Immunogenicity of the Plasmodium falciparum glutamate-rich protein expressed by vaccinia virus

Research output: Contribution to journalJournal articleResearchpeer-review

The glurp gene of Plasmodium falciparum F32 has been inserted into a vaccinia virus, and the recombinant virus was designated VVG4. Expression of glurp in VVG4-infected Vero cells was analyzed by immunoprecipitation and revealed a primary GLURP product of approximately 220,000 Da; GLURP was detected both intracellularly and in culture supernatants. To study the immunogenicity of vaccinia virus-expressed GLURP, mice were immunized with VVG4 and serum samples were analyzed for antibody reactivity with three polypeptides, covering almost the entire GLURP molecule; these three polypeptides were produced in recombinant form in Escherichia coli. The immune response was primarily directed against a carboxy-terminal repeat region. The mouse anti-GLURP serum recognized authentic GLURP by immunoprecipitation analysis from P. falciparum grown in vitro. These results demonstrate that vaccinia virus-expressed glurp product can induce a humoral immune response against GLURP derived from blood-stage parasites.

Original languageEnglish
JournalInfection and Immunity
Volume62
Issue number8
Pages (from-to)3270-5
Number of pages6
ISSN0019-9567
Publication statusPublished - Aug 1994
Externally publishedYes

    Research areas

  • Animals, Base Sequence, Female, Humans, Malaria Vaccines/immunology, Mice, Mice, Inbred BALB C, Molecular Sequence Data, Molecular Weight, Plasmodium falciparum/immunology, Protozoan Proteins/biosynthesis, Protozoan Vaccines, Vaccines, Synthetic/immunology, Vaccinia virus/genetics

ID: 203012623