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磷霉素对浮游及生物被膜相关多重耐药性尿路致病性临床分离株的疗效。

Efficacy of Fosfomycin against Planktonic and Biofilm-Associated MDR Uropathogenic Clinical Isolates.

作者信息

Dzib-Baak Haziel Eleazar, Uc-Cachón Andrés Humberto, Dzul-Beh Angel de Jesús, Rosado-Manzano Rey Fernando, Gracida-Osorno Carlos, Molina-Salinas Gloria María

机构信息

Unidad de Investigación Médica Yucatán, Instituto Mexicano del Seguro Social, Mérida 97150, Mexico.

Unidad Médica de Alta Especialidad, Instituto Mexicano del Seguro Social, Mérida 97150, Mexico.

出版信息

Trop Med Infect Dis. 2022 Sep 8;7(9):235. doi: 10.3390/tropicalmed7090235.

Abstract

Urinary tract infections (UTI) are a severe public health problem and are caused mainly by the uropathogenic (UPEC). Antimicrobial resistance and limited development of new antimicrobials have led to the reuse of old antibiotics such as fosfomycin. The aim of this study was to evaluate the in vitro efficacy of fosfomycin on a collection of multidrug-resistant (MDR) UPEC and the degradative activity on biofilm producers. A total of 100 MDR UPEC clinical isolates were collected from patients at Mexican second- and third-level hospitals. Microorganism identification was performed using an automated system, the evaluation of the susceptibility of clinical isolates to fosfomycin was performed using the resazurin microtiter assay, and the identification of biofilm producers and the effect of fosfomycin in biofilms were evaluated using the crystal violet method. Among planktonic MDR UPEC, 93% were susceptible to fosfomycin. Eighty-three MDR UPEC were categorized as weak (39.8%), moderate (45.2%), and strong (14.5%) biofilm producers. Fosfomycin exhibited degradative activity ranging from 164.4 µg/mL to 1045 µg/mL. Weak producers required statistically lower concentrations of fosfomycin to destroy the biofilm, contrary to moderate and strong producers. In conclusion, fosfomycin could be an option for the treatment of infections caused by MDR UPEC, for which the antimicrobial treatment is more often becoming limited.

摘要

尿路感染(UTI)是一个严重的公共卫生问题,主要由尿路致病性大肠杆菌(UPEC)引起。抗菌药物耐药性以及新抗菌药物研发的局限性导致了诸如磷霉素等旧抗生素的重新使用。本研究的目的是评估磷霉素对一系列多重耐药(MDR)UPEC的体外疗效以及对生物膜形成菌的降解活性。从墨西哥二级和三级医院的患者中总共收集了100株MDR UPEC临床分离株。使用自动化系统进行微生物鉴定,使用刃天青微量滴定法评估临床分离株对磷霉素的敏感性,并使用结晶紫法评估生物膜形成菌的鉴定以及磷霉素在生物膜中的作用。在浮游的MDR UPEC中,93%对磷霉素敏感。83株MDR UPEC被分类为弱(39.8%)、中度(45.2%)和强(14.5%)生物膜形成菌。磷霉素表现出的降解活性范围为164.4 µg/mL至1045 µg/mL。与中度和强生物膜形成菌相反,弱生物膜形成菌破坏生物膜所需的磷霉素浓度在统计学上较低。总之,对于抗菌治疗往往越来越受限的MDR UPEC引起的感染,磷霉素可能是一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c1f/9505523/2bcc1bd96ba7/tropicalmed-07-00235-g001.jpg

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