Human infections by Marburg (MBG) and Ebola (EBO) viruses result in lethal
hemorrhagic fever. To identify cellular entry factors employed by MBG virus
, noninfectible cells transduced with an expression library were challenged
with a selectable pseudotype virus packaged by MBG glycoproteins (GP). A c
DNA encoding the folate receptor-alpha (FR-alpha) was recovered from cells
exhibiting reconstitution of viral entry. A FR-alpha cDNA was recovered in
a similar strategy employing EBO pseudotypes. FR-alpha expression in Jurkat
cells facilitated MBG or EBO entry, and FR-blocking reagents inhibited inf
ection by MBG or EBO. Finally, FR-alpha bound cells expressing MBG or EBO G
P and mediated syncytia formation triggered by MBG GP. Thus, FR-alpha is a
significant cofactor for cellular entry for MBG and EBO viruses.