| Literature DB >> 34610295 |
Rita E Chen1, Brittany K Smith2, John M Errico2, David N Gordon3, Emma S Winkler1, Laura A VanBlargan4, Chandni Desai2, Scott A Handley2, Kimberly A Dowd3, Emerito Amaro-Carambot3, M Jane Cardosa5, Carlos A Sariol6, Esper G Kallas7, Rafick-Pierre Sékaly8, Nikos Vasilakis9, Daved H Fremont10, Stephen S Whitehead3, Theodore C Pierson3, Michael S Diamond11.
Abstract
Although divergent dengue viruses (DENVs) have been isolated in insects, nonhuman primates, and humans, their relationships to the four canonical serotypes (DENV 1-4) are poorly understood. One virus isolated from a dengue patient, DKE-121, falls between genotype and serotype levels of sequence divergence to DENV-4. To examine its antigenic relationship to DENV-4, we assessed serum neutralizing and protective activity. Whereas DENV-4-immune mouse sera neutralize DKE-121 infection, DKE-121-immune sera inhibit DENV-4 less efficiently. Passive transfer of DENV-4 or DKE-121-immune sera protects mice against homologous, but not heterologous, DENV-4 or DKE-121 challenge. Antigenic cartography suggests that DENV-4 and DKE-121 are related but antigenically distinct. However, DENV-4 vaccination confers protection against DKE-121 in nonhuman primates, and serum from humans immunized with a tetravalent vaccine neutralize DENV-4 and DKE-121 infection equivalently. As divergent DENV strains, such as DKE-121, may meet criteria for serotype distinction, monitoring their capacity to impact dengue disease and vaccine efficacy appears warranted.Entities:
Keywords: antibody; dengue; divergent; genotype; neutralization; pathogenesis; protection; serotype
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Year: 2021 PMID: 34610295 PMCID: PMC8595868 DOI: 10.1016/j.chom.2021.09.006
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 31.316