Liu Ying, Zhou Feng, Wang Xuan-Ang, Chen Xi-Meng, Zheng Lan-Lan, Chen Hong-Ying, Ma Shi-Jie
Ministry of Education Key Laboratory for Animal Pathogens and Biosafety, College of Veterinary Medicine, Henan Agricultural University, Zhengdong New District Longzi Lake #15, Zhengzhou, Henan Province, 450046, P.R. China.
Henan Seed Industry Development Center, Zhengzhou, Henan Province, 450000, P.R. China.
Arch Virol. 2025 Apr 29;170(6):114. doi: 10.1007/s00705-025-06304-7.
Bovine viral diarrhea virus (BVDV) is one of the major pathogens hindering the development of the global beef industry. To investigate the epidemic profile and genetic diversity of this virus, a total of 77 fecal samples were collected from cattle with diarrhea in Henan, Sichuan, Shandong, and Hebei provinces of China during 2023-2024 and screened for the presence of BVDV using reverse transcription polymerase chain reaction (RT-PCR). The results showed that 35 of the 77 bovine samples (45%) were positive for BVDV, with the highest positive rate of 26% (20/77) in Henan province. The 5'-UTR sequences of the viruses from 21 positive samples and the whole-genome sequence from one sample (BVDV-385) were determined and analyzed. The 5'-UTR sequences from this study were 74.7-96.4% identical to those of 23 reference sequences. Phylogenetic analysis based on the 5'-UTR sequences indicated that 20 of the strains belonged to the subtype BVDV-1m, while only one, BVDV-385 from Henan province, belonged to genotype BVDV-3. Analysis of the genome sequence of strain BVDV-385 showed that its E2 protein has a unique amino acid (aa) deletion and ten unique aa substitutions, and its NS5B protein has seven unique aa substitutions. The variations were predicted to affect four potential linear B cell epitopes in the E2 protein and to introduce a potential non-canonical N-glycosylation site (574 NPS) in the NS5B protein. The results of this study contribute to our understanding of the genetic diversity of BVDV in China.
牛病毒性腹泻病毒(BVDV)是阻碍全球牛肉产业发展的主要病原体之一。为了调查该病毒的流行概况和遗传多样性,2023年至2024年期间,在中国河南、四川、山东和河北省共采集了77份腹泻牛的粪便样本,并采用逆转录聚合酶链反应(RT-PCR)检测其中是否存在BVDV。结果显示,77份牛样本中有35份(45%)BVDV呈阳性,河南省的阳性率最高,为26%(20/77)。测定并分析了21份阳性样本中病毒的5'-UTR序列以及1份样本(BVDV-385)的全基因组序列。本研究中的5'-UTR序列与23条参考序列的同源性为74.7%-96.4%。基于5'-UTR序列的系统发育分析表明,其中20株属于BVDV-1m亚型,而仅1株来自河南省的BVDV-385属于BVDV-3基因型。对BVDV-385毒株的基因组序列分析表明,其E2蛋白存在一个独特的氨基酸(aa)缺失和十个独特的aa替换,其NS5B蛋白有七个独特的aa替换。这些变异预计会影响E2蛋白中的四个潜在线性B细胞表位,并在NS5B蛋白中引入一个潜在的非典型N-糖基化位点(574 NPS)。本研究结果有助于我们了解中国BVDV的遗传多样性。