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A comparative analysis of methylome profiles of Campylobacter jejuni sheep abortion isolate and gastroenteric strains using PacBio data

Campylobacter jejuni is a leading cause of human gastrointestinal disease and small ruminant abortions in the United States. The recent emergence of a highly virulent, tetracycline-resistant C. jejuni subsp. jejuni sheep abortion clone (clone SA) in the United States, and that strain's associat...

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Autores principales: Mou, Kathy T., Muppirala, Usha K., Severin, Andrew J., Clark, Tyson A., Boitano, Matthew, Plummer, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294202/
https://www.ncbi.nlm.nih.gov/pubmed/25642218
http://dx.doi.org/10.3389/fmicb.2014.00782
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author Mou, Kathy T.
Muppirala, Usha K.
Severin, Andrew J.
Clark, Tyson A.
Boitano, Matthew
Plummer, Paul J.
author_facet Mou, Kathy T.
Muppirala, Usha K.
Severin, Andrew J.
Clark, Tyson A.
Boitano, Matthew
Plummer, Paul J.
author_sort Mou, Kathy T.
collection PubMed
description Campylobacter jejuni is a leading cause of human gastrointestinal disease and small ruminant abortions in the United States. The recent emergence of a highly virulent, tetracycline-resistant C. jejuni subsp. jejuni sheep abortion clone (clone SA) in the United States, and that strain's association with human disease, has resulted in a heightened awareness of the zoonotic potential of this organism. Pacific Biosciences' Single Molecule, Real-Time sequencing technology was used to explore the variation in the genome-wide methylation patterns of the abortifacient clone SA (IA3902) and phenotypically distinct gastrointestinal-specific C. jejuni strains (NCTC 11168 and 81-176). Several notable differences were discovered that distinguished the methylome of IA3902 from that of 11168 and 81-176: identification of motifs novel to IA3902, genome-specific hypo- and hypermethylated regions, strain level variability in genes methylated, and differences in the types of methylation motifs present in each strain. These observations suggest a possible role of methylation in the contrasting disease presentations of these three C. jejuni strains. In addition, the methylation profiles between IA3902 and a luxS mutant were explored to determine if variations in methylation patterns could be identified that might explain the role of LuxS-dependent methyl recycling in IA3902 abortifacient potential.
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spelling pubmed-42942022015-01-30 A comparative analysis of methylome profiles of Campylobacter jejuni sheep abortion isolate and gastroenteric strains using PacBio data Mou, Kathy T. Muppirala, Usha K. Severin, Andrew J. Clark, Tyson A. Boitano, Matthew Plummer, Paul J. Front Microbiol Microbiology Campylobacter jejuni is a leading cause of human gastrointestinal disease and small ruminant abortions in the United States. The recent emergence of a highly virulent, tetracycline-resistant C. jejuni subsp. jejuni sheep abortion clone (clone SA) in the United States, and that strain's association with human disease, has resulted in a heightened awareness of the zoonotic potential of this organism. Pacific Biosciences' Single Molecule, Real-Time sequencing technology was used to explore the variation in the genome-wide methylation patterns of the abortifacient clone SA (IA3902) and phenotypically distinct gastrointestinal-specific C. jejuni strains (NCTC 11168 and 81-176). Several notable differences were discovered that distinguished the methylome of IA3902 from that of 11168 and 81-176: identification of motifs novel to IA3902, genome-specific hypo- and hypermethylated regions, strain level variability in genes methylated, and differences in the types of methylation motifs present in each strain. These observations suggest a possible role of methylation in the contrasting disease presentations of these three C. jejuni strains. In addition, the methylation profiles between IA3902 and a luxS mutant were explored to determine if variations in methylation patterns could be identified that might explain the role of LuxS-dependent methyl recycling in IA3902 abortifacient potential. Frontiers Media S.A. 2015-01-14 /pmc/articles/PMC4294202/ /pubmed/25642218 http://dx.doi.org/10.3389/fmicb.2014.00782 Text en Copyright © 2015 Mou, Muppirala, Severin, Clark, Boitano and Plummer. 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
Mou, Kathy T.
Muppirala, Usha K.
Severin, Andrew J.
Clark, Tyson A.
Boitano, Matthew
Plummer, Paul J.
A comparative analysis of methylome profiles of Campylobacter jejuni sheep abortion isolate and gastroenteric strains using PacBio data
title A comparative analysis of methylome profiles of Campylobacter jejuni sheep abortion isolate and gastroenteric strains using PacBio data
title_full A comparative analysis of methylome profiles of Campylobacter jejuni sheep abortion isolate and gastroenteric strains using PacBio data
title_fullStr A comparative analysis of methylome profiles of Campylobacter jejuni sheep abortion isolate and gastroenteric strains using PacBio data
title_full_unstemmed A comparative analysis of methylome profiles of Campylobacter jejuni sheep abortion isolate and gastroenteric strains using PacBio data
title_short A comparative analysis of methylome profiles of Campylobacter jejuni sheep abortion isolate and gastroenteric strains using PacBio data
title_sort comparative analysis of methylome profiles of campylobacter jejuni sheep abortion isolate and gastroenteric strains using pacbio data
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294202/
https://www.ncbi.nlm.nih.gov/pubmed/25642218
http://dx.doi.org/10.3389/fmicb.2014.00782
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