Complete sequence analysis of human norovirus GII.17 detected in South Korea

Epidemiol Infect. 2019 Jan:147:e203. doi: 10.1017/S0950268819000943.

Abstract

Norovirus, a major cause of gastroenteritis in people of all ages worldwide, was first reported in South Korea in 1999. The most common causal agents of pediatric acute gastroenteritis are norovirus and rotavirus. While vaccination has reduced the pediatric rotavirus infection rate, norovirus vaccines have not been developed. Therefore, prediction and prevention of norovirus are very important. Norovirus is divided into genogroups GI-GVII, with GII.4 being the most prevalent. However, in 2012-2013, GII.17 showed a higher incidence than GII.4 and a novel variant, GII.P17-GII.17, appeared. In this study, 204 stool samples collected in 2013-2014 were screened by reverse transcriptase-polymerase chain reaction; 11 GI (5.39%) and 45 GII (22.06%) noroviruses were identified. GI.4, GI.5, GII.4, GII.6 and GII.17 were detected. The whole genomes of the three norovirus GII.17 were sequenced. The whole genome of GII.17 consists of three open reading frames of 5109, 1623 and 780 bp. Compared with 20 GII.17 strains isolated in other countries, we observed numerous changes in the protruding P2 domain of VP1 in the Korean GII.17 viruses. Our study provided genome information that might aid in epidemic prevention, epidemiology studies and vaccine development.

Keywords: GII.17.; Gastroenteritis; norovirus; phylogenetic tree; sequence analysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caliciviridae Infections / epidemiology
  • Caliciviridae Infections / virology*
  • Feces / virology
  • Gastroenteritis / epidemiology
  • Gastroenteritis / virology*
  • Genotype*
  • Humans
  • Incidence
  • Molecular Epidemiology
  • Norovirus / classification
  • Norovirus / genetics*
  • Norovirus / isolation & purification*
  • Open Reading Frames
  • Phylogeny
  • Republic of Korea / epidemiology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis*
  • Sequence Homology
  • Whole Genome Sequencing*