新型四环素衍生物紫檀环素体外抗脓肿分枝杆菌活性的研究。

IF 2.9 3区 医学 Q2 INFECTIOUS DISEASES
Infection and Drug Resistance Pub Date : 2025-10-04 eCollection Date: 2025-01-01 DOI:10.2147/IDR.S538789
Qinlong Yu, Xiaoqin Niu, Bailong Hou, Minjie Mao, Li Zhu, Weifeng Shen, Wei Wang
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引用次数: 0

摘要

目的:评价齐凡环素对脓肿分枝杆菌的体外抗菌活性。方法:采集2019 - 2024年嘉兴市某三级医院患者呼吸道分离的脓肿分枝杆菌。利用全基因组测序(WGS)对所有分离株进行种、亚型和erm 41基因多态性鉴定。采用微量肉汤稀释法检测患儿对齐那环素及13种比较药的敏感性,并评价齐那环素与7种抗菌药物的联合用药效果。结果:共收集到67株脓肿分枝杆菌,并进行全基因组测序。基因组分析鉴定出60株脓肿分枝杆菌亚种。脓肿分枝杆菌亚种7株。massiliense。其中脓肿分枝杆菌亚种。其中57株为erm41 T28基因型,其余3株为erm41 C28基因型。在我们的研究中,齐凡环素(MIC50/MIC90, 0.06/0.25 mg/L)的MIC50和MIC90分别比替加环素(MIC50/MIC90, 0.12/0.5 mg/L)低2倍,比奥马达环素(MIC50/MIC90, 0.25/0.5 mg/L)低4倍和2倍。与环丙沙星、莫西沙星、甲氧苄啶-磺胺甲恶唑、头孢西丁、强力霉素、亚胺培南和克拉霉素相比,齐万环素除阿米卡星和利奈唑外,抗菌活性显著优于环丙沙星、莫西沙星、甲氧苄啶-磺胺甲恶唑。齐凡环素与7种治疗脓肿分枝杆菌的抗菌药物联合使用无显著相互作用。结论:齐凡环素对脓肿分枝杆菌具有良好的体外抗菌活性,有可能作为脓肿分枝杆菌多药联合治疗方案的替代药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In vitro Activity of the Novel Tetracyclines Derivative, Zifanocycline Against <i>Mycobacterium abscessus</i>.

In vitro Activity of the Novel Tetracyclines Derivative, Zifanocycline Against Mycobacterium abscessus.

Objective: This study aimed to evaluate the in vitro antibacterial activity of zifanocycline against Mycobacterium abscessus.

Methods: From 2019 to 2024, Mycobacterium abscessus isolates from the respiratory tract of patients were collected at a tertiary hospital in Jiaxing City. All isolates were identified for species, subtypes, and the erm 41 gene polymorphism using whole-genome sequencing (WGS). Susceptibility to zifanocycline and 13 comparators was tested using the broth microdilution method, and the combined effects of zifanocycline and seven antibacterial drugs were evaluated.

Results: A total of 67 strains of Mycobacterium abscessus were collected and subjected to whole-genome sequencing. Genomic analysis identified 60 strains of Mycobacterium abscessus subsp. abscessus and 7 strains of Mycobacterium abscessus subsp. massiliense. Among the Mycobacterium abscessus subsp. abscessus strains, 57 exhibited the erm41 T28 genotype, whereas the remaining three showed the erm41 C28 genotype. In our study, zifanocycline (MIC50/MIC90, 0.06/0.25 mg/L) demonstrated a 2-fold lower MIC50 and MIC90 compared to tigecycline (MIC50/MIC90, 0.12/0.5 mg/L), and a 4-fold and 2-fold lower MIC50 and MIC90, respectively, compared to omadacycline (MIC50/MIC90, 0.25/0.5 mg/L). In addition to amikacin and linezolid, zifanocycline demonstrated significantly superior antibacterial activity compared with ciprofloxacin, moxifloxacin, trimethoprim-sulfamethoxazole, cefoxitin, doxycycline, imipenem, and clarithromycin. The combination of zifanocycline and the seven antibacterial drugs used for the treatment of Mycobacterium abscessus showed no significant interactions.

Conclusion: Zifanocycline exhibits positive antibacterial activity against Mycobacterium abscessus in vitro and has potential as an alternative agent in multidrug combination therapy regimens for the treatment of this pathogen.

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来源期刊
Infection and Drug Resistance
Infection and Drug Resistance Medicine-Pharmacology (medical)
CiteScore
5.60
自引率
7.70%
发文量
826
审稿时长
16 weeks
期刊介绍: About Journal Editors Peer Reviewers Articles Article Publishing Charges Aims and Scope Call For Papers ISSN: 1178-6973 Editor-in-Chief: Professor Suresh Antony An international, peer-reviewed, open access journal that focuses on the optimal treatment of infection (bacterial, fungal and viral) and the development and institution of preventative strategies to minimize the development and spread of resistance.
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