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2022 - 2023年中国广西和江苏省J亚群禽白血病病毒的分离与分子特征

Isolation and molecular characteristic of subgroup J avian leukosis virus in Guangxi and Jiangsu provinces of China during 2022-2023.

作者信息

Wang Zeming, Wang Shengnan, Li Jingwen, Miao Tiantian, Luo Yi, Shen Tianjie, Zhang Qi, Li Tianzi, Wu Jiayan, Ma Lihua, Xiang Ruping, Zhang Jun, Wan Zhimin, Xie Quan, Shao Hongxia, Qin Aijian, Ye Jianqiang, Li Tuofan

机构信息

Key Laboratory of Jiangsu Preventive Veterinary Medicine, Key Laboratory for Avian Preventive Medicine, Ministry of Education, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, PR China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu, PR China; Joint International Research Laboratory of Agriculture and Agri-Product Safety, the Ministry of Education of China, Yangzhou University, Yangzhou, Jiangsu, PR China.

Key Laboratory of Jiangsu Preventive Veterinary Medicine, Key Laboratory for Avian Preventive Medicine, Ministry of Education, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, PR China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu, PR China; Joint International Research Laboratory of Agriculture and Agri-Product Safety, the Ministry of Education of China, Yangzhou University, Yangzhou, Jiangsu, PR China; Institutes of Agricultural Science and Technology Development, Yangzhou University, Yangzhou, Jiangsu, PR China.

出版信息

Poult Sci. 2025 May 7;104(8):105272. doi: 10.1016/j.psj.2025.105272.

Abstract

Subgroup J avian leukosis virus (ALV-J) has significantly affected the global poultry industry, with rapid mutations and frequent outbreaks in the poultry industry of China, challenging the current eradication strategies. In this study, virus isolation, identification, and complete genome sequencing of suspected ALV-J-infected samples collected from Guangxi and Jiangsu provinces during 2022-2023 were performed. Four ALV-J strains (designated as, GXZM01, GXZM02, JSZM02, and JSZM963) were successfully isolated and sequenced, with genome lengths ranging from 7487 to 7636 bp and a homology of 82.8 %-96.5 % with the reference ALV-J strains. The amino acid sequences of the gag and pol genes of the isolated strains showed relatively high conservation, with homologies of 95-100 % and 97.1-99.5 % compared with the reference strains, respectively. Analysis of the 3'UTR revealed that the 4 ALV-J isolates show different type of mutations compared to the reference strains, with all the isolates containing a 175 bp deletion at the r-TM, while the JSZM02 strain uniquely showed a 127 bp deletion in the E element. The homology of Env protein and Gp85 protein between the 4 isolates and the reference strains ranged from 86.5 to 95.6 % and 83.7 to 93.8 %, respectively. Notably, in comparison with ALV-J prototype strain HPRS-103, we found that a distinct deletion of 11 aa located at 209-219 aa of Gp85 protein of GXZM02 strain which located at the receptor-binding domain (RBD) and partially overlapped with hypervariable region2 (hr2). Structural prediction analysis revealed that the Gp85 proteins of these ALV-J strains exhibited certain differences in the number of α-helices and β-sheets. Importantly, viral growth kinetic showed that the replication ability of GXZM02 was the weakest one among the 4 isolates, which is potentially related to the deletion in the RBD. Our findings contribute to enrich the epidemiological data on ALV-J and reveal the evolution of prevalent ALV-J strains in clinic, which will provide scientific basis for ALV prevention and control.

摘要

J亚群禽白血病病毒(ALV-J)已对全球家禽业造成重大影响,在中国家禽业中其突变迅速且疫情频发,对当前的根除策略构成挑战。本研究对2022年至2023年期间从广西和江苏省采集的疑似感染ALV-J的样本进行了病毒分离、鉴定及全基因组测序。成功分离并测序了4株ALV-J毒株(分别命名为GXZM01、GXZM02、JSZM02和JSZM963),基因组长度在7487至7636 bp之间,与参考ALV-J毒株的同源性为82.8%-96.5%。分离毒株的gag和pol基因氨基酸序列显示出较高的保守性,与参考毒株的同源性分别为95%-100%和97.1%-99.5%。对3'UTR的分析表明,与参考毒株相比,这4株ALV-J分离株呈现出不同类型的突变,所有分离株在r-TM处均有175 bp的缺失,而JSZM02毒株在E元件中独特地出现了127 bp的缺失。4株分离株与参考毒株之间Env蛋白和Gp85蛋白的同源性分别为86.5%至95.6%和83.7%至93.8%。值得注意的是,与ALV-J原型毒株HPRS-103相比,我们发现GXZM02毒株Gp85蛋白位于受体结合域(RBD)的209-219 aa处有11个氨基酸的明显缺失,且部分与高变区2(hr2)重叠。结构预测分析表明,这些ALV-J毒株的Gp85蛋白在α螺旋和β折叠的数量上存在一定差异。重要的是,病毒生长动力学显示,GXZM02的复制能力在4株分离株中最弱,这可能与RBD中的缺失有关。我们的研究结果有助于丰富ALV-J的流行病学数据,并揭示临床中流行的ALV-J毒株的进化情况,为ALV的防控提供科学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/550a/12141838/76fd19de345c/gr1.jpg

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