Cargando…
The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens
BACKGROUND: Campylobacter is the leading cause of foodborne diarrhoeal illness in humans and is mostly acquired from consumption or handling of contaminated poultry meat. In the absence of effective licensed vaccines and inhibitors, selection for chickens with increased resistance to Campylobacter c...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835825/ https://www.ncbi.nlm.nih.gov/pubmed/27090510 http://dx.doi.org/10.1186/s12864-016-2612-7 |
_version_ | 1782427677003612160 |
---|---|
author | Psifidi, A. Fife, M. Howell, J. Matika, O. van Diemen, P. M. Kuo, R. Smith, J. Hocking, P. M. Salmon, N. Jones, M. A. Hume, D. A. Banos, G. Stevens, M. P. Kaiser, P. |
author_facet | Psifidi, A. Fife, M. Howell, J. Matika, O. van Diemen, P. M. Kuo, R. Smith, J. Hocking, P. M. Salmon, N. Jones, M. A. Hume, D. A. Banos, G. Stevens, M. P. Kaiser, P. |
author_sort | Psifidi, A. |
collection | PubMed |
description | BACKGROUND: Campylobacter is the leading cause of foodborne diarrhoeal illness in humans and is mostly acquired from consumption or handling of contaminated poultry meat. In the absence of effective licensed vaccines and inhibitors, selection for chickens with increased resistance to Campylobacter could potentially reduce its subsequent entry into the food chain. Campylobacter intestinal colonisation levels are influenced by the host genetics of the chicken. In the present study, two chicken populations were used to investigate the genetic architecture of avian resistance to colonisation: (i) a back-cross of two White Leghorn derived inbred lines [(6(1) x N) x N] known to differ in resistance to Campylobacter colonisation and (ii) a 9(th) generation advanced intercross (6(1) x N) line. RESULTS: The level of colonisation with Campylobacter jejuni following experimental infection was found to be a quantitative trait. A back-cross experiment using 1,243 fully informative single nucleotide polymorphism (SNP) markers revealed quantitative trait loci (QTL) on chromosomes 7, 11 and 14. In the advanced intercross line study, the location of the QTL on chromosome 14 was confirmed and refined and two new QTLs were identified located on chromosomes 4 and 16. Pathway and re-sequencing data analysis of the genes located in the QTL candidate regions identified potential pathways, networks and candidate resistance genes. Finally, gene expression analyses were performed for some of the candidate resistance genes to support the results. CONCLUSION: Campylobacter resistance in chickens is a complex trait, possibly involving the Major Histocompatibility Complex, innate and adaptive immune responses, cadherins and other factors. Two of the QTLs for Campylobacter resistance are co-located with Salmonella resistance loci, indicating that it may be possible to breed simultaneously for enhanced resistance to both zoonoses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2612-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4835825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48358252016-04-20 The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens Psifidi, A. Fife, M. Howell, J. Matika, O. van Diemen, P. M. Kuo, R. Smith, J. Hocking, P. M. Salmon, N. Jones, M. A. Hume, D. A. Banos, G. Stevens, M. P. Kaiser, P. BMC Genomics Research Article BACKGROUND: Campylobacter is the leading cause of foodborne diarrhoeal illness in humans and is mostly acquired from consumption or handling of contaminated poultry meat. In the absence of effective licensed vaccines and inhibitors, selection for chickens with increased resistance to Campylobacter could potentially reduce its subsequent entry into the food chain. Campylobacter intestinal colonisation levels are influenced by the host genetics of the chicken. In the present study, two chicken populations were used to investigate the genetic architecture of avian resistance to colonisation: (i) a back-cross of two White Leghorn derived inbred lines [(6(1) x N) x N] known to differ in resistance to Campylobacter colonisation and (ii) a 9(th) generation advanced intercross (6(1) x N) line. RESULTS: The level of colonisation with Campylobacter jejuni following experimental infection was found to be a quantitative trait. A back-cross experiment using 1,243 fully informative single nucleotide polymorphism (SNP) markers revealed quantitative trait loci (QTL) on chromosomes 7, 11 and 14. In the advanced intercross line study, the location of the QTL on chromosome 14 was confirmed and refined and two new QTLs were identified located on chromosomes 4 and 16. Pathway and re-sequencing data analysis of the genes located in the QTL candidate regions identified potential pathways, networks and candidate resistance genes. Finally, gene expression analyses were performed for some of the candidate resistance genes to support the results. CONCLUSION: Campylobacter resistance in chickens is a complex trait, possibly involving the Major Histocompatibility Complex, innate and adaptive immune responses, cadherins and other factors. Two of the QTLs for Campylobacter resistance are co-located with Salmonella resistance loci, indicating that it may be possible to breed simultaneously for enhanced resistance to both zoonoses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2612-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-18 /pmc/articles/PMC4835825/ /pubmed/27090510 http://dx.doi.org/10.1186/s12864-016-2612-7 Text en © Psifidi et al. 2016 Open AccessThis 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 Psifidi, A. Fife, M. Howell, J. Matika, O. van Diemen, P. M. Kuo, R. Smith, J. Hocking, P. M. Salmon, N. Jones, M. A. Hume, D. A. Banos, G. Stevens, M. P. Kaiser, P. The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens |
title | The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens |
title_full | The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens |
title_fullStr | The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens |
title_full_unstemmed | The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens |
title_short | The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens |
title_sort | genomic architecture of resistance to campylobacter jejuni intestinal colonisation in chickens |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835825/ https://www.ncbi.nlm.nih.gov/pubmed/27090510 http://dx.doi.org/10.1186/s12864-016-2612-7 |
work_keys_str_mv | AT psifidia thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT fifem thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT howellj thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT matikao thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT vandiemenpm thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT kuor thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT smithj thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT hockingpm thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT salmonn thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT jonesma thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT humeda thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT banosg thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT stevensmp thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT kaiserp thegenomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT psifidia genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT fifem genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT howellj genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT matikao genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT vandiemenpm genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT kuor genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT smithj genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT hockingpm genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT salmonn genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT jonesma genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT humeda genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT banosg genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT stevensmp genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens AT kaiserp genomicarchitectureofresistancetocampylobacterjejuniintestinalcolonisationinchickens |