Identifying the Role of E2 Domains on Alphavirus Neutralization and Protective Immune Responses

James Weger-Lucarelli, Matthew T. Aliota, Attapon Kamlangdee, Jorge E. Osorio

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Background: Chikungunya virus (CHIKV) and other alphaviruses are the etiologic agents of numerous diseases in both humans and animals. Despite this, the viral mediators of protective immunity against alphaviruses are poorly understood, highlighted by the lack of a licensed human vaccine for any member of this virus genus. The alphavirus E2, the receptor-binding envelope protein, is considered to be the predominant target of the protective host immune response. Although envelope protein domains have been studied for vaccine and neutralization in flaviviruses, their role in alphaviruses is less characterized. Here, we describe the role of the alphavirus E2 domains in neutralization and protection through the use of chimeric viruses. Methodology/Principal Findings: Four chimeric viruses were constructed in which individual E2 domains of CHIKV were replaced with the corresponding domain from Semliki Forest virus (SFV) (ΔDomA/ΔDomB/ΔDomC/ ΔDomA+B). Vaccination studies in mice (both live and inactivated virus) revealed that domain B was the primary determinant of neutralization. Neutralization studies with CHIKV immune serum from humans were consistent with mouse studies, as ΔDomB was poorly neutralized. Conclusions/Significance: Using chimeric viruses, it was determined that the alphavirus E2 domain B was the critical target of neutralizing antibodies in both mice and humans. Therefore, chimeric viruses may have more relevance for vaccine discovery than peptide-based approaches, which only detect linear epitopes. This study provides new insight into the role of alphavirus E2 domains on neutralization determinants and may be useful for the design of novel therapeutic technologies.

Original languageEnglish (US)
Article numbere0004163
JournalPLoS neglected tropical diseases
Volume9
Issue number10
DOIs
StatePublished - Oct 16 2015

Bibliographical note

Funding Information:
Funding: This work was supported by NIH grant #AI093491-02. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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