Institute of Microbiology, Dept. of Medical Sciences, Magna Graecia University, Via Tommaso Campanella 115, 88100 Catanzaro, Italy.
Mol Cell Probes. 2011 Oct-Dec;25(5-6):238-42. doi: 10.1016/j.mcp.2011.07.001. Epub 2011 Jul 28.
We describe a SYBR Green I-based real-time PCR targeting Bartonella quintana transcriptional regulatory protein (bqtR) gene, recently found as invariant gene among different B. quintana strains. Melting curve analysis allowed us to discriminate between B. quintana and Bartonella henselae amplified products. We also show its usefulness in the management of a blood culture-negative patient affected by enlarged cervical lymphonodes and long-lasting fever. B. quintana DNA detection in patient whole blood samples and blood culture bottles was confirmed by sequencing and analyzing amplified products.
我们描述了一种基于 SYBR Green I 的实时 PCR 方法,该方法针对最近发现的不同 Bartonella quintana 菌株中不变的转录调节蛋白(bqtR)基因。熔解曲线分析允许我们区分 Bartonella quintana 和 Bartonella henselae 的扩增产物。我们还展示了它在处理患有颈淋巴结肿大和长期发热的血培养阴性患者中的用途。通过测序和分析扩增产物,确认了患者全血样本和血培养瓶中的 B. quintana DNA 检测。