Evaluation of the in vitro efficacy of antimicrobials against Enterobacterales with multiple carbapenemase enzymes.

IF 1.7 Q4 MICROBIOLOGY
Reena Rajan, Gopinathan Sasikala
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引用次数: 0

Abstract

Background and objectives: High-dose of carbapenems and combination therapies with new β-lactam/β-lactamase inhibitors and polymyxin B/tigecycline have been considered for treatment of carbapenem resistant Enterobacterales infection. The research was conducted to evaluate the in vitro potency of aminoglycosides, ceftazidime/avibactam/aztreonam and tigecycline against isolates of Enterobacteriaceae with multiple carbapenemase enzymes.

Materials and methods: 42 genotypically confirmed carbapenem resistant Enterobacterales (twenty-nine NDM producers, nine NDM and OXA-48 producers, three NDM and VIM producers and one NDM combined with VIM and OXA 48 producer) were included. Minimum inhibitory concentration for carbapenems, aminoglycosides and tigecycline was determined by Vitek 2. Ceftazidime/avibactam/aztreonam synergy was observed by disk diffusion methodology.

Results: The in vitro efficacy of aminoglycosides was observed against Escherichia coli (E. coli) isolates with NDM and VIM genes. Low tigecycline susceptibility was observed among Klebsiella pneumoniae (K. pneumoniae) isolates with NDM and OXA-48 genes. Ceftazidime -avibactam/aztreonam combination displayed good in vitro activity against dual carbapenemase producers of E. coli isolates (NDM with OXA-48 and NDM with VIM genes) and Klebsiella pneumoniae (combination of NDM, VIM and OXA-48 genes).

Conclusion: Ceftazidime/avibactam/aztreonam, aminoglycosides and tigecycline displayed in vitro activity against dual carbapenemase producers of E. coli and K. pneumoniae.

含多种碳青霉烯酶的肠杆菌抗菌药物的体外疗效评价。
背景与目的:高剂量碳青霉烯类药物和新型β-内酰胺/β-内酰胺酶抑制剂与多粘菌素B/替加环素联合治疗碳青霉烯类耐药肠杆菌感染已被考虑。研究氨基糖苷类、头孢他啶/阿维巴坦/氨曲南和替加环素对含多种碳青霉烯酶的肠杆菌科分离株的体外药效。材料与方法:纳入42株经基因典型鉴定的耐碳青霉烯类肠杆菌,其中29株产NDM, 9株产NDM和OXA-48, 3株产NDM和VIM, 1株产NDM与VIM和OXA-48合产。用Vitek 2测定碳青霉烯类、氨基糖苷类和替加环素的最低抑菌浓度。采用圆盘扩散法观察头孢他啶/阿维巴坦/氨曲南的协同作用。结果:观察氨基糖苷类药物对NDM和VIM基因大肠杆菌的体外抑菌效果。肺炎克雷伯菌NDM和OXA-48基因分离株对替加环素的敏感性较低。头孢他啶-阿维巴坦/氨曲南联合对大肠杆菌(含OXA-48基因的NDM和含VIM基因的NDM)和肺炎克雷伯菌(含NDM、VIM和OXA-48基因的NDM)的双重碳青霉烯酶产生菌具有良好的体外活性。结论:头孢他啶/阿维巴坦/氨曲南、氨基糖苷类和替加环素对大肠杆菌和肺炎克雷伯菌的双碳青霉烯酶产生菌具有体外活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
7.10%
发文量
96
审稿时长
12 weeks
期刊介绍: The Iranian Journal of Microbiology (IJM) is an international, multi-disciplinary, peer-reviewed journal that provides rapid publication of the most advanced scientific research in the areas of basic and applied research on bacteria and other micro-organisms, including bacteria, viruses, yeasts, fungi, microalgae, and protozoa concerning the development of tools for diagnosis and disease control, epidemiology, antimicrobial agents, clinical microbiology, immunology, Genetics, Genomics and Molecular Biology. Contributions may be in the form of original research papers, review articles, short communications, case reports, technical reports, and letters to the Editor. Research findings must be novel and the original data must be available for review by the Editors, if necessary. Studies that are preliminary, of weak originality or merely descriptive as well as negative results are not appropriate for the journal. Papers considered for publication must be unpublished work (except in an abstract form) that is not under consideration for publication anywhere else, and all co-authors should have agreed to the submission. Manuscripts should be written in English.
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