AgResearch, National Centre for Biosecurity and Infectious Disease, Wallaceville, P.O. Box 40063, Upper Hutt, New Zealand.
Infect Immun. 2010 Mar;78(3):1383-9. doi: 10.1128/IAI.01020-09. Epub 2009 Dec 28.
Mycobacterium avium subsp. paratuberculosis (basonym M. paratuberculosis) is the causative agent of paratuberculosis, a chronic enteritis of ruminants. To control the considerable economic effect that paratuberculosis has on the livestock industry, a vaccine that induces protection with minimal side effects is required. We employed transposon mutagenesis and allelic exchange to develop three potential vaccine candidates, which were then tested for virulence with macrophages, mice, and goats. All three models identified the WAg906 mutant as being the most attenuated, but some differences in the levels of attenuation were evident among the models when testing the other strains. In a preliminary mouse vaccine experiment, limited protection was induced by WAg915, as evidenced by a reduced bacterial load in spleens and livers 12 weeks following intraperitoneal challenge with M. paratuberculosis K10. While we found macrophages and murine models to be rapid and cost-effective alternatives for the initial screening of M. paratuberculosis mutants for attenuation, it appears necessary to do the definitive assessment of attenuation with a ruminant model.
分支杆菌亚种。副结核(原名 M. paratuberculosis)是副结核病的病原体,这是一种反刍动物的慢性肠炎。为了控制副结核病对畜牧业造成的巨大经济影响,需要一种诱导最小副作用保护的疫苗。我们采用转座子诱变和等位基因交换开发了三种潜在的疫苗候选物,然后用巨噬细胞、小鼠和山羊对它们的毒力进行了测试。所有三种模型都将 WAg906 突变体鉴定为最衰减的,但在测试其他菌株时,模型之间的衰减水平存在一些差异。在初步的小鼠疫苗实验中,WAg915 诱导了有限的保护,这表明在腹腔内用 M. paratuberculosis K10 攻毒 12 周后,脾脏和肝脏中的细菌载量减少。虽然我们发现巨噬细胞和鼠模型是快速和具有成本效益的替代方法,用于对 M. paratuberculosis 突变体进行衰减的初步筛选,但似乎有必要用反刍动物模型对衰减进行明确评估。