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无需 DNA 提取的直接实时 PCR 检测和流感嗜血杆菌血清分型。

Direct Real-Time PCR for the Detection and Serotyping of Haemophilus influenzae without DNA Extraction.

机构信息

Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Preventiongrid.416738.f, Atlanta, Georgia, USA.

IHRC Inc., Contractor to Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Preventiongrid.416738.f, Atlanta, Georgia, USA.

出版信息

J Clin Microbiol. 2022 Apr 20;60(4):e0211121. doi: 10.1128/jcm.02111-21. Epub 2022 Mar 21.

Abstract

To monitor the burden and changes in Haemophilus influenzae (Hi) disease, direct real-time PCR (drt-PCR) assays have been developed for Hi detection in monoplex form and its six serotypes in triplex form, directly from cerebrospinal fluid (CSF) specimens. These assays target the gene for the species detection (Hi-) and serotype-specific genes in region II of the capsule biosynthesis locus (Hi-abf and Hi-cde), identified through comparative analysis of Hi and non-Hi whole-genome sequences. The lower limit of detection (LLD) is 293 CFU/mL for the Hi- assay and ranged from 11 to 130 CFU/mL for the triplex serotyping assays. Using culture as a reference method, the sensitivity and specificity of Hi-, Hi-abf, and Hi-cde were 100%. Triplex serotyping assays also showed 100% agreement for each serotype compared to their corresponding monoplex serotyping assay. These highly sensitive and specific drt-PCR assays do not require DNA extraction and thereby reduce the time, cost, and handling required to process CSF specimens. Furthermore, triplex drt-PCR assays combine the detection of three serotypes in a single reaction, further improving testing efficiency, which is critical for laboratories that process high volumes of Hi specimens for surveillance and diagnostic purposes.

摘要

为了监测流感嗜血杆菌(Hi)疾病的负担和变化,已经开发了直接实时 PCR(drt-PCR)检测方法,用于从脑脊液(CSF)标本中单重形式和三重形式直接检测 Hi 及其六个血清型。这些检测方法针对种属检测(Hi-)和荚膜生物合成基因座区域 II 中血清型特异性基因(Hi-abf 和 Hi-cde)的基因,通过对 Hi 和非 Hi 全基因组序列的比较分析确定。Hi-检测的最低检测限(LLD)为 293 CFU/mL,三重血清分型检测的范围为 11 至 130 CFU/mL。使用培养作为参考方法,Hi-、Hi-abf 和 Hi-cde 的敏感性和特异性均为 100%。与相应的单重血清分型检测相比,三重血清分型检测对于每个血清型也显示出 100%的一致性。这些高度敏感和特异性的 drt-PCR 检测方法不需要 DNA 提取,从而减少了处理 CSF 标本所需的时间、成本和处理。此外,三重 drt-PCR 检测方法将三种血清型的检测结合在一个反应中,进一步提高了检测效率,这对于处理大量 Hi 标本进行监测和诊断目的的实验室至关重要。

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