The evolutionary origins of human-associated bacteriophage communities are poorly understood.To address this question, we examined fecal phageomes of 23 wild non-human primate taxa, including multiple representatives of all the major primate radiations, and find relatives of the majority of human-associated phages. Primate taxa have distinct phageome compositions that exhibit a clear phylosymbiotic signal, and phage-superhost co-divergence is detected for 44 individual phages. Within species, neighboring social groups harbor evolutionarily and compositionally distinct phageomes, structured by superhost social behavior. However, captive non-human primate phageomes are more similar to humans than their wild counterparts, revealing replacement of wild-associated phages with human-associated ones. Together, our results suggest that potentially labile primate-phage associations persisted across millions of years of evolution, potentially facilitated by transmission between groupmates.
One Sentence Summary:Relatives of human-associated phages in wild primates reveal ancient but dynamic superhostphage associations shaped by social transmission.
Main Text:Mammals harbor diverse communities of microorganisms, the majority of which are bacteria in the gastrointestinal tract. Gut bacterial communities in turn host diverse bacteriophage communities that influence their structure, function, colonization patterns, and ultimately superhost health (the superhost is the host for bacteria that in turn host the bacteriophages; 1).