Stoffregen William C, Olsen Steven C, Bricker Betsy J
Bacterial Diseases of Livestock Research Unit, National Animal Disease Center, Agricultural Research Service, USDA, Ames, IA 50010, USA.
Am J Vet Res. 2006 Oct;67(10):1802-8. doi: 10.2460/ajvr.67.10.1802.
To determine the immunogenicity and efficacy of Brucella abortus strain RB51 (SRB51) as a vaccine in domestic pigs.
Sixty-eight 6-week-old crossbred domestic pigs and twenty-four 4-month-old gilts.
In experiment 1, pigs were vaccinated IM (n = 51) with 2 x 10(10) CFUs of SRB51 or sham inoculated (17). Periodic blood samples were obtained to perform blood cultures, serologic evaluations, and cell-mediated immunity assays. Necropsies were performed at selected times between weeks 1 and 23 after vaccination to determine vaccine clearance. In experiment 2, gilts were similarly vaccinated (n = 18) or sham inoculated (8) and similar samples were obtained after vaccination. Gilts were bred and challenged conjunctivally with 5.0 x 10(7) CFUs of virulent Brucella suis strain 3B. Necropsies were performed on gilts and on fetuses or neonates after abortion or parturition, respectively. Bacterial cultures and serologic evaluations were performed on samples obtained at necropsy to determine vaccine efficacy.
Humoral and cell-mediated immune responses did not differ between vaccinates and controls. After vaccination, SRB51 was not isolated from blood cultures of either group and was isolated from lymphoid tissues of 3 pigs at 2 weeks (n = 2) and 4 weeks (1) after vaccination. No differences were found in isolation of B suis or in seroconversion between vaccinated and control gilts and between their neonates or aborted fetuses.
Parenteral vaccination with SRB51 does not induce humoral or cell-mediated immune responses. Vaccination with SRB51 did not protect gilts or their neonates and fetuses from virulent challenge with B suis.
确定流产布鲁氏菌RB51菌株(SRB51)作为家猪疫苗的免疫原性和效力。
68头6周龄的杂交家猪和24头4月龄的后备母猪。
在实验1中,51头猪通过肌肉注射接种2×10¹⁰CFU的SRB51,17头猪进行假接种。定期采集血样进行血培养、血清学评估和细胞介导免疫测定。在接种后第1至23周的选定时间进行尸检,以确定疫苗清除情况。在实验2中,18头后备母猪同样接种疫苗或假接种,接种后采集类似样本。后备母猪进行配种,并通过结膜接种5.0×10⁷CFU的强毒猪布鲁氏菌3B菌株进行攻毒。分别在后备母猪流产或分娩后对其以及胎儿或新生儿进行尸检。对尸检时采集的样本进行细菌培养和血清学评估,以确定疫苗效力。
接种疫苗组和对照组之间的体液免疫和细胞介导免疫反应没有差异。接种疫苗后,两组的血培养均未分离出SRB51,接种后2周(n = 2)和4周(1头)时,从3头猪的淋巴组织中分离出该菌株。接种疫苗的后备母猪及其对照组之间,以及它们的新生儿或流产胎儿之间,在猪布鲁氏菌的分离或血清转化方面没有差异。
肌肉注射SRB51不能诱导体液免疫或细胞介导免疫反应。接种SRB51不能保护后备母猪及其新生儿和胎儿免受猪布鲁氏菌强毒株的攻击。