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用于检测狂犬病病毒属所有七种基因型的逆转录聚合酶链反应。

RT-PCR for detection of all seven genotypes of Lyssavirus genus.

作者信息

Vázquez-Morón S, Avellón A, Echevarría J E

机构信息

Instituto de Salud Carlos III, Centro Nacional de Microbiología, Servicio de Microbiología Diagnóstica, Aislamiento y Detección de Virus, Ctra. Majadahonda-Pozuelo Km2, 28220 Majadahonda, Madrid, Spain.

出版信息

J Virol Methods. 2006 Aug;135(2):281-7. doi: 10.1016/j.jviromet.2006.03.008. Epub 2006 May 19.

Abstract

The Lyssavirus genus includes seven species or genotypes named 1-7. Rabies genotypes correlate with geographical distribution and specific hosts. Co-circulation of different lyssaviruses, imported cases, and the presence of unknown viruses, such as Aravan, Khujand, Irkut and West Caucasian Bat Virus, make it necessary to use generic methods able to detect all lyssaviruses. Primer sequences were chosen from conserved regions in all genotypes in order to optimise a generic RT-PCR. Serial dilutions of 12 RNA extracts from all seven Lyssavirus genotypes were examined to compare the sensitivity of the RT-PCR standardised in this study with a published RT-PCR optimised for EBLV1 detection and capable of amplifying RNA from all seven lyssaviruses. All seven genotypes were detected by both RT-PCRs, however, the sensitivity was higher with the new version of the test. Twenty samples submitted for rabies diagnosis were tested by the new RT-PCR. Eight out of 20 samples from six dogs, one horse and one bat were found positive, in agreement with immunofluorescence results. Seven samples from terrestrial mammals were genotype 1 and one from a bat was genotype 5. In conclusion, this method can be used to complement immunofluorescence for the diagnosis of rabies, enabling the detection of unexpected lyssaviruses during rabies surveillance.

摘要

狂犬病病毒属包括7个种或基因型,分别命名为1 - 7型。狂犬病基因型与地理分布和特定宿主相关。不同狂犬病病毒的共同流行、输入性病例以及未知病毒(如阿拉万病毒、胡占德病毒、伊尔库茨克病毒和西高加索蝙蝠病毒)的存在,使得有必要采用能够检测所有狂犬病病毒的通用方法。从所有基因型的保守区域中选择引物序列,以优化通用逆转录聚合酶链反应(RT-PCR)。对来自所有7种狂犬病病毒基因型的12份RNA提取物进行系列稀释,以比较本研究中标准化的RT-PCR与已发表的针对欧洲蝙蝠狂犬病病毒1型(EBLV1)检测优化且能够扩增所有7种狂犬病病毒RNA的RT-PCR的灵敏度。两种RT-PCR均检测到了所有7种基因型,然而,新版本检测的灵敏度更高。用新的RT-PCR对送检狂犬病诊断的20份样本进行检测。来自6只狗、1匹马和1只蝙蝠的20份样本中有8份呈阳性,与免疫荧光结果一致。来自陆生哺乳动物的7份样本为1型,来自1只蝙蝠的1份样本为5型。总之,该方法可用于补充狂犬病诊断中的免疫荧光检测,在狂犬病监测期间能够检测到意外的狂犬病病毒。

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