Leff L G, Kernan R M, McArthur J V, Shimkets L J
Department of Microbiology and Savannah River Ecology Laboratory, University of Georgia, Athens 30602, USA.
Appl Environ Microbiol. 1995 Apr;61(4):1634-6. doi: 10.1128/aem.61.4.1634-1636.1995.
Burkholderia (Pseudomonas) cepacia is a common environmental bacterium which can be pathogenic for plants and humans. In this study, four strategies were used to identify aquatic isolates: API test strips, hybridization with species-specific DNA probes for the 16S and 23S rRNA genes, fatty acid methyl ester (FAME) profiles, and growth on selective medium (TB-T agar [C. Hagedorn, W. D. Gould, T. R. Bardinelli, and D. R. Gustarson, Appl. Environ. Microbiol. 53:2265-2268, 1987]). Only 59% of the isolates identified as B. cepacia with the API test strips were confirmed as B. cepacia by using fatty acid profiles. The 23S rRNA probe generated a few false-positive results but dramatically underestimated the number of B. cepacia isolates (i.e., 40% of the colonies that did not hybridize to the probe were B. cepacia, as determined by FAME). The 16S rRNA probe generated more false-positive results than the 23S rRNA probe but was effective in identifying the majority of the B. cepacia isolates. The selective medium was only partially successful in recovering B. cepacia. Use of the B. cepacia-specific 16S rRNA probe was the most efficient and accurate way of identifying B. cepacia.
洋葱伯克霍尔德菌(假单胞菌属)是一种常见的环境细菌,可对植物和人类致病。在本研究中,采用了四种策略来鉴定水生分离株:API测试条、与16S和23S rRNA基因的种特异性DNA探针杂交、脂肪酸甲酯(FAME)谱分析以及在选择性培养基(TB-T琼脂[C. Hagedorn、W. D. Gould、T. R. Bardinelli和D. R. Gustarson,《应用与环境微生物学》53:2265 - 2268,1987年])上生长。通过API测试条鉴定为洋葱伯克霍尔德菌的分离株中,只有59%通过脂肪酸谱分析被确认为洋葱伯克霍尔德菌。23S rRNA探针产生了一些假阳性结果,但显著低估了洋葱伯克霍尔德菌分离株的数量(即,通过FAME分析确定,未与该探针杂交的菌落中有40%是洋葱伯克霍尔德菌)。16S rRNA探针产生的假阳性结果比23S rRNA探针更多,但在鉴定大多数洋葱伯克霍尔德菌分离株方面是有效的。选择性培养基在回收洋葱伯克霍尔德菌方面仅部分成功。使用洋葱伯克霍尔德菌特异性16S rRNA探针是鉴定洋葱伯克霍尔德菌最有效和准确的方法。