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利用有限超基因组模型的改进方法对金黄色葡萄球菌、肺炎链球菌和流感嗜血杆菌病原体进行比较性超基因组分析。

Comparative supragenomic analyses among the pathogens Staphylococcus aureus, Streptococcus pneumoniae, and Haemophilus influenzae using a modification of the finite supragenome model.

机构信息

Center for Genomic Sciences, Allegheny-Singer Research Institute, Pittsburgh, PA 15212, USA.

出版信息

BMC Genomics. 2011 Apr 13;12:187. doi: 10.1186/1471-2164-12-187.

Abstract

BACKGROUND

Staphylococcus aureus is associated with a spectrum of symbiotic relationships with its human host from carriage to sepsis and is frequently associated with nosocomial and community-acquired infections, thus the differential gene content among strains is of interest.

RESULTS

We sequenced three clinical strains and combined these data with 13 publically available human isolates and one bovine strain for comparative genomic analyses. All genomes were annotated using RAST, and then their gene similarities and differences were delineated. Gene clustering yielded 3,155 orthologous gene clusters, of which 2,266 were core, 755 were distributed, and 134 were unique. Individual genomes contained between 2,524 and 2,648 genes. Gene-content comparisons among all possible S. aureus strain pairs (n = 136) revealed a mean difference of 296 genes and a maximum difference of 476 genes. We developed a revised version of our finite supragenome model to estimate the size of the S. aureus supragenome (3,221 genes, with 2,245 core genes), and compared it with those of Haemophilus influenzae and Streptococcus pneumoniae. There was excellent agreement between RAST's annotations and our CDS clustering procedure providing for high fidelity metabolomic subsystem analyses to extend our comparative genomic characterization of these strains.

CONCLUSIONS

Using a multi-species comparative supragenomic analysis enabled by an improved version of our finite supragenome model we provide data and an interpretation explaining the relatively larger core genome of S. aureus compared to other opportunistic nasopharyngeal pathogens. In addition, we provide independent validation for the efficiency and effectiveness of our orthologous gene clustering algorithm.

摘要

背景

金黄色葡萄球菌与人类宿主从带菌到败血症的一系列共生关系有关,并且经常与医院获得性和社区获得性感染有关,因此菌株之间的差异基因含量很有意义。

结果

我们对三个临床株进行了测序,并将这些数据与 13 个公共人类分离株和一个牛株相结合,进行了比较基因组分析。所有基因组都使用 RAST 进行注释,然后对它们的基因相似性和差异性进行了描绘。基因聚类产生了 3155 个直系同源基因簇,其中 2266 个是核心基因,755 个是分布基因,134 个是独特基因。单个基因组包含 2524 到 2648 个基因。对所有可能的金黄色葡萄球菌菌株对(n=136)进行基因含量比较,发现平均差异为 296 个基因,最大差异为 476 个基因。我们对有限超基因组模型进行了修订,以估计金黄色葡萄球菌超基因组的大小(3221 个基因,其中 2245 个是核心基因),并将其与流感嗜血杆菌和肺炎链球菌的超基因组大小进行了比较。RAST 的注释和我们的 CDS 聚类过程非常吻合,这为代谢组学亚系统分析提供了高保真度,从而扩展了我们对这些菌株的比较基因组特征的研究。

结论

使用改进后的有限超基因组模型进行多物种比较超基因组分析,我们提供了数据和解释,说明了金黄色葡萄球菌相对于其他机会性鼻咽病原体具有相对较大的核心基因组的原因。此外,我们还为我们的直系同源基因聚类算法的效率和有效性提供了独立验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0af/3094309/39140a2728ec/1471-2164-12-187-1.jpg

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