Identification of a novel human polyomavirus in organs of the gastrointestinal tract

Polyomaviruses are small, non-enveloped viruses with a circular double-stranded DNA genome. Using a generic polyomavirus PCR targeting the VP1 major structural protein gene, a novel polyomavirus was initially identified in resected human liver tissue and provisionally named Human Polyomavirus 12 (HP...

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Published in:PloS one Vol. 8; no. 3; p. e58021
Main Authors: Korup, Sarah, Rietscher, Janita, Calvignac-Spencer, Sébastien, Trusch, Franziska, Hofmann, Jörg, Moens, Ugo, Sauer, Igor, Voigt, Sebastian, Schmuck, Rosa, Ehlers, Bernhard
Format: Journal Article
Language:English
Published: United States Public Library of Science 13-03-2013
Public Library of Science (PLoS)
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Summary:Polyomaviruses are small, non-enveloped viruses with a circular double-stranded DNA genome. Using a generic polyomavirus PCR targeting the VP1 major structural protein gene, a novel polyomavirus was initially identified in resected human liver tissue and provisionally named Human Polyomavirus 12 (HPyV12). Its 5033 bp genome is predicted to encode large and small T antigens and the 3 structural proteins VP1, VP2 and VP3. Phylogenetic analyses did not reveal a close relationship to any known human or animal polyomavirus. Investigation of organs, body fluids and excretions of diseased individuals and healthy subjects with both HPyV12-specific nested PCR and quantitative real-time PCR revealed additional virus-positive samples of resected liver, cecum and rectum tissues and a positive fecal sample. A capsomer-based IgG ELISA was established using the major capsid protein VP1 of HPyV12. Seroprevalences of 23% and 17%, respectively, were determined in sera from healthy adults and adolescents and a pediatric group of children. These data indicate that the virus naturally infects humans and that primary infection may already occur in childhood.
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: SK JR SCS FT JH IS SV RS UM BE. Performed the experiments: SK JR SCS FT JH SV RS. Analyzed the data: SK JR SCS FT JH UM IS SV RS BE. Contributed reagents/materials/analysis tools: JH SV RS BE. Wrote the paper: SK JR SCS FT JH UM SV RS BE.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0058021