Dengue Virus NS1 Binds Ephrin B1 to Trigger Endothelial Dysfunction
Felix PahmeieriD, Sabrina Hammond, Charlotte FloryiD, Xinyi FengiD, S. LeeiD, Erika Vanessa Jiménez-PosadaiD, Elias Michael DuarteiD, Jaime Andrés Cardona-OspinaiD, Aquena H. BalliD, Nharae E. Lee, Kayla Leung, Laurentia V. TjangiD, P. Robert BeattyiD, Scott B. BieringiD, Pietro ScaturroiD, Eva HarrisiD
Abstract
Dengue virus (DENV), a member of the Flaviviridae family, is the most prevalent and medically important mosquito-borne viral pathogen. Infected cells secrete the viral non-structural protein 1 (NS1) into the bloodstream, where it can interact with endothelial cells to induce vascular leak. Host factors involved in NS1-mediated endothelial dysfunction are incompletely understood, leading us to investigate the host interactome of DENV NS1 in endothelial cells via a comparative mass spectrometry approach. We identified ephrin B1 (EFNB1) as a critical host factor in NS1-mediated endothelial barrier dysfunction and show that phosphorylation of EFNB1 is necessary for induction of barrier dysfunction. Further, we map the interface of the EFNB1-NS1 complex through biochemical and computational approaches, and we show that EFNB1-Fc-fusion proteins can act as decoys to block NS1-induced barrier dysfunction in vitro and in vivo. This study provides insights into the mechanism of flavivirus NS1-mediated endothelial barrier dysfunction and new avenues to target vascular leak.
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