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厌氧菌中的抗菌药物耐药性。

Antimicrobial resistance in anaerobes.

作者信息

Rasmussen B A, Bush K, Tally F P

机构信息

Infectious Disease Section, Wyeth-Ayerst Research, Pearl River, New York 10965, USA.

出版信息

Clin Infect Dis. 1997 Jan;24 Suppl 1:S110-20. doi: 10.1093/clinids/24.supplement_1.s110.

Abstract

The development of antibiotic resistance in anaerobic bacteria has a tremendous impact on the selection of antimicrobial agents for empirical therapy. Susceptibility studies have documented the emergence of antimicrobial resistance and indicate distinct differences in resistance patterns related to individual hospitals, geographic regions, and antibiotic-prescribing regimens. Resistance to beta-lactam drugs, clindamycin, tetracyclines, and 5-nitroimidazoles (metronidazole) has been observed. The prime mechanism for resistance to beta-lactam agents is the production of beta-lactamases. Resistance to clindamycin is mediated by modification of the ribosome. Tetracycline resistance is mediated by both tetracycline efflux and ribosomal protection. 5-Nitroimidazole resistance appears to be caused by a combination of decreased antibiotic uptake and decreased nitroreductase activity. The level of chloramphenicol susceptibility remains quite high, whereas uniform resistance to aminoglycosides and quinolones is observed. Understanding the mechanisms of resistance is critical for both informed selection of antimicrobial therapy and the design of new antimicrobial agents.

摘要

厌氧菌中抗生素耐药性的发展对经验性治疗抗菌药物的选择产生了巨大影响。药敏研究记录了抗菌药物耐药性的出现,并表明与各个医院、地理区域和抗生素处方方案相关的耐药模式存在明显差异。已观察到对β-内酰胺类药物、克林霉素、四环素和5-硝基咪唑类(甲硝唑)的耐药性。对β-内酰胺类药物耐药的主要机制是β-内酰胺酶的产生。对克林霉素的耐药性是由核糖体修饰介导的。四环素耐药性由四环素外排和核糖体保护介导。5-硝基咪唑类耐药性似乎是由抗生素摄取减少和硝基还原酶活性降低共同引起的。氯霉素的敏感水平仍然很高,而对氨基糖苷类和喹诺酮类则观察到普遍耐药。了解耐药机制对于明智地选择抗菌治疗和设计新型抗菌药物都至关重要。

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