Polymorphisms in the TLR4 and TLR5 gene are significantly associated with inflammatory bowel disease in German shepherd dogs

• Published in: PloS one 2010-12, Vol.5 (12), p.e15740-e15740
• Main Authors: Kathrani, Aarti, House, Arthur, Catchpole, Brian, Murphy, Angela, German, Alex, Werling, Dirk, Allenspach, Karin
• Format: Article
• Language: English
• Subjects: Alleles; Analysis; Animals; Antigens; Biology; Case-Control Studies; Chemokines; Diarrhea; Disease Models, Animal; DNA Mutational Analysis; Dogs; Female; Genes; Genetic aspects; Genomes; Haplotypes; Humans; Immune system; Infectious diseases; Inflammation; Inflammatory bowel disease; Inflammatory bowel diseases; Inflammatory Bowel Diseases - metabolism; Intestine; Linkage Disequilibrium; Male; Medicine; Mutation; Pathogenesis; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Proteins; Receptors; Risk; Salmonella; Salmonella Enteritidis; Single nucleotide polymorphisms; Single-nucleotide polymorphism; Studies; TLR2 protein; TLR4 protein; TLR5 protein; Toll-Like Receptor 2 - metabolism; Toll-Like Receptor 4 - genetics; Toll-Like Receptor 4 - metabolism; Toll-Like Receptor 5 - genetics; Toll-Like Receptor 5 - metabolism; Toll-like receptors; Veterinary colleges; Veterinary Science; Vomiting
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0015740

Inflammatory bowel disease (IBD) is considered to be the most common cause of vomiting and diarrhoea in dogs, and the German shepherd dog (GSD) is particularly susceptible. The exact aetiology of IBD is unknown, however associations have been identified between specific single-nucleotide polymorphisms (SNPs) in Toll-like receptors (TLRs) and human IBD. However, to date, no genetic studies have been undertaken in canine IBD. The aim of this study was to investigate whether polymorphisms in canine TLR 2, 4 and 5 genes are associated with IBD in GSDs. Mutational analysis of TLR2, TLR4 and TLR5 was performed in 10 unrelated GSDs with IBD. Four non-synonymous SNPs (T23C, G1039A, A1571T and G1807A) were identified in the TLR4 gene, and three non-synonymous SNPs (G22A, C100T and T1844C) were identified in the TLR5 gene. The non-synonymous SNPs identified in TLR4 and TLR5 were evaluated further in a case-control study using a SNaPSHOT multiplex reaction. Sequencing information from 55 unrelated GSDs with IBD were compared to a control group consisting of 61 unrelated GSDs. The G22A SNP in TLR5 was significantly associated with IBD in GSDs, whereas the remaining two SNPs were found to be significantly protective for IBD. Furthermore, the two SNPs in TLR4 (A1571T and G1807A) were in complete linkage disequilibrium, and were also significantly associated with IBD. The TLR5 risk haplotype (ACC) without the two associated TLR4 SNP alleles was significantly associated with IBD, however the presence of the two TLR4 SNP risk alleles without the TLR5 risk haplotype was not statistically associated with IBD. Our study suggests that the three TLR5 SNPs and two TLR4 SNPs; A1571T and G1807A could play a role in the pathogenesis of IBD in GSDs. Further studies are required to confirm the functional importance of these polymorphisms in the pathogenesis of this disease.