VISAVET Health Surveillance Centre, Complutense University of Madrid, Avda. Puerta de Hierro, 28040 Madrid, Spain.
Hipra Scientific S.L.U., Avda. La Selva 135, 17170 Amer, Spain.
Res Vet Sci. 2021 Mar;135:486-494. doi: 10.1016/j.rvsc.2020.11.017. Epub 2020 Nov 25.
Salmonella enterica serovar Abortusovis (S. Abortusovis) infection is one of the most important causes of infectious late-term abortion as well as birth of weak lambs in sheep in many countries throughout the world. Implementation of protocols based on the application of effective vaccines is one of the most effective approaches for controlling this disease, but variable efficacy has been reported, possibly related to factors associated with the host, the vaccine, the parameters used for determining efficacy and the challenge protocols. In this context, a new commercial inactivated vaccine (INMEVA; Laboratorios Hipra S.A., Spain) was evaluated in 20 control and 17 vaccinated gestating ewes, subcutaneously challenged at 90 days of gestation with 5 × 10 colony-forming units (cfu) of a wild strain of S. Abortusovis. Incidence of reproductive failures, bacterial vaginal excretion (by real time PCR), and lamb survival were evaluated as indicators of the vaccine's level of protection. Moreover, humoral response (by ELISA test in serum samples) was studied. Vaccination was showed to be safe under the study conditions. Vaccine efficacy was demonstrated in two different ways: i) it significantly decreased the percentage of abortions [29.4% (5/17) in the vaccinated group compared to the control group (65%; 13/20)] and ii) there was a significant reduction of the overall vaginal excretion in the sampling period (3.05 log cfu/mL ± 0.84 in the vaccinated group vs. 5.68 ± 0.67 in the control group). Given these results, the vaccine evaluated can be considered as an effective alternative for controlling S. Abortusovis infection in ovine flocks.
流产布鲁氏菌(S. Abortusovis)感染是导致世界许多国家绵羊传染性晚期流产和弱羔羊出生的最重要原因之一。实施基于应用有效疫苗的方案是控制这种疾病的最有效方法之一,但据报道其效果存在差异,这可能与宿主、疫苗、用于确定疗效的参数和挑战方案相关的因素有关。在此背景下,对一种新的商业灭活疫苗(INMEVA;Laboratorios Hipra S.A.,西班牙)进行了评估,将 20 只对照和 17 只妊娠母羊在妊娠 90 天经皮下接种 5×10 个菌落形成单位(cfu)野生流产布鲁氏菌,作为疫苗保护水平的指标,评估了生殖失败、细菌阴道排出(实时 PCR)和羔羊存活率。此外,还研究了体液反应(通过血清样本 ELISA 试验)。在研究条件下,疫苗接种是安全的。疫苗的有效性通过两种不同的方式得到证明:i)显著降低了流产的百分比[接种组 29.4%(17/58),而对照组为 65%(20/31)];ii)在整个采样期间阴道总排出量显著减少(接种组 3.05 log cfu/mL±0.84,对照组 5.68±0.67)。鉴于这些结果,评估的疫苗可被视为控制绵羊流产布鲁氏菌感染的有效替代方案。