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J Antibiot (Tokyo) ; 71(4): 447-455, 2018 03.
Article in English | MEDLINE | ID: mdl-29371644

ABSTRACT

The alarming issue of antibiotic resistance expansion requires a continuous search for new and efficient antibacterial agents. Here we describe the design of new tools to screen for target-specific inhibitors of the bacterial Rho factor directly inside eukaryotic cells. Rho factor is a global regulator of gene expression which is essential to most bacteria, especially Gram-negative. Since Rho has no functional or structural homolog in eukaryotes, it constitutes a valuable and well known bacterial target as evidenced by its inhibition by the natural antibiotic, Bicyclomycin. Our screening tools are based on perturbation of mRNA processing and packaging reactions in the nucleus of eukaryotic cells by the RNA-dependent helicase/translocase activity of bacterial Rho factor leading to a growth defect phenotype. In this approach, any compound that impedes Rho activity should restore growth to yeast or human cells expressing Rho protein, providing valuable means to screen for target-specific antibacterial agents within the environment of a eukaryotic cell. The yeast tool expressing E. coli Rho factor was validated using Bicyclomycin as the control antibacterial agent. The validation of the screening tool was further extended with a stable human cell line expressing Rho factor conditionally. Finally, we show that Rho factors from different bacterial pathogens can also be designed as yeast-based screening tools which can reveal subtle variations in the functional features of the proteins.


Subject(s)
Anti-Bacterial Agents/pharmacology , Rho Factor/drug effects , Yeasts/drug effects , Bacterial Infections/microbiology , Cell Line , Cell Survival/drug effects , Drug Evaluation, Preclinical , Escherichia coli/drug effects , Escherichia coli/genetics , Gram-Negative Bacteria/drug effects , HEK293 Cells , Humans , Saccharomyces cerevisiae/drug effects , Transcription, Genetic
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