Functional investigation of grass carp reovirus nonstructural protein NS80
© Cai et al; licensee BioMed Central Ltd. 2011
Received: 11 January 2011
Accepted: 14 April 2011
Published: 14 April 2011
Grass Carp Reovirus (GCRV), a highly virulent agent of aquatic animals, has an eleven segmented dsRNA genome encased in a multilayered capsid shell, which encodes twelve proteins including seven structural proteins (VP1-VP7), and five nonstructural proteins (NS80, NS38, NS31, NS26, and NS16). It has been suggested that the protein NS80 plays an important role in the viral replication cycle that is similar to that of its homologous protein μNS in the genus of Orthoreovirus.
As a step to understanding the basis of the part played by NS80 in GCRV replication and particle assembly, we used the yeast two-hybrid (Y2H) system to identify NS80 interactions with proteins NS38, VP4, and VP6 as well as NS80 and NS38 self-interactions, while no interactions appeared in the four protein pairs NS38-VP4, NS38-VP6, VP4-VP4, and VP4-VP6. Bioinformatic analyses of NS80 with its corresponding proteins were performed with all currently available homologous protein sequences in ARVs (avian reoviruses) and MRVs (mammalian reoviruses) to predict further potential functional domains of NS80 that are related to VFLS (viral factory-like structures) formation and other roles in viral replication. Two conserved regions spanning from aa (amino acid) residues of 388 to 433, and 562 to 580 were discovered in this study. The second conserved region with corresponding conserved residues Tyr565, His569, Cys571, Asn573, and Glu576 located between the two coiled-coils regions (aa ~513-550 and aa ~615-690) in carboxyl-proximal terminus were supposed to be essential to form VFLS, so that aa residues ranging from 513 to 742 of NS80 was inferred to be the smallest region that is necessary for forming VFLS. The function of the first conserved region including Ala395, Gly419, Asp421, Pro422, Leu438, and Leu443 residues is unclear, but one-third of the amino-terminal region might be species specific, dominating interactions with other viral components.
Our results in this study together with those from previous investigations indicate the protein NS80 might play a central role in VFLS formation and viral components recruitment in GCRV particle assembly, similar to the μNS protein in ARVs and MRVs.
Grass carp reovirus (GCRV) is a tentative member in the Aquareovirus genus of the Reoviridae family which shares a common genome of 9 to 12 double-stranded RNA (dsRNA) segments packaged within a multilayered icosahedral capsid shell . Different from most identified aquareoviruses, GCRV has been recognized as one of the most pathogenic agents amongst Aquareovirus isolates, which has caused a severe epidemic outbreak of hemorrhagic disease affecting a vast majority (~85%) of fingerling and yearling grass carp in southern China [2, 3]. GCRV serves as a good model for studying viral replication and pathogenesis of Aquareovirus due to its high virulence.
Studies revealed that there is a close evolutionary relationship between MRVs (mammalian reoviruses) and Aquareovirus. Recent progress on 3D structural reconstruction of single particles of GCRV by cryo-electron microscopy (CryoEM) confirmed the high similarities in the structures of viral proteins between GCRV and MRVs [5–8]. Previous investigations indicate that GCRV eleven genomic dsRNA segments (named S1-S11) encoded seven structural proteins (VP1-VP7) and five nonstructural proteins (NS80, NS38, NS31, NS26, and NS16) . Comparative studies revealed that mature GCRV particles consists of five core proteins VP1, VP2, VP3, VP4, and VP6 which are respectively homologous to λ2, λ3, λ1, μ2, and σ2 in MRVs; and two outer capsid proteins VP5 and VP7 which are analogues of μ1 and σ3 in MRVs [4–7]. However, there is no special cell attachment protein in GCRV that is homologous to MRVs σ1, hinting at different viral attachment mechanisms in GCRV and MRVs.
While the structural proteins are of great importance for GCRV entry into cells during its infection, nonstructural proteins are believed to be indispensable in replication and nascent virus particle assembly. Recent progress on nonstructural proteins in genus Orthoreovirus including MRVs and ARVs (avian reoviruses) suggests that μNS serves as a versatile protein which could form viral factory-like structures (VFLS) and recruit proteins σNS, λ1, λ2, λ3, μ2, σ2, and core particles to VFLS [9–21]. As such, NS80 might act as a scaffolding protein and a leading performer associated with the highly efficient viral replication and/or accurate assembly of progeny core particles during GCRV infection. Apart from the central role played by μNS in VFLS formation, nonstructural protein σNS, core protein μ2 and σ2 as well as RNA transcription related proteins λ1, λ2, and λ3 are also crucial accessories in VFLS formation in associating with μNS[17, 20]. σNS is known to interact directly with μNS and act as a plus single-stranded RNA (ssRNA) binding protein involved in recruiting mRNAs to VFLS for reovirus genomic dsRNA synthesis and assembly [10, 21–23]. The core protein μ2 is known to be a cellular microtubule associated protein that is linked to the VFLS morphology formation (showed either globular or filamentous). It displays both ssRNA and dsRNA binding abilities that might function in reovirus transcription [11, 24–30] and also exhibits both nucleoside and RNA triphosphatase activities[28, 29]. Moreover, another core protein σ2 that is known to play a role in stabilizing the core shell and outer capsid, has also been detected to interact with μNS and performs dsRNA-binding ability but shows no enzymatic activity [21, 31, 32].
Much progress has been made in identifying the multiple roles played by μNS in viral replication and assembly in MRVs/ARVs, but little is known about the properties of NS80 protein in Aquareovirus. Previously, we characterized that the full-length and carboxyl-proximal region (aa 335-742) of NS80 are able to form VFLS in both infected and transfected cells. To extend our understanding of this multifunctional protein, we investigated interactions of NS80 with itself and with the proteins NS38, VP4 and VP6 using the yeast two-hybrid system. Bioinformatic analysis was also conducted to identfy and define the potential functional domains of NS80 that are related to VFLS formation and other roles in GCRV replication and assembly. Our results provide valuable information for further detailed experimental design of NS80 to determine the functional domains and explore currently unknown functions.
Virus and cell lines
GCRV strain named GCRV873, maintained in this laboratory was used in this study. CIK (Ctenopharyngodon idellus kidney) cells were employed for GCRV propagation. The GCRV particles were purified from the infected CIK cells and used for genomic RNA extraction. The first strand cDNA was synthesized using GCRV total genomic RNA as a template that is described elsewhere .
Construction of recombinant plasmids
Primers used for PCR amplification and sequencing of GCRV target gene in this study
In vivo yeast two-hybrid assay and identification
Matchmaker™ GAL4 Two-Hybrid System 3 Kit, yeast selective media and other necessary reagents used in yeast transformation and Y2H assay were purchased from Clontech Laboratories, Inc. After testing the bait and prey constructs for autoactivation and toxicity, a total of twelve yeast co-transformations were performed to identify interactions of NS80-NS80 (pGBKT7-NS80 & pGADT7-NS80), NS80-NS38 (pGBKT7-NS80 & pGADT7-NS38), NS80-VP4 (pGBKT7-NS80 & pGADT7-VP4), NS80-VP6 (pGBKT7-NS80 & pGADT7-VP6), NS38-NS38 (pGBKT7-NS38 & pGADT7-NS38), NS38-VP4 (pGBKT7-NS38 & pGADT7-VP4), NS38-VP6 (pGBKT7-NS38 & pGADT7-VP6), VP4-VP4 (pGBKT7-VP4 & pGADT7-VP4), VP4-VP6 (pGBKT7-VP4& pGADT7-VP6), VP6-VP6 (pGBKT7-VP6& pGADT7-VP6), 53-T (pGBKT7-53 & pGADT7-T, positive control), and Lam-T (pGBKT7-Lam & pGADT7-T, negative control). Briefly, for each transformation, 100 ng of bait recombinant plasmid and 100 ng of prey recombinant plasmid were mixed and transformed into Saccharomyces cerevisiae AH109 in small scale reactions according to the Clontech Kit User Manual (PT3247-1). The transformants were then grown at 30°C on SD (synthetically defined) medium. Each yeast transformation was grown on both plates of SD/-Leu-Trp (D ouble D ropo ut, ab. DDO) and SD/-Ade-His-Leu-Trp (Q uadruple D ropo ut, ab. QDO).
Yeast AH109 transformants were inoculated into 5 mL DDO broth and incubated, shaking at 30°C until OD600 reached an approximate concentration of 0.4-0.6. Aspirated 5 μL of the each cultured transformant and inoculated onto both plates of DDO and QDO containing 1 × BU salts (pH 7.0) and X-Gal (ab. DDO/X and QDO/X, respectively). The remaining cultures were centrifuged and used to isolate the co-transformed plasmids by E.Z.N.A.™ Yeast Plasmid Kit (Omega, USA) and PCR identification performed. For preparation of yeast cultures and protein extracts, we referred to the Clontech Yeast Protocols Handbook (PT3024-1). The Urea/SDS method recommended in this instruction was used to extract yeast total proteins. For Western blotting, NS80 specific antiserum that was previously described was employed as primary antibody . The alkaline phosphatase coupled goat anti-rabbit IgG (Sigma, USA) was used as secondary antibody. The result was visualized by developing with NBT/BCIP AP substrate solution (Promega, USA) according to the manufacturer's instructions.
Phylogenetic and bioinformatic analyses
For phylogenetic analysis, NS80 deduced amino acid sequence and related reference sequences were checked manually and edited by using ClustalX software .The MEGA 3.1 software package was used to construct NS80's phylogenetic tree by the neighbor-joining distance method . The reliability of the inferred tree was tested with 1000 bootstrap replicates.
For bioinformatic analyses, a total of three online programs were used to analyze sequences of NS80 and its homologues extracted from NCBI GenBank database. NS80 primary structure alignment was performed by running the NCBI blastp search tool (http://blast.ncbi.nlm.nih.gov/Blast.cgi). The Multicoil program was used to predict NS80 α-helical coiled-coil regions and generate custom figures (http://groups.csail.mit.edu/cb/multicoil/cgi-bin/multicoil.cgi). Multiple sequence alignment (MSA) was performed by the ClustalW program to obtain conserved regions and residues (http://myhits.isb-sib.ch/cgi-bin/clustalw).
Identification of GCRV NS80, NS38, VP4, and VP6 interactions by Y2H assay
GCRV NS80, NS38, VP4, and VP6 encoding genes were cloned into the Clontech Y2H bait plasmid pGBKT7 and prey plasmid pGADT7 respectively, and the following eight constructs: pGBKT7-NS80, pGADT7-NS80, pGBKT7-NS38, pGADT7-NS38, pGBKT7-VP4, pGADT7-VP4, pGBKT7-VP6, and pGADT7-VP6 were successfully obtained. The validities of these recombinant plasmids were confirmed by sequencing.
To analyze yeast plasmid inserts, all the respective co-transformed bait and prey recombinant plasmids were isolated and could be amplified by PCR identification (data not shown). Moreover, the NS80 protein expression could be detected by Western blotting using NS80 rabbit antiserum as the first antibody (data not shown). These results indicated that the bait and prey plasmids could well replicate and express in yeast cells.
Phylogenetic characterization of GCRV NS80
Bioinformatic analyses of GCRV NS80
Since Fields and Song firstly described the yeast two-hybrid system , it has been become a powerful genetic approach to identify protein-protein interaction (PPI) in vivo. The system can be applied in three scenarios: novel PPI identification, putative PPI confirmation, and definition of interacting domains. For application in reovirus PPI identification, Becker et al. reported MRV μNS could interact with σNS but not with outer capsid protein σ3 using the Clontech Y2H system . Another recent associated investigation indicated that ARV μNS could interact with itself using the Clontech mammalian two-hybrid system . In this study, the protein NS80 was first identified to have interactions with NS38, VP4 and VP6 except for NS80 and NS38 self-interactions, indicating that the NS80 and NS38 proteins are capable of both homologous and heterogenous interactions. At the same time, no interactions could be detected between protein pairs NS38-VP4, NS38-VP6, VP4-VP4, VP4-VP6, suggesting dominant protein interactions happened in NS80 during the viral life cycle. However, for VP6 self-interaction, we could not draw a definite conclusion, since three reporter genes including HIS3 (synthesis of histidine), ADE2 (synthesis of adenine), and lacZ (expression of β-galactosidase) should be simultaneously activated to define positive interactions, but only lacZ was expressed in the Y2H assay. Taking into consideration that blue colonies formed on DDO/X plates, maybe this was caused by protein misfolding, and further confirmation, by using another PPI system is necessary.
Bioinformatic analysis is a very useful tool for predict protein function and functional domains and was applied to provide information related to NS80 function. Blastp analysis indicated GCRV NS80 and MRVs/ARVs μNS only displayed weak identities in the carboxyl-proximal region, however, this region is required for formation of VFLS of NS80 in Aquareovirus and μNS in Orthoreovirus and remains relatively conserved amongst different host species. It has been proved that the MRVs μNS carboxyl-terminal one-third region (aa 471-721) is the smallest region necessary for forming VFLS , and the GCRV NS80 carboxyl-terminal region (aa 335-742) has been characterized to have the same phenotype. It is important to note, however, this region spanning from aa residues 335 to 742 is apparently sufficient but not essential for this phenotype. Based on our analysis, the necessary or smallest region for VFLS formation in NS80 is located in aa residues 513-742, although this needs to be experimentally confirmed in subsequent studies. We also note that it has been reported that the second conserved region of NS80 and five conserved amino acid residues (Tyr565, His569, Cys571, Asn573 and Glu576) located between the two coiled-coils are thought to be necessary and crucial to the VFLS formation, and which has been proved to cause the loss of the VFLS formation phenotype in MRVs/ARVs by mutating either the conserved His or Cys residue or by truncating this region [17, 20].
As previously reported in MRVs, the first 40 residues of the μNS N-terminus are sufficient for interaction with both σNS (NS38's homolog) and μ2 (VP4's homolog), and the region of 173-221 residues is sufficient for interaction with σ2 (VP6's homolog) . Although we have experimentally proved NS80 interacts with NS38, VP4, and VP6, we could not predict the interacting domains because no conserved residues were discovered in the corresponding position by either blastp or MSF analyses. The μNS amino-terminal region of 1-221 residues was sufficient to interact with σNS, λ1, λ2, μ2, and σ2 , however, no conserved residues were identified in the NS80 amino-terminal region by aligning analogous proteins from the genera of Aquareovirus and Orthoreovirus using the ClustalW program, which indicates the amino-terminal region is highly divergent. It is likely that the N-terminal functional regions of NS80 are species special to dominate interactions with related components.
The NS80/μNS is approximately divided into three regions, the carboxyl-terminal one-third region is involved in VFLS formation and the amino-terminal one-third region may be associated with protein recruitments. But the roles of the middle one-third region have never been investigated and remain unknown. Based on our bioinformatic analysis, the presence of a conserved region (aa ~388-443 for NS80) including six conserved amino acid residues (Ala395, Gly419, Asp421, Pro422, Leu438, and Leu443 for NS80) located in this region is reported here for the first time, which suggests novel functions might be explored in NS80/μNS.
In this study, we established that NS80 interacted with itself, NS38, VP4, or VP6 and the NS38 self-interaction, characterized the phylogenesis of NS80, and proposed the potential functional regions. The results contribute a basic understanding of NS80 VFLS formation and interaction with other proteins during GCRV replication and particle assembly, moreover, the study provides valuable information for further experimental design and investigation of NS80 functions.
Based on our investigation, it is suggested that GCRV NS80 shares common roles with MRVs/ARVs μNS in VFLS formation and other viral components recruitment during viral replication and assembly. Our findings give a better understanding of NS80 functions and also provide guidance for the further study of this multifunctional protein.
We thank Dr.Lep Rayner for editing our manuscript, and Dr.Simon Rayner for bioinformatic analyses advice. This work was supported in part by grants from the National Natural Science Foundation of China (30871940, 31072233) ,and National Basic Research Program of China (973 Program, 2009CB118701).
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