ABSTRACT mazEF is a toxin-antitoxin module located on chromosomes of most bacteria. MazF toxins are endoribonucleases antagonized by MazE antitoxins. Previously, we characterized several quorum sensing peptides called " e xtracellular d eath f actors" (EDFs). When secreted from bacterial cultures, EDFs induce interspecies cell death. EDFs also enhance the endoribonucleolytic activity of Escherichia coli MazF. Mycobacterium tuberculosis carries several mazEF modules. Among them, the endoribonucleolytic activities of MazF proteins mt-1, mt-3, and mt-6 were identified. MazF-mt6 and MazF-mt-3 cleave M.?tuberculosis rRNAs. Here we report the in vitro effects of EDFs on the endoribonucleolytic activities of M.?tuberculosis MazFs. Escherichia coli EDF ( Ec EDF) and the three Pseudomonas aeruginosa EDFs ( Pa EDFs) individually enhance the endoribonucleolytic activities of MazF-mt6 and MazF-mt3 and overcome the inhibitory effect of MazE-mt3 or MazE-mt6 on the endoribonucleolytic activities of the respective toxins. We propose that these EDFs can serve as a basis for a novel class of antibiotics against M.?tuberculosis . IMPORTANCE Mycobacterium tuberculosis is one of the leading causes of death from infectious disease. M.?tuberculosis is highly drug resistant, and drug delivery to the infected site is very difficult. In previous studies, we showed that e xtracellular d eath f actors (EDFs) can work as quorum sensing molecules which participate in interspecies bacterial cell death. In this study, we demonstrated the role of different EDFs in the endoribonucleolytic activities of M.?tuberculosis MazFs. Escherichia coli EDF ( Ec EDF) and the three Pseudomonas aeruginosa EDFs ( Pa EDFs) individually enhance the endoribonucleolytic activities of MazF-mt6 and MazF-mt3. The current report provides a basis for the use of the EDF peptides Ec EDF and Pa EDF as novel antibiotics against M.?tuberculosis .
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