临床药物治疗杂志2024,Vol.22Issue(7) :1-5.DOI:10.3969/j.issn.1672-3384.2024.07.001

耐碳青霉烯类大肠埃希菌对替加环素的耐药机制及治疗

The resistance mechanism of carbapenem-resistant Escherichia coli to tigecycline and therapies

李娟
临床药物治疗杂志2024,Vol.22Issue(7) :1-5.DOI:10.3969/j.issn.1672-3384.2024.07.001

耐碳青霉烯类大肠埃希菌对替加环素的耐药机制及治疗

The resistance mechanism of carbapenem-resistant Escherichia coli to tigecycline and therapies

李娟1
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作者信息

  • 1. 合肥市第二人民医院 药学部,安徽 合肥,230011
  • 折叠

摘要

大肠埃希菌是一种常见的共生菌和致病菌,作为肠道和尿路感染及败血症的主要致病菌,给全球的医疗卫生系统带来了巨大的负担.近年来,由于临床上抗菌药物的滥用,导致耐碳青霉烯类大肠埃希菌(CREO)产生,对临床治疗是一个严峻挑战.替加环素是治疗CREO的一线用药之一,但CREO可对替加环素产生耐药性.CREO对替加环素的耐药机制包括外排泵过表达、质粒介导的耐药基因、脂多糖核心生物合成途径基因突变等.本文综述了CREO对替加环素的耐药机制,探讨对耐替加环素CERO的治疗.

Abstract

Escherichia coli is a common commensal and pathogenic bacterium in the human microflora.As a major causative agent of enteric,septicemia,and urinary tract infections,Escherichia coli poses a huge burden on healthcare systems worldwide.In recent years,the misuse of antimicrobial agents in clinical practice has led to the emergence of carbapenem-resistant Escherichia coli(CREO),posing a serious challenge to clinical treatment.Tigecycline is considered to be one of the first-line therapies for the treatment of CREO.However,CREO can become resistant to tigecycline.The mechanisms of resistance in CREO to tigecycline include overexpression of efflux pumps,plasmid-mediated resistance genes,and gene mutations in the lipopolysaccharide core biosynthesis path way.This article reviews the resistance mechanism of CREO and explores the current alternative therapies for tigecycline-resistant CERO.

关键词

大肠埃希菌/替加环素/耐药性/耐药机制/治疗

Key words

Escherichia coli/tigecycline/drug resistance/resistance mechanisms/treatment

引用本文复制引用

出版年

2024
临床药物治疗杂志
北京药学会

临床药物治疗杂志

CSTPCD
影响因子:1.07
ISSN:1672-3384
参考文献量3
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