Li Yuanyi, Gottschalk Marcelo, Esgleas Miriam, Lacouture Sonia, Dubreuil J Daniel, Willson Philip, Harel Josee
Groupe de Recherche sur les Maladies Infectieuses du Porc, Faculté de Médecine Vétérinaire, Université de Montréal, C.P. 5000, St.-Hyacinthe, Québec J2S 7C6, Canada.
Clin Vaccine Immunol. 2007 Aug;14(8):937-43. doi: 10.1128/CVI.00046-07. Epub 2007 Jun 13.
Sao is a Streptococcus suis surface protein recently identified as a potential vaccine candidate. In this study, recombinant Sao in combination with Quil A provided cross-protection against S. suis serotype 2 disease in mouse and pig vaccination protocols. Subcutaneous immunization of mice elicited strong immunoglobulin G (IgG) antibody responses. All four IgG subclasses were induced, with the IgG2a titer being the highest, followed by those of IgG1, IgG2b, and IgG3. Challenge of the mice with S. suis strain 31533 resulted in a mortality rate of 80% for the control group, which received Quil A only. In contrast, all of the mice immunized with Sao survived. In a pig vaccination protocol, intramuscular immunization with Sao also elicited significant humoral antibody responses, and both the IgG1 and IgG2 subclasses were induced, with a predominance of IgG2 production. In vitro assay showed that Sao-induced antibodies significantly promoted the ability of porcine neutrophils in opsonophagocytic killing of S. suis. An aerosol challenge of the pigs with S. suis strain 166 resulted in clinical signs characteristic of S. suis infection in diseased pigs. The vaccine group showed significantly better survival, lower clinical scores, and less S. suis recovery from postmortem tissue samples than did the control group. Furthermore, this study also revealed that although challenge S. suis strains express Sao size variants, recombinant Sao conferred cross-protection. These data demonstrate that recombinant Sao formulated with Quil A triggers strong opsonizing antibody responses which confer efficient immunity against challenge infection with heterologous S. suis type 2.
Sao是一种最近被鉴定为潜在疫苗候选物的猪链球菌表面蛋白。在本研究中,重组Sao与Quil A联合使用,在小鼠和猪的疫苗接种方案中提供了针对猪链球菌2型疾病的交叉保护。小鼠皮下免疫引发了强烈的免疫球蛋白G(IgG)抗体反应。诱导了所有四种IgG亚类,其中IgG2a滴度最高,其次是IgG1、IgG2b和IgG3。用猪链球菌31533菌株攻击小鼠,仅接受Quil A的对照组死亡率为80%。相比之下,所有用Sao免疫的小鼠都存活了下来。在猪的疫苗接种方案中,用Sao进行肌肉注射免疫也引发了显著的体液抗体反应,诱导了IgG1和IgG2亚类,以IgG2产生为主。体外试验表明,Sao诱导的抗体显著促进了猪中性粒细胞对猪链球菌的调理吞噬杀伤能力。用猪链球菌166菌株对猪进行气溶胶攻击,患病猪出现了猪链球菌感染的特征性临床症状。与对照组相比,疫苗组的存活率显著更高,临床评分更低,死后组织样本中猪链球菌的回收率更低。此外,本研究还表明,尽管攻击的猪链球菌菌株表达Sao大小变体,但重组Sao仍能提供交叉保护。这些数据表明,与Quil A配制的重组Sao引发了强烈的调理抗体反应,从而对异源猪链球菌2型的攻击感染提供了有效的免疫力。