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Discovery of a Novel Polyomavirus in Acute Diarrheal Samples from Children

Polyomaviruses are small circular DNA viruses associated with chronic infections and tumors in both human and animal hosts. Using an unbiased deep sequencing approach, we identified a novel, highly divergent polyomavirus, provisionally named MX polyomavirus (MXPyV), in stool samples from children. T...

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Autores principales: Yu, Guixia, Greninger, Alexander L., Isa, Pavel, Phan, Tung G., Martínez, Miguel Angel, de la Luz Sanchez, Maria, Contreras, Juan Francisco, Santos-Preciado, José Ignacio, Parsonnet, Julie, Miller, Steve, DeRisi, Joseph L., Delwart, Eric, Arias, Carlos F., Chiu, Charles Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498111/
https://www.ncbi.nlm.nih.gov/pubmed/23166671
http://dx.doi.org/10.1371/journal.pone.0049449
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author Yu, Guixia
Greninger, Alexander L.
Isa, Pavel
Phan, Tung G.
Martínez, Miguel Angel
de la Luz Sanchez, Maria
Contreras, Juan Francisco
Santos-Preciado, José Ignacio
Parsonnet, Julie
Miller, Steve
DeRisi, Joseph L.
Delwart, Eric
Arias, Carlos F.
Chiu, Charles Y.
author_facet Yu, Guixia
Greninger, Alexander L.
Isa, Pavel
Phan, Tung G.
Martínez, Miguel Angel
de la Luz Sanchez, Maria
Contreras, Juan Francisco
Santos-Preciado, José Ignacio
Parsonnet, Julie
Miller, Steve
DeRisi, Joseph L.
Delwart, Eric
Arias, Carlos F.
Chiu, Charles Y.
author_sort Yu, Guixia
collection PubMed
description Polyomaviruses are small circular DNA viruses associated with chronic infections and tumors in both human and animal hosts. Using an unbiased deep sequencing approach, we identified a novel, highly divergent polyomavirus, provisionally named MX polyomavirus (MXPyV), in stool samples from children. The ∼5.0 kB viral genome exhibits little overall homology (<46% amino acid identity) to known polyomaviruses, and, due to phylogenetic variation among its individual proteins, cannot be placed in any existing taxonomic group. PCR-based screening detected MXPyV in 28 of 834 (3.4%) fecal samples collected from California, Mexico, and Chile, and 1 of 136 (0.74%) of respiratory samples from Mexico, but not in blood or urine samples from immunocompromised patients. By quantitative PCR, the measured titers of MXPyV in human stool at 10% (weight/volume) were as high as 15,075 copies. No association was found between the presence of MXPyV and diarrhea, although girls were more likely to shed MXPyV in the stool than boys (p = 0.012). In one child, viral shedding was observed in two stools obtained 91 days apart, raising the possibility of chronic infection by MXPyV. A multiple sequence alignment revealed that MXPyV is a closely related variant of the recently reported MWPyV and HPyV10 polyomaviruses. Further studies will be important to determine the association, if any, of MXPyV with disease in humans.
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spelling pubmed-34981112012-11-19 Discovery of a Novel Polyomavirus in Acute Diarrheal Samples from Children Yu, Guixia Greninger, Alexander L. Isa, Pavel Phan, Tung G. Martínez, Miguel Angel de la Luz Sanchez, Maria Contreras, Juan Francisco Santos-Preciado, José Ignacio Parsonnet, Julie Miller, Steve DeRisi, Joseph L. Delwart, Eric Arias, Carlos F. Chiu, Charles Y. PLoS One Research Article Polyomaviruses are small circular DNA viruses associated with chronic infections and tumors in both human and animal hosts. Using an unbiased deep sequencing approach, we identified a novel, highly divergent polyomavirus, provisionally named MX polyomavirus (MXPyV), in stool samples from children. The ∼5.0 kB viral genome exhibits little overall homology (<46% amino acid identity) to known polyomaviruses, and, due to phylogenetic variation among its individual proteins, cannot be placed in any existing taxonomic group. PCR-based screening detected MXPyV in 28 of 834 (3.4%) fecal samples collected from California, Mexico, and Chile, and 1 of 136 (0.74%) of respiratory samples from Mexico, but not in blood or urine samples from immunocompromised patients. By quantitative PCR, the measured titers of MXPyV in human stool at 10% (weight/volume) were as high as 15,075 copies. No association was found between the presence of MXPyV and diarrhea, although girls were more likely to shed MXPyV in the stool than boys (p = 0.012). In one child, viral shedding was observed in two stools obtained 91 days apart, raising the possibility of chronic infection by MXPyV. A multiple sequence alignment revealed that MXPyV is a closely related variant of the recently reported MWPyV and HPyV10 polyomaviruses. Further studies will be important to determine the association, if any, of MXPyV with disease in humans. Public Library of Science 2012-11-14 /pmc/articles/PMC3498111/ /pubmed/23166671 http://dx.doi.org/10.1371/journal.pone.0049449 Text en © 2012 Yu 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
Yu, Guixia
Greninger, Alexander L.
Isa, Pavel
Phan, Tung G.
Martínez, Miguel Angel
de la Luz Sanchez, Maria
Contreras, Juan Francisco
Santos-Preciado, José Ignacio
Parsonnet, Julie
Miller, Steve
DeRisi, Joseph L.
Delwart, Eric
Arias, Carlos F.
Chiu, Charles Y.
Discovery of a Novel Polyomavirus in Acute Diarrheal Samples from Children
title Discovery of a Novel Polyomavirus in Acute Diarrheal Samples from Children
title_full Discovery of a Novel Polyomavirus in Acute Diarrheal Samples from Children
title_fullStr Discovery of a Novel Polyomavirus in Acute Diarrheal Samples from Children
title_full_unstemmed Discovery of a Novel Polyomavirus in Acute Diarrheal Samples from Children
title_short Discovery of a Novel Polyomavirus in Acute Diarrheal Samples from Children
title_sort discovery of a novel polyomavirus in acute diarrheal samples from children
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498111/
https://www.ncbi.nlm.nih.gov/pubmed/23166671
http://dx.doi.org/10.1371/journal.pone.0049449
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