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经直肠前列腺活检男性的直肠拭子分离出的肠杆菌科中氟喹诺酮耐药的分子机制:靶向预防的原理。

The molecular mechanisms of fluoroquinolone resistance found in rectal swab isolates of Enterobacterales from men undergoing a transrectal prostate biopsy: the rationale for targeted prophylaxis.

机构信息

Department of Bacteriology, National Institute of Public Health NIH - National Research Institute, Chocimska 24, 00-791, Warsaw, Poland.

Department of Urology, St. Anna Hospital, A. Mickiewicza 39, 05-500, Piaseczno, Poland.

出版信息

Ann Clin Microbiol Antimicrob. 2021 Dec 7;20(1):81. doi: 10.1186/s12941-021-00487-y.

Abstract

BACKGROUND

Transrectal ultrasound-guided prostate biopsy (TRUS-Bx) is considered an essential urological procedure for the histological diagnosis of prostate cancer. It is, however, considered a "contaminated" procedure which may lead to infectious complications. Recent studies suggest a significant share of fluoroquinolone-resistant rectal flora in post-biopsy infections.

METHODS

The molecular mechanisms of fluoroquinolone resistance, including PMQR (plasmid-mediated quinolone resistance) as well as mutation in the QRDRs (quinolone-resistance determining regions) of gyrA, gyrB, parC and parE, among Enterobacterales isolated from 32 of 48 men undergoing a prostate biopsy between November 2015 and April 2016 were investigated. Before the TRUS-Bx procedure, all the patients received an oral antibiotic containing fluoroquinolones.

RESULTS

In total, 41 Enterobacterales isolates were obtained from rectal swabs. The MIC of ciprofloxacin and the presence of common PMQR determinants were investigated in all the isolates. Nine (21.9%) isolates carried PMQR with qnrS as the only PMQR agent detected. DNA sequencing of the QRDRs in 18 Enterobacterales (E. coli n = 17 and E. cloacae n = 1) isolates with ciprofloxacin MIC ≥ 0.25 mg/l were performed. Substitutions in the following codons were found: GyrA-83 [Ser → Leu, Phe] and 87 [Asp → Asn]; GyrB codon-605 [Met → Leu], ParC codons-80 [Ser → Ile, Arg] and 84 [Glu → Gly, Met, Val, Lys], ParE codons-458 [Ser → Ala], 461 [Glu → Ala] and 512 [Ala → Thr]. Six isolates with ciprofloxacin MIC ≥ 2 mg/l had at least one mutation in GyrA together with qnrS.

CONCLUSIONS

This study provides information on the common presence of PMQRs among Enterobacterales isolates with ciprofloxacin MIC ≥ 0.25 mg/l, obtained from men undergoing TRUS-Bx. This fact may partially explain why some men develop post-TRUS-Bx infections despite ciprofloxacin prophylaxis.

摘要

背景

经直肠超声引导前列腺活检(TRUS-Bx)被认为是前列腺癌组织学诊断的重要泌尿外科程序。然而,它被认为是一种“污染”程序,可能导致感染并发症。最近的研究表明,在活检后感染中,肠杆菌科的氟喹诺酮耐药直肠菌群有很大一部分。

方法

本研究调查了 2015 年 11 月至 2016 年 4 月期间接受前列腺活检的 48 名男性中的 32 名男性的 32 名男性的分子机制,包括 PMQR(质粒介导的喹诺酮耐药)以及 gyrA、gyrB、parC 和 parE 的 QRDRs(喹诺酮耐药决定区)中的突变。在 TRUS-Bx 程序之前,所有患者都接受了含有氟喹诺酮的口服抗生素。

结果

共从直肠拭子中获得 41 株肠杆菌科分离株。对所有分离株进行了环丙沙星 MIC 和常见 PMQR 决定因素的检测。9 株(21.9%)分离株携带 PMQR,仅检测到 qnrS 为唯一的 PMQR 因子。对 18 株肠杆菌科(大肠杆菌 n = 17 和阴沟肠杆菌 n = 1)分离株的 QRDRs 进行了 DNA 测序,这些分离株的环丙沙星 MIC≥0.25mg/l。在以下密码子中发现了取代:GyrA-83 [Ser→Leu,Phe] 和 87 [Asp→Asn];GyrB 密码子-605 [Met→Leu]、ParC 密码子-80 [Ser→Ile、Arg] 和 84 [Glu→Gly、Met、Val、Lys]、ParE 密码子-458 [Ser→Ala]、461 [Glu→Ala] 和 512 [Ala→Thr]。6 株环丙沙星 MIC≥2mg/l 的分离株至少在 GyrA 中带有一个突变,同时带有 qnrS。

结论

本研究提供了有关接受 TRUS-Bx 男性的环丙沙星 MIC≥0.25mg/l 的肠杆菌科分离株中常见 PMQRs 的信息。这一事实可能部分解释了为什么一些男性在接受 TRUS-Bx 后会出现感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c2/8650336/0a958b90b820/12941_2021_487_Fig1_HTML.jpg

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