Literature DB >> 29471118

The dynamics of norovirus genotypes and genetic analysis of a novel recombinant GII.P12-GII.3 among infants and children in Bangkok, Thailand between 2014 and 2016.

Michittra Boonchan1, Ratigorn Guntapong2, Napas Sripirom3, Kriangsak Ruchusatsawat2, Phakapun Singchai2, Pimpha Rungnobhakhun3, Ratana Tacharoenmuang2, Hiroto Mizushima4, Masashi Tatsumi4, Naokazu Takeda4, Somchai Sangkitporn2, Jutarat Mekmullica3, Kazushi Motomura5.   

Abstract

Norovirus (NoV) is the leading cause of viral acute gastroenteritis among all age groups in the world. We performed a molecular epidemiological study of the NoVs prevalent in Bangkok between November 2014 and July 2016 to investigate the emergence of new NoV variants in Thailand. A total of 332 stool specimens were collected from hospitalized pediatric patients with acute gastroenteritis in Bangkok, Thailand. NoVs were detected by real-time PCR. The genome of the N-terminal/shell domain was amplified, the nucleotide sequence was determined, and phylogenetic analyses were performed. GII NoV was detected in 58 (17.5%) of the 332 specimens. GII.17, a genotype strain prevalent from 2014 to mid-2015, was hardly detected and replaced by the GII.3 genotype strain. Entire genome sequencing followed by phylogenetic analysis of the GII.3 genotype strains indicated that they are new recombinant viruses, because the genome encoding ORF1 is derived from a GII.12 genotype strain, whereas that encoding ORF2-3 is from a GII.3 genotype strain. The putative recombination breakpoints with the highest statistical significance were located around the border of 3Dpol and ORF2. The change in the prevalent strain of NoV seems to be linked to the emergence of new forms of recombinant viruses. These findings suggested that the swapping of the structural and non-structural proteins of NoV is a common mechanism by which new epidemic variants are generated in nature.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bangkok; GII.3; Norovirus; Recombinant virus; Thailand

Mesh:

Substances:

Year:  2018        PMID: 29471118     DOI: 10.1016/j.meegid.2018.02.028

Source DB:  PubMed          Journal:  Infect Genet Evol        ISSN: 1567-1348            Impact factor:   3.342


  3 in total

1.  Human Norovirus Propagation in Human Induced Pluripotent Stem Cell-Derived Intestinal Epithelial Cells.

Authors:  Shintaro Sato; Kota Hisaie; Shiho Kurokawa; Akio Suzuki; Naomi Sakon; Yohei Uchida; Yoshikazu Yuki; Hiroshi Kiyono
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2018-12-10

2.  Coding-Complete Genome Sequence of a Recombinant Human Norovirus Strain Identified as Subtype GII.p12_GII.3.

Authors:  Byung-Joo Park; Hee-Seop Ahn; Sang-Hoon Han; Hyeon-Jeong Go; Eu-Lim Lyoo; Changsun Choi; Jinjong Myoung; Joong-Bok Lee; Seung-Yong Park; Chang-Seon Song; Sang-Won Lee; In-Soo Choi
Journal:  Microbiol Resour Announc       Date:  2020-01-30

3.  Identification of Human Norovirus GII.3 Blockade Antibody Epitopes.

Authors:  Yufang Yi; Shuxia Wang; Xiaoli Wang; Pei Xiong; Qingwei Liu; Chao Zhang; Feifei Yin; Zhong Huang
Journal:  Viruses       Date:  2021-10-13       Impact factor: 5.048

  3 in total

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