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通过限制性片段长度多态性(RFLP)分析对GII.4和GIIb诺如病毒RT-PCR扩增产物进行基因分型。

Genotyping of GII.4 and GIIb norovirus RT-PCR amplicons by RFLP analysis.

作者信息

Ramirez Stefania, Giammanco Giovanni M, De Grazia Simona, Colomba Claudia, Martella Vito, Arista Serenella

机构信息

Department of Hygiene and Microbiology, University of Palermo, via del Vespro 133, Palermo, Italy.

出版信息

J Virol Methods. 2008 Feb;147(2):250-6. doi: 10.1016/j.jviromet.2007.09.005. Epub 2007 Oct 22.

Abstract

GII.4 and GIIb/Hilversum norovirus (NoV) strains appear to have a prominent epidemiological role in outbreaks or sporadic cases of human gastroenteritis. Sequence analysis, although laborious, is the reference method used for characterization of noroviruses. In this study a screening test is proposed to characterize GIIb and GII.4 NoVs based on restriction fragment length polymorphism (RFLP) analysis of amplicons obtained from the RNA-dependent RNA polymerase (RdRp) region. Virtual analysis of 793 RdRp sequences of GGI and GGII NoVs, retrieved from GenBank, and representative of global geographical origins on a long-time period, permitted the selection of four restriction enzymes, XmnI, AhdI, BstXI, and AcuI, suitable for correct identification of GIIb and GII.4 NoV genotypes. Experimental analysis by the RT-PCR RFLP analysis of 41 NoV strains detected in Palermo during the years 2002-2005 allowed to recognize all the Italian strains as belonging to GIIb/Hilversum or GII.4, and sequence analysis confirmed these results. The PCR-RFLP protocol developed in this study proved to be a simple and reliable proxy for sequence-based classification of the GIIb/Hilversum and GII.4 NoV variants displaying high specificity (100%) and sensitivity (94%).

摘要

GII.4型和GIIb/希尔弗瑟姆诺如病毒(NoV)毒株似乎在人类肠胃炎的暴发或散发病例中具有重要的流行病学作用。序列分析虽然费力,但却是用于诺如病毒鉴定的参考方法。在本研究中,我们提出了一种基于对从RNA依赖的RNA聚合酶(RdRp)区域获得的扩增子进行限制性片段长度多态性(RFLP)分析来鉴定GIIb和GII.4型诺如病毒的筛选试验。对从GenBank中检索到的、代表全球长期地理来源的793个GGI和GGII型诺如病毒的RdRp序列进行虚拟分析,从而选出了四种限制性内切酶,即XmnI、AhdI、BstXI和AcuI,它们适用于正确鉴定GIIb和GII.4型诺如病毒基因型。通过对2002年至2005年期间在巴勒莫检测到的41株诺如病毒进行RT-PCR RFLP分析的实验分析,得以识别出所有意大利毒株均属于GIIb/希尔弗瑟姆型或GII.4型,序列分析也证实了这些结果。本研究中开发的PCR-RFLP方案被证明是一种简单可靠的替代方法,可用于对GIIb/希尔弗瑟姆型和GII.4型诺如病毒变体进行基于序列的分类,显示出高特异性(100%)和敏感性(94%)。

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