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肠出血性大肠杆菌O157:H7致病岛负调控因子的鉴定

Identification of a negative regulator for the pathogenicity island of enterohemorrhagic Escherichia coli O157:H7.

作者信息

Lio Joaquim Chan-Wang, Syu Wan-Jr

机构信息

Institute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.

出版信息

J Biomed Sci. 2004 Nov-Dec;11(6):855-63. doi: 10.1007/BF02254371.

Abstract

Enterohemorrhagic Escherichia coli (EHEC) forms histological lesions termed attaching and effacing lesions (A/E lesions) on infected large intestine tissue. The major virulence factors involved in A/E lesions reside on a locus of enterocyte effacement (LEE), a pathogenicity island. The LEE comprises 41 specific open reading frames, of which most are organized in 5 major operons, LEE1, LEE2, LEE3, LEE4, and tir(LEE5). The expression of LEE genes is regulated in a complicated manner by environmental factors such as temperature, osmolarity, and quorum sensing. Current knowledge is that regulation is hierarchical: a pivotal positive regulator, ler, is first stimulated, which in turn activates the expression of other operons. Herein, we report on the presence of a negative regulation protein located within the LEE. L0044 is 372 bp in length and is located outside of the 5 major operons. An isogenic L0044 deletion mutant displayed loss of the repression phenotype and increased synthesis of several LEE proteins when bacteria were cultured under repressive conditions that disfavor expression of LEE proteins. Reciprocally, trans expression of L0044 suppressed the expression of the LEE. Furthermore, mRNA of ler increased as a result of deleting L0044, and disrupting ler in a L0044-deleted background reversed the loss of the repression phenotype. Thus, L0044 plays a role in regulating the expression of virulence genes in EHEC by modulating the activation of ler.

摘要

肠出血性大肠杆菌(EHEC)在感染的大肠组织上形成称为紧密黏附与消除性病变(A/E病变)的组织学损伤。参与A/E病变的主要毒力因子位于肠细胞消除位点(LEE),这是一个致病岛。LEE由41个特定的开放阅读框组成,其中大多数被组织成5个主要操纵子,即LEE1、LEE2、LEE3、LEE4和tir(LEE5)。LEE基因的表达受温度、渗透压和群体感应等环境因素的复杂调控。目前的认识是,这种调控是分层的:一个关键的正调控因子ler首先被激活,进而激活其他操纵子的表达。在此,我们报告在LEE内存在一种负调控蛋白。L0044长度为372 bp,位于5个主要操纵子之外。当细菌在不利于LEE蛋白表达的抑制条件下培养时,同基因L0044缺失突变体表现出抑制表型丧失和几种LEE蛋白合成增加。相反,L0044的反式表达抑制了LEE的表达。此外,删除L0044导致ler的mRNA增加,在L0044缺失背景下破坏ler可逆转抑制表型的丧失。因此,L0044通过调节ler的激活在调控EHEC毒力基因表达中发挥作用。

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