Locus of a Virus Neutralization Epitope on the Japanese Encephalitis Virus Envelope Protein Determined by Use of Long PCR-Based Region-Specific Random Mutagenesis

• Published in: Virology (New York, N.Y.) N.Y.), 2001-09, Vol.287 (2), p.417-426
• Main Authors: Morita, Kouichi, Tadano, Masayuki, Nakaji, Shun, Kosai, Kosuke, Mathenge, Edward G.M., Pandey, Basu D., Hasebe, Futoshi, Inoue, Shingo, Igarashi, Akira
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Monoclonal - immunology; Antibody Affinity; Cells, Cultured; Encephalitis Virus, Japanese - genetics; Encephalitis Virus, Japanese - immunology; Epitopes - immunology; Japanese encephalitis virus; long PCR; Membrane Glycoproteins - genetics; Membrane Glycoproteins - immunology; Mice; Mutagenesis; neutralization escape mutant; Neutralization Tests; Polymerase Chain Reaction; Recombinant Proteins - immunology; recombinant virus; Recombination, Genetic; Viral Envelope Proteins - genetics; Viral Envelope Proteins - immunology
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1006/viro.2001.1048

We prepared recombinant Japanese encephalitis (JE) virus populations possessing random mutations at the envelope (E) protein region by a long PCR-based method. Neutralization-resistant mutants were selected from these populations by application of JE-specific virus neutralizing monoclonal antibody (mAb) 503, which possessed a 51,200-fold neutralization titer. We classified the mutants into three groups, each bearing two amino acid alterations at the E protein region: 52, Gln–Arg, and 136, Lys–Glu; 136, Lys–Glu, and 275, Ser–Pro; and 126, Ile–Thr, and 136, Lys–Glu, respectively. Three different genetically engineered variants, each bearing a single mutation, 126, Ile–Thr; 136, Lys–Glu; and 275, Ser–Pro, respectively, showed partial but not complete recovery of reactivity to mAb 503. Our results indicate that the amino acid substitutions at amino acid positions 52, 126, 136, and 275 altered the structure of the neutralization epitope for mAb 503 on the E protein. All these mutations were clustered at the junction of domains I and II of the E protein and it is likely that the epitope for mAb 503 is composed of at least E0-e, D0-a, and k strands of the E protein. We also demonstrated the efficacy of the long PCR-based recombinant virus technique as a useful tool for the creation of a variety of mutants bearing random mutations at targeted areas of the virus genome.