Rémond Michelle, Da Costa Bruno, Riffault Sabine, Parida Satya, Breard Emmanuel, Lebreton Françoise, Zientara Stephan, Delmas Bernard
UMR 1161 Virologie AFSSA-INRA-ENVA, F-94706 Maisons-Alfort, France.
Vaccine. 2009 Jan 1;27(1):93-8. doi: 10.1016/j.vaccine.2008.10.036. Epub 2008 Nov 5.
An antigen delivery system based on subviral particles formed by the self-assembly of the capsid protein of infectious bursal disease virus and carrying foreign peptides at the top of the projection domain was investigated. We report here the effective insertion of the foot-and-mouth disease virus (FMDV) immunodominant epitope in one of the four external loops of the subviral particles. Out of the two loops tested, one of them tolerated an insert of 12 amino acids without disrupting the subviral particle assembly. The subviral particles reacted with neutralizing FMDV type O1 monoclonal and polyclonal antibodies and elicited a neutralizing antibody response in immunized mice. Furthermore, we found that they have the potential for the detection of FMDV antibodies in a competitive ELISA for diagnostic.
研究了一种基于传染性法氏囊病病毒衣壳蛋白自组装形成的亚病毒颗粒的抗原递送系统,该系统在突出结构域顶端携带外源肽。我们在此报告口蹄疫病毒(FMDV)免疫显性表位有效插入亚病毒颗粒四个外部环之一中。在测试的两个环中,其中一个环可耐受12个氨基酸的插入而不破坏亚病毒颗粒组装。亚病毒颗粒与O1型口蹄疫病毒中和单克隆抗体和多克隆抗体发生反应,并在免疫小鼠中引发中和抗体反应。此外,我们发现它们有潜力用于在竞争性ELISA诊断中检测口蹄疫病毒抗体。