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对具有新毒力见解的大肠杆菌 CFT073 进行基因组重新注释。

Genome reannotation of Escherichia coli CFT073 with new insights into virulence.

机构信息

State Key Laboratory for Turbulence and Complex Systems, and Department of Biomedical Engineering, College of Engineering, Peking University, Beijing 100871, China.

出版信息

BMC Genomics. 2009 Nov 22;10:552. doi: 10.1186/1471-2164-10-552.

Abstract

BACKGROUND

As one of human pathogens, the genome of Uropathogenic Escherichia coli strain CFT073 was sequenced and published in 2002, which was significant in pathogenetic bacterial genomics research. However, the current RefSeq annotation of this pathogen is now outdated to some degree, due to missing or misannotation of some essential genes associated with its virulence. We carried out a systematic reannotation by combining automated annotation tools with manual efforts to provide a comprehensive understanding of virulence for the CFT073 genome.

RESULTS

The reannotation excluded 608 coding sequences from the RefSeq annotation. Meanwhile, a total of 299 coding sequences were newly added, about one third of them are found in genomic island (GI) regions while more than one fifth of them are located in virulence related regions pathogenicity islands (PAIs). Furthermore, there are totally 341 genes were relocated with their translational initiation sites (TISs), which resulted in a high quality of gene start annotation. In addition, 94 pseudogenes annotated in RefSeq were thoroughly inspected and updated. The number of miscellaneous genes (sRNAs) has been updated from 6 in RefSeq to 46 in the reannotation. Based on the adjustment in the reannotation, subsequent analysis were conducted by both general and case studies on new virulence factors or new virulence-associated genes that are crucial during the urinary tract infections (UTIs) process, including invasion, colonization, nutrition uptaking and population density control. Furthermore, miscellaneous RNAs collected in the reannotation are believed to contribute to the virulence of strain CFT073. The reannotation including the nucleotide data, the original RefSeq annotation, and all reannotated results is freely available via http://mech.ctb.pku.edu.cn/CFT073/.

CONCLUSION

As a result, the reannotation presents a more comprehensive picture of mechanisms of uropathogenicity of UPEC strain CFT073. The new genes change the view of its uropathogenicity in many respects, particularly by new genes in GI regions and new virulence-associated factors. The reannotation thus functions as an important source by providing new information about genomic structure and organization, and gene function. Moreover, we expect that the detailed analysis will facilitate the studies for exploration of novel virulence mechanisms and help guide experimental design.

摘要

背景

作为人类病原体之一,尿路致病性大肠杆菌 CFT073 株的基因组于 2002 年被测序并公布,这在病原细菌基因组学研究中具有重要意义。然而,由于与该病原体毒力相关的一些重要基因缺失或注释错误,目前该病原体的 RefSeq 注释在某种程度上已经过时。我们通过结合自动化注释工具和人工努力,对其进行了系统的重新注释,从而提供了对 CFT073 基因组毒力的全面了解。

结果

重新注释排除了 RefSeq 注释中的 608 个编码序列。同时,共新增了 299 个编码序列,其中约三分之一位于基因组岛(GI)区域,超过五分之一位于与毒力相关的致病岛(PAI)区域。此外,共有 341 个基因的翻译起始位点(TIS)发生了重新定位,从而实现了高质量的基因起始注释。此外,RefSeq 注释中的 94 个假基因也经过了全面检查和更新。重新注释中,miscellaneous 基因(sRNAs)的数量从 RefSeq 的 6 个增加到了 46 个。基于重新注释的调整,通过对新的毒力因子或新的与尿路感染(UTI)过程中至关重要的毒力相关基因的一般和案例研究,对新的毒力因子或新的与毒力相关的基因进行了后续分析,包括入侵、定植、营养吸收和种群密度控制。此外,重新注释中收集的 miscellaneous RNA 被认为有助于 CFT073 株的毒力。核苷酸数据、原始 RefSeq 注释和所有重新注释的结果可通过 http://mech.ctb.pku.edu.cn/CFT073/ 免费获取。

结论

重新注释提供了 UPEC 菌株 CFT073 尿路致病性的更全面的机制图。新基因在许多方面改变了其尿路致病性的观点,特别是 GI 区域的新基因和新的毒力相关因子。重新注释因此作为一个重要的信息来源,提供了关于基因组结构和组织以及基因功能的新信息。此外,我们期望详细的分析将有助于探索新的毒力机制的研究,并有助于指导实验设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19a3/2785843/1aa8214bdf22/1471-2164-10-552-1.jpg

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