Human DDX3X Unwinds Japanese Encephalitis and Zika Viral 5′ Terminal Regions

Flavivirus genus includes many deadly viruses such as the Japanese encephalitis virus (JEV) and Zika virus (ZIKV). The 5&prime
terminal regions (TR) of flaviviruses interact with human proteins and such interactions are critical for viral replication. One of the human proteins identified to interact with the 5&prime
TR of JEV is the DEAD-box helicase, DDX3X. In this study, we in vitro transcribed the 5&prime
TR of JEV and demonstrated its direct interaction with recombinant DDX3X (Kd of 1.66 &plusmn
0.21 &micro
M) using microscale thermophoresis (MST). Due to the proposed structural similarities of 5&prime
and 3&prime
TRs of flaviviruses, we investigated if the ZIKV 5&prime
TR could also interact with human DDX3X. Our MST studies suggested that DDX3X recognizes ZIKV 5&prime
TR with a Kd of 7.05 &plusmn
0.75 &micro
M. Next, we performed helicase assays that suggested that the binding of DDX3X leads to the unwinding of JEV and ZIKV 5&prime
TRs. Overall, our data indicate, for the first time, that DDX3X can directly bind and unwind in vitro transcribed flaviviral TRs. In summary, our work indicates that DDX3X could be further explored as a therapeutic target to inhibit Flaviviral replication