Comparison of testing methods assessing the in vitro efficacy of the combination of aztreonam with avibactam on multidrug-resistant Gram-negative bacilli

IF 4.6 2区 医学 Q1 MICROBIOLOGY Annals of Clinical Microbiology and Antimicrobials Pub Date : 2024-05-25 DOI:10.1186/s12941-024-00708-0
Corentin Deckers, Florian Bélik, Olivier Denis, Pierre Bogaerts, Isabel Montesinos, Catherine Berhin, Warda Bouchahrouf, Martin Hoebeke, Stephanie Evrard, Nicolas Gilliard, Merve Okur, Te-Din Huang
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Abstract

Aztreonam-avibactam (ATM-AVI) combination shows promising effectiveness on most carbapenemase-producing Gram-negatives, yet standardized antibiotic susceptibility testing (AST) methods for evaluating the combination in clinical laboratories is lacking. We aimed to evaluate different ATM-AVI AST approaches. 96 characterized carbapenem-resistant clinical isolates belonging to 9 Enterobacterales (EB; n = 80) and P. aeruginosa (PA; n = 16) species, including 90 carbapenemase producers and 72 strains resistant to both CAZ-AVI and ATM, were tested. Paper disk elution (DE; Bio-Rad) and E-test gradient strips stacking (SS; bioMérieux) were performed for the ATM + CAZ-AVI combination. MIC Test Strip (MTS; Liofilchem) was evaluated for ATM-AVI MIC determination. Results were interpreted applying ATM clinical breakpoints of the EUCAST guidelines and compared to the broth microdilution method (Sensititre, Thermofisher). According to broth microdilution method, 93% of EB and 69% of PA were tested susceptible to ATM-AVI. The synergistic effect of ATM-AVI was of 95% for EB, but of only 17% for PA. The MTS method yielded higher categorical and essential agreement (CA/EA) rates for both EB (89%/91%) and PA (94%/94%) compared to SS, where the rates were 87%/83% for EB and 81%/81% for PA. MTS and SS yielded 2 and 3 major discrepancies, respectively, while 3 very major discrepancies each were observed for both methods. Concerning the DE method, CA reached 91% for EB and 81% for PA, but high number of very major discrepancies were observed for EB (n = 6; 8%) and for PA (n = 3; 19%). The ATM-AVI association displayed excellent in vitro activity against highly resistant clinical Enterobacterales strains. MTS method offers accurate ATM-AVI AST results, while the SS method might serve as better alternative then DE method in assessing the efficacy of ATM + CAZ-AVI combination. However, further investigation is needed to confirm the methods' ability to detect ATM-AVI resistance.
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评估阿曲霉素与阿维菌素复方制剂对耐多药革兰氏阴性杆菌体外疗效的测试方法比较
阿奇霉素-阿维菌素(ATM-AVI)组合对大多数产碳青霉烯酶的革兰氏阴性菌有很好的疗效,但临床实验室缺乏评估该组合的标准化抗生素药敏试验(AST)方法。我们旨在评估不同的 ATM-AVI AST 方法。我们对 96 株特征化的耐碳青霉烯类临床分离株进行了测试,这些分离株属于 9 种肠杆菌属(EB;n = 80)和铜绿假单胞菌属(PA;n = 16),其中包括 90 株碳青霉烯酶产生株和 72 株对 CAZ-AVI 和 ATM 均耐药的菌株。对 ATM + CAZ-AVI 组合进行了纸盘洗脱(DE;Bio-Rad)和 E 测试梯度条堆叠(SS;生物梅里埃)。MIC测试带(MTS;Liofilchem)用于测定ATM-AVI的MIC。检测结果根据欧盟 CAST 指南的 ATM 临床断点进行解释,并与肉汤微量稀释法(Sensititre,Thermofisher)进行比较。根据肉汤微稀释法,93% 的 EB 和 69% 的 PA 对 ATM-AVI 易感。ATM-AVI 对 EB 的增效作用为 95%,但对 PA 的增效作用仅为 17%。与 SS 相比,MTS 方法对 EB(89%/91%)和 PA(94%/94%)的分类和基本一致率(CA/EA)更高,EB 为 87%/83%,PA 为 81%/81%。MTS 和 SS 分别产生了 2 次和 3 次重大差异,而两种方法各出现了 3 次非常重大的差异。在 DE 方法中,EB 的 CA 达到 91%,PA 达到 81%,但 EB(n = 6;8%)和 PA(n = 3;19%)出现了大量的极不一致。ATM-AVI 联合物对高耐药性临床肠杆菌菌株具有出色的体外活性。MTS 法可提供准确的 ATM-AVI AST 结果,而 SS 法在评估 ATM + CAZ-AVI 组合的疗效方面可能比 DE 法更好。不过,要确认这些方法检测 ATM-AVI 耐药性的能力,还需要进一步的研究。
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来源期刊
CiteScore
8.60
自引率
0.00%
发文量
49
审稿时长
>12 weeks
期刊介绍: Annals of Clinical Microbiology and Antimicrobials considers good quality, novel and international research of more than regional relevance. Research must include epidemiological and/or clinical information about isolates, and the journal covers the clinical microbiology of bacteria, viruses and fungi, as well as antimicrobial treatment of infectious diseases. Annals of Clinical Microbiology and Antimicrobials is an open access, peer-reviewed journal focusing on information concerning clinical microbiology, infectious diseases and antimicrobials. The management of infectious disease is dependent on correct diagnosis and appropriate antimicrobial treatment, and with this in mind, the journal aims to improve the communication between laboratory and clinical science in the field of clinical microbiology and antimicrobial treatment. Furthermore, the journal has no restrictions on space or access; this ensures that the journal can reach the widest possible audience.
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