TY - JOUR
T1 - Epidemiology and molecular evolution of GI.1 sapovirus in the recent era
AU - Hoque, Sheikh A.
AU - Akari, Yuki
AU - Khamrin, Pattara
AU - Phan, Tung
AU - Onda, Yuko
AU - Okitsu, Shoko
AU - Komoto, Satoshi
AU - Hayakawa, Satoshi
AU - Komine- Aizawa, Shihoko
AU - Yuki, Yoshikazu
AU - Kiyono, Hiroshi
AU - Ushijima, Hiroshi
N1 - Publisher Copyright:
© 2024 Wiley Periodicals LLC.
PY - 2024/9
Y1 - 2024/9
N2 - Sapovirus (SaV) infection is increasing worldwide. Herein, we provided evidence of a significant increase in SaV infection in Japan during 2010–2022, primarily due to the considerable (p = 0.0003) rise of the GI.1 genotype. Furthermore, we found that all major and minor SaV outbreaks in Japan, including the largest SaV outbreak in 2021–2022, were caused by the GI.1 genotype. Therefore, to get insight into the underlying molecular mechanism behind this rising trend of the SaV GI.1 type, we selected 15 SaV GI.1 outbreak strains for complete genome analysis through next-generation sequencing. Phylogenetically, our strains remained clustered in different branches in lineages I and II among the GI.1 genotype. We showed all amino acid (aa) substitutions in different open reading frames (ORFs) in these strains. Importantly, we have demonstrated that the strains involved in the largest SaV outbreak in Japan in 2021–2022 belonged to lineage II and possessed the third ORF. We have identified some unique aa mutations in these major outbreak strains in the NS1 and NS6-NS7 regions that are thought to be associated with viral pathogenicity, cell tropism, and epidemiological competence. Thus, in addition to enriching the database of SaV's complete sequences, this study provides insights into its important mutations.
AB - Sapovirus (SaV) infection is increasing worldwide. Herein, we provided evidence of a significant increase in SaV infection in Japan during 2010–2022, primarily due to the considerable (p = 0.0003) rise of the GI.1 genotype. Furthermore, we found that all major and minor SaV outbreaks in Japan, including the largest SaV outbreak in 2021–2022, were caused by the GI.1 genotype. Therefore, to get insight into the underlying molecular mechanism behind this rising trend of the SaV GI.1 type, we selected 15 SaV GI.1 outbreak strains for complete genome analysis through next-generation sequencing. Phylogenetically, our strains remained clustered in different branches in lineages I and II among the GI.1 genotype. We showed all amino acid (aa) substitutions in different open reading frames (ORFs) in these strains. Importantly, we have demonstrated that the strains involved in the largest SaV outbreak in Japan in 2021–2022 belonged to lineage II and possessed the third ORF. We have identified some unique aa mutations in these major outbreak strains in the NS1 and NS6-NS7 regions that are thought to be associated with viral pathogenicity, cell tropism, and epidemiological competence. Thus, in addition to enriching the database of SaV's complete sequences, this study provides insights into its important mutations.
KW - GI.1 genotype
KW - ORFs
KW - deduced amino acid sequences
KW - epidemics
KW - molecular evolution
KW - phylogenetic analysis
KW - sapovirus
UR - https://www.scopus.com/pages/publications/85203582760
UR - https://www.scopus.com/inward/citedby.url?scp=85203582760&partnerID=8YFLogxK
U2 - 10.1002/jmv.29904
DO - 10.1002/jmv.29904
M3 - Article
C2 - 39264064
AN - SCOPUS:85203582760
SN - 0146-6615
VL - 96
JO - Journal of Medical Virology
JF - Journal of Medical Virology
IS - 9
M1 - e29904
ER -