Short CommunicationHSPA5 is an essential host factor for Ebola virus infection

- Targeting HSPA5 chaperone activity inhibits EBOV.
- EBOV transcript and protein production is impaired in the absence of HSPA5.
- Targeting HSPA5 in vivo protects mice from lethal EBOV.

Development of novel strategies targeting the highly virulent ebolaviruses is urgently required. A proteomic study identified the ER chaperone HSPA5 as an ebolavirus-associated host protein. Here, we show using the HSPA5 inhibitor (-)- epigallocatechin gallate (EGCG) that the chaperone is essential for virus infection, thereby demonstrating a functional significance for the association. Furthermore, in vitro and in vivo gene targeting impaired viral replication and protected animals in a lethal infection model. These findings demonstrate that HSPA5 is vital for replication and can serve as a viable target for the design of host-based countermeasures.