Peer-reviewed veterinary case report
Clostridium toxins not linked to bleeding diarrhea in dogs
By Busch, K et al.·Published in The Veterinary record·2015·Clinic of Small Animal Medicine, Germany·View original on PubMed →
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Original publication title: Clostridium perfringens enterotoxin and Clostridium difficile toxin A/B do not play a role in acute haemorrhagic diarrhoea syndrome in dogs.
- Species:
- dog
Plain-English summary
A group of 54 dogs with sudden, severe diarrhea and vomiting (known as acute hemorrhagic diarrhea syndrome or AHDS) were tested for certain bacteria and toxins to see if they were causing the symptoms. The tests showed that while some dogs had the bacteria Clostridium perfringens and Clostridium difficile, these were not linked to the severity of their illness or how long they needed to stay in the hospital. This means that these bacteria and their toxins likely do not contribute to AHDS in dogs. The dogs were treated for their symptoms, and the study suggests that other factors are responsible for this condition.
People also search for: dog diarrhea treatment · why is my dog vomiting · acute hemorrhagic diarrhea syndrome in dogs
Abstract
Although an association between clostridial pathogens and canine idiopathic acute haemorrhagic diarrhoea syndrome (AHDS) has been described, the relevance of those bacteria and their toxins remains unclear. The aim of this study was to evaluate the association between severity of clinical signs and presence of Clostridium perfringens enterotoxin (CPE) and Clostridium difficile toxin A/B (CDT A/B) in faeces of dogs with AHDS. Faecal samples of 54 dogs with idiopathic AHDS were tested by qualitative CPE and CDT A/B ELISA, and PCR was performed to detect enterotoxin genes of C. perfringens (cpe) and toxin B genes of C. difficile (cdt b). Prevalence of cdt b and CDT A/B in dogs with AHDS was 10/54 and 2/54 versus 3/23 and 0/23 in control dogs. Prevalence of cpe was 35/54 in affected versus 9/23 in control dogs. Prevalence of CPE in dogs with AHDS (13/54) was higher compared with control dogs (0/23). No significant difference was detected between CPE-positive and -negative and between cpe-positive and -negative dogs in severity of clinical signs, duration of hospitalisation, mortality rate and selected laboratory parameters. This study suggests that CPE and CDT A/B do not play a role in idiopathic AHDS, are not associated with clinical parameters in affected dogs and cannot be used to predict disease outcome.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/25467148/