Gee Jay E, Sacchi Claudio T, Glass Mindy B, De Barun K, Weyant Robbin S, Levett Paul N, Whitney Anne M, Hoffmaster Alex R, Popovic Tanja
Meningitis and Special Pathogens Branch, Division of Bacterial and Mycotic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
J Clin Microbiol. 2003 Oct;41(10):4647-54. doi: 10.1128/JCM.41.10.4647-4654.2003.
Burkholderia pseudomallei and B. mallei, the causative agents of melioidosis and glanders, respectively, are designated category B biothreat agents. Current methods for identifying these organisms rely on their phenotypic characteristics and an extensive set of biochemical reactions. We evaluated the use of 16S rRNA gene sequencing to rapidly identify these two species and differentiate them from each other as well as from closely related species and genera such as Pandoraea spp., Ralstonia spp., Burkholderia gladioli, Burkholderia cepacia, Burkholderia thailandensis, and Pseudomonas aeruginosa. We sequenced the 1.5-kb 16S rRNA gene of 56 B. pseudomallei and 23 B. mallei isolates selected to represent a wide range of temporal, geographic, and origin diversity. Among all 79 isolates, a total of 11 16S types were found based on eight positions of difference. Nine 16S types were identified in B. pseudomallei isolates based on six positions of difference, with differences ranging from 0.5 to 1.5 bp. Twenty-two of 23 B. mallei isolates showed 16S rRNA gene sequence identity and were designated 16S type 10, whereas the remaining isolate was designated type 11. This report provides a basis for rapidly identifying and differentiating B. pseudomallei and B. mallei by molecular methods.
类鼻疽和鼻疽的病原体分别为伯克霍尔德菌属假鼻疽杆菌和鼻疽杆菌,它们被指定为B类生物威胁因子。目前鉴定这些微生物的方法依赖于它们的表型特征以及一系列广泛的生化反应。我们评估了使用16S rRNA基因测序来快速鉴定这两个物种,并将它们彼此区分开来,同时也与密切相关的物种和属如潘多拉菌属、罗尔斯通菌属、唐菖蒲伯克霍尔德菌、洋葱伯克霍尔德菌、泰国伯克霍尔德菌和铜绿假单胞菌区分开来。我们对56株假鼻疽杆菌和23株鼻疽杆菌分离株的1.5 kb 16S rRNA基因进行了测序,这些分离株的选择代表了广泛的时间、地理和来源多样性。在所有79株分离株中,基于8个差异位置共发现了11种16S类型。基于6个差异位置在假鼻疽杆菌分离株中鉴定出9种16S类型,差异范围为0.5至1.5 bp。23株鼻疽杆菌分离株中的22株显示出16S rRNA基因序列同一性,被指定为16S类型10,而其余分离株被指定为类型11。本报告为通过分子方法快速鉴定和区分假鼻疽杆菌和鼻疽杆菌提供了依据。