Flynn C M, Kelley C M, Barrett M S, Jones R N
Department of Pathology, University of Iowa College of Medicine, Iowa City 52242, USA.
J Clin Microbiol. 1997 Aug;35(8):2083-6. doi: 10.1128/jcm.35.8.2083-2086.1997.
Mycobacterium marinum, a well-recognized cutaneous pathogen, is usually treated by chemotherapy without available standardized in vitro susceptibility testing information. In this study, we have attempted to apply the stable-gradient method (Etest; AB Biodisk, Solna, Sweden) to susceptibility testing of M. marinum in order to assess the activities of eight antimicrobial agents against 60 recent clinical strains of M. marinum collected from 10 geographic sites within the United States. Two plated media (5% sheep blood Mueller-Hinton agar and Middlebrook 7H11 agar) were compared, and 7H11 agar was found to be superior in supporting the growth of all strains. Four reference strains of M. marinum were tested on five occasions with eight drugs (160 tests) in order to evaluate Etest reproducibility. Results were observed to be within 1 log2 dilution of the all-test median MIC for 97.5% of the Etests. Our MIC results for the 60 strains clearly demonstrate the best in vitro potency against M. marinum isolates to be as follows (rank order): trimethoprim-sulfamethoxazole (MIC at which 90% of the isolates are inhibited [MIC90], 0.25 and 4.25 microg/ml, respectively) = ethambutol > clarithromycin (MIC90, 1 microg/ml) > minocycline = doycycline (MIC90, 4 microg/ml) > amikacin (MIC90, 8 microg/ml). Rifampin was only marginally active against the M. marinum strains tested (MIC90, at the National Committee for Clinical Laboratory Standards) breakpoint of 1 microg/ml), and ciprofloxacin was not active (MIC90, 8 microg/ml). These data should enhance the empiric drug selection for contemporary M. marinum infections and also provide evidence that the Etest can be utilized to guide chemotherapy with alternative agents.
海分枝杆菌是一种公认的皮肤病原体,通常采用化疗进行治疗,但目前尚无可用的标准化体外药敏试验信息。在本研究中,我们尝试应用梯度扩散法(Etest;AB生物盘公司,瑞典索尔纳)对海分枝杆菌进行药敏试验,以评估8种抗菌药物对从美国10个地理区域收集的60株近期临床分离的海分枝杆菌的活性。比较了两种平板培养基(5%羊血Mueller-Hinton琼脂和Middlebrook 7H11琼脂),发现7H11琼脂在支持所有菌株生长方面表现更优。对4株海分枝杆菌参考菌株进行了5次8种药物的测试(共160次测试),以评估Etest的重复性。结果显示,97.5%的Etest结果在所有测试的MIC中位数的1 log2稀释范围内。我们对60株菌株的MIC结果清楚地表明,对海分枝杆菌分离株体外活性最佳的药物如下(按活性排序):甲氧苄啶-磺胺甲恶唑(90%分离株被抑制时的MIC [MIC90],分别为0.25和4.25微克/毫升)=乙胺丁醇>克拉霉素(MIC90,1微克/毫升)>米诺环素=多西环素(MIC90,4微克/毫升)>阿米卡星(MIC90,8微克/毫升)。利福平对所测试的海分枝杆菌菌株活性仅略高于国家临床实验室标准委员会设定的1微克/毫升的断点,环丙沙星无活性(MIC90,8微克/毫升)。这些数据应有助于为当代海分枝杆菌感染的经验性药物选择提供依据,也为Etest可用于指导替代药物化疗提供了证据。