Alanine Substitution Inactivates Cross-Reacting Epitopes in Dengue Virus Recombinant Envelope Proteins

• Published in: Viruses Vol. 12; no. 2; p. 208
• Main Authors: Zomosa-Signoret, Viviana C, Morales-González, Karina R, Estrada-Rodríguez, Ana E, Rivas-Estilla, Ana M, Devèze-García, M Cristina, Galaviz-Aguilar, Edgar, Vidaltamayo, Román
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI 13.02.2020; MDPI AG
• Subjects: Alanine - immunology; Amino Acid Substitution; Antibodies, Viral - blood; Cross Reactions; dengue; Dengue - immunology; Dengue - virology; Dengue Virus - classification; Dengue Virus - genetics; Dengue Virus - immunology; epitope inactivation; Epitope Mapping; Epitopes - genetics; Epitopes - immunology; Humans; Recombinant Proteins - genetics; Recombinant Proteins - immunology; Serogroup; serological methods; Viral Envelope Proteins - genetics; Viral Envelope Proteins - immunology; zika; epitope inactivation; serological methods; dengue; Zika
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v12020208

The expansion of the habitat of mosquitoes belonging to the genus puts nearly half of the world's population at risk of contracting dengue fever, and a significant fraction will develop its serious hemorrhagic complication, which can be fatal if not diagnosed properly and treated in a timely fashion. Although several diagnostic methods have been approved for dengue diagnostics, their applicability is limited in rural areas of developing countries by sample preparation costs and methodological requirements, as well as cross-reactivity among the different serotypes of the Dengue virus and other flavivirus, such as the Zika virus. For these reasons, it is necessary to generate more specific antigens to improve serological methods that could be cheaper and used in field operations. Here, we describe a strategy for the inactivation of cross-reacting epitopes on the surface of the Dengue virus envelope protein through the synthetic generation of recombinant peptide sequences, where key amino acid residues from Dengue virus serotype 1 (DENV-1) and 2 (DENV-2) are substituted by alanine residues. The proteins thus generated are recognized by 88% of sera from Dengue NS1+ patients and show improved serotype specificity because they do not react with the antibodies present in seroconverted, PCR-serotyped DEN-4 infected patients.