Ceftolozane/Tazobactam Susceptibility Testing in Extended-Spectrum Betalactamase- and Carbapenemase-Producing Gram-Negative Bacteria of Various Clonal Lineages.

European Journal of Microbiology & Immunology Pub Date : 2019-02-08 eCollection Date: 2019-03-18 DOI:10.1556/1886.2019.00001
Carlo Pazzini, Parviz Ahmad-Nejad, Beniam Ghebremedhin
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引用次数: 10

Abstract

Nowadays, multidrug-resistant bacteria are considered as an increasing serious threat to public health worldwide. Global and local surveillance data are helpful in the application of the most efficient antimicrobial agent in bacterial infections. In the current study, we aimed to analyze the activity of the previously cleared agent ceftolozane/ tazobactam (C/T) in African and European multidrug-resistant Gram-negative bacteria. Susceptibility testing was performed on 147 extended-spectrum β-lactamase (107 Escherichia coli and 40 Klebsiella pneumoniae) and 103 carbapenemase-producing Gram-negative bacteria using Etest according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) clinical breakpoints. Among the extended-spectrum β-lactamase producing isolates, 91 Escherichia coli isolates (85%) and 23 Klebsiella pneumoniae isolates (57.5%) were susceptible towards C/T whereas out of the 103 carbapenemase-producing isolates 102 (99.0%) were C/T-resistant. C/T should be included in susceptibility testing to fairly administer this antimicrobial agent in infections caused by multidrug-resistant bacteria. It may be considered as a therapy option for infections caused by extended-spectrum β-lactamase-producing bacteria once susceptibility to this antimicrobial combination has been confirmed.

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不同克隆系产β -内酰胺酶和碳青霉烯酶的革兰氏阴性菌的增谱药敏试验
目前,耐多药细菌被认为是世界范围内日益严重的公共卫生威胁。全球和地方监测数据有助于在细菌感染中应用最有效的抗菌药物。在目前的研究中,我们的目的是分析先前清除的药物ceftolozane/ tazobactam (C/T)在非洲和欧洲多重耐药革兰氏阴性菌中的活性。采用Etest对147种广谱β-内酰胺酶(107种大肠埃希菌和40种肺炎克雷伯菌)和103种产碳青霉烯酶的革兰氏阴性菌进行药敏试验,试验结果符合欧洲抗菌药物敏感性试验委员会(EUCAST)的临床分点。在产β-内酰胺酶的广谱菌株中,91株大肠埃希菌(85%)和23株肺炎克雷伯菌(57.5%)对C/T敏感,103株碳青霉烯酶产菌株中102株(99.0%)对C/T耐药。应将C/T纳入药敏试验,以便在多重耐药细菌引起的感染中公平地使用这种抗微生物药物。一旦证实对这种抗菌药物组合的敏感性,它可能被认为是由广谱β-内酰胺酶产生细菌引起的感染的一种治疗选择。
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