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Genome-Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene

The enteropathogen Campylobacter jejuni is a major worldwide health and economic burden, being one of the leading causes of bacterial gastroenteritis and commonly linked to postinfectious onset of autoimmune disease. Chickens are a major vector for human infection and even though variation in avian...

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Autores principales: Connell, Sarah, Meade, Kieran G., Allan, Brenda, Lloyd, Andrew T., Downing, Tim, O’Farrelly, Cliona, Bradley, Daniel G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656734/
https://www.ncbi.nlm.nih.gov/pubmed/23550144
http://dx.doi.org/10.1534/g3.113.006031
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author Connell, Sarah
Meade, Kieran G.
Allan, Brenda
Lloyd, Andrew T.
Downing, Tim
O’Farrelly, Cliona
Bradley, Daniel G.
author_facet Connell, Sarah
Meade, Kieran G.
Allan, Brenda
Lloyd, Andrew T.
Downing, Tim
O’Farrelly, Cliona
Bradley, Daniel G.
author_sort Connell, Sarah
collection PubMed
description The enteropathogen Campylobacter jejuni is a major worldwide health and economic burden, being one of the leading causes of bacterial gastroenteritis and commonly linked to postinfectious onset of autoimmune disease. Chickens are a major vector for human infection and even though variation in avian colonization level is heritable, no previous studies have identified regions of the genome associated with colonization resistance. We performed a genome-wide association study of resistance to C. jejuni colonization in the avian intestine by controlling for population structure, which revealed a risk locus with genome-wide significance spanning the T-cadherin (CDH13) gene. A second possible risk locus was also identified close to calmodulin (CALM1), a calcium-activated modulator of cadherin function. In addition, gene expression analysis of mRNA sequencing profiles revealed that the relative expression of the two genes is significantly associated with colonization resistance. Functional studies have previously demonstrated involvement of cadherins and calmodulin in C. jejuni intracellular invasion and colonization of human intestinal epithelial cells in vitro. Consistent with this finding, our analysis reveals that variation surrounding these genes is associated with avian colonization resistance in vivo and highlights their potential as possible targets for control of the bacterium in avian and human populations.
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spelling pubmed-36567342013-05-18 Genome-Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene Connell, Sarah Meade, Kieran G. Allan, Brenda Lloyd, Andrew T. Downing, Tim O’Farrelly, Cliona Bradley, Daniel G. G3 (Bethesda) Investigations The enteropathogen Campylobacter jejuni is a major worldwide health and economic burden, being one of the leading causes of bacterial gastroenteritis and commonly linked to postinfectious onset of autoimmune disease. Chickens are a major vector for human infection and even though variation in avian colonization level is heritable, no previous studies have identified regions of the genome associated with colonization resistance. We performed a genome-wide association study of resistance to C. jejuni colonization in the avian intestine by controlling for population structure, which revealed a risk locus with genome-wide significance spanning the T-cadherin (CDH13) gene. A second possible risk locus was also identified close to calmodulin (CALM1), a calcium-activated modulator of cadherin function. In addition, gene expression analysis of mRNA sequencing profiles revealed that the relative expression of the two genes is significantly associated with colonization resistance. Functional studies have previously demonstrated involvement of cadherins and calmodulin in C. jejuni intracellular invasion and colonization of human intestinal epithelial cells in vitro. Consistent with this finding, our analysis reveals that variation surrounding these genes is associated with avian colonization resistance in vivo and highlights their potential as possible targets for control of the bacterium in avian and human populations. Genetics Society of America 2013-05-01 /pmc/articles/PMC3656734/ /pubmed/23550144 http://dx.doi.org/10.1534/g3.113.006031 Text en Copyright © 2013 Connell et al.
spellingShingle Investigations
Connell, Sarah
Meade, Kieran G.
Allan, Brenda
Lloyd, Andrew T.
Downing, Tim
O’Farrelly, Cliona
Bradley, Daniel G.
Genome-Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene
title Genome-Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene
title_full Genome-Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene
title_fullStr Genome-Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene
title_full_unstemmed Genome-Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene
title_short Genome-Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene
title_sort genome-wide association analysis of avian resistance to campylobacter jejuni colonization identifies risk locus spanning the cdh13 gene
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656734/
https://www.ncbi.nlm.nih.gov/pubmed/23550144
http://dx.doi.org/10.1534/g3.113.006031
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