| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4361611 | Cell Host & Microbe | 2011 | 8 Pages |
SummaryAlphaviruses, including several emerging human pathogens, are a large family of mosquito-borne viruses with Sindbis virus being a prototypical member of the genus. The host factor requirements and receptors for entry of this class of viruses remain obscure. Using a Drosophila system, we identified the divalent metal ion transporter natural resistance-associated macrophage protein (NRAMP) as a host cell surface molecule required for Sindbis virus binding and entry into Drosophila cells. Consequently, flies mutant for dNRAMP were protected from virus infection. NRAMP2, the ubiquitously expressed vertebrate homolog, mediated binding and infection of Sindbis virus into mammalian cells, and murine cells deficient for NRAMP2 were nonpermissive to infection. Alphavirus glycoprotein chimeras demonstrated that the requirement for NRAMP2 is at the level of Sindbis virus entry. Given the conserved structure of alphavirus glycoproteins, and the widespread use of transporters for viral entry, other alphaviruses may use conserved multipass membrane proteins for infection.
► Drosophila NRAMP, a metal ion transporter, is required for Sindbis virus infection ► dNRAMP is required for binding, entry, and infection of Drosophila cells and adult flies ► Sindbis virus infection is sensitive to iron treatment ► NRAMP2 is required for Sindbis virus entry and infection of mammalian cells
