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Evaluation of polymorphisms in inflammatory mediator and cellular adhesion genes as risk factors for feline infectious peritonitis

Research output: Contribution to journalArticle

Original languageEnglish
Number of pages7
JournalJournal of Feline Medicine and Surgery
Early online date2 Aug 2019
DOIs
DateAccepted/In press - 1 Jul 2019
DateE-pub ahead of print (current) - 2 Aug 2019

Abstract

Objectives
Feline infectious peritonitis (FIP) is a high mortality infectious disease. Single nucleotide polymorphisms (SNPs) in the genes encoding interferon gamma (IFNG), tumour necrosis factor alpha (TNFA) and DC-SIGN (CD209) have been associated with increased and decreased risk of developing FIP. This study was designed to determine whether these associations were present in a UK population of pedigree cats using samples from cats euthanased with a confirmed diagnosis (FIP, n=22; non-FIP, n=10) or clinically healthy cats over 11 years of age (n=3).

Methods
DNA was extracted from tissue (n=32) or blood (n=3) and PCR performed for regions of IFNG, TNFA and CD209. PCR amplicons were sequenced, each SNP genotype determined, and genotype/allele frequency for each SNP and FIP status compared.

Results
No significant association was found between genotype and FIP status for any SNP analysed. There was a trend for the heterozygous CT genotype at both IFNG g.401 and g.408 to be associated with FIP (P=0.13), but this genotype was also found in a substantial proportion of non-FIP cats. There was also a trend for the heterozygous CT genotype at IFNG g.428 to be associated with FIP (P=0.06), although most cats with FIP had the CC genotype at this locus. No associations were found between any allele at TNFA g.-421, CD209 g.1900, CD209 g.2276, CD209 g.2392 and CD209 g.2713 and FIP.

Conclusions and relevance
The use of the IFNG, TNFA and CD209 SNPs described to predict risk of FIP cannot currently be recommended.

    Research areas

  • gamma interferon, genetic risk factor, pyrosequencing, Feline coronavirus

Documents

Documents

  • Full-text PDF (accepted author manuscript)

    Rights statement: This is the author accepted manuscript (AAM). The final published version (version of record) is available online via Sage at https://doi.org/10.1177%2F1098612X19865637 . Please refer to any applicable terms of use of the publisher.

    Accepted author manuscript, 262 KB, PDF document

    Embargo ends: 2/08/20

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    Licence: Other

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