巴尔通体
rpoB公司
生物
聚合酶链反应
挑剔的有机体
巴尔通氏体
实时聚合酶链反应
病毒学
微生物学
基因
遗传学
16S核糖体RNA
细菌
血清学
抗体
作者
Anna Vesty,Gillian Henderson,Matthew Blakiston,Aakash V. Chhibber,Andrew Fox-Lewis,Sally Roberts,Indira Basu
标识
DOI:10.1016/j.pathol.2021.10.014
摘要
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.
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