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Association of the chicken MHC B haplotypes with resistance to avian coronavirus
Clinical respiratory illness was compared in five homozygous chicken lines, originating from homozygous B2, B8, B12 and B19, and heterozygous B2/B12 birds after infection with either of two strains of the infectious bronchitis virus (IBV). All chickens used in these studies originated from White Leg...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103219/ https://www.ncbi.nlm.nih.gov/pubmed/23178407 http://dx.doi.org/10.1016/j.dci.2012.10.006 |
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author | Banat, Ghida R. Tkalcic, Suzana Dzielawa, Jennifer A. Jackwood, Mark W. Saggese, Miguel D. Yates, Linda Kopulos, Renee Briles, W.E. Collisson, Ellen W. |
author_facet | Banat, Ghida R. Tkalcic, Suzana Dzielawa, Jennifer A. Jackwood, Mark W. Saggese, Miguel D. Yates, Linda Kopulos, Renee Briles, W.E. Collisson, Ellen W. |
author_sort | Banat, Ghida R. |
collection | PubMed |
description | Clinical respiratory illness was compared in five homozygous chicken lines, originating from homozygous B2, B8, B12 and B19, and heterozygous B2/B12 birds after infection with either of two strains of the infectious bronchitis virus (IBV). All chickens used in these studies originated from White Leghorn and Ancona linages. IBV Gray strain infection of MHC homozygous B12 and B19 haplotype chicks resulted in severe respiratory disease compared to chicks with B2/B2 and B5/B5 haplotypes. Demonstrating a dominant B2 phenotype, B2/B12 birds were also more resistant to IBV. Respiratory clinical illness in B8/B8 chicks was severe early after infection, while illness resolved similar to the B5 and B2 homozygous birds. Following M41 strain infection, birds with B2/B2 and B8/B8 haplotypes were again more resistant to clinical illness than B19/B19 birds. Real time RT-PCR indicated that infection was cleared more efficiently in trachea, lungs and kidneys of B2/B2 and B8/B8 birds compared with B19/B19 birds. Furthermore, M41 infected B2/B2 and B8/B8 chicks performed better in terms of body weight gain than B19/B19 chicks. These studies suggest that genetics of B defined haplotypes might be exploited to produce chicks resistant to respiratory pathogens or with more effective immune responses. |
format | Online Article Text |
id | pubmed-7103219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71032192020-03-31 Association of the chicken MHC B haplotypes with resistance to avian coronavirus Banat, Ghida R. Tkalcic, Suzana Dzielawa, Jennifer A. Jackwood, Mark W. Saggese, Miguel D. Yates, Linda Kopulos, Renee Briles, W.E. Collisson, Ellen W. Dev Comp Immunol Article Clinical respiratory illness was compared in five homozygous chicken lines, originating from homozygous B2, B8, B12 and B19, and heterozygous B2/B12 birds after infection with either of two strains of the infectious bronchitis virus (IBV). All chickens used in these studies originated from White Leghorn and Ancona linages. IBV Gray strain infection of MHC homozygous B12 and B19 haplotype chicks resulted in severe respiratory disease compared to chicks with B2/B2 and B5/B5 haplotypes. Demonstrating a dominant B2 phenotype, B2/B12 birds were also more resistant to IBV. Respiratory clinical illness in B8/B8 chicks was severe early after infection, while illness resolved similar to the B5 and B2 homozygous birds. Following M41 strain infection, birds with B2/B2 and B8/B8 haplotypes were again more resistant to clinical illness than B19/B19 birds. Real time RT-PCR indicated that infection was cleared more efficiently in trachea, lungs and kidneys of B2/B2 and B8/B8 birds compared with B19/B19 birds. Furthermore, M41 infected B2/B2 and B8/B8 chicks performed better in terms of body weight gain than B19/B19 chicks. These studies suggest that genetics of B defined haplotypes might be exploited to produce chicks resistant to respiratory pathogens or with more effective immune responses. Elsevier Ltd. 2013-04 2012-11-22 /pmc/articles/PMC7103219/ /pubmed/23178407 http://dx.doi.org/10.1016/j.dci.2012.10.006 Text en Copyright © 2012 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Banat, Ghida R. Tkalcic, Suzana Dzielawa, Jennifer A. Jackwood, Mark W. Saggese, Miguel D. Yates, Linda Kopulos, Renee Briles, W.E. Collisson, Ellen W. Association of the chicken MHC B haplotypes with resistance to avian coronavirus |
title | Association of the chicken MHC B haplotypes with resistance to avian coronavirus |
title_full | Association of the chicken MHC B haplotypes with resistance to avian coronavirus |
title_fullStr | Association of the chicken MHC B haplotypes with resistance to avian coronavirus |
title_full_unstemmed | Association of the chicken MHC B haplotypes with resistance to avian coronavirus |
title_short | Association of the chicken MHC B haplotypes with resistance to avian coronavirus |
title_sort | association of the chicken mhc b haplotypes with resistance to avian coronavirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103219/ https://www.ncbi.nlm.nih.gov/pubmed/23178407 http://dx.doi.org/10.1016/j.dci.2012.10.006 |
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