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Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam

Respiratory syncytial virus (RSV) is a major cause of acute respiratory infections (ARIs) in children worldwide and can cause high mortality, especially in developing countries. However, information on the clinical and molecular characteristics of RSV infection in developing countries is limited. Fr...

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Autores principales: Tran, Dinh Nguyen, Pham, Thi Minh Hong, Ha, Manh Tuan, Tran, Thi Thu Loan, Dang, Thi Kim Huyen, Yoshida, Lay-Myint, Okitsu, Shoko, Hayakawa, Satoshi, Mizuguchi, Masashi, Ushijima, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551923/
https://www.ncbi.nlm.nih.gov/pubmed/23349659
http://dx.doi.org/10.1371/journal.pone.0045436
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author Tran, Dinh Nguyen
Pham, Thi Minh Hong
Ha, Manh Tuan
Tran, Thi Thu Loan
Dang, Thi Kim Huyen
Yoshida, Lay-Myint
Okitsu, Shoko
Hayakawa, Satoshi
Mizuguchi, Masashi
Ushijima, Hiroshi
author_facet Tran, Dinh Nguyen
Pham, Thi Minh Hong
Ha, Manh Tuan
Tran, Thi Thu Loan
Dang, Thi Kim Huyen
Yoshida, Lay-Myint
Okitsu, Shoko
Hayakawa, Satoshi
Mizuguchi, Masashi
Ushijima, Hiroshi
author_sort Tran, Dinh Nguyen
collection PubMed
description Respiratory syncytial virus (RSV) is a major cause of acute respiratory infections (ARIs) in children worldwide and can cause high mortality, especially in developing countries. However, information on the clinical and molecular characteristics of RSV infection in developing countries is limited. From April 2010 to May 2011, 1,082 nasopharyngeal swabs were collected from children with ARI admitted to the Children's Hospital 2, Ho Chi Minh City, Vietnam. Samples were screened for RSV and genotyped by reverse transcription-PCR and sequencing. Demographic and clinical data was also recorded. RSV was found in 23.8% (257/1,082) of samples. RSV A was the dominant subgroup, accounting for 91.4% (235/257), followed by RSV B, 5.1% (13/257), and 9 cases (3.5%) were mixed infection of these subgroups. The phylogenetic analysis revealed that all group A strains belonged to the GA2 genotype. All group B strains belonged to the recently identified BA genotype, and further clustered into 2 recently described subgenotypes BA9 and BA10. One GA2 genotype strain had a premature stop codon which shortened the G protein length. RSV infection was significantly associated with younger age and higher severity score than those without. Co-infection with other viruses did not affect disease severity. RSV A caused more severe disease than RSV B. The results from this study will not only contribute to the growing database on the molecular diversity of RSV circulating worldwide but may be also useful in clinical management and vaccine development.
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spelling pubmed-35519232013-01-24 Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam Tran, Dinh Nguyen Pham, Thi Minh Hong Ha, Manh Tuan Tran, Thi Thu Loan Dang, Thi Kim Huyen Yoshida, Lay-Myint Okitsu, Shoko Hayakawa, Satoshi Mizuguchi, Masashi Ushijima, Hiroshi PLoS One Research Article Respiratory syncytial virus (RSV) is a major cause of acute respiratory infections (ARIs) in children worldwide and can cause high mortality, especially in developing countries. However, information on the clinical and molecular characteristics of RSV infection in developing countries is limited. From April 2010 to May 2011, 1,082 nasopharyngeal swabs were collected from children with ARI admitted to the Children's Hospital 2, Ho Chi Minh City, Vietnam. Samples were screened for RSV and genotyped by reverse transcription-PCR and sequencing. Demographic and clinical data was also recorded. RSV was found in 23.8% (257/1,082) of samples. RSV A was the dominant subgroup, accounting for 91.4% (235/257), followed by RSV B, 5.1% (13/257), and 9 cases (3.5%) were mixed infection of these subgroups. The phylogenetic analysis revealed that all group A strains belonged to the GA2 genotype. All group B strains belonged to the recently identified BA genotype, and further clustered into 2 recently described subgenotypes BA9 and BA10. One GA2 genotype strain had a premature stop codon which shortened the G protein length. RSV infection was significantly associated with younger age and higher severity score than those without. Co-infection with other viruses did not affect disease severity. RSV A caused more severe disease than RSV B. The results from this study will not only contribute to the growing database on the molecular diversity of RSV circulating worldwide but may be also useful in clinical management and vaccine development. Public Library of Science 2013-01-22 /pmc/articles/PMC3551923/ /pubmed/23349659 http://dx.doi.org/10.1371/journal.pone.0045436 Text en © 2013 Tran 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
Tran, Dinh Nguyen
Pham, Thi Minh Hong
Ha, Manh Tuan
Tran, Thi Thu Loan
Dang, Thi Kim Huyen
Yoshida, Lay-Myint
Okitsu, Shoko
Hayakawa, Satoshi
Mizuguchi, Masashi
Ushijima, Hiroshi
Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam
title Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam
title_full Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam
title_fullStr Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam
title_full_unstemmed Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam
title_short Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam
title_sort molecular epidemiology and disease severity of human respiratory syncytial virus in vietnam
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551923/
https://www.ncbi.nlm.nih.gov/pubmed/23349659
http://dx.doi.org/10.1371/journal.pone.0045436
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