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Increasing resistance to beta-lactam antibiotics among clinical isolates of Enterococcus faecium: a 22-year review at one institution.

机译:粪肠球菌临床分离株对β-内酰胺抗生素的耐药性增加:在一家机构进行的22年回顾。

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摘要

To identify any change in the antibiotic resistance of Enterococcus faecium, we examined the antibiotic susceptibilities of clinical strains (n = 84) isolated at one institution during the 22 years since 1968. A significant increase in resistance to penicillin was observed during the study period: the MICs of penicillin for 50 and 90% of isolates tested were 16 and 64 micrograms/ml, respectively, from 1969 to 1988 (n = 48; geometric mean MIC, 14 micrograms/ml) , whereas they were 256 and 512 micrograms/ml, respectively, from 1989 to 1990 (n = 36; geometric mean MIC, 123 micrograms/ml) (P less than 0.001). A comparable increase in resistance to ampicillin was also noted (P less than 0.001). No strains produced detectable beta-lactamase. In contrast, susceptibilities to vancomycin, teicoplanin, and ciprofloxacin remained stable. High-level resistance to gentamicin was observed in none of 48 isolates from 1969 to 1988, but was present in 22 of 36 strains (61%) from 1989 to 1990 (P less than 0.001) and was significantly associated with resistance (MIC, greater than or equal to 128 micrograms/ml) to penicillin (P less than 0.001). To assess the potential evolution of antibiotic resistance in this species, clinical isolates (n = 24) were compared with strains isolated in 1968 from a human population in the Solomon Islands that was never exposed to antibiotics. Solomon Island isolates were significantly more susceptible than all clinical strains to penicillin, ampicillin, and vancomycin (P less than 0.001 for each), but they exhibited no differences in susceptibility to teicoplanin or ciprofloxacin. The penicillin-binding affinity of penicillin-binding protein 5 (PBP 5) in penicillin-resistant clinical strains (MIC, 512 micrograms/ml) was notably lower than that in strains with more typical susceptibilities, suggesting an alteration in this PBP as a possible mechanism for increased penicillin resistance. Solomon Island strains most susceptible to penicillin demonstrated a prominent PBP 5* and the absence of PBP 5. These changes in the antibiotic resistance of E. faecium emphasize the importance of identifying this species in patients with serious enterococcal infections and the necessity of assessing its susceptibility to both beta-lactams and aminoglycosides if effective therapy is to be identified.
机译:为了确定粪肠球菌的抗生素耐药性是否发生任何变化,我们检查了自1968年以来的22年中在一所机构中分离出的临床菌株(n = 84)的抗生素敏感性。在研究期间,观察到的对青霉素的耐药性显着增加:从1969年到1988年,测试的50%和90%分离株的青霉素MIC分别为16和64微克/毫升(n = 48;几何平均MIC,14微克/毫升),而它们的256和512微克/毫升分别从1989年到1990年(n = 36;几何平均MIC,123微克/毫升)(P小于0.001)。还发现对氨苄西林的抗药性有可比的增加(P小于0.001)。没有菌株产生可检测的β-内酰胺酶。相反,对万古霉素,替考拉宁和环丙沙星的敏感性保持稳定。从1969年至1988年,在48株菌株中均未观察到对庆大霉素的高水平抗药性,但在1989年至1990年期间,在36株菌株中有22株(61%)存在庆大霉素(P小于0.001),并且与抗药性显着相关(MIC,更大小于或等于128微克/毫升)的青霉素(P小于0.001)。为了评估该物种对抗生素耐药性的潜在演变,将临床分离株(n = 24)与1968年从从未接触过抗生素的所罗门群岛人群中分离出的菌株进行了比较。与所有临床菌株相比,所罗门群岛分离株对青霉素,氨苄青霉素和万古霉素的敏感度更高(每种P均小于0.001),但它们对替考拉宁或环丙沙星的敏感性没有差异。耐青霉素临床菌株(MIC,512微克/毫升)中青霉素结合蛋白5(PBP 5)的青霉素结合亲和力明显低于典型药敏性较弱的菌株,这表明该PBP可能发生改变增强青霉素耐药性的机制。对青霉素最敏感的所罗门岛菌株显示出突出的PBP 5 *和PBP 5不存在。这些粪肠球菌的耐药性变化强调了在严重肠球菌感染患者中鉴定该菌种的重要性以及评估其敏感性的必要性。如果要确定有效的治疗方法,则应同时使用β-内酰胺和氨基糖苷。

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