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用于“分型”非洲马瘟病毒的血清型特异性引物和基于凝胶的 RT-PCR 检测方法:来自非洲的毒株鉴定。

Serotype specific primers and gel-based RT-PCR assays for 'typing' African horse sickness virus: identification of strains from Africa.

机构信息

Vector-borne Disease Programme, Institute for Animal Health, Pirbright Laboratory, Pirbright, Woking, Surrey, United Kingdom.

出版信息

PLoS One. 2011;6(10):e25686. doi: 10.1371/journal.pone.0025686. Epub 2011 Oct 20.

Abstract

African horse sickness is a devastating, transboundary animal disease, that is 'listed' by the Office International des Epizooties (OIE). Although attenuated, inactivated and subunit vaccines have been developed for African horse sickness virus (AHSV), these are serotype-specific and their effective deployment therefore relies on rapid and reliable identification of virus type. AHSV serotype is controlled by the specificity of interactions between neutralising antibodies, and components of the outer-capsid, particularly protein VP2 (encoded by AHSV genome segment 2 (Seg-2)). We report the development and evaluation of novel gel based reverse transcription-PCR (RT-PCR) assays targeting AHSV Seg-2, which can be used to very significantly increase the speed and reliability of detection and identification (compared to virus neutralisation tests) of the nine serotypes of AHSV. Primer sets were designed targeting regions of Seg-2 that are conserved between strains within each of the AHSV serotype (types 1 to 9). These assays were evaluated using multiple AHSV strains from the orbivirus reference collection at IAH (www.reoviridae.org/dsRNA_virus_proteins/ReoID/AHSV-isolates.htm). In each case the Seg-2 primers showed a high level of specificity and failed to cross-amplify the most closely related heterologous AHSV types, or other related orbiviruses (such as bluetongue virus (BTV), or equine encephalosis virus (EEV)). The assays are rapid and sensitive, and can be used to detect and type viral RNA in blood, tissue samples, or cultivated viral suspensions within 24 h. They were used to identify AHSV strains from recent outbreaks in sub-Saharan African countries. These methods also generate cDNAs suitable for sequencing and phylogenetic analyses of Seg-2, identifying distinct virus lineages within each virus-type and helping to identify strain movements/origins. The RT-PCR methods described here provide a robust and versatile tool for rapid and specific detection and identification of AHSV serotypes 1 to 9.

摘要

非洲马瘟是一种具有毁灭性的、跨界的动物疾病,被国际动物卫生组织(OIE)“列出”。尽管已经开发出针对非洲马瘟病毒(AHSV)的减毒、灭活和亚单位疫苗,但这些疫苗都是血清型特异性的,因此其有效部署依赖于对病毒类型的快速可靠识别。AHSV 血清型由中和抗体和外壳蛋白 VP2(由 AHSV 基因组片段 2(Seg-2)编码)等成分之间的特异性相互作用控制。我们报告了针对 AHSV Seg-2 的新型凝胶逆转录 PCR(RT-PCR)检测方法的开发和评估,与病毒中和试验相比,这些方法可显著提高检测和鉴定 AHSV 九个血清型的速度和可靠性。针对每个 AHSV 血清型(1 至 9 型)内株之间保守的 Seg-2 区域设计了引物组。使用来自 IAH 的 orbivirus 参考收藏中的多种 AHSV 株评估了这些检测方法(www.reoviridae.org/dsRNA_virus_proteins/ReoID/AHSV-isolates.htm)。在每种情况下,Seg-2 引物都表现出高度的特异性,并且不会交叉扩增最密切相关的异源 AHSV 类型或其他相关 orbiviruses(如蓝舌病病毒(BTV)或马脑炎病毒(EEV))。这些检测方法快速且灵敏,可用于在 24 小时内检测和鉴定血液、组织样本或培养病毒悬浮液中的病毒 RNA。它们用于鉴定来自撒哈拉以南非洲国家最近暴发的 AHSV 株。这些方法还生成适合 Seg-2 测序和系统发育分析的 cDNA,鉴定每个病毒型内的独特病毒谱系,并有助于识别菌株的传播/起源。本文描述的 RT-PCR 方法为快速特异性检测和鉴定 AHSV 血清型 1 至 9 提供了一种强大而通用的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9502/3197586/91069d61f6e6/pone.0025686.g001.jpg

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