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Evaluation and Validation of a Real-Time PCR Assay for Detection and Quantitation of Human Adenovirus 14 from Clinical Samples

机译:从临床样品中检测和定量人腺病毒14的实时PCR分析的评估和验证

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摘要

In 2007, the Centers for Disease Control and Prevention (CDC) reported that Human adenovirus type 14 (HAdV-14) infected 106 military personnel and was responsible for the death of one U.S. soldier at Lackland Air Force Base in Texas. Identification of the responsible adenovirus, which had not previously been seen in North America and for which rapid diagnostic tools were unavailable, required retrospective analysis at reference laboratories. Initial quarantine measures were also reliant on relatively slow traditional PCR analysis at other locations. To address this problem, we developed a real-time PCR assay that detects a 225 base pair sequence in the HAdV-14a hexon gene. Fifty-one oropharyngeal swab specimens from the Naval Health Research Center, San Diego, CA and Advanced Diagnostic Laboratory, Lackland AFB, TX were used to validate the new assay. The described assay detected eight of eight and 19 of 19 confirmed HAdV-14a clinical isolates in two separate cohorts from respiratory disease outbreaks. The real-time PCR assay had a wide dynamic range, detecting from 102 to 107 copies of genomic DNA per reaction. The assay did not cross-react with other adenoviruses, influenza, respiratory syncytial virus, or common respiratory tract bacteria. The described assay is easy to use, sensitive and specific for HAdV-14a in clinical throat swab specimens, and very rapid since turnaround time is less than four hours to obtain an answer.
机译:2007年,疾病控制与预防中心(CDC)报告说,14型人腺病毒(HAdV-14)感染了106名军人,并导致德克萨斯州拉克兰空军基地的一名美军士兵死亡。要鉴定负责任的腺病毒,以前在北美还没有发现过这种病毒,而对于这种腺病毒没有快速诊断工具,需要在参考实验室进行回顾性分析。最初的隔离措施还依赖于其他位置相对较慢的传统PCR分析。为了解决这个问题,我们开发了一种实时PCR检测方法,可检测HAdV-14a六邻体基因中的225个碱基对序列。来自加利福尼亚州圣地亚哥海军健康研究中心和得克萨斯州拉克兰空军基地高级诊断实验室的五十一个口咽拭子标本用于验证该新方法。所描述的测定法在来自呼吸系统疾病暴发的两个独立队列中检测到了八个已确诊的HAdV-14a临床分离株中的八个,以及八个中的十九个。实时PCR分析具有广泛的动态范围,每个反应可检测102至107个基因组DNA。该测定与其他腺病毒,流行性感冒,呼吸道合胞病毒或常见的呼吸道细菌没有交叉反应。所描述的测定法易于使用,对临床咽拭子标本中的HAdV-14a敏感且具有特异性,并且由于周转时间少于4小时才能获得答案,因此检测速度非常快。

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