Fekete T
Section of Infectious Diseases, Temple University Health Sciences Center, Philadelphia, Pennsylvania 19140.
Clin Microbiol Rev. 1993 Jan;6(1):22-33. doi: 10.1128/CMR.6.1.22.
Antimicrobial susceptibility testing (AST) of Neisseria gonorrhoeae has been under development since the early days of antimicrobial agents. However, it is rarely applied to clinical isolates today. The history of the various in vitro tests to determine the susceptibility of N. gonorrhoeae to antibiotics is rich with evidence that these results predict response to therapy for almost all agents tested. Further, AST is a useful and important aspect of strain characterization and disease epidemiology in conjunction with the more specific but laborious techniques of auxotyping, serotyping, and plasmid analysis. Current technology has overcome many of the objections to AST for N. gonorrhoeae with standardization of test media and the development of an accurate disk diffusion AST method that is suited to most clinical laboratories regardless of volume or level of technical expertise. Ironically, the very low level of resistance to the current primary treatment strategy in the United States, ceftriaxone or another potent cephalosporin, makes the use of AST somewhat superfluous.
自抗菌药物问世以来,淋病奈瑟菌的药敏试验(AST)就一直在发展。然而,如今它很少应用于临床分离株。各种用于确定淋病奈瑟菌对抗生素敏感性的体外试验的历史充分证明,这些结果几乎能预测所有受试药物的治疗反应。此外,结合更为特异但繁琐的菌型分型、血清分型和质粒分析技术,药敏试验是菌株特征分析和疾病流行病学的一个有用且重要的方面。当前技术通过对试验培养基进行标准化以及开发出一种适用于大多数临床实验室(无论规模大小或技术专业水平高低)的准确纸片扩散法药敏试验,克服了许多针对淋病奈瑟菌药敏试验的反对意见。具有讽刺意味的是,在美国,目前主要治疗策略(头孢曲松或另一种强效头孢菌素)的耐药水平极低,这使得药敏试验的使用略显多余。