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首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Molecular sub-grouping of enterovirus reference and wild type strains into distinct genetic clusters using a simple RFLP assay.
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Molecular sub-grouping of enterovirus reference and wild type strains into distinct genetic clusters using a simple RFLP assay.

机译:使用简单的RFLP分析,将肠病毒参考和野生型菌株的分子亚群分为不同的遗传簇。

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摘要

RFLP analysis and sequencing of RT-PCR amplicons in previous studies revealed the existence of intra-serotypic variability in the 5'-UTR of human enteroviruses, complicating the use of this method to serotype isolates. During the present study, the available sequences of many enterovirus reference and wild type strains were analysed in an attempt to discover restriction sites that would rapidly and reliably aid the classification of human enteroviruses into specific sub-groups on the basis of their 5'-UTR for diagnostic and/or epidemiological purposes. Despite intratypic genetic variability in the 5'-UTR, the results of the sequence analysis, as well as data from the RFLP analysis of 61 enterovirus reference strains from 60 different serotypes and 123 clinical isolates showed that one restriction endonuclease, HpaII, may contribute to a reliable sub-classification of CAVs and the rest of enteroviruses, on the basis of 5'-UTR, into five genetic groups, which could be particularly useful in clinical and epidemiological studies. Although more sequence data from enterovirus reference and wild type strains may be required for the elaboration of a precise molecular identification system, the more possible genotypic classification into distinct clusters, as shown with the restriction enzyme HpaII, and the determination of the biological significance of this grouping (pathogenesis, epidemiology) might constitute an alternative means of enterovirus identification against conventional classification into distinct serotypes.
机译:在先前的研究中,RFLP分析和RT-PCR扩增子的测序揭示了人类肠病毒5'-UTR中存在血清型内变异性,使该方法对血清型分离株的使用变得复杂。在本研究中,分析了许多肠道病毒参考和野生型菌株的可用序列,以试图发现限制性位点,这些限制性位点可根据其5'-UTR快速,可靠地帮助将人类肠道病毒分类为特定亚组。用于诊断和/或流行病学目的。尽管5'-UTR具有典型的遗传变异性,但序列分析的结果以及来自60种不同血清型和123种临床分离株的61种肠病毒参考菌株的RFLP分析数据表明,一种限制性核酸内切酶HpaII可能有助于在5'-UTR的基础上,将CAV和其余肠道病毒的可靠子分类分为五个基因组,这在临床和流行病学研究中尤其有用。尽管可能需要更多来自肠道病毒参考菌株和野生型菌株的序列数据来构建精确的分子鉴定系统,但如限制性酶HpaII所示,将基因型更可能分为不同的簇,并确定其生物学意义。分组(发病机制,流行病学)可能构成针对常规分类为不同血清型的肠道病毒鉴定的另一种方法。

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