耐碳青霉烯类肠杆菌科
替加环素
粘菌素
肠杆菌科
生物
质粒
阿兹屈南
碳青霉烯
微生物学
抗生素耐药性
头孢他啶/阿维巴坦
抗药性
基因
遗传学
抗生素
亚胺培南
大肠杆菌
作者
Robert F. Potter,Alaric W. D’Souza,Gautam Dantas
标识
DOI:10.1016/j.drup.2016.09.002
摘要
Carbapenems, our one-time silver bullet for multidrug resistant bacterial infections, are now threatened by widespread dissemination of carbapenem-resistant Enterobacteriaceae (CRE). Successful expansion of Enterobacteriaceae clonal groups and frequent horizontal gene transfer of carbapenemase expressing plasmids are causing increasing carbapenem resistance. Recent advances in genetic and phenotypic detection facilitate global surveillance of CRE diversity and prevalence. In particular, whole genome sequencing enabled efficient tracking, annotation, and study of genetic elements colocalized with carbapenemase genes on chromosomes and on plasmids. Improved characterization helps detail the co-occurrence of other antibiotic resistance genes in CRE isolates and helps identify pan-drug resistance mechanisms. The novel β-lactamase inhibitor, avibactam, combined with ceftazidime or aztreonam, is a promising CRE treatment compared to current colistin or tigecycline regimens. To halt increasing CRE-associated morbidity and mortality, we must continue quality, cooperative monitoring and urgently investigate novel treatments.
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