主要促进者超家族
流出
支原体
溴化乙锭
结核分枝杆菌
微生物学
泰特
生物
氯霉素
抑制因子
多重耐药
电泳迁移率测定
抗药性
转录因子
突变体
抗生素
肺结核
基因
遗传学
DNA
医学
病理
作者
Xue Li,Ping Li,Cao Ruan,Long xiang Xie,Yinzhong Gu,Li Jiang,Qin Yi,Xi Lv,Jianping Xie
标识
DOI:10.1016/j.abb.2019.04.010
摘要
Development of extensively drug resistant (XDR) strains and multidrug resistant (MDR) in Mycobacterium tuberculosis is caused by an efflux mechanism of antibiotics in the bacteria. Rv0191, predicted to a major facilitator superfamily transporter of efflux pump, contributes to elevated expression in some clinical isolates. To characterize the role of Rv0191 which might be involved in antibiotics resistance, Mycobacterium smegmatis was taken as a type strains to do drug susceptibility, ethidium bromide (EB) accumulation assay and electrophoretic mobility shift assay. M. smegmatis Ms0232 mutant became more susceptible to chloramphenicol and showed different cell surface properties. Rv1353c, a TetR family transcription factor, can downregulate the transcription of Rv0191. Rv1353c overexpression strain became more sensitive to chloramphenicol. Together, these findings indicate that Rv1353c encodes a transcriptional repressor that directly interacts with the Rv0191 promoter and modulates the expression of Rv0191. This provided a new player in mycobacteria chloramphenicol resistance.
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