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联合粘菌素与呋喃酮 C-30 挽救革兰氏阴性菌的粘菌素耐药性 及 。

Combining Colistin with Furanone C-30 Rescues Colistin Resistance of Gram-Negative Bacteria and .

机构信息

Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical Universitygrid.414906.e, Wenzhou, China.

Department of Medical Lab Science, School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China.

出版信息

Microbiol Spectr. 2021 Dec 22;9(3):e0123121. doi: 10.1128/Spectrum.01231-21. Epub 2021 Nov 3.

Abstract

The spread of multidrug-resistant (MDR) Gram-negative bacteria (GNB) has led to serious public health problems worldwide. Colistin, as a "last resort" for the treatment of MDR bacterial infections, has been used significantly in recent years and has led to the continuous emergence of colistin-resistant strains. In this study, we aimed to investigate the synergistic effect on the antimicrobial and antibiofilm activities of a colistin/furanone C-30 combination against colistin-resistant GNB and . According to antimicrobial resistance profiles, most of the colistin-resistant strains we collected showed MDR phenotypes. The checkerboard method and time-kill curve showed that the combination with furanone C-30 increases the antibacterial activity of colistin significantly. In addition, the furanone C-30/colistin combination can not only inhibit the formation of bacterial biofilm but also has a better eradication effect on preformed mature biofilms. The result of scanning electron microscopy (SEM) demonstrated that the furanone C-30/colistin combination led to a significant reduction in the number of cells in biofilms. Furthermore, furanone C-30 at 50 μg/ml did not cause any additional toxicity to RAW264.7 cells according to a cytotoxicity assay. In infection experiments, the furanone C-30/colistin combination increased the survival rate of infected Galleria mellonella larvae as well as decreased the microbial load in a mouse thigh infection model. The synergistic effect of the furanone C-30/colistin combination against colistin-resistant GNB is encouraging, and this work may shed light on a new therapeutic approach to combat colistin-resistant pathogens. Colistin is among the few antibiotics effective against multidrug-resistant Gram-negative bacteria (GNB) clinical isolates. However, colistin-resistant GNB strains have emerged in recent years. Therefore, the combination of colistin and nonantibacterial drugs has attracted much attention. In this study, the furanone C-30/colistin combination showed good antibacterial and antibiofilm activity and . In addition, increased membrane permeability leads to the synergistic effect of the furanone C-30/colistin combination. Because of the low cytotoxicity of furanone C-30, this combination has good application prospects in clinical anti-infective therapy. This finding might shed light on the discovery of combination therapy for infections caused by colistin-resistant GNB pathogens.

摘要

多药耐药(MDR)革兰氏阴性菌(GNB)的传播已在全球范围内导致严重的公共卫生问题。多粘菌素作为治疗 MDR 细菌感染的“最后手段”,近年来被大量使用,并导致不断出现多粘菌素耐药株。在这项研究中,我们旨在研究多粘菌素/呋喃酮 C-30 联合应用对多粘菌素耐药 GNB 和 的抗菌和抗生物膜活性的协同作用。根据抗生素耐药性特征,我们收集的大多数多粘菌素耐药菌株均表现出 MDR 表型。棋盘法和时间杀伤曲线显示,呋喃酮 C-30 可显著增强多粘菌素的抗菌活性。此外,呋喃酮 C-30/多粘菌素联合用药不仅能抑制细菌生物膜的形成,而且对成熟生物膜的清除效果更好。扫描电子显微镜(SEM)的结果表明,呋喃酮 C-30/多粘菌素联合用药导致生物膜中细胞数量显著减少。此外,细胞毒性测定表明,呋喃酮 C-30 在 50μg/ml 时对 RAW264.7 细胞没有造成任何额外的毒性。在 感染实验中,呋喃酮 C-30/多粘菌素联合用药提高了感染家蚕幼虫的存活率,并降低了小鼠大腿感染模型中的微生物负荷。呋喃酮 C-30/多粘菌素联合用药对多粘菌素耐药 GNB 的协同作用令人鼓舞,这项工作可能为对抗多粘菌素耐药病原体提供新的治疗方法。多粘菌素是少数几种对多药耐药革兰氏阴性菌(GNB)临床分离株有效的抗生素之一。然而,近年来多粘菌素耐药 GNB 菌株已经出现。因此,多粘菌素与非抗菌药物的联合应用引起了广泛关注。在这项研究中,呋喃酮 C-30/多粘菌素联合用药表现出良好的抗菌和抗生物膜活性。此外,增加细胞膜通透性导致呋喃酮 C-30/多粘菌素联合用药的协同作用。由于呋喃酮 C-30 的细胞毒性低,这种联合用药在临床抗感染治疗中有很好的应用前景。这一发现可能为发现多粘菌素耐药 GNB 病原体感染的联合治疗方法提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e7e/8567244/f1f973a5c9f3/spectrum.01231-21-f001.jpg

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