Wu Chia-wei, Livesey Michael, Schmoller Shelly K, Manning Elizabeth J B, Steinberg Howard, Davis William C, Hamilton Mary Jo, Talaat Adel M
The Laboratory of Bacterial Genomics, Department of Pathobiological Sciences, University of Wisconsin-Madison, 1656 Linden Drive, Madison, WI 53706-1581, USA.
Infect Immun. 2007 May;75(5):2110-9. doi: 10.1128/IAI.01739-06. Epub 2007 Feb 12.
Infection with Mycobacterium avium subsp. paratuberculosis causes Johne's disease in cattle and is a serious problem for the dairy industry worldwide. Development of models to mimic aspects of Johne's disease remains an elusive goal because of the chronic nature of the disease. In this report, we describe a surgical approach employed to characterize the very early stages of infection of calves with M. avium subsp. paratuberculosis. To our surprise, strains of M. avium subsp. paratuberculosis were able to traverse the intestinal tissues within 1 h of infection in order to colonize distant organs, such as the liver and lymph nodes. Both the ileum and the mesenteric lymph nodes were persistently infected for months following intestinal deposition of M. avium subsp. paratuberculosis despite a lack of fecal shedding of mycobacteria. During the first 9 months of infection, humoral immune responses were not detected. Nonetheless, using flow cytometric analysis, we detected a significant change in the cells participating in the inflammatory responses of infected calves compared to cells in a control animal. Additionally, the levels of cytokines detected in both the ileum and the lymph nodes indicated that there were TH1-type-associated cellular responses but not TH2-type-associated humoral responses. Finally, surgical inoculation of a wild-type strain and a mutant M. avium subsp. paratuberculosis strain (with an inactivated gcpE gene) demonstrated the ability of the model which we developed to differentiate between the wild-type strain and a mutant strain of M. avium subsp. paratuberculosis deficient in tissue colonization and invasion. Overall, novel insights into the early stages of Johne's disease were obtained, and a practical model of mycobacterial invasiveness was developed. A similar approach can be used for other enteric bacteria.
鸟分枝杆菌副结核亚种感染会导致牛患副结核病,这是全球乳制品行业面临的一个严重问题。由于该疾病具有慢性特征,开发能够模拟副结核病某些方面的模型仍然是一个难以实现的目标。在本报告中,我们描述了一种手术方法,用于表征犊牛感染鸟分枝杆菌副结核亚种的早期阶段。令我们惊讶的是,鸟分枝杆菌副结核亚种菌株能够在感染后1小时内穿过肠道组织,以便在肝脏和淋巴结等远处器官定植。在肠道接种鸟分枝杆菌副结核亚种后,尽管没有分枝杆菌的粪便排出,但回肠和肠系膜淋巴结持续感染了数月。在感染的前9个月内,未检测到体液免疫反应。尽管如此,通过流式细胞术分析,我们发现与对照动物的细胞相比,感染犊牛参与炎症反应的细胞有显著变化。此外,在回肠和淋巴结中检测到的细胞因子水平表明存在与TH1型相关的细胞反应,但没有与TH2型相关的体液反应。最后,对野生型菌株和鸟分枝杆菌副结核亚种突变菌株(gcpE基因失活)进行手术接种,证明了我们开发的模型能够区分野生型菌株和在组织定植和侵袭方面存在缺陷的鸟分枝杆菌副结核亚种突变菌株。总体而言,我们获得了对副结核病早期阶段的新见解,并开发了一种实用的分枝杆菌侵袭模型。类似的方法可用于其他肠道细菌。