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肠道细菌兼致病共生菌普通拟杆菌,在人肠道上皮细胞系中,以菌株和生长阶段依赖的方式激活核因子κB。

The gut bacterium and pathobiont Bacteroides vulgatus activates NF-κB in a human gut epithelial cell line in a strain and growth phase dependent manner.

作者信息

Ó Cuív Páraic, de Wouters Tomas, Giri Rabina, Mondot Stanislas, Smith Wendy J, Blottière Hervé M, Begun Jakob, Morrison Mark

机构信息

The University of Queensland Diamantina Institute, The University of Queensland, Translational Research Institute, Brisbane, QLD, Australia; CSIRO Preventative Health Flagship Research Program, Queensland, Australia.

Micalis Institute, INRA, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.

出版信息

Anaerobe. 2017 Oct;47:209-217. doi: 10.1016/j.anaerobe.2017.06.002. Epub 2017 Jun 3.

Abstract

The gut microbiota is increasingly implicated in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC) although the identity of the bacteria that underpin these diseases has remained elusive. The pathobiont Bacteroides vulgatus has been associated with both diseases although relatively little is known about how its growth and functional activity might drive the host inflammatory response. We identified an ATP Binding Cassette (ABC) export system and lipoprotein in B. vulgatus ATCC 8482 and B. vulgatus PC510 that displayed significant sequence similarity to an NF-κB immunomodulatory regulon previously identified on a CD-derived metagenomic fosmid clone. Interestingly, the ABC export system was specifically enriched in CD subjects suggesting that it may be important for colonization and persistence in the CD gut environment. Both B. vulgatus ATCC 8482 and PC510 activated NF-κB in a strain and growth phase specific manner in a HT-29/kb-seap-25 enterocyte like cell line. B. vulgatus ATCC 8482 also activated NF-κB in a Caco-2-NF-κBluc enterocyte like and an LS174T-NF-κBluc goblet cell like cell lines, and induced NF-κB-p65 subunit nuclear translocation and IL-6, IL-8, CXCL-10 and MCP-1 gene expression. Despite this, NF-κB activation was not coincident with maximal expression of the ABC exporter or lipoprotein in B. vulgatus PC510 suggesting that the regulon may be necessary but not sufficient for the immunomodulatory effects.

摘要

肠道微生物群越来越多地被认为与克罗恩病(CD)和溃疡性结肠炎(UC)的发病机制有关,尽管引发这些疾病的细菌身份仍然难以捉摸。致病性拟杆菌已被认为与这两种疾病都有关联,尽管对于其生长和功能活性如何驱动宿主炎症反应了解相对较少。我们在普通拟杆菌ATCC 8482和普通拟杆菌PC510中鉴定出一种ATP结合盒(ABC)输出系统和脂蛋白,它们与先前在一个源自CD的宏基因组fosmid克隆上鉴定出的NF-κB免疫调节操纵子显示出显著的序列相似性。有趣的是,ABC输出系统在CD患者中特异性富集,这表明它对于在CD肠道环境中的定殖和持续存在可能很重要。普通拟杆菌ATCC 8482和PC510在HT-29/kb-seap-25肠上皮样细胞系中以菌株和生长阶段特异性方式激活NF-κB。普通拟杆菌ATCC 8482还在Caco-2-NF-κBluc肠上皮样细胞系和LS174T-NF-κBluc杯状细胞样细胞系中激活NF-κB,并诱导NF-κB-p65亚基的核转位以及IL-6、IL-8、CXCL-10和MCP-1基因表达。尽管如此,NF-κB的激活与普通拟杆菌PC510中ABC输出蛋白或脂蛋白的最大表达并不一致,这表明该操纵子对于免疫调节作用可能是必要的,但并不充分。

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