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首页> 外文期刊>Microbiology and biotechnology letters >Comparative Genomic Analysis of Lactobacillus rhamnosus BFE5264, a Probiotic Strain Isolated from Traditional Maasai Fermented Milk
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Comparative Genomic Analysis of Lactobacillus rhamnosus BFE5264, a Probiotic Strain Isolated from Traditional Maasai Fermented Milk

机译:乳酸杆菌BFE5264的比较基因组分析,传统马赛发酵牛奶中分离的益生菌菌株

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Lactobacillus rhamnosus BFE5264, isolated from a Maasai fermented milk product ("kule naoto"), was previously shown to exhibit bile acid resistance, cholesterol assimilation, and adhesion to HT29-MTX cells in vitro. In this study, we re-annotated andanalyzed the previously reported complete genome sequence of strain BFE5264. The genome consists of a circular chromosome of 3,086,152 bp and a putative plasmid, which is the largest one identified among L. rhamnosus strains. Among the 2,883 predicted protein-coding genes, those with carbohydrate-related functions were the most abundant. Genome analysis of strain BFE5264 revealed two consecutive CRISPR regions and no known virulence factors or antimicrobial resistance genes. In addition, previously known highly variable regions in the genomes of L. rhamnosus strains were also evident in strain BFE5264. Pairwise comparison with the most studied probiotic strain L. rhamnosus GG revealed strain BFE5264-specific deletions, probably due to insertion sequence-mediated recombination. The latter was associated with loss of the spaCBA pilin gene cluster and exopolysaccharide biosynthetic genes. Comparative genomic analysis of the sequences from all available L. rhamnosus strains revealed that they were clustered into two groups, being within the same species boundary based on the average nucleotide identities. Strain BFE5264 had a sister group relationship with the group that contained strain GG, but neither ANI-based hierarchical clustering nor core-gene-based phylogenetic tree construction showed a clear distinctive pattern associated with the isolation source, implying that the genotype alone cannot account for their ecological niches. These results provide insights into the probiotic mechanisms of strainBFE5264 at the genomic level.
机译:从Maasai发酵乳制品(“kule naoto”)中分离的乳杆菌菌菌菌菌菌菌菌菌株(“Kule naoto”),以表现出胆汁酸性抗性,胆固醇同化和对HT29-MTX细胞的粘附性。在这项研究中,我们重新注释并分析了先前报道的菌株BFE5264的完整基因组序列。基因组由3,086,152bp的圆形染色体和推定的质粒组成,这是L. rhamosus菌株中鉴定的最大的质粒。在2,883个预测的蛋白质编码基因中,含有碳水化合物相关功能的蛋白质中最丰富的蛋白质编码基因。菌株BFE5264的基因组分析显示出两个连续的克切区区域,没有已知的毒力因子或抗微生物抗性基因。另外,在菌株BFE5264中也显而易见的L. rhamosus菌株的先前已知的高度可变区。与最研究的益生菌菌株L.Rhamnosus GG的成对比较显示出菌株BFE5264特异性缺失,可能是由于插入序列介导的重组。后者与SpacBA菌素基因簇和外偶糖生物合成基因的损失有关。来自所有可用L. rhamosus菌株的序列的比较基因组分析显示将它们聚集成两组,基于平均核苷酸同一性在相同的物种边界内。菌株BFE5264与含有菌株GG的组进行患者群体关系,但既不是基于ANI的分层聚类,也没有基于核心基因的系统发育树施工显示出与隔离源相关的明显独特的模式,这意味着单独的基因型不能解释他们的生态利基。这些结果提供了对基因组水平菌株BFE5264的益生菌机制的见解。

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