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DNA腺嘌呤甲基转移酶的过量表达会改变小肠结肠炎耶尔森菌的运动性、侵袭性以及脂多糖O抗原的组成。

Overproduction of DNA adenine methyltransferase alters motility, invasion, and the lipopolysaccharide O-antigen composition of Yersinia enterocolitica.

作者信息

Fälker Stefan, Schilling Jennifer, Schmidt M Alexander, Heusipp Gerhard

机构信息

Institut für Infektiologie, Zentrum für Molekularbiologie der Entzündung, Westfälische Wilhelms-Universität Münster, 48149 Münster, Germany.

出版信息

Infect Immun. 2007 Oct;75(10):4990-7. doi: 10.1128/IAI.00457-07. Epub 2007 Aug 6.

Abstract

DNA adenine methyltransferase (Dam) not only regulates basic cellular functions but also interferes with the proper expression of virulence factors in various pathogens. We showed previously that for the human pathogen Yersinia enterocolitica, overproduction of Dam results in increased invasion of epithelial cells. Since invasion and motility are coordinately regulated in Y. enterocolitica, we analyzed the motility of a Dam-overproducing (Dam(OP)) strain and found it to be highly motile. In Dam(OP) strains, the operon encoding the master regulator of flagellum biosynthesis, flhDC, is upregulated. We show that the increased invasion is not due to enhanced expression of known and putative Y. enterocolitica invasion and adhesion factors, such as Inv, YadA, Ail, Myf fibrils, Pil, or Flp pili. However, overproduction of Dam no longer results in increased invasion for an inv mutant strain, indicating that Inv is necessary for increased invasion after overproduction of Dam. Since we show that overproduction of Dam results in an increased amount of rough lipopolysaccharide (LPS) molecules lacking O-antigen side chains, this implies that reduced steric hindrance by LPS might contribute to increased invasion by a Y. enterocolitica Dam(OP) strain. Our data add an important new aspect to the various virulence-associated phenotypes influenced by DNA methylation in Y. enterocolitica and indicate that Dam targets regulatory processes modulating the composition and function of the bacterial surface.

摘要

DNA腺嘌呤甲基转移酶(Dam)不仅调节细胞的基本功能,还会干扰多种病原体中致病因子的正常表达。我们之前发现,对于人类病原体小肠结肠炎耶尔森菌而言,Dam的过量表达会导致其对上皮细胞的侵袭增加。由于小肠结肠炎耶尔森菌的侵袭和运动是协同调节的,我们分析了Dam过量表达(Dam(OP))菌株的运动能力,发现其具有高度运动性。在Dam(OP)菌株中,编码鞭毛生物合成主要调节因子的操纵子flhDC上调。我们发现,侵袭增加并非由于已知和假定的小肠结肠炎耶尔森菌侵袭及黏附因子(如Inv、YadA、Ail、Myf菌毛、菌毛或Flp菌毛)的表达增强所致。然而,Dam的过量表达对inv突变株不再导致侵袭增加,这表明Inv是Dam过量表达后侵袭增加所必需的。由于我们发现Dam的过量表达会导致缺乏O抗原侧链的粗糙脂多糖(LPS)分子数量增加,这意味着LPS空间位阻的降低可能有助于小肠结肠炎耶尔森菌Dam(OP)菌株的侵袭增加。我们的数据为小肠结肠炎耶尔森菌中受DNA甲基化影响的各种毒力相关表型增添了一个重要的新方面,并表明Dam靶向调节细菌表面组成和功能的调控过程。

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