RNA interference defends against viral infection in plant and animal cells. The nematode Caenorhabditis elegans and its natural pathogen, the positive-strand RNA virus Orsay, have recently emerged as a new animal model of host-virus interaction. Using a genome-wide association study in C. elegans wild populations and quantitative trait locus mapping, we identify a 159 base-pair deletion in the conserved drh-1 gene (encoding a RIG-I-like helicase) as a major determinant of viral sensitivity. We show that DRH-1 is required for the initiation of an antiviral RNAi pathway and the generation of virus-derived siRNAs (viRNAs). In mammals, RIG-I-domain containing proteins trigger an interferon-based innate immunity pathway in response to RNA virus infection. Our work in C. elegans demonstrates that the RIG-I domain has an ancient role in viral recognition. We propose that RIG-I acts as modular viral recognition factor that couples viral recognition to different effector pathways including RNAi and interferon responses.https://doi.org/10.7554/eLife.00994.001
Most organisms—from bacteria to mammals—have at least a rudimentary immune system that can detect and defend against pathogens, particularly viruses. This defense mechanism, which is known as the innate immune system, uses sensor proteins to recognize viral RNA, and then mobilizes other immune components to attack the invaders.
The specific mechanisms used to destroy viruses differ between species. In mammals, a protein called RIG-1 binds to viral RNA and activates a signaling pathway that leads to the production of interferons: immune proteins named after their ability to ‘interfere’ with viral replication. Plants and insects do not use interferons, but instead use a mechanism called RNA interference, in which long double-stranded RNAs are cleaved into shorter fragments.
The nematode worm C. elegans also deploys RNA interference against viruses but, in contrast to insects and plants, worms do not possess a specific set of RNA interference enzymes that participate solely in the antiviral response. They do, however, express a protein called DRH-1 that is related to the RIG-I protein found in mammals.
To investigate whether DRH-1 contributes to innate immunity in C. elegans, Ashe et al. infected 97 strains of C. elegans from around the world with a virus, and showed that some strains were more sensitive to the virus than others, with certain strains showing complete resistance. By comparing a sensitive strain with a resistant one, Ashe et al. revealed that viral sensitivity was caused by a mutation in the gene encoding DRH-1.
Further experiments showed that DRH-1 is required for the first step in RNA interference. Ashe et al. have thus identified a conserved role for RIG-1 in initiating antiviral responses, and propose that the protein couples virus recognition to distinct defense mechanisms in different evolutionary groups.https://doi.org/10.7554/eLife.00994.002
The arms races between pathogens and their hosts have led to the evolution of sophisticated mechanisms to provide immunity against infection. Whilst adaptive immunity is specific to vertebrates, innate mechanisms are present in all multicellular organisms, allowing cells to recognize specific pathogens and instigate appropriate responses. RNA viruses are important pathogens of many multicellular organisms, which replicate without a DNA intermediate using RNA dependent RNA polymerase. Successful neutralization of invading RNA viruses by cells thus requires the viral genome to be recognized within the sea of endogenous RNA.
The primary innate immune sensors for RNA viruses in mammals are RIG-I and its homolog MDA-5 (Schlee, 2013). Viral recognition by RIG-I and MDA-5 triggers activation of downstream signaling, mediated by the proteins’ N-terminal CARD domains, and results in the activation of the interferon pathway (Yoneyama et al., 2004). Initial recognition of viral RNA is likely to be mediated by the DExD/H-box helicase domain and the C-terminal RIG-I domain. Though the precise ligands that activate RIG-I family proteins are not fully defined, MDA-5 appears to bind long dsRNA (Gitlin et al., 2006), whilst RIG-I seems to recognize the 5′ end of double stranded RNA, but only if it has a 5′ triphosphate (Pichlmair et al., 2006). As all known RNA polymerases leave a triphosphate at the 5′ end of newly synthesized RNA, the presence of a 5′ triphosphate is likely to be a signature of RNA virus replication and thus allow viral replication intermediates to be distinguished from endogenous mRNA, which will predominantly display a 5′ cap (Rehwinkel and Reis e Sousa, 2010).
In plants and insects, interferon signaling is not involved in antiviral defense. Instead, the RNA interference (RNAi) pathway provides robust defense against RNA viral infection (Ding and Voinnet, 2007; Ding, 2010). The initial step in protection against positive strand RNA virus infection in plants and insects is detection and subsequent cleavage of the double-stranded replication intermediate by members of the Dicer family of endonucleases. Insects and plants possess dedicated Dicer enzymes responsible specifically for this antiviral response, Dicer-like 4 (and to a lesser extent Dicer-like 1) in plants, and Dicer2 in insects (Bouché et al., 2006; Deleris et al., 2006; Fusaro et al., 2006; Galiana-Arnoux et al., 2006; van Rij et al., 2006; Diaz-Pendon et al., 2007). The small RNAs thus generated feed into the canonical RNAi machinery and can be used to silence the viral genome.
In the nematode C. elegans, the RNAi pathway is best characterized as a response to artificial introduction of dsRNA by feeding or injection. However, exposing C. elegans to virus-derived dsRNA using transgenes or infection with mammalian viruses also triggers an RNAi response (Lu et al., 2005; Schott et al., 2005; Wilkins et al., 2005; Yigit et al., 2006). Additionally, we have shown previously that this response is also initiated upon infection with a positive strand RNA virus, named the Orsay virus, which infects C. elegans in the wild through horizontal transmission. Disruption of this pathway through mutation of the core components of the RNAi machinery results in greatly increased viral infection levels. Interestingly, the Orsay virus infects a wild isolate named JU1580 (from which the Orsay virus was isolated) to much higher levels than the N2 strain (Félix et al., 2011).
Despite these advances, our understanding of how RNAi-mediated antiviral defense in C. elegans is orchestrated is still limited. One major unsolved problem is how viral dsRNA within the cell is recognized in order to initiate the antiviral response. In contrast to the situation in both plants and insects, C. elegans only has one Dicer enzyme (Knight and Bass, 2001; Yigit et al., 2006); it is expected therefore that the activity of Dicer in different small RNA pathways will be controlled by different partner proteins within distinct complexes (Yigit et al., 2006; Thivierge et al., 2012).
In this regard it is intriguing that C. elegans encodes three homologues of the mammalian viral recognition protein RIG-I: DRH-1, DRH-2 and DRH-3. The three RIG-I family members do not contain the CARD domains required for interferon induction; consistently they have yet to be implicated in signaling pathways. However, they do possess the RIG-I C-terminal domain and the helicase domains, potentially enabling them to recognize viral RNA. So far study of these genes has connected them to the RNA interference response. DRH-1 was initially characterized as a protein interacting with DCR-1, RDE-1 and RDE-4 (Tabara et al., 2002; Duchaine et al., 2006; Sijen et al., 2007). RNAi of drh-1 was not found to be required for RNAi per se but result in a defect in RNAi of a second gene (Tabara et al., 2002), however it remains unclear whether this effect was solely due to knockdown of drh-1. More recent studies did not observe defects in endogenous or exogenous small RNA pathways in drh-1 mutants (Gu et al., 2009; Lu et al., 2009). However, drh-1 mutants were found to be defective in the silencing of a flockhouse virus-derived replicon (Lu et al., 2009). drh-1 and drh-2 are the result of a recent gene duplication event that occurred after the last common ancestor of C. elegans and its closest known sister clade including C. briggsae (www.wormbase.org) (Stein et al., 2003), and drh-2 is the upstream gene in an operon containing drh-1. drh-2 has lost some of its functional domains due to frame-shift mutations and its function remains unclear, although it has been suggested to act as a negative regulator of RNAi (Lu et al., 2009). DRH-3 is required for endogenous small RNA pathways in the germline and efficient exogenous RNAi (Gu et al., 2009), and is found in at least two distinct protein complexes including the ERI Complex (ERIC) (Gu et al., 2009; Thivierge et al., 2012). Thus, an intriguing possibility is that RIG-I family genes in C. elegans initiate RNAi rather than the interferon response.
Here we discover a naturally occurring deletion in the gene drh-1 that is widespread in C. elegans populations despite predisposing individuals to viral sensitivity. We show that the increased viral sensitivity caused by this deletion results from a failure of the RNAi pathway. Mutations in drh-1 almost completely abolish the production of primary siRNAs, allowing us to place DRH-1 at the top of a hierarchical RNAi response. Our data supports a model whereby the conserved RNA virus recognition capability of drh-1 allows it to recruit the RNAi machinery to defend C. elegans from viral infection.
To explore intraspecific variation in viral resistance in C. elegans, we assayed a worldwide set of 97 wild C. elegans isolates that had previously been genotyped (Andersen et al., 2012). To assess viral sensitivity, we infected each isolate in triplicate and quantified the viral load after 7 days by qRT-PCR. Viral loads of the 97 isolates varied widely over five orders of magnitude (Figure 1—figure supplement 1A). Genome-wide association for viral load revealed a single peak covering a 6 Mb region in the middle of chromosome IV (Figure 1A). However, further mapping resolution is limited by the low natural recombination frequency in the species (Cutter et al., 2009; Andersen et al., 2012).
We therefore focused on genetic variation in viral sensitivity between the N2 and JU1580 isolates. We first assayed viral sensitivity in 110 F2 recombinant families (Figure 1—figure supplement 1B). Whole-genome sequencing of a pool of the 20 most sensitive families revealed linkage to chromosome IV (Figure 1—figure supplement 1C). To narrow down the candidate region, we introgressed the center of chromosome IV (IV:3,329,219 to IV:11,083,410) of JU1580 into N2 animals (yielding strain JU2170). As expected, JU2170 showed similar viral load to JU1580 (Figure 1—figure supplement 2). We then screened for recombinants in this region after crossing JU2170 with N2. This allowed us to restrict the candidate region to a 155 kb interval carried by a virus-sensitive recombinant strain named JU2196 (Figure 1B, Figure 1—figure supplement 2).
Genome sequencing of the JU1580 isolate and alignment to the N2 reference strain revealed 20 single nucleotide polymorphisms (SNPs), including one non-synonymous SNP, and one 159 base indel in the 155 kb region (Figure 1—figure supplement 2). The 159 base deletion in the JU1580 genome, named niDf250 (IV:6,607,635-6,607,793), lies within the drh-1 gene locus (Figure 1C). drh-1 is a homolog of the mammalian RIG-I family genes, whose products bind virus-derived RNAs, acting as pattern recognition receptors (Parameswaran et al., 2010; Yoneyama and Fujita, 2010), and trigger antiviral innate immune responses in mammals (Yoneyama et al., 2004). C. elegans expresses three RIG-I-like proteins: DRH-1, DRH-2 and DRH-3. The niDf250 deletion covers most of drh-1 exon 19 and part of exon 20 (Figure 1C) and was confirmed using genomic PCR (Figure 1D). drh-1 mRNA levels are unchanged in JU1580 (Figure 1E) and the resulting transcript is predicted to encode a truncated protein of 987 amino acids, identical to the N2 form of DRH-1 up to amino acid 973 but with a novel C-terminus (Figure 1F). Importantly, this truncates the RIG-I C-terminal domain (amino acids 885–1014), thought to be required for RNA recognition specificity (Kowalinski et al., 2011; Figure 1F).
To establish a potential role for DRH-1 in Orsay antiviral resistance we tested whether a drh-1 deletion in the N2 background was sufficient to impart viral sensitivity, as assayed by viral load. Indeed, the drh-1(ok3495) mutant displayed an increased viral load compared to N2 animals, similar to that of JU1580 (Figure 1G). Conversely, transgenic JU1580 animals carrying a fosmid containing the N2 allele of drh-1 were resistant to Orsay infection (Figure 1G). Therefore, variation at the drh-1 locus explains the difference in viral load between N2 and JU1580.
An inactivating mutation in a pathogen-resistance gene could be expected to be a rare deleterious variant in natural populations, yet the wild niDf250 allele is found at an intermediate frequency at the global level, in 22/97 (23%) of the tested wild isolates. The deletion is found in about one third of isolates from Europe and Africa (21/64, 33%) with a high incidence in France (14/30, 47%), but is rarer (1/30) in those from the Americas and the Pacific regions (Figure 2A). As expected, the presence of the deletion correlated strongly with viral load in the infection experiment (Figure 1—figure supplement 1A; Wilcoxon test on viral load of isolates carrying each drh-1 allele, p=1.3×10−9). Thus, surprisingly, the derived drh-1 allele has spread to intermediate frequency in natural populations, despite rendering the animals susceptible to viral infection.
A possible interpretation for the spread of the sensitive drh-1 allele might be that high Orsay viral load has no deleterious effect on fitness. However, in laboratory conditions, we found that viral infection leads to delayed and decreased total progeny of JU1580 and drh-1(ok3495) mutant animals relative to uninfected animals, whilst infection of N2 had no significant effect (Figure 2—figure supplement 1). Furthermore, we performed a competition experiment between N2 and JU2196, which contains the drh-1 region from JU1580 introgressed into the N2 background (Figure 1B). N2 rapidly outcompetes JU2196 in the presence of viral infection, but not its absence, confirming that the increased viral infection resulting from the drh-1 deletion is indeed detrimental for fitness (Figure 2B). In the absence of viral infection, we could not detect in standard laboratory conditions over 10 generations of competition any positive or negative effect of the drh-1 deletion and the introgressed surrounding region. Thus the natural drh-1 deletion impairs fitness only in the presence of viral infection.
To characterize the evolutionary history of the drh-1 region, we first focused on the 6 Mb region detected by genome-wide association. This region presents three main haplotypes among the 97 wild isolates (Andersen et al., 2012): the N2 haplotype, the JU1580 haplotype and a distant haplotypic group (including RW7000 and QX1211), as well as a few recombinants (Figure 2C, Figure 2—figure supplement 2). The drh-1(niDf250) allele is exclusively found in isolates carrying the JU1580 haplotype in the 6 Mb region and in a few recombinants with either the N2 or distant haplotypes (Figure 2C). The JU1580 and N2 haplotypes show fewer fixed differences in RAD polymorphic sites between them (24 SNPs) than with the divergent haplotype group (63 and 57 SNPs, respectively). In addition, from our whole-genome JU1580 sequencing data, N2 and JU1580 display a very low level of molecular diversity in the central region of chromosome IV (Figure 2D). Moreover, we observe a strong decrease in molecular diversity between IV:4529464 to IV:6662701 in isolates carrying the niDf250 allele (Figure 2E, lines), but not in those carrying the drh-1 (N2) allele. Thus, the divergence between the N2 and JU1580 haplotypes in this region, including the niDf250 deletion, appears recent relative to much of the species’ genetic diversity. Furthermore, the niDf250 allele is in high or even full linkage disequilibrium with a large region of chromosome IV (Figure 2E, dots). This lack of diversity and the high linkage disequilibrium around niDf250 suggest a partial sweep of the haplotype linked to niDf250. They also imply that the sensitive drh-1 allele may have spread by hitch-hiking with a favorable allele.
Having established the major role of drh-1 allelic variation in natural variation of antiviral defense in C. elegans, we wished to understand the molecular mechanisms of DRH-1 action in the antiviral response. We previously showed that disruption of small RNA pathway genes such as rde-1, which encodes an Argonaute protein essential for RNAi in response to exogenous dsRNA (RDE-1), renders N2 animals as sensitive to the Orsay virus as JU1580 (Félix et al., 2011). DRH-1 interacts with the double-stranded RNA (dsRNA) binding protein RDE-4 and the dsRNA-specific endonuclease Dicer (DCR-1), both of which act upstream of RDE-1 in exogenous RNAi (Tabara et al., 1999; Parrish and Fire, 2001; Barber et al., 2010) However, DRH-1 is dispensable for exogenous RNAi (Gu et al., 2009). We therefore wondered if DRH-1 could act specifically to promote DCR-1 processing of long dsRNA that is produced during viral RNA replication. Indeed, we find that DCR-1 is required for viral resistance in the N2 strain (Figure 3A). We therefore postulated that the antiviral response involves siRNAs processed by DCR-1, which may initiate a cascade of events analogous to canonical C. elegans RNAi.
In C. elegans, the RNAi pathway is divided into primary and secondary steps. Long dsRNA is processed by DCR-1 to generate a primary siRNA duplex ∼23 nucleotides (nt) in length with 5′ monophosphates and 2 nt 3′ overhangs. By examining libraries derived solely from small RNAs with 5′ monophosphates (5′ dependent libraries), we could interrogate the primary siRNA response specifically. In wild-type N2 animals, infection with virus leads to generation of predominantly 23 nt small RNAs with no first nucleotide bias, mapping both sense and antisense to the viral genome in equal proportions (Figure 3B). These small RNAs are likely primary DCR-1 products generated from the double-stranded intermediate of viral replication, consistent with the small RNA response against single-strand RNA viruses in insects (Flynt et al., 2009). Furthermore, overlapping RNAs mapping to complementary strands of the viral genome showed the 2 nt 3′ overhang characteristic of Dicer products (p<10−9, χ2 test against a uniform distribution of overhang length) (Figure 3C). The same viRNA pattern was observed in rde-1 mutants lacking the primary siRNA Argonaute protein RDE-1 (Figure 3D). Thus rde-1 mutants are proficient in primary viRNA formation despite being sensitive to viral infection (Figure 3—figure supplement 1) (Félix et al., 2011). In contrast, JU1580 animals showed a markedly different pattern (Figure 3E). First, a much higher proportion of small RNAs derived from the sense strand than the antisense strand (88% vs 49% in N2). Second, the size distribution of viRNAs was flattened, with a greatly reduced proportion of 23 nt RNAs and an increased proportion of 15–20 nt RNAs. These shorter viRNAs were not present in libraries prepared from uninfected JU1580 or N2 controls (Figure 3—figure supplement 2A) and appeared to be derived from regions of strong secondary structure within the virus (Figure 3—figure supplement 3). The drh-1 mutant (in an N2 strain background) displayed an identical viRNA pattern to JU1580 (Figure 3F). Thus JU1580 and drh-1 mutant strains are deficient in primary siRNA generation against the virus.
Primary siRNAs act upstream of an amplification step by triggering the synthesis of secondary siRNAs antisense to targeted RNAs (Sijen et al., 2001). Secondary siRNAs are synthesized by RNA-dependent RNA polymerases (RdRPs), and bind to a number of secondary siRNA-specific Argonaute proteins to bring about target silencing (Yigit et al., 2006). Secondary siRNAs have a modal length of 22 nt, are 5′ triphosphorylated, have a strong preference for a 5′ guanine (G), and are referred to as 22G siRNAs (22Gs). Small RNAs can be enzymatically treated prior to adaptor ligation to allow sequencing (5′ independent) of both primary and secondary siRNAs (Pak and Fire, 2007; Sijen et al., 2007). N2 animals infected with Orsay virus showed a robust secondary 22G siRNA response, primarily antisense to the viral genome (Figure 4A, Figure 4—figure supplement 1). In contrast, rde-1 mutants lacked 22G siRNAs, consistent with a role for RDE-1 in initiating the secondary siRNA response (Figure 4B, Figure 4—figure supplement 1). In addition, mutants lacking DRH-3 or the RdRP RRF-1 and a strain deficient in 12 worm Argonaute proteins (WAGO-1 through 12) that bind secondary siRNAs (MAGO-12) (Yigit et al., 2006) lacked 22G viRNAs, but still produced primary siRNAs (Figure 4F,L,M). The above have previously been implicated in secondary siRNA generation in other contexts (Yigit et al., 2006; Pak and Fire, 2007; Sijen et al., 2007) and drh-3, rrf-1 and MAGO-12 mutant strains are also sensitive to viral infection similar to rde-1 (Figure 3—figure supplement 1). Taken together these data show that a canonical secondary siRNA pathway is engaged to amplify the antiviral response.
drh-1 mutants and JU1580 animals displayed the same profile of sense siRNAs in 5′ independent libraries as in 5′ dependent libraries (Figures 3E–F and 4C,E). Mutants deficient in the adjacent gene drh-2 have a viRNA profile similar to N2 (Figure 4I) and are as resistant to viral infection as N2 (Figure 3—figure supplement 1), implying that this gene is not involved in the antiviral siRNA pathway. Moreover transgenic JU1580 animals carrying the drh-1 gene from N2 showed the same overall viRNA profile as N2 (Figure 4D, Figure 4—figure supplement 1), further supporting the conclusion that drh-1 deficiency is primarily responsible for the defective siRNA synthesis and virus sensitivity in JU1580. Importantly however, there were residual antisense 22G siRNAs present in both JU1580 and drh-1 mutants. This suggests that the few DCR-1 products with the correct length in drh-1 mutants can still be used to generate secondary siRNAs as in N2, implying that drh-1 is not essential for the secondary siRNA pathway. Consistent with this interpretation, the reduced 23 nucleotide long primary siRNA products in JU1580 still displayed a 2 nucleotide 3′ overhang characteristic of DCR-1 activity (Figure 4—figure supplement 2).
Furthermore, residual 22G siRNAs are also present in mutants deficient in the DCR-1 accessory factor RDE-4, which is required for efficient DCR-1 activity in the exogenous RNAi pathway (Figure 4J; Tabara et al., 1999; Parrish and Fire, 2001). Additionally, drh-1 mutants displayed no difference in endogenous 22G siRNAs mapping antisense to protein-coding genes, whilst, in agreement with previous data (Gu et al., 2009), drh-3 mutants showed markedly reduced levels of endogenous siRNAs (Figure 4—figure supplement 3). Together with our observation that drh-1 mutants are deficient in primary viRNA production, this suggests that DRH-1 acts early in the antiviral siRNA pathway and is not required for downstream amplification steps. These observations are in contrast to earlier work describing a role for DRH-1 downstream of secondary siRNA production in a flockhouse virus replicon model (Lu et al., 2009).
To further test this interpretation, we examined double mutant strains. The prominent 23 nt peak for sense and antisense viRNAs attributed to DCR-1 activity present in drh-3 and rde-1 single mutants was absent in both drh-3; drh-1 and drh-1; rde-1 double mutants (Figure 4G,H). This is consistent with the idea that DRH-1 acts upstream of DRH-3 and RDE-1 in the antiviral siRNA pathway and acts in concert with DCR-1. The rde-4; drh-1 double mutant showed a further reduction in primary 23 nucleotide long Dicer products compared to the drh-1 single mutant (Figure 3—figure supplement 2). Furthermore, residual antisense 22G siRNAs in drh-1 mutants (Figure 4E) were mostly absent in rde-4; drh-1 double mutants (Figure 4K). These data support the conclusion that residual DCR-1 activity on viral dsRNA in drh-1 mutants is dependent on RDE-4. Thus, the double mutant data confirms the position of DRH-1 as an upstream factor essential for the generation of robust levels of antiviral siRNA in response to infection.
Overall our data support a key and unique role for the C. elegans RIG-I-like protein DRH-1 in primary siRNA synthesis by either guiding DCR-1 activity to the viral genome or assisting DCR-1 processing of the double-stranded viral RNA. We suggest that the physical interaction between DRH-1 and DCR-1, and the potential for DRH-1 to recognize the viral genome as foreign, possibly through its well-conserved RIG-I domain, may enable DRH-1 to recruit DCR-1 to the double-stranded replicating viral genome and instigate a hierarchical antiviral siRNA response (Figure 5). Our data also show that the role of DRH-1 in viral recognition is distinct from that of its paralogs. Given the sequence and domain similarities between DRH-1, DRH-2 and DRH-3, it will be of interest to determine the mode of RNA recognition by DRH-2 and DRH-3 in the future.
Our findings imply that parallel RNAi pathways are involved in recognition of viral infection, aberrant endogenous transcripts and exogenous RNAi (exo-RNAi) in an experimental setting. It is interesting therefore that DRH-1 is found in a protein complex with DCR-1 and RDE-4 even in the absence of infection (Thivierge et al., 2012). This might suggest that this complex limits the availability of DCR-1 for exo-RNAi. However, drh-1 and N2 worms respond equally to exo-RNAi, suggesting that this is not the case (Figure 4—figure supplement 4). The constitutive nature of the DCR/DRH-1 complex may allow cells to respond much more rapidly to the presence of viral replication intermediates. Recent observations from Rui Lu and colleagues are in agreement with our findings (Guo et al., 2013).
Antiviral small RNAs generated by Dicer are an evolutionarily conserved mechanism for fighting infection by positive-strand RNA viruses (Aliyari and Ding, 2009). However, there must be some mechanism to distinguish between the viral genome and cellular RNAs. Drosophila and plants have a dedicated Dicer enzyme responsible for viral dsRNA recognition. We suggest that in C. elegans DRH-1 may perform this function. The absence of a role for drh-1 in the endogenous small RNA pathway (Figure 4—figure supplement 3; Gu et al., 2009) supports the idea that it encodes a viral-specific recognition factor. In mammals, the C-terminal domain of the DRH-1 ortholog RIG-I is able to recognize the 5′ triphosphate on viral genomes in the context of the double-stranded replication intermediate (Hornung et al., 2006; Pichlmair et al., 2006; Rehwinkel et al., 2010). The C-terminal domain is conserved in DRH-1, thus suggesting that DRH-1 might use a recognition mechanism analogous to RIG-I to recruit DCR-1 to the Orsay virus RNA. In support of this, 5′ RACE experiments from total RNA from infected animals using Orsay virus specific primers fail to detect product unless the 5′ triphosphate is removed prior to adaptor ligation (Figure 4—figure supplement 3), suggesting that the majority of Orsay genomic RNA molecules are indeed phosphorylated at the 5′ end.
It is interesting that the recognition function of DRH-1 may be conserved with mammalian RIG-I whilst the effector pathways are apparently distinct. It will therefore be intriguing to examine whether any part of the function of DRH-1 in antiviral RNAi might be conserved in mammals. As yet, although small RNA responses have been analyzed in mammalian cells infected with viruses (Parameswaran et al., 2010) it is not clear whether these have a significant role in the defense of viral infection or whether they display any similarities to antiviral RNAi pathway in plants or nematodes. Examining whether cells deficient in RIG-I show alterations in small RNA pathways upon viral infection may help to address this question. Equally, it will be interesting to identify whether DRH-1 has a signaling role in C. elegans upon viral infection. Such studies might indicate whether the gene expression or the RNAi function is the ancestral role of RIG-I-like genes.
RIG-I and MDA-5 respond to viral infection with changes in cytoplasmic localization that result in the activation of the interferon response (Nakhaei et al., 2009). In addition, RIG-I and MDA-5 are themselves interferon-induced genes. It will therefore be of great interest to explore the behavior of DRH-1 upon viral infection. A recent genome-wide analysis of gene expression upon Orsay virus infection in C. elegans did not detect any significant changes in drh-1 transcript levels (Sarkies et al., 2013). Furthermore, a GFP-DRH-1 fusion protein did not show marked alterations in expression levels or subcellular localization upon infection with the Orsay virus (our unpublished observations). It will be important to analyze the behavior of the endogenous DRH-1 protein upon infection in future studies.
Our discovery of an inactivating deletion in drh-1 carried by many wild isolates of C. elegans is consistent with the rapid evolution under strong selection known to characterize proteins involved in immunity, including antiviral RNAi defense (Obbard et al., 2006; Vasseur et al., 2011). Yet it is puzzling that a derived allele with deleterious consequences in the presence of viral infection is found at intermediate frequency. One possible explanation might be the low natural occurrence of infecting viruses, meaning that the drh-1 deletion is effectively neutral. In support of this argument we have not been able to detect similar intestinal symptoms of viral infection in our extensive C. elegans sampling (Félix and Duveau, 2012), including in other years of sampling in the Orsay orchard. Alternatively the drh-1 deletion may have hitch-hiked to fixation with a closely linked beneficial mutation. Such a phenomenon is likely to be common in C. elegans natural populations due to the low effective outcrossing rate, which results in high linkage disequilibrium, especially when associated with a positive selective sweep (Cutter et al., 2009). Indeed we find that the natural drh-1 deletion allele is in high linkage disequilibrium with the surrounding region of chromosome IV (Figure 2E). A related possibility is that the drh-1 deletion itself might have a positive fitness effect in some natural conditions. Although we did not detect a fitness advantage for the region surrounding the drh-1 deletion under laboratory conditions, we cannot test all possible natural conditions, thus a beneficial effect for the drh-1 deletion or its surrounding region remains a possibility. Interestingly, RIG-I appears to have been lost in several clades, including chickens (Zou et al., 2009; Barber et al., 2010; Table 1), which might explain the increased sensitivity of chickens to avian influenza virus when compared to ducks (Barber et al., 2010).
In conclusion, we found that the RIG-I domain has an ancient role in antiviral immunity outside of mammals, yet that this broad conservation in animals is compatible with recurrent losses in insects, ducks, and down to some C. elegans isolates. Our results further indicate that the conserved biochemical activity of RIG-I is viral recognition, whereas downstream effector pathways, such as RNAi and interferon responses, may differ between C. elegans and mammals.
Virus filtrate was prepared as described previously (Félix et al., 2011).
We used 97 natural isolates that have been partly sequenced in a previous study using RAD-sequencing (Andersen et al., 2012). We first submitted each isolate to a bleaching treatment that eliminates horizontally transmitted symbionts such as the Orsay virus (Félix et al., 2011). For each isolate, we infected two 55-mm plates containing five young adults, in triplicate. Cultures were incubated with the Orsay virus at 23°C for 7 days. Maintenance over more than 4 days after infection was performed by transferring a piece of agar (approximately 0.1 cm3) every 2–3 days to a new plate with food. For each infection batch, JU1580 was infected as a control. At 7 days post-infection, nematodes from two plates were collected in M9 and RNA was extracted as described previously (Félix et al., 2011).
cDNA was generated from 1 μg total RNA with random primers using Superscript III (Life Technologies, Foster City, CA). cDNA was diluted to 1:10 for RT-qPCR analysis. RT-qPCR was performed using LightCycler 480 SYBR Green I Master (Roche, Mannheim, Germany). The amplification was performed on a LightCycler 480 Real Time PCR System (Roche). Each sample was normalized to eft-2, and then viral RNA1 (primers GW194 and GW195 in the 97) or RNA2 (oTB17 and oTB18 in the recombinant analysis) levels were compared to the level present in a reference RNA extract obtained from infected JU1580 animals.
Association mapping was performed using the EMMA package with the default kinship matrix (Kang et al., 2008). The mapped trait was the log-transformed mean value of the qPCR on the RNA1 of the Orsay virus.
JU1580 hermaphrodites were crossed to N2 males. 11 heterozygous larvae (stage L4) of the F1 cross progeny were picked singly in 35-mm plates and allowed to self. 110 recombinant F2 larvae (stage L4) were picked as individuals into 35-mm Petri dishes. F2 animals were cultured at 20°C for 24 hr and then inoculated with 10 µl of Orsay virus filtrate. After 4 days of culture at 20°C, the F2 animals and their F3/F4 progeny were resuspended into M9 and washed three times in 1 ml of M9. Animals were pelleted in approximately 20 µl of M9 after the last wash. 5 N2 and 5 JU1580 animals were treated in the same way than the recombinant F2 animals to serve as controls.
To measure the viral load in the infected F2 families, 5 µl of nematode pellets were added to 45 µl of lysis solution (with 1:100 DNase I) from the Power SYBR Green Cells-to-Ct kit (Ambion, Austin, TX). The lysis mixtures were freeze-thawed 10 times using liquid nitrogen and a hot water bath, and then vortexed for 30 min in 96-well plates. 5 µl of Stop Solution (Ambion) were added to each lysis mixture to complete the RNA extraction step. The cDNA synthesis and the qPCRs were then performed using the Power SYBR Green Cells-to-Ct kit (Ambion). We used 2 µl of cDNA (equivalent of cDNA contained in 0.09 µl of nematode pellet) as a template for the qPCR. The level of viral RNA was normalized to gapdh.
DNA from JU1580 or pools of 20 N2 × JU1580 recombinant lines was isolated and DNA libraries were prepared for high-throughput sequencing using the Nextera DNA sample prep kit from Illumina. Sequencing was 150 paired end sequencing was performed on a Illumina MiSeq instrument. The JU1580 genomic reads are accessible at the NCBI Short Read Archive under the accession number: SRS369862.
Processing of Illumina reads, mapping and variation detection was performed using the CLC Genomics Workbench 5 (version 5.5.1). N2 reference genome and annotation used was WormBase release WS220 (www.wormbase.org). SNP and indel analysis was performed using the R statistical environment.
N2 males were crossed to JU1580 hermaphrodites, and the F1 males outcrossed to N2 hermaphrodites. As niDf250 had already been identified in the genome sequence analysis, F2 animals were genotyped by PCR for the presence of its JU1580 allele in the 6 Mb central region of chromosome IV with primers oTB40 and oTB43 (Supplementary file 1B). From one heterozygous animal, 20 homozygous niDf250 F3 animals were selected and crossed to N2 males to start another cycle of introgression. We repeated this cycle twice and in the final cycle 20 homozygous niDf250 F3 animals were isolated. We used a pyrosequencing genotyping method (PyroMark Q96 ID instrument; Biotage) to select among these 20 animals those with the full 6 Mb central region of chromosome IV from JU1580 into the N2 genetic background, and only this region. We genotyped six SNPs on chromosome IV (one at either end of the chromosome, one at either end of the 6 Mb region and two within this region), three SNPs on chromosomes I, III, V, X and two on II. We thus obtained an introgressed line, called JU2170. To obtain recombinants within the 6 Mb central region of chromosome IV for fine mapping, JU2170 hermaphrodites were crossed to N2 males. From 20 F1 heterozygous hermaphrodites, we isolated 300 F2 individuals and selected for recombinants between the two SNPs at either end of the region (IV: 3,877,431 and IV: 11,083,410). We thus obtained five recombinants. We further narrowed down the recombination break point by genotyping inside the candidate region (Figure 1—figure supplement 2).
SNPs were genotyped by pyrosequencing, using a PyroMark Q96 ID instrument from Biotage (Uppsala, Sweden). The PSQ Assay Design software was used to design pyrosequencing primers. To biotinylate one strand in the PCR reaction, we added a universal tag on one primer, as described (Aydin et al., 2006). For each strain, 10 adult animals were mixed with 10 μl of worm lysis buffer (Fay and Bender, 2008; Félix et al., 2011) containing proteinase K at 100 μg/ml. After lysis at 60°C for 1 hr and proteinase K inactivation at 95°C for 15 min, we added 1 μl of worm lysate to 50 μl of PCR mix composed of: 0.25 μl of GoTaq DNA polymerase (Promega, Madison, Wisconsin), 5 μl of dNTP at 2 mM, 10 μl of 5x GoTaq buffer, 0.17 μl of non-biotinylated primer at 10 mM, and 0.87 μl of corresponding universal biotinylated primers at 10 mM, and 1 μl of the reverse primer. Single-stranded DNA was then purified and the pyrosequencing reaction was performed following the manufacturer’s indications. Primers are listed in Supplementary file 1B.
Non-synchronized animals were cultured in a 55-mm plate and collected in M9 just before starvation. RNA extraction and RT-qPCR were performed as described previously (Félix et al., 2011).
JU1580 animals were transformed as described (Mello and Fire, 1995) with the fosmid WRM0640dC01 that contains the entire length of the drh-1 gene and its operon CEOP4647. The injection mix contained 10 ng/µl of fosmid DNA, 5 ng/µl of the co-marker transgene myo-3::gfp::unc-54, 85 ng/µl of 1 kb DNA ladder (Invitrogen), 20 mM potassium phosphate pH 7.5, and 3 mM potassium citrate pH 7.5. The transgene was then integrated via X-ray irradiation as described (Fire, 1986). We controlled that the transgenic copy of drh-1 was transcriptionally active in transformed animals by qRT-PCR on a portion of the mRNA that is deleted in the wild JU1580 strain.
For all strains mentioned in Figures 3 and 4, as well as for the strain PD8753 that carries a balanced mutation in dcr-1, one or two young adults were inoculated with 20 µl of viral filtrate for 4 days at 20°C (or 15°C for mago-12 animals) in 55-mm plates in five biological replicates.
4 days after infection, all animals except those from the PD8753 strain were collected in M9; RNA extraction and RT-qPCR were performed as described previously (2). Aliquots of RNA were kept apart for small RNA libraries (see below). For the infected progeny of PD8753 parents, 16 dcr-1 and 16 dcr-1/+ adults per replicate were selected under the fluorescent microscope (i.e., the balancer chromosome carries a gfp reporter) and lysed individually in 10 µl of lysis solution (with 1:100 DNase I) from the Power SYBR Green Cells-to-Ct kit (Ambion). The lysis mixtures were pooled for each replicates and the qRT-PCR was performed as indicated above for the F2 families.
Preparation of RNA used for small RNA libraries is described above. For 5′ independent libraries, 3–5 μg of total RNA was pre-treated with 5′ polyphosphatase (Epicenter) following the manufacturer’s instructions. Small RNA libraries were generated from either polyphosphatase treated or total RNA (3–5 μg) using the TruSeq Small RNA kit (Illumina) following the manufacturer’s instructions. Small RNA libraries were sequenced using the Illumina MiSeq. Small RNA sequence data were submitted to the Gene Expression Omnibus (GEO) under accession number GSE41693.
Small RNA libraries were sequenced using the Illumina MiSeq. Fastq files generated by the machine had adaptors removed using the program Cutadapt v1, and were converted into Fasta files using a custom Perl script. For alignment to the viral genome, Fasta files were trimmed to leave only reads of between 15 and 30 nucleotides using a custom Perl script and were aligned using Bowtie (version 0.12.7) to RNA1 and RNA2 of the Orsay virus genome (Félix et al., 2011), reporting only the best single alignment with up to one mismatch allowed. Sam files from Bowtie were converted into bam files using the SAMtools utility (Li and Durbin, 2009) and bam files were converted into bed files using the BedTools utility (Quinlan and Hall, 2010). Bed files were read into the R environment and plots of the length and first nucleotide as well as read distribution along RNA2 were generated using custom scripts written in R. The level of virus as measured by qRT-PCR was observed to correlate non-linearly with the total level of sense small RNAs in different N2 wild-type samples, thus data were normalized to all viral siRNAs or all sense viRNAs to illustrate differences in read distribution between different samples. Analysis of the overlap to identify potential DCR-1 signatures was carried out by selecting reads of the same length coming from opposite strands on the viral genome, which overlapped by at least one nucleotide. The number of reads overlapping by every possible length either 3′ or 5′ was compared to that expected were the entire distribution uniform using a χ2 test. Only one overlap was statistically significantly enriched with a cut-off of p<0.05 as indicated in the text. For alignment to the C. elegans genome to analyze any potential changes in 22G levels, fasta files were trimmed to leave only reads of between 18 and 30 nucleotides, and the fasta files were collapsed using the FastX Toolkit. Reads matching to microRNA precursors downloaded from miRbase (Kozomara and Griffiths-Jones, 2011) were removed using a custom Perl script, and the remaining reads were aligned to the Ce6 genome (WS190) using Bowtie, reporting the best match with no mismatches (parameters—best–k 1–v 0). After converting bam files to bed files as above, 22Gs mapping antisense to the Ce6/WS190 UCSC annotations of genes (sangerGene.txt) downloaded from the UCSC genome browser website, were then selected from the alignments using a custom Perl script. Genes with abundant 22G reads in N2 wild-type worms were further selected by setting a cut-off of at least five reads in at least one of the N2 wild-type samples and duplicate or overlapping annotations were removed. Comparison of mutants to N2 wild-type was carried out after normalizing to the total number of aligned reads in each library. Secondary structure analysis of the viral genome was performed using RNA-fold (McCaskill, 1990) on a 50 bp window sliding by increments of 20 bp. A Z-score for the secondary structure strength of each window was calculated by comparing the ensemble free energy mean ensemble free energy for 100 random shuffles of the 50 bp window.
Total RNA isolated from infected animals as described above was ligated to the 5′ adaptor from the Illumina Truseq small RNA kit either with or without prior treatment with 5′ polyphosphatase. Only monophosphorylated 5′ ends will be able to ligate to the adaptor, as for the small RNA sequencing. Ligated products were then reverse transcribed using a primer specific for RNA1. The resulting cDNA was then analysed by standard Taq PCR and gel electrophoresis using either primers designed to amplify within the 5′ end of the viral genome as a positive control or primers to amplify from the adaptor into the 5′ end, thus determining whether the adaptor was able to ligate efficiently to the 5´ end (Figure 4—figure supplement 3B).
For each of the 97 isolates, 97 SNPs included in the 6 Mb central region of chromosome IV associated with Orsay virus sensitivity were extracted from RAD-sequencing data (Andersen et al., 2012). DNAsp allowed us to classify all isolates in 28 different haplotypes for this region. The neighbor-net network (Bryant and Moulton, 2004) was then drawn using the SplitTree software (Librado and Rozas, 2009). The average number of differences per polymorphic RAD site along chromosome IV was calculated using DNAsp (Huson and Bryant, 2006) using a sliding window of 25 SNPs every 10 SNPs. The linkage disequilibrium (D′ ) between drh-1 alleles and polymorphic RAD sites on chromosome IV was calculated by DNAsp.
For each strain, we seeded ten 55-mm NGM plates with five L4 animals on each. 5 of the 10 plates were infected with the Orsay virus. Before starvation was reached, we transferred a piece of agar (4 × 4 mm at the surface, 1 cm to the bottom of the plate) from each of the five plates of each treatment (to maximize infection probability) to a single 90 mm NGM plate. 40 L4 animals (F2 progeny from the infected animals) were then isolated for each treatment. Each scored individual was transferred into a new plate 24, 36, 48, 60, 72, 96 and 120 hr after the L4 stage, and progeny number was scored 48 hr after each transfer (most were then at the L4 and adult animals). To ease scoring, some plates were cooled to 4°C after 48 hr and scored within 2 days. N2 and the drh-1 mutant in the N2 background (RB2519) were assayed in parallel. JU1580 and JU1580 rescue (SX2377) were independently blind tested in parallel.
From the same starting populations, we in addition isolated for the survival assay ten animals on nine 55 mm diameter NGM plates (n = 90). Each pool of 10 animals was then transferred to a new plate every 24 hr. Survival was assessed every day by scoring the capacity of each animal to react to stimulation (shaking plates and touching them with a pick). Dead animals were removed from the plate. We also measured the lifespan of each parent from the progeny scoring (n = 40).
Each F2 population was fixed and prepared for FISH as previously described (Kowalinski et al., 2011) using custom Stellaris (Biosearch Technologies) probes for the Orsay virus RNA1 molecule (Supplementary file 1B) labeled with Quasar 670 Dye. Standard fluorescence microscopy was performed using an upright Zeiss AxioImager M1 equipped with a Pixis 1024B camera (Princeton instruments) and a Lumen 200 metal arc lamp (Prior Scientific). A L4 larva was scored as infected when we could see a signal inside at least one intestinal cell. The proportion of infected L4 individuals was the following: 35.0% (n = 109) of JU1580; 3.4% (n = 121) of SX2377; 53.0% (n = 103) of RB2519; 9.0% (n = 100) of N2 animals.
The lmer function from the R package « lme4 » was used to determine the effect of the treatment on the dynamics of progeny production by comparing with an ANOVA the Akaike Information Criterion of a model involving both time, treatment and their interaction to that of a null model involving only time. For the longevity assay, we used the survdiff function (log rank test) of the R package « survival » as to test the effect of the treatment.
The N2 and JU2196 genotypes were competed in the presence or absence of the virus. JU2196 is a near isogenic line with the 4.4 Mb central part of chromosome IV from JU1580 into the N2 background (Figure 1—figure supplement 2A). Both strains were cleaned and roughly synchronized by bleaching. Once the bleached embryos had developed to adulthood, we let them lay embryos for 1 hr and half to further synchronize the populations. After letting the embryos hatch overnight, we started the competition experiment with L2 hermaphrodite larvae in a 1:1 ratio (20 plates with 10 N2 and 10 JU2196 animals on each), adding 50 μl of Orsay virus preparation on half of these plates and 50 μl of M9 solution in the other. Populations were harvested 5 days later with M9 solution under sterile conditions in microfuge tubes. After 2 min of centrifugation at 3000 rpm, the supernatant was removed and a fraction of the pellet containing 100–400 animals (generally 2 μl) was transferred to a new NGM plate. After this initial transfer, transfers were repeated approximately every 36 hr, before starvation. We did not observe a high occurrence of males in this experiment, thus it is unlikely that the tested chromosome IV region recombined.
At each transfer, 2 μl of the pellet was mixed with 18 μl of worm lysis buffer containing proteinase K at 100 μg/ml. The product of the worm lysis was then used as a PCR template using the pyrosequencing primers IV_6124501 Forward and Reverse (Supplementary file 1B). We quantified the proportion of the drh-1(N2) allele using the quantitative option of the pyrosequencer (PyroMark Q96 ID instrument; Biotage). To measure the accuracy of this quantification method, a standard curve was performed with different known proportions of alleles (known proportions of genomic DNA). The correlation between observed and real allele frequencies exceeded 0.983 and the average standard deviation calculated from five replicates of observed frequencies was 6%.
The lmer function from the R package « lme4 » was used to determine the effect of the treatment on the genotype frequency by comparing with an ANOVA the Akaike Information Criterion of a model involving both time, treatment and their interaction to that of a null model involving only time.
unc-22 and empty vector RNAi bacteria were grown for 6 hr at 37°C. unc-22 bacteria were then serially diluted with the empty vector bacteria and seeded onto NGM agar plates containing IPTG (1 mM) and carbenicillin (25 μg/ml). After drying overnight, N2, drh-1 or eri-1 worms were added and then grown at 20°C for 4 days. Each strain was tested in triplicate at each dilution and 15 animals selected at random from each plate were scored for either twitching or paralysis phenotypes.
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Detlef WeigelReviewing Editor; Max Planck Institute for Developmental Biology, Germany
eLife posts the editorial decision letter and author response on a selection of the published articles (subject to the approval of the authors). An edited version of the letter sent to the authors after peer review is shown, indicating the substantive concerns or comments; minor concerns are not usually shown. Reviewers have the opportunity to discuss the decision before the letter is sent (see review process). Similarly, the author response typically shows only responses to the major concerns raised by the reviewers.
Thank you for sending your work entitled “A deletion polymorphism in the C. elegans RIG-I homolog disables viral RNA dicing and antiviral immunity” for consideration at eLife. Your article has been favorably evaluated by a Senior editor (Detlef Weigel) and 2 reviewers.
The Senior editor has assembled the following comments to help you prepare a revised submission.
Ashe and colleagues use an appealing mix of quantitative and molecular genetics to identify and characterize a natural polymorphism in the C. elegans DRH-1 gene that affects production of viral-derived primary siRNAs. The gene emerged from an analysis of natural variation in sensitivity to the Orsay virus, and by a combination of GWAS, introgression mapping, and whole-genome sequencing, the authors managed to pin down a small deletion as a major-effect locus. Using mostly if not exclusively genetics, the authors provide evidence that DRH-1 is likely to specifically recruit the Dicer protein DCR-1 to viral dsRNA substrates. This clearly is a new finding, especially in an organism with a single Dicer. While we find the work very interesting, a minimal set of additional experiments would help support the inferences of the genetic analyses by answering the following questions: 1) Does viral infection affect the expression and subcellular location of DRH-1 protein, as assayed with a GFP fusion?
2) Is there evidence that EXO RNAi is enhanced in drh-1 mutants because absence of DRH-1-bound Dicer would increase Dicer pools? That DRH-1 is not involved in endosiRNA production is consistent with a specific role for SRH-3 in bringing Dicer onto endosiRNA substrates. If the answer to the initial question is yes, this could support the scenario for the possible benefit of the drh-1 deletion in a significant fraction of the wild accessions because of enhanced environmental RNAi (which may confer unknown fitness advantages).
3) A critical experiment for supporting the proposed model would be whether the naturally found truncated form of DRH-1 indeed fails to interact with DCR-1 and RDE-4. We understand that antibodies are not available to test this. Thus, mechanistic inferences about DRH-1 action should be toned down in the revision.https://doi.org/10.7554/eLife.00994.021
1) Does viral infection affect the expression and subcellular location of DRH-1 protein, as assayed with a GFP fusion?
With regard to changes in drh-1 mRNA levels we have recently published a study analysing gene expression changes upon Orsay virus infection (Sarkies et al., Genome Research 2013). We observed no statistically significant changes in drh-1 transcript levels upon infection in wild-type (N2) animals. Thus drh-1 is unlikely to be transcriptionally regulated upon viral infection.
With regards to the subcellular localization of DRH-1 protein, we agree with the reviewers that the cell biology of viral infection in C. elegans is of great interest, including changes in the subcellular localization of DRH-1 before and after viral infection. However, we do not agree that this analysis relates directly to the manuscript that we have submitted: any change or lack of change in subcellular localization would neither strengthen nor contradict our model. Furthermore, we believe that a thorough analysis of DRH-1 behaviour upon infection would have to include analysis of the subcellular dynamics of the Orsay virus in order to be meaningful. Since we do not fully understand this yet, a combined analysis should be the focus of an independent future study. Nevertheless, we have generated a transgenic line expressing a DRH-1-GFP fusion protein. We found that these transgenic animals localize GFP diffusely in the cytoplasm of intestinal and other cells (Author response image 1 below, transgene driven by a “ubiquitous” promoter, sur-5). We observed that the cytoplasmic localization of GFP does not change in response to infection with the Orsay virus. However, in the absence of a suitable antibody that works in immunofluorescence, we are unable to assess the localization of the endogenous protein, thus we cannot rule out that changes in DRH-1 subcellular localization occur upon infection. We should therefore be cautious about the interpretation of such a negative result and we would prefer not to include these data in the manuscript. We have therefore added a paragraph to the Discussion referencing the gene expression paper, and we have referred to the results of the DRH-1GFP fusion protein analysis as data not shown.
2) Is there evidence that EXO RNAi is enhanced in drh-1 mutants because absence of DRH-1-bound Dicer would increase Dicer pools? That DRH-1 is not involved in endosiRNA production is consistent with a specific role for DRH-3 in bringing Dicer onto endosiRNA substrates. If the answer to the initial question is yes, this could support the scenario for the possible benefit of the drh-1 deletion in a significant fraction of the wild accessions because of enhanced environmental RNAi (which may confer unknown fitness advantages).
The reviewers have raised an interesting point. We therefore performed RNAi experiments using a dilution series of unc-22 RNAi (see Materials and methods) and found that exo-RNAi is not enhanced in drh-1 mutants, while it is enhanced in eri-1 mutants. We conclude that there is no evidence that DCR-1 interaction with RDE-4 and DRH-1 limits its availability for exo-RNAi. We have included this data as Figure 4–figure supplement 4. We also added a discussion point to the Discussion.
3) A critical experiment for supporting the proposed model would be whether the naturally found truncated form of DRH-1 indeed fails to interact with DCR-1 and RDE-4. We understand that antibodies are not available to test this. Thus, mechanistic inferences about DRH-1 action should be toned down in the revision.
The truncated DRH-1 (nDf250) might fail to interact with RDE-4/DRH-1, the Orsay RNA, or both. By analogy to RIG-I we suggest that DRH-1 (niDf250) fails to recognize the Orsay RNA. However, we agree with the reviewers: we have toned down our mechanistic inferences by suggesting that DRH-1 may be necessary for either recognition of viral RNA or correct Dicer processing “assisting DCR-1 processing of the double-stranded viral RNA.”https://doi.org/10.7554/eLife.00994.022
- Jérémie Le Pen
- Eric A Miska
- Eric A Miska
- Eric A Miska
- Marie-Anne Félix
- Tony Bélicard
- Marie-Anne Félix
- Lise Frézal
- Marie-Anne Félix
- Marie-Anne Félix
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We thank M Tanguy and J Rehwinkel for critical insights into viral biology, C Bradshaw and G Allen for Bioinformatics support and S Moss, I Nuez and A Richaud for laboratory management. We are grateful to C Franz and the D Wang laboratory for viral filtrate preparations, to E Andersen for help with the whole-genome association, and to M De Bono for reagents. Some strains were provided by the CGC, which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440). Some deletion mutations were provided by the International C. elegans Gene Knockout Consortium which is funded by the National Institute of Health, the Canadian Institute for Health Research, Genome Canada, Genome BC, and the Michael Smith Foundation. Fosmids were provided by D Moerman laboratory. AA was supported by a Herchel-Smith postdoctoral fellowship. PS was supported by a research fellowship at Gonville and Caius College, Cambridge.
- Detlef Weigel, Max Planck Institute for Developmental Biology, Germany
- Received: May 24, 2013
- Accepted: August 20, 2013
- Version of Record published: October 8, 2013 (version 1)
© 2013, Ashe 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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