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中国四个省份牛病毒性腹泻病毒的分子检测与基因分型

Molecular detection and genotyping of bovine viral diarrhea virus in four provinces of China.

作者信息

Liu Ying, Zhou Feng, Wang Xuan-Ang, Chen Xi-Meng, Zheng Lan-Lan, Chen Hong-Ying, Ma Shi-Jie

机构信息

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.

出版信息

Arch Virol. 2025 Apr 29;170(6):114. doi: 10.1007/s00705-025-06304-7.

Abstract

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.

摘要

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。

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