HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Fusion PCR generated Japanese encephalitis virus/dengue 4 virus chimera exhibits lack of neuroinvasiveness, attenuated neurovirulence, and a dual-flavi immune response in mice.

Abstract
The first flavivirus chimera encoding dengue 4 virus (D4) PrM and E structural proteins in a Japanese encephalitis virus (JEV) backbone was successfully generated using the long-PCR based cDNA-fragment stitching (LPCRcFS) technique, demonstrating the technique's applicability for rapid preparation of flavivirus chimeras. The JEV/D4 chimera multiplied at levels equal to JEV and D4 in the mosquito cell line C6/36, while in a mouse neuronal cell line (N2a) JEV replicated efficiently, but JEV/D4 and D4 did not. In mouse challenge experiments, JEV/D4 showed a lack of neuroinvasiveness similar to D4 when inoculated intraperitoneally, but demonstrated attenuated neurovirulence (LD50=3.17 x 10(4) f.f.u.) when inoculated intracranially. It was also noted that mice receiving intraperitoneal challenge with JEV/D4 possessed D4-specific neutralization antibody and in addition clearly showed resistance to JEV intraperitoneal challenge (at 100 x LD50). This suggests that immunity to anti-JEV non-structural protein(s) offers protection against JEV infection in vivo. Dengue secondary infection was also simulated by challenging mice pre-immunized with dengue 2 virus, with D4 or JEV/D4. Mice showed higher secondary antibody response to challenge with JEV/D4 than to D4, at 210,000 and 37,000 averaged ELISA units, respectively. Taken together, aside from demonstrating the LPCRcFS technique, it could be concluded that the PrM and E proteins are the major determinant of neuroinvasiveness for JEV. It is also expected that the JEV/D4 chimera with its pathogenicity in mice and atypical immune profile, could have applications in dengue prophylactic research, in vivo efficacy assessment of dengue vaccines and development of animal research on models of dengue secondary infection.
AuthorsEdward Gitau Matumbi Mathenge, Maria Del Carmen Parquet, Yasutomo Funakoshi, Seiji Houhara, Pooi Fong Wong, Akitoyo Ichinose, Futoshi Hasebe, Shingo Inoue, Kouichi Morita
JournalThe Journal of general virology (J Gen Virol) Vol. 85 Issue Pt 9 Pg. 2503-2513 (Sep 2004) ISSN: 0022-1317 [Print] England
PMID15302944 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Viral
  • Antigens, Viral
  • Recombinant Fusion Proteins
  • Viral Envelope Proteins
  • prM protein, Flavivirus
  • glycoprotein E, Flavivirus
Topics
  • Animals
  • Antibodies, Viral (blood)
  • Antigens, Viral (genetics)
  • Cell Line
  • Culicidae
  • Dengue (blood, virology)
  • Dengue Virus (genetics, immunology, pathogenicity)
  • Disease Models, Animal
  • Encephalitis Virus, Japanese (genetics, immunology, pathogenicity)
  • Encephalitis, Japanese (blood, pathology, virology)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Neutralization Tests
  • Paralysis (pathology)
  • Polymerase Chain Reaction
  • Recombinant Fusion Proteins (biosynthesis)
  • Recombination, Genetic
  • Species Specificity
  • Viral Envelope Proteins (genetics, immunology)
  • Virulence

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: