Authors

Sébastien Calvignac-Spencer, Robert Koch-Institut
Sripriya Murthy, Robert Koch-Institut
Kathryn O’Brien, University of Plymouth
Anthony Agbor, African Parks Network
Samuel Angedakin, Max Planck Institute for Evolutionary Anthropology
Mimi Arandjelovic, Max Planck Institute for Evolutionary Anthropology
Emmanuel Ayuk Ayimisin, Max Planck Institute for Evolutionary Anthropology
Emma Bailey, Max Planck Institute for Evolutionary Anthropology
Richard A. Bergl, North Carolina Zoological Park
Gregory Brazzola, Max Planck Institute for Evolutionary Anthropology
Paula Dieguez, Max Planck Institute for Evolutionary Anthropology
Manasseh Eno-Nku, WWF Cameroon
Henk Eshuis, Max Planck Institute for Evolutionary Anthropology
Barbara Fruth, Liverpool John Moores University
Thomas R. Gillespie, Emory University
Yisa Ginath, Max Planck Institute for Evolutionary Anthropology
Maryke Gray, Batavia Coast Maritime Institute
Ilka Herbinger, World Wildlife Fund (WWF) Germany
Sorrel Jones, Max Planck Institute for Evolutionary Anthropology
Laura Kehoe, University of British Columbia
Hjalmar Kühl, German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig
Deo Kujirakwinja, Wildlife Conservation Society
Kevin Lee, Arizona State University
Nadège F. Madinda, Max Planck Institute for Evolutionary Anthropology
Guillain Mitamba, Wildlife Conservation Society
Emmanuel Muhindo, Wildlife Conservation Society
Radar Nishuli, Institut Congolais pour la Conservation de la Nature
Lucy J. Ormsby, Max Planck Institute for Evolutionary Anthropology
Klara J. Petrzelkova, Czech Academy of Sciences
Andrew J. Plumptre, BirdLife International
Volker Sommer
Heegde M Ter
Angelique Todd
Raymond Tokunda
Erin Wessling
Michael A. Jarvis
Fabian H. Leendertz
Bernhard Ehlers
Sébastien Calvignac-Spencer

Abstract

Herpesviruses are thought to have evolved in very close association with their hosts. This is notably the case for cytomegaloviruses (CMVs; genus Cytomegalovirus) infecting primates, which exhibit a strong signal of co-divergence with their hosts. Some herpesviruses are however known to have crossed species barriers. Based on a limited sampling of CMV diversity in the hominine (African great ape and human) lineage, we hypothesized that chimpanzees and gorillas might have mutually exchanged CMVs in the past. Here, we performed a comprehensive molecular screening of all 9 African great ape species/subspecies, using 675 fecal samples collected from wild animals. We identified CMVs in eight species/subspecies, notably generating the first CMV sequences from bonobos. We used this extended dataset to test competing hypotheses with various degrees of co-divergence/number of host switches while simultaneously estimating the dates of these events in a Bayesian framework. The model best supported by the data involved the transmission of a gorilla CMV to the panine (chimpanzee and bonobo) lineage and the transmission of a panine CMV to the gorilla lineage prior to the divergence of chimpanzees and bonobos, more than 800,000 years ago. Panine CMVs then co-diverged with their hosts. These results add to a growing body of evidence suggesting that viruses with a double-stranded DNA genome (including other herpesviruses, adenoviruses, and papillomaviruses) often jumped between hominine lineages over the last few million years.

Publication Date

2019-07-01

Publication Title

Virus Evolution

Volume

5

Issue

2

Embargo Period

2024-01-04

Keywords

cytomegalovirus, hominine, host switch, codivergence, dsDNA virus

10.1093/ve/vez015" data-hide-no-mentions="true">

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