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Improved Detection of Rhinoviruses by Nucleic Acid Sequence-Based Amplification after Nucleotide Sequence Determination of the 5′ Noncoding Regions of Additional Rhinovirus Strains

机译:确定其他鼻病毒株5'非编码区的核苷酸序列后,通过基于核酸序列的扩增改进鼻病毒的检测。

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摘要

The isothermal nucleic acid sequence-based amplification (NASBA) system was applied for the detection of rhinoviruses using primers targeted at the 5′ noncoding region (5′ NCR) of the viral genome. The nucleotide sequence of the 5′ NCRs of 34 rhinovirus isolates was determined to map the most conserved regions and design more appropriate primers and probes. The assay amplified RNA extracted from 30 rhinovirus reference strains and 88 rhinovirus isolates, it did not amplify RNA from 49 enterovirus isolates and other respiratory viruses. The assay allows one to discriminate between group A and B rhinoviruses. Sensitivities for the detection of group B and group A rhinoviruses was 20 and 200 50% tissue culture infective doses, respectively.
机译:基于等温核酸序列的扩增(NASBA)系统用于鼻病毒的检测,使用针对病毒基因组5'非编码区(5'NCR)的引物。确定了34个鼻病毒分离株5'NCR的核苷酸序列,以定位最保守的区域并设计更合适的引物和探针。该测定法扩增了从30株鼻病毒参考菌株和88株鼻病毒分离物中提取的RNA,但并未扩增49株肠病毒和其他呼吸道病毒中的RNA。该测定法可以区分A组和B组鼻病毒。 B组和A组鼻病毒的检测灵敏度分别为20和200 50%组织培养感染剂量。

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