首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Development of Reverse Transcription-PCR (Oligonucleotide Probing) Enzyme-Linked Immunosorbent Assays for Diagnosis and Preliminary Typing of Foot-and-Mouth Disease: a New System Using Simple and Aqueous-Phase Hybridization
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Development of Reverse Transcription-PCR (Oligonucleotide Probing) Enzyme-Linked Immunosorbent Assays for Diagnosis and Preliminary Typing of Foot-and-Mouth Disease: a New System Using Simple and Aqueous-Phase Hybridization

机译:口蹄疫的诊断和初步分型的逆转录PCR(寡核苷酸探测)酶联免疫吸附测定方法的发展:一种使用简单和水相杂交的新系统

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摘要

A reverse transcription-PCR (RT-PCR)–enzyme-linked immunosorbent assay system that detects a relatively conserved region within the RNA genome of all seven serotypes of foot-and-mouth disease virus (FMDV) has been developed. The high specificity of the assay is achieved by including a rapid hybridization step with a biotin-labeled internal oligonucleotide. The assay is highly sensitive, fast, and easy to perform. A similar assay, based on a highly variable region of the FMDV genome and employing a single asymmetric RT-PCR and multiple hybridization oligonucleotides, was developed to demonstrate the method's ability to type FMDV. Based on our theoretical and practical knowledge of the methodology, we predict that similar assays are applicable to diagnosis and strain differentiation in any system amenable to PCR amplification.
机译:已经开发了一种逆转录PCR(RT-PCR)–酶联免疫吸附测定系统,该系统可检测口蹄疫病毒(FMDV)的所有七种血清型的RNA基因组内相对保守的区域。通过包括与生物素标记的内部寡核苷酸的快速杂交步骤来实现测定的高特异性。该测定法高度灵敏,快速且易于执行。基于FMDV基因组的高度可变区域并采用单个不对称RT-PCR和多种杂交寡核苷酸的类似测定方法得到了开发,以证明该方法能够对FMDV进行分型。基于我们对方法学的理论和实践知识,我们预测相似的分析法可用于任何适合PCR扩增的系统中的诊断和菌株分化。

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