Wadsworth Center, New York State Department of Health, PO Box 22002, Albany, NY 12201-2002, USA.
Mol Cell Probes. 2013 Apr;27(2):86-9. doi: 10.1016/j.mcp.2012.11.003. Epub 2012 Nov 26.
Our laboratory has developed a simple two-step multiplex real-time PCR for use on isolates of Haemophilus influenzae for molecular serotype identification and the detection of capsular gene targets. The assay consists of a 2-plex real-time PCR targeting the capsule transport gene (bexA), and serotype b specific gene (bcsB), and a 5-plex real-time PCR detecting serotypes a, c, d, e, and f targeting Region II serotype-specific genes. Both real-time PCR assays are highly sensitive (<8 CFU) for all serotypes and 100% specific when tested by a panel of more than 40 bacterial organisms. A retrospective study of 214 isolates received between 1998 and 2011 were tested and compared against the traditional slide agglutination test (SAT) resulting in 100% concordance. We demonstrate that this two-step real-time PCR approach is more sensitive than previously published PCR assays and provides a simple alternative to the SAT. Reliable, rapid and sensitive H. influenzae serotyping is critical for identifying new emerging strains for epidemiological surveillance.
我们的实验室开发了一种简单的两步多重实时 PCR 方法,用于流感嗜血杆菌分离株的分子血清型鉴定和荚膜基因靶标的检测。该检测方法由针对荚膜转运基因 (bexA) 和血清型 b 特异性基因 (bcsB) 的 2 重实时 PCR 以及针对区域 II 血清型特异性基因的检测 a、c、d、e 和 f 血清型的 5 重实时 PCR 组成。所有血清型的两种实时 PCR 检测方法均具有高度敏感性(<8 CFU),并且在经过超过 40 种细菌的检测面板测试时具有 100%的特异性。对 1998 年至 2011 年间收到的 214 株分离株进行了回顾性研究,并与传统的玻片凝集试验(SAT)进行了比较,结果完全一致。我们证明,这种两步实时 PCR 方法比以前发表的 PCR 检测方法更敏感,为 SAT 提供了一种简单的替代方法。可靠、快速和敏感的流感嗜血杆菌血清分型对于识别新出现的菌株进行流行病学监测至关重要。