Gottfredsson M, Erlendsdóttir H, Sigfússon A, Gudmundsson S
Department of Immunology, Landspítalinn National University Hospital, and University of Iceland Medical School, Reykjavik.
Antimicrob Agents Chemother. 1998 May;42(5):1005-11. doi: 10.1128/AAC.42.5.1005.
Changes in bacterial ultrastructure after antibiotic exposure and during the postantibiotic effect (PAE) have been demonstrated by electron microscopy (EM). However, EM is qualitative and subject to individual interpretation. In contrast, flow cytometry gives qualitative and quantitative information. The sizes and nucleic acid contents of Escherichia coli and Pseudomonas aeruginosa were studied during antimicrobial exposure as well as during the PAE period by staining the organisms with propidium iodide and analyzing them with flow cytometry and fluorescence microscopy. The effects of ampicillin, ceftriaxone, ciprofloxacin, gentamicin, and rifampin were studied for E. coli, whereas for P. aeruginosa imipenem and ciprofloxacin were investigated. After exposure of E. coli to ampicillin, ceftriaxone, and ciprofloxacin, filamentous organisms were observed by fluorescence microscopy. These changes in morphology were reflected by increased forward light scatter (FSC) and nucleic acid content as measured by flow cytometry. For the beta-lactams the extent of filamentation increased in a dose-dependent manner after drug removal, resulting in formation of distinct subpopulations of bacteria. These changes peaked at 20 to 35 min, and bacteria returned to normal after 90 min after drug removal. In contrast, the subpopulations induced by ciprofloxacin did not return to normal until > 180 min after the end of the classically defined PAE. Rifampin resulted in formation of small organisms with low FSC, whereas no distinctive characteristics were noted after gentamicin exposure. For P. aeruginosa an identifiable subpopulation of large globoid cells and increased nucleic acid content was detected after exposure to imipenem. These changes persisted past the PAE, as defined by viability counting. Swollen organisms with increased FSC were detected after ciprofloxacin exposure, even persisting during bacterial growth. In summary, for beta-lactam antibiotics and ciprofloxacin, the PAE is characterized by dynamic formation of enlarged cell populations of increased nucleic acid content, whereas rifampin induces a decrease in size and nucleic acid content in the organisms. Flow cytometry is an ideal method for future studies of bacterial phenotypic characteristics during the PAE.
抗生素暴露后及抗生素后效应(PAE)期间细菌超微结构的变化已通过电子显微镜(EM)得到证实。然而,EM是定性的,且易受个人解读影响。相比之下,流式细胞术可提供定性和定量信息。通过用碘化丙啶对大肠杆菌和铜绿假单胞菌进行染色,并用流式细胞术和荧光显微镜对其进行分析,研究了抗菌药物暴露期间以及PAE期间这些细菌的大小和核酸含量。研究了氨苄西林、头孢曲松、环丙沙星、庆大霉素和利福平对大肠杆菌的影响,而对于铜绿假单胞菌则研究了亚胺培南和环丙沙星的影响。大肠杆菌暴露于氨苄西林、头孢曲松和环丙沙星后,通过荧光显微镜观察到丝状菌体。这些形态变化通过流式细胞术测量的前向光散射(FSC)增加和核酸含量增加得以体现。对于β-内酰胺类抗生素,药物去除后丝状化程度呈剂量依赖性增加,导致形成不同的细菌亚群。这些变化在20至35分钟达到峰值,药物去除后90分钟细菌恢复正常。相比之下,环丙沙星诱导的亚群直到经典定义的PAE结束后>180分钟才恢复正常。利福平导致形成FSC低的小菌体,而庆大霉素暴露后未观察到明显特征。对于铜绿假单胞菌,暴露于亚胺培南后检测到一个可识别的大球状细胞亚群且核酸含量增加。这些变化在通过活菌计数定义的PAE之后仍然存在。环丙沙星暴露后检测到FSC增加的肿胀菌体,甚至在细菌生长期间持续存在。总之,对于β-内酰胺类抗生素和环丙沙星,PAE的特征是动态形成核酸含量增加的扩大细胞群体,而利福平诱导菌体大小和核酸含量降低。流式细胞术是未来研究PAE期间细菌表型特征的理想方法。