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益生菌双歧杆菌可保护小鼠免受产志贺毒素大肠杆菌O157:H7的致命感染。

Probiotic bifidobacteria protect mice from lethal infection with Shiga toxin-producing Escherichia coli O157:H7.

作者信息

Asahara Takashi, Shimizu Kensuke, Nomoto Koji, Hamabata Takashi, Ozawa Ayako, Takeda Yoshifumi

机构信息

Yakult Central Institute for Microbiological Research, Kunitachi, Tokyo 186-8650, Japan.

出版信息

Infect Immun. 2004 Apr;72(4):2240-7. doi: 10.1128/IAI.72.4.2240-2247.2004.

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.

摘要

在致死性小鼠产志贺毒素大肠杆菌(STEC)感染模型中,研究了益生菌双歧杆菌对产志贺毒素大肠杆菌O157:H7的抗感染活性。只要给小鼠饮用含链霉素(5 mg/ml)的水,通过口服短双歧杆菌养乐多菌株(对硫酸链霉素天然耐药)就能在小鼠肠道实现稳定定植。在感染对照组中观察到的以体重显著减轻及随后死亡为特征的STEC感染致病性,在短双歧杆菌定植组中受到显著抑制。此外,短双歧杆菌定植组中肠道内STEC细胞的志贺毒素(Stx)产生几乎被完全抑制。对几种对链霉素天然耐药的双歧杆菌菌株的抗STEC活性进行比较发现,尽管双歧双歧杆菌ATCC 15696和链状双歧杆菌ATCC 27539(T)等菌株能达到与有效菌株(如短双歧杆菌养乐多菌株和假链状双歧杆菌DSM 20439)相似的高菌量水平,但它们并未赋予抗感染活性。与感染对照组(乙酸浓度28 mM;pH 7.15)相比,有效菌株产生高浓度的乙酸(56 mM)并降低肠道pH值(至pH 6.75);这些作用被认为与这些菌株的抗感染活性有关,因为发现高浓度乙酸和低pH值的组合在体外STEC生长过程中能抑制Stx产生。

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