Arenas-Gamboa Angela M, Ficht Thomas A, Davis Donald S, Elzer Philip H, Kahl-McDonagh Melissa, Wong-Gonzalez Alfredo, Rice-Ficht Allison C
Department of Veterinary Pathobiology, Texas A&M University and Texas Agricultural Experiment Station, College Station, Texas 77845-1114, USA.
J Wildl Dis. 2009 Oct;45(4):1021-9. doi: 10.7589/0090-3558-45.4.1021.
Bison (Bison bison) and elk (Cervus elaphus nelsoni) in the Greater Yellowstone Area (GYA), USA, are infected with Brucella abortus, the causative agent of bovine brucellosis, and they serve as a wildlife reservoir for the disease. Bovine brucellosis recently has been transmitted from infected elk to cattle in Montana, Wyoming, and Idaho and has resulted in their loss of brucellosis-free status. An efficacious Brucella vaccine with a delivery system suitable for wildlife would be a valuable tool in a disease prevention and control program. We evaluated Strain 19 (S19) in a sustained release vehicle consisting of alginate microspheres containing live vaccine. In a challenge study using red deer (Cervus elaphus elaphus) as a model for elk, alginate, a naturally occurring polymer combined with a protein of Fasciola hepatica vitelline protein B was used to microencapsulate S19. Red deer were orally or subcutaneously immunized with 1.5 x 10(10) colony-forming units (CFUs) using microencapsulated S19. Humoral and cellular profiles were analyzed bimonthly throughout the study. The vaccinated red deer and nonvaccinated controls were challenged 1 yr postimmunization conjunctivally with 1 x 10(9) CFUs of B. abortus strain 2308. Red deer vaccinated with oral microencapsulated S19 had a statistically significant lower bacterial tissue load compared with controls. These data indicate for the first time that protection against Brucella-challenge can be achieved by combining a commonly used vaccine with a novel oral delivery system such as alginate-vitelline protein B microencapsulation. This system is a potential improvement for efficacious Brucella-vaccine delivery to wildlife in the GYA.
美国大黄石地区(GYA)的美洲野牛(Bison bison)和麋鹿(Cervus elaphus nelsoni)感染了牛布鲁氏菌病的病原体牛布鲁氏菌(Brucella abortus),它们是这种疾病的野生动物宿主。牛布鲁氏菌病最近已从受感染的麋鹿传播到蒙大拿州、怀俄明州和爱达荷州的牛群中,并导致这些地区失去了无布鲁氏菌病的状态。一种有效的布鲁氏菌疫苗以及适合野生动物的给药系统将是疾病预防和控制计划中的宝贵工具。我们评估了由含有活疫苗的海藻酸盐微球组成的缓释载体中的19号菌株(S19)。在一项以马鹿(Cervus elaphus elaphus)作为麋鹿模型的攻毒研究中,使用与肝片吸虫卵黄蛋白B的一种蛋白质结合的天然聚合物海藻酸盐对S19进行微囊化。使用微囊化的S19以1.5×10¹⁰菌落形成单位(CFUs)对马鹿进行口服或皮下免疫。在整个研究过程中每两个月分析一次体液和细胞情况。免疫1年后,用1×10⁹CFUs的牛布鲁氏菌2308菌株对结膜进行攻毒,对接种疫苗的马鹿和未接种疫苗的对照马鹿进行攻毒。与对照相比,口服微囊化S19疫苗的马鹿的细菌组织载量在统计学上显著更低。这些数据首次表明,通过将常用疫苗与新型口服给药系统(如海藻酸盐 - 卵黄蛋白B微囊化)相结合,可以实现对布鲁氏菌攻毒的保护。该系统对于向GYA的野生动物有效递送布鲁氏菌疫苗是一种潜在的改进。