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高致病性牛病毒性腹泻病毒BJ-11揭示了与犊牛毒力相关的基因进化。

Highly pathogenic bovine viral diarrhea virus BJ-11 unveils genetic evolution related to virulence in calves.

作者信息

Zhang Yuanyuan, Cheng Jing, Guo Yu, Hu Yibin, Zhao Zhuo, Liu Wenxiao, Zhou Linyi, Wu Peize, Cheng Chunjie, Yang Chun, Yang Jing, Du Enqi, Li Yongqing

机构信息

Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China.

College of Veterinary Medicine, Northwest A&F University, Yangling, China.

出版信息

Front Microbiol. 2025 Jan 14;15:1540358. doi: 10.3389/fmicb.2024.1540358. eCollection 2024.

DOI:10.3389/fmicb.2024.1540358
PMID:39877754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11772275/
Abstract

Bovine viral diarrhea virus (BVDV) is the causative agent of bovine viral diarrhea, which causes significant economic loss to the global livestock industry. Despite the widespread use of inactivated BVDV vaccines, highly pathogenic strains continue to emerge. In China, regional variations in BVDV subtypes, morbidities, and symptoms, however, only the BVDV 1a subtype vaccine is currently approved. Therefore, this study is to gain insight into the biological characteristics and genetic variation of BVDV strains prevalent in Beijing. Meanwhile, this will provide a theoretical foundation and technical support for the prevention and control of BVDV, as well as raise awareness of the potential for virulence enhancement caused by the unregulated use of BVDV vaccines. In this study, A BVDV strain, BJ-11, was isolated from calves that died of diarrhea and vaccinated of BVDV. To evaluate its virulence, newborn calves were experimentally infected with the BJ-11. Clinical signs included fever, diarrhea, bloody stools, anorexia, and death in some cases. A marked reduction in leukocyte and lymphocyte counts were observed, accompanied by an increase in neutrophil counts. Histopathological changes manifested as severe lung lesions. Phylogenetic analysis indicated that BJ-11 belongs to the BVDV 1b subtype, genetically closest to the JL-1 strain. Analysis of the E2 glycosylation site disappeared (298SYT) in one of the four common glycosylation sites in the BVDV-1, which has been reported to affect the ability of the virus to infect and an additional glycosylation site (122NGS). These results indicate that BJ-11 is a highly pathogenic strain evolved from a low-virulence ancestor and should be served as a challenge strain. Simultaneously, these results contribute to a broader understanding of BVDV and whether imperfect vaccination strategies lead to reversal of immunosuppressive virulence.

摘要

牛病毒性腹泻病毒(BVDV)是牛病毒性腹泻的病原体,给全球畜牧业造成了巨大的经济损失。尽管灭活的BVDV疫苗被广泛使用,但高致病性毒株仍不断出现。在中国,BVDV亚型、发病率和症状存在区域差异,然而目前仅批准了BVDV 1a亚型疫苗。因此,本研究旨在深入了解北京地区流行的BVDV毒株的生物学特性和基因变异。同时,这将为BVDV的防控提供理论基础和技术支持,并提高对BVDV疫苗使用不当导致毒力增强可能性的认识。在本研究中,从死于腹泻且接种过BVDV疫苗的犊牛中分离出一株BVDV毒株BJ - 11。为评估其毒力,将新生犊牛用BJ - 11进行实验性感染。临床症状包括发热、腹泻、血便、厌食,部分病例出现死亡。观察到白细胞和淋巴细胞计数显著减少,同时中性粒细胞计数增加。组织病理学变化表现为严重的肺部病变。系统发育分析表明,BJ - 11属于BVDV 1b亚型,在基因上与JL - 1毒株最为接近。分析发现BVDV - 1四个常见糖基化位点之一的E2糖基化位点消失(298SYT),据报道这会影响病毒的感染能力,并且出现了一个额外的糖基化位点(122NGS)。这些结果表明,BJ - 11是一株从低毒力祖先进化而来的高致病性毒株,应作为攻毒毒株。同时,这些结果有助于更广泛地了解BVDV以及不完善的疫苗接种策略是否会导致免疫抑制毒力的逆转。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/7a42ef0f7f51/fmicb-15-1540358-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/2ca7426790bc/fmicb-15-1540358-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/e50b46ad2ec2/fmicb-15-1540358-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/11ce925933e3/fmicb-15-1540358-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/092c7f462b7c/fmicb-15-1540358-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/82d5f24d6d25/fmicb-15-1540358-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/56edcc222296/fmicb-15-1540358-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/4d794bf0464f/fmicb-15-1540358-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/2f4f6830785c/fmicb-15-1540358-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/7a42ef0f7f51/fmicb-15-1540358-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/2ca7426790bc/fmicb-15-1540358-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/e50b46ad2ec2/fmicb-15-1540358-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/11ce925933e3/fmicb-15-1540358-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/092c7f462b7c/fmicb-15-1540358-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/82d5f24d6d25/fmicb-15-1540358-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/56edcc222296/fmicb-15-1540358-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/4d794bf0464f/fmicb-15-1540358-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/2f4f6830785c/fmicb-15-1540358-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6924/11772275/7a42ef0f7f51/fmicb-15-1540358-g009.jpg

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