Cargando…
The Moraxella catarrhalis phase-variable DNA methyltransferase ModM3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media
BACKGROUND: Moraxella catarrhalis is a leading cause of otitis media (OM) and chronic obstructive pulmonary disease (COPD). M. catarrhalis contains a Type III DNA adenine methyltransferase (ModM) that is phase-variably expressed (i.e., its expression is subject to random, reversible ON/OFF switching...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902483/ https://www.ncbi.nlm.nih.gov/pubmed/31818247 http://dx.doi.org/10.1186/s12866-019-1660-y |
_version_ | 1783477677294878720 |
---|---|
author | Blakeway, Luke V. Tan, Aimee Jurcisek, Joseph A. Bakaletz, Lauren O. Atack, John M. Peak, Ian R. Seib, Kate L. |
author_facet | Blakeway, Luke V. Tan, Aimee Jurcisek, Joseph A. Bakaletz, Lauren O. Atack, John M. Peak, Ian R. Seib, Kate L. |
author_sort | Blakeway, Luke V. |
collection | PubMed |
description | BACKGROUND: Moraxella catarrhalis is a leading cause of otitis media (OM) and chronic obstructive pulmonary disease (COPD). M. catarrhalis contains a Type III DNA adenine methyltransferase (ModM) that is phase-variably expressed (i.e., its expression is subject to random, reversible ON/OFF switching). ModM has six target recognition domain alleles (modM1–6), and we have previously shown that modM2 is the predominant allele, while modM3 is associated with OM. Phase-variable DNA methyltransferases mediate epigenetic regulation and modulate pathogenesis in several bacteria. ModM2 of M. catarrhalis regulates the expression of a phasevarion containing genes important for colonization and infection. Here we describe the phase-variable expression of modM3, the ModM3 methylation site and the suite of genes regulated within the ModM3 phasevarion. RESULTS: Phase-variable expression of modM3, mediated by variation in length of a 5′-(CAAC)(n)-3′ tetranucleotide repeat tract in the open reading frame was demonstrated in M. catarrhalis strain CCRI-195ME with GeneScan fragment length analysis and western immunoblot. We determined that ModM3 is an active N6-adenine methyltransferase that methylates the sequence 5′-AC(m6)ATC-3′. Methylation was detected at all 4446 5′-ACATC-3′ sites in the genome when ModM3 is expressed. RNASeq analysis identified 31 genes that are differentially expressed between modM3 ON and OFF variants, including five genes that are involved in the response to oxidative and nitrosative stress, with potential roles in biofilm formation and survival in anaerobic environments. An in vivo chinchilla (Chinchilla lanigera) model of otitis media demonstrated that transbullar challenge with the modM3 OFF variant resulted in an increased middle ear bacterial load compared to a modM3 ON variant. In addition, co-infection experiments with NTHi and M. catarrhalis modM3 ON or modM3 OFF variants revealed that phase variation of modM3 altered survival of NTHi in the middle ear during early and late stage infection. CONCLUSIONS: Phase variation of ModM3 epigenetically regulates the expression of a phasevarion containing multiple genes that are potentially important in the progression of otitis media. |
format | Online Article Text |
id | pubmed-6902483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69024832019-12-11 The Moraxella catarrhalis phase-variable DNA methyltransferase ModM3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media Blakeway, Luke V. Tan, Aimee Jurcisek, Joseph A. Bakaletz, Lauren O. Atack, John M. Peak, Ian R. Seib, Kate L. BMC Microbiol Research Article BACKGROUND: Moraxella catarrhalis is a leading cause of otitis media (OM) and chronic obstructive pulmonary disease (COPD). M. catarrhalis contains a Type III DNA adenine methyltransferase (ModM) that is phase-variably expressed (i.e., its expression is subject to random, reversible ON/OFF switching). ModM has six target recognition domain alleles (modM1–6), and we have previously shown that modM2 is the predominant allele, while modM3 is associated with OM. Phase-variable DNA methyltransferases mediate epigenetic regulation and modulate pathogenesis in several bacteria. ModM2 of M. catarrhalis regulates the expression of a phasevarion containing genes important for colonization and infection. Here we describe the phase-variable expression of modM3, the ModM3 methylation site and the suite of genes regulated within the ModM3 phasevarion. RESULTS: Phase-variable expression of modM3, mediated by variation in length of a 5′-(CAAC)(n)-3′ tetranucleotide repeat tract in the open reading frame was demonstrated in M. catarrhalis strain CCRI-195ME with GeneScan fragment length analysis and western immunoblot. We determined that ModM3 is an active N6-adenine methyltransferase that methylates the sequence 5′-AC(m6)ATC-3′. Methylation was detected at all 4446 5′-ACATC-3′ sites in the genome when ModM3 is expressed. RNASeq analysis identified 31 genes that are differentially expressed between modM3 ON and OFF variants, including five genes that are involved in the response to oxidative and nitrosative stress, with potential roles in biofilm formation and survival in anaerobic environments. An in vivo chinchilla (Chinchilla lanigera) model of otitis media demonstrated that transbullar challenge with the modM3 OFF variant resulted in an increased middle ear bacterial load compared to a modM3 ON variant. In addition, co-infection experiments with NTHi and M. catarrhalis modM3 ON or modM3 OFF variants revealed that phase variation of modM3 altered survival of NTHi in the middle ear during early and late stage infection. CONCLUSIONS: Phase variation of ModM3 epigenetically regulates the expression of a phasevarion containing multiple genes that are potentially important in the progression of otitis media. BioMed Central 2019-12-09 /pmc/articles/PMC6902483/ /pubmed/31818247 http://dx.doi.org/10.1186/s12866-019-1660-y Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Blakeway, Luke V. Tan, Aimee Jurcisek, Joseph A. Bakaletz, Lauren O. Atack, John M. Peak, Ian R. Seib, Kate L. The Moraxella catarrhalis phase-variable DNA methyltransferase ModM3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media |
title | The Moraxella catarrhalis phase-variable DNA methyltransferase ModM3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media |
title_full | The Moraxella catarrhalis phase-variable DNA methyltransferase ModM3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media |
title_fullStr | The Moraxella catarrhalis phase-variable DNA methyltransferase ModM3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media |
title_full_unstemmed | The Moraxella catarrhalis phase-variable DNA methyltransferase ModM3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media |
title_short | The Moraxella catarrhalis phase-variable DNA methyltransferase ModM3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media |
title_sort | moraxella catarrhalis phase-variable dna methyltransferase modm3 is an epigenetic regulator that affects bacterial survival in an in vivo model of otitis media |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902483/ https://www.ncbi.nlm.nih.gov/pubmed/31818247 http://dx.doi.org/10.1186/s12866-019-1660-y |
work_keys_str_mv | AT blakewaylukev themoraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT tanaimee themoraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT jurcisekjosepha themoraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT bakaletzlaureno themoraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT atackjohnm themoraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT peakianr themoraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT seibkatel themoraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT blakewaylukev moraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT tanaimee moraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT jurcisekjosepha moraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT bakaletzlaureno moraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT atackjohnm moraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT peakianr moraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia AT seibkatel moraxellacatarrhalisphasevariablednamethyltransferasemodm3isanepigeneticregulatorthataffectsbacterialsurvivalinaninvivomodelofotitismedia |