A Genetically Engineered Rotavirus NSP2 Phosphorylation Mutant Impaired in Viroplasm Formation and Replication Shows an Early Interaction between vNSP2 and Cellular Lipid Droplets

Abstract

Many RNA viruses replicate in cytoplasmic compartments (virus factories or viroplasms) composed of viral and cellular proteins, but the mechanisms required for their formation remain largely unknown. Rotavirus (RV) replication in viroplasms requires interactions between virus nonstructural proteins NSP2 and NSP5, which are associated with components of lipid droplets (LDs). We previously identified two forms of NSP2 in RV-infected cells, a cytoplasmically dispersed form (dNSP2) and a viroplasm-specific form (vNSP2), which interact with hypophosphorylated and hyperphosphorylated NSP5, respectively, indicating that a coordinated phosphorylation cascade controls viroplasm assembly. The cellular kinase CK1α phosphorylates NSP2 on serine 313, triggering the localization of vNSP2 to sites of viroplasm assembly and its association with hyperphosphorylated NSP5. Using reverse genetics, we generated a rotavirus with a phosphomimetic NSP2 (S313D) mutation to directly evaluate the role of CK1α NSP2 phosphorylation in viroplasm formation. Recombinant rotavirus NSP2 S313D (rRV NSP2 S313D) is significantly delayed in viroplasm formation and in virus replication and interferes with wild-type RV replication in coinfection. Taking advantage of the delay in viroplasm formation, the NSP2 phosphomimetic mutant was used as a tool to observe very early events in viroplasm assembly. We show that (i) viroplasm assembly correlates with NSP5 hyperphosphorylation and (ii) vNSP2 S313D colocalizes with RV-induced LDs without NSP5, suggesting that vNSP2 phospho-S313 is sufficient for interacting with LDs and may be the virus factor required for RV-induced LD formation. Further studies with the rRV NSP2 S313D virus are expected to reveal new aspects of viroplasm and LD initiation and assembly. IMPORTANCE Reverse genetics was used to generate a recombinant rotavirus with a single phosphomimetic mutation in nonstructural protein 2 (NSP2 S313D) that exhibits delayed viroplasm formation, delayed replication, and an interfering phenotype during coinfection with wild-type rotavirus, indicating the importance of this amino acid during virus replication. Exploiting the delay in viroplasm assembly, we found that viroplasm-associated NSP2 colocalizes with rotavirus-induced lipid droplets prior to the accumulation of other rotavirus proteins that are required for viroplasm formation and that NSP5 hyperphosphorylation is required for viroplasm assembly. These data suggest that NSP2 phospho-S313 is sufficient for interaction with lipid droplets and may be the virus factor that induces lipid droplet biogenesis in rotavirus-infected cells. Lipid droplets are cellular organelles critical for the replication of many viral and bacterial pathogens, and thus, understanding the mechanism of NSP2-mediated viroplasm/lipid droplet initiation and interaction will lead to new insights into this important host-pathogen interaction.

Rotavirus as an Expression Platform of Domains of the SARS-CoV-2 Spike Protein

“…In some cases, support plasmids expressing capping enzymes [African swine fever virus NP868R [ 25 ] or vaccinia virus D1L/D12R [ 15 ]] or fusion proteins [avian reovirus p10FAST [ 15 ]] are co-transfected with the pT7 vectors to enhance recovery of recombinant viruses. Rotavirus reverse genetics systems have been used to mutate several of the viral genome segments and to generate virus strains that express reporter proteins [ 17 , 19 , 26 , 27 , 28 , 29 , 30 ].…”

Rotavirus as an Expression Platform of the SARS-CoV-2 Spike Protein

“…In some cases, support plasmids expressing capping enzymes [African swine fever virus NP868R (22) or vaccinia virus D1L/D12R (18)] or fusion proteins [avian reovirus p10FAST (18)] are co-transfected with the pT7 vectors to enhance recovery of recombinant viruses. Rotavirus reverse genetics systems have been used to mutate several of the viral genome segments and to generate virus strains that express reporter proteins (13,17,(23)(24)(25)(26).…”

Recent advances in rotavirus reverse genetics and its utilization in basic research and vaccine development

“…During the short time span after its initial development, plasmid-only-based RV RGSs have been used extensively in diverse areas of RV research, including studies of the functions of RV proteins [ 146 ], the generation of RV reassortants [ 147 ], stable RV reporter expression systems [ 148 ], and novel vaccine platforms [ 149 ]. Thus, it can be envisioned that RGSs will be extensively employed in the rotavirus field in the future to study multiple facets of rotavirus biology that were not possible to investigate prior to the era of rotavirus RGSs.…”