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分子伴侣DnaK参与猪布鲁氏菌在U937衍生吞噬细胞内的生长。

Participation of the molecular chaperone DnaK in intracellular growth of Brucella suis within U937-derived phagocytes.

作者信息

Köhler S, Teyssier J, Cloeckaert A, Rouot B, Liautard J P

机构信息

Institut National de la Santé et de la Recherche Médicale U-431, Université Montpellier II, France.

出版信息

Mol Microbiol. 1996 May;20(4):701-12. doi: 10.1111/j.1365-2958.1996.tb02510.x.

Abstract

In the intracellular bacterium Brucella suis, the molecular chaperone DnaK was induced under heat-shock conditions and at low pH. Insertional inactivation of dnaK and dnaJ within the dnaK/J locus led to the conclusion that DnaK, but not DnaJ, was required for growth at 37 degrees C in vitro. Viability of the dnaK null mutant was also greatly affected at low pH. Under conditions allowing intracellular multiplication, the infection of U937-derived phagocytes resulted in long-lasting DnaK induction in the wild-type bacteria. In infection experiments performed with both mutants at the reduced temperature of 30 degrees C, the dnaK mutant of B. suis survived but failed to multiply within U937 cells, whereas the wild-type strain and the dnaJ mutant multiplied normally. Complementation of the dnaK mutant with the cloned dnaK gene restored growth at 37 degrees C, increased resistance to acid pH, and increased intracellular multiplication. This is the first report of the effects of dnaK inactivation in a pathogenic species, and of the temperature-independent contribution of DnaK to intracellular multiplication of the pathogen B. suis.

摘要

在细胞内细菌猪布鲁氏菌中,分子伴侣DnaK在热休克条件和低pH值下被诱导表达。dnaK/J基因座内的dnaK和dnaJ插入失活表明,体外37℃生长需要DnaK而非DnaJ。dnaK缺失突变体在低pH值下的生存能力也受到极大影响。在允许细胞内增殖的条件下,野生型细菌感染源自U937的吞噬细胞会导致DnaK持续诱导表达。在30℃的低温下对两种突变体进行感染实验时,猪布鲁氏菌的dnaK突变体能够存活,但无法在U937细胞内增殖,而野生型菌株和dnaJ突变体则能正常增殖。用克隆的dnaK基因对dnaK突变体进行互补,可恢复其在37℃的生长能力,增强对酸性pH值的抗性,并增加细胞内增殖。这是关于致病物种中dnaK失活影响以及DnaK对猪布鲁氏菌病原体细胞内增殖的温度非依赖性贡献的首次报道。

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