Molecular ecology and natural history of simian foamy virus infection in wild-living chimpanzees.

Weimin Liu1 Michael Worobey Yingying Li Brandon F Keele Frederic Bibollet-Ruche Yuanyuan Guo Paul A Goepfert Mario L Santiago Jean-Bosco N Ndjango Cecile Neel Stephen L Clifford Crickette Sanz Shadrack Kamenya Michael L Wilson Anne E Pusey Nicole Gross-Camp Christophe Boesch Vince Smith Koichiro Zamma Michael A Huffman John C Mitani David P Watts Martine Peeters George M Shaw William M Switzer Paul M Sharp Beatrice H Hahn
Affiliations 1 institutions
  1. Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.

Abstract

Identifying microbial pathogens with zoonotic potential in wild-living primates can be important to human health, as evidenced by human immunodeficiency viruses types 1 and 2 (HIV-1 and HIV-2) and Ebola virus. Simian foamy viruses (SFVs) are ancient retroviruses that infect Old and New World monkeys and apes. Although not known to cause disease, these viruses are of public health interest because they have the potential to infect humans and thus provide a more general indication of zoonotic exposure risks. Surprisingly, no information exists concerning the prevalence, geographic distribution, and genetic diversity of SFVs in wild-living monkeys and apes. Here, we report the first comprehensive survey of SFVcpz infection in free-ranging chimpanzees (Pan troglodytes) using newly developed, fecal-based assays. Chimpanzee fecal samples (n = 724) were collected at 25 field sites throughout equatorial Africa and tested for SFVcpz-specific antibodies (n = 706) or viral nucleic acids (n = 392). SFVcpz infection was documented at all field sites, with prevalence rates ranging from 44% to 100%. In two habituated communities, adult chimpanzees had significantly higher SFVcpz infection rates than infants and juveniles, indicating predominantly horizontal rather than vertical transmission routes. Some chimpanzees were co-infected with simian immunodeficiency virus (SIVcpz); however, there was no evidence that SFVcpz and SIVcpz were epidemiologically linked. SFVcpz nucleic acids were recovered from 177 fecal samples, all of which contained SFVcpz RNA and not DNA. Phylogenetic analysis of partial gag (616 bp), pol-RT (717 bp), and pol-IN (425 bp) sequences identified a diverse group of viruses, which could be subdivided into four distinct SFVcpz lineages according to their chimpanzee subspecies of origin. Within these lineages, there was evidence of frequent superinfection and viral recombination. One chimpanzee was infected by a foamy virus from a Cercopithecus monkey species, indicating cross-species transmission of SFVs in the wild. These data indicate that SFVcpz (i) is widely distributed among all chimpanzee subspecies; (ii) is shed in fecal samples as viral RNA; (iii) is transmitted predominantly by horizontal routes; (iv) is prone to superinfection and recombination; (v) has co-evolved with its natural host; and (vi) represents a sensitive marker of population structure that may be useful for chimpanzee taxonomy and conservation strategies.

Supporting text Virus Host Location
Africa, Central 2 Animals 1948 Ape Diseases 7 Base Sequence 52 DNA, Mitochondrial 5 Ecology 6 Ecosystem 36 Feces 113 Genetics, Microbial 1 Humans 1440 Molecular Sequence Data 160 Pan troglodytes 20 Phylogeny 805 Retroviridae Infections 17 Simian foamy virus 8

Evidence records

6 total
Zoonotic Surveillance
3 records · 3 evidence types
Evidence type
1 records
OVE584
Key finding

SFVcpz viral RNA was detected in fecal samples from free-ranging chimpanzees across equatorial Africa.

Virus
Host
Location
Supporting text

Here, we report the first comprehensive survey of SFVcpz infection in free-ranging chimpanzees (Pan troglodytes) using newly developed, fecal-based assays. Chimpanzee fecal samples (n = 724) were collected at 25 field sites throughout equatorial Africa and tested for SFVcpz-specific antibodies (n = 706) or viral nucleic acids (n = 392).

Method
fecal-based assays | nucleic acid detection
Sample type
fecal samples
Geographic raw
equatorial Africa
Evidence type
1 records
OVE585
Key finding

Chimpanzee fecal samples collected across equatorial Africa showed SFVcpz-specific antibody signals indicating prior viral exposure in wild populations.

Virus
Host
Location
Not specified
Supporting text

Chimpanzee fecal samples (n = 724) were collected at 25 field sites throughout equatorial Africa and tested for SFVcpz-specific antibodies (n = 706).

Method
antibody testing | serological assay for SFVcpz-specific antibodies
Sample type
fecal samples
Evidence type
1 records
OVE586
Key finding

SFVcpz is widely distributed among all subspecies of wild chimpanzees throughout equatorial Africa, supporting its role as a long-term natural reservoir in these populations.

Virus
Host
Location
Supporting text

Chimpanzee fecal samples (n = 724) were collected at 25 field sites throughout equatorial Africa and tested for SFVcpz-specific antibodies (n = 706) or viral nucleic acids (n = 392). SFVcpz infection was documented at all field sites, with prevalence rates ranging from 44% to 100%.

Method
fecal-based assays | antibody detection | viral RNA detection | phylogenetic analysis
Sample type
fecal samples
Geographic raw
equatorial Africa
Transmission Evidence
1 records · 1 evidence types
Evidence type
1 records
OVE587
Key finding

A foamy virus originating from a Cercopithecus monkey species infected a wild chimpanzee, demonstrating natural cross-species transmission among non-human primates.

Virus
Host
Location
Supporting text

One chimpanzee was infected by a foamy virus from a Cercopithecus monkey species, indicating cross-species transmission of SFVs in the wild.

Method
fecal-based viral nucleic acid detection | phylogenetic analysis of gag, pol-RT, and pol-IN sequences
Study design
field surveillance and phylogenetic analysis
Transmission direction
animal-to-animal
Geographic raw
wild
Genomic Evolution
2 records · 2 evidence types
Evidence type
1 records
OVE589
Key finding

Simian foamy viruses infecting chimpanzees (SFVcpz) show frequent recombination among viral lineages based on sequence analysis.

Virus
Host
Not specified
Location
Not specified
Supporting text

Within these lineages, there was evidence of frequent superinfection and viral recombination.

Event type
recombination
Genes or segments
gag | pol-RT | pol-IN
Evidence type
1 records
OVE588
Key finding

Phylogenetic analysis of SFVcpz sequences revealed four distinct viral lineages corresponding to chimpanzee subspecies.

Virus
Host
Location
Not specified
Supporting text

Phylogenetic analysis of partial gag (616 bp), pol-RT (717 bp), and pol-IN (425 bp) sequences identified a diverse group of viruses, which could be subdivided into four distinct SFVcpz lineages according to their chimpanzee subspecies of origin.

Genes or proteins
gag | pol-RT | pol-IN
Analysis methods
phylogenetic analysis