Leya Mwense, Kim Won Kyong, Cho Jeong Sang, Yu Eun-Chae, Kim Young-Jee, Yeo Yoonhwan, Lyoo Kwang-Soo, Yang Myeon-Sik, Han Sang-Seop, Lee John Hwa, Tark Dongseob, Hur Jin, Kim Bumseok
College of Veterinary Medicine, Chonbuk National University, Iksan 54596, Korea.
Korea Zoonosis Research Institute, Chonbuk National University, Iksan 54596, Korea.
J Vet Sci. 2018 Sep 30;19(5):643-652. doi: 10.4142/jvs.2018.19.5.643.
is an intracellular pathogen with a cellular infection mechanism similar to that of , making it a suitable choice for use in an anti- immune boost system. This study explores the efficacy of a Typhimurium delivery-based combination vaccine for four heterologous antigens ( lumazine synthase, proline racemase subunit A, outer-membrane protein 19, and Cu/Zn superoxide dismutase) targeting brucellosis in goats. We inoculated the attenuated delivery-based vaccine combination subcutaneously at two different inoculation levels; 5 × 10 colony-forming unit (CFU)/mL (Group B) and 5 × 10 CFU/mL (Group C) and challenged the inoculations with virulent at 6 weeks post-immunization. Serum immunoglobulin G titers against individual antigens in immunized goats (Group C) were significantly higher than those of the non-immunized goats (Group A) at 3 and 6 weeks after vaccination. Upon antigenic stimulation, interferon-γ from peripheral blood mononuclear cells was significantly elevated in Groups B and C compared to that in Group A. The immunized goats had a significantly higher level of protection as demonstrated by the low bacterial loads in most tissues from the goats challenged with . Relative real-time polymerase chain reaction results revealed that the expression of antigens was lower in spleen, kidney, and lung of immunized goats than of non-immunized animals. Also, treatment with our combination vaccine ameliorated histopathological lesions induced by the infection. Overall, the Typhimurium delivery-based combination vaccine was effective in delivering immunogenic proteins, making it potentially useful in protecting livestock from brucellosis.
是一种细胞内病原体,其细胞感染机制与[某种病原体]相似,这使其成为用于抗[病原体名称]免疫增强系统的合适选择。本研究探讨了基于鼠伤寒沙门氏菌递送的联合疫苗针对四种异源布鲁氏菌抗原(核黄素合酶、脯氨酸消旋酶亚基A、外膜蛋白19和铜/锌超氧化物歧化酶)在山羊中预防布鲁氏菌病的效果。我们以两种不同接种水平皮下接种基于减毒鼠伤寒沙门氏菌递送的联合疫苗;5×10菌落形成单位(CFU)/mL(B组)和5×10⁶CFU/mL(C组),并在免疫后6周用强毒[病原体名称]对接种动物进行攻毒。接种疫苗的山羊(C组)在接种后3周和6周时,针对各抗原的血清免疫球蛋白G滴度显著高于未免疫山羊(A组)。在抗原刺激后,与A组相比,B组和C组外周血单核细胞产生的干扰素-γ显著升高。攻毒后,接种疫苗的山羊大多数组织中的细菌载量较低,表明其具有显著更高的保护水平。相对实时聚合酶链反应结果显示,接种疫苗的山羊脾脏、肾脏和肺中布鲁氏菌抗原的表达低于未免疫动物。此外,我们的联合疫苗治疗减轻了由[病原体名称]感染引起的组织病理学损伤。总体而言,基于鼠伤寒沙门氏菌递送的联合疫苗在递送免疫原性布鲁氏菌蛋白方面是有效的,使其在保护家畜免受布鲁氏菌病感染方面具有潜在用途。