Evaluation of gradient strip diffusion for susceptibility testing of aztreonam-avibactam in metallo-β-lactamase-producing Enterobacterales.

IF 6.1 2区 医学 Q1 MICROBIOLOGY Journal of Clinical Microbiology Pub Date : 2024-11-13 Epub Date: 2024-09-30 DOI:10.1128/jcm.00649-24
Jamie K Lemon, Cheryl Jankowsi-Romano, Scott Duong, Stefan Juretschko, Vincent A Streva
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Abstract

The emergence of metallo-β-lactamase (MBL)-producing Enterobacterales presents unique clinical treatment challenges. Recently developed β-lactam/ β-lactamase inhibitor combination agents, while effective against other carbapenemase-producing organisms, are notably ineffective against MBL producers. While MBLs do not hydrolyze monobactams (aztreonam), many MBL-producing organisms are resistant to aztreonam through alternate mechanisms, leaving cefiderocol as the sole monotherapy treatment option recommended for MBL producers. Recent guidelines for the treatment of MBL-harboring organisms have added combination therapy with aztreonam and ceftazidime-avibactam, using ceftazidime-avibactam as a source of the β-lactamase inhibitor avibactam. Current laboratory testing options for the combination of aztreonam-avibactam are limited to broth microdilution (BMD) and broth disk elution (BDE) methods, which are not practical in most clinical laboratories. In this study, we evaluated the performance of aztreonam/avibactam gradient strips on 103 MBL-producing Enterobacterales patient isolates as well as an additional 31 isolates from the CDC AR Bank. All MBL Enterobacterales patient isolates included in this study harbored a New Delhi metallo-β-lactamase (blaNDM) gene. Essential agreement of gradient strip minimal inhibitory concentrations (MICs) for patient isolates compared to BMD was 93.2%. While there are no established breakpoints for aztreonam-avibactam, category agreement (CA) for patient isolates was 97.1% when using the CLSI aztreonam breakpoints. There were no major or very major errors observed. There were three minor errors. Precision for aztreonam-avibactam gradient strip diffusion was 100%. These data demonstrate that the use of gradient strip diffusion for aztreonam-avibactam MIC determination in MBL-producing Enterobacterales is a viable option for clinical laboratories.

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评估梯度条带扩散法在产金-β-内酰胺酶肠杆菌中对阿曲南唑-阿维菌素的药敏试验。
产金属-β-内酰胺酶(MBL)肠杆菌的出现给临床治疗带来了独特的挑战。最近开发的 β-内酰胺/β-内酰胺酶抑制剂复方制剂虽然对其他产碳青霉烯酶的微生物有效,但对 MBL 生产者明显无效。虽然 MBL 不会水解单内酰胺(阿曲南),但许多产生 MBL 的病菌会通过其他机制对阿曲南产生耐药性,因此头孢哌酮成为针对 MBL 生产者推荐的唯一单一疗法。最近,治疗产生 MBL 的微生物的指南增加了唑曲南和头孢唑肟-阿维菌素的联合疗法,使用头孢唑肟-阿维菌素作为 β-内酰胺酶抑制剂阿维菌素的来源。目前对阿曲南类-阿维菌素复方制剂的实验室检测方法仅限于肉汤微量稀释法(BMD)和肉汤盘洗脱法(BDE),而这两种方法在大多数临床实验室并不实用。在本研究中,我们对 103 例产生 MBL 的肠杆菌患者分离物以及另外 31 例来自疾病预防控制中心 AR 库的分离物进行了唑曲南/阿维菌素梯度条的性能评估。本研究中的所有 MBL 肠杆菌患者分离物均携带新德里金属-β-内酰胺酶(blaNDM)基因。患者分离物的梯度条带最小抑菌浓度 (MIC) 与 BMD 的基本一致率为 93.2%。虽然目前还没有确立阿兹曲南-阿维巴坦的断点,但在使用 CLSI 阿兹曲南断点时,患者分离物的类别一致性(CA)为 97.1%。没有发现重大或非常重大的错误。有三个轻微错误。阿兹菌素-阿维菌素梯度条带扩散的精确度为 100%。这些数据表明,使用梯度条带扩散法测定产甲氧苄啶肠杆菌的阿兹菌素-阿维菌素 MIC 值是临床实验室的可行选择。
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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
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