Evidence map›Paper›PMID 42514641›Full record

ArticleVeterinary sciences2026

Molecular Epidemiological Survey of Porcine Rotavirus in the Guangxi Region from 2020 to 2025 and Isolation and Identification of the G9P[23] Strain CH-GXGL-PoRV-3151-2021.

Shuo Zhao, Xianhua Wu, Ying He, Jinmu Lin, Xinlin Zhong, Baojiang Lin, Wen Zhao, Xinting Xu, Qunpeng Duan, Xunye Yang and 11 more

Abstract read
In one paragraph

Article in Veterinary sciences, 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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2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Shuo ZhaoAnimal Science and Technology College, Guangxi University, Nanning 530004, China.ORCID 0009-0008-5965-0362
Xianhua WuAnimal Science and Technology College, Guangxi University, Nanning 530004, China.
Ying HeKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Jinmu LinPeople's Government of Xinjing Town, Baise 533899, China.
Xinlin ZhongAnimal Science and Technology College, Guangxi University, Nanning 530004, China.
Baojiang LinGuangxi Reclamation Yongxin Animal Husbandry Group Xijiang Co., Ltd., Guigang 537104, China.
Wen ZhaoAnimal Science and Technology College, Guangxi University, Nanning 530004, China.
Xinting XuKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Qunpeng DuanAnimal Science and Technology College, Guangxi University, Nanning 530004, China.
Xunye YangKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Han ShaoAnimal Science and Technology College, Guangxi University, Nanning 530004, China.
Ying PengKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Yilan XuKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Tingting ChenKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Chenyu QuanKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Bingxia LuKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Wenfeng WangKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Yang QinKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Zhongwei ChenKey Laboratory of Veterinary Biotechnology of Guangxi, Guangxi Veterinary Research Institute, Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs, Nanning 530001, China.
Yangqing LuAnimal Science and Technology College, Guangxi University, Nanning 530004, China.
Yibin QinAnimal Science and Technology College, Guangxi University, Nanning 530004, China.

Funding

Guangxi Basic Research Operating Expenses Special Fund 22-4Guangxi Basic Research Operating Expenses Special Fund 23-3Guangxi Key R&D Project Guike AB25069246Nanning Municipal Science and Technology Heavy Sky Special Project 20232039National Modern Agricultural Industrial Technology System Guangxi Innovation Team Development Project myetxgxentd-2023-15-02Self-Financed Agricultural Science and Technology Projects in Guangxi Z2023034Self-Financed Agricultural Science and Technology Projects in Guangxi Z2202225
6 · The paper itself

Abstract

Porcine rotavirus (PoRV) has emerged as a primary pathogen causing viral diarrhea in pigs, resulting in significant economic losses. This study was conducted to systematically characterize the epidemiology and genotypic characteristics of PoRV in Guangxi, China. A total of 870 diarrheic pig samples were collected from Guangxi during 2020-2025. The qRT-PCR results indicated an overall PoRV-positive rate of 41.38% (360/870), and the annual positivity rate showed an overall upward trend. The genetic evolutionary analysis of the VP4, VP6, and VP7 genes indicated that PoRV predominantly belonged to the A group and the predominant P genotype observed was P[13] (76.83%), while the G genotypes were G5 (36.56%) and G9 (33.33%). The most prevalent genotype combinations were G9P[13]I5 and G5P[13]I5. CH-GXGL-PoRV-3151-2021, a PoRV strain isolated from positive samples, was identified via RT-PCR, qRT-PCR, whole-genome sequencing, and IFA. This strain was assigned the 11-segment genotype constellation G9-P[23]-I5-R1-C1-M1-A8-N1-T1-E1-H1 based on whole-genome sequencing. NSP1 and NSP2 showed high similarity to human rotavirus strains, whereas VP1-VP4, VP6, VP7, and NSP3-NSP5 showed high similarity to porcine rotavirus strains. This study indicates the widespread circulation of PoRV in Guangxi, with multiple G genotypes, including G9, G5, G4, G3, G2, and G26, being detected. The isolated G9P[23]I5 strain exhibits the same genotype as the strains that have become increasingly prevalent in recent years. This strain may represent a possible reassortant between porcine and human rotaviruses. This study offers significant insights into the epidemiology of PoRV and the prevalent genotypes in Guangxi, thereby supporting the development of targeted prevention strategies and novel vaccines.

Indexed as

genotypingmolecular epidemiologyphylogenetic analysesporcine rotavirusvirus isolation

Identifiers

PMID42514641
PMCPMC13417820

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