Novak Ryan T, Glass Mindy B, Gee Jay E, Gal Daniel, Mayo Mark J, Currie Bart J, Wilkins Patricia P
Meningitis and Special Pathogens Branch, Division of Bacterial and Mycotic Diseases, National Center for Infectious Diseases, CDC, Atlanta, GA 30333, USA.
J Clin Microbiol. 2006 Jan;44(1):85-90. doi: 10.1128/JCM.44.1.85-90.2006.
Here we report on the development of a discriminatory real-time assay for the rapid identification of Burkholderia pseudomallei isolates and the evaluation of this assay for sensitivity against related species and detection in spiked human blood samples. The assay targets a 115-base-pair region within orf2 of the B. pseudomallei type III secretion system gene cluster and distinguishes B. pseudomallei from other microbial species. Assay performance was evaluated with 224 geographically, temporally, and clinically diverse B. pseudomallei isolates from the Centers for Disease Control and Prevention strain collection. This represents the first real-time PCR for rapid and sensitive identification of B. pseudomallei that has been tested for cross-reactivity with 23 Burkholderia mallei, 5 Burkholderia thailandensis, and 35 Burkholderia and 76 non-Burkholderia organisms which have historically presented diagnostic challenges. The assay performed with 100% specificity. The limit of detection was found to be 76 femtograms of DNA (equivalent to 5.2 x 10(3) genome equivalents per ml) in a single PCR. In spiked human blood, the assay could detect as few as 8.4 x 10(3) CFU per ml. This rapid assay is a valuable tool for identification of B. pseudomallei and may improve diagnosis in regions endemic for melioidosis.
在此,我们报告一种用于快速鉴定类鼻疽伯克霍尔德菌分离株的鉴别性实时检测方法的开发,以及对该检测方法针对相关菌种的敏感性和在加标人血样本中的检测情况的评估。该检测方法针对类鼻疽伯克霍尔德菌III型分泌系统基因簇的orf2内一个115碱基对的区域,可将类鼻疽伯克霍尔德菌与其他微生物菌种区分开来。使用来自疾病控制和预防中心菌株库的224株在地理、时间和临床方面具有多样性的类鼻疽伯克霍尔德菌分离株对检测性能进行了评估。这是首个用于快速、灵敏鉴定类鼻疽伯克霍尔德菌的实时PCR方法,该方法已针对与23株鼻疽伯克霍尔德菌、5株泰国伯克霍尔德菌、35株伯克霍尔德菌属细菌以及76株非伯克霍尔德菌属微生物的交叉反应性进行了测试,这些微生物历来都带来诊断挑战。该检测方法的特异性为100%。在单次PCR中,检测限为76飞克DNA(相当于每毫升5.2×10³个基因组当量)。在加标人血中,该检测方法每毫升可检测低至8.4×10³个菌落形成单位。这种快速检测方法是鉴定类鼻疽伯克霍尔德菌的宝贵工具,可能会改善类鼻疽病流行地区的诊断。