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发酵乳杆菌 3872 作为防治空肠弯曲菌感染的潜在工具。

Lactobacillus fermentum 3872 as a potential tool for combatting Campylobacter jejuni infections.

机构信息

a The School of Life Sciences, Pharmacy and Chemistry, SEC Faculty , Kingston University , Kingston Upon Thames , UK.

出版信息

Virulence. 2017 Nov 17;8(8):1753-1760. doi: 10.1080/21505594.2017.1362533. Epub 2017 Aug 25.

DOI:10.1080/21505594.2017.1362533
PMID:28766992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5810503/
Abstract

Due to the global spread of multidrug resistant pathogenic bacteria, alternative approaches in combating infectious diseases are required. One such approach is the use of probiotics. Lactobacillus fermentum 3872 is a promising probiotic bacterium producing a range of antimicrobial compounds, such as hydrogen peroxide and lactic acid. In addition, previous studies involving genome sequencing and analysis of L. fermentum 3872 allowed the identification of a gene encoding a cell surface protein referred to as collagen binding protein (CBP) (not found in other strains of the species, according to the GenBank database), consisting of a C-terminal cell wall anchor domain (LPXT), multiple repeats of 'B domains' that form stalks presenting an "A domain" required for adhesion. In this study, we found that the CBP of L. fermentum 3872 binds to collagen I present on the surface of the epithelial cells lining the gastrointestinal tract. Moreover, we found that this host receptor is also used for attachment by the major gastrointestinal pathogen, Campylobacter jejuni. Furthermore, we identified an adhesin involved in such interaction and demonstrated that both L. fermentum 3872 and its CBP can inhibit binding of this pathogen to collagen I. Combined with the observation that C. jejuni growth is affected in the acidic environment produced by L. fermentum 3872, the finding provides a good basis for further investigation of this strain as a potential tool for fighting Campylobacter infections.

摘要

由于多药耐药病原菌在全球范围内的传播,需要寻找对抗传染病的替代方法。其中一种方法是使用益生菌。发酵乳杆菌 3872 是一种有前途的益生菌,它能产生多种抗菌化合物,如过氧化氢和乳酸。此外,先前涉及 L. fermentum 3872 基因组测序和分析的研究,鉴定出一种编码细胞表面蛋白的基因,称为胶原蛋白结合蛋白(CBP)(根据 GenBank 数据库,在该物种的其他菌株中未发现),它由一个 C 端细胞壁锚定域(LPXT)、多个“B 结构域”的重复组成,这些结构域形成了呈现粘附所需“A 结构域”的柄。在这项研究中,我们发现 L. fermentum 3872 的 CBP 与胃肠道上皮细胞表面的胶原蛋白 I 结合。此外,我们发现这种宿主受体也被胃肠道主要病原体空肠弯曲菌用于附着。此外,我们鉴定出一种参与这种相互作用的黏附素,并证明 L. fermentum 3872 及其 CBP 都可以抑制该病原体与胶原蛋白 I 的结合。结合 C. jejuni 的生长在 L. fermentum 3872 产生的酸性环境中受到影响这一观察结果,这一发现为进一步研究该菌株作为对抗空肠弯曲菌感染的潜在工具提供了良好的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/a95142ae366e/kvir-08-08-1362533-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/498aa629525d/kvir-08-08-1362533-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/0f847edb9c01/kvir-08-08-1362533-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/d4059655c8ef/kvir-08-08-1362533-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/7cca203bd3c8/kvir-08-08-1362533-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/de6a8c0a6cca/kvir-08-08-1362533-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/a95142ae366e/kvir-08-08-1362533-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/498aa629525d/kvir-08-08-1362533-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/0f847edb9c01/kvir-08-08-1362533-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/d4059655c8ef/kvir-08-08-1362533-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/7cca203bd3c8/kvir-08-08-1362533-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/de6a8c0a6cca/kvir-08-08-1362533-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/5810503/a95142ae366e/kvir-08-08-1362533-g006.jpg

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