Evidence map›Paper›PMID 42469826›Full record

ArticleBMC veterinary research2026

Development of a TaqMan RT-qPCR for the detection and genotyping of bovine viral diarrhea virus types 1, 2, and HoBi-like pestivirus.

Yangyang Xiao, Qianqian Dong, Yifei Wu, Yang Yang, Jinchao Wang, Tao He, Qinghua Luo, Bowen Li, Tianying Chi, Ang Li and 2 more

Abstract read
In one paragraph

Article in BMC veterinary research, 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

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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

12 authors.

Yangyang Xiao *College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang, 832000, China.
Qianqian Dong *College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang, 832000, China.
Yifei WuSchool of Biological & Chemical Engineering, Chongqing University of Education, Chongqing, 400067, China.
Yang YangCollege of Life Sciences, Northwest A&F University, Yangling, Shaanxi, 712100, China.
Jinchao WangSub-center of the China Animal Health and Epidemiology Center for the National Center for Veterinary Culture Collection, Qingdao, Shandong, 266032, China.
Tao HeCollege of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang, 832000, China.
Qinghua LuoSub-center of the China Animal Health and Epidemiology Center for the National Center for Veterinary Culture Collection, Qingdao, Shandong, 266032, China.
Bowen LiSub-center of the China Animal Health and Epidemiology Center for the National Center for Veterinary Culture Collection, Qingdao, Shandong, 266032, China.
Tianying ChiSub-center of the China Animal Health and Epidemiology Center for the National Center for Veterinary Culture Collection, Qingdao, Shandong, 266032, China.
Ang LiSub-center of the China Animal Health and Epidemiology Center for the National Center for Veterinary Culture Collection, Qingdao, Shandong, 266032, China.
Jinliang ShengCollege of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang, 832000, China. sjlshz@126.com.
Faxing WuSub-center of the China Animal Health and Epidemiology Center for the National Center for Veterinary Culture Collection, Qingdao, Shandong, 266032, China. wufaxing@cahec.cn.

Funding

National Natural Science Foundation of China Grant No. 32460872)Qingdao Municipal Science & Technology Benefiting-the-People Demonstration Project Grant No.25-1-5-xdny-30-nsh
6 · The paper itself

Abstract

backgroundHoBi-like pestivirus (HoBiPeV), as a newly discovered virus species in recent years, poses a serious threat to the global cattle industry due to its wide transmission and high pathogenicity. The genetic sequence of HoBiPeV exhibits significant differences when compared to the known strains of BVDV-1 (Pestivirus bovis) and BVDV-2 (Pestivirus tauri).Current detection methods are typically limited to identifying BVDV-1 and BVDV-2, and are unable to effectively differentiate HoBiPeV from the other two genotypes. To facilitate the rapid detection and differentiation of various genotypes, this study developed a pair of universal primers along with three TaqMan probes based on the 5' UTR sequences of the BVDV-1, BVDV-2, and HoBiPeV available in GenBank. A one-step multiplex TaqMan RT-qPCR detection method was developed.

resultsThe results showed that this method could specifically detect the three genotypes of BVDV without cross-reactivity. It exhibited high sensitivity, with a minimum detection limit of 1 × 10¹copies/µL. The amplification efficiencies were 104.6%, 102.9%, and 117.7%, respectively, demonstrating a strong linear relationship (R

conclusionsThis method not only significantly enhances the detection rate of HoBiPeV but also reveals the potential prevalence of this genotype in cattle populations, providing valuable insights for updating existing epidemiological databases and informing the selection of vaccine strains. The method is applicable in areas such as the detection of raw materials and intermediates during vaccine production, quality control of dairy products, and large-scale virus monitoring. It also exhibits broad application value in epidemiological investigations and the prevention and control of viral diseases in cattle farms.

Indexed as

Diarrhea Virus 1, Bovine ViralDiarrhea Virus 2, Bovine ViralDiarrhea Viruses, Bovine ViralPestivirusReal-Time Polymerase Chain Reaction5' Untranslated RegionsAnimalsBovine Virus Diarrhea-Mucosal DiseaseCattleGenotypePestivirus InfectionsSensitivity and Specificity5' Untranslated RegionsBovine viral diarrhea virusDetectionDifferentiationMultiplex RT-qPCRTaqMan probes

Identifiers

PMID42469826
PMCPMC13670847

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