Abstract

In parallel with the """"""""Jennerian"""""""" and modified """"""""Jennerian"""""""" approach to vaccination against rotavirus diarrhea in which an oral live attenuated rotavirus vaccine is generated, we are pursuing other exploratory approaches to vaccination. A complete rotavirus particle consists of three capsid layers: an outer layer consisting of VP4 and VP7, an intermediate layer consisting of VP6 and an inner core consisting primarily of VP2. In this project, taking advantage of (i) the availability in our laboratory of various baculovirus recombinants expressing rotavirus proteins including VP2, VP4, VP6 and VP7 and (ii) properties of selected rotavirus structural proteins to self-assemble spontaneously and form virus-like particles (VLPs) upon co-expression in insect cells, we are pursuing the construction of recombinant rotavirus VLP subunit vaccines that can be delivered via various routes including intranasally. By co-infecting insect cells with recombinant baculoviruses expressing simian rotavirus SA11 VP2 and VP6 and human rotavirus AU32 VP7 (G9), we analyzed last year various factors involved in VLP assembly in an effort to optimize the expression system and enhance the yield of VLPs. This year, in order to increase the yield of VLP production, we cloned the human rotavirus Wa genes 2 and 6 into a single baculovirus transfer vector. Efforts will be made to produce 2/6 VLPs composed of human rotavirus Wa strain VP2 and VP6 proteins.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000914-02
Application #
6809350
Study Section
(LID)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2003
Total Cost
Indirect Cost

  Institution

Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code