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Molecular genetic characterisation of norovirus GII.17 strains circulating in South Korea in 2024
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View Affiliations Hide AffiliationsCorrespondence:Sun-Whan Parksunwhan korea.kr
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Citation style for this article: . Molecular genetic characterisation of norovirus GII.17 strains circulating in South Korea in 2024. Euro Surveill. 2026;31(13):pii=2500372. https://doi.org/10.2807/1560-7917.ES.2026.31.13.2500372 Received: 28 May 2025; Accepted: 16 Sept 2025
Abstract
In South Korea, norovirus outbreaks have been predominantly attributed to the GII.4 genotype; however, since mid-2024, strains harbouring the GII.17 genotype are being detected more frequently, raising concerns about a potential shift in the dominant circulating strain and resulting public health implications.
We aimed to analyse the nt sequences of the gene encoding the viral protein 1 (VP1), the major capsid protein, of the GII.17 norovirus strains detected in South Korea in 2024, compare them with the corresponding nt sequences of the GII.17 Kawasaki 2014 lineage strains and evaluate whether GII.17 has the potential to replace the long-dominant GII.4 genotype.
We obtained 11 complete VP1 sequences from stool specimens collected across six regions in South Korea (Busan, Daejeon, Gangwon-do, Gyeongsangbuk-do, Incheon, Jeollanam-do) in 2024 and compared them with the VP1 sequence of the reference strain (GII.17 Kawasaki 2014) to identify genetic changes.
Key amino acid substitutions (R299P, N378D and K388R) were identified in the P2 domain of the VP1, which is a major antigenic site. Notably, N378D corresponds to D374 in the GII.4 genotype, which is a position involved in histo-blood group antigen (HBGA) binding, and K388R, adjacent to other antigenic sites, may alter the surface charge of the capsid.
The data provide molecular evidence that the emerging GII.17 strain in South Korea may evade the host immune surveillance machinery and exhibit altered receptor binding, underscoring the public health threat posed by this strain and the need for enhanced genomic surveillance and effective vaccine development.
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