Lifestyle and the presence of helminths is associated with gut microbiome composition in Cameroonians

Author:

Rubel Meagan A.,Abbas Arwa,Taylor Louis J.,Connell Andrew,Tanes Ceylan,Bittinger Kyle,Ndze Valantine N.,Fonsah Julius Y.,Ngwang Eric,Essiane André,Fokunang Charles,Njamnshi Alfred K.,Bushman Frederic D.,Tishkoff Sarah A.

Abstract

Abstract Background African populations provide a unique opportunity to interrogate host-microbe co-evolution and its impact on adaptive phenotypes due to their genomic, phenotypic, and cultural diversity. We integrate gut microbiome 16S rRNA amplicon and shotgun metagenomic sequence data with quantification of pathogen burden and measures of immune parameters for 575 ethnically diverse Africans from Cameroon. Subjects followed pastoralist, agropastoralist, and hunter-gatherer lifestyles and were compared to an urban US population from Philadelphia. Results We observe significant differences in gut microbiome composition across populations that correlate with subsistence strategy and country. After these, the variable most strongly associated with gut microbiome structure in Cameroonians is the presence of gut parasites. Hunter-gatherers have high frequencies of parasites relative to agropastoralists and pastoralists. Ascaris lumbricoides, Necator americanus, Trichuris trichiura, and Strongyloides stercoralis soil-transmitted helminths (“ANTS” parasites) significantly co-occur, and increased frequency of gut parasites correlates with increased gut microbial diversity. Gut microbiome composition predicts ANTS positivity with 80% accuracy. Colonization with ANTS, in turn, is associated with elevated levels of TH1, TH2, and proinflammatory cytokines, indicating an association with multiple immune mechanisms. The unprecedented size of this dataset allowed interrogation of additional questions—for example, we find that Fulani pastoralists, who consume high levels of milk, possess an enrichment of gut bacteria that catabolize galactose, an end product of lactose metabolism, and of bacteria that metabolize lipids. Conclusions These data document associations of bacterial microbiota and eukaryotic parasites with each other and with host immune responses; each of these is further correlated with subsistence practices.

Funder

National Science Foundation

Wenner-Gren Foundation

National Institutes of Health

University of Pennsylvania

The Louis and Clark Fund

Penn Center for AIDS Research

PennCHoP Microbiome Program

Leakey Foundation

Publisher

Springer Science and Business Media LLC

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