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Fic Proteins of Campylobacter fetus subsp. venerealis Form a Network of Functional Toxin–Antitoxin Systems

Enzymes containing the FIC (filamentation induced by cyclic AMP) domain catalyze post-translational modifications of target proteins. In bacteria the activity of some Fic proteins resembles classical toxin–antitoxin (TA) systems. An excess of toxin over neutralizing antitoxin can enable bacteria to...

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Autores principales: Sprenger, Hanna, Kienesberger, Sabine, Pertschy, Brigitte, Pöltl, Lisa, Konrad, Bettina, Bhutada, Priya, Vorkapic, Dina, Atzmüller, Denise, Feist, Florian, Högenauer, Christoph, Gorkiewicz, Gregor, Zechner, Ellen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651007/
https://www.ncbi.nlm.nih.gov/pubmed/29089929
http://dx.doi.org/10.3389/fmicb.2017.01965
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author Sprenger, Hanna
Kienesberger, Sabine
Pertschy, Brigitte
Pöltl, Lisa
Konrad, Bettina
Bhutada, Priya
Vorkapic, Dina
Atzmüller, Denise
Feist, Florian
Högenauer, Christoph
Gorkiewicz, Gregor
Zechner, Ellen L.
author_facet Sprenger, Hanna
Kienesberger, Sabine
Pertschy, Brigitte
Pöltl, Lisa
Konrad, Bettina
Bhutada, Priya
Vorkapic, Dina
Atzmüller, Denise
Feist, Florian
Högenauer, Christoph
Gorkiewicz, Gregor
Zechner, Ellen L.
author_sort Sprenger, Hanna
collection PubMed
description Enzymes containing the FIC (filamentation induced by cyclic AMP) domain catalyze post-translational modifications of target proteins. In bacteria the activity of some Fic proteins resembles classical toxin–antitoxin (TA) systems. An excess of toxin over neutralizing antitoxin can enable bacteria to survive some stress conditions by slowing metabolic processes and promoting dormancy. The cell can return to normal growth when sufficient antitoxin is present to block toxin activity. Fic genes of the human and animal pathogen Campylobacter fetus are significantly associated with just one subspecies, which is specifically adapted to the urogenital tract. Here, we demonstrate that the fic genes of virulent isolate C. fetus subsp. venerealis 84-112 form multiple TA systems. Expression of the toxins in Escherichia coli caused filamentation and growth inhibition phenotypes reversible by concomitant antitoxin expression. Key active site residues involved in adenylylation by Fic proteins are conserved in Fic1, Fic3 and Fic4, but degenerated in Fic2. We show that both Fic3 and the non-canonical Fic2 disrupt assembly and function of E. coli ribosomes when expressed independently of a trans-acting antitoxin. Toxicity of the Fic proteins is controlled by different mechanisms. The first involves intramolecular regulation by an inhibitory helix typical for Fic proteins. The second is an unusual neutralization by heterologous Fic–Fic protein interactions. Moreover, a small interacting antitoxin called Fic inhibitory protein 3, which appears unrelated to known Fic antitoxins, has the novel capacity to bind and neutralize Fic toxins encoded in cis and at distant sites. These findings reveal a remarkable system of functional crosstalk occurring between Fic proteins expressed from chromosomal and extrachromosomal modules. Conservation of fic genes in other bacteria that either inhabit or establish pathology in the urogenital tract of humans and animals underscores the significance of these factors for niche-specific adaptation and virulence.
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spelling pubmed-56510072017-10-31 Fic Proteins of Campylobacter fetus subsp. venerealis Form a Network of Functional Toxin–Antitoxin Systems Sprenger, Hanna Kienesberger, Sabine Pertschy, Brigitte Pöltl, Lisa Konrad, Bettina Bhutada, Priya Vorkapic, Dina Atzmüller, Denise Feist, Florian Högenauer, Christoph Gorkiewicz, Gregor Zechner, Ellen L. Front Microbiol Microbiology Enzymes containing the FIC (filamentation induced by cyclic AMP) domain catalyze post-translational modifications of target proteins. In bacteria the activity of some Fic proteins resembles classical toxin–antitoxin (TA) systems. An excess of toxin over neutralizing antitoxin can enable bacteria to survive some stress conditions by slowing metabolic processes and promoting dormancy. The cell can return to normal growth when sufficient antitoxin is present to block toxin activity. Fic genes of the human and animal pathogen Campylobacter fetus are significantly associated with just one subspecies, which is specifically adapted to the urogenital tract. Here, we demonstrate that the fic genes of virulent isolate C. fetus subsp. venerealis 84-112 form multiple TA systems. Expression of the toxins in Escherichia coli caused filamentation and growth inhibition phenotypes reversible by concomitant antitoxin expression. Key active site residues involved in adenylylation by Fic proteins are conserved in Fic1, Fic3 and Fic4, but degenerated in Fic2. We show that both Fic3 and the non-canonical Fic2 disrupt assembly and function of E. coli ribosomes when expressed independently of a trans-acting antitoxin. Toxicity of the Fic proteins is controlled by different mechanisms. The first involves intramolecular regulation by an inhibitory helix typical for Fic proteins. The second is an unusual neutralization by heterologous Fic–Fic protein interactions. Moreover, a small interacting antitoxin called Fic inhibitory protein 3, which appears unrelated to known Fic antitoxins, has the novel capacity to bind and neutralize Fic toxins encoded in cis and at distant sites. These findings reveal a remarkable system of functional crosstalk occurring between Fic proteins expressed from chromosomal and extrachromosomal modules. Conservation of fic genes in other bacteria that either inhabit or establish pathology in the urogenital tract of humans and animals underscores the significance of these factors for niche-specific adaptation and virulence. Frontiers Media S.A. 2017-10-17 /pmc/articles/PMC5651007/ /pubmed/29089929 http://dx.doi.org/10.3389/fmicb.2017.01965 Text en Copyright © 2017 Sprenger, Kienesberger, Pertschy, Pöltl, Konrad, Bhutada, Vorkapic, Atzmüller, Feist, Högenauer, Gorkiewicz and Zechner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Sprenger, Hanna
Kienesberger, Sabine
Pertschy, Brigitte
Pöltl, Lisa
Konrad, Bettina
Bhutada, Priya
Vorkapic, Dina
Atzmüller, Denise
Feist, Florian
Högenauer, Christoph
Gorkiewicz, Gregor
Zechner, Ellen L.
Fic Proteins of Campylobacter fetus subsp. venerealis Form a Network of Functional Toxin–Antitoxin Systems
title Fic Proteins of Campylobacter fetus subsp. venerealis Form a Network of Functional Toxin–Antitoxin Systems
title_full Fic Proteins of Campylobacter fetus subsp. venerealis Form a Network of Functional Toxin–Antitoxin Systems
title_fullStr Fic Proteins of Campylobacter fetus subsp. venerealis Form a Network of Functional Toxin–Antitoxin Systems
title_full_unstemmed Fic Proteins of Campylobacter fetus subsp. venerealis Form a Network of Functional Toxin–Antitoxin Systems
title_short Fic Proteins of Campylobacter fetus subsp. venerealis Form a Network of Functional Toxin–Antitoxin Systems
title_sort fic proteins of campylobacter fetus subsp. venerealis form a network of functional toxin–antitoxin systems
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651007/
https://www.ncbi.nlm.nih.gov/pubmed/29089929
http://dx.doi.org/10.3389/fmicb.2017.01965
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