Upregulation of Toll-Like Receptors in Chronic Enteropathies in Dogs

Background: Inflammatory bowel disease (IBD) is thought to result from a dysregulated interaction between the host immune system and commensal microflora. Toll‐like receptors (TLRs) recognize microbe‐associated molecular patterns (MAMPs), but their role in enteropathies in dogs is unknown. Hypothesi...

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Veröffentlicht in:Journal of veterinary internal medicine 2008-05, Vol.22 (3), p.553-560
Hauptverfasser: Burgener, I.A, Konig, A, Allenspach, K, Sauter, S.N, Boisclair, J, Doherr, M.G, Jungi, T.W
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container_end_page 560
container_issue 3
container_start_page 553
container_title Journal of veterinary internal medicine
container_volume 22
creator Burgener, I.A
Konig, A
Allenspach, K
Sauter, S.N
Boisclair, J
Doherr, M.G
Jungi, T.W
description Background: Inflammatory bowel disease (IBD) is thought to result from a dysregulated interaction between the host immune system and commensal microflora. Toll‐like receptors (TLRs) recognize microbe‐associated molecular patterns (MAMPs), but their role in enteropathies in dogs is unknown. Hypothesis: That there is a dysregulation of TLRs recognizing bacterial MAMPs in dogs with IBD. Animals: Sixteen healthy beagles and 12 dogs with steroid‐treated (ST) and 23 dogs with food‐responsive (FR) diarrhea. Methods: Prospective, observational study. mRNA expression of canine TLR2, 4, and 9 was evaluated by quantitative real‐time RT‐PCR in duodenal and colonic biopsies obtained before and after standard therapy. Samples from control dogs were taken at necropsy, with additional biopsies of stomach, jejunum, ileum, and mesenteric lymph node in 6 dogs. Results: There were significant differences (P≤ .017) in expression of TLR2, 4, and 9 between the 6 sampled locations in healthy control dogs (lymph node > small intestine ≥ colon). Before therapy, ST expressed more mRNA than control dogs for all 3 receptors (P < .05). There were no significant differences between pretreatment and posttreatment values, even though 32/35 dogs improved clinically. No associations were found when comparing receptor mRNA expression with either histology or clinical activity scores. Conclusions and Clinical Importance: Bacteria‐responsive TLR2, 4, and 9 are upregulated in duodenal and colonic mucosa in IBD. This might lead to increased inflammation through interaction with the commensal flora. The absence of significant changes after therapy despite clinical improvement might point toward the existence of a genetic predisposition to IBD as described in human IBD.
doi_str_mv 10.1111/j.1939-1676.2008.0093.x
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Toll‐like receptors (TLRs) recognize microbe‐associated molecular patterns (MAMPs), but their role in enteropathies in dogs is unknown. Hypothesis: That there is a dysregulation of TLRs recognizing bacterial MAMPs in dogs with IBD. Animals: Sixteen healthy beagles and 12 dogs with steroid‐treated (ST) and 23 dogs with food‐responsive (FR) diarrhea. Methods: Prospective, observational study. mRNA expression of canine TLR2, 4, and 9 was evaluated by quantitative real‐time RT‐PCR in duodenal and colonic biopsies obtained before and after standard therapy. Samples from control dogs were taken at necropsy, with additional biopsies of stomach, jejunum, ileum, and mesenteric lymph node in 6 dogs. Results: There were significant differences (P≤ .017) in expression of TLR2, 4, and 9 between the 6 sampled locations in healthy control dogs (lymph node &gt; small intestine ≥ colon). Before therapy, ST expressed more mRNA than control dogs for all 3 receptors (P &lt; .05). There were no significant differences between pretreatment and posttreatment values, even though 32/35 dogs improved clinically. No associations were found when comparing receptor mRNA expression with either histology or clinical activity scores. Conclusions and Clinical Importance: Bacteria‐responsive TLR2, 4, and 9 are upregulated in duodenal and colonic mucosa in IBD. This might lead to increased inflammation through interaction with the commensal flora. The absence of significant changes after therapy despite clinical improvement might point toward the existence of a genetic predisposition to IBD as described in human IBD.</description><identifier>ISSN: 0891-6640</identifier><identifier>EISSN: 1939-1676</identifier><identifier>DOI: 10.1111/j.1939-1676.2008.0093.x</identifier><identifier>PMID: 18466244</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Animals ; Case-Control Studies ; Chronic Disease ; Commensal bacteria ; Dog Diseases - genetics ; Dog Diseases - metabolism ; Dogs ; Female ; Food Hypersensitivity - genetics ; Food Hypersensitivity - metabolism ; Food Hypersensitivity - veterinary ; Food-responsive diarrhea ; Gastrointestinal Tract - metabolism ; Gastrointestinal Tract - pathology ; Gene Expression Regulation ; Inflammatory bowel disease ; Inflammatory Bowel Diseases - genetics ; Inflammatory Bowel Diseases - metabolism ; Inflammatory Bowel Diseases - veterinary ; Intestinal Diseases - genetics ; Intestinal Diseases - metabolism ; Intestinal Diseases - veterinary ; Male ; Microbe-associated molecular patterns ; Mucosal immunity ; receptors ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Toll-Like Receptors - genetics ; Toll-Like Receptors - metabolism ; Up-Regulation</subject><ispartof>Journal of veterinary internal medicine, 2008-05, Vol.22 (3), p.553-560</ispartof><rights>Copyright © 2008 by the American College of Veterinary Internal Medicine</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5233-6ff74ac04d0bd3d0ec21c000236238679eab8dce7019c7a69176860bffa7097c3</citedby><cites>FETCH-LOGICAL-c5233-6ff74ac04d0bd3d0ec21c000236238679eab8dce7019c7a69176860bffa7097c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1939-1676.2008.0093.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1939-1676.2008.0093.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,11562,27924,27925,45574,45575,46052,46476</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1939-1676.2008.0093.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18466244$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burgener, I.A</creatorcontrib><creatorcontrib>Konig, A</creatorcontrib><creatorcontrib>Allenspach, K</creatorcontrib><creatorcontrib>Sauter, S.N</creatorcontrib><creatorcontrib>Boisclair, J</creatorcontrib><creatorcontrib>Doherr, M.G</creatorcontrib><creatorcontrib>Jungi, T.W</creatorcontrib><title>Upregulation of Toll-Like Receptors in Chronic Enteropathies in Dogs</title><title>Journal of veterinary internal medicine</title><addtitle>J Vet Intern Med</addtitle><description>Background: Inflammatory bowel disease (IBD) is thought to result from a dysregulated interaction between the host immune system and commensal microflora. Toll‐like receptors (TLRs) recognize microbe‐associated molecular patterns (MAMPs), but their role in enteropathies in dogs is unknown. Hypothesis: That there is a dysregulation of TLRs recognizing bacterial MAMPs in dogs with IBD. Animals: Sixteen healthy beagles and 12 dogs with steroid‐treated (ST) and 23 dogs with food‐responsive (FR) diarrhea. Methods: Prospective, observational study. mRNA expression of canine TLR2, 4, and 9 was evaluated by quantitative real‐time RT‐PCR in duodenal and colonic biopsies obtained before and after standard therapy. Samples from control dogs were taken at necropsy, with additional biopsies of stomach, jejunum, ileum, and mesenteric lymph node in 6 dogs. Results: There were significant differences (P≤ .017) in expression of TLR2, 4, and 9 between the 6 sampled locations in healthy control dogs (lymph node &gt; small intestine ≥ colon). Before therapy, ST expressed more mRNA than control dogs for all 3 receptors (P &lt; .05). There were no significant differences between pretreatment and posttreatment values, even though 32/35 dogs improved clinically. No associations were found when comparing receptor mRNA expression with either histology or clinical activity scores. Conclusions and Clinical Importance: Bacteria‐responsive TLR2, 4, and 9 are upregulated in duodenal and colonic mucosa in IBD. This might lead to increased inflammation through interaction with the commensal flora. 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There were no significant differences between pretreatment and posttreatment values, even though 32/35 dogs improved clinically. No associations were found when comparing receptor mRNA expression with either histology or clinical activity scores. Conclusions and Clinical Importance: Bacteria‐responsive TLR2, 4, and 9 are upregulated in duodenal and colonic mucosa in IBD. This might lead to increased inflammation through interaction with the commensal flora. The absence of significant changes after therapy despite clinical improvement might point toward the existence of a genetic predisposition to IBD as described in human IBD.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>18466244</pmid><doi>10.1111/j.1939-1676.2008.0093.x</doi><tpages>8</tpages></addata></record>
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source Wiley Online Library (Open Access Collection)
subjects Animals
Case-Control Studies
Chronic Disease
Commensal bacteria
Dog Diseases - genetics
Dog Diseases - metabolism
Dogs
Female
Food Hypersensitivity - genetics
Food Hypersensitivity - metabolism
Food Hypersensitivity - veterinary
Food-responsive diarrhea
Gastrointestinal Tract - metabolism
Gastrointestinal Tract - pathology
Gene Expression Regulation
Inflammatory bowel disease
Inflammatory Bowel Diseases - genetics
Inflammatory Bowel Diseases - metabolism
Inflammatory Bowel Diseases - veterinary
Intestinal Diseases - genetics
Intestinal Diseases - metabolism
Intestinal Diseases - veterinary
Male
Microbe-associated molecular patterns
Mucosal immunity
receptors
RNA, Messenger - genetics
RNA, Messenger - metabolism
Toll-Like Receptors - genetics
Toll-Like Receptors - metabolism
Up-Regulation
title Upregulation of Toll-Like Receptors in Chronic Enteropathies in Dogs
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