1990
DOI: 10.11150/kansenshogakuzasshi1970.64.1425
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Preventive Effect of Clostridium butyricum M588 against the Proliferation of Clostridium difficile during Antimicrobial Therapy

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Cited by 12 publications
(7 citation statements)
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“…The analysis of the KEGG categories revealed that vitamin, amino acid and O-glycan biosynthesis were the most enriched metabolic pathways. C. butyricum ferments in the cecum and thus provides a large number of SCFA, amino acids, vitamins and other metabolites to the host ( Kuroiwa et al., 1990 ; Yang et al., 2012 ). These abundant nutrients are transported into epithelial cells of the cecal mucosa through the upregulation of carrier genes, such as solute carrier family 7 member 11 ( SLC7A11 ), low-density lipoprotein-related protein 2 ( LRP2 ), translocator protein 2 ( TSPO2 ), hemoglobin subunit mu ( HBM ), hemoglobin subunit alpha 1 ( HBA1 ) and ENSGALG00000050921 (very-long-chain fatty acid-CoA ligase activity), which might shed light on the mechanisms through which dietary supplementation with C. butyricum can improve growth performance ( Table 1 ).…”
Section: Discussionmentioning
confidence: 99%
“…The analysis of the KEGG categories revealed that vitamin, amino acid and O-glycan biosynthesis were the most enriched metabolic pathways. C. butyricum ferments in the cecum and thus provides a large number of SCFA, amino acids, vitamins and other metabolites to the host ( Kuroiwa et al., 1990 ; Yang et al., 2012 ). These abundant nutrients are transported into epithelial cells of the cecal mucosa through the upregulation of carrier genes, such as solute carrier family 7 member 11 ( SLC7A11 ), low-density lipoprotein-related protein 2 ( LRP2 ), translocator protein 2 ( TSPO2 ), hemoglobin subunit mu ( HBM ), hemoglobin subunit alpha 1 ( HBA1 ) and ENSGALG00000050921 (very-long-chain fatty acid-CoA ligase activity), which might shed light on the mechanisms through which dietary supplementation with C. butyricum can improve growth performance ( Table 1 ).…”
Section: Discussionmentioning
confidence: 99%
“…C. difficile is a common pathogen responsible for a large proportion of AAD cases, and in a human study C. butyricum administration was associated with decreased fecal levels of C. difficile as well as the toxin it produces. 79 More recently, Woo and colleagues demonstrated that in vitro co-culture of C. difficile with CBM 588 decreased the pathogen’s toxicity in a dose-dependent manner. 80 Oka et al .…”
Section: Evidence From Murine Models Of Diseasementioning
confidence: 99%
“…Shimbo et al (2005) and Imase et al (2008) observed stabilising effects on the intestinal microbiota when CBM 588 was administered as a supplement during the antibiotic eradication of Helicobacter pylori infection. Furthermore, it has been found that CBM 588 is able to suppress the production of Clostridium difficile toxins after antimicrobial therapy in humans and also to inhibit some strains of Vibrio cholerae, Aeromonas hydrophila, and Shigella flexneri in mixed cultures (Kuroiwa et al 1990). CBM 588 was also tested in rats, wherein it was able to mitigate the symptoms of dextran sulphate sodium-induced colitis and also increased the counts of lactobacilli in their gut (Okamoto et al 2000).…”
mentioning
confidence: 99%