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The Fecal Viral Flora of Wild Rodents

The frequent interactions of rodents with humans make them a common source of zoonotic infections. To obtain an initial unbiased measure of the viral diversity in the enteric tract of wild rodents we sequenced partially purified, randomly amplified viral RNA and DNA in the feces of 105 wild rodents...

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Autores principales: Phan, Tung G., Kapusinszky, Beatrix, Wang, Chunlin, Rose, Robert K., Lipton, Howard L., Delwart, Eric L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164639/
https://www.ncbi.nlm.nih.gov/pubmed/21909269
http://dx.doi.org/10.1371/journal.ppat.1002218
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author Phan, Tung G.
Kapusinszky, Beatrix
Wang, Chunlin
Rose, Robert K.
Lipton, Howard L.
Delwart, Eric L.
author_facet Phan, Tung G.
Kapusinszky, Beatrix
Wang, Chunlin
Rose, Robert K.
Lipton, Howard L.
Delwart, Eric L.
author_sort Phan, Tung G.
collection PubMed
description The frequent interactions of rodents with humans make them a common source of zoonotic infections. To obtain an initial unbiased measure of the viral diversity in the enteric tract of wild rodents we sequenced partially purified, randomly amplified viral RNA and DNA in the feces of 105 wild rodents (mouse, vole, and rat) collected in California and Virginia. We identified in decreasing frequency sequences related to the mammalian viruses families Circoviridae, Picobirnaviridae, Picornaviridae, Astroviridae, Parvoviridae, Papillomaviridae, Adenoviridae, and Coronaviridae. Seventeen small circular DNA genomes containing one or two replicase genes distantly related to the Circoviridae representing several potentially new viral families were characterized. In the Picornaviridae family two new candidate genera as well as a close genetic relative of the human pathogen Aichi virus were characterized. Fragments of the first mouse sapelovirus and picobirnaviruses were identified and the first murine astrovirus genome was characterized. A mouse papillomavirus genome and fragments of a novel adenovirus and adenovirus-associated virus were also sequenced. The next largest fraction of the rodent fecal virome was related to insect viruses of the Densoviridae, Iridoviridae, Polydnaviridae, Dicistroviriade, Bromoviridae, and Virgaviridae families followed by plant virus-related sequences in the Nanoviridae, Geminiviridae, Phycodnaviridae, Secoviridae, Partitiviridae, Tymoviridae, Alphaflexiviridae, and Tombusviridae families reflecting the largely insect and plant rodent diet. Phylogenetic analyses of full and partial viral genomes therefore revealed many previously unreported viral species, genera, and families. The close genetic similarities noted between some rodent and human viruses might reflect past zoonoses. This study increases our understanding of the viral diversity in wild rodents and highlights the large number of still uncharacterized viruses in mammals.
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spelling pubmed-31646392011-09-09 The Fecal Viral Flora of Wild Rodents Phan, Tung G. Kapusinszky, Beatrix Wang, Chunlin Rose, Robert K. Lipton, Howard L. Delwart, Eric L. PLoS Pathog Research Article The frequent interactions of rodents with humans make them a common source of zoonotic infections. To obtain an initial unbiased measure of the viral diversity in the enteric tract of wild rodents we sequenced partially purified, randomly amplified viral RNA and DNA in the feces of 105 wild rodents (mouse, vole, and rat) collected in California and Virginia. We identified in decreasing frequency sequences related to the mammalian viruses families Circoviridae, Picobirnaviridae, Picornaviridae, Astroviridae, Parvoviridae, Papillomaviridae, Adenoviridae, and Coronaviridae. Seventeen small circular DNA genomes containing one or two replicase genes distantly related to the Circoviridae representing several potentially new viral families were characterized. In the Picornaviridae family two new candidate genera as well as a close genetic relative of the human pathogen Aichi virus were characterized. Fragments of the first mouse sapelovirus and picobirnaviruses were identified and the first murine astrovirus genome was characterized. A mouse papillomavirus genome and fragments of a novel adenovirus and adenovirus-associated virus were also sequenced. The next largest fraction of the rodent fecal virome was related to insect viruses of the Densoviridae, Iridoviridae, Polydnaviridae, Dicistroviriade, Bromoviridae, and Virgaviridae families followed by plant virus-related sequences in the Nanoviridae, Geminiviridae, Phycodnaviridae, Secoviridae, Partitiviridae, Tymoviridae, Alphaflexiviridae, and Tombusviridae families reflecting the largely insect and plant rodent diet. Phylogenetic analyses of full and partial viral genomes therefore revealed many previously unreported viral species, genera, and families. The close genetic similarities noted between some rodent and human viruses might reflect past zoonoses. This study increases our understanding of the viral diversity in wild rodents and highlights the large number of still uncharacterized viruses in mammals. Public Library of Science 2011-09-01 /pmc/articles/PMC3164639/ /pubmed/21909269 http://dx.doi.org/10.1371/journal.ppat.1002218 Text en Phan et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Phan, Tung G.
Kapusinszky, Beatrix
Wang, Chunlin
Rose, Robert K.
Lipton, Howard L.
Delwart, Eric L.
The Fecal Viral Flora of Wild Rodents
title The Fecal Viral Flora of Wild Rodents
title_full The Fecal Viral Flora of Wild Rodents
title_fullStr The Fecal Viral Flora of Wild Rodents
title_full_unstemmed The Fecal Viral Flora of Wild Rodents
title_short The Fecal Viral Flora of Wild Rodents
title_sort fecal viral flora of wild rodents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164639/
https://www.ncbi.nlm.nih.gov/pubmed/21909269
http://dx.doi.org/10.1371/journal.ppat.1002218
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