Arenas-Gamboa Angela M, Ficht Thomas A, Davis Donald S, Elzer Philip H, Wong-Gonzalez Alfredo, Rice-Ficht Allison C
Department of Veterinary Pathobiology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, 4467 TAMU, College Station, Texas 77843-4467, USA.
J Wildl Dis. 2009 Jan;45(1):165-73. doi: 10.7589/0090-3558-45.1.165.
Brucellosis is an important zoonotic disease of nearly worldwide distribution. The occurrence of the infection in humans is largely dependent on the prevalence of brucellosis in animal reservoirs, including wildlife. The current vaccine used for cattle Brucella abortus strain RB51, has proven ineffective in protecting bison (Bison bison) and elk (Cervus nelsoni) from infection and abortion. To test possible improvements in vaccine efficacy, a novel approach of immunization was examined from April 2004 to November 2006 using alginate composite microspheres containing a nonimmunogenic, eggshell-precursor protein of the parasite Fasciola hepatica (Vitelline protein B, VpB) to deliver live vaccine strain RB51. Red deer (Cervus elaphus), used as a model for elk, were vaccinated orally (PO) or subcutaneously (SC) with 1.5x10(10) viable organisms per animal. Humoral responses postvaccination (immunoglobulin G [IgG] levels), assessed at different time points, indicated that capsules containing live RB51 elicited an anti-Brucella specific IgG response. Furthermore, the encapsulated vaccine elicited a cell-mediated response that the nonencapsulated vaccinates failed to produce. Finally, red deer were challenged with B. abortus strain 19 by conjunctival exposure. Only animals that received encapsulated RB51 vaccine by either route exhibited a significant reduction in bacterial counts in their spleens. These data suggest that alginate-VpB microspheres provide a method to enhance the RB51 vaccine performance in elk.
布鲁氏菌病是一种重要的人畜共患病,几乎遍布全球。人类感染的发生在很大程度上取决于动物宿主(包括野生动物)中布鲁氏菌病的流行情况。目前用于牛的布鲁氏菌流产菌株RB51疫苗,已被证明在保护野牛(美洲野牛)和麋鹿(加拿大马鹿)免受感染和流产方面无效。为了测试疫苗效力可能的改进方法,2004年4月至2006年11月研究了一种新的免疫方法,即使用含有寄生虫肝片吸虫非免疫原性卵壳前体蛋白(卵黄蛋白B,VpB)的海藻酸盐复合微球来递送活疫苗菌株RB51。以马鹿作为麋鹿的模型,每只动物口服(PO)或皮下注射(SC)1.5×10¹⁰个活生物体进行接种。在不同时间点评估接种后的体液反应(免疫球蛋白G [IgG]水平),结果表明含有活RB51的胶囊引发了抗布鲁氏菌特异性IgG反应。此外,封装疫苗引发了细胞介导的反应,而未封装的疫苗接种则未能产生这种反应。最后,通过结膜暴露用布鲁氏菌流产菌株19对马鹿进行攻毒。只有通过任何一种途径接受封装RB51疫苗的动物,其脾脏中的细菌数量显著减少。这些数据表明,海藻酸盐-VpB微球提供了一种提高RB51疫苗对麋鹿免疫效果的方法。