Skip to main content
Top
Published in: BMC Infectious Diseases 1/2019

Open Access 01-12-2019 | Acute Gastroenteritis | Research article

Genetic diversity and epidemiology of Genogroup II noroviruses in children with acute sporadic gastroenteritis in Shanghai, China, 2012–2017

Authors: Lijuan Lu, Huaqing Zhong, Menghua Xu, Liyun Su, Lingfeng Cao, Ran Jia, Jin Xu

Published in: BMC Infectious Diseases | Issue 1/2019

Login to get access

Abstract

Background

Noroviruses (NoVs) are considered an important cause of acute gastroenteritis (AGE) across all age groups, especially in children under 5 years of age. We investigated the epidemiology of noroviruses in outpatient children from the Children’s Hospital of Fudan University in Shanghai, China.

Methods

Stool specimens were collected between January 2012 and December 2017 from 1433 children under 5 years of age with acute gastroenteritis. All samples were analysed by conventional reverse transcription-polymerase chain reaction (RT-PCR) for genogroup II NoVs amplifying both the RNA-dependent RNA polymerase (RdRp) and partial capsid genes. The Norovirus Genotyping Tool v.2.0 (https://​www.​rivm.​nl/​mpf/​typingtool/​norovirus/​) was used for genotyping the strains, and phylogenetic analyses were conducted by MEGA 6.0.

Results

From 2012 to 2017, GII NoVs were detected in 15.4% (220/1433) of the samples, with the highest detection rate in children aged 7–12 months (19.2%, 143/746). The seasons with the highest prevalence of GII NoVs infection were autumn and winter. Based on genetic analysis of RdRp, GII.Pe (74.5%%, 137/184) was the most predominant RdRp genotype from 2013 to 2017, while GII.P4 played a dominant role in 2012 (55.6%, 21/36). Among the capsid genotypes, the most prevalent NoV genotype from 2012 to 2017 was GII.4 (74.1%, 163/220). On the basis of genetic analysis of RdRp and capsid sequences, the strains were clustered into − 19 RdRp/capsid genotypes, and 12 of them were discordant, such as GII.Pe/GII.4-Sydney_2012, GII.P12/GII.3, GII.P7/GII.6, GII.Pe/GII.3, and GII.P16/GII.2. Starting with 2013, GII.Pe/GII.4-Sydney_2012 had completely replaced the pandemic GII.P4-2006b/GII.4-2006b subtype and was detected in children across all age groups.

Conclusions

The present study shows high detection rates and the genetic diversity of circulating NoV GII genotypes in paediatric AGE samples from Shanghai. The findings emphasize the importance of continuous molecular surveillance of emerging NoV strains.
Literature
2.
go back to reference Ahmed SM, Hall AJ, Robinson AE, Verhoef L, Premkumar P, Parashar UD, et al. Global prevalence of norovirus in cases of gastroenteritis: a systematic review and meta-analysis. Lancet Infect Dis. 2014;14(8):725–30.PubMedCrossRef Ahmed SM, Hall AJ, Robinson AE, Verhoef L, Premkumar P, Parashar UD, et al. Global prevalence of norovirus in cases of gastroenteritis: a systematic review and meta-analysis. Lancet Infect Dis. 2014;14(8):725–30.PubMedCrossRef
3.
go back to reference Patel MM, Widdowson MA, Glass RI, Akazawa K, Vinjé J, Parashar UD. Systematic literature review of role of noroviruses in sporadic gastroenteritis. Emerg Infect Dis. 2008;14(8):1224–31.PubMedPubMedCentralCrossRef Patel MM, Widdowson MA, Glass RI, Akazawa K, Vinjé J, Parashar UD. Systematic literature review of role of noroviruses in sporadic gastroenteritis. Emerg Infect Dis. 2008;14(8):1224–31.PubMedPubMedCentralCrossRef
4.
go back to reference Anderson EJ. Prevention and treatment of viral diarrhea in pediatrics. Expert Rev Anti-Infect Ther. 2010;8(2):205–17.PubMedCrossRef Anderson EJ. Prevention and treatment of viral diarrhea in pediatrics. Expert Rev Anti-Infect Ther. 2010;8(2):205–17.PubMedCrossRef
5.
go back to reference Lopman BA, Steele D, Kirkwood CD, Parashar UD. The vast and varied global burden of norovirus: prospects for prevention and control. PLoS Med. 2016;13(4):e1001999.PubMedPubMedCentralCrossRef Lopman BA, Steele D, Kirkwood CD, Parashar UD. The vast and varied global burden of norovirus: prospects for prevention and control. PLoS Med. 2016;13(4):e1001999.PubMedPubMedCentralCrossRef
6.
go back to reference Jiang X, Wang M, Wang K, Estes MK. Sequence and genomic organization of Norwalk virus. Virology. 1993;195(1):51–61.PubMedCrossRef Jiang X, Wang M, Wang K, Estes MK. Sequence and genomic organization of Norwalk virus. Virology. 1993;195(1):51–61.PubMedCrossRef
7.
go back to reference Thorne LG, Goodfellow IG. Norovirus gene expression and replication. J Gen Virol. 2014;95(Pt 2):278–91.PubMedCrossRef Thorne LG, Goodfellow IG. Norovirus gene expression and replication. J Gen Virol. 2014;95(Pt 2):278–91.PubMedCrossRef
9.
go back to reference Hoa Tran TN, Trainor E, Nakagomi T, Cunliffe NA, Nakagomi O. Molecular epidemiology of noroviruses associated with acute sporadic gastroenteritis in children: global distribution of genogroups, genotypes and GII.4 variants. J Clin Virol. 2013;56(3):185–93.PubMedCrossRef Hoa Tran TN, Trainor E, Nakagomi T, Cunliffe NA, Nakagomi O. Molecular epidemiology of noroviruses associated with acute sporadic gastroenteritis in children: global distribution of genogroups, genotypes and GII.4 variants. J Clin Virol. 2013;56(3):185–93.PubMedCrossRef
10.
go back to reference van Beek J, de Graaf M, Al-Hello H, Allen DJ, Ambert-Balay K, Botteldoorn N, et al. Molecular surveillance of norovirus, 2005-16: an epidemiological analysis of data collected from the NoroNet network. Lancet Infect Dis. 2018;18(5):545–53.PubMedCrossRef van Beek J, de Graaf M, Al-Hello H, Allen DJ, Ambert-Balay K, Botteldoorn N, et al. Molecular surveillance of norovirus, 2005-16: an epidemiological analysis of data collected from the NoroNet network. Lancet Infect Dis. 2018;18(5):545–53.PubMedCrossRef
11.
12.
go back to reference Kroneman A, Vega E, Vennema H, Vinjé J, White PA, Hansman G, et al. Proposal for a unified norovirus nomenclature and genotyping. Arch Virol. 2013;158(10):2059–68.PubMedPubMedCentralCrossRef Kroneman A, Vega E, Vennema H, Vinjé J, White PA, Hansman G, et al. Proposal for a unified norovirus nomenclature and genotyping. Arch Virol. 2013;158(10):2059–68.PubMedPubMedCentralCrossRef
13.
go back to reference Di Felice E, Mauroy A, Pozzo FD, Thiry D, Ceci C, Di Martino B, et al. Bovine noroviruses: a missing component of calf diarrhoea diagnosis. Vet J. 2016;207:53–62.PubMedCrossRef Di Felice E, Mauroy A, Pozzo FD, Thiry D, Ceci C, Di Martino B, et al. Bovine noroviruses: a missing component of calf diarrhoea diagnosis. Vet J. 2016;207:53–62.PubMedCrossRef
14.
go back to reference Supadej K, Khamrin P, Kumthip K, Kochjan P, Yodmeeklin A, Ushijima H, et al. Wide variety of recombinant strains of norovirus GII in pediatric patients hospitalized with acute gastroenteritis in Thailand during 2005 to 2015. Infect Genet Evol. 2017;52:44–51.PubMedCrossRef Supadej K, Khamrin P, Kumthip K, Kochjan P, Yodmeeklin A, Ushijima H, et al. Wide variety of recombinant strains of norovirus GII in pediatric patients hospitalized with acute gastroenteritis in Thailand during 2005 to 2015. Infect Genet Evol. 2017;52:44–51.PubMedCrossRef
15.
go back to reference Andrade JSR, Fumian TM, Leite JPG, Assis MR, Bello G, Mir D, et al. Detection and molecular characterization of emergent GII.P17/GII.17 norovirus in Brazil, 2015. Infect Genet Evol. 2017;51:28–32.PubMedCrossRef Andrade JSR, Fumian TM, Leite JPG, Assis MR, Bello G, Mir D, et al. Detection and molecular characterization of emergent GII.P17/GII.17 norovirus in Brazil, 2015. Infect Genet Evol. 2017;51:28–32.PubMedCrossRef
16.
go back to reference Fu JG, Shi C, Xu C, Lin Q, Zhang J, Yi QH, et al. Outbreaks of acute gastroenteritis associated with a re-emerging GII.P16-GII.2 norovirus in the spring of 2017 in Jiangsu, China. PLoS One. 2017;12(12):e0186090.PubMedPubMedCentralCrossRef Fu JG, Shi C, Xu C, Lin Q, Zhang J, Yi QH, et al. Outbreaks of acute gastroenteritis associated with a re-emerging GII.P16-GII.2 norovirus in the spring of 2017 in Jiangsu, China. PLoS One. 2017;12(12):e0186090.PubMedPubMedCentralCrossRef
17.
go back to reference Lu QB, Huang DD, Zhao J, Wang HY, Zhang XA, Xu HM, et al. An increasing prevalence of recombinant GII norovirus in pediatric patients with diarrhea during 2010-2013 in China. Infect Genet Evol. 2015;31:48–52.PubMedCrossRef Lu QB, Huang DD, Zhao J, Wang HY, Zhang XA, Xu HM, et al. An increasing prevalence of recombinant GII norovirus in pediatric patients with diarrhea during 2010-2013 in China. Infect Genet Evol. 2015;31:48–52.PubMedCrossRef
18.
go back to reference Xue C, Pan L, Zhu W, Wang Y, Fu H, Cui C, et al. Molecular epidemiology of genogroup II norovirus infections in acute gastroenteritis patients during 2014-2016 in Pudong new area, Shanghai, China. Gut Pathog. 2018;10:7.PubMedPubMedCentralCrossRef Xue C, Pan L, Zhu W, Wang Y, Fu H, Cui C, et al. Molecular epidemiology of genogroup II norovirus infections in acute gastroenteritis patients during 2014-2016 in Pudong new area, Shanghai, China. Gut Pathog. 2018;10:7.PubMedPubMedCentralCrossRef
19.
go back to reference Pan L, Xue C, Fu H, Liu D, Zhu L, Cui C, et al. The novel norovirus genotype GII.17 is the predominant strain in diarrheal patients in Shanghai, China. Gut Pathog. 2016;8:49.PubMedPubMedCentralCrossRef Pan L, Xue C, Fu H, Liu D, Zhu L, Cui C, et al. The novel norovirus genotype GII.17 is the predominant strain in diarrheal patients in Shanghai, China. Gut Pathog. 2016;8:49.PubMedPubMedCentralCrossRef
20.
go back to reference Lu L, Jia R, Zhong H, Xu M, Su L, Cao L, et al. Molecular characterization and multiple infections of rotavirus, norovirus, sapovirus, astrovirus and adenovirus in outpatients with sporadic gastroenteritis in Shanghai, China, 2010-2011. Arch Virol. 2015;160(5):1229–38.PubMedCrossRef Lu L, Jia R, Zhong H, Xu M, Su L, Cao L, et al. Molecular characterization and multiple infections of rotavirus, norovirus, sapovirus, astrovirus and adenovirus in outpatients with sporadic gastroenteritis in Shanghai, China, 2010-2011. Arch Virol. 2015;160(5):1229–38.PubMedCrossRef
21.
go back to reference Zeng M, Xu X, Zhu C, Chen J, Zhu Q, Lin S, et al. Clinical and molecular epidemiology of norovirus infection in childhood diarrhea in China. J Med Virol. 2012;84(1):145–51.PubMedCrossRef Zeng M, Xu X, Zhu C, Chen J, Zhu Q, Lin S, et al. Clinical and molecular epidemiology of norovirus infection in childhood diarrhea in China. J Med Virol. 2012;84(1):145–51.PubMedCrossRef
22.
go back to reference Lu L, Zhong H, Xu M, Su L, Cao L, Dong N, et al. Molecular epidemiology of human calicivirus infections in children with acute diarrhea in Shanghai: a retrospective comparison between inpatients and outpatients treated between 2006 and 2011. Arch Virol. 2014;159(7):1613–21.PubMedCrossRef Lu L, Zhong H, Xu M, Su L, Cao L, Dong N, et al. Molecular epidemiology of human calicivirus infections in children with acute diarrhea in Shanghai: a retrospective comparison between inpatients and outpatients treated between 2006 and 2011. Arch Virol. 2014;159(7):1613–21.PubMedCrossRef
23.
go back to reference Farsi M, Roodbari F, Nejati B, Arashkia A, Jalilvand S, Nateghian A, et al. Prevalence and genetic diversity of norovirus genogroup II in children less than 5 years of age with acute gastroenteritis in Tehran, Iran. Med Microbiol Immunol. 2018;207(3–4):201–10.PubMedCrossRef Farsi M, Roodbari F, Nejati B, Arashkia A, Jalilvand S, Nateghian A, et al. Prevalence and genetic diversity of norovirus genogroup II in children less than 5 years of age with acute gastroenteritis in Tehran, Iran. Med Microbiol Immunol. 2018;207(3–4):201–10.PubMedCrossRef
24.
go back to reference Hassine-Zaafrane M, Sdiri-Loulizi K, Kaplon J, Salem IB, Pothier P, Aouni M, et al. Prevalence and genetic diversity of norovirus infection in Tunisian children (2007-2010). J Med Virol. 2013;85(6):1100–10.PubMedCrossRef Hassine-Zaafrane M, Sdiri-Loulizi K, Kaplon J, Salem IB, Pothier P, Aouni M, et al. Prevalence and genetic diversity of norovirus infection in Tunisian children (2007-2010). J Med Virol. 2013;85(6):1100–10.PubMedCrossRef
25.
go back to reference Esteves A, Nordgren J, Tavares C, Fortes F, Dimbu R, Saraiva N, et al. Genetic diversity of norovirus in children under 5 years of age with acute gastroenteritis from Angola. Epidemiol Infect. 2018;146(5):551–7.PubMedCrossRef Esteves A, Nordgren J, Tavares C, Fortes F, Dimbu R, Saraiva N, et al. Genetic diversity of norovirus in children under 5 years of age with acute gastroenteritis from Angola. Epidemiol Infect. 2018;146(5):551–7.PubMedCrossRef
26.
go back to reference Xue Y, Pan H, Hu J, Wu H, Li J, Xiao W, et al. Epidemiology of norovirus infections among diarrhea outpatients in a diarrhea surveillance system in Shanghai, China: a cross-sectional study. BMC Infect Dis. 2015;15:183.PubMedPubMedCentralCrossRef Xue Y, Pan H, Hu J, Wu H, Li J, Xiao W, et al. Epidemiology of norovirus infections among diarrhea outpatients in a diarrhea surveillance system in Shanghai, China: a cross-sectional study. BMC Infect Dis. 2015;15:183.PubMedPubMedCentralCrossRef
28.
go back to reference Tan D, Deng L, Wang M, Li X, Ma Y, Liu W. High prevalence and genetic diversity of noroviruses among children with sporadic acute gastroenteritis in Nanning City, China, 2010-2011. J Med Virol. 2015;87(3):498–503.PubMedCrossRef Tan D, Deng L, Wang M, Li X, Ma Y, Liu W. High prevalence and genetic diversity of noroviruses among children with sporadic acute gastroenteritis in Nanning City, China, 2010-2011. J Med Virol. 2015;87(3):498–503.PubMedCrossRef
29.
go back to reference Siafakas N, Zerva L, Hatzaki D, Lebessi E, Chronopoulou G, Paraskakis I, et al. Molecular epidemiology of noroviruses in children in South Greece, 2013-2015. J Med Virol. 2018;90(11):1703–11.PubMedCrossRef Siafakas N, Zerva L, Hatzaki D, Lebessi E, Chronopoulou G, Paraskakis I, et al. Molecular epidemiology of noroviruses in children in South Greece, 2013-2015. J Med Virol. 2018;90(11):1703–11.PubMedCrossRef
30.
go back to reference Zhang P, Chen L, Fu Y, Ji L, Wu X, Xu D, et al. Clinical and molecular analyses of norovirus-associated sporadic acute gastroenteritis: the emergence of GII.17 over GII.4, Huzhou, China, 2015. BMC Infect Dis. 2016;16(1):717.PubMedPubMedCentralCrossRef Zhang P, Chen L, Fu Y, Ji L, Wu X, Xu D, et al. Clinical and molecular analyses of norovirus-associated sporadic acute gastroenteritis: the emergence of GII.17 over GII.4, Huzhou, China, 2015. BMC Infect Dis. 2016;16(1):717.PubMedPubMedCentralCrossRef
31.
go back to reference Bruggink LD, Dunbar NL, Marshall JA. Emergence of GII.E as a major ORF 1 norovirus genotype and its associated ORF 2 GII.4 variant forms. Infect Genet Evol. 2014;22:157–63.PubMedCrossRef Bruggink LD, Dunbar NL, Marshall JA. Emergence of GII.E as a major ORF 1 norovirus genotype and its associated ORF 2 GII.4 variant forms. Infect Genet Evol. 2014;22:157–63.PubMedCrossRef
32.
go back to reference Fu JG, Ai J, Zhang J, Wu QB, Qi X, Ji H, et al. Molecular epidemiology of genogroup II norovirus infection among hospitalized children with acute gastroenteritis in Suzhou (Jiangsu, China) from 2010 to 2013. J Med Virol. 2016;88(6):954–60.PubMedCrossRef Fu JG, Ai J, Zhang J, Wu QB, Qi X, Ji H, et al. Molecular epidemiology of genogroup II norovirus infection among hospitalized children with acute gastroenteritis in Suzhou (Jiangsu, China) from 2010 to 2013. J Med Virol. 2016;88(6):954–60.PubMedCrossRef
33.
go back to reference Xue L, Dong R, Wu Q, Li Y, Cai W, Kou X, et al. Molecular epidemiology of noroviruses associated with sporadic gastroenteritis in Guangzhou, China, 2013-2015. Arch Virol. 2016;161(5):1377–84.PubMedCrossRef Xue L, Dong R, Wu Q, Li Y, Cai W, Kou X, et al. Molecular epidemiology of noroviruses associated with sporadic gastroenteritis in Guangzhou, China, 2013-2015. Arch Virol. 2016;161(5):1377–84.PubMedCrossRef
34.
go back to reference Lu J, Sun L, Fang L, Yang F, Mo Y, Lao J, et al. Gastroenteritis outbreaks caused by norovirus GII.17, Guangdong Province, China, 2014-2015. Emerg Infect Dis. 2015;21(7):1240–2.PubMedPubMedCentralCrossRef Lu J, Sun L, Fang L, Yang F, Mo Y, Lao J, et al. Gastroenteritis outbreaks caused by norovirus GII.17, Guangdong Province, China, 2014-2015. Emerg Infect Dis. 2015;21(7):1240–2.PubMedPubMedCentralCrossRef
36.
go back to reference Chen H, Qian F, Xu J, Chan M, Shen Z, Zai S, et al. A novel norovirus GII.17 lineage contributed to adult gastroenteritis in Shanghai, China, during the winter of 2014–2015. Emerg Microb Infect. 2015;4(11):e67. Chen H, Qian F, Xu J, Chan M, Shen Z, Zai S, et al. A novel norovirus GII.17 lineage contributed to adult gastroenteritis in Shanghai, China, during the winter of 2014–2015. Emerg Microb Infect. 2015;4(11):e67.
37.
go back to reference Dang Thanh H, Than VT, Nguyen TH, Lim I, Kim W. Emergence of norovirus GII.17 variants among children with acute gastroenteritis in South Korea. PLoS One. 2016;11(5):e0154284.PubMedPubMedCentralCrossRef Dang Thanh H, Than VT, Nguyen TH, Lim I, Kim W. Emergence of norovirus GII.17 variants among children with acute gastroenteritis in South Korea. PLoS One. 2016;11(5):e0154284.PubMedPubMedCentralCrossRef
38.
go back to reference Nakamura N, Kobayashi S, Minagawa H, Matsushita T, Sugiura W, Iwatani Y. Molecular epidemiology of enteric viruses in patients with acute gastroenteritis in Aichi prefecture, Japan, 2008/09-2013/14. J Med Virol. 2016;88(7):1180–6.PubMedCrossRef Nakamura N, Kobayashi S, Minagawa H, Matsushita T, Sugiura W, Iwatani Y. Molecular epidemiology of enteric viruses in patients with acute gastroenteritis in Aichi prefecture, Japan, 2008/09-2013/14. J Med Virol. 2016;88(7):1180–6.PubMedCrossRef
39.
go back to reference Howard LM, Mwape I, Siwingwa M, Simuyandi M, Guffey MB, Stringer JS, et al. Norovirus infections in young children in Lusaka Province, Zambia: clinical characteristics and molecular epidemiology. BMC Infect Dis. 2017;17(1):92.PubMedPubMedCentralCrossRef Howard LM, Mwape I, Siwingwa M, Simuyandi M, Guffey MB, Stringer JS, et al. Norovirus infections in young children in Lusaka Province, Zambia: clinical characteristics and molecular epidemiology. BMC Infect Dis. 2017;17(1):92.PubMedPubMedCentralCrossRef
40.
go back to reference Hoa-Tran TN, Nakagomi O, Dao AT, Nguyen AT, Agbemabiese CA, Vu HM, et al. Molecular epidemiology of noroviruses detected in Vietnamese children with acute gastroenteritis from 2012 to 2015. J Med Microbiol. 2017;66(1):34–45.PubMedCrossRef Hoa-Tran TN, Nakagomi O, Dao AT, Nguyen AT, Agbemabiese CA, Vu HM, et al. Molecular epidemiology of noroviruses detected in Vietnamese children with acute gastroenteritis from 2012 to 2015. J Med Microbiol. 2017;66(1):34–45.PubMedCrossRef
41.
go back to reference Bruggink LD, Moselen JM, Marshall JA. Genotype analysis of noroviruses associated with gastroenteritis outbreaks in childcare centres, Victoria, Australia, 2012-2015. Epidemiol Infect. 2017;145(9):1933–41.PubMedCrossRef Bruggink LD, Moselen JM, Marshall JA. Genotype analysis of noroviruses associated with gastroenteritis outbreaks in childcare centres, Victoria, Australia, 2012-2015. Epidemiol Infect. 2017;145(9):1933–41.PubMedCrossRef
42.
go back to reference Rahman M, Rahman R, Nahar S, Hossain S, Ahmed S, Golam Faruque AS, et al. Norovirus diarrhea in Bangladesh, 2010-2014: prevalence, clinical features, and genotypes. J Med Virol. 2016;88(10):1742–50.PubMedCrossRef Rahman M, Rahman R, Nahar S, Hossain S, Ahmed S, Golam Faruque AS, et al. Norovirus diarrhea in Bangladesh, 2010-2014: prevalence, clinical features, and genotypes. J Med Virol. 2016;88(10):1742–50.PubMedCrossRef
43.
go back to reference Mans J, Murray TY, Nadan S, Netshikweta R, Page NA, Taylor MB. Norovirus diversity in children with gastroenteritis in South Africa from 2009 to 2013: GII.4 variants and recombinant strains predominate. Epidemiol Infect. 2016;144(5):907–16.PubMedCrossRef Mans J, Murray TY, Nadan S, Netshikweta R, Page NA, Taylor MB. Norovirus diversity in children with gastroenteritis in South Africa from 2009 to 2013: GII.4 variants and recombinant strains predominate. Epidemiol Infect. 2016;144(5):907–16.PubMedCrossRef
44.
go back to reference Makhaola K, Moyo S, Lechiile K, Goldfarb DM, Kebaabetswe LP. Genetic and epidemiological analysis of norovirus from children with gastroenteritis in Botswana, 2013-2015. BMC Infect Dis. 2018;18(1):246.PubMedPubMedCentralCrossRef Makhaola K, Moyo S, Lechiile K, Goldfarb DM, Kebaabetswe LP. Genetic and epidemiological analysis of norovirus from children with gastroenteritis in Botswana, 2013-2015. BMC Infect Dis. 2018;18(1):246.PubMedPubMedCentralCrossRef
45.
go back to reference Wu X, Han J, Chen L, Xu D, Shen Y, Zha Y, et al. Prevalence and genetic diversity of noroviruses in adults with acute gastroenteritis in Huzhou, China, 2013-2014. Arch Virol. 2015;160(7):1705–13.PubMedPubMedCentralCrossRef Wu X, Han J, Chen L, Xu D, Shen Y, Zha Y, et al. Prevalence and genetic diversity of noroviruses in adults with acute gastroenteritis in Huzhou, China, 2013-2014. Arch Virol. 2015;160(7):1705–13.PubMedPubMedCentralCrossRef
46.
go back to reference Chen C, Yan JB, Wang HL, Li P, Li KF, Wu B, et al. Molecular epidemiology and spatiotemporal dynamics of norovirus associated with sporadic acute gastroenteritis during 2013-2017, Zhoushan Islands, China. PLoS One. 2018;13(7):e0200911.PubMedPubMedCentralCrossRef Chen C, Yan JB, Wang HL, Li P, Li KF, Wu B, et al. Molecular epidemiology and spatiotemporal dynamics of norovirus associated with sporadic acute gastroenteritis during 2013-2017, Zhoushan Islands, China. PLoS One. 2018;13(7):e0200911.PubMedPubMedCentralCrossRef
47.
go back to reference Mahar JE, Kirkwood CD. Characterization of norovirus strains in Australian children from 2006 to 2008: prevalence of recombinant strains. J Med Virol. 2011;83(12):2213–9.PubMedCrossRef Mahar JE, Kirkwood CD. Characterization of norovirus strains in Australian children from 2006 to 2008: prevalence of recombinant strains. J Med Virol. 2011;83(12):2213–9.PubMedCrossRef
48.
go back to reference Phan TG, Kuroiwa T, Kaneshi K, Ueda Y, Nakaya S, Nishimura S, et al. Changing distribution of norovirus genotypes and genetic analysis of recombinant GIIb among infants and children with diarrhea in Japan. J Med Virol. 2006;78(7):971–8.PubMedCrossRef Phan TG, Kuroiwa T, Kaneshi K, Ueda Y, Nakaya S, Nishimura S, et al. Changing distribution of norovirus genotypes and genetic analysis of recombinant GIIb among infants and children with diarrhea in Japan. J Med Virol. 2006;78(7):971–8.PubMedCrossRef
49.
go back to reference Bruggink LD, Moselen JM, Marshall JA. The comparative molecular epidemiology of GII.P7_GII.6 and GII.P7_GII.7 norovirus outbreaks in Victoria, Australia, 2012-2014. Intervirology. 2016;59(1):60–5.PubMedCrossRef Bruggink LD, Moselen JM, Marshall JA. The comparative molecular epidemiology of GII.P7_GII.6 and GII.P7_GII.7 norovirus outbreaks in Victoria, Australia, 2012-2014. Intervirology. 2016;59(1):60–5.PubMedCrossRef
50.
go back to reference Nagasawa K, Matsushima Y, Motoya T, Mizukoshi F, Ueki Y, Sakon N, et al. Phylogeny and immunoreactivity of norovirus GII.P16-GII.2, Japan, winter 2016-17. Emerg Infect Dis. 2018;24(1):144–8.PubMedPubMedCentralCrossRef Nagasawa K, Matsushima Y, Motoya T, Mizukoshi F, Ueki Y, Sakon N, et al. Phylogeny and immunoreactivity of norovirus GII.P16-GII.2, Japan, winter 2016-17. Emerg Infect Dis. 2018;24(1):144–8.PubMedPubMedCentralCrossRef
51.
go back to reference Bidalot M, Théry L, Kaplon J, De Rougemont A, Ambert-Balay K. Emergence of new recombinant noroviruses GII.p16-GII.4 and GII.p16-GII.2, France, winter 2016 to 2017. Euro Surveill. 2017;22(15):30508.PubMedPubMedCentralCrossRef Bidalot M, Théry L, Kaplon J, De Rougemont A, Ambert-Balay K. Emergence of new recombinant noroviruses GII.p16-GII.4 and GII.p16-GII.2, France, winter 2016 to 2017. Euro Surveill. 2017;22(15):30508.PubMedPubMedCentralCrossRef
52.
go back to reference Kwok K, Niendorf S, Lee N, Hung TN, Chan LY, Jacobsen S, et al. Increased Detection of Emergent Recombinant Norovirus GII.P16-GII.2 Strains in Young Adults, Hong Kong, China, 2016–2017. Emerg Infect Dis. 2017;23(11):1852–5.PubMedPubMedCentralCrossRef Kwok K, Niendorf S, Lee N, Hung TN, Chan LY, Jacobsen S, et al. Increased Detection of Emergent Recombinant Norovirus GII.P16-GII.2 Strains in Young Adults, Hong Kong, China, 2016–2017. Emerg Infect Dis. 2017;23(11):1852–5.PubMedPubMedCentralCrossRef
54.
go back to reference Lu J, Fang L, Sun L, Zeng H, Li Y, Zheng H, et al. Association of GII.P16-GII.2 recombinant norovirus strain with increased norovirus outbreaks, Guangdong, China, 2016. Emerg Infect Dis. 2017;23(7):1188–90.PubMedPubMedCentralCrossRef Lu J, Fang L, Sun L, Zeng H, Li Y, Zheng H, et al. Association of GII.P16-GII.2 recombinant norovirus strain with increased norovirus outbreaks, Guangdong, China, 2016. Emerg Infect Dis. 2017;23(7):1188–90.PubMedPubMedCentralCrossRef
Metadata
Title
Genetic diversity and epidemiology of Genogroup II noroviruses in children with acute sporadic gastroenteritis in Shanghai, China, 2012–2017
Authors
Lijuan Lu
Huaqing Zhong
Menghua Xu
Liyun Su
Lingfeng Cao
Ran Jia
Jin Xu
Publication date
01-12-2019
Publisher
BioMed Central
Published in
BMC Infectious Diseases / Issue 1/2019
Electronic ISSN: 1471-2334
DOI
https://doi.org/10.1186/s12879-019-4360-1

Other articles of this Issue 1/2019

BMC Infectious Diseases 1/2019 Go to the issue