Genomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs

Abstract Background Immunoglobulin A (IgA) deficiency, chronic enteropathies and exocrine pancreatic insufficiency (EPI) have a high prevalence in German Shepherd dogs (GSD). This prospective study determined the prevalence of faecal IgA deficiency (IgAD) in GSD and investigated several candidate ge...

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Autores principales: Niels Grützner, Romy M. Heilmann, Ursula Tress, Iain R. Peters, Jan S. Suchodolski, Jörg M. Steiner
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Publicado: Wiley 2021
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spelling oai:doaj.org-article:a6b892a429d04bf3946a633c929023d62021-11-19T17:14:25ZGenomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs2053-109510.1002/vms3.603https://doaj.org/article/a6b892a429d04bf3946a633c929023d62021-11-01T00:00:00Zhttps://doi.org/10.1002/vms3.603https://doaj.org/toc/2053-1095Abstract Background Immunoglobulin A (IgA) deficiency, chronic enteropathies and exocrine pancreatic insufficiency (EPI) have a high prevalence in German Shepherd dogs (GSD). This prospective study determined the prevalence of faecal IgA deficiency (IgAD) in GSD and investigated several candidate genes and the canine genome for a region or locus co‐segregating with IgAD in GSD. Faecal IgA concentrations were quantified and genomic DNA was extracted from 8 GSD with an undetectable faecal IgA (classified as IgAD) and 80 non‐IgAD GSD. The canine minimal screening set II microsatellite markers were genotyped, with evidence of an association at p < 1.0 × 10−3. Faecal IgA concentrations were also tested for an association with patient clinical and biochemical variables. Results Allele frequencies observed using the candidate gene approach were not associated with faecal IgAD in GSD. In the genome‐wide association study (GWAS), the microsatellite marker FH2361 on canine chromosome 33 approached statistical significance for a link with IgAD in GSD (p = 1.2 × 10−3). A subsequent GWAS in 11 GSD with EPI and 80 control GSD revealed a significant association between EPI and FH2361 (p = 8.2 × 10−4). Conclusions The lack of an association with the phenotype of faecal IgAD in GSD using the candidate gene approach and GWAS might suggests that faecal IgAD in GSD is a relative or transient state of deficiency. However, the prevalence of faecal IgAD in GSD appears to be low (<3%). The relationship between faecal IgAD, EPI and loci close to FH2361 on canine chromosome 33 in GSD warrants further investigation.Niels GrütznerRomy M. HeilmannUrsula TressIain R. PetersJan S. SuchodolskiJörg M. SteinerWileyarticlecalgranulincanine trypsin‐like immunoreactivityfaecal IgAGerman Shepherd dogintestineVeterinary medicineSF600-1100ENVeterinary Medicine and Science, Vol 7, Iss 6, Pp 2144-2155 (2021)
institution DOAJ
collection DOAJ
language EN
topic calgranulin
canine trypsin‐like immunoreactivity
faecal IgA
German Shepherd dog
intestine
Veterinary medicine
SF600-1100
spellingShingle calgranulin
canine trypsin‐like immunoreactivity
faecal IgA
German Shepherd dog
intestine
Veterinary medicine
SF600-1100
Niels Grützner
Romy M. Heilmann
Ursula Tress
Iain R. Peters
Jan S. Suchodolski
Jörg M. Steiner
Genomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs
description Abstract Background Immunoglobulin A (IgA) deficiency, chronic enteropathies and exocrine pancreatic insufficiency (EPI) have a high prevalence in German Shepherd dogs (GSD). This prospective study determined the prevalence of faecal IgA deficiency (IgAD) in GSD and investigated several candidate genes and the canine genome for a region or locus co‐segregating with IgAD in GSD. Faecal IgA concentrations were quantified and genomic DNA was extracted from 8 GSD with an undetectable faecal IgA (classified as IgAD) and 80 non‐IgAD GSD. The canine minimal screening set II microsatellite markers were genotyped, with evidence of an association at p < 1.0 × 10−3. Faecal IgA concentrations were also tested for an association with patient clinical and biochemical variables. Results Allele frequencies observed using the candidate gene approach were not associated with faecal IgAD in GSD. In the genome‐wide association study (GWAS), the microsatellite marker FH2361 on canine chromosome 33 approached statistical significance for a link with IgAD in GSD (p = 1.2 × 10−3). A subsequent GWAS in 11 GSD with EPI and 80 control GSD revealed a significant association between EPI and FH2361 (p = 8.2 × 10−4). Conclusions The lack of an association with the phenotype of faecal IgAD in GSD using the candidate gene approach and GWAS might suggests that faecal IgAD in GSD is a relative or transient state of deficiency. However, the prevalence of faecal IgAD in GSD appears to be low (<3%). The relationship between faecal IgAD, EPI and loci close to FH2361 on canine chromosome 33 in GSD warrants further investigation.
format article
author Niels Grützner
Romy M. Heilmann
Ursula Tress
Iain R. Peters
Jan S. Suchodolski
Jörg M. Steiner
author_facet Niels Grützner
Romy M. Heilmann
Ursula Tress
Iain R. Peters
Jan S. Suchodolski
Jörg M. Steiner
author_sort Niels Grützner
title Genomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs
title_short Genomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs
title_full Genomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs
title_fullStr Genomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs
title_full_unstemmed Genomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs
title_sort genomic association and further characterisation of faecal immunoglobulin a deficiency in german shepherd dogs
publisher Wiley
publishDate 2021
url https://doaj.org/article/a6b892a429d04bf3946a633c929023d6
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AT iainrpeters genomicassociationandfurthercharacterisationoffaecalimmunoglobulinadeficiencyingermanshepherddogs
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