Primate phageomes are structured by superhost phylogeny and environment.

Journal Article (Journal Article)

Humans harbor diverse communities of microorganisms, the majority of which are bacteria in the gastrointestinal tract. These gut bacterial communities in turn host diverse bacteriophage (hereafter phage) communities that have a major impact on their structure, function, and, ultimately, human health. However, the evolutionary and ecological origins of these human-associated phage communities are poorly understood. To address this question, we examined fecal phageomes of 23 wild nonhuman primate taxa, including multiple representatives of all the major primate radiations. We find relatives of the majority of human-associated phages in wild primates. Primate taxa have distinct phageome compositions that exhibit a clear phylosymbiotic signal, and phage-superhost codivergence is often detected for individual phages. Within species, neighboring social groups harbor compositionally and evolutionarily distinct phageomes, which are structured by superhost social behavior. Captive nonhuman primate phageome composition is intermediate between that of their wild counterparts and humans. Phage phylogenies reveal replacement of wild great ape-associated phages with human-associated ones in captivity and, surprisingly, show no signal for the persistence of wild-associated phages in captivity. Together, our results suggest that potentially labile primate-phage associations have persisted across millions of years of evolution. Across primates, these phylosymbiotic and sometimes codiverging phage communities are shaped by transmission between groupmates through grooming and are dramatically modified when primates are moved into captivity.

Full Text

Duke Authors

Cited Authors

  • Gogarten, JF; Rühlemann, M; Archie, E; Tung, J; Akoua-Koffi, C; Bang, C; Deschner, T; Muyembe-Tamfun, J-J; Robbins, MM; Schubert, G; Surbeck, M; Wittig, RM; Zuberbühler, K; Baines, JF; Franke, A; Leendertz, FH; Calvignac-Spencer, S

Published Date

  • April 2021

Published In

Volume / Issue

  • 118 / 15

Start / End Page

  • e2013535118 -

PubMed ID

  • 33876746

Pubmed Central ID

  • PMC8053973

Electronic International Standard Serial Number (EISSN)

  • 1091-6490

International Standard Serial Number (ISSN)

  • 0027-8424

Digital Object Identifier (DOI)

  • 10.1073/pnas.2013535118


  • eng