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编码VP7基因的限制性片段长度多态性分析的应用:爱尔兰和全球轮状病毒分离株的精细比较

Application of restriction fragment length polymorphism analysis of VP7-encoding genes: fine comparison of Irish and global rotavirus isolates.

作者信息

O'Halloran F, Lynch M, Cryan B, Fanning S

机构信息

Molecular Diagnostics Unit, Cork Institute of Technology, Bishopstown, Ireland.

出版信息

J Clin Microbiol. 2002 Feb;40(2):524-31. doi: 10.1128/JCM.40.2.524-531.2002.

Abstract

A restriction fragment length polymorphism (RFLP) detection assay was developed to examine the genetic relationship(s) among VP7-encoding genes from 100 Irish rotavirus isolates and 30 randomly selected global rotavirus isolates (from the current databases). RFLP analysis of the VP7 gene segments was performed independently with three enzymes (RsaI, AluI, and EcoRV) in separate reactions by direct digestion of the DNA product amplified by reverse transcriptase (RT)-mediated PCR (RT-PCR) or by using computational methods. Thirty-six RFLP patterns were identified for all 130 strains, and of these, only nine patterns were associated with the Irish isolates. A correlation between the G type of the Irish isolates and certain single or combined enzyme profiles was apparent. These data suggested that the Irish wild-type rotavirus population was homogeneous and could be distinguished by RFLP analysis from global isolates of the same serotype(s). The deduced amino acid sequences of the VP7 RT-PCR products from six Irish isolates known to be of the G serotype revealed significant amino acid substitutions within major antigenic regions. In addition, these data identified the existence of at least two genetic lineages within serotype G1 strains which were distinguishable by RFLP analysis.

摘要

开发了一种限制性片段长度多态性(RFLP)检测方法,以研究100株爱尔兰轮状病毒分离株和30株随机选择的全球轮状病毒分离株(来自当前数据库)中VP7编码基因之间的遗传关系。通过逆转录酶(RT)介导的PCR(RT-PCR)扩增的DNA产物直接消化,或使用计算方法,分别用三种酶(RsaI、AluI和EcoRV)在单独的反应中对VP7基因片段进行RFLP分析。在所有130株菌株中鉴定出36种RFLP模式,其中只有9种模式与爱尔兰分离株相关。爱尔兰分离株的G型与某些单一或组合酶谱之间存在明显的相关性。这些数据表明,爱尔兰野生型轮状病毒群体是同质的,并且可以通过RFLP分析与相同血清型的全球分离株区分开来。已知为G血清型的6株爱尔兰分离株的VP7 RT-PCR产物推导的氨基酸序列显示,主要抗原区域内存在显著的氨基酸取代。此外,这些数据确定了血清型G1菌株中至少存在两个可通过RFLP分析区分的遗传谱系。

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