Coussens Paul M, Jeffers Abra, Colvin Christopher
Department of Animal Science and Center for Animal Functional Genomics, Michigan State University, East Lansing, MI 48824, USA.
Microb Pathog. 2004 Feb;36(2):93-108. doi: 10.1016/j.micpath.2003.09.007.
Mycobacterium avium subspecies paratuberculosis (M. paratuberculosis) is the causative agent of Johne's disease in ruminants. M. paratuberculosis is a slow-growing intracellular bacterium and infections with M. paratuberculosis can persist in a subclinical state for several years. An early and appropriate T cell-mediated cytotoxic response (Th1-like) to M. paratuberculosis infection is often replaced with an antibody or Th 2-like response as infected animals move toward a progressively more clinical state. The reasons for this shift in immune response are unknown. Recent studies suggest that in vitro exposure of peripheral blood mononuclear cells (PBMCs) from Johne's disease positive cows to M. paratuberculosis for 18-24 h results in suppressed expression of numerous immune cell genes. This effect appears at odds with the notion that immune cells from infected cows would respond to M. paratuberculosis-specific antigens in a vigorous and positive manner. In this report, we detail experiments designed to test the hypothesis that many positive changes in PBMC gene expression induced by M. paratuberculosis in vitro are transient, being rapidly suppressed by as yet unknown mechanisms. Our results demonstrate that, indeed, in vitro stimulation with M. paratuberculosis induces rapid changes in infected cow PBMC gene expression (within 2-4 h of exposure) and that many of these changes are no longer evident by 8-16 h of exposure to M. paratuberculosis. Although precise mechanisms responsible for rapid M. paratuberculosis-mediated activation of PBMC gene expression and the loss thereof remain to be determined, our novel results suggest that PBMCs from Johne's disease positive cows are indeed capable of vigorously responding to M. paratuberculosis and that, for many genes, this response is tempered within 8 h of exposure.
副结核分枝杆菌鸟亚种(副结核分枝杆菌)是反刍动物约翰氏病的病原体。副结核分枝杆菌是一种生长缓慢的细胞内细菌,副结核分枝杆菌感染可在亚临床状态下持续数年。随着感染动物病情逐渐发展至临床状态,对副结核分枝杆菌感染的早期且适当的T细胞介导的细胞毒性反应(类Th1反应)常被抗体或类Th2反应所取代。这种免疫反应转变的原因尚不清楚。最近的研究表明,将约翰氏病阳性奶牛的外周血单核细胞(PBMC)在体外暴露于副结核分枝杆菌18 - 24小时会导致众多免疫细胞基因的表达受到抑制。这种效应似乎与受感染奶牛的免疫细胞会以积极且有力的方式对副结核分枝杆菌特异性抗原作出反应这一观点相悖。在本报告中,我们详细阐述了旨在检验以下假设的实验:副结核分枝杆菌在体外诱导的PBMC基因表达中的许多正向变化是短暂的,会被未知机制迅速抑制。我们的结果表明,事实上,用副结核分枝杆菌进行体外刺激会在受感染奶牛的PBMC基因表达中诱导快速变化(在暴露后2 - 4小时内),并且在暴露于副结核分枝杆菌8 - 16小时后,其中许多变化不再明显。尽管负责副结核分枝杆菌介导的PBMC基因表达快速激活及其丧失的精确机制仍有待确定,但我们的新结果表明,约翰氏病阳性奶牛的PBMC确实能够有力地对副结核分枝杆菌作出反应,而且对于许多基因来说,这种反应在暴露8小时内就会减弱。