期刊
PLOS PATHOGENS
卷 17, 期 11, 页码 -出版社
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.ppat.1009675
关键词
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资金
- Bundesministerium fur Bildung und Forschung SuLaMa/BMBF [FKZ 01LL0914]
- Deutsche Forschungsgemeinschaft, DFG [SPP 1596, Ga 342/19-1]
Recent studies have shown that MHC gene diversity can indirectly influence host health by shaping the bacterial community, which in turn affects immune responses to parasite infections. Research on non-human primates in Madagascar found that both MHC class I and II gene diversity impacted the composition of the gut microbiota, which further predicted the likelihood of adenovirus and helminth infections. This highlights the importance of considering the microbiome in understanding parasite-mediated MHC selection.
Until recently, the study of major histocompability complex (MHC) mediated immunity has focused on the direct link between MHC diversity and susceptibility to parasite infection. However, MHC genes can also influence host health indirectly through the sculpting of the bacterial community that in turn shape immune responses. We investigated the links between MHC class I and II gene diversity gut microbiome diversity and micro- (adenovirus, AdV) and macro- (helminth) parasite infection probabilities in a wild population of non-human primates, mouse lemurs of Madagascar. This setup encompasses a plethora of underlying interactions between parasites, microbes and adaptive immunity in natural populations. Both MHC classes explained shifts in microbiome composition and the effect was driven by a few select microbial taxa. Among them were three taxa (Odoribacter, Campylobacter and Prevotellaceae-UCG-001) which were in turn linked to AdV and helminth infection status, correlative evidence of the indirect effect of the MHC via the microbiome. Our study provides support for the coupled role of MHC diversity and microbial flora as contributing factors of parasite infection. Author summary The selective pressure of the major histocompatibility complex (MHC) on microbial communities, and the potential role of this interaction in driving parasite resistance has been largely neglected. Using a natural population of the primate Microcebus griseorufus, we provide correlative evidence of two outstanding findings: that MHCI and MHCII diversity shapes the composition of the gut microbiota; and that select taxa associated with MHC diversity predicted adenovirus and helminth infection status. Our study highlights the importance of incorporating the microbiome when investigating parasite-mediated MHC selection.
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