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首页> 外文期刊>Journal of Clinical Microbiology >Simultaneous Detection of Rift Valley Fever, Bluetongue, Rinderpest, and Peste des Petits Ruminants Viruses by a Single-Tube Multiplex Reverse Transcriptase-PCR Assay Using a Dual-Priming Oligonucleotide System
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Simultaneous Detection of Rift Valley Fever, Bluetongue, Rinderpest, and Peste des Petits Ruminants Viruses by a Single-Tube Multiplex Reverse Transcriptase-PCR Assay Using a Dual-Priming Oligonucleotide System

机译:使用双引物寡核苷酸系统通过单管多重逆转录酶-PCR分析法同时检测裂谷热,蓝舌病,牛瘟和小瘟疫反刍动物病毒

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摘要

The aim of this study was to develop a highly sensitive and specific one-step multiplex reverse transcriptase PCR assay for the simultaneous and differential detection of Rift Valley Fever virus (RVFV), bluetongue virus (BTV), rinderpest virus (RPV), and Peste des petits ruminants virus (PPRV). These viruses cause mucosal lesions in cattle, sheep, and goats, and they are difficult to differentiate from one another based solely on their clinical presentation in suspected disease cases. In this study, we developed a multiplex reverse transcriptase PCR to detect these viruses using a novel dual-priming oligonucleotide (DPO). The DPO contains two separate priming regions joined by a polydeoxyinosine linker, which blocks extension of nonspecifically primed templates and consistently allows high PCR specificity even under less-than-optimal PCR conditions. A total of 19 DPO primers were designed to detect and discriminate between RVFV, BTV, RPV, and PPRV by the generation of 205-, 440-, 115-, and 243-bp cDNA products, respectively. The multiplex reverse transcriptase PCR described here enables the early diagnosis of these four viruses and may also be useful as part of a testing regime for cattle, sheep, or goats exhibiting similar clinical signs, including mucosal lesions.
机译:这项研究的目的是开发一种高灵敏度和特异性的一步多重逆转录酶PCR检测方法,用于同时和差异检测裂谷热病毒(RVFV),蓝舌病毒(BTV),牛瘟病毒(RPV)和Peste小反刍动物病毒(PPRV)。这些病毒在牛,羊和山羊中引起粘膜损伤,很难仅根据其在可疑疾病病例中的临床表现就相互区分。在这项研究中,我们开发了一种多重逆转录酶PCR技术,可以使用新型的双引物寡核苷酸(DPO)检测这些病毒。 DPO包含由聚脱氧肌苷连接子连接的两个独立的引物区域,该引物区域阻止非特异性引物模板的延伸,即使在低于最佳的PCR条件下,也始终具有较高的PCR特异性。总共设计了19种DPO引物,分别通过产生205、440、115和243 bp cDNA产物来检测和区分RVFV,BTV,RPV和PPRV。此处描述的多重逆转录酶PCR可以对这四种病毒进行早期诊断,并且还可以用作牛,羊或山羊表现出类似临床体征(包括粘膜病变)的测试方案的一部分。

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