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Evolutionary dynamics of GII.17 norovirus
BACKGROUND: During the winter of 2014–2015, a rarely reported norovirus (NoV) genotype GII.17 was found to have increased its frequency in norovirus outbreaks in East Asia, surpassing the GII.4 NoV infections. GII.17 genotype has been detected for over three decades in the world. The aim of this stu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797681/ https://www.ncbi.nlm.nih.gov/pubmed/29404222 http://dx.doi.org/10.7717/peerj.4333 |
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author | Sang, Shaowei Yang, Xiaoyun |
author_facet | Sang, Shaowei Yang, Xiaoyun |
author_sort | Sang, Shaowei |
collection | PubMed |
description | BACKGROUND: During the winter of 2014–2015, a rarely reported norovirus (NoV) genotype GII.17 was found to have increased its frequency in norovirus outbreaks in East Asia, surpassing the GII.4 NoV infections. GII.17 genotype has been detected for over three decades in the world. The aim of this study is to examine the evolutionary dynamics of GII.17 over the last four decades. METHODS: NoV GII.17 sequences with complete or nearly complete VP1 were downloaded from GenBank and the phylogenetic analyses were then conducted. RESULTS: The maximum likelihood analysis showed that GII.17 genotype could be divided into four different clades (Clades A–D). The strains detected after 2012, which could be the cause of the outbreaks, were separated into Clades C–D with their mean amino acid distance being 4.5%. Bayesian Markov chain Monte Carlo analyses indicated that the rate of nucleotide substitution per sites was 1.68 × 10(−3) nucleotide substitutions/site/year and the time of the most recent common ancestor was 1840. The P2 subdomain of GII.17 was highly variable with 44% (56/128) amino acids variations including two insertions at positions 295–296 and one deletion at position 385 (Clades C and D) and one insertion at position 375 (Clade D). Variations existed in Epitopes A, B and D corresponding to GII.4 and human histo-blood group antigens binding site I in P2 subdomain. CONCLUSION: The novel GII.17 strains that caused outbreaks in 2013–2015 may have two new variants. The evolvement of HBGAs binding site and epitopes in P2 subdomain might contribute to the novel GII.17 strains predominance in some regions. |
format | Online Article Text |
id | pubmed-5797681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57976812018-02-05 Evolutionary dynamics of GII.17 norovirus Sang, Shaowei Yang, Xiaoyun PeerJ Epidemiology BACKGROUND: During the winter of 2014–2015, a rarely reported norovirus (NoV) genotype GII.17 was found to have increased its frequency in norovirus outbreaks in East Asia, surpassing the GII.4 NoV infections. GII.17 genotype has been detected for over three decades in the world. The aim of this study is to examine the evolutionary dynamics of GII.17 over the last four decades. METHODS: NoV GII.17 sequences with complete or nearly complete VP1 were downloaded from GenBank and the phylogenetic analyses were then conducted. RESULTS: The maximum likelihood analysis showed that GII.17 genotype could be divided into four different clades (Clades A–D). The strains detected after 2012, which could be the cause of the outbreaks, were separated into Clades C–D with their mean amino acid distance being 4.5%. Bayesian Markov chain Monte Carlo analyses indicated that the rate of nucleotide substitution per sites was 1.68 × 10(−3) nucleotide substitutions/site/year and the time of the most recent common ancestor was 1840. The P2 subdomain of GII.17 was highly variable with 44% (56/128) amino acids variations including two insertions at positions 295–296 and one deletion at position 385 (Clades C and D) and one insertion at position 375 (Clade D). Variations existed in Epitopes A, B and D corresponding to GII.4 and human histo-blood group antigens binding site I in P2 subdomain. CONCLUSION: The novel GII.17 strains that caused outbreaks in 2013–2015 may have two new variants. The evolvement of HBGAs binding site and epitopes in P2 subdomain might contribute to the novel GII.17 strains predominance in some regions. PeerJ Inc. 2018-02-01 /pmc/articles/PMC5797681/ /pubmed/29404222 http://dx.doi.org/10.7717/peerj.4333 Text en ©2018 Sang and Yang http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Epidemiology Sang, Shaowei Yang, Xiaoyun Evolutionary dynamics of GII.17 norovirus |
title | Evolutionary dynamics of GII.17 norovirus |
title_full | Evolutionary dynamics of GII.17 norovirus |
title_fullStr | Evolutionary dynamics of GII.17 norovirus |
title_full_unstemmed | Evolutionary dynamics of GII.17 norovirus |
title_short | Evolutionary dynamics of GII.17 norovirus |
title_sort | evolutionary dynamics of gii.17 norovirus |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797681/ https://www.ncbi.nlm.nih.gov/pubmed/29404222 http://dx.doi.org/10.7717/peerj.4333 |
work_keys_str_mv | AT sangshaowei evolutionarydynamicsofgii17norovirus AT yangxiaoyun evolutionarydynamicsofgii17norovirus |