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Genetic susceptibility to feline infectious peritonitis in Birman cats

Genetic factors are presumed to influence the incidence of feline infectious peritonitis (FIP), especially among pedigreed cats. However, proof for the existence of such factors has been limited and mainly anecdotal. Therefore, we sought evidence for genetic susceptibility to FIP using feline high d...

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Autores principales: Golovko, Lyudmila, Lyons, Leslie A., Liu, Hongwei, Sørensen, Anne, Wehnert, Suzanne, Pedersen, Niels C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342855/
https://www.ncbi.nlm.nih.gov/pubmed/23619280
http://dx.doi.org/10.1016/j.virusres.2013.04.006
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author Golovko, Lyudmila
Lyons, Leslie A.
Liu, Hongwei
Sørensen, Anne
Wehnert, Suzanne
Pedersen, Niels C.
author_facet Golovko, Lyudmila
Lyons, Leslie A.
Liu, Hongwei
Sørensen, Anne
Wehnert, Suzanne
Pedersen, Niels C.
author_sort Golovko, Lyudmila
collection PubMed
description Genetic factors are presumed to influence the incidence of feline infectious peritonitis (FIP), especially among pedigreed cats. However, proof for the existence of such factors has been limited and mainly anecdotal. Therefore, we sought evidence for genetic susceptibility to FIP using feline high density single nucleotide polymorphism (SNP) arrays in a genome-wide association study (GWAS). Birman cats were chosen for GWAS because they are highly inbred and suffer a high incidence of FIP. DNA from 38 Birman cats that died of FIP and 161 healthy cats from breeders in Denmark and USA were selected for genotyping using 63K SNPs distributed across the feline genome. Danish and American Birman cats were closely related and the populations were therefore combined and analyzed in two manners: (1) all cases (FIP) vs. all controls (healthy) regardless of age, and (2) cases 1½ years of age and younger (most susceptible) vs. controls 2 years of age and older (most resistant). GWAS of the second cohort was most productive in identifying significant genome-wide associations between case and control cats. Four peaks of association with FIP susceptibility were identified, with two being identified on both analyses. Five candidate genes ELMO1, RRAGA, TNFSF10, ERAP1 and ERAP2, all relevant to what is known about FIP virus pathogenesis, were identified but no single association was fully concordant with the disease phenotype. Difficulties in doing GWAS in cats and interrogating complex genetic traits were discussed.
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spelling pubmed-43428552015-02-27 Genetic susceptibility to feline infectious peritonitis in Birman cats Golovko, Lyudmila Lyons, Leslie A. Liu, Hongwei Sørensen, Anne Wehnert, Suzanne Pedersen, Niels C. Virus Res Article Genetic factors are presumed to influence the incidence of feline infectious peritonitis (FIP), especially among pedigreed cats. However, proof for the existence of such factors has been limited and mainly anecdotal. Therefore, we sought evidence for genetic susceptibility to FIP using feline high density single nucleotide polymorphism (SNP) arrays in a genome-wide association study (GWAS). Birman cats were chosen for GWAS because they are highly inbred and suffer a high incidence of FIP. DNA from 38 Birman cats that died of FIP and 161 healthy cats from breeders in Denmark and USA were selected for genotyping using 63K SNPs distributed across the feline genome. Danish and American Birman cats were closely related and the populations were therefore combined and analyzed in two manners: (1) all cases (FIP) vs. all controls (healthy) regardless of age, and (2) cases 1½ years of age and younger (most susceptible) vs. controls 2 years of age and older (most resistant). GWAS of the second cohort was most productive in identifying significant genome-wide associations between case and control cats. Four peaks of association with FIP susceptibility were identified, with two being identified on both analyses. Five candidate genes ELMO1, RRAGA, TNFSF10, ERAP1 and ERAP2, all relevant to what is known about FIP virus pathogenesis, were identified but no single association was fully concordant with the disease phenotype. Difficulties in doing GWAS in cats and interrogating complex genetic traits were discussed. Elsevier B.V. 2013-07 2013-04-22 /pmc/articles/PMC4342855/ /pubmed/23619280 http://dx.doi.org/10.1016/j.virusres.2013.04.006 Text en Copyright © 2013 Elsevier B.V. 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
Golovko, Lyudmila
Lyons, Leslie A.
Liu, Hongwei
Sørensen, Anne
Wehnert, Suzanne
Pedersen, Niels C.
Genetic susceptibility to feline infectious peritonitis in Birman cats
title Genetic susceptibility to feline infectious peritonitis in Birman cats
title_full Genetic susceptibility to feline infectious peritonitis in Birman cats
title_fullStr Genetic susceptibility to feline infectious peritonitis in Birman cats
title_full_unstemmed Genetic susceptibility to feline infectious peritonitis in Birman cats
title_short Genetic susceptibility to feline infectious peritonitis in Birman cats
title_sort genetic susceptibility to feline infectious peritonitis in birman cats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342855/
https://www.ncbi.nlm.nih.gov/pubmed/23619280
http://dx.doi.org/10.1016/j.virusres.2013.04.006
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