首页> 外文期刊>Veterinary Research: A Journal on Animal Infection >A highly sensitive and specific gel-based multiplex RT-PCR assay for the simultaneous and differential diagnosis of African swine fever and Classical swine fever in clinical samples
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A highly sensitive and specific gel-based multiplex RT-PCR assay for the simultaneous and differential diagnosis of African swine fever and Classical swine fever in clinical samples

机译:一种高度灵敏,基于凝胶的特异性多重RT-PCR检测试剂盒,可同时和鉴别诊断临床样品中的非洲猪瘟和古典猪瘟

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摘要

The development and standardisation of a novel, highly sensitive and specific one-step hot start multiplex RT-PCR assay is presented for the simultaneous and differential diagnosis of African swine fever (ASF) and Classical swine fever (CSF). The method uses two primer sets, each one specific for the corresponding virus, amplifying DNA fragments different in length, allowing a gel-based differential detection of the PCR products. Universal detection of ASF and CSF virus strains was achieved through selection of primers in conserved viral genome regions. The detection range was confirmed by analysis of a large collection of isolates of the two viruses. The high specificity of the assay was proven by testing related viruses, uninfected cell line cultures and healthy pig tissues. Additional confirmatory tests of the ASF and CSF virus amplicon specificity, based on restriction endonuclease analysis with BsmA I or Ban II, respectively, are also described. The analysis of whole blood and serum samples from experimentally infected animals proved the usefulness of the method for an early diagnosis of both diseases, even before the appearance of the first clinical signs. A study of 150 positive field samples from several ASF and CSF outbreaks showed the suitability of this method for a rapid (less than five hours), sensitive and specific differential diagnosis in clinical samples. In addition, a highly sensitive and specific uniplex RT-PCR for CSFV was also developed and standardised as a powerful tool for fast and early diagnosis of the disease.
机译:提出了一种新颖,高度灵敏,特异的一步热启动多重RT-PCR检测方法的开发和标准化方法,用于同时诊断非洲猪瘟(ASF)和经典猪瘟(CSF)。该方法使用两个引物组,每个引物组对相应的病毒具有特异性,可扩增长度不同的DNA片段,从而可以对PCR产物进行基于凝胶的差异检测。通过选择保守的病毒基因组区域中的引物,实现了对ASF和CSF病毒株的通用检测。通过分析两种病毒的大量分离物,确认了检测范围。通过检测相关病毒,未感染的细胞系培养物和健康的猪组织证明了该测定法的高特异性。还描述了分别基于分别用BsmA I或Ban II进行限制性核酸内切酶分析的ASF和CSF病毒扩增子特异性的其他验证性测试。对来自实验感染动物的全血和血清样本的分析证明了该方法对早期诊断这两种疾病的有效性,甚至在出现第一个临床症状之前也是如此。对来自多个ASF和CSF暴发的150个阳性场样品的研究表明,该方法适用于临床样品中的快速(少于5小时),灵敏和特异的鉴别诊断。此外,还开发了用于CSFV的高度灵敏且特异的单重RT-PCR,并将其标准化为快速,早期诊断疾病的强大工具。

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