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关键枢纽和瓶颈基因区分了巨噬细胞对毒力和减毒牛分枝杆菌的反应。

Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis.

机构信息

Animal Genomics Laboratory, UCD School of Agriculture and Food Science, University College Dublin , Dublin , Ireland ; Systems Biology Ireland, UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin , Dublin , Ireland.

Animal Genomics Laboratory, UCD School of Agriculture and Food Science, University College Dublin , Dublin , Ireland.

出版信息

Front Immunol. 2014 Oct 1;5:422. doi: 10.3389/fimmu.2014.00422. eCollection 2014.

Abstract

Mycobacterium bovis is an intracellular pathogen that causes tuberculosis in cattle. Following infection, the pathogen resides and persists inside host macrophages by subverting host immune responses via a diverse range of mechanisms. Here, a high-density bovine microarray platform was used to examine the bovine monocyte-derived macrophage transcriptome response to M. bovis infection relative to infection with the attenuated vaccine strain, M. bovis Bacille Calmette-Guérin. Differentially expressed genes were identified (adjusted P-value ≤0.01) and interaction networks generated across an infection time course of 2, 6, and 24 h. The largest number of biological interactions was observed in the 24-h network, which exhibited scale-free network properties. The 24-h network featured a small number of key hub and bottleneck gene nodes, including IKBKE, MYC, NFKB1, and EGR1 that differentiated the macrophage response to virulent and attenuated M. bovis strains, possibly via the modulation of host cell death mechanisms. These hub and bottleneck genes represent possible targets for immuno-modulation of host macrophages by virulent mycobacterial species that enable their survival within a hostile environment.

摘要

牛分枝杆菌是一种细胞内病原体,可引起牛的结核病。感染后,该病原体通过多种机制颠覆宿主免疫反应,在宿主巨噬细胞中存活和持续存在。在这里,使用高密度牛微阵列平台检查了牛单核细胞衍生的巨噬细胞转录组对 M. bovis 感染的反应,相对于感染减毒疫苗株 M. bovis Bacille Calmette-Guérin。鉴定了差异表达的基因(调整后的 P 值≤0.01),并在 2、6 和 24 小时的感染时间过程中生成了相互作用网络。在 24 小时网络中观察到最多的生物相互作用,该网络具有无标度网络特性。24 小时网络的关键枢纽和瓶颈基因节点数量较少,包括 IKBKE、MYC、NFKB1 和 EGR1,它们区分了巨噬细胞对强毒和弱毒 M. bovis 菌株的反应,可能通过调节宿主细胞死亡机制。这些枢纽和瓶颈基因可能是毒力分枝杆菌物种对宿主巨噬细胞进行免疫调节的潜在靶点,使它们能够在恶劣的环境中存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4adc/4181336/ba3b6fb0fe73/fimmu-05-00422-g001.jpg

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