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脂 A 酰化在小肠结肠炎耶尔森菌毒力中的作用。

Role of lipid A acylation in Yersinia enterocolitica virulence.

机构信息

Fundación Caubet- CIMERA Illes Balears, 07110 Bunyola, Spain.

出版信息

Infect Immun. 2010 Jun;78(6):2768-81. doi: 10.1128/IAI.01417-09. Epub 2010 Apr 12.

Abstract

Yersinia enterocolitica is an important human pathogen. Y. enterocolitica must adapt to the host environment, and temperature is an important cue regulating the expression of most Yersinia virulence factors. Here, we report that Y. enterocolitica 8081 serotype O:8 synthesized tetra-acylated lipid A at 37 degrees C but that hexa-acylated lipid A predominated at 21 degrees C. By mass spectrometry and genetic methods, we have shown that the Y. enterocolitica msbB, htrB, and lpxP homologues encode the acyltransferases responsible for the addition of C(12), C(14) and C(16:1), respectively, to lipid A. The expression levels of the acyltransferases were temperature regulated. Levels of expression of msbB and lpxP were higher at 21 degrees C than at 37 degrees C, whereas the level of expression of htrB was higher at 37 degrees C. At 21 degrees C, an lpxP mutant was the strain most susceptible to polymyxin B, whereas at 37 degrees C, an htrB mutant was the most susceptible. We present evidence that the lipid A acylation status affects the expression of Yersinia virulence factors. Thus, expression of flhDC, the flagellar master regulatory operon, was downregulated in msbB and lpxP mutants, with a concomitant decrease in motility. Expression of the phospholipase yplA was also downregulated in both mutants. inv expression was downregulated in msbB and htrB mutants, and consistent with this finding, invasion of HeLa cells was diminished. However, the expression of rovA, the positive regulator of inv, was not affected in the mutants. The levels of pYV-encoded virulence factors Yops and YadA in the acyltransferase mutants were not affected. Finally, we show that only the htrB mutant was attenuated in vivo.

摘要

小肠结肠炎耶尔森菌是一种重要的人类病原体。小肠结肠炎耶尔森菌必须适应宿主环境,而温度是调节大多数耶尔森氏菌毒力因子表达的重要线索。在这里,我们报告说,血清型 O:8 的小肠结肠炎耶尔森菌 8081 在 37°C 时合成四酰化脂质 A,但在 21°C 时六酰化脂质 A 占主导地位。通过质谱和遗传方法,我们已经表明,小肠结肠炎耶尔森菌 msbB、htrB 和 lpxP 同源物分别编码负责将 C(12)、C(14)和 C(16:1)添加到脂质 A 的酰基转移酶。酰基转移酶的表达水平受温度调节。msbB 和 lpxP 的表达水平在 21°C 时高于 37°C,而 htrB 的表达水平在 37°C 时更高。在 21°C 时,lpxP 突变体对多粘菌素 B 最敏感,而在 37°C 时,htrB 突变体最敏感。我们提供的证据表明,脂质 A 的酰化状态会影响耶尔森氏菌毒力因子的表达。因此,在 msbB 和 lpxP 突变体中,flagellar 主调控操纵子 flhDC 的表达下调,同时运动性降低。在这两种突变体中,磷脂酶 yplA 的表达也下调。msbB 和 htrB 突变体中 inv 的表达下调,与这一发现一致的是,HeLa 细胞的侵袭性降低。然而,突变体中 rovA 的表达不受影响,rovA 是 inv 的正调控因子。在酰基转移酶突变体中,pYV 编码的毒力因子 Yops 和 YadA 的水平没有受到影响。最后,我们表明只有 htrB 突变体在体内减弱。

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