Hamilton H L, Follett D M, Siegfried L M, Czuprynski C J
Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison 53706.
Infect Immun. 1989 Jan;57(1):225-30. doi: 10.1128/iai.57.1.225-230.1989.
In this study gnotobiotic mice were inoculated with a human isolate of Mycobacterium paratuberculosis (strain Linda; ATCC 43015) in an attempt to investigate the pathogenesis of intestinal paratuberculosis. Mycobacterium paratuberculosis-monoassociated nu/+ mice developed a persistent low-level intestinal infection but did not support progressive bacillary multiplication. In contrast, monoassociated nu/nu mice eventually harbored approximately 10(7) M. paratuberculosis per g of intestinal tissue. Acid-fast bacilli and granulomas were observed in the intestinal mucosa and livers of nu/nu but not nu/+ mice. Similar results were obtained after intragastric inoculation of M. paratuberculosis into nu/+ and nu/nu flora-defined mice. These observations suggest that the presence of an intact cellular immune system is important for limiting intestinal multiplication of M. paratuberculosis. The results of this study may be relevant to our understanding of the pathogenesis of Johne's disease in ruminants and of human inflammatory bowel diseases that have a mycobacterial etiology (e.g., some cases of Crohn's disease and Mycobacterium avium-Mycobacterium intracellulare enteritis in patients with acquired immunodeficiency syndrome).
在本研究中,将无菌小鼠接种人副结核分枝杆菌分离株(琳达菌株;ATCC 43015),以研究肠道副结核病的发病机制。副结核分枝杆菌单关联的nu/+小鼠发生了持续性低水平肠道感染,但不支持杆菌的进行性增殖。相比之下,单关联的nu/nu小鼠最终每克肠道组织中含有约10(7)个副结核分枝杆菌。在nu/nu小鼠而非nu/+小鼠的肠道黏膜和肝脏中观察到抗酸杆菌和肉芽肿。将副结核分枝杆菌经胃内接种到nu/+和nu/nu菌群确定的小鼠后也获得了类似结果。这些观察结果表明,完整的细胞免疫系统对于限制副结核分枝杆菌在肠道内的增殖很重要。本研究结果可能与我们对反刍动物约翰氏病以及有分枝杆菌病因的人类炎症性肠病(例如,某些克罗恩病病例以及获得性免疫缺陷综合征患者的鸟分枝杆菌-胞内分枝杆菌肠炎)发病机制的理解有关。