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A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae

Non-typeable Haemophilus influenzae contains an N(6)-adenine DNA-methyltransferase (ModA) that is subject to phase-variable expression (random ON/OFF switching). Five modA alleles, modA2, modA4, modA5, modA9 and modA10, account for over two-thirds of clinical otitis media isolates surveyed. Here, we...

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Autores principales: Atack, John M., Srikhanta, Yogitha N., Fox, Kate L., Jurcisek, Joseph A., Brockman, Kenneth L., Clark, Tyson A., Boitano, Matthew, Power, Peter M., Jen, Freda E.-C., McEwan, Alastair G., Grimmond, Sean M., Smith, Arnold L., Barenkamp, Stephen J., Korlach, Jonas, Bakaletz, Lauren O., Jennings, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525171/
https://www.ncbi.nlm.nih.gov/pubmed/26215614
http://dx.doi.org/10.1038/ncomms8828
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author Atack, John M.
Srikhanta, Yogitha N.
Fox, Kate L.
Jurcisek, Joseph A.
Brockman, Kenneth L.
Clark, Tyson A.
Boitano, Matthew
Power, Peter M.
Jen, Freda E.-C.
McEwan, Alastair G.
Grimmond, Sean M.
Smith, Arnold L.
Barenkamp, Stephen J.
Korlach, Jonas
Bakaletz, Lauren O.
Jennings, Michael P.
author_facet Atack, John M.
Srikhanta, Yogitha N.
Fox, Kate L.
Jurcisek, Joseph A.
Brockman, Kenneth L.
Clark, Tyson A.
Boitano, Matthew
Power, Peter M.
Jen, Freda E.-C.
McEwan, Alastair G.
Grimmond, Sean M.
Smith, Arnold L.
Barenkamp, Stephen J.
Korlach, Jonas
Bakaletz, Lauren O.
Jennings, Michael P.
author_sort Atack, John M.
collection PubMed
description Non-typeable Haemophilus influenzae contains an N(6)-adenine DNA-methyltransferase (ModA) that is subject to phase-variable expression (random ON/OFF switching). Five modA alleles, modA2, modA4, modA5, modA9 and modA10, account for over two-thirds of clinical otitis media isolates surveyed. Here, we use single molecule, real-time (SMRT) methylome analysis to identify the DNA-recognition motifs for all five of these modA alleles. Phase variation of these alleles regulates multiple proteins including vaccine candidates, and key virulence phenotypes such as antibiotic resistance (modA2, modA5, modA10), biofilm formation (modA2) and immunoevasion (modA4). Analyses of a modA2 strain in the chinchilla model of otitis media show a clear selection for ON switching of modA2 in the middle ear. Our results indicate that a biphasic epigenetic switch can control bacterial virulence, immunoevasion and niche adaptation in an animal model system.
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spelling pubmed-45251712015-09-04 A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae Atack, John M. Srikhanta, Yogitha N. Fox, Kate L. Jurcisek, Joseph A. Brockman, Kenneth L. Clark, Tyson A. Boitano, Matthew Power, Peter M. Jen, Freda E.-C. McEwan, Alastair G. Grimmond, Sean M. Smith, Arnold L. Barenkamp, Stephen J. Korlach, Jonas Bakaletz, Lauren O. Jennings, Michael P. Nat Commun Article Non-typeable Haemophilus influenzae contains an N(6)-adenine DNA-methyltransferase (ModA) that is subject to phase-variable expression (random ON/OFF switching). Five modA alleles, modA2, modA4, modA5, modA9 and modA10, account for over two-thirds of clinical otitis media isolates surveyed. Here, we use single molecule, real-time (SMRT) methylome analysis to identify the DNA-recognition motifs for all five of these modA alleles. Phase variation of these alleles regulates multiple proteins including vaccine candidates, and key virulence phenotypes such as antibiotic resistance (modA2, modA5, modA10), biofilm formation (modA2) and immunoevasion (modA4). Analyses of a modA2 strain in the chinchilla model of otitis media show a clear selection for ON switching of modA2 in the middle ear. Our results indicate that a biphasic epigenetic switch can control bacterial virulence, immunoevasion and niche adaptation in an animal model system. Nature Pub. Group 2015-07-28 /pmc/articles/PMC4525171/ /pubmed/26215614 http://dx.doi.org/10.1038/ncomms8828 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Atack, John M.
Srikhanta, Yogitha N.
Fox, Kate L.
Jurcisek, Joseph A.
Brockman, Kenneth L.
Clark, Tyson A.
Boitano, Matthew
Power, Peter M.
Jen, Freda E.-C.
McEwan, Alastair G.
Grimmond, Sean M.
Smith, Arnold L.
Barenkamp, Stephen J.
Korlach, Jonas
Bakaletz, Lauren O.
Jennings, Michael P.
A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae
title A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae
title_full A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae
title_fullStr A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae
title_full_unstemmed A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae
title_short A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae
title_sort biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable haemophilus influenzae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525171/
https://www.ncbi.nlm.nih.gov/pubmed/26215614
http://dx.doi.org/10.1038/ncomms8828
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