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首页> 外文期刊>Journal of Medical Microbiology: An Official Journal of the Pathological Society of Great Britain and Ireland >In vitro time-kill studies of antimicrobial agents against blood isolates of imipenem-resistant Acinetobacter baumannii, including colistin- or tigecycline-resistant isolates
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In vitro time-kill studies of antimicrobial agents against blood isolates of imipenem-resistant Acinetobacter baumannii, including colistin- or tigecycline-resistant isolates

机译:对抗亚胺培南耐药鲍曼不动杆菌血液分离物的抗菌剂的体外时间杀灭研究,包括对大肠粘菌素或替加环素耐药的分离物

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The emergence of colistin or tigecycline resistance as well as imipenem resistance in Acinetobacter baumannii poses a great therapeutic challenge. The bactericidal and synergistic effects of several combinations of antimicrobial agents against imipenem-, colistin- or tigecycline-resistant A. baumannii isolates were investigated by in vitro time-kill experiments. Six imipenem-resistant A. baumannii blood isolates were examined in this study, including colistin- and tigecycline-susceptible, colistin-resistant but tigecycline-susceptible, and colistin-susceptible but tigecycline-resistant isolates. Time-kill studies were performed using five antimicrobial agents singly or in combinations (imipenem plus colistin, imipenem plus ampicillin-sulbactam, colistin plus rifampicin, colistin plus tigecycline, and tigecycline plus rifampicin) at concentrations of 0.5× and 1× their MICs. Only imipenem was consistently effective as a single agent against all six A. baumannii isolates. Although the effectiveness of combinations of 0.5× MIC antimicrobial agents was inconsistent, combination regimens using 1× MIC of the antimicrobial agents displayed excellent bactericidal activities against all six A. baumannii isolates. Among the combinations of 0.5× MIC antimicrobial agents, the combination of colistin and tigecycline showed synergistic or bactericidal effects against four of the isolates. This in vitro time-kill analysis suggests that antimicrobial combinations are effective for killing imipenem-resistant A. baumannii isolates, even if they are simultaneously resistant to either colistin or tigecycline. However, the finding that the combinations of 0.5× MIC antimicrobial agents were effective on only some isolates may warrant further investigation of the doses of combination agents needed to kill resistant A. baumannii.
机译:鲍曼不动杆菌中大肠菌素或替加环素耐药性以及亚胺培南耐药性的出现提出了巨大的治疗挑战。通过体外时间杀灭实验研究了几种抗微生物剂组合对亚胺培南,大肠菌素或替加环素耐药的鲍曼不动杆菌的杀菌和协同作用。在这项研究中检查了六种对亚胺培南耐药的鲍曼不动杆菌血液分离株,包括对大肠菌素和替加环素敏感,对大肠菌素耐药但对替加环素敏感,对大肠菌素敏感但对替加环素耐药的分离株。使用五种抗微生物剂分别或以其MIC的浓度分别使用五种抗菌剂(亚胺培南加粘菌素,亚胺培南加氨苄青霉素-舒巴坦,粘菌素加利福平,粘菌素加替加环素和替加环素加利福霉素)进行时间杀灭研究。仅亚胺培南作为单一试剂始终有效地对抗所有六个鲍曼不动杆菌。尽管0.5x MIC抗菌剂联合使用的效果不一致,但使用1x MIC的抗菌剂联合治疗方案对所有六个鲍曼不动杆菌均显示出优异的杀菌活性。在0.5x MIC抗菌剂的组合中,粘菌素和替加环素的组合对其中的四个分离物显示出协同或杀菌作用。这项体外时间杀灭分析表明,即使它们同时对大肠菌素或替加环素具有抗性,抗菌药物组合也可有效杀死对亚胺培南耐药的鲍曼不动杆菌。但是,发现0.5x MIC抗菌剂的组合仅对某些分离物有效,这一发现可能需要进一步研究杀死抗性鲍曼不动杆菌所需的组合剂的剂量。

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