ID | 65100 |
フルテキストURL | |
著者 |
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
|
抄録 | 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.
|
キーワード | antimicrobial resistance
Escherichia coli
urinary tract infections
flomoxef
ST131
|
発行日 | 2023-03-06
|
出版物タイトル |
Antibiotics
|
巻 | 12巻
|
号 | 3号
|
出版者 | MDPI
|
開始ページ | 522
|
ISSN | 2079-6382
|
資料タイプ |
学術雑誌論文
|
言語 |
英語
|
OAI-PMH Set |
岡山大学
|
著作権者 | © 2023 by the authors.
|
論文のバージョン | publisher
|
PubMed ID | |
DOI | |
Web of Science KeyUT | |
関連URL | isVersionOf https://doi.org/10.3390/antibiotics12030522
|
ライセンス | 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
|