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首页> 外文期刊>Microbial Ecology: An International Journal >Aggregation Factor as an Inhibitor of Bacterial Binding to Gut Mucosa
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Aggregation Factor as an Inhibitor of Bacterial Binding to Gut Mucosa

机译:聚集因子作为细菌与肠粘膜结合的抑制剂

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摘要

Modern research in the area of probiotics is largely devoted to discovering factors that promote the adherence of probiotic candidates to host mucosal surfaces. The aim of the present study was to test the role of aggregation factor (AggL) and mucin-binding protein (MbpL) from Lactococcus sp. in adhesion to gastrointestinal mucosa. In vitro, ex vivo, and in vivo experiments in rats were used to assess the adhesive potential of these two proteins expressed in heterologous host Lactobacillus salivarius BGHO1. Although there was no influence of MbpL protein expression on BGHO1 adhesion to gut mucosa, expression of AggL had a negative effect on BGHO1 binding to ileal and colonic rat mucosa, as well as to human HT29-MTX cells and porcine gastric mucin in vitro. Because AggL did not decrease the adhesion of bacteria to intestinal fragments in ex vivo tests, where peristaltic simulation conditions were missing, we propose that intestinal motility could be a crucial force for eliminating aggregation-factor-bearing bacteria. Bacterial strains expressing aggregation factor could facilitate the removal of pathogens through the coaggregation mechanism, thus balancing gut microbial ecosystems in people affected by intestinal bacteria overgrowth.
机译:益生菌领域的现代研究主要致力于发现促进益生菌候选物粘附于宿主粘膜表面的因素。本研究的目的是测试乳球菌的聚集因子(AggL)和粘蛋白结合蛋白(MbpL)的作用。在胃肠粘膜的粘附。使用大鼠的体外,离体和体内实验评估异源宿主唾液乳杆菌BGHO1中表达的这两种蛋白的黏附潜能。尽管MbpL蛋白表达对BGHO1对肠粘膜的粘附没有影响,但是AggL的表达对BGHO1与回肠和结肠大鼠粘膜以及人HT29-MTX细胞和猪胃粘蛋白的结合具有负面影响。由于在缺少蠕动模拟条件的离体测试中,AggL不会降低细菌对肠碎片的粘附性,因此我们提出肠运动性可能是消除带有聚集因子的细菌的关键力量。表达聚集因子的细菌菌株可通过共聚集机制促进病原体的去除,从而平衡肠道细菌过度生长影响人群的肠道微生物生态系统。

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