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1.
Toxicological Research ; : 99-106, 2013.
Article in English | WPRIM | ID: wpr-59642

ABSTRACT

Clostridium difficile infection (CDI) has become a significant threat to public health. Although broad-spectrum antibiotic therapy is the primary treatment option for CDI, its use has evident limitations. Probiotics have been proved to be effective in the treatment of CDI and are a promising therapeutic option for CDI. In this study, 4 strains of lactic acid bacteria (LAB), namely, Lactobacillus rhamnosus (LR5), Lactococ-cuslactis (SL3), Bifidobacterium breve (BR3), and Bifidobacterium lactis (BL3) were evaluated for their anti-C. difficile activity. Co-culture incubation of C. difficile (106 and 1010 CFU/ml) with each strain of LAB indicated that SL3 possessed the highest antimicrobial activity over a 24-hr period. The cell-free supernatants of the 4 LAB strains exhibited MIC50 values between 0.424 mg/ml (SL3) and 1.318 (BR3) mg/ml. These results may provide a basis for alternative therapies for the treatment of C. difficile-associated gut disorders.


Subject(s)
Bacteria , Bifidobacterium , Clostridium , Clostridioides difficile , Coculture Techniques , Complementary Therapies , Lactic Acid , Lacticaseibacillus rhamnosus , Probiotics , Public Health , Pyridines , Sprains and Strains , Thiazoles
2.
Journal of Veterinary Science ; : 165-167, 2009.
Article in English | WPRIM | ID: wpr-54362

ABSTRACT

The effect of extracellular beta-(1-->3), (1-->6)-glucan, produced by Paenibacillus polymyxa JB115, on nitric oxide (NO) production in RAW264.7 macrophages was investigated. beta-glucan induced the production of NO by RAW264.7 macrophages in a concentration- and time-dependent manner. Moreover, beta-glucan stimulation increased the mRNA expression of iNOS, COX-2 and IL-6 in RAW264.7 macrophages in a concentration-dependent manner.


Subject(s)
Animals , Mice , Bacillus/metabolism , Cell Line , Cyclooxygenase 2/biosynthesis , Interleukin-6/biosynthesis , Lipopolysaccharides/pharmacology , Macrophages/drug effects , Nitric Oxide/biosynthesis , Nitric Oxide Synthase Type II/biosynthesis , RNA, Messenger/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction , beta-Glucans/metabolism
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