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Probiotic bifidobacteria protect mice from lethal infection with Shiga toxin-producing Escherichia coli O157:H7
Takashi Asahara1, Kensuke Shimizu, Koji Nomoto
1Yakult Central Institute for Microbiological Research, Kunitachi, Tokyo 186-8650, Japan.
Abstract:
The anti-infectious activity of probiotic Bifidobacteria against Shiga toxin-producing Escherichia coli (STEC) O157:H7 was examined in a fatal mouse STEC infection model. Stable colonization of the murine intestines was achieved by the oral administration of Bifidobacterium breve strain Yakult (naturally resistant to streptomycin sulfate) as long as the mice were treated with streptomycin in their drinking water (5 mg/ml). The pathogenicity of STEC infection, characterized by marked body weight loss and subsequent death, observed in the infected controls was dramatically inhibited in the B. breve-colonized group. Moreover, Stx production by STEC cells in the intestine was almost completely inhibited in the B. breve-colonized group. A comparison of anti-STEC activity among several Bifidobacterium strains with natural resistance to streptomycin revealed that strains such as Bifidobacterium bifidum ATCC 15696 and Bifidobacterium catenulatum ATCC 27539(T) did not confer an anti-infectious activity, despite achieving high population levels similar to those of effective strains, such as B. breve strain Yakult and Bifidobacterium pseudocatenulatum DSM 20439. The effective strains produced a high concentration of acetic acid (56 mM) and lowered the pH of the intestine (to pH 6.75) compared to the infected control group (acetic acid concentration, 28 mM; pH, 7.15); these effects were thought to be related to the anti-infectious activity of these strains because the combination of a high concentration of acetic acid and a low pH was found to inhibit Stx production during STEC growth in vitro.
Insights
Probiotic Bifidobacteria, specifically Bifidobacterium breve, effectively inhibited Shiga toxin-producing Escherichia coli (STEC) O157:H7 infection in mice. This probiotic action was linked to increased acetic acid production and lower gut pH, reducing toxin output.
Area of Science:
- Microbiology
- Gastroenterology
- Immunology
Background:
- Shiga toxin-producing Escherichia coli (STEC) O157:H7 causes severe infections.
- Probiotics are being investigated for their potential to combat bacterial pathogens.
Purpose of the Study:
- To evaluate the anti-infectious efficacy of probiotic Bifidobacteria against STEC O157:H7 in a murine model.
- To identify specific Bifidobacterium strains and their mechanisms of action against STEC.
Main Methods:
- Oral administration of Bifidobacterium breve strain Yakult to streptomycin-treated mice to achieve intestinal colonization.
- Infection of mice with STEC O157:H7 and monitoring of clinical signs (weight loss, mortality).
- Measurement of Shiga toxin (Stx) production and analysis of gut environment (pH, acetic acid concentration).
Main Results:
- Bifidobacterium breve colonization significantly inhibited STEC O157:H7 pathogenicity, reducing weight loss and mortality.
- Shiga toxin production by STEC in the intestine was nearly completely inhibited in B. breve-colonized mice.
- Effective anti-STEC strains, like B. breve Yakult, produced high acetic acid levels and lowered intestinal pH, unlike ineffective strains.
Conclusions:
- Bifidobacterium breve demonstrates significant anti-infectious activity against STEC O157:H7 in a mouse model.
- The anti-infectious effect is associated with acetic acid production and pH reduction, which inhibit Shiga toxin production.
- Specific Bifidobacterium strains vary in their efficacy against STEC, highlighting the importance of strain selection.
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