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Future Microbiol ; 12: 867-879, 2017 08.
Article in English | MEDLINE | ID: mdl-28686056

ABSTRACT

AIM: We investigated a proteome profile, protein-protein interaction and morphological changes of Mycobacterium tuberculosis after different times of eupomatenoid-5 (EUP-5) induction to evaluate the cellular response to the drug-induced damages. METHODS: The bacillus was induced to sub-minimal inhibitory concentration of EUP-5 at 12 h, 24 h and 48 h. The proteins were separated by 2D gel electrophoresis, identified by LC/MS-MS. Scanning electron microscopy and Search Tool for the Retrieval of Interacting Genes/Proteins analyses were performed. RESULTS: EUP-5 impacts mainly in M. tuberculosis proteins of intermediary metabolism and interactome suggests a multisite disturbance that contributes to bacilli death. Scanning electron microscopy revealed the loss of bacillary form. CONCLUSION: Some of the differentially expressed proteins have the potential to be drug targets such as citrate synthase (Rv0896), phosphoglycerate kinase (Rv1437), ketol-acid reductoisomerase (Rv3001c) and ATP synthase alpha chain (Rv1308).


Subject(s)
Benzofurans/pharmacology , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/metabolism , Phenols/pharmacology , Proteomics , Bacterial Proteins/drug effects , Bacterial Proteins/metabolism , Benzofurans/chemistry , Citrate (si)-Synthase/drug effects , Electrophoresis, Gel, Two-Dimensional , Genes, Bacterial/drug effects , Humans , Ketol-Acid Reductoisomerase/drug effects , Microbial Sensitivity Tests , Microscopy, Electron, Scanning , Mycobacterium tuberculosis/cytology , Mycobacterium tuberculosis/enzymology , Phenols/chemistry , Phosphoglycerate Kinase/drug effects , Protein Interaction Domains and Motifs , Proteome/analysis , Tandem Mass Spectrometry , Time Factors , Tuberculosis/drug therapy , Tuberculosis/microbiology
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