Brunet B, de Barbeyrac B, Renaudin H, Bébéar C
Laboratoire de Bacteriologie, Hopital Pellegrin, Bordeaux, France.
Eur J Clin Microbiol Infect Dis. 1989 Jul;8(7):636-8. doi: 10.1007/BF01968147.
Five wild-type strains of tetracycline-resistant Ureaplasma Ureaplasma urealyticum and one tetracycline-sensitive Ureaplasma urealyticum strain were tested for presence of the tetM sequence by hybridization assays. Two sorts of probes were used, a plasmid containing the tetM fragment and the tetM fragment alone. Two sorts of label were used for each, digoxigenin and radio-labelling. Both purified DNA at various concentrations and non-purified DNA in the pellet from a 10 ml culture were used as targets. The digoxigenin-labelled whole plasmid probe was as specific as the insert alone when hybridized with non-purified DNA, and was more sensitive than radio-labelled probes.
通过杂交试验检测了五株四环素抗性解脲脲原体野生型菌株和一株四环素敏感解脲脲原体菌株中tetM序列的存在情况。使用了两种探针,一种是含有tetM片段的质粒,另一种是单独的tetM片段。每种探针都使用了两种标记,地高辛和放射性标记。不同浓度的纯化DNA以及来自10毫升培养物沉淀中的未纯化DNA都用作靶标。当地高辛标记的完整质粒探针与未纯化DNA杂交时,其特异性与单独的插入片段相同,并且比放射性标记探针更敏感。