Real-Time PCR Detection of Mycoplasma pneumoniae, Chlamydia pneumoniae and Legionella pneumophila in Respiratory Specimens Using the ARIES® System

Subathra Marimuthu, L. Wolf, J. Summersgill
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Abstract

Background: Mycoplasma pneumoniae (Mpn), Chlamydia pneumoniae (Cpn), and Legionella pneumophila (Lpn) can cause both epidemic and endemic occurrences of acute respiratory disease and are responsible for up to 22% of cases of community acquired pneumonia. Due to the limited availability of FDA-approved molecular diagnostic assays, we developed and evaluated a multiplexed Real-time PCR assay for the detection of these agents in two respiratory specimen types on the Luminex ARIES ® instrument. The instrument provides for nucleic acid extraction plus PCR amplification and target detection in the same cassette. The ARIES ® instrument generates a cycle threshold value and a confirmatory melt curve value for each reaction, including results for an internal sample processing control. The limit of detection for Mpn, Cpn and Lpn, was 100 CFU/ mL, 1000 CFU/mL and 100 CFU/mL, respectively. In addition, accuracy, precision, specificity and stability studies were conducted to validate the assay for diagnostic use. Between November 2016 and June 2017, a total of 836 patient specimens were processed in our reference laboratory, with six positive Mpn and two positive Lpn. No specimens were positive for Cpn during this time period. The availability of a robust multiplex PCR assay greatly enhances the ability to rapidly diagnose infections caused by these three agents causing atypical pneumonia.
应用ARIES®系统实时荧光定量PCR检测呼吸道标本中肺炎支原体、肺炎衣原体和嗜肺军团菌
背景:肺炎支原体(Mpn)、肺炎衣原体(Cpn)和嗜肺军团菌(Lpn)可引起急性呼吸道疾病的流行和地方性发生,并导致高达22%的社区获得性肺炎病例。由于fda批准的分子诊断方法的可用性有限,我们开发并评估了一种多重实时荧光定量PCR方法,用于在Luminex ARIES®仪器上检测两种呼吸道标本类型中的这些药物。该仪器提供了核酸提取加PCR扩增和目标检测在同一盒。ARIES®仪器为每个反应生成循环阈值和确认熔融曲线值,包括内部样品处理控制的结果。Mpn、Cpn和Lpn的检出限分别为100 CFU/mL、1000 CFU/mL和100 CFU/mL。此外,还进行了准确性、精密度、特异性和稳定性研究,以验证该分析的诊断用途。2016年11月至2017年6月,我院参比实验室共处理患者标本836份,其中Mpn阳性6份,Lpn阳性2份。在此期间,没有标本呈Cpn阳性。强大的多重PCR检测的可用性大大提高了快速诊断由这三种引起非典型肺炎的病原体引起的感染的能力。
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