Brown B A, Wallace R J, Onyi G O, De Rosas V, Wallace R J
Department of Microbiology, University of Texas Health Center, Tyler 75710.
Antimicrob Agents Chemother. 1992 Jan;36(1):180-4. doi: 10.1128/AAC.36.1.180.
Susceptibilities to erythromycin by broth microdilution were compared with those to the newer macrolide clarithromycin for 223 isolates of rapidly growing mycobacteria belonging to seven taxonomic groups. Seventy-nine random isolates were also tested against azithromycin and roxithromycin. The MIC of clarithromycin for 90% of strains tested (MIC90) was 0.25 microgram/ml for isolates of Mycobacterium chelonae subsp. chelonae and 0.5 microgram/ml for M. chelonae subsp. abscessus, with 100% of strains inhibited by less than or equal to 1 microgram/ml. Clarithromycin was 10 to 50 times more active than erythromycin and four- to eightfold more active than the other newer macrolides against M. chelonae. MICs of clarithromycin frequently increased with prolonged incubation with isolates of M. chelonae subsp. abscessus but not M. chelonae subsp. chelonae. MICs of clarithromycin were much higher for M. fortuitum bv. fortuitum (MIC50, 2.0 microgram/ml; MIC90, greater than 8.0 microgram/ml). The three newer macrolides had comparable activity against M. fortuitum bv. peregrinum (MIC90s of 0.5 to 2.0 microgram/ml compared with erythromycin MIC90s of greater than 8.0 microgram/ml). Overall, clarithromycin was the most active agent, inhibiting all isolates of M. chelonae subsp. chelonae, M. chelonae subsp. abscessus, M. fortuitum bv. peregrinum, and the M. chelonae-like organisms and 35% of M. fortuitum bv. fortuitum at less than or equal to 1 microgram/ml. Clinical trials of the newer macrolides, especially clarithromycin, against these environmental mycobacterial species appear to be warranted.
采用肉汤微量稀释法,比较了223株属于7个分类群的快速生长分枝杆菌对红霉素和新型大环内酯类药物克拉霉素的敏感性。还对79株随机分离株进行了阿奇霉素和罗红霉素的测试。对于龟分枝杆菌龟亚种的分离株,克拉霉素对90%测试菌株的最低抑菌浓度(MIC90)为0.25微克/毫升,对于龟分枝杆菌脓肿亚种为0.5微克/毫升,100%的菌株在小于或等于1微克/毫升时受到抑制。克拉霉素对龟分枝杆菌的活性比红霉素高10至50倍,比其他新型大环内酯类药物高4至8倍。克拉霉素的MIC通常随着与龟分枝杆菌脓肿亚种分离株孵育时间的延长而增加,但与龟分枝杆菌龟亚种孵育时不会增加。对于偶然分枝杆菌偶然生物变种,克拉霉素的MIC要高得多(MIC50为2.0微克/毫升;MIC90大于8.0微克/毫升)。三种新型大环内酯类药物对偶然分枝杆菌迁徙生物变种的活性相当(MIC90为0.5至2.0微克/毫升,而红霉素的MIC90大于8.0微克/毫升)。总体而言,克拉霉素是最具活性的药物,在小于或等于1微克/毫升时可抑制所有龟分枝杆菌龟亚种、龟分枝杆菌脓肿亚种、偶然分枝杆菌迁徙生物变种、类龟分枝杆菌和35%的偶然分枝杆菌偶然生物变种。针对这些环境分枝杆菌物种进行新型大环内酯类药物,尤其是克拉霉素的临床试验似乎是有必要的。