Molecular epidemiology and genetic diversity of norovirus among hospitalized children with acute gastroenteritis in Tianjin, China, 2018-2020

被引:18
作者
Fang, Yulian [1 ]
Dong, Zhaoying [2 ]
Liu, Yan [3 ]
Wang, Wei [1 ]
Hou, Mengzhu [1 ]
Wu, Jinying [1 ]
Wang, Lu [1 ]
Zhao, Yu [4 ]
机构
[1] Tianjin Univ, Tianjin Pediat Res Inst, Tianjin Key Lab Birth Defects Prevent & Treatment, Tianjin Childrens Hosp,Childrens Hosp, 238 Longyan Rd, Tianjin 300134, Peoples R China
[2] Tianjin Union Med Ctr, Dept Neurol, 190 Jieyuan Rd, Tianjin 300121, Peoples R China
[3] Tianjin Med Univ, Clin Pediat Coll, 238 Longyan Rd, Tianjin 300134, Peoples R China
[4] Tianjin Univ, Dept Digest, Tianjin Childrens Hosp, Childrens Hosp, 238 Longyan Rd, Tianjin 300134, Peoples R China
关键词
Norovirus; Acute gastroenteritis; Genotype; RdRp; Capsid; Children; GII.4; VARIANTS; UNITED-STATES; PREVALENCE; STRAINS; RECOMBINATION; INFECTION; EVOLUTION; DIARRHEA; FEATURES; PRIMERS;
D O I
10.1186/s12879-021-06375-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Norovirus (NoV) is a major cause of viral acute gastroenteritis (AGE) in children worldwide. Epidemiological analysis with respect to the virus strains is limited in China. This study aimed to investigate the prevalence, patterns, and molecular characteristics of NoV infection among children with AGE in China. Methods A total 4848 stool samples were collected from children who were admitted with AGE in Tianjin Children's Hospital from August 2018 to July 2020. NoV was preliminarily detected using real-time reverse transcription polymerase chain reaction (RT-PCR). Partial sequences of the RNA-dependent RNA polymerase (RdRp) and capsid genes of positive samples were amplified by conventional RT-PCR and then sequenced. The NoV genotype was determined by online Norovirus Typing Tool Version 2.0, and phylogenetic analysis was conducted using MEGA 6.0. Results The prevalence of NoV was 26.4% (1280/4848). NoV was detected in all age groups, with the 7-12 months group having the highest detection rate (655/2014, 32.5%). NoV was detected during most part of the year with higher frequency in winter than other seasons. Based on the genetic analysis of RdRp, GII. Pe was the most predominant genotype detected at 70.7% (381/539) followed by GII.P12 at 25.4% (137/539). GII.4 was the most predominant capsid genotype detected at 65.3% (338/518) followed by GII.3 at 26.8% (139/518). Based on the genetic analysis of RdRp and capsid sequences, the strains were clustered into 10 RdRp-capsid genotypes: GII.Pe-GII.4 Sydney 2012 (65.5%), GII.P12-GII.3 (27.2%), GII.P16-GII.2 (1.8%), GII.P12-GII.2 (0.2%), GII.P17-GII.17 (1.1%), GII.Pe-GII.3 (1.8%), GII.Pe-GII.2 (1.1%), GII.Pe-GII.1 (0.4%), GII.16-GII.4 Sydney 2012 (0.7%), and GII.P7-GII.6 (0.2%). The predominant NoV genotypes changed from GII.Pe-GII.4 Sydney 2012 and GII.P12-GII.3 between August 2018 and July 2019 to GII.Pe-GII.4 Sydney 2012 and GII.P16-GII.2 between August 2019 and July 2020. The patients with GII.Pe-GII.4 Sydney 2012 genotype were more likely to suffer from vomiting symptom than those with GII.P12-GII.3. Conclusions NoV is an important pathogen responsible for viral AGE among children in China. GII.Pe-GII.4 Sydney 2012 and GII.P12-GII.3 were major recombinant genotypes. Knowledge of circulating genotypes and seasonal trends is of great importance for disease prevention and surveillance.
引用
收藏
页数:9
相关论文
共 37 条
[11]  
Dang Wen, 2019, Zhonghua Yufang Yixue Zazhi, V53, P811, DOI 10.3760/cma.j.issn.0253-9624.2019.08.003
[12]   Molecular epidemiology of genogroup II norovirus infection among hospitalized children with acute gastroenteritis in Suzhou (Jiangsu, China) from 2010 to 2013 [J].
Fu, Jian-Guang ;
Ai, Jing ;
Zhang, Jun ;
Wu, Qing-Bin ;
Qi, Xian ;
Ji, Hong ;
Jin, Miao ;
Liu, Cheng ;
Wang, Shen-Jiao ;
Shan, Jun ;
Bao, Chang-Jun ;
Tang, Fen-Yang ;
Zhu, Ye-Fei .
JOURNAL OF MEDICAL VIROLOGY, 2016, 88 (06) :954-960
[13]   Evolutionary and Molecular Analysis of Complete Genome Sequences of Norovirus From Brazil: Emerging Recombinant Strain GII.P16/GII.4 [J].
Hernandez, Juliana Merces ;
Silva, Luciana Damascena ;
Sousa Junior, Edivaldo Costa ;
Cardoso, Jedson Ferreira ;
Amaral Reymao, Tammy Kathlyn ;
Rodrigues Portela, Ana Caroline ;
Silva de Lima, Clayton Pereira ;
Teixeira, Dielle Monteiro ;
Souza Lucena, Maria Silvia ;
Teixeira Nunes, Marcio Roberto ;
Gabbay, Yvone Benchimol .
FRONTIERS IN MICROBIOLOGY, 2020, 11
[14]  
Imade Paul Erhunmwunse, 2015, Int J Microbiol, V2015, P685821, DOI 10.1155/2015/685821
[15]   Molecular epidemiology of rotavirus and norovirus in Ile-Ife, Nigeria: High prevalence of G12P[8] rotavirus strains and detection of a rare norovirus genotype [J].
Japhet, Margaret Oluwatoyin ;
Adesina, Olufisayo Adeyemi ;
Famurewa, Oladiran ;
Svensson, Lennart ;
Nordgren, Johan .
JOURNAL OF MEDICAL VIROLOGY, 2012, 84 (09) :1489-1496
[16]   Genogroup-specific PCR primers for detection of Norwalk-like viruses [J].
Kojima, S ;
Kageyama, T ;
Fukushi, S ;
Hoshino, FB ;
Shinohara, M ;
Uchida, K ;
Natori, K ;
Takeda, N ;
Katayama, K .
JOURNAL OF VIROLOGICAL METHODS, 2002, 100 (1-2) :107-114
[17]  
Koo Hoonmo L, 2013, J Pediatric Infect Dis Soc, V2, P57, DOI 10.1093/jpids/pis070
[18]   The epidemiology of Norovirus in the Middle East and North Africa (MENA) region: a systematic review [J].
Kreidieh, Khalil ;
Charide, Rana ;
Dbaibo, Ghassan ;
Melhem, Nada M. .
VIROLOGY JOURNAL, 2017, 14
[19]   Proposal for a unified norovirus nomenclature and genotyping [J].
Kroneman, Annelies ;
Vega, Everardo ;
Vennema, Harry ;
Vinje, Jan ;
White, Peter A. ;
Hansman, Grant ;
Green, Kim ;
Martella, Vito ;
Katayama, Kazuhiko ;
Koopmans, Marion .
ARCHIVES OF VIROLOGY, 2013, 158 (10) :2059-2068
[20]   Molecular Evolution of Human Norovirus GII.2 Clusters [J].
Li, Xingguang ;
Liu, Haizhou ;
Rife Magalis, Brittany ;
Pond, Sergei L. Kosakovsky ;
Volz, Erik M. .
FRONTIERS IN MICROBIOLOGY, 2021, 12