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Full-Genomic Analysis of a Human Norovirus Recombinant GII.12/13 Novel Strain Isolated from South Korea

Norovirus (NoV) genogroups I and II are frequently recognized as the main causes of acute gastroenteritis and outbreaks of non-bacterial foodborne diseases. Furthermore, variants and recombinant strains of this virus are continuously emerging worldwide. The aim of this study was to identify NoV stra...

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Autores principales: Won, Yu-Jung, Park, Jeong-Woong, Han, Sang-ha, Cho, Han-Gil, Kang, Lae-Hyung, Lee, Sung-Geun, Ryu, Sang-Ryeol, Paik, Soon-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877344/
https://www.ncbi.nlm.nih.gov/pubmed/24391985
http://dx.doi.org/10.1371/journal.pone.0085063
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author Won, Yu-Jung
Park, Jeong-Woong
Han, Sang-ha
Cho, Han-Gil
Kang, Lae-Hyung
Lee, Sung-Geun
Ryu, Sang-Ryeol
Paik, Soon-Young
author_facet Won, Yu-Jung
Park, Jeong-Woong
Han, Sang-ha
Cho, Han-Gil
Kang, Lae-Hyung
Lee, Sung-Geun
Ryu, Sang-Ryeol
Paik, Soon-Young
author_sort Won, Yu-Jung
collection PubMed
description Norovirus (NoV) genogroups I and II are frequently recognized as the main causes of acute gastroenteritis and outbreaks of non-bacterial foodborne diseases. Furthermore, variants and recombinant strains of this virus are continuously emerging worldwide. The aim of this study was to identify NoV strains and to investigate and characterize rare genotypes. Stool samples (n = 500) were collected from patients with symptoms of acute gastroenteritis in Korea between December 2004 and November 2007. For analysis of the samples, rapid genotype screening was performed using reverse transcriptase-polymerase chain reaction. Full sequencing, using a newly designed set of 12 primers, revealed GII-12/13 strain. The partial sequence of GII-12/13 strain was compared with published NoV (GII-1 - 14) sequences targeting RdRp and capsid regions using phylogenetic analysis with the SimPlot program, which could evaluate recombination breakpoints. SimPlot analysis was also performed with the strain GII-12/Gifu-96/JPN (AB045603) for the RdRp region and with GII-13/G5175B-83/AUS(DQ379714) for the capsid region. NoV was detected in 19 of the 500 stool samples (3.8%). Genogroup GII-4 was found most frequently (n = 9, 1.8%), followed by GII-3 (n = 4, 0.8%), GII-6 (n = 3, 0.6%), GI-6 (n = 2, 0.4%), and GII-12/13 (n = 1, 0.2%). Importantly, we identified a novel NoV recombinant strain, C9-439 (KF289337), indicating potential risks, which suggested that, recombination occurred in the region between open reading frames 1 and 2 of the GII-12/13 strain and that breakpoints occurred in the polymerase region.
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spelling pubmed-38773442014-01-03 Full-Genomic Analysis of a Human Norovirus Recombinant GII.12/13 Novel Strain Isolated from South Korea Won, Yu-Jung Park, Jeong-Woong Han, Sang-ha Cho, Han-Gil Kang, Lae-Hyung Lee, Sung-Geun Ryu, Sang-Ryeol Paik, Soon-Young PLoS One Research Article Norovirus (NoV) genogroups I and II are frequently recognized as the main causes of acute gastroenteritis and outbreaks of non-bacterial foodborne diseases. Furthermore, variants and recombinant strains of this virus are continuously emerging worldwide. The aim of this study was to identify NoV strains and to investigate and characterize rare genotypes. Stool samples (n = 500) were collected from patients with symptoms of acute gastroenteritis in Korea between December 2004 and November 2007. For analysis of the samples, rapid genotype screening was performed using reverse transcriptase-polymerase chain reaction. Full sequencing, using a newly designed set of 12 primers, revealed GII-12/13 strain. The partial sequence of GII-12/13 strain was compared with published NoV (GII-1 - 14) sequences targeting RdRp and capsid regions using phylogenetic analysis with the SimPlot program, which could evaluate recombination breakpoints. SimPlot analysis was also performed with the strain GII-12/Gifu-96/JPN (AB045603) for the RdRp region and with GII-13/G5175B-83/AUS(DQ379714) for the capsid region. NoV was detected in 19 of the 500 stool samples (3.8%). Genogroup GII-4 was found most frequently (n = 9, 1.8%), followed by GII-3 (n = 4, 0.8%), GII-6 (n = 3, 0.6%), GI-6 (n = 2, 0.4%), and GII-12/13 (n = 1, 0.2%). Importantly, we identified a novel NoV recombinant strain, C9-439 (KF289337), indicating potential risks, which suggested that, recombination occurred in the region between open reading frames 1 and 2 of the GII-12/13 strain and that breakpoints occurred in the polymerase region. Public Library of Science 2013-12-31 /pmc/articles/PMC3877344/ /pubmed/24391985 http://dx.doi.org/10.1371/journal.pone.0085063 Text en © 2013 Won 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
Won, Yu-Jung
Park, Jeong-Woong
Han, Sang-ha
Cho, Han-Gil
Kang, Lae-Hyung
Lee, Sung-Geun
Ryu, Sang-Ryeol
Paik, Soon-Young
Full-Genomic Analysis of a Human Norovirus Recombinant GII.12/13 Novel Strain Isolated from South Korea
title Full-Genomic Analysis of a Human Norovirus Recombinant GII.12/13 Novel Strain Isolated from South Korea
title_full Full-Genomic Analysis of a Human Norovirus Recombinant GII.12/13 Novel Strain Isolated from South Korea
title_fullStr Full-Genomic Analysis of a Human Norovirus Recombinant GII.12/13 Novel Strain Isolated from South Korea
title_full_unstemmed Full-Genomic Analysis of a Human Norovirus Recombinant GII.12/13 Novel Strain Isolated from South Korea
title_short Full-Genomic Analysis of a Human Norovirus Recombinant GII.12/13 Novel Strain Isolated from South Korea
title_sort full-genomic analysis of a human norovirus recombinant gii.12/13 novel strain isolated from south korea
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877344/
https://www.ncbi.nlm.nih.gov/pubmed/24391985
http://dx.doi.org/10.1371/journal.pone.0085063
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