Snydman D R, Jacobus N V, McDermott L A, Supran S, Cuchural G J, Finegold S, Harrell L, Hecht D W, Iannini P, Jenkins S, Pierson C, Rihs J, Gorbach S L
Departments of Medicine, Pathology, and Community Health, New England Medical Center, Tufts University School of Medicine, Boston, Massachusetts 02111-1526, USA.
Antimicrob Agents Chemother. 1999 Oct;43(10):2417-22. doi: 10.1128/AAC.43.10.2417.
Antimicrobial resistance, including plasmid-mediated resistance, among the species of the Bacteroides fragilis group is well documented. An analysis of the in vitro susceptibility of B. fragilis group species referred between 1995 and 1996 as well as during a 7-year (1990 to 1996), prospective, multicenter survey of over 4,000 clinical isolates of B. fragilis group species was undertaken to review trends in the percent resistance to and geometric mean MICs of the antibiotics tested. There was a trend toward a decrease in the geometric mean MICs of most beta-lactam antibiotics, while the percent resistance to most agents was less affected. Within the species B. fragilis, the geometric mean MICs showed significant (P < 0.05) decreases for piperacillin-tazobactam, ticarcillin-clavulanate, piperacillin, ticarcillin, ceftizoxime, cefotetan, and cefmetazole; a significant increase was observed for clindamycin and cefoxitin. For the non-B. fragilis species, a significant decrease in the geometric mean MICs was observed for meropenem, ampicillin-sulbactam, ticarcillin-clavulanate, piperacillin, ticarcillin, ceftizoxime, and cefmetazole; a significant increase was observed for cefoxitin. Significant increases in percent resistance were observed within the B. fragilis strains for ticarcillin and ceftizoxime and within the non-B. fragilis isolates for cefotetan. Significant increases in percent resistance among all B. fragilis group species were observed for clindamycin, while imipenem showed no significant change in resistance trends. The trend analysis for trovafloxacin was limited to 3 years, since the quinolone was tested only in 1994, 1995, and 1996. During the 7 years analyzed, there was no resistance to metronidazole or chloramphenicol observed. The data demonstrate that resistance among the B. fragilis group species has decreased in the past several years, the major exception being clindamycin. The majority of the resistance decrease has been for the beta-lactams in B. fragilis, compared to other species. The reasons for these changes are not readily apparent.
脆弱拟杆菌群各菌种中存在包括质粒介导耐药性在内的抗菌药物耐药性,这已得到充分记载。对1995年至1996年以及在一项为期7年(1990年至1996年)的前瞻性多中心调查中提交的4000多株脆弱拟杆菌群临床分离株的体外药敏性进行了分析,以回顾所测试抗生素的耐药百分比和几何平均最低抑菌浓度(MIC)的趋势。大多数β-内酰胺类抗生素的几何平均MIC呈下降趋势,而对大多数药物的耐药百分比受影响较小。在脆弱拟杆菌菌种内,哌拉西林-他唑巴坦、替卡西林-克拉维酸、哌拉西林、替卡西林、头孢唑肟、头孢替坦和头孢美唑的几何平均MIC显著(P<0.05)下降;克林霉素和头孢西丁的几何平均MIC显著升高。对于非脆弱拟杆菌菌种,美罗培南、氨苄西林-舒巴坦、替卡西林-克拉维酸、哌拉西林、替卡西林、头孢唑肟和头孢美唑的几何平均MIC显著下降;头孢西丁的几何平均MIC显著升高。在脆弱拟杆菌菌株中,替卡西林和头孢唑肟的耐药百分比显著增加,在非脆弱拟杆菌分离株中,头孢替坦的耐药百分比显著增加。在所有脆弱拟杆菌群菌种中,克林霉素的耐药百分比显著增加,而亚胺培南的耐药趋势无显著变化。曲伐沙星的趋势分析仅限于3年,因为该喹诺酮类药物仅在1994年、1995年和1996年进行了测试。在分析的7年中,未观察到对甲硝唑或氯霉素的耐药性。数据表明,在过去几年中,脆弱拟杆菌群菌种的耐药性有所下降,主要例外是克林霉素。与其他菌种相比,脆弱拟杆菌中耐药性下降主要是针对β-内酰胺类药物。这些变化的原因尚不清楚。