Zuo Fanglei, Appaswamy Amulya, Gebremariam Hanna G, Jonsson Ann-Beth
Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden.
Front Microbiol. 2019 Dec 3;10:2770. doi: 10.3389/fmicb.2019.02770. eCollection 2019.
We have previously shown that Kx110A1, a human stomach isolate, can colonize mouse stomach and reduce the initial colonization of . Here, we investigated the role of sortase-dependent proteins (SDPs) involved in these functions by the construction of a mutant for , the gene encoding the housekeeping sortase that covalently anchors SDPs to the cell surface. The mutant showed a decrease in hydrophobicity and autoaggregation under acidic conditions, indicating the effect of SDPs on cell surface properties. Correspondingly, the mutant lost the capacity to adhere to gastric epithelial cells, thus resulting in an inability to provide a physical barrier to prevent adherence. These results indicate that sortase A is a key determinant of the cell surface properties of Kx110A1 and contributes to -mediated exclusion of . Understanding the molecular mechanisms by which lactobacilli antagonize might contribute to the development of novel therapeutic strategies that take advantage of health-promoting bacteria and reduce the burden of antibiotic resistance.
我们之前已经表明,人胃分离株Kx110A1能够定殖于小鼠胃部并减少[未提及的某种细菌]的初始定殖。在此,我们通过构建[未提及的某种细菌]的突变体来研究分选酶依赖性蛋白(SDPs)在这些功能中的作用,[未提及的某种细菌]是编码看家分选酶的基因,该酶将SDPs共价锚定到细胞表面。[未提及的某种细菌]突变体在酸性条件下疏水性和自聚集性降低,表明SDPs对细胞表面特性有影响。相应地,[未提及的某种细菌]突变体失去了黏附胃上皮细胞的能力,从而导致无法提供物理屏障来阻止[未提及的某种细菌]黏附。这些结果表明分选酶A是Kx110A1细胞表面特性的关键决定因素,并有助于[未提及的某种细菌]介导的对[未提及的某种细菌]的排斥。了解乳酸菌拮抗[未提及的某种细菌]的分子机制可能有助于开发利用促进健康细菌并减轻抗生素耐药性负担的新型治疗策略。