粘菌素
肺炎克雷伯菌
多粘菌素
生物
微生物学
耐碳青霉烯类肠杆菌科
抗生素耐药性
抗生素
替加环素
肠杆菌科
碳青霉烯
多重耐药
基因
遗传学
大肠杆菌
作者
Jenna M. Kuhn,Y. Peter Di
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2023-01-12
卷期号:15 (1): 270-270
被引量:4
标识
DOI:10.3390/pharmaceutics15010270
摘要
The emergence and dissemination of carbapenem-resistant Klebsiella pneumoniae (KP), one of the carbapenem-resistant Enterobacteriaceae (CRE), is now an emerging cause of antibiotic-resistant nosocomial infections associated with high rates of morbidity and mortality. Colistin, or polymyxin E, is a last-resort peptide antibiotic used to treat multidrug-resistant (MDR) Gram-negative bacterial infections including KP. Unfortunately, resistance to colistin is rising with increasing use in the clinical setting. Although clinical evidence links certain mutations to colistin resistance (COL-R) in KP, the origination and association of the mutations remain unclear. We hypothesize that the timing of COL-R mutations influences the development and progression of KP resistance to colistin. We performed planktonic and biofilm in vitro experimental evolutions of KP strain ATCC 43816 under increasing colistin concentrations to characterize the temporal regulation of critical COL-R mutations throughout COL-R progression. The resistance generation and mutation profiles of independently evolved bacterial populations with different lifestyles were compared. Genes with various functions theorize the timeline in which key mutations are generated and their roles in the progression of COL-R. Our results aim to advance the research and development of effective therapeutics to treat MDR bacterial infection as the dissemination of CRE continues to be a severe public health threat.
科研通智能强力驱动
Strongly Powered by AbleSci AI