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小反刍兽慢病毒基质蛋白编码区gag的系统发育分析:比较分析及分子流行病学应用

Phylogenetic analysis of the gag region encoding the matrix protein of small ruminant lentiviruses: comparative analysis and molecular epidemiological applications.

作者信息

Pisoni Giuliano, Bertoni Giuseppe, Boettcher Paul, Ponti Wilma, Moroni Paolo

机构信息

Department of Veterinary Pathology, Hygiene and Public Health, University of Milano, via Celoria 10, 20133 Milano, Italy.

出版信息

Virus Res. 2006 Mar;116(1-2):159-67. doi: 10.1016/j.virusres.2005.09.012. Epub 2005 Nov 15.

DOI:10.1016/j.virusres.2005.09.012
PMID:16293335
Abstract

Little sequence information exists on the matrix-protein (MA) encoding region of small ruminant lentiviruses (SRLV). Fifty-two novel sequences were established and permitted a first phylogenetic analysis of this region of the SRLV genome. The variability of the MA encoding region is higher compared to the gag region encoding the capsid protein and surprisingly close to that reported for the env gene. In contrast to primate lentiviruses, the deduced amino acid sequences of the N- and C-terminal domains of MA are variable. This permitted to pinpoint a basic domain in the N-terminal domain that is conserved in all lentiviruses and likely to play an important functional role. Additionally, a seven amino acid insertion was detected in all MVV strains, which may be used to differentiate CAEV and MVV isolates. A molecular epidemiology analysis based on these sequences indicates that the Italian lentivirus strains are closely related to each other and to the CAEV-CO strain, a prototypic strain isolated three decades ago in the US. This suggests a common origin of the SRLV circulating in the monitored flocks, possibly related to the introduction of infected goats in a negative population. Finally, this study shows that the MA region is suitable for phylogenetic studies and may be applied to monitor SRLV eradication programs.

摘要

关于小反刍兽慢病毒(SRLV)的基质蛋白(MA)编码区的序列信息很少。已建立了52个新序列,并对SRLV基因组的该区域进行了首次系统发育分析。与编码衣壳蛋白的gag区域相比,MA编码区的变异性更高,且令人惊讶地与env基因报道的变异性相近。与灵长类慢病毒不同,MA的N端和C端结构域的推导氨基酸序列是可变的。这使得能够确定N端结构域中一个在所有慢病毒中都保守且可能发挥重要功能作用的碱性结构域。此外,在所有梅迪 - 维斯纳病毒(MVV)毒株中检测到一个七氨基酸插入,这可用于区分山羊关节炎 - 脑炎病毒(CAEV)和MVV分离株。基于这些序列的分子流行病学分析表明,意大利慢病毒毒株彼此之间以及与30年前在美国分离的原型毒株CAEV - CO密切相关。这表明在所监测的羊群中传播的SRLV有共同起源,可能与将感染山羊引入阴性群体有关。最后,这项研究表明MA区域适用于系统发育研究,并可用于监测SRLV根除计划。

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