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Epidemiological and molecular analysis of human norovirus infections in Taiwan during 2011 and 2012
BACKGROUND: The human norovirus (NV) circulates worldwide and is a major cause of epidemics, which have increased in Taiwan since 2002. NV in acute gastroenteritis (AGE) and non-acute gastroenteritis (asymptomatic) patients, including children and adults, have not been previously examined in Taiwan;...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725169/ https://www.ncbi.nlm.nih.gov/pubmed/23875971 http://dx.doi.org/10.1186/1471-2334-13-338 |
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author | Tang, Meng-Bin Chen, Chien-Hsien Chen, Shou-Chien Chou, Yu-Ching Yu, Chia-Peng |
author_facet | Tang, Meng-Bin Chen, Chien-Hsien Chen, Shou-Chien Chou, Yu-Ching Yu, Chia-Peng |
author_sort | Tang, Meng-Bin |
collection | PubMed |
description | BACKGROUND: The human norovirus (NV) circulates worldwide and is a major cause of epidemics, which have increased in Taiwan since 2002. NV in acute gastroenteritis (AGE) and non-acute gastroenteritis (asymptomatic) patients, including children and adults, have not been previously examined in Taiwan; therefore, we examined the epidemiology and phylogeny of NV in AGE and asymptomatic patients of all ages. METHODS: 253 stool samples were collected from August 2011 to July 2012 (including 155 AGE and 98 asymptomatic samples in Taiwan) and analyzed using reverse transcription-polymerase chain reaction (RT-PCR) for NV. Primers targeting the RNA-polymerase gene were used for RT-PCR to allow DNA sequencing of Taiwan NV strains and phylogenetic analyses. RESULTS: NV was detected in 24 (9.5%) of 253 stool specimens using RT-PCR. NV was isolated from all age groups (1 to 86 y) and those NV-positive samples were major identified from inpatients (79.2%, 19/24). Statistical analysis showed that the NV infectious rate of AGE patients was statistically significant (P < 0.05) for age, season and water type, respectively. Phylogenetic analyses of the RdRp region sequence showed that 24 NV isolates belonged to Genogroup II Genotype 4 (GII.4). They were closely related to the epidemic strain in Taiwan in 2006, the GII.4-2006b pandemic strain in 2006, and the GII.4-New Orleans strain in 2010. CONCLUSION: This study is the first to examine NV in sporadic AGE and asymptomatic patients in Taiwan. Furthermore, epidemic strains of isolated GII.4 were predominant in Taiwan during 2011 and 2012. |
format | Online Article Text |
id | pubmed-3725169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37251692013-07-28 Epidemiological and molecular analysis of human norovirus infections in Taiwan during 2011 and 2012 Tang, Meng-Bin Chen, Chien-Hsien Chen, Shou-Chien Chou, Yu-Ching Yu, Chia-Peng BMC Infect Dis Research Article BACKGROUND: The human norovirus (NV) circulates worldwide and is a major cause of epidemics, which have increased in Taiwan since 2002. NV in acute gastroenteritis (AGE) and non-acute gastroenteritis (asymptomatic) patients, including children and adults, have not been previously examined in Taiwan; therefore, we examined the epidemiology and phylogeny of NV in AGE and asymptomatic patients of all ages. METHODS: 253 stool samples were collected from August 2011 to July 2012 (including 155 AGE and 98 asymptomatic samples in Taiwan) and analyzed using reverse transcription-polymerase chain reaction (RT-PCR) for NV. Primers targeting the RNA-polymerase gene were used for RT-PCR to allow DNA sequencing of Taiwan NV strains and phylogenetic analyses. RESULTS: NV was detected in 24 (9.5%) of 253 stool specimens using RT-PCR. NV was isolated from all age groups (1 to 86 y) and those NV-positive samples were major identified from inpatients (79.2%, 19/24). Statistical analysis showed that the NV infectious rate of AGE patients was statistically significant (P < 0.05) for age, season and water type, respectively. Phylogenetic analyses of the RdRp region sequence showed that 24 NV isolates belonged to Genogroup II Genotype 4 (GII.4). They were closely related to the epidemic strain in Taiwan in 2006, the GII.4-2006b pandemic strain in 2006, and the GII.4-New Orleans strain in 2010. CONCLUSION: This study is the first to examine NV in sporadic AGE and asymptomatic patients in Taiwan. Furthermore, epidemic strains of isolated GII.4 were predominant in Taiwan during 2011 and 2012. BioMed Central 2013-07-22 /pmc/articles/PMC3725169/ /pubmed/23875971 http://dx.doi.org/10.1186/1471-2334-13-338 Text en Copyright © 2013 Tang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tang, Meng-Bin Chen, Chien-Hsien Chen, Shou-Chien Chou, Yu-Ching Yu, Chia-Peng Epidemiological and molecular analysis of human norovirus infections in Taiwan during 2011 and 2012 |
title | Epidemiological and molecular analysis of human norovirus infections in Taiwan during 2011 and 2012 |
title_full | Epidemiological and molecular analysis of human norovirus infections in Taiwan during 2011 and 2012 |
title_fullStr | Epidemiological and molecular analysis of human norovirus infections in Taiwan during 2011 and 2012 |
title_full_unstemmed | Epidemiological and molecular analysis of human norovirus infections in Taiwan during 2011 and 2012 |
title_short | Epidemiological and molecular analysis of human norovirus infections in Taiwan during 2011 and 2012 |
title_sort | epidemiological and molecular analysis of human norovirus infections in taiwan during 2011 and 2012 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725169/ https://www.ncbi.nlm.nih.gov/pubmed/23875971 http://dx.doi.org/10.1186/1471-2334-13-338 |
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