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大肠杆菌 ACRB 中近端结合口袋 Arg717 取代导致临床相关耐药谱差异。

Proximal Binding Pocket Arg717 Substitutions in Escherichia coli AcrB Cause Clinically Relevant Divergencies in Resistance Profiles.

机构信息

SANKEN (The Institute of Scientific and Industrial Research), Osaka Universitygrid.136593.b, Ibaraki, Osaka, Japan.

Graduate School of Pharmaceutical Sciences, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.

出版信息

Antimicrob Agents Chemother. 2022 Apr 19;66(4):e0239221. doi: 10.1128/aac.02392-21. Epub 2022 Mar 21.

Abstract

Recent mutations in RND efflux pumps in clinical strains have further increased multidrug resistance. We show that R717L and R717Q substitutions (found in azithromycin-resistant Salmonella enterica spp.) in the Escherichia coli efflux pump AcrB dramatically increase macrolide, as well as fluoroquinolone, resistance. On the other hand, cells became more susceptible to novobiocin and β-lactam cloxacillin. We urge the control of, and adjustments to, treatments with antibiotics and the need for novel antibiotics and efflux pump inhibitors.

摘要

近年来,临床分离株中 RND 外排泵的突变进一步增加了多重耐药性。我们发现,大肠杆菌外排泵 AcrB 中的 R717L 和 R717Q 取代(在耐阿奇霉素的沙门氏菌属中发现)可显著增加大环内酯类和氟喹诺酮类药物的耐药性。另一方面,细胞对新生霉素和β-内酰胺类药物氯唑西林的敏感性增加。我们敦促控制和调整抗生素的治疗方法,并需要新型抗生素和外排泵抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f1c/9017336/da9dc78cbb50/aac.02392-21-f001.jpg

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