Grimont P A, Grimont F, Desplaces N, Tchen P
J Clin Microbiol. 1985 Mar;21(3):431-7. doi: 10.1128/jcm.21.3.431-437.1985.
A procedure for preparing a DNA probe to be used in the specific detection of Legionella pneumophila by dot or colony hybridization has been devised. When total DNA from L. pneumophila was used as a radioactive probe, cross-hybridization occurred with DNA from many other species belonging to various families (including Legionellaceae, Enterobacteriaceae, Pseudomonadaceae, and Vibrionaceae). Cross-hybridizing restriction fragments in L. pneumophila ATCC 33152 DNA were identified on Southern blots. When unlabeled DNA from strain ATCC 33152 was cleaved by endonuclease BamHI, the DNA fragments cross-hybridizing with the labeled DNA from all of the other species and genera tested (or with Escherichia coli 16 + 23 S RNA) had a size of 21.4 and 16.2 kilobase pairs (major bands) and 28.0, 12.8, and 10.1 kilobase pairs (minor bands). BamHI restriction fragments of L. pneumophila DNA deprived of the cross-hybridizing fragments were pooled and used as a probe for the detection of L. pneumophila. This probe proved to be specific for L. pneumophila in colony and dot hybridization. It can potentially be used for the detection of L. pneumophila in clinical and water samples. The procedure described can be readily applied to the preparation of probes specific for phylogenetically isolated bacterial species other than L. pneumophila.
已设计出一种制备DNA探针的方法,该探针可用于通过斑点杂交或菌落杂交特异性检测嗜肺军团菌。当使用嗜肺军团菌的总DNA作为放射性探针时,会与来自其他多个不同科的物种(包括军团菌科、肠杆菌科、假单胞菌科和弧菌科)的DNA发生交叉杂交。在Southern印迹上鉴定出嗜肺军团菌ATCC 33152 DNA中的交叉杂交限制片段。当用内切酶BamHI切割来自ATCC 33152菌株的未标记DNA时,与所有测试的其他物种和属的标记DNA(或与大肠杆菌16 + 23 S RNA)交叉杂交的DNA片段大小为21.4和16.2千碱基对(主要条带)以及28.0、12.8和10.1千碱基对(次要条带)。将去除交叉杂交片段的嗜肺军团菌DNA的BamHI限制片段汇集起来,并用作检测嗜肺军团菌的探针。该探针在菌落杂交和斑点杂交中被证明对嗜肺军团菌具有特异性。它有可能用于检测临床和水样中的嗜肺军团菌。所述方法可很容易地应用于制备针对除嗜肺军团菌以外的系统发育上孤立的细菌物种的特异性探针。