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A genomic region involved in the formation of adhesin fibers in Bacillus cereus biofilms

机译:蜡样芽胞杆菌生物膜中粘附素纤维形成的基因组区域

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摘要

Bacillus cereus is a bacterial pathogen that is responsible for many recurrent disease outbreaks due to food contamination. Spores and biofilms are considered the most important reservoirs of B. cereus in contaminated fresh vegetables and fruits. Biofilms are bacterial communities that are difficult to eradicate from biotic and abiotic surfaces because of their stable and extremely strong extracellular matrix. These extracellular matrixes contain exopolysaccharides, proteins, extracellular DNA, and other minor components. Although B. cereus can form biofilms, the bacterial features governing assembly of the protective extracellular matrix are not known. Using the well-studied bacterium B. subtilis as a model, we identified two genomic loci in B. cereus, which encodes two orthologs of the amyloid-like protein TasA of B. subtilis and a SipW signal peptidase. Deletion of this genomic region in B. cereus inhibited biofilm assembly; notably, mutation of the putative signal peptidase SipW caused the same phenotype. However, mutations in tasA or calY did not completely prevent biofilm formation; strains that were mutated for either of these genes formed phenotypically different surface attached biofilms. Electron microscopy studies revealed that TasA polymerizes to form long and abundant fibers on cell surfaces, whereas CalY does not aggregate similarly. Heterologous expression of this amyloid-like cassette in a B. subtilis strain lacking the factors required for the assembly of TasA amyloid-like fibers revealed (i) the involvement of this B. cereus genomic region in formation of the air-liquid interphase pellicles and (ii) the intrinsic ability of TasA to form fibers similar to the amyloid-like fibers produced by its B. subtilis ortholog.
机译:蜡状芽孢杆菌是一种细菌性病原体,它是由于食物污染导致许多复发性疾病暴发的原因。孢子和生物膜被认为是蜡状芽孢杆菌在受污染的新鲜蔬菜和水果中最重要的贮藏库。生物膜是细菌群落,由于其稳定且极其坚固的细胞外基质,很难从生物和非生物表面清除。这些细胞外基质包含胞外多糖,蛋白质,细胞外DNA和其他次要成分。尽管蜡状芽孢杆菌可以形成生物膜,但支配保护性细胞外基质组装的细菌特征尚不清楚。使用经过深入研究的枯草芽孢杆菌作为模型,我们在蜡状芽孢杆菌中鉴定了两个基因组位点,它们编码了枯草芽孢杆菌淀粉样蛋白TasA的两个直系同源基因和SipW信号肽酶。蜡状芽孢杆菌中该基因组区域的删除抑制了生物膜的组装。值得注意的是,推定的信号肽酶SipW的突变引起了相同的表型。但是,tasA或calY突变并不能完全阻止生物膜的形成。这些基因之一突变的菌株形成表型不同的表面附着生物膜。电子显微镜研究表明,TasA聚合形成细胞表面上长而丰富的纤维,而CalY不会类似地聚集。该淀粉样蛋白样盒在枯草芽孢杆菌菌株中的异源表达缺乏组装TasA淀粉样蛋白纤维所需的因子,显示(i)蜡样芽孢杆菌基因组区域参与了气液间膜和(ii)TasA形成与其枯草芽孢杆菌直系同源物产生的淀粉样蛋白样纤维相似的内在能力。

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