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ID 65100
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Sakaeda, Kazuma Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Sadahira, Takuya Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
Maruyama, Yuki Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Iwata, Takehiro Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Kaken ID
Watanabe, Masami Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Kaken ID publons researchmap
Wada, Koichiro Koichiro Wada Department of Urology, School of Medicine, Shimane University ORCID researchmap
Araki, Motoo Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID publons researchmap
Abstract
We carried out a molecular biological analysis of extended-spectrum beta-lactamase (ESBL)-producing E. coli strains and their sensitivity to flomoxef (FMOX). Sequence type (ST) analysis by multilocus sequence typing (MLST) and classification of ESBL genotypes by multiplex PCR were performed on ESBL-producing E. coli strains isolated from urine samples collected from patients treated at our institution between 2008 and 2018. These sequences were compared with results for antimicrobial drug susceptibility determined using a micro-liquid dilution method. We also analyzed cases treated with FMOX at our institution to examine its clinical efficacy. Of the 911 E. coli strains identified, 158 (17.3%) were ESBL-producing. Of these, 67.7% (107/158) were strain ST-131 in ST analysis. Nearly all (154/158; 97.5%) were CTX-M genotypes, with M-14 and M-27 predominating. The isolated strains were sensitive to FMOX in drug susceptibility tests. Among the patient samples, 33 cases received FMOX, and of these, 5 had ESBL-producing E. coli. Among these five cases, three received FMOX for surgical prophylaxis as urinary carriers of ESBL-producing E. coli, and postoperative infections were prevented in all three patients. The other two patients received FMOX treatment for urinary tract infections. FMOX treatment was successful for one, and the other was switched to carbapenem. Our results suggest that FMOX has efficacy for perioperative prophylactic administration in urologic surgery involving carriers of ESBL-producing bacteria and for therapeutic administration for urinary tract infections. Use of FMOX avoids over-reliance on carbapenems or beta-lactamase inhibitors and thus is an effective antimicrobial countermeasure.
Keywords
antimicrobial resistance
Escherichia coli
urinary tract infections
flomoxef
ST131
Published Date
2023-03-06
Publication Title
Antibiotics
Volume
volume12
Issue
issue3
Publisher
MDPI
Start Page
522
ISSN
2079-6382
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2023 by the authors.
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Related Url
isVersionOf https://doi.org/10.3390/antibiotics12030522
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https://creativecommons.org/licenses/by/4.0/
Citation
Sakaeda, K.; Sadahira, T.; Maruyama, Y.; Iwata, T.;Watanabe, M.;Wada, K.; Araki, M. The Genotypic and Phenotypic Characteristics Contributing to Flomoxef Sensitivity in Clinical Isolates of ESBL-Producing E. coli Strains from Urinary Tract Infections. Antibiotics 2023, 12, 522. https://doi.org/10.3390/antibiotics12030522