Cargando…

Evaluation of Interferon-Gamma Polymorphisms as a Risk factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats—a Large Cohort Study

Feline infectious peritonitis (FIP) is a common infectious cause of death in cats, with heritable host factors associated with altered risk of disease. To assess the role of feline interferon-gamma gene (fIFNG) variants in this risk, the allele frequencies of two single nucleotide polymorphisms (SNP...

Descripción completa

Detalles Bibliográficos
Autores principales: Barker, Emi N., Lait, Philippa, Ressel, Lorenzo, Blackwell, Emily-Jayne, Tasker, Séverine, Kedward-Dixon, Helen, Kipar, Anja, Helps, Christopher R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399832/
https://www.ncbi.nlm.nih.gov/pubmed/32635137
http://dx.doi.org/10.3390/pathogens9070535
_version_ 1783566223000207360
author Barker, Emi N.
Lait, Philippa
Ressel, Lorenzo
Blackwell, Emily-Jayne
Tasker, Séverine
Kedward-Dixon, Helen
Kipar, Anja
Helps, Christopher R.
author_facet Barker, Emi N.
Lait, Philippa
Ressel, Lorenzo
Blackwell, Emily-Jayne
Tasker, Séverine
Kedward-Dixon, Helen
Kipar, Anja
Helps, Christopher R.
author_sort Barker, Emi N.
collection PubMed
description Feline infectious peritonitis (FIP) is a common infectious cause of death in cats, with heritable host factors associated with altered risk of disease. To assess the role of feline interferon-gamma gene (fIFNG) variants in this risk, the allele frequencies of two single nucleotide polymorphisms (SNPs) (g.401 and g.408) were determined for non-pedigree cats either with confirmed FIP (n = 59) or from the general population (cats enrolled in a large lifetime longitudinal study; n = 264). DNA was extracted from buccal swabs or tissue samples. A pyrosequencing assay to characterize the fIFNG SNPs was designed, optimized and subsequently performed on all samples. Genotype and allele frequency were calculated for each population. Characterization of the target SNPs was possible for 56 of the cats with FIP and 263 of the cats from the general population. The SNPs were in complete linkage disequilibrium with each other. There was an association between FIP status and genotype (χ(2); p = 0.028), with a reduced risk of developing FIP (χ(2); p = 0.0077) associated with the genotype TT at both positions. These results indicate that, although fIFNG variants may be associated with altered risk of disease, the prevalence of individual variants within both populations limits application of their characterization to breeding purposes.
format Online
Article
Text
id pubmed-7399832
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-73998322020-08-17 Evaluation of Interferon-Gamma Polymorphisms as a Risk factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats—a Large Cohort Study Barker, Emi N. Lait, Philippa Ressel, Lorenzo Blackwell, Emily-Jayne Tasker, Séverine Kedward-Dixon, Helen Kipar, Anja Helps, Christopher R. Pathogens Article Feline infectious peritonitis (FIP) is a common infectious cause of death in cats, with heritable host factors associated with altered risk of disease. To assess the role of feline interferon-gamma gene (fIFNG) variants in this risk, the allele frequencies of two single nucleotide polymorphisms (SNPs) (g.401 and g.408) were determined for non-pedigree cats either with confirmed FIP (n = 59) or from the general population (cats enrolled in a large lifetime longitudinal study; n = 264). DNA was extracted from buccal swabs or tissue samples. A pyrosequencing assay to characterize the fIFNG SNPs was designed, optimized and subsequently performed on all samples. Genotype and allele frequency were calculated for each population. Characterization of the target SNPs was possible for 56 of the cats with FIP and 263 of the cats from the general population. The SNPs were in complete linkage disequilibrium with each other. There was an association between FIP status and genotype (χ(2); p = 0.028), with a reduced risk of developing FIP (χ(2); p = 0.0077) associated with the genotype TT at both positions. These results indicate that, although fIFNG variants may be associated with altered risk of disease, the prevalence of individual variants within both populations limits application of their characterization to breeding purposes. MDPI 2020-07-03 /pmc/articles/PMC7399832/ /pubmed/32635137 http://dx.doi.org/10.3390/pathogens9070535 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Barker, Emi N.
Lait, Philippa
Ressel, Lorenzo
Blackwell, Emily-Jayne
Tasker, Séverine
Kedward-Dixon, Helen
Kipar, Anja
Helps, Christopher R.
Evaluation of Interferon-Gamma Polymorphisms as a Risk factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats—a Large Cohort Study
title Evaluation of Interferon-Gamma Polymorphisms as a Risk factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats—a Large Cohort Study
title_full Evaluation of Interferon-Gamma Polymorphisms as a Risk factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats—a Large Cohort Study
title_fullStr Evaluation of Interferon-Gamma Polymorphisms as a Risk factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats—a Large Cohort Study
title_full_unstemmed Evaluation of Interferon-Gamma Polymorphisms as a Risk factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats—a Large Cohort Study
title_short Evaluation of Interferon-Gamma Polymorphisms as a Risk factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats—a Large Cohort Study
title_sort evaluation of interferon-gamma polymorphisms as a risk factor in feline infectious peritonitis development in non-pedigree cats—a large cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399832/
https://www.ncbi.nlm.nih.gov/pubmed/32635137
http://dx.doi.org/10.3390/pathogens9070535
work_keys_str_mv AT barkeremin evaluationofinterferongammapolymorphismsasariskfactorinfelineinfectiousperitonitisdevelopmentinnonpedigreecatsalargecohortstudy
AT laitphilippa evaluationofinterferongammapolymorphismsasariskfactorinfelineinfectiousperitonitisdevelopmentinnonpedigreecatsalargecohortstudy
AT ressellorenzo evaluationofinterferongammapolymorphismsasariskfactorinfelineinfectiousperitonitisdevelopmentinnonpedigreecatsalargecohortstudy
AT blackwellemilyjayne evaluationofinterferongammapolymorphismsasariskfactorinfelineinfectiousperitonitisdevelopmentinnonpedigreecatsalargecohortstudy
AT taskerseverine evaluationofinterferongammapolymorphismsasariskfactorinfelineinfectiousperitonitisdevelopmentinnonpedigreecatsalargecohortstudy
AT kedwarddixonhelen evaluationofinterferongammapolymorphismsasariskfactorinfelineinfectiousperitonitisdevelopmentinnonpedigreecatsalargecohortstudy
AT kiparanja evaluationofinterferongammapolymorphismsasariskfactorinfelineinfectiousperitonitisdevelopmentinnonpedigreecatsalargecohortstudy
AT helpschristopherr evaluationofinterferongammapolymorphismsasariskfactorinfelineinfectiousperitonitisdevelopmentinnonpedigreecatsalargecohortstudy