. Andrew A Lover
  4. John M Marshall
  5. Bouasy Hongvanthong
  6. Hugh JW Sturrock
  7. Adam Bennett
(2021)
Spatio-temporal associations between deforestation and malaria incidence in Lao PDR
eLife 10:e56974.
https://doi.org/10.7554/eLife.56974

Share this article

https://doi.org/10.7554/eLife.56974

Further reading

  1. How does cutting down forests influence the spread of malaria?

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    Background:

    Few national-level studies have evaluated the impact of ‘hybrid’ immunity (vaccination coupled with recovery from infection) from the Omicron variants of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).

    Methods:

    From May 2020 to December 2022, we conducted serial assessments (each of ~4000–9000 adults) examining SARS-CoV-2 antibodies within a mostly representative Canadian cohort drawn from a national online polling platform. Adults, most of whom were vaccinated, reported viral test-confirmed infections and mailed self-collected dried blood spots (DBSs) to a central lab. Samples underwent highly sensitive and specific antibody assays to spike and nucleocapsid protein antigens, the latter triggered only by infection. We estimated cumulative SARS-CoV-2 incidence prior to the Omicron period and during the BA.1/1.1 and BA.2/5 waves. We assessed changes in antibody levels and in age-specific active immunity levels.

    Results:

    Spike levels were higher in infected than in uninfected adults, regardless of vaccination doses. Among adults vaccinated at least thrice and infected more than 6 months earlier, spike levels fell notably and continuously for the 9-month post-vaccination. In contrast, among adults infected within 6 months, spike levels declined gradually. Declines were similar by sex, age group, and ethnicity. Recent vaccination attenuated declines in spike levels from older infections. In a convenience sample, spike antibody and cellular responses were correlated. Near the end of 2022, about 35% of adults above age 60 had their last vaccine dose more than 6 months ago, and about 25% remained uninfected. The cumulative incidence of SARS-CoV-2 infection rose from 13% (95% confidence interval 11–14%) before omicron to 78% (76–80%) by December 2022, equating to 25 million infected adults cumulatively. However, the coronavirus disease 2019 (COVID-19) weekly death rate during the BA.2/5 waves was less than half of that during the BA.1/1.1 wave, implying a protective role for hybrid immunity.

    Conclusions:

    Strategies to maintain population-level hybrid immunity require up-to-date vaccination coverage, including among those recovering from infection. Population-based, self-collected DBSs are a practicable biological surveillance platform.

    Funding:

    Funding was provided by the COVID-19 Immunity Task Force, Canadian Institutes of Health Research, Pfizer Global Medical Grants, and St. Michael’s Hospital Foundation. PJ and ACG are funded by the Canada Research Chairs Program.