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2011年从中国南方鸡群中分离出的传染性法氏囊病病毒的分子特征及系统发育分析

Molecular characterization and phylogenetic analysis of infectious bursal disease viruses isolated from chicken in South China in 2011.

作者信息

Liu Di, Zhang Xiang-Bin, Yan Zhuan-Qiang, Chen Feng, Ji Jun, Qin Jian-Ping, Li Hai-Yan, Lu Jun-Peng, Xue Yu, Liu Jia-Jia, Xie Qing-Mei, Ma Jing-Yun, Xue Chun-Yi, Bee Ying-Zuo

机构信息

College of Animal Science, South China Agricultural University, Guangzhou, 510642, China.

出版信息

Trop Anim Health Prod. 2013 Jun;45(5):1107-12. doi: 10.1007/s11250-012-0333-8. Epub 2012 Dec 2.

Abstract

Infectious bursal disease virus (IBDV) is a double-stranded RNA virus that causes immunosuppressive disease in young chickens. Thousands of cases of IBDV infection are reported each year in South China, and these infections can result in considerable economic losses to the poultry industry. To monitor variations of the virus during the outbreaks, 30 IBDVs were identified from vaccinated chicken flocks from nine provinces in South China in 2011. VP2 fragments from different virus strains were sequenced and analyzed by comparison with the published sequences of IBDV strains from China and around the world. Phylogenetic analysis of hypervariable regions of the VP2 (vVP2) gene showed that 29 of the isolates were very virulent (vv) IBDVs, and were closely related to vvIBDV strains from Europe and Asia. Alignment analysis of the deduced amino acid (aa) sequences of vVP2 showed the 29 vv isolates had high uniformity, indicated low variability and slow evolution of the virus. The non-vvIBDV isolate JX2-11 was associated with higher than expected mortality, and had high deduced aa sequence similarity (99.2 %) with the attenuated vaccine strain B87 (BJ). The present study has demonstrated the continued circulation of IBDV strains in South China, and emphasizes the importance of reinforcing IBDV surveillance.

摘要

传染性法氏囊病病毒(IBDV)是一种双链RNA病毒,可导致雏鸡发生免疫抑制性疾病。中国南方每年报告数千例IBDV感染病例,这些感染会给家禽业造成相当大的经济损失。为监测疫情期间该病毒的变异情况,2011年从中国南方9个省份的免疫鸡群中鉴定出30株IBDV。对不同病毒株的VP2片段进行测序,并与已发表的来自中国及世界各地的IBDV毒株序列进行比较分析。VP2(vVP2)基因高变区的系统发育分析表明,其中29株分离株为超强毒(vv)IBDV,与来自欧洲和亚洲的vvIBDV毒株密切相关。vVP2推导氨基酸(aa)序列的比对分析表明,这29株vv分离株具有高度一致性,表明该病毒变异性低、进化缓慢。非vvIBDV分离株JX2-11与高于预期的死亡率有关,且与弱毒疫苗株B87(BJ)的推导aa序列相似度高(99.2%)。本研究证明了IBDV毒株在中国南方持续传播,并强调了加强IBDV监测的重要性。

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