猪布鲁氏菌粗菌苗口服或非肠注射对野猪的免疫原性和效果

S. Olsen, P. Boggiatto, J. Wilson-Welder, P. Nol, J. Rhyan, N. Srirangathan
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引用次数: 2

摘要

猪布鲁氏菌毒株353-1是一种临床安全的稳定疫苗毒株,在常规的布鲁氏菌病监测试验中不会引起阳性血清学反应,并且在接种后诱导猪的体液和细胞免疫。在这项研究中,我们评估了口服或肠外接种353-1菌株1.9 x 1010菌落形成单位(CFU)后的组织清除率和免疫反应,并比较了疫苗接种和对照治疗在实验性结膜攻击后对猪乙型流感病毒感染的保护效果。与未接种菌株的猪相比,口服或亲代接种353-1菌株的野猪在接种后所有采样时间的布鲁氏菌平均ELISA滴度均高于未接种菌株的猪(P < 0.05)。与未接种疫苗的PBMC相比,父母在12周或17周接种353-1疫苗或在接种后12周口服疫苗的PBMC表现出更大的抗原特异性增殖反应(P < 0.05)。在尸体解剖时,与口服或肠外接种疫苗相比,未接种疫苗的野猪在大多数组织中具有更高的标准管凝集滴度和播散性感染(P < 0.05)定植(CFU/gm)。在实验攻毒后4周,没有从注射疫苗收集的任何组织中恢复毒力攻毒菌株。尽管从一些样品中恢复了低水平的攻毒菌株,但口服疫苗在大多数组织中的定植与肠外疫苗没有差异(P < 0.05),但与未接种疫苗的猪相比,组织定植减少了(P < 0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunogenicity and Efficacy of a Rough Brucella suis Vaccine Delivered Orally or Parenterally to Feral Swine
Brucella suis strain 353-1 is a stable vaccine strain that is clinically safe, does not cause positive serologic responses on conventional brucellosis surveillance tests, and induces humoral and cellular immunity in swine after vaccination. In this study, we evaluated tissue clearance and immunologic responses after oral or parenteral vaccination of feral swine with 1.9 x 1010 colony-forming units (CFU) of strain 353-1, and compared efficacy of vaccination and control treatments in protecting against infection after experimental conjunctival challenge with a virulent B. suis strain. Feral swine vaccinated orally or parentally with strain 353-1 had greater (P < 0.05) mean ELISA titers to Brucella at all sampling times after vaccination when compared to non-vaccinated swine. PBMC from swine parentally vaccinated with 353-1 at 12 or 17 weeks, or oral vaccinates at 12 weeks after vaccination, demonstrated greater (P < 0.05) antigen-specific proliferative responses when compared to responses of PBMC from non-vaccinates. At necropsy, 4 weeks after experimental challenge with virulent B. suis, non-vaccinated feral swine had greater standard tube agglutination titers and disseminated infection with higher (P < 0.05) colonization (CFU/gm) in most tissues as compared to oral or parenteral vaccinates. The virulent challenge strain was not recovered from any tissues collected from parenteral vaccinates at 4 weeks after experimental challenge. Although the challenge strain was recovered at low levels from some samples, tissue colonization in most tissues of oral vaccinates did not differ (P > 0.05) from parenteral vaccinates, but was reduced (P < 0.05) when compared to colonization in non-vaccinated swine.
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