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感染高毒力结核分枝杆菌TT372的豚鼠的全基因组反应。

Whole genome response in guinea pigs infected with the high virulence strain Mycobacterium tuberculosis TT372.

作者信息

Aiyaz Mohamed, Bipin Chand, Pantulwar Vinay, Mugasimangalam Raja, Shanley Crystal A, Ordway Diane J, Orme Ian M

出版信息

Tuberculosis (Edinb). 2014 Dec;94(6):606-15. doi: 10.1016/j.tube.2014.10.001.

Abstract

In this study we conducted a microarray-based whole genomic analysis of gene expression in the lungs after exposure of guinea pigs to a low dose aerosol of the Atypical Beijing Western Cape TT372 strain of Mycobacterium tuberculosis, after harvesting lung tissues three weeks after infection at a time that effector immunity is starting to peak. The infection resulted in a very large up-regulation of multiple genes at this time, particularly in the context of a "chemokine storm" in the lungs. Overall gene expression was considerably reduced in animals that had been vaccinated with BCG two months earlier, but in both cases strong signatures featuring gamma interferon [IFNγ] and tumor necrosis factor [TNFα] were observed indicating the potent TH1 response in these animals. Even though their effects are not seen until later in the infection, even at this early time point gene expression patterns associated with the potential emergence of regulatory T cells were observed. Genes involving lung repair, response to oxidative stress, and cell trafficking were strongly expressed, but interesting these gene patterns differed substantially between the infected and vaccinated/infected groups of animals. Given the importance of this species as a relevant and cost-effective small animal model of tuberculosis, this approach has the potential to provide new information regarding the effects of vaccination on control of the disease process.

摘要

在本研究中,我们对豚鼠暴露于非典型北京西开普TT372株结核分枝杆菌低剂量气溶胶后,在感染三周后收获肺组织(此时效应免疫开始达到峰值)时的肺组织基因表达进行了基于微阵列的全基因组分析。此时感染导致多个基因大量上调,尤其是在肺部“趋化因子风暴”的背景下。两个月前接种卡介苗的动物总体基因表达大幅降低,但在两种情况下均观察到以γ干扰素[IFNγ]和肿瘤坏死因子[TNFα]为特征的强烈信号,表明这些动物中存在有效的TH1反应。即使在感染后期才观察到它们的作用,但即使在这个早期时间点,也观察到了与调节性T细胞潜在出现相关的基因表达模式。涉及肺修复、氧化应激反应和细胞运输的基因强烈表达,但有趣的是,这些基因模式在感染组与接种疫苗/感染组动物之间有很大差异。鉴于该物种作为一种相关且具有成本效益的结核病小动物模型的重要性,这种方法有可能提供有关疫苗接种对疾病进程控制效果的新信息。

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