» Articles » PMID: 23300577

The Fecal Microbiome in Dogs with Acute Diarrhea and Idiopathic Inflammatory Bowel Disease

Abstract

Background: Recent molecular studies have revealed a highly complex bacterial assembly in the canine intestinal tract. There is mounting evidence that microbes play an important role in the pathogenesis of acute and chronic enteropathies of dogs, including idiopathic inflammatory bowel disease (IBD). The aim of this study was to characterize the bacterial microbiota in dogs with various gastrointestinal disorders.

Methodology/principal Findings: Fecal samples from healthy dogs (n = 32), dogs with acute non-hemorrhagic diarrhea (NHD; n = 12), dogs with acute hemorrhagic diarrhea (AHD; n = 13), and dogs with active (n = 9) and therapeutically controlled idiopathic IBD (n = 10) were analyzed by 454-pyrosequencing of the 16S rRNA gene and qPCR assays. Dogs with acute diarrhea, especially those with AHD, had the most profound alterations in their microbiome, as significant separations were observed on PCoA plots of unweighted Unifrac distances. Dogs with AHD had significant decreases in Blautia, Ruminococcaceae including Faecalibacterium, and Turicibacter spp., and significant increases in genus Sutterella and Clostridium perfringens when compared to healthy dogs. No significant separation on PCoA plots was observed for the dogs with IBD. Faecalibacterium spp. and Fusobacteria were, however, decreased in the dogs with clinically active IBD, but increased during time periods of clinically insignificant IBD, as defined by a clinical IBD activity index (CIBDAI).

Conclusions: Results of this study revealed a bacterial dysbiosis in fecal samples of dogs with various GI disorders. The observed changes in the microbiome differed between acute and chronic disease states. The bacterial groups that were commonly decreased during diarrhea are considered to be important short-chain fatty acid producers and may be important for canine intestinal health. Future studies should correlate these observed phylogenetic differences with functional changes in the intestinal microbiome of dogs with defined disease phenotypes.

Citing Articles

Exploring Gut Microbiota-Targeted Therapies for Canine Idiopathic Epilepsy.

Blanquet L, Serra D, Marrinhas C, Almeida A Int J Mol Sci. 2025; 26(4).

PMID: 40004205 PMC: 11855791. DOI: 10.3390/ijms26041742.


Shaping the human gut microbiota: The role of canine companionship, lifestyle choices, and sp.

Pavlickova Z, Pafco B, Ilik V, Andersen L, Jirku M, Brozova K One Health. 2025; 20:100979.

PMID: 39944406 PMC: 11815985. DOI: 10.1016/j.onehlt.2025.100979.


Sustainable, greenhouse gas derived fermented protein in canine diets-a pilot study.

Babu R, Padmanabhan S, Ganesan R, Subbian E, Van T, Eri R Front Vet Sci. 2025; 11:1477182.

PMID: 39867602 PMC: 11758626. DOI: 10.3389/fvets.2024.1477182.


Effects of Chenpi ( cv. ) on serum antioxidant enzymes, inflammatory factors, and intestinal health in Beagle dogs.

Wang W, Xu L, Zhang Y, Cao Y, Yang Y, Liu G Front Microbiol. 2025; 15():1415860.

PMID: 39839098 PMC: 11747223. DOI: 10.3389/fmicb.2024.1415860.


Apparent total tract nutrient digestibility of frozen raw, freeze-dried raw, fresh, and extruded dog foods and their effects on serum metabolites and fecal characteristics, metabolites, and microbiota of healthy adult dogs.

Geary E, Oba P, Templeman J, Swanson K Transl Anim Sci. 2024; 8:txae163.

PMID: 39687915 PMC: 11648562. DOI: 10.1093/tas/txae163.


References
1.
Sokol H, Seksik P, Furet J, Firmesse O, Nion-Larmurier I, Beaugerie L . Low counts of Faecalibacterium prausnitzii in colitis microbiota. Inflamm Bowel Dis. 2009; 15(8):1183-9. DOI: 10.1002/ibd.20903. View

2.
Gurjar A, Hegde N, Love B, Jayarao B . Real-time multiplex PCR assay for rapid detection and toxintyping of Clostridium perfringens toxin producing strains in feces of dairy cattle. Mol Cell Probes. 2007; 22(2):90-5. DOI: 10.1016/j.mcp.2007.08.001. View

3.
Jergens A, Schreiner C, Frank D, Niyo Y, Ahrens F, Eckersall P . A scoring index for disease activity in canine inflammatory bowel disease. J Vet Intern Med. 2003; 17(3):291-7. DOI: 10.1111/j.1939-1676.2003.tb02450.x. View

4.
Gontcharova V, Youn E, Wolcott R, Hollister E, Gentry T, Dowd S . Black Box Chimera Check (B2C2): a Windows-Based Software for Batch Depletion of Chimeras from Bacterial 16S rRNA Gene Datasets. Open Microbiol J. 2011; 4:47-52. PMC: 3040993. DOI: 10.2174/1874285801004010047. View

5.
Marks S, Rankin S, Byrne B, Weese J . Enteropathogenic bacteria in dogs and cats: diagnosis, epidemiology, treatment, and control. J Vet Intern Med. 2011; 25(6):1195-208. DOI: 10.1111/j.1939-1676.2011.00821.x. View