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首页> 外文期刊>Research in Microbiology >Group X hybrid histidine kinase Chk1 is dispensable for stress adaptation, host-pathogen interactions and virulence in the opportunistic yeast Candida guilliermondii
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Group X hybrid histidine kinase Chk1 is dispensable for stress adaptation, host-pathogen interactions and virulence in the opportunistic yeast Candida guilliermondii

机译:组X杂交组氨酸激酶CHK1可用于应力适应,宿主 - 病原体相互作用和毒力,在机会酵母念珠菌甘肃菲尔迪

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Hybrid histidine kinases (HHKs) progressively emerge as prominent sensing proteins in the fungal kingdom and as ideal targets for future therapeutics. The group X HHK is of major interest, since it was demonstrated to play an important role in stress adaptation, host pathogen interactions and virulence in some yeast and mold models, and particularly Chk1, that corresponds to the sole group X HHK in Candida albicans. In the present work, we investigated the role of Chk1 in the low-virulence species Candida guilliermondii, in order to gain insight into putative conservation of the role of group X HHK in opportunistic yeasts. We demonstrated that disruption of the corresponding gene CHK1 does not influence growth, stress tolerance, drug susceptibility, protein glycosylation or cell wall composition in C. guilliermondii. In addition, we showed that loss of CHK1 does not affect C. guilliermondii ability to interact with macrophages and to stimulate cytokine production by human peripheral blood mononuclear cells. Finally, the C. guilliermondii chk1 null mutant was found to be as virulent as the wild-type strain in the experimental model Galleria mellonella. Taken together, our results demonstrate that group X HHK function is not conserved in Candida species. (C) 2017 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
机译:杂交组氨酸激酶(HHK)逐渐出现在真菌王国中的突出传感蛋白质,也是未来治疗剂的理想目标。 X HHK群体具有重大兴趣,因为它被证明在一些酵母和模型模型中的应力适应,宿主病原体相互作用和毒力中起重要作用,特别是Chk1,其对应于Candida albicans的唯一组X HHK。在目前的工作中,我们调查了CHK1在低毒力物种Candida Guilliermondii中的作用,以便深入了解X HHK集团在机会酵母中的作用。我们证明了相应的基因CHK1的破坏不会影响C.Guilliermondii中的生长,应力耐受性,药物敏感性,蛋白质糖基化或细胞壁组合物。此外,我们表明,CHK1的丧失不会影响与巨噬细胞相互作用的C.Guilliermondii能力,并通过人外周血单核细胞刺激细胞因子产生。最后,发现C.Guilliermondii CHK1缺突突变体是实验模型中梅隆菌的野生型菌株的毒力。我们的结果一起携带,X X HHK函数在念珠菌物种中不保守。 (c)2017年Institut Pasteur。由Elsevier Masson SA出版。版权所有。

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