Cooney Meagan A, Steele James L, Steinberg Howard, Talaat Adel M
Laboratory of Bacterial Genomics, Department of Pathobiological Sciences, University of Wisconsin-Madison Madison, WI, USA.
Food Science, University of Wisconsin-Madison Madison, WI, USA.
Front Cell Infect Microbiol. 2014 Feb 5;4:11. doi: 10.3389/fcimb.2014.00011. eCollection 2014.
Mycobacterium avium subsp. paratuberculosis (M. paratuberculosis) the causative agent of Johne's disease, is one of the most serious infectious diseases in dairy cattle worldwide. Due to the chronic nature of this disease and no feasible control strategy, it is essential to have an efficient animal model which is representative of the natural route of infection as well as a viable treatment option. In this report, we evaluated the effect of different doses of M. paratuberculosis in their ability to colonize murine tissues following oral delivery and the ability of Lactobacillus casei ATCC 334, a nascent probiotic, to combat paratuberculosis. Oral inoculation of mice was able to establish paratuberculosis in a dose-dependent manner. Two consecutive doses of approximately 10(9) CFU per mouse resulted in a disseminated infection, whereas lower doses were not efficient to establish infection. All inoculated mice were colonized with M. paratuberculosis, maintained infection for up to 24 weeks post infection and generated immune responses that reflect M. paratuberculosis infection in cattle. Notably, oral administration of L. casei ATCC 334 did not reduce the level of M. paratuberculosis colonization in treated animals. Interestingly, cytokine responses and histology indicated a trend for the immunomodulation and reduction of pathology in animals receiving L. casei ATCC 334 treatment. Overall, a reproducible oral model of paratuberculosis in mice was established that could be used for future vaccine experiments. Although the L. casei ATCC 334 was not a promising candidate for controlling paratuberculosis, we established a protocol to screen other probiotic candidates.
副结核分枝杆菌(M. paratuberculosis)是约内氏病的病原体,是全球奶牛中最严重的传染病之一。由于这种疾病的慢性性质以及缺乏可行的控制策略,拥有一个能代表自然感染途径的高效动物模型以及可行的治疗方案至关重要。在本报告中,我们评估了不同剂量的副结核分枝杆菌经口服后在小鼠组织中定植的能力,以及新生益生菌干酪乳杆菌ATCC 334对抗副结核病的能力。给小鼠口服接种能够以剂量依赖的方式引发副结核病。每只小鼠连续两次接种约10⁹CFU可导致播散性感染,而较低剂量则无法有效引发感染。所有接种的小鼠都被副结核分枝杆菌定植,在感染后长达24周内维持感染,并产生反映牛副结核分枝杆菌感染的免疫反应。值得注意的是,口服给予干酪乳杆菌ATCC 334并未降低治疗动物体内副结核分枝杆菌的定植水平。有趣的是,细胞因子反应和组织学表明,接受干酪乳杆菌ATCC 334治疗的动物存在免疫调节和病理减轻的趋势。总体而言,建立了一种可重复的小鼠副结核病口服模型,可用于未来的疫苗实验。虽然干酪乳杆菌ATCC 334不是控制副结核病的有前景的候选菌株,但我们建立了一个方案来筛选其他益生菌候选菌株。