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Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis
There are four outcomes to feline coronavirus (FCoV) infection: the development of feline infectious peritonitis (FIP, which is immune-mediated), subclinical infection, development of healthy lifelong carriers and a small minority of cats who resist infection (Addie and Jarrett, Veterinary Record 14...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
ESFM and AAFP. Published by Elsevier Ltd.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129417/ https://www.ncbi.nlm.nih.gov/pubmed/15123149 http://dx.doi.org/10.1016/j.jfms.2003.12.010 |
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author | Addie, Diane D Kennedy, Lorna J Ryvar, Ruth Willoughby, K Gaskell, R.M Ollier, W.E.R Nart, Pablo Radford, Alan D |
author_facet | Addie, Diane D Kennedy, Lorna J Ryvar, Ruth Willoughby, K Gaskell, R.M Ollier, W.E.R Nart, Pablo Radford, Alan D |
author_sort | Addie, Diane D |
collection | PubMed |
description | There are four outcomes to feline coronavirus (FCoV) infection: the development of feline infectious peritonitis (FIP, which is immune-mediated), subclinical infection, development of healthy lifelong carriers and a small minority of cats who resist infection (Addie and Jarrett, Veterinary Record 148 (2001) 649). Examination of the FCoV genome has shown that the same strain of virus can produce different clinical manifestations, suggesting that host genetic factors may also play a role in the outcome of infection. FIP is most prevalent amongst pedigree cats, although how much of this is due to them living in large groups (leading to higher virus challenge and stress which predisposes to FIP) and how much is due to genetic susceptibility is not known. If host genetics could be shown to play a role in disease, it may allow the detection of cats with a susceptibility to FIP and the development of increased population resistance through selective breeding. The feline leucocyte antigen (FLA) complex contains many genes that are central to the control of the immune response. In this preliminary study, we used clonal sequence analysis or reference strand conformational analysis (RSCA) to analyse the class II FLA–DRB of 25 cats for which the outcome of FCoV exposure was known. Individual cats were shown to have between two and six FLA–DRB alleles. There was no statistically significant association between the number of alleles and the outcome of FCoV infection. No particular allele appeared to be associated with either the development of FIP, resistance to FCoV, or the carrier status. However, the analysis was complicated by apparent breed variation in FLA–DRB and the small number of individuals in this study. |
format | Online Article Text |
id | pubmed-7129417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | ESFM and AAFP. Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71294172020-04-08 Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis Addie, Diane D Kennedy, Lorna J Ryvar, Ruth Willoughby, K Gaskell, R.M Ollier, W.E.R Nart, Pablo Radford, Alan D J Feline Med Surg Article There are four outcomes to feline coronavirus (FCoV) infection: the development of feline infectious peritonitis (FIP, which is immune-mediated), subclinical infection, development of healthy lifelong carriers and a small minority of cats who resist infection (Addie and Jarrett, Veterinary Record 148 (2001) 649). Examination of the FCoV genome has shown that the same strain of virus can produce different clinical manifestations, suggesting that host genetic factors may also play a role in the outcome of infection. FIP is most prevalent amongst pedigree cats, although how much of this is due to them living in large groups (leading to higher virus challenge and stress which predisposes to FIP) and how much is due to genetic susceptibility is not known. If host genetics could be shown to play a role in disease, it may allow the detection of cats with a susceptibility to FIP and the development of increased population resistance through selective breeding. The feline leucocyte antigen (FLA) complex contains many genes that are central to the control of the immune response. In this preliminary study, we used clonal sequence analysis or reference strand conformational analysis (RSCA) to analyse the class II FLA–DRB of 25 cats for which the outcome of FCoV exposure was known. Individual cats were shown to have between two and six FLA–DRB alleles. There was no statistically significant association between the number of alleles and the outcome of FCoV infection. No particular allele appeared to be associated with either the development of FIP, resistance to FCoV, or the carrier status. However, the analysis was complicated by apparent breed variation in FLA–DRB and the small number of individuals in this study. ESFM and AAFP. Published by Elsevier Ltd. 2004-04 2004-02-25 /pmc/articles/PMC7129417/ /pubmed/15123149 http://dx.doi.org/10.1016/j.jfms.2003.12.010 Text en Copyright © 2004 ESFM and AAFP. Published by 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 Addie, Diane D Kennedy, Lorna J Ryvar, Ruth Willoughby, K Gaskell, R.M Ollier, W.E.R Nart, Pablo Radford, Alan D Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis |
title | Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis |
title_full | Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis |
title_fullStr | Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis |
title_full_unstemmed | Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis |
title_short | Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis |
title_sort | feline leucocyte antigen class ii polymorphism and susceptibility to feline infectious peritonitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129417/ https://www.ncbi.nlm.nih.gov/pubmed/15123149 http://dx.doi.org/10.1016/j.jfms.2003.12.010 |
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