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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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 |
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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 |
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