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维罗霉素恢复多药耐药革兰氏阴性病原体对抗粘菌素的敏感性。

Valnemulin restores colistin sensitivity against multidrug-resistant gram-negative pathogens.

机构信息

Department of Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, China.

Institute for Brain Science and Disease, Chongqing Medical University, Chongqing, China.

出版信息

Commun Biol. 2024 Sep 12;7(1):1122. doi: 10.1038/s42003-024-06805-2.

Abstract

Colistin is one of the last-resort antibiotics in treating infections caused by multidrug-resistant (MDR) pathogens. Unfortunately, the emergence of colistin-resistant gram-negative strains limit its clinical application. Here, we identify an FDA-approved drug, valnemulin (Val), exhibit a synergistic effect with colistin in eradicating both colistin-resistant and colistin-susceptible gram-negative pathogens both in vitro and in the mouse infection model. Furthermore, Val acts synergistically with colistin in eliminating intracellular bacteria in vitro. Functional studies and transcriptional analysis confirm that the combinational use of Val and colistin could cause membrane permeabilization, proton motive force dissipation, reduction in intracellular ATP level, and suppression in bacterial motility, which result in bacterial membrane disruption and finally cell death. Our findings reveal the potential of Val as a colistin adjuvant to combat MDR bacterial pathogens and treat recalcitrant infections.

摘要

黏菌素是治疗多重耐药(MDR)病原体感染的最后手段之一。不幸的是,黏菌素耐药革兰氏阴性菌株的出现限制了其临床应用。在这里,我们发现一种已获得 FDA 批准的药物,沃尼妙林(Val),在体外和小鼠感染模型中,与黏菌素联合使用具有协同作用,可根除黏菌素耐药和敏感的革兰氏阴性病原体。此外,Val 与黏菌素在体外协同作用以消除细胞内细菌。功能研究和转录分析证实,Val 和黏菌素的联合使用可导致膜通透性增加、质子动力势耗散、细胞内 ATP 水平降低以及细菌运动能力下降,从而导致细菌膜破裂,最终导致细胞死亡。我们的研究结果表明,Val 有潜力作为黏菌素佐剂,用于对抗 MDR 细菌病原体和治疗难治性感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c925/11390741/e837fa97e034/42003_2024_6805_Fig1_HTML.jpg

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