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检测整合子接合元件中 bla 基因在引起尿道炎的 4 株广泛耐药流感嗜血杆菌中的存在。

Detection of bla in an integrative and conjugative element in four extensively drug-resistant Haemophilus parainfluenzae strains causing urethritis.

机构信息

Microbiology Department, Hospital Universitari de Bellvitge, IDIBELL-UB, Barcelona, Spain.

Microbiology Department, Hospital Universitari de Bellvitge, IDIBELL-UB, Barcelona, Spain; Research Network for Respiratory Diseases (CIBERES), ISCIII, Madrid, Spain.

出版信息

Int J Antimicrob Agents. 2023 Nov;62(5):106991. doi: 10.1016/j.ijantimicag.2023.106991. Epub 2023 Sep 28.

Abstract

Haemophilus parainfluenzae is a commensal organism with rising numbers of multidrug-resistant (MDR) strains. This pathogen is of increasing clinical relevance in urogenital infection. The aim of this work was to identify and characterise the molecular mechanisms of resistance associated with four cephalosporin-resistant H. parainfluenzae strains collected from patients with urethritis. Antimicrobial resistance was determined by microdilution following European Committee on Antimicrobial Susceptibility Testing criteria. Strains were then analysed by whole-genome sequencing to determine clonal relationship and the molecular basis of antimicrobial resistance. Finally, a phylogenetic analysis was performed on all urogenital MDR strains of H. parainfluenzae previously isolated in our hospital. All strains were resistant to β-lactams, macrolides, tetracycline, fluoroquinolones, chloramphenicol, cotrimoxazole, and aminoglycosides. The resistance profile was compatible with the presence of an extended-spectrum β-lactamase (ESBL). Whole-genome sequencing detected bla that conferred high minimum inhibitory concentrations to cephalosporins in two novel integrative and conjugative elements (ICEHpaHUB6 and ICEHpaHUB7) that also harboured a bla β-lactamase. This study shows a novel bla ESBL carried in an integrative conjugative element in four extensively drug-resistant H. parainfluenzae strains. This resistance determinant could be transmitted to other sexually transmitted pathogens and this is a cause for concern.

摘要

副流感嗜血杆菌是一种共生菌,其具有越来越多的多药耐药(MDR)菌株。这种病原体在泌尿生殖道感染中的临床相关性日益增加。这项工作的目的是鉴定和描述与从尿道炎患者中分离的四株头孢菌素耐药副流感嗜血杆菌菌株相关的耐药分子机制。采用微量稀释法按照欧洲抗菌药物敏感性试验委员会标准确定抗菌药物耐药性。然后通过全基因组测序分析来确定克隆关系和抗菌药物耐药的分子基础。最后,对我院以前分离的所有泌尿生殖道 MDR 副流感嗜血杆菌菌株进行了系统发育分析。所有菌株均对β-内酰胺类、大环内酯类、四环素类、氟喹诺酮类、氯霉素、复方磺胺甲噁唑和氨基糖苷类药物耐药。耐药谱与存在扩展谱β-内酰胺酶(ESBL)相符。全基因组测序在两个新的整合和共轭元件(ICEHpaHUB6 和 ICEHpaHUB7)中检测到bla,该元件赋予头孢菌素高最小抑菌浓度,该元件还携带 blaβ-内酰胺酶。这项研究显示了四个广泛耐药的副流感嗜血杆菌菌株中新型 bla ESBL 携带在整合共轭元件中。这种耐药决定因素可能会传播给其他性传播病原体,这令人担忧。

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