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One dog’s waste is another dog’s wealth : a pilot study of fecal microbiota transplantation in dogs with acute hemorrhagic diarrhea syndrome
One dog’s waste is another dog’s wealth : a pilot study of fecal microbiota transplantation in dogs with acute hemorrhagic diarrhea syndrome
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One dog’s waste is another dog’s wealth : a pilot study of fecal microbiota transplantation in dogs with acute hemorrhagic diarrhea syndrome
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One dog’s waste is another dog’s wealth : a pilot study of fecal microbiota transplantation in dogs with acute hemorrhagic diarrhea syndrome
One dog’s waste is another dog’s wealth : a pilot study of fecal microbiota transplantation in dogs with acute hemorrhagic diarrhea syndrome

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One dog’s waste is another dog’s wealth : a pilot study of fecal microbiota transplantation in dogs with acute hemorrhagic diarrhea syndrome
One dog’s waste is another dog’s wealth : a pilot study of fecal microbiota transplantation in dogs with acute hemorrhagic diarrhea syndrome
Journal Article

One dog’s waste is another dog’s wealth : a pilot study of fecal microbiota transplantation in dogs with acute hemorrhagic diarrhea syndrome

2021
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Overview
Canine acute hemorrhagic diarrhea syndrome (AHDS) has been associated in some studies with Clostridioides perfringens overgrowth and toxin-mediated necrosis of the intestinal mucosa. We aimed to determine the effect of a single fecal microbiota transplantation (FMT) on clinical scores and fecal microbiomes of 1 and 7 dogs with AHDS from New Zealand and South Africa. We hypothesized that FMT would improve AHDS clinical scores and increase microbiota alpha-diversity and short-chain fatty acid (SCFA)-producing microbial communities’ abundances in dogs with AHDS after FMT. We sequenced the V3-V4 region of the 16S-rRNA gene in the feces of AHDS FMT-recipients and sham-treated control dogs, and their healthy donors at admission, discharge, and 30 days post-discharge. There were no significant differences in median AHDS clinical scores between FMT-recipients and sham-treated controls at admission or discharge (P = 0.22, P = 0.41). At admission, the Shannon diversity index (SDI) was lower in AHDS dogs than healthy donors (P = 0.002). The SDI did not change from admission to 30 days in sham-treated dogs yet increased in FMT-recipients from admission to discharge (P = 0.04) to levels not different than donors (P = 0.33) but significantly higher than sham-treated controls (P = 0.002). At 30 days, the SDI did not differ between FMT recipients, sham-treated controls, and donors (P = 0.88). Principal coordinate analysis of the Bray-Curtis index separated post-FMT and donor dogs from pre-FMT and sham-treated dogs (P = 0.009) because of increased SCFA-producing genera’s abundances after FMT. A single co-abundance subnetwork contained many of the same OTUs found to be differentially abundant in FMT-recipients, and the abundance of this module was increased in FMT-recipients at discharge and 30 days, compared to shamtreated controls. We conclude in this small pilot study FMT did not have any clinical benefit.