Peer-reviewed veterinary case report
Bacterial and fungal DNA found in dog skin inflammation lesions
By Rosa, Fabio B et al.·Published in Veterinary pathology·2018·1 Department of Veterinary Pathobiology, United States·View original on PubMed →
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Original publication title: Analysis of Bacterial and Fungal Nucleic Acid in Canine Sterile Granulomatous and Pyogranulomatous Dermatitis and Panniculitis.
- Species:
- dog
Plain-English summary
A group of dogs with skin problems called sterile granulomatous and pyogranulomatous dermatitis (SGPD) was studied to see if bacteria or fungi were causing their lesions. Researchers looked at skin samples from both affected dogs and healthy dogs and found that while certain bacteria were more common in the dogs with SGPD, the overall diversity of bacteria and fungi was similar between the two groups. This suggests that the skin lesions in these dogs are likely not caused by infections but are instead sterile. Understanding this can help veterinarians treat SGPD more effectively.
People also search for: dog skin problems treatment · sterile granulomatous dermatitis in dogs · bacteria on dog skin
Abstract
Next generation sequencing (NGS) studies are revealing a diverse microbiota on the skin of dogs. The skin microbiota of canine sterile granulomatous and pyogranulomatous dermatitis (SGPD) has yet to be investigated using NGS techniques. NGS targeting the 16S rRNA and ITS-1 region of bacterial and fungal DNA, respectively, were used to investigate if bacterial and fungal DNA were associated with skin lesions in cases of canine SGPD. The study included 20 formalin-fixed paraffin-embedded (FFPE) skin samples and 12 fresh samples from SGPD-affected dogs, and 10 FFPE and 10 fresh samples from healthy dogs. DNA was extracted from deep dermis and panniculus, and microbial DNA was amplified using primers targeting the bacterial 16S rRNA V1-V3 and fungal ITS-1 regions. The amplified DNA was utilized for NGS on an Illumina MiSeq instrument. The sequences were processed using QIIME. No differences in fungal or bacterial alpha diversity were observed between the SGPD and control samples. Beta diversity analysis demonstrated differences in the bacterial communities between SGPD and control, but not in the fungal communities. Compared to controls, the family Erysipelotrichaceae and genus Staphylococcus were significantly more abundant in the SGPD FFPE samples, and genus Corynebacterium were more abundant in fresh samples. The bacteria found to be more abundant in SGPD are common inhabitants of skin surfaces, and likely secondary contaminants in SGPD cases. This study provides additional evidence that SGPD lesions are likely sterile.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/29145794/