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产CTX-M-15 型酶大肠埃希菌在使用匹美西林治疗过程中发生 CTX-M-127 型突变,导致对美西林耐药。

Mutational change of CTX-M-15 to CTX-M-127 resulting in mecillinam resistant Escherichia coli during pivmecillinam treatment of a patient.

机构信息

Department of Clinical Microbiology, Rigshospitalet, Copenhagen, Denmark.

Department of Clinical Microbiology, Hvidovre Hospital, Hvidovre, Denmark.

出版信息

Microbiologyopen. 2019 Dec;8(12):e941. doi: 10.1002/mbo3.941. Epub 2019 Oct 1.

Abstract

Pivmecillinam (amdinocillin pivoxil) is the recommended first-choice antibiotic used to treat urinary tract infections (UTIs) in Denmark. The frequency of mutation to mecillinam (MEC) resistance is described as high in vitro; however, treatment of UTI has a good clinical response and prevalence of mecillinam resistance in Escherichia coli remains low despite many years of use. We describe occurrence of in vivo mecillinam resistance in a clinical isolate of ESBL-producing E. coli following pivmecillinam treatment. The identified phenotypic differences in the mecillinam resistant isolate compared with the original mecillinam susceptible isolate were a full-length LPS with O-antigen (O25), mecillinam resistance and a lower MIC for ceftazidime. Regarding genotype, the resistant isolate differed with a mutation in bla to bla , loss of a part of a plasmid and a genomic island, respectively, and insertion of a transposase in wbbL, causing the rough phenotype. The observed mecillinam resistance is expected to be caused by the mutation in bla with additional contribute from the serotype shift. We continue to recommend the use of pivmecillinam as first-line treatment for UTI.

摘要

匹美西林(氨丁卡西林匹肟)是丹麦推荐用于治疗尿路感染(UTI)的首选抗生素。体外研究表明,其对美西林(MEC)耐药性的突变频率很高;然而,尽管使用多年,治疗 UTI 仍具有良好的临床疗效,且大肠埃希菌对美西林的耐药率仍然较低。我们描述了在 ESBL 产生大肠埃希菌的临床分离株中,在使用匹美西林治疗后出现的体内美西林耐药性。与原始美西林敏感分离株相比,耐美西林分离株的表型差异为具有完整 O 抗原(O25)的全长 LPS、美西林耐药性和头孢他啶 MIC 值降低。就基因型而言,耐药分离株在 bla 中发生突变,导致 bla ,部分质粒和基因组岛丢失,以及 wbbL 中的转座酶插入,导致粗糙表型。观察到的美西林耐药性预计是由 bla 中的突变引起的,同时还与血清型转变有关。我们继续推荐将匹美西林作为 UTI 的一线治疗药物。

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