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Comparative Genomic Analyses of Seventeen Streptococcus pneumoniae Strains: Insights into the Pneumococcal Supragenome

机译:十七个肺炎链球菌菌株的比较基因组分析:肺炎球菌超基因组的见解。

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摘要

The distributed-genome hypothesis (DGH) states that pathogenic bacteria possess a supragenome that is much larger than the genome of any single bacterium and that these pathogens utilize genetic recombination and a large, noncore set of genes as a means of diversity generation. We sequenced the genomes of eight nasopharyngeal strains of Streptococcus pneumoniae isolated from pediatric patients with upper respiratory symptoms and performed quantitative genomic analyses among these and nine publicly available pneumococcal strains. Coding sequences from all strains were grouped into 3,170 orthologous gene clusters, of which 1,454 (46%) were conserved among all 17 strains. The majority of the gene clusters, 1,716 (54%), were not found in all strains. Genic differences per strain pair ranged from 35 to 629 orthologous clusters, with each strain's genome containing between 21 and 32% noncore genes. The distribution of the orthologous clusters per genome for the 17 strains was entered into the finite-supragenome model, which predicted that (i) the S. pneumoniae supragenome contains more than 5,000 orthologous clusters and (ii) 99% of the orthologous clusters (∼3,000) that are represented in the S. pneumoniae population at frequencies of ≥0.1 can be identified if 33 representative genomes are sequenced. These extensive genic diversity data support the DGH and provide a basis for understanding the great differences in clinical phenotype associated with various pneumococcal strains. When these findings are taken together with previous studies that demonstrated the presence of a supragenome for Streptococcus agalactiae and Haemophilus influenzae, it appears that the possession of a distributed genome is a common host interaction strategy.
机译:分布式基因组假说(DGH)指出,致病细菌的超基因组比任何一种细菌的基因组都要大得多,并且这些病原体利用基因重组和大量的非核心基因集作为多样性产生的一种手段。我们对从患有上呼吸道症状的儿科患者中分离出的八株肺炎链球菌肺炎链球菌菌株的基因组进行了测序,并对这九种可公开获得的肺炎球菌菌株进行了定量基因组分析。来自所有菌株的编码序列被分组为3170个直系同源基因簇,其中在所有17个菌株中保守了1454个(46%)。在所有菌株中均未发现大多数基因簇,即1,716个(54%)。每个菌株对的遗传差异范围为35至629个直系同源簇,每个菌株的基因组包含21%至32%的非核心基因。将这17个菌株的直系同源簇的分布输入到有限超基因组模型中,该模型预测(i)肺炎链球菌超基因组包含超过5,000个直系同源簇,以及(ii)99%的直系同源簇(〜如果对33个代表性基因组进行了测序,则可以鉴定出在肺炎链球菌群体中以≥0.1的频率出现的3,000个)。这些广泛的基因多样性数据支持DGH,并为理解与各种肺炎球菌菌株相关的临床表型的巨大差异提供了基础。当将这些发现与以前的研究一起证明无乳链球菌和流感嗜血杆菌存在超基因组时,似乎拥有一个分布式基因组是一种常见的宿主相互作用策略。

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