Blanchard A, Crabb D M, Dybvig K, Duffy L B, Cassell G H
Department of Microbiology, University of Alabama, Birmingham 35294.
FEMS Microbiol Lett. 1992 Aug 15;74(2-3):277-81. doi: 10.1016/0378-1097(92)90442-q.
Tetracycline resistance in Mycoplasma hominis and Ureaplasma urealyticum has been associated with the tetM determinant and has recently been increasing in incidence. We report here a rapid method for detection of the tetM determinant based on the use of the polymerase chain reaction (PCR) to amplify a 397-bp DNA fragment from the tetM gene and verification of specificity using the restriction enzyme TaqI. Analysis of 42 U. urealyticum and 49 M. hominis isolates indicates that the PCR method may be clinically useful for determination of tetracycline sensitivity, as tetM is presently the only known determinant associated with tetracycline resistance in these two organisms. All of the tetM-positive M. hominis isolates were sensitive to doxycycline, indicating that tetM does not necessarily confer resistance to this antibiotic.
人型支原体和解脲脲原体中的四环素耐药性与tetM决定簇有关,且其发病率最近一直在上升。我们在此报告一种基于聚合酶链反应(PCR)的快速检测tetM决定簇的方法,该方法用于从tetM基因扩增出一个397 bp的DNA片段,并使用限制性内切酶TaqI验证特异性。对42株解脲脲原体和49株人型支原体分离株的分析表明,PCR方法在临床上可能有助于确定四环素敏感性,因为tetM目前是这两种微生物中与四环素耐药性相关的唯一已知决定簇。所有tetM阳性的人型支原体分离株对强力霉素敏感,这表明tetM不一定赋予对这种抗生素的耐药性。