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Serologic Evidence of Frequent Human Infection with WU and KI Polyomaviruses

WU polyomavirus (WUPyV) and KI polyomavirus (KIPyV) are novel human polyomaviruses. They were originally identified in human respiratory secretions, but the extent of human infection caused by these viruses has not been described to date. To determine the seroepidemiology of WUPyV and KIpyIV, we use...

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Autores principales: Nguyen, Nang L., Le, Binh-Minh, Wang, David
Formato: Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2815979/
https://www.ncbi.nlm.nih.gov/pubmed/19751580
http://dx.doi.org/10.3201/eid1508.090270
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author Nguyen, Nang L.
Le, Binh-Minh
Wang, David
author_facet Nguyen, Nang L.
Le, Binh-Minh
Wang, David
author_sort Nguyen, Nang L.
collection PubMed
description WU polyomavirus (WUPyV) and KI polyomavirus (KIPyV) are novel human polyomaviruses. They were originally identified in human respiratory secretions, but the extent of human infection caused by these viruses has not been described to date. To determine the seroepidemiology of WUPyV and KIpyIV, we used an ELISA to screen serum samples from 419 patients at the St. Louis Children’s Hospital and Barnes-Jewish Hospital during 2007–2008. The age-stratified deidentified samples were examined for antibodies to the major capsid proteins of WUPyV and KIPyV. Seropositivity for each virus was similar; antibody levels were high in the youngest age group (<6 months), decreased to a nadir in the next age group (6 to <12 months), and then steadily increased with subsequent age groups, eventually reaching a plateau of ≈80% for WUPyV and ≈70% for KIPyV. These results demonstrate that both KIPyV and WUPyV cause widespread infection in the human population.
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spelling pubmed-28159792010-02-23 Serologic Evidence of Frequent Human Infection with WU and KI Polyomaviruses Nguyen, Nang L. Le, Binh-Minh Wang, David Emerg Infect Dis Research WU polyomavirus (WUPyV) and KI polyomavirus (KIPyV) are novel human polyomaviruses. They were originally identified in human respiratory secretions, but the extent of human infection caused by these viruses has not been described to date. To determine the seroepidemiology of WUPyV and KIpyIV, we used an ELISA to screen serum samples from 419 patients at the St. Louis Children’s Hospital and Barnes-Jewish Hospital during 2007–2008. The age-stratified deidentified samples were examined for antibodies to the major capsid proteins of WUPyV and KIPyV. Seropositivity for each virus was similar; antibody levels were high in the youngest age group (<6 months), decreased to a nadir in the next age group (6 to <12 months), and then steadily increased with subsequent age groups, eventually reaching a plateau of ≈80% for WUPyV and ≈70% for KIPyV. These results demonstrate that both KIPyV and WUPyV cause widespread infection in the human population. Centers for Disease Control and Prevention 2009-08 /pmc/articles/PMC2815979/ /pubmed/19751580 http://dx.doi.org/10.3201/eid1508.090270 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Research
Nguyen, Nang L.
Le, Binh-Minh
Wang, David
Serologic Evidence of Frequent Human Infection with WU and KI Polyomaviruses
title Serologic Evidence of Frequent Human Infection with WU and KI Polyomaviruses
title_full Serologic Evidence of Frequent Human Infection with WU and KI Polyomaviruses
title_fullStr Serologic Evidence of Frequent Human Infection with WU and KI Polyomaviruses
title_full_unstemmed Serologic Evidence of Frequent Human Infection with WU and KI Polyomaviruses
title_short Serologic Evidence of Frequent Human Infection with WU and KI Polyomaviruses
title_sort serologic evidence of frequent human infection with wu and ki polyomaviruses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2815979/
https://www.ncbi.nlm.nih.gov/pubmed/19751580
http://dx.doi.org/10.3201/eid1508.090270
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