Rab1A functioned as a binding protein involved in Macrobrachium rosenbergii Taihu virus infection.

Macrobrachium rosenbergii Taihu virus (MrTV) is a virulent pathogen that mainly threatens M. rosenbergii larvae. Rab proteins, which are essential for controlling intracellular membrane trafficking, are hijacked by multiple viruses to complete their life cycle. In this paper, we studied the function of M. rosenbergii Rab1A (MrRab1A) in the MrTV infection. Upon MrTV infection, the transcription level of MrRab1A was significantly up-regulated, indicating MrRab1A was a MrTV responsive gene and might be important for MrTV infection. Co-IP and co-localization assays revealed that MrRab1A could directly bind with MrTV and its capsid protein VP3. Moreover, the in vivo neutralization assay demonstrated that pre-incubation of MrTV with recombinant MrRab1A could partially block MrTV infection. These findings indicated that MrRab1A functioned as a virus-binding protein involved in MrTV infection, which shed new light on the mechanism of MrTV infection and provided a potential target for developing anti-MrTV therapies. • We identified MrRab1A as a binding protein of MrTV for the first time. • The transcription level of MrRab1A was significantly increased upon MrTV infection. • Co-IP and co-localization assays revealed that MrRab1A could bind with MrTV. • Preincubation of MrTV with rMrRab1A could partially block MrTV infection. [ABSTRACT FROM AUTHOR]