Cauchard S, Bertrand F, Barrier-Battut I, Jacquet S, Laurentie M, Barbey C, Laugier C, Deville S, Cauchard J
ANSES, Dozulé Laboratory for Equine Diseases, Bacteriology and Parasitology Unit, 14430 Goustranville, France.
SEPPIC, 22 Terrasse Bellini, Paris La Défense, France.
Vet Immunol Immunopathol. 2014 Feb 15;157(3-4):164-74. doi: 10.1016/j.vetimm.2013.12.003. Epub 2013 Dec 17.
Rhodococcus equi is the most common infectious cause of mortality in foals between 1 and 6 months of age. Because of an increase in the number of antibiotic-resistant strains, the optimization of a prophylactic strategy is a key factor in the comprehensive management of R. equi pneumonia. The objectives of this study were to assess the safety and immunogenicity of R. equi-secreted proteins (ReSP) co-administered with either the nanoparticular adjuvant Montanide™ IMS 3012 VG, or a new polymeric adjuvant Montanide™ PET GEL A, and to further investigate the most immunogenic proteins for subsequent immunization/challenge experiments in the development of a vaccine against rhodoccocal pneumonia. The approach involved two phases. The first phase aimed to investigate the safety of vaccination in six adult horses. The second phase aimed to determine the safety and immunogenicity of vaccination in twelve 3-week-old foals. We set out to develop a method based on ultrasound measurements for safety assessment in adult horses in order to evaluate any in situ changes at the injection site, in the skin or the underlying muscle, with quantitative and qualitative data revealing that administration of ReSP combined with the Pet Gel A adjuvant led to an increase in local inflammation, associated with 4- to 7-fold higher levels of anti-R. equi IgGa, IgGb and IgGT, compared to administration of ReSP associated with IMS 3012 adjuvant, but without any impact on animal demeanor. Investigations were then performed in foals with serological and clinical follow-up until 6 months of age. Interestingly, we observed in foals a much lower incidence of adverse local tissue reactions at the injection site than in adult horses, with transient and moderate swelling for the group that received ReSP combined with Pet Gel A. Immunized foals with Pet Gel A adjuvant exhibited a similar response in both IgGa and IgGT levels, but a lower response in IgGb levels, compared to adult horses, with a subisotype profile that may however reflect a bias favorable to R. equi resistance. From the crude extract of secreted proteins, dot-blot screening enabled identification of cholesterol oxidase, mycolyl transferase 3, and PSP (probable secreted protein) as the most immunogenic candidates. Taken together, these results are encouraging in developing a vaccine for foals.
马红球菌是1至6月龄幼驹最常见的致死性感染病因。由于抗生素耐药菌株数量增加,优化预防策略是马红球菌肺炎综合管理的关键因素。本研究的目的是评估与纳米颗粒佐剂Montanide™ IMS 3012 VG或新型聚合物佐剂Montanide™ PET GEL A共同给药的马红球菌分泌蛋白(ReSP)的安全性和免疫原性,并进一步研究在开发抗红球菌肺炎疫苗的后续免疫/攻毒实验中最具免疫原性的蛋白。该方法包括两个阶段。第一阶段旨在研究六匹成年马接种疫苗的安全性。第二阶段旨在确定12匹3周龄幼驹接种疫苗的安全性和免疫原性。我们着手开发一种基于超声测量的方法用于成年马的安全性评估,以评估注射部位、皮肤或其下方肌肉的任何原位变化,定量和定性数据显示,与Pet Gel A佐剂联合使用ReSP会导致局部炎症增加,与抗马红球菌IgGa、IgGb和IgGT水平高出4至7倍相关,相比之下,与IMS 3012佐剂联合使用ReSP时则不然,但对动物行为没有任何影响。然后对幼驹进行了血清学和临床随访调查,直至6月龄。有趣的是,我们观察到幼驹注射部位局部组织不良反应的发生率远低于成年马,接受ReSP与Pet Gel A联合使用的组出现短暂和中度肿胀。与成年马相比,用Pet Gel A佐剂免疫的幼驹在IgGa和IgGT水平上表现出相似的反应,但在IgGb水平上反应较低,其亚型分布可能反映了对马红球菌抗性有利的偏差。通过分泌蛋白的粗提物,斑点印迹筛选能够鉴定出胆固醇氧化酶、分枝菌酸转移酶3和PSP(可能的分泌蛋白)是最具免疫原性的候选物。综上所述,这些结果对于开发幼驹疫苗是令人鼓舞的。