Evidence map›Paper›PMID 42310243›Full record

ArticleArchives of virology2026

Molecular epidemiology of DS-1-like G1P[8] rotavirus strains in Vietnam, 2012-2016: Evolutionary dynamics of an unusual rotavirus reassortant.

Pham Thi Tam, Manh Hung Vu, Thi Nguyen Hoa-Tran, Thi Hai Anh Dao, The Anh Nguyen, Thi Hong Duong, Thi Thanh Huyen Dang, Thanh Trung Nguyen, Hong Mai Hoang, Thi Viet Ha Nguyen and 10 more

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Article in Archives of virology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

20 authors.

Pham Thi TamNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Manh Hung VuNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Thi Nguyen Hoa-TranNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam. trnghoasuk@gmail.com.ORCID http://orcid.org/0000-0001-6887-7317
Thi Hai Anh DaoNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
The Anh NguyenNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Thi Hong DuongNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Thi Thanh Huyen DangNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Thanh Trung NguyenNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Hong Mai HoangNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Thi Viet Ha NguyenNational Children's Hospital, Hanoi, Vietnam.
Thuy Huong NguyenCenter for Research and Production of Vaccines and Biologicals, Hanoi, Vietnam.
Grabovac VarjaWorld Health Organization Regional Office for the Western Pacific, Manila, Philippines.
Thomas SarahMurdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Julie E BinesMurdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Celeste M DonatoMurdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Futoshi HasebeInstitute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Toshio KodamaInstitute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Haruka AbeInstitute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Toyoko NakagomiGraduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Osamu NakagomiGraduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

Funding

Japan Agency for Medical Research and Development (AMED) JP20wm0125006 and JP25wm0125006Japan Agency for Medical Research and Development (AMED) JP25wm0125006
6 · The paper itself

Abstract

The segmented genome of Rotavirus alphagastroenteritidis facilitates the emergence of unusual reassortants, increasingly documented in the post-vaccine era. However, their long-term evolutionary dynamics and population-level persistence remain poorly understood. We investigated G1P[8] strains detected through hospital-based surveillance in northern and central Vietnam from 2012 to 2016. Electropherotyping, whole-genome sequencing, and phylogenetic analyses were performed to define genomic constellations and reconstruct evolutionary dynamics of DS-1-like reassortants. We documented four-year circulation patterns of DS-1-like G1P[8] strains, emerging in 2012/2013, peaking in mid-2014, and declining by 2016. Among 44 strains exhibiting short electropherotypes, at least three sequential genotype constellations (A-C) were identified: Constellation A likely arose in northern Vietnam through inter-genogroup reassortment between Wa-like G1P[8] (VP7/VP4) and DS-1-like G2P[4] strains; A related variant in central Vietnam suggested regional transmission from contemporaneous strains reported in Thailand and Japan; Constellation B involved acquisition of a Wa-like NSP2 gene; Constellation C included additional reassortment with bovine-like NSP2 and NSP4 genes from a co-circulating G8P[8] strain. No significant differences in clinical severity were observed between DS-1-like and Wa-like infections, and no cases of either genotype were detected among fully vaccinated children. Overall, this study describes a stepwise reassortment process involving intergenogroup, intragenogroup, and potential zoonotic events. Genomic diversification in this setting was not associated with increased virulence or evidence of immune escape. These findings highlight the need for continued genomic surveillance and broader sampling to better resolve the evolutionary dynamics of rotavirus reassortants.

Indexed as

Evolution, MolecularReassortant VirusesRotavirusRotavirus InfectionsAnimalsGenome, ViralGenotypeHumansMolecular EpidemiologyPhylogenyRNA, ViralVietnamRNA, Viral

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