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Development and evaluation of dual-target real-time polymerase chain reaction assays to detect Bordetella spp.

机译:开发和评估双目标实时聚合酶链反应测定法,以检测博德特氏菌。

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Novel, highly specific, and sensitive real-time polymerase chain reaction (PCR) assays using 2 targets, insertion sequence (IS481) and pertussis toxin subunit 1 (ptxS1), were developed to detect Bordetella pertussis and to differentiate between relevant Bordetella spp. Sixty-four non-Bordetella isolates were negative by both assays, demonstrating the specificity of the assays. B. pertussis, Bordetella parapertussis, and Bordetella holmesii isolates were specifically identified using the assays. The lower limit of detection was less than 10 genomic equivalents per reaction for the IS481 and ptxS1 assays. These assays were evaluated using 145 human clinical specimens obtained during cough-illness outbreak investigations, and PCR results were compared with Bordetella spp. culture results. Twenty-seven (18.6%) specimens had late positive cycle threshold (Ct) values (35
机译:开发了新颖,高度特异性和灵敏的实时聚合酶链反应(PCR)检测方法,使用两个靶标(插入序列(IS481)和百日咳毒素亚基1(ptxS1))来检测百日咳博德特氏菌并区分相关的博德特氏菌。两种测定法中有64种非博德氏菌分离物均为阴性,证明了测定法的特异性。百日咳博德特氏菌,副百日咳博德特氏菌和霍姆氏博德特氏菌的分离株可通过这些检测方法进行鉴定。对于IS481和ptxS1分析,每个反应的检测下限小于10个基因组当量。使用在咳嗽暴发调查中获得的145个人临床标本对这些测定进行了评估,并将PCR结果与Bordetella spp进行了比较。文化成果。使用IS481分析的二十七个(18.6%)标本具有晚期阳性循环阈值(Ct)值(35 <或= Ct <40),使用ptxS1分析和培养物具有相应的阴性结果,被认为是不确定的。讨论了在咳嗽暴发期间使用PCR检测和结果解释的指南。

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