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Dengue viruses cluster antigenically but not as discrete serotypes
Author(s) -
Leah C. Katzelnick,
Judith M. Fonville,
Gregory D. Gromowski,
José BustosArriaga,
Angela Green,
Sarah L. James,
Louis Lau,
Magelda Montoya,
Chunling Wang,
Laura A. VanBlargan,
Colin A. Russell,
Hlaing Myat Thu,
Theodore C. Pierson,
Philippe Buchy,
John Aaskov,
Jorge L. MuñozJordán,
Nikos Vasilakis,
Robert V. Gibbons,
Robert B. Tesh,
Albert D. M. E. Osterhaus,
Ron A. M. Fouchier,
Anna P. Durbin,
Cameron P. Simmons,
Edward C. Holmes,
Eva Harris,
Stephen S. Whitehead,
Derek J. Smith
Publication year - 2015
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aac5017
Subject(s) - dengue fever , virology , serotype , antigenic variation , dengue virus , biology , original antigenic sin , antigen , dengue vaccine , cluster (spacecraft) , virus , antibody , antibody dependent enhancement , immunology , antigenic drift , influenza a virus , computer science , programming language
The four genetically divergent dengue virus (DENV) types are traditionally classified as serotypes. Antigenic and genetic differences among the DENV types influence disease outcome, vaccine-induced protection, epidemic magnitude, and viral evolution. We characterized antigenic diversity in the DENV types by antigenic maps constructed from neutralizing antibody titers obtained from African green monkeys and after human vaccination and natural infections. Genetically, geographically, and temporally, diverse DENV isolates clustered loosely by type, but we found that many are as similar antigenically to a virus of a different type as to some viruses of the same type. Primary infection antisera did not neutralize all viruses of the same DENV type any better than other types did up to 2 years after infection and did not show improved neutralization to homologous type isolates. That the canonical DENV types are not antigenically homogeneous has implications for vaccination and research on the dynamics of immunity, disease, and the evolution of DENV.

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