Assessment of broth disk elution method for aztreonam in combination with ceftazidime/avibactam against Enterobacterales isolates.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-09-03 DOI:10.1128/spectrum.00953-24
Peipei Song, Jian Xu, Lan Jiang, Qin Zhang, Chenggui Liu
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Abstract

The combination of aztreonam with ceftazidime/avibactam is considered a potential therapeutic approach for the treatment of infections caused by metallo-β-lactamase (MBL)-producing isolates. In this study, in vitro antibacterial activity of aztreonam with avibactam against 204 carbapenemase-producing Enterobacterales was determined by broth disk elution (BDE) method of two detection volumes (5- and 2-mL broth), with broth microdilution (BMD) method as a reference. For the BDE-5mL test, the categorical agreement (CA) of ATM+CZA-lo tube (aztreonam/ceftazidime/avibactam: 6/6/4 mg/L) was 99.5%, with 0.5% major error (ME) and 0% very major error (VME); the CA of 2ATM+CZA-lo tube (12/6/4 mg/L) was 100%, with no ME and VME. For the BDE-2mL test, the CA of ATM+2CZA-hi tube (15/10/4 mg/L) was 98.5%, with 0% ME and 37.5% VME; the CA of 2ATM+2CZA-hi tube (30/10/4 mg/L) was 97.1%, with 0% ME and 75% VME. The BDE-5 mL test is an economical and practical method for clinical microbiology laboratories to determine the antibacterial susceptibility of aztreonam with avibactam against Enterobacterales, especially the 2ATM+CZA-lo tube with a final concentration of 12/6/4 mg/L of aztreonam/ceftazidime/avibactam.

Importance: Infections caused by metallo-β-lactamase (MBL)-producing Enterobacterales are increasingly reported worldwide, and it is a significant challenge for clinical infection treatment. MBLs are adept at hydrolyzing almost all traditional β-lactam antibiotics except aztreonam, and the enzyme activity cannot be inhibited by traditional or novel β-lactamase inhibitors. The good thing is that the combination of aztreonam with ceftazidime/avibactam has been proven to be one of the potential therapeutic approaches for treating infections related with MBL-producing isolates. Broth microdilution (BMD) method is recommended as a reference method for its accuracy, but it is too complex to perform in most routine laboratories. Finding a more convenient, practical, and accurate susceptibility testing method for aztreonam/avibactam in clinical microbiology laboratories is very necessary. Here, we evaluated the performance of broth disk elution (BDE) method for aztreonam in combination with ceftazidime/avibactam against Enterobacterales isolates, with BMD as a reference.

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肉汤盘洗脱法评估阿兹曲南与头孢他啶/阿维菌素联合治疗肠杆菌分离物的效果。
在治疗由产金属-β-内酰胺酶(MBL)分离菌株引起的感染时,阿兹曲南与头孢他啶/阿维巴坦联用被认为是一种潜在的治疗方法。本研究以肉汤微量稀释法(BMD)为参照,采用两种检测容量(5 毫升和 2 毫升肉汤)的肉汤盘洗脱法(BDE)测定了阿曲南加阿维巴坦对 204 种产碳青霉烯酶肠杆菌的体外抗菌活性。在 BDE-5 毫升检测中,ATM+CZA-lo 管(阿曲南/头孢唑肟/阿维菌素:6/6/4 毫克/升)的分类一致性(CA)为 99.5%,主要误差(ME)为 0.5%,极主要误差(VME)为 0%;2ATM+CZA-lo 管(12/6/4 毫克/升)的分类一致性(CA)为 100%,无主要误差和极主要误差。在 BDE-2 毫升检测中,ATM+2CZA-hi 管(15/10/4 毫克/升)的 CA 为 98.5%,ME 为 0%,VME 为 37.5%;2ATM+2CZA-hi 管(30/10/4 毫克/升)的 CA 为 97.1%,ME 为 0%,VME 为 75%。BDE-5 mL 试验是临床微生物实验室测定阿曲南加阿维菌素对肠杆菌抗菌敏感性的一种经济实用的方法,特别是 2ATM+2CZA-lo 管(阿曲南/头孢唑肟/阿维菌素的最终浓度为 12/6/4 mg/L):由产金属-β-内酰胺酶(MBL)肠杆菌引起的感染在全球范围内的报道越来越多,这对临床感染治疗是一个重大挑战。除阿曲南外,MBLs 几乎能水解所有传统的 β-内酰胺类抗生素,传统或新型 β-内酰胺酶抑制剂均无法抑制其酶活性。好在阿兹曲南与头孢唑肟/阿维菌素联用已被证明是治疗与产生 MBL 的分离菌相关的感染的潜在治疗方法之一。肉汤微量稀释(BMD)法因其准确性而被推荐为参考方法,但这种方法过于复杂,大多数常规实验室都无法采用。在临床微生物实验室中寻找一种更方便、实用、准确的阿兹曲南/阿维菌素药敏试验方法是非常必要的。在此,我们以肉汤盘洗脱法(BDE)为参照,评估了肉汤盘洗脱法对阿曲南及头孢他啶/阿维菌素联合治疗肠杆菌属分离株的效果。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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