The combined dual β-lactams and diazabicyclooctane β-lactamase inhibitor is highly effective against Mycobacterium abscessus species in vitro.

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES Journal of global antimicrobial resistance Pub Date : 2025-02-25 DOI:10.1016/j.jgar.2025.02.015
Kana Misawa, Tomoyasu Nishimura, Maiko Yoshikawa, Rina Shimamura, Shoko Kashimura, Yuki Enoki, Kazuaki Taguchi, Kazuaki Matsumoto, Naoki Hasegawa
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Abstract

Background: Mycobacterium abscessus pulmonary disease is a refractory infectious disease. Since the number of patients infected with Mycobacterium abscessus species (MABS) is increasing worldwide, developing an effective treatment is urgent. We previously reported that nacubactam, a diazabicyclooctane (DBO) β-lactamase inhibitor, could inhibit MABS β-lactamase. Few reports have indicated that dual β-lactams were effective with a DBO β-lactamase inhibitor against MABS.

Objectives: To determine which dual β-lactams have high antibacterial activity against MABS in the presence and absence of nacubactam.

Methods: Antimicrobial susceptibility tests were conducted through a checkerboard assay of 27 β-lactams using the broth microdilution method for three subspecies type strains and 20 clinical isolates of MABS. The number of intracellular and extracellular bacteria was measured using human macrophages infected with M. abscessus treated with effective combinations confirmed in susceptibility tests.

Results: In antimicrobial susceptibility tests, 91 combinations of dual β-lactams with nacubactam exhibited synergistic effects on M. abscessus JCM13569. Among them, the combination of cefazolin, cefotiam, cefoxitin, or cefuroxime with imipenem and nacubactam exhibited highly synergistic effects, resulting in low minimum inhibitory concentrations (MICs) against MABS clinical isolates. Without nacubactam, the combination of imipenem and cefoxitin showed the lowest MIC. In experiments using human macrophages infected with M. abscessus, these dual β-lactam combinations reduced the number of intracellular and extracellular bacteria compared to those of single β-lactam.

Conclusions: The combination of cefazolin, cefotiam, cefoxitin, or cefuroxime with imipenem and nacubactam was highly effective against MABS. Without nacubactam, the combination of cefoxitin and imipenem was effective.

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背景:脓肿分枝杆菌肺病是一种难治性传染病。由于全球感染脓肿分枝杆菌(MABS)的患者人数不断增加,开发有效的治疗方法迫在眉睫。我们曾报道过一种二氮杂双环辛烷(DBO)β-内酰胺酶抑制剂纳库巴坦能抑制 MABS β-内酰胺酶。很少有报告指出双 β-内酰胺与 DBO β-内酰胺酶抑制剂对 MABS 有效:确定哪些双 β-内酰胺类药物在纳库巴坦存在和不存在的情况下对 MABS 具有较高的抗菌活性:方法:采用肉汤微量稀释法对 MABS 的 3 个亚种类型菌株和 20 个临床分离菌株进行了 27 种 β-内酰胺类药物的抗菌药敏感性试验。用人巨噬细胞感染脓肿疽杆菌后,用药敏试验确认的有效组合物对细胞内和细胞外的细菌数量进行了测定:结果:在抗菌药药敏试验中,91 种双 β-内酰胺类药物与纳库巴坦的组合对 JCM13569 型脓肿病菌有协同作用。其中,头孢唑啉、头孢替安、头孢西丁或头孢呋辛与亚胺培南和纳库巴坦的组合具有高度协同作用,对 MABS 临床分离株的最低抑菌浓度(MIC)较低。在不使用纳库巴坦的情况下,亚胺培南和头孢西丁的组合显示出最低的 MIC 值。在使用感染了脓肿霉菌的人体巨噬细胞进行的实验中,与单一β-内酰胺类药物相比,这些双β-内酰胺类药物组合可减少细胞内和细胞外细菌的数量:结论:头孢唑啉、头孢替安、头孢西丁或头孢呋辛与亚胺培南和纳库巴坦联合用药对 MABS 非常有效。在不使用纳可巴坦的情况下,头孢西丁和亚胺培南联用也很有效。
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
Journal of global antimicrobial resistance
Journal of global antimicrobial resistance INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
8.70
自引率
2.20%
发文量
285
审稿时长
34 weeks
期刊介绍: The Journal of Global Antimicrobial Resistance (JGAR) is a quarterly online journal run by an international Editorial Board that focuses on the global spread of antibiotic-resistant microbes. JGAR is a dedicated journal for all professionals working in research, health care, the environment and animal infection control, aiming to track the resistance threat worldwide and provides a single voice devoted to antimicrobial resistance (AMR). Featuring peer-reviewed and up to date research articles, reviews, short notes and hot topics JGAR covers the key topics related to antibacterial, antiviral, antifungal and antiparasitic resistance.
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