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原型肠聚集性大肠杆菌 042 株的全基因组序列和比较代谢组学分析。

Complete genome sequence and comparative metabolic profiling of the prototypical enteroaggregative Escherichia coli strain 042.

机构信息

Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.

出版信息

PLoS One. 2010 Jan 20;5(1):e8801. doi: 10.1371/journal.pone.0008801.

Abstract

BACKGROUND

Escherichia coli can experience a multifaceted life, in some cases acting as a commensal while in other cases causing intestinal and/or extraintestinal disease. Several studies suggest enteroaggregative E. coli are the predominant cause of E. coli-mediated diarrhea in the developed world and are second only to Campylobacter sp. as a cause of bacterial-mediated diarrhea. Furthermore, enteroaggregative E. coli are a predominant cause of persistent diarrhea in the developing world where infection has been associated with malnourishment and growth retardation.

METHODS

In this study we determined the complete genomic sequence of E. coli 042, the prototypical member of the enteroaggregative E. coli, which has been shown to cause disease in volunteer studies. We performed genomic and phylogenetic comparisons with other E. coli strains revealing previously uncharacterised virulence factors including a variety of secreted proteins and a capsular polysaccharide biosynthetic locus. In addition, by using Biolog Phenotype Microarrays we have provided a full metabolic profiling of E. coli 042 and the non-pathogenic lab strain E. coli K-12. We have highlighted the genetic basis for many of the metabolic differences between E. coli 042 and E. coli K-12.

CONCLUSION

This study provides a genetic context for the vast amount of experimental and epidemiological data published thus far and provides a template for future diagnostic and intervention strategies.

摘要

背景

大肠杆菌可以经历多方面的生活,在某些情况下作为共生菌,而在其他情况下则导致肠道和/或肠道外疾病。几项研究表明,聚集性大肠杆菌是发达国家中大肠杆菌介导的腹泻的主要原因,仅次于弯曲杆菌属,是细菌性腹泻的主要原因。此外,聚集性大肠杆菌是发展中国家持续性腹泻的主要原因,感染与营养不良和生长迟缓有关。

方法

在这项研究中,我们确定了大肠杆菌 042 的全基因组序列,大肠杆菌 042 是聚集性大肠杆菌的典型代表,已被证明在志愿者研究中会引起疾病。我们对其他大肠杆菌菌株进行了基因组和系统发育比较,揭示了以前未被描述的毒力因子,包括各种分泌蛋白和荚膜多糖生物合成基因座。此外,通过使用 Biolog 表型微阵列,我们对大肠杆菌 042 和非致病性实验室菌株大肠杆菌 K-12 进行了全面的代谢谱分析。我们强调了大肠杆菌 042 和大肠杆菌 K-12 之间许多代谢差异的遗传基础。

结论

本研究为迄今为止发表的大量实验和流行病学数据提供了遗传背景,并为未来的诊断和干预策略提供了模板。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d967/2808357/24ef1384eeb8/pone.0008801.g001.jpg

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