Involvement of Surfactant Protein D in Ebola Virus Infection Enhancement via Glycoprotein Interaction
Anne-Laure Favier (CRSSA), Olivier Reynard, Evelyne Gout (IBS - UMR, 5075), Martin Van Eijk, Henk Haagsman, Erika Crouch (Department of Pathology, And Immunology), Viktor Volchkov, Christophe Peyrefitte, Nicole Thielens (IBS, - UMR 5075)

TL;DR
This study uncovers that surfactant protein D interacts with Ebola virus glycoprotein and enhances infection in vitro, revealing a novel host factor that may facilitate viral spread.
Contribution
It demonstrates for the first time that surfactant protein D can enhance Ebola virus infection through direct glycoprotein interaction.
Findings
hSP-D interacts specifically with Ebola GP.
hSP-D enhances Ebola virus infection in vitro.
Similar effects observed with porcine SP-D and Reston virus.
Abstract
Since the largest 2014-2016 Ebola virus disease outbreak in West Africa, understanding of Ebola virus infection has improved, notably the involvement of innate immune mediators. Amongst them, collectins are important players in the antiviral innate immune defense. A screening of Ebola glycoprotein (GP)-collectins interactions revealed the specific interaction of human surfactant protein D (hSP-D), a lectin expressed in lung and liver, two compartments where Ebola was found in vivo. Further analyses have demonstrated an involvement of hSP-D in the enhancement of virus infection in several in vitro models. Similar effects were observed for porcine SP-D (pSP-D). In addition, both hSP-D and pSP-D interacted with Reston virus (RESTV) GP and enhanced pseudoviral infection in pulmonary cells. Thus, our study reveals a novel partner of Ebola GP that may participate to enhance viral spread.
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