期刊论文详细信息
BMC Molecular and Cell Biology
MazEF-rifampicin interaction suggests a mechanism for rifampicin induced inhibition of persisters
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Alexander, Cyrus1  Guru, Ankeeta1  Pradhan, Pinkilata1  Mallick, Sunanda1  Mahanandia, Nimai Charan4  Subudhi, Bharat Bhusan5  Beuria, Tushar Kant1 
[1] Institute of Life Sciences;Manipal Academy of Higher Education;Regional Centre for Biotechnology;Animal Biotechnology Centre, National Dairy Research Institute;Drug Development and Analysis, School of Pharmaceutical Sciences, Siksha ‘O’ Anusandhan Deemed to be University
关键词: TA system;    MazEF;    Rifampicin;    Bacterial persistence;   
DOI  :  10.1186/s12860-020-00316-8
学科分类:内科医学
来源: Colegio Oficial de Psicologos
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【 摘 要 】

Persistence is a natural phenomenon whereby a subset of a population of isogenic bacteria either grow slow or become dormant conferring them with the ability to withstand various stresses including antibiotics. In a clinical setting bacterial persistence often leads to the recalcitrance of various infections increasing the treatment time and cost. Additionally, some studies also indicate that persistence can also pave way for the emergence of resistant strains. In a laboratory setting this persistent phenotype is enriched in nutritionally deprived environments. Consequently, in a batch culture the late stationary phase is enriched with persistent bacteria. The mechanism of persister cell formation and its regulation is not well understood. Toxin-antitoxin (TA) systems have been implicated to be responsible for bacterial persistence and rifampicin is used to treat highly persistent bacterial strains. The current study tries to explore a possible interaction between rifampicin and the MazEF TA system that furthers the former’s success rate in treating persistent bacteria. In the current study we found that the population of bacteria in the death phase of a batch culture consists of metabolically inactive live cells resembling persisters, which showed higher membrane depolarization as compared to the log phase bacteria. We also observed an increase in the expression of the MazEF TA modules in this phase. Since rifampicin is used to kill the persisters, we assessed the interaction of rifampicin with MazEF complex. We showed that rifampicin moderately interacts with MazEF complex with 1:1 stoichiometry. Our study suggests that the interaction of rifampicin with MazEF complex might play an important role in inhibition of persisters.

【 授权许可】

CC BY|CC0   

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