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金黄色葡萄球菌致病岛3的特征及表达分析。对葡萄球菌致病岛进化的启示。

Characterization and expression analysis of Staphylococcus aureus pathogenicity island 3. Implications for the evolution of staphylococcal pathogenicity islands.

作者信息

Yarwood Jeremy M, McCormick John K, Paustian Michael L, Orwin Paul M, Kapur Vivek, Schlievert Patrick M

机构信息

Department of Microbiology, University of Minnesota Medical School, 420 Delaware Street SE, Minneapolis, MN 55455, USA.

出版信息

J Biol Chem. 2002 Apr 12;277(15):13138-47. doi: 10.1074/jbc.M111661200. Epub 2002 Jan 30.

Abstract

We describe the complete sequence of the 15.9-kb staphylococcal pathogenicity island 3 encoding staphylococcal enterotoxin serotypes B, K, and Q. The island, which meets the generally accepted definition of pathogenicity islands, contains 24 open reading frames potentially encoding proteins of more than 50 amino acids, including an apparently functional integrase. The element is bordered by two 17-bp direct repeats identical to those found flanking staphylococcal pathogenicity island 1. The island has extensive regions of homology to previously described pathogenicity islands, particularly staphylococcal pathogenicity islands 1 and bov. The expression of 22 of the 24 open reading frames contained on staphylococcal pathogenicity island 3 was detected either in vitro during growth in a laboratory medium or serum or in vivo in a rabbit model of toxic shock syndrome using DNA microarrays. The effect of oxygen tension on staphylococcal pathogenicity island 3 gene expression was also examined. By comparison with the known staphylococcal pathogenicity islands in the context of gene expression described here, we propose a model of pathogenicity island origin and evolution involving specialized transduction events and addition, deletion, or recombination of pathogenicity island "modules."

摘要

我们描述了编码葡萄球菌肠毒素血清型B、K和Q的15.9 kb葡萄球菌致病岛3的完整序列。该致病岛符合致病岛的普遍公认定义,包含24个开放阅读框,可能编码50多个氨基酸的蛋白质,其中包括一个明显具有功能的整合酶。该元件由两个17 bp的直接重复序列界定,这两个重复序列与在葡萄球菌致病岛1侧翼发现的重复序列相同。该致病岛与先前描述的致病岛有广泛的同源区域,特别是葡萄球菌致病岛1和bov。使用DNA微阵列,在实验室培养基或血清中生长的体外培养条件下,或在中毒性休克综合征兔模型的体内条件下,检测到了葡萄球菌致病岛3上24个开放阅读框中的22个的表达。还研究了氧张力对葡萄球菌致病岛3基因表达的影响。通过在此处描述的基因表达背景下与已知的葡萄球菌致病岛进行比较,我们提出了一个致病岛起源和进化的模型,该模型涉及专门的转导事件以及致病岛“模块”的添加、缺失或重组。

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