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Quorum Sensing Extracellular Death Peptides Enhance the Endoribonucleolytic Activities of Mycobacterium tuberculosis MazF Toxins
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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
.
Title: Quorum Sensing Extracellular Death Peptides Enhance the Endoribonucleolytic Activities of
Mycobacterium tuberculosis
MazF Toxins
Description:
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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