Nov. 17, 2010 The types of gut bacteria that populate the guts of primates depend on the species of the host as well as where the host lives and what they eat. A study led by Howard Ochman at Yale University examines the gut microbial communities in great apes, showing that a host's species, rather than their diet, has the greatest effect on gut bacteria diversity.
These findings will publish next week in the online, open access journal PLoS Biology.
"Bacteria are crucial to human health. They enhance the immune system, protect against toxins, and assist in the maturation and renewal of intestinal cells," says Ochman. Gut microbes outnumber our own cells by 10 to 1 but little is known about how certain species come to populate our stomachs, which are sterile at birth. What causes this variation within microbial communities has been a matter of debate. Some scientists have argued that diet and habitat play the most prominent roles. However, Ochman and colleagues found that diversity in the composition of these gut communities, not including those occasional transients and unwelcome visitors such as pathogenic bacteria, depends primarily upon the host species.
Using genetic markers, the team measured the diversity and abundance of various microbial species found in fecal matter of five great ape species collected in their native ranges and discovered that bacterial populations assorted to species. Moreover, the relationships of the microbial communities matched that of their host. In other words, not only is it possible to differentiate chimpanzees from humans by examining the microbial populations within their guts, but these gut microbes have been tracking the evolution of their hosts for millions of years.
Funding: This work was supported in part by National Institutes of Health grants GM56120 and GM74735 to HO; AI065371 to MW; and AI50529, AI58715, and AI27767 to BHH.
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- Ochman H, Worobey M, Kuo C-H, Ndjango J-BN, Peeters M, et al. Evolutionary Relationships of Wild Hominids Recapitulated by Gut Microbial Communities. PLoS Biol, 8(11): e1000546 DOI: 10.1371/journal.pbio.1000546
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