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基于 ssrA 靶点的实时 PCR 技术检测人临床样本中巴尔通体种属及测序鉴定种属水平的评价

Evaluation of ssrA-targeted real time PCR for the detection of Bartonella species in human clinical samples and reflex sequencing for species-level identification.

机构信息

Microbiology, LabPlus, Auckland City Hospital, Auckland, New Zealand.

Microbiology, LabPlus, Auckland City Hospital, Auckland, New Zealand.

出版信息

Pathology. 2022 Jun;54(4):449-452. doi: 10.1016/j.pathol.2021.10.014. Epub 2022 Feb 3.

Abstract

The genus Bartonella includes species capable of causing disease in animals and humans. Due to its fastidious nature, direct detection of Bartonella causing human infection relies largely on molecular microbiological methods. Thus, it is imperative that diagnostic assays in use have the ability to detect a range of Bartonella species associated with human disease. In this study, we compared the performance of a real time polymerase chain reaction (PCR) assay targeting the ssrA gene to conventional rpoB-targeted PCR and sequencing for detection and differentiation of Bartonella species in human clinical samples. The real time ssrA PCR performed better for non-Bartonella henselae species, detecting B. clarridgeiae and B. quintana DNA in heart valve specimens that were not detected by rpoB PCR, and improved the sensitivity of B. henselae detection in blood specimens. Our findings suggest the real time ssrA PCR assay is suitable for detection and identification of Bartonella species in human clinical specimens.

摘要

巴通体属包括能够引起动物和人类疾病的物种。由于其苛刻的性质,直接检测引起人类感染的巴通体在很大程度上依赖于分子微生物学方法。因此,使用中的诊断检测必须能够检测与人类疾病相关的一系列巴通体物种。在这项研究中,我们比较了靶向 ssrA 基因的实时聚合酶链反应(PCR)检测与常规 rpoB 靶向 PCR 和测序,用于检测和区分人类临床样本中的巴通体物种。实时 ssrA PCR 对非汉塞巴尔通体物种的检测性能更好,能够检测到心瓣膜标本中的 B. clarridgeiae 和 B. quintana DNA,而 rpoB PCR 则无法检测到,并且提高了血液标本中 B. henselae 的检测灵敏度。我们的研究结果表明,实时 ssrA PCR 检测适用于检测和鉴定人类临床标本中的巴通体物种。

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