Guangli Hu , Zhiqing Zhao , Liguo Gao , Rui Geng , Shengjin Liu , Hao Zhang , Yongchang Cao , Hanqin Shen , Chunyi Xue
{"title":"Assessment of genetic diversity and pathogenicity of porcine rotavirus A, and immunogenicity of a bivalent inactivated vaccine in southern China","authors":"Guangli Hu , Zhiqing Zhao , Liguo Gao , Rui Geng , Shengjin Liu , Hao Zhang , Yongchang Cao , Hanqin Shen , Chunyi Xue","doi":"10.1016/j.vetmic.2026.110893","DOIUrl":null,"url":null,"abstract":"<div><div>Porcine group A rotavirus (PoRVA) is a widespread enteric pathogen that causes severe diarrheal outbreaks in swine herds, leading to considerable economic losses in China’s pig farming industry. From 2022–2024, a systematic surveillance was conducted across southern China, during which 5425 diarrheic samples were collected to assess the epidemiology of PoRVA. The results showed that PoRVA infections peaked in winter and spring, with monthly positivity rates ranging from 36 % to 68 % in southern regions. Genotyping of 103 VP4/VP7 sequences revealed the predominant VP7 genotypes G5 (43.69 %), G4 (23.39 %), and G9 (15.53 %), as well as the major VP4 genotypes P[13] (68.93 %), P[6] (10.68 %), and P[23] (9.71 %). Two PoRVA strains were successfully isolated from positive intestinal samples collected in Guangdong and Jiangsu provinces, designated RVA/Pig/China/JS/2024/G9P[23] (JS2024) and RVA/Pig/China/GD/2024/G5P[13] (GD2024), respectively. Experimental infection demonstrated that both isolates caused severe watery diarrhea in 3-day-old colostrum-deprived piglets, resulting in mortality rates of 40 % (2/5) for JS2024 and 20 % (1/5) for GD2024. A bivalent inactivated vaccine prepared with the two isolates (10^8 TCID<sub>50</sub>/mL per antigen, administered twice at a 14-day interval) elicited robust neutralizing antibody responses against both G5 and G9 genotypes. Furthermore, maternal immunization with the bivalent vaccine in pregnant sows resulted in efficient transfer of maternal antibodies to neonatal piglets. Piglets born to vaccinated sows exhibited significantly higher pre-challenge neutralizing antibody titers, developed only mild clinical diarrhea following JS2024 or GD2024 challenge, displayed substantially reduced fecal viral shedding, and showed 100 % survival, in contrast to unvaccinated litters, which experienced severe diarrhea, high viral loads, and mortality. Collectively, these findings suggest that both isolates are promising vaccine candidates and provide essential data for future PoRVA prevention and control strategies.</div></div>","PeriodicalId":23551,"journal":{"name":"Veterinary microbiology","volume":"314 ","pages":"Article 110893"},"PeriodicalIF":2.8000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary microbiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378113526000246","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/22 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Porcine group A rotavirus (PoRVA) is a widespread enteric pathogen that causes severe diarrheal outbreaks in swine herds, leading to considerable economic losses in China’s pig farming industry. From 2022–2024, a systematic surveillance was conducted across southern China, during which 5425 diarrheic samples were collected to assess the epidemiology of PoRVA. The results showed that PoRVA infections peaked in winter and spring, with monthly positivity rates ranging from 36 % to 68 % in southern regions. Genotyping of 103 VP4/VP7 sequences revealed the predominant VP7 genotypes G5 (43.69 %), G4 (23.39 %), and G9 (15.53 %), as well as the major VP4 genotypes P[13] (68.93 %), P[6] (10.68 %), and P[23] (9.71 %). Two PoRVA strains were successfully isolated from positive intestinal samples collected in Guangdong and Jiangsu provinces, designated RVA/Pig/China/JS/2024/G9P[23] (JS2024) and RVA/Pig/China/GD/2024/G5P[13] (GD2024), respectively. Experimental infection demonstrated that both isolates caused severe watery diarrhea in 3-day-old colostrum-deprived piglets, resulting in mortality rates of 40 % (2/5) for JS2024 and 20 % (1/5) for GD2024. A bivalent inactivated vaccine prepared with the two isolates (10^8 TCID50/mL per antigen, administered twice at a 14-day interval) elicited robust neutralizing antibody responses against both G5 and G9 genotypes. Furthermore, maternal immunization with the bivalent vaccine in pregnant sows resulted in efficient transfer of maternal antibodies to neonatal piglets. Piglets born to vaccinated sows exhibited significantly higher pre-challenge neutralizing antibody titers, developed only mild clinical diarrhea following JS2024 or GD2024 challenge, displayed substantially reduced fecal viral shedding, and showed 100 % survival, in contrast to unvaccinated litters, which experienced severe diarrhea, high viral loads, and mortality. Collectively, these findings suggest that both isolates are promising vaccine candidates and provide essential data for future PoRVA prevention and control strategies.
期刊介绍:
Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal.
Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge.
Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.