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Evaluation of Type-Specific Real-Time PCR Assays Using the LightCycler and J.B.A.I.D.S. for Detection of Adenoviruses in Species HAdV-C

机译:使用LightCycler和J.B.A.I.D.S.评估特定类型的实时PCR分析用于检测HAdV-C物种中的腺病毒

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摘要

Sporadically, HAdVs from species HAdV-C are detected in acute respiratory disease outbreaks. To rapidly type these viruses, we designed real-time PCR assays that detect and discriminate between adenovirus types HAdV-C1, -C2, -C5, and -C6. Sixteen clinical isolates from the California Department of Public Health were used to validate the new assays. Type-specific TaqMan real-time PCR assays were designed and used independently to successfully identify 16 representative specimens. The lower limit of detection for our LightCycler singleplex real-time PCR assays were calculated to be 100, 100, 100, and 50 genomic copies per reaction for HAdV-C1, HAdV-C2, HAdV-C5 and HAdV-C6, respectively. The results for the singleplex J.B.A.I.D.S. assays were similar. Our assays did not cross-react with other adenoviruses outside of species HAdV-C, respiratory syncytial virus, influenza, or respiratory disease causing bacteria. These assays have the potential to be useful as diagnostic tools for species HAdV-C infection.
机译:在急性呼吸道疾病暴发中,散发性地检测到HAdV-C物种的HAdV。为了快速分型这些病毒,我们设计了实时PCR分析方法,用于检测和区分腺病毒类型HAdV-C1,-C2,-C5和-C6。来自加利福尼亚公共卫生部的十六种临床分离株用于验证新测定。设计类型特定的TaqMan实时PCR分析,并独立使用,以成功鉴定16个代表性标本。对于我们的LightCycler单重实时PCR检测,检测到的下限分别为HAdV-C1,HAdV-C2,HAdV-C5和HAdV-C6每个反应100、100、100和50个基因组拷贝。单重J.B.A.I.D.S.的结果测定方法相似。我们的检测方法并未与HAdV-C物种,呼吸道合胞病毒,流感或引起呼吸道疾病的细菌以外的其他腺病毒发生交叉反应。这些测定法有可能用作HAdV-C物种感染的诊断工具。

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