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Review |
Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK
Correspondence
Polly Roy
polly.roy{at}lshtm.ac.uk
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ABSTRACT |
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 TOP ABSTRACT BackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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Published online ahead of print on 03/06/2008 as DOI 10.1099/vir.0.2008/002089-0.
BTV genome segments, encoded proteins, their locations and functions are shown in a supplementary table available with the online version of this paper.
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Background |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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). For both farmers and the public, the outlook for 2008 is necessarily cautious as this is a newly emerging disease in key livestock, sheep and cattle that had not previously been considered a threat. Bluetongue virus (BTV), which is the causative agent of the disease, has been known for >100 years. Its inexorable spread from its origins in South Africa has led to European colonization over the last 10 years such that its occurrence in the UK was but a matter of time (EFSA, 2007). BTV causes haemorrhagic disease in ruminants and, as such, represents a major economic threat in many parts of the world. It can infect both wild ruminants and domestic livestock, causing disease in sheep, goats and cattle with mortality reaching 70 % in some breeds of sheep. BTV is endemic in many tropical and subtropical countries. The virus is transmitted by several species of biting midges (gnats) in the genus Culicoides (Fig. 1) and, similar to the other arboviruses, the distribution and seasonal activity of these insect vectors determines both the distribution and occurrence of disease in animals (Purse et al., 2005). There are at least 24 serotypes (BTV-1,-2, etc.), with most prevalent in South Africa (Erasmus, 1985). In Europe however, only a handful of the serotypes (BTV-1, -2, -4, -8, -9 and -16) circulate and it is not clear exactly how a particular serotype of the virus arrives or why some seem more successful than others. The lack of a gradual spread of one dominant serotype would suggest that repeated importation of infected animals or the long distance movement of Culicoides vectors are the cause.
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). Many of these viruses are pathogenic to animals and some also infect or are pathogenic for humans (genera Orthoreovirus, Rotavirus, Coltivirus and Seadornavirus) (Mertens et al., 2005). Orbiviruses (14 related serogroups, some 140 members) infect animals, plants and insects and are transmitted by arthropods, such as mosquitoes, gnats and ticks. Many of these viruses cause diseases in animals or plants, often with high economic impacts in agriculture and animal health. Although BTV and the related epizootic haemorrhagic disease virus (EHDV) of deer, African horse sickness virus (AHSV) and equine encephalosis virus (EEV) are all transmitted by gnats (Culicoides) and can cause high morbidity and mortality in animals, BTV is the more common throughout the world, often causing serious periodic outbreaks (Erasmus, 1985). As a result of its economic significance, BTV has been the subject of extensive molecular, genetic and structural studies and now represents the best characterized of all the orbiviruses (Roy, 2007). Viruses of the family Reoviridae, including BTV and other orbiviruses, are characterized primarily by their genome of 10–12 segments of linear, double-stranded RNA (dsRNA). Almost all of these separate segments represent single genes, generating a total of 10–13 viral proteins. The virions are non-lipid-containing icosahedral capsid structures, usually with an outer capsid layer surrounding an inner capsid or core that contains the genome. Shortly after cell entry, this outer capsid is removed to release the inner capsid within which the genome remains sequestered from the cellular triggers of innate immunity. Cores must necessarily, therefore, carry all the transcription machinery of the virus, synthesizing and extruding multiple-capped positive-sense RNAs from each genomic segment into the host cell cytoplasm. Current models for the transcription of the dsRNA genome are based on the polymerase complex contacting the template RNA and the nascent transcript being directed out of the core particle through a pore on its surface. This requires the efficient co-ordination of some half-a-dozen enzyme activities, including helicase, polymerase and RNA capping activity. Considerable advances have been made in recent years in understanding the replicase complexes of these viruses, including BTV. Each of the BTV proteins that form the complex has been expressed as a recombinant protein, purified and used to develop an in vitro assay system for activity. This, in turn, has led to the detailed mapping of the structure–function relationships among each core component. In some cases, three-dimensional structural studies have complemented these analyses to reveal the fine level of structural detail associated with proteins of the BTV inner capsid, and their function alone and in combination. This review will be centred on the molecular dissection of these proteins and will discuss recent data that demonstrate how the combined activities of the core enzymes result in the release of infectious transcripts that are necessary and sufficient to establish viral infection.
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Overview of BTV replication |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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), resulting in some differences at a finer level. Also, there are several structural differences in virus particles and protein organizations between these viruses and thus it is conceivable that some stages of BTV replication would be unique.
In mammalian cells, BTV entry proceeds via virus attachment to a receptor on the plasma membrane (Eaton & Hyatt, 1989). Through a combination of biochemical and confocal microscopy studies, together with specific inhibitors and RNA interference, it has recently been shown that BTV enters cells by clathrin-mediated endocytosis and pH-dependent penetration (Forzan et al., 2007).
The outer capsid proteins of BTV, which are non-glycosylated, are responsible for virus entry and penetration and their structural organizations must facilitate these processes. Image processing of virion micrographs obtained from cryo-electron microscopy (cryo-EM) shows a well-ordered morphology with a unique icosahedral organization (Hewat et al., 1992a, 1994; Nason et al., 2004). The icosahedral virion particle has a diameter of approximately 88 nm and the outer layer is composed of 180 VP2 molecules and 360 VP5 molecules. The 180 VP2 molecules form 60 spike-like, sail-shaped structures while the 360 VP5 molecules are arranged in 120 globular structures and are located more internally than the VP2 spikes. The VP2 spikes extend 3 nm beyond the main body of the particle and are responsible for virus attachment to the cell surface and receptor-mediated endocytosis of the virion (Eaton & Hyatt, 1989; Forzan et al., 2007). BTV entry into the cytoplasm requires endosomal acidic pH which allows the globular VP5 protein to permeabilize the endosomal membrane via its amino terminal ‘pore-forming’ peptide, analogous to the fusion peptides of envelope viruses (Hassan et al., 2001; Forzan et al., 2004, 2007). The membrane penetration activity of VP5 was dramatically shown when VP5 was presented appropriately on the cell-surface and induced cell–cell fusion, confirming that it has the capability to destabilize cellular membranes (Forzan et al., 2004). Critically, VP5 only exhibits its membrane-destabilizing properties after it has undergone a low-pH-triggered activation step, which presumably mimics the endosomal environment encountered during cell entry and possibly triggers a change in the conformation of the protein (Forzan et al., 2007). VP5 lacks the autocatalytic cleavage and N-terminal myristoyl group present in the entry proteins of reoviruses and rotaviruses and does not require proteolytic activation, in contrast to some other viral fusion proteins (Espejo et al., 1981; Estes et al., 1981; Smee et al., 1981; Nibert et al., 1991; Colman & Lawrence, 2003). In the case of rotavirus, the penetration of virus into the cells' cytoplasm (and probably also the uncoating of the virus particle) is dependent upon trypsin activation of viral outer capsid protein VP4. It is noteworthy that the structural organization of the outer capsid proteins of rotavirus and reovirus are very different from that of BTV (Nason et al., 2004; Zhang et al., 2005; see review by Pesavento et al., 2006), although in all three groups of viruses the outer capsid proteins perform essentially same function, i.e. entry, membrane penetration and release of transcriptionally active inner capsid into the cytoplasm.
Thus, for BTV the current model posits that VP2 makes initial contact with the host cell and triggers receptor-mediated endocytosis of the virus particle; VP5 then undergoes a low-pH-triggered conformational change that results in the destabilization of the endosomal membrane (Forzan et al., 2007). It is likely that the change in conformation of VP5 that promotes membrane destabilization, forming a protein layer with intrinsic outside-in curvature, weakens the contacts between VP5 and the underlying outer layer of the core (Forzan et al., 2004, 2007). This allows core particles, from which both outer capsid proteins have been lost, to be released into the cytoplasm and initiate genome replication (Van Dijk & Huismans, 1982; Huismans et al., 1987). In addition to being transcriptionally active, cores generated in vitro by proteolytic treatment of purified BTV also retain infectivity for the insect vector and vector-derived cells, indicating that core proteins can also mediate cell attachment and penetration (Mertens et al., 1987).
The core is a multi-enzyme complex composed of two major proteins (VP7 and VP3) and three enzymically active minor proteins (VP1, VP4 and VP6) in addition to the ten segments of dsRNA genome (approx. 19 000 base pairs in total) (Verwoerd et al., 1970, 1972; Fukusho et al., 1989 and see reviews by Roy et al., 1990a; Roy, 1995). Core enzymes transcribe the ten viral genome segments, as well as cap and methylate full-length mRNA copies of each segment (Van Dijk & Huismans, 1982). The mRNAs are not polyadenylated. In the current model of replication, the mRNA molecules synthesized by the parental cores represent the only transfer of genetic information to the next generation of progeny particles. Transcription occurs inside the viral core and involves the extrusion of ‘capped’ and methylated mRNA species that are subsequently translated into viral proteins in the cytoplasm of an infected cell. The genomic dsRNA segments are never released from the core. Biochemical and EM evidence suggests that all ten genome segments are transcribed simultaneously, similar to the reovirus (Gillies et al., 1971; Huismans & Verwoerd, 1973; Bartlett et al., 1974), although the ten mRNA species are not synthesized at the same rate for BTV (Verwoerd & Huismans, 1972).
Newly produced viral proteins later interact with sequestered viral mRNA species within cytoplasmic viral inclusion bodies (VIBs) to form proviral particles. These proviral particles are believed to be the sites of dsRNA synthesis and the further production of mRNA prior to eventual formation of complete virus particles and extrusion/release from an infected cell (Lecatsas, 1968; Eaton et al., 1990). The VIBs predominantly consist of the viral-coded non-structural protein, NS2, which is synthesized abundantly in virus-infected cells and is responsible for recruiting both the core proteins and newly synthesized transcripts (Thomas et al., 1990; Kar & Roy, 2003; Lymperopoulos et al., 2003, 2006; Modrof et al., 2005). Although the exact mechanism of genome encapsidation is still not clear, current data suggests that VIBs are the genome encapsidation and assembly sites of the cores. However, outer capsid proteins are not recruited by NS2 and the assembly of outer capsid on the core does not take place within the VIBs. The two outer capsid proteins are processed independently of each other and outside of the VIBs (Bhattacharya et al., 2007; Kar et al., 2007). The smallest of the NS proteins (NS3), which is encoded by the smallest RNA segment (S10), is the only glycosylated protein encoded by BTV and is found associated with both VP2 and VP5 (French et al., 1989; Wu et al., 1992; Beaton et al., 2002). Current data suggest that NS3 is involved in both maturation and release of virus (Hyatt et al., 1993; Beaton et al., 2002; Wirblich et al., 2006). Unlike NS2 and NS3, much less is known of the role of the largest NS protein, NS1, which is encoded by RNA segment 6 and synthesizes large numbers of tubular structures in the infected cells (Huismans & Els, 1979; Urakawa & Roy, 1988). This is a unique feature of BTV and other orbiviruses and neither rotavirus- nor reovirus-infected cells exhibit such tubular structures. Current data suggest that NS1 is an essential protein and is involved in virus replication and morphogenesis (Owens et al., 2004). The assembly roles of the outer capsid and NS proteins in the virus life cycle will not be discussed further in this review as these have recently been reviewed elsewhere (Roy, 2005; Noad & Roy, 2006). However, the functions assigned to each of the ten proteins are summarized in Supplementary Table S1 (available with the online version of this paper).
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The architecture of BTV core particles that facilitate the synthesis and release of viral transcripts |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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, 1988). This has facilitated three-dimensional structural analyses which have revealed that the icosahedral surface of the core (73 nm in diameter) has a triangulation number of 13 in a left-handed configuration (T=13l) and is solely made up of 260 trimers of VP7 that are attached onto an inner, thin protein shell (59 nm in diameter) (Prasad et al., 1992; Grimes et al., 1997, 1998). The core possesses channels at both the icosahedral threefold and the fivefold axes (Fig. 2). The three minor proteins, together with genomic RNA, are enclosed by the inner thin shell which is formed essentially by 120 VP3 molecules arranged in 12 decamers. The structural architecture of this layer is also shared by other members of the family, emphasizing the importance of this architecture in capsid assembly for these viruses (see review by Stuart & Grimes, 2006). It is likely that assembly of this layer initiates the assembly of the core. Indeed, VP3 expressed alone, or VP3 and VP7 expressed together can assemble into single shells (although often not very stable) or highly stable double-shelled particles in the absence of the minor proteins and genomic RNA (French & Roy, 1990; Hewat et al., 1992b). The self-assembly capability of VP3 indicates that VP3 amino acid sequences not only determine the fold and overall structure of the protein but also the overall size of the complete capsid. The assembly of VP3 must, therefore, also dictate the organization of the other structural components of the particles that are attached to it or that interact with it, both internally and externally. This notion was further supported by demonstrating that VP3–VP7 recombinant core-like particles also encapsidate the internal minor proteins following co-expression (Loudon & Roy, 1991; Nason et al., 2004). Reconstructions of recombinant particles consisting of only VP3 and VP7 revealed essentially the same size and architecture as that of the authentic cores, while the particles composed of VP3 and VP7, together with two internal proteins, VP1 and VP4, exhibited an extra flower-shaped density directly beneath the icosahedral fivefold axes and attached to the underside of the VP3 layer (Fig. 2) (Loudon & Roy, 1991; Nason et al., 2004). Further, when the core crystals were soaked in transcription buffer, the fivefold pores expanded, indicating that, during transcription, they act as the exit site for mRNA, while low molecular mass metabolites such as nucleotides use separate sites for entry (Diprose et al., 2001). Thus, it appears that there are selective channels for the entry and exit of substrates and by-products into and out of the core, all facilitated by the expansion of the core (Diprose et al., 2001).
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; Gouet et al., 1999). The estimated volume of this density was consistent with the molecular mass (approx. 13.1x106 Da) of the BTV genome (19 219 bp; Fukusho et al., 1989), thus implying that these helical layers are the genomic dsRNA segments. The packaging order of these layers appears to be imposed by grooves that form tracks for the RNA on the inside of the VP3 layer, but without any specific interactions (Grimes et al., 1998; Gouet et al., 1999). Such an organization would facilitate the movement of RNA within the core during transcription activity. |
Dissecting the enzymic function(s) of the core proteins |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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; Silverstein et al., 1970) and was subsequently confirmed by others in the field.
The structural integrity of the core particle appears to be essential for maintaining an efficient transcriptional activity which, in turn, requires the efficient co-ordination of a series of enzyme activities. The BTV core possesses only three minor proteins (VP1, VP4 and VP6) which are responsible for synthesizing the ‘capped’ and methylated transcripts of each dsRNA segment that are released from the transcribing core into the cytoplasm. In addition to polymerase and capping enzymes, a BTV helicase may also be required to unwind the dsRNA genome prior to the initiation and during the synthesis of mRNA species (Fig. 3). Initial assignment of each catalytic activity was based on the predicted amino acid sequence of each protein (Fukusho et al., 1989; and see review by Roy, 1992). The predicted enzyme activity of each protein was subsequently confirmed by experimental studies. Using individual recombinant proteins and in vitro assay systems, it has been possible to delineate the specific catalytic activities provided by each and to confirm that indeed the three core-associated minor proteins, VP1, VP4 and VP6, are solely responsible for synthesizing the ‘capped’ and methylated transcripts of each dsRNA segments. The catalytic activity of each protein established by in vitro systems, together with structural information now available, gives an unambiguous assignment for each protein as discussed below.
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VP6 as a RNA helicase protein |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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). Sequence comparisons of a large number of helicases from different organisms have identified these common functional motifs, including putative sequences for RNA binding, ATP binding/hydrolysis and helicase function (Schmid & Linder, 1992; Kadare & Haenni, 1997; de la Cruz et al., 1999; Dillingham & Kowalczykowski, 2001; Tai et al., 2001). RNA helicases also have a particular signature sequence, the DEAD-box or ‘DECH-box’, which is responsible for forming the protein–ATP complex in the presence of Mg2+ (de la Cruz et al., 1999; Dillingham & Kowalczykowski, 2001). The smallest BTV core protein, VP6 (35.7 kDa), has a high proportion of hydrophilic and positively charged residues and binds both single-stranded and double-stranded RNA (Roy et al., 1990b). Moreover, in the presence of ATP and magnesium ions, the purified soluble VP6 can bind either blunt-ended RNA duplexes or those with short 5' or 3' overhangs and unwind the duplex efficiently in vitro (Fig. 4) (Stauber et al., 1997). These two processes, translocation and strand separation, occur simultaneously during nucleic acid unwinding and use energy from the ATP hydrolysis (Bayliss & Smith, 1996; Paolini et al., 2000; McDougal & Guarino, 2001; White et al., 2001). It is therefore likely that BTV may use VP6 as a helicase, either to unwind the dsRNA ahead of the transcriptase protein or to separate the parental and newly synthesized RNAs following transcription. A number of functional motifs such as ATP-binding/ATPase activity, RNA-binding and RNA-unwinding domains can be recognized in the VP6 protein when it is compared with other available helicases. When these putative functional sites were altered by site-specific mutagenesis, the functional activity of each VP6 mutant derivative was reduced or lost in comparison with wild-type VP6, emphasizing that VP6 is probably the helicase protein of BTV (Kar & Roy, 2003). In particular, substitution at a single residue in the commonly conserved (RxGRxxR) RNA-binding motif (RRGRTGR, aa 205–211) of BTV VP6 severely affected RNA binding and inhibited RNA-unwinding activity. Similarly, changes in the first arginine in the RKGRVGR motif of the vaccinia virus NPH II protein or hepatitis C virus NS3 helicase protein severely reduced RNA-binding activity (Gross & Shuman, 1995; Tai et al., 2001). Mutational analysis in HCV NS3 strongly suggests that the first arginine residue forms hydrogen bonds with the key residues involved in RNA binding (Lin & Kim, 1999; Tai et al., 2001). Moreover, in this substitution mutant, ATP hydrolysis was also impaired, indicating that all three functions are interlinked and depend on the same specific sequences within the structure of the protein. The data also suggest that VP6 helicase activity, like all other helicases, is dependent on ATP hydrolysis.
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; Bird et al., 1998; Lohman et al., 1998). The soluble VP6 is a monomer, but very rapidly forms stable hexamers, particularly in the presence of ssRNA and dsRNA (Fig. 4). These VP6–RNA complexes form discrete ring-like structures (Fig. 4, Kar et al., 2004). Such ring-like structures are shared by a number of other RNA helicases (Gogol et al., 1991; Sedman & Stenlund, 1998; Fouts et al., 1999). Thus, accumulating data indicate that VP6 is a typical RNA helicase protein with all the functional and structural criteria shared with other viral and cellular helicase proteins. |
The largest protein VP1 is the RNA-dependent RNA polymerase |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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; Urakawa et al., 1989). Subsequent studies have used a purified recombinant protein for an in vitro polymerase assay. These data showed that the soluble BTV VP1 is an active enzyme which exhibits a processive replicase activity in the absence of any other viral proteins and initiates BTV minus-strand synthesis de novo (Boyce et al., 2004). The in vitro reaction conditions for VP1 replicase activity used in these experiments were equivalent to those of the optimal transcriptase activity of intact BTV core particles, which indicated that there is no major change in polymerase activity caused by dissociation of VP1 from the rest of the core complex (Van Dijk & Huismans, 1980, 1988; Mertens et al., 1984). These data contrast with those of rotavirus and reovirus. In rotavirus it has been suggested that the assigned polymerase protein (VP1) alone is incapable of performing the polymerase activity in an in vitro assay system, being only functional when it was attached to the inner shell (Chen et al., 1994; Patton et al., 1997; Tortorici et al., 2003). Similarly, it was reported that the assigned polymerase protein of reovirus was incapable of synthesizing de novo RNA on its own, although it was shown that a short RNA oligonucleotide could be generated by the protein (Tao et al., 2002). While the BTV VP1 in vitro replicase activity was low, the activity was detectable for at least 24 h at 37 °C. VP1 was able to copy each of the plus-strand RNA segments fully, from the smallest BTV RNA (822 nt) to the largest BTV plus-strand RNA of 3954 nt. Each product was a complete duplex and was RNase I resistant, but RNase III sensitive, dsRNA. Further, the minus-strand product was formed by de novo initiation rather than extension of a terminal hairpin-like structure in the template RNA. Surprisingly, given the well-documented template-specific binding of the polymerase of rotavirus (Patton, 1996; Patton et al., 1997; Patton & Chen, 1999; Tortorici et al., 2003), BTV VP1 replicated template RNAs that did not contain the conserved terminal hexanucleotide common to all BTV genome segments. This was also true of templates with termini that bore no resemblance at all to these conserved sequences, although the polymerase did have a preference for templates with a terminal C nucleotide. Interestingly, the reovirus 
3 polymerase, which has been shown to be a poly(C)-dependent poly(G) polymerase (Starnes & Joklik, 1993), is also capable of initiating dsRNA synthesis on a non-viral template in the absence of other viral and cellular proteins (Tao et al., 2002). Thus, BTV and reovirus polymerases show some common characteristics that are quite distinct from rotavirus, which has a polymerase that is only active in the presence of the core protein VP2 (Patton et al., 1997; Tortorici et al., 2003). The BTV replicase activity appears to be much more similar to that reported for the dsRNA bacteriophage 
6 polymerase protein P2 with respect to non-specificity. However, P2 does have a preference for templates with the authentic phage-RNA-like dinucleotide at the 3' end of the template RNA, but it will catalyse dsRNA synthesis on any template ssRNA (Makeyev & Bamford, 2000a, b, 2001).
The replicase activity of VP1 alone is low, with only a small minority of the potential template molecules being replicated. It is probable that other viral proteins might act normally to modulate the efficient activity of VP1 in the assembling core particle and probably also provide template specificity. Indeed, the evidence from other viral replicase systems would seem to suggest that polymerase activities (e.g. hepatitis C virus polymerase) are highly regulated in vivo (Piccininni et al., 2002; Shirota et al., 2002).
The confirmation of VP1 as the BTV polymerase protein was further provided by generating a structural model and by reconstitution studies. Since all DNA and RNA polymerases share a similar structure, and as RdRps are more similar to each other than to other polymerases, it was possible to postulate a VP1 3D structure based on several available RdRp crystal structures (Wehrfritz et al., 2007). All RdRp proteins adopt the typical polymerase structure of a right hand, complete with fingers, palm and thumb subdomains. Co-crystallization of these enzymes with nucleoside triphosphates (NTP), or with oligonucleotides, has mapped substrate-binding sites, while the binding of divalent cations, Mg2+ or Mn2+, has been mapped to the catalytic sites, normally characterized by a Gly-Asp-Asp (GDD) motif (Ng et al., 2002; Tao et al., 2002; Choi et al., 2004; Ferrer-Orta et al., 2004). The active site of these polymerases is at the centre of the molecule, in the centre of the palm domain. An additional domain, N-terminal to the fingers, that anchors the tips of the fingers to the thumb is also present in these RdRps (Tao et al., 2002; Choi et al., 2004). Beyond several conserved motifs, there is little primary sequence conservation among the RdRps of the RNA viruses in general, or among those of the dsRNA viruses. Reovirus 3, which has a total of 1267 aa, is a similar size to BTV VP1 (1302 aa). The polymerase domain (PD) of 3 is located in the centre of the molecule (Tao et al., 2002). In addition to PD, unlike the other RdRp, 3 also possesses a large N-terminal domain (NTD) as well as a C-terminal domain (CTD) (Tao et al., 2002). The NTD of 3 covers one side of the active site, and anchors the fingertips to the thumb. The CTD of 3, which covers the catalytic cleft on the other side, forms a bracelet structure with two tightly sealed circles. The opening in the centre of the bracelet forms the exit route for the nascent dsRNA (Tao et al., 2002).
BTV VP1 has a GDD motif at positions 763–765 surrounded by the other sequence motifs characteristic of polymerase proteins (Roy et al., 1988; Bruenn, 1991, 2003), which suggests that VP1 may have a single, central polymerase domain, similar to reovirus 3. When submitted to a web-based server, 500 amino acid residues (aa 581–880) in the central region of VP1 that include the GDD sequence produced alignments with the RdRps of two positive-sense ssRNA viruses, rabbit haemorrhagic disease virus (RHDV) and poliovirus (PV) (Wehrfritz et al., 2007). To generate a spatially restrained three-dimensional model of the polymerase domain of VP1, the final polymerase sequence alignments were then submitted together to the MODELLER program (Sali et al., 1995). The model shows a typical polymerase structure of VP1 with the canonical structure of a right hand with ‘fingers’, ‘palm’, and ‘thumb’ (Fig. 5). The ‘fingers’ subdomain has three 
helices and four β strands, in contrast with other RdRps which have eight helices and five or more β strands (Hansen et al., 1997; Ng et al., 2002; Choi et al., 2004; Ferrer-Orta et al., 2004; Appleby et al., 2005).
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helices. This is an arrangement universally found in polymerases. The architecture of the ‘palm’ region is the most highly conserved structure of all known polymerases and many of its features are shared across all families of RNA and DNA polymerases, including the VP1 model (O'Reilly & Kao, 1998). The aspartate residues in motif C, which are predicted to be responsible for divalent cation co-ordination, are at positions 764 and 765 of VP1. Two additional aspartate residues believed to be involved in either metal ion co-ordination or the binding of NTPs are positioned in motif A at residues 669 and 674 in the VP1 model (Appleby et al., 2005; Wehrfritz et al., 2007)
The ‘thumb’ subdomain of modelled VP1 has three helices linked by loops. The ‘thumb’ subdomain of RdRps generally have four or more helices that are preceded by a short β strand that is located between the ‘palm’ and the ‘thumb’ subdomains (Ng et al., 2002; Tao et al., 2002). In VP1, there is a gap in the polymerase domain alignment which indicates that this β-strand is missing in VP1. The ‘thumb’ of reovirus 3 polymerase also has only three helices.
Reovirus 3 is the only RdRp from the family Reoviridae for which the structure has been solved. The initial search of the SAM T-02 server database, using the central portion of BTV VP1, did not identify the equivalent regions of reovirus 3 or bacteriophage 6 P2, the structures of which are known (Butcher et al., 2001; Tao et al., 2002). However, a subsequent search of the FUGUE server database (Shi et al., 2001) using the full-length VP1 recovered an alignment spanning the entire length of the VP1 protein with the sequence of reovirus 3, suggesting that the polymerase domain of VP1 could also be modelled on 3. The modelled regions that were obtained from this alignment showed a polymerase-type structure similar to the model already obtained and similar to the polymerase domain of 3. A comparison of the root mean square deviation (RMSD) value between the complete polymerase domain model derived from PV and RHDV and the polymerase domain of reovirus 3 indicated a 2.0 Å deviation (Wehrfritz et al., 2007).
The 3 structure was also used to model the amino-terminal and carboxy-terminal regions of BTV VP1. The models of both regions exhibited a high degree of structural similarity with these two regions of the 3 structure (Fig. 5). The VP1 NTD and CTD of VP1 gave RMSD values of 0.9 and 0.72 Å, respectively, when compared with the corresponding regions of reovirus 3. The NTD model of BTV VP1 showed a crescent-shaped, -β protein which was predicted to fit over the PD model, anchoring the fingertips to the thumb in a similar fashion to that of 3 (Tao et al., 2002). However, unlike 3, in which a cap recognition site has been located in the NTD, no obvious cap recognition residues in VP1 were detected from the alignment used.
The modelled CTD of VP1 has a bracelet structure like that of 3. In 3 this bracelet structure forms a pore through which the newly formed genomic dsRNA leaves the polymerase. This VP1 domain putatively has 20 helices and 6 β strands, similar to the C-terminal region of 3, indicating a very close structural similarity in this region of the molecule, and that the CTD of BTV VP1 also must form an exit pore for the nascent dsRNA (Fig. 5). One region in VP1 was impossible to model (Fig. 5), and this unmodelled region may be a binding site for either of the two other enzymic proteins, VP4 or VP6.
To obtain biological evidence that the GDD motif located within the centre of the palm domain is essential for catalytic activity of VP1, this motif was mutated (DD764–765AA) in a recombinant VP1 protein. When tested in vitro, the recombinant mutant protein showed complete loss of catalytic activity, emphasizing that the PD model is likely to be correct (Wehrfritz et al., 2007). Further, to verify the model structure biologically, three constructs were designed to express each of the three domains, PD, NTD and CTD, separately in an Escherichia coli expression system. Each expressed fragment was then purified in soluble form and tested for its role in NTP-binding and polymerase activity. Neither the NTD nor the CTD showed any NTP-binding or RdRp activity. Only the PD alone showed efficient NTP-binding activity, although it had no RdRp activity. Similarly, when the PD fragment was mixed either with NTD or with CTD, again no RdRp activity was achieved. In contrast, when soluble PD fragment was mixed together with the purified NTD and CTD fragments in vitro, the RdRp activity was reconstituted (Fig. 5) (Wehrfritz et al., 2007). This suggested that, although PD possesses the catalytic activity, the other two domains are needed to stabilize the protein, further emphasizing that the structure–function relationship of VP1 is analogous to the reovirus 3, for which the structure has shown that the PD requires the other two domains to stabilize the protein. BTV VP1 is the first polymerase protein to be dissected into three component parts from which a fully functional activity could be reconstituted.
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The second largest minor protein VP4 is the mRNA capping enzyme |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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; Shatkin & Both, 1976). The ‘cap’ structure stabilizes the newly synthesized mRNAs and allows efficient translation initiation of mRNAs (Rottman et al., 1974; Furuichi et al., 1975; Urushibara et al., 1975; Wei et al., 1975; Shatkin & Both, 1976; Parker & Song, 2004). Many eukaryotic viruses, including members of the family Reoviridae, also ‘cap’ the 5' termini of the RNA transcripts they synthesize. While many viruses use the cellular capping machinery, BTV and reoviruses encode their own capping enzymes. Since the newly synthesized transcripts of these viruses are readily capped prior to their release from the cores, the catalytic activities required for ‘cap’ formation must be provided by one or more proteins within the core. Current models for the transcription of the dsRNA genome of members of the family Reoviridae are based on the polymerase complex contacting the template RNA and the nascent transcript being directed out of the core particle through a pore on its surface. In the case of reovirus, this pore is associated with a turret-like structure on the surface of the core that is formed from pentamers of a structural protein which possesses capping activity (Zhang et al., 2003). For rotavirus and BTV, where there are no turret structures present, the capping activity is associated with minor structural components that are located within the inner capsids (Le Blois et al., 1992; Patton & Chen, 1999).
Formation of the cap structure requires at least three key enzymic activities: (i) an RNA triphosphatase (RTase) that hydrolyses the 5'-triphosphate terminus of the mRNA to a diphosphate; (ii) a guanylyltransferase (GTase) that caps the diphosphate terminus with GMP via a 5'-5' triphosphate linkage, and (iii) a guanine-N7-methyltransferase (N7MTase) that adds a methyl group to the N7 position of the blocking guanosine. For BTV and reovirus transcripts, an additional nucleoside-2'-O-methyltransferase (2'OMTase) is also required. This enzyme is responsible for methylating the 2'-hydroxyl group of the ribose of the first nucleotide (namely type 1 cap). For BTV, based on the predicted amino acid sequence, the second largest minor protein, VP4 (76.4 kDa), was predicted to possess some of these catalytic activities. Through the use of highly purified VP4 and recombinant CLPs containing VP4, it was shown that VP4 possesses RNA 5' triphosphatase activity and can covalently bind GMP via a phosphoamide linkage as well as catalyse a GTP--PPi exchange reaction, both characteristic features of guanylyltransferase enzymes (Martinez Costas et al., 1998; Ramadevi et al., 1998b). Further direct evidence of VP4 capping activity was obtained by demonstrating in vitro transfer of GMP to the 5' end of in vitro-synthesized BTV ssRNA transcripts to form a cap structure. Moreover, VP4 was able to catalyse the conversion of unmethylated GpppG or in vitro-produced uncapped BTV RNA transcripts to a full cap structure, m7GpppGm, in the presence of S-adenosyl-L-methionine (AdoMet). Analysis of the methylated products of the reaction by HPLC identified both methyltransferase type 1 and type 2 activities associated with VP4, demonstrating that the complete BTV capping reaction is associated with this one protein (Ramadevi et al., 1998b). Thus, VP4 alone is responsible for the complete ‘cap’ structure at the 5' ends of BTV transcripts. Cellular methyltransferase proteins typically appear to encode only a single activity (Reddy et al., 1992), whereas a number of viral methyltransferases, such as that encoded by vaccinia virus, have an additional enzymic activity such as GTase (Martin et al., 1975; Martin & Moss, 1976). The nsP1 proteins of Semliki Forest virus and Sindbis virus (both positive-strand RNA viruses) also encode both methyltransferase and GTase activities (Mi et al., 1989; Laakkonen et al., 1994). In vaccinia virus, RTase, GTase and N7MTase are components of a capping enzyme complex containing two subunits of 95 kDa and 31 kDa (Venkatesan et al., 1980). However, 2'OMTase activity is mediated by an additional protein VP39 (Benchimol-Barbosa et al., 2002). In contrast to these viruses, BTV VP4 maximizes its coding capacity by catalysing all of the capping and methylation steps necessary to form the complete type 1 cap structure. The protein also possesses an additional catalytic activity, an inorganic pyrophosphatase activity, which may aid the transcription activity within the virus by removing inorganic pyrophosphate which is an inhibitor of the polymerase reaction (Martinez Costas et al., 1998). BTV VP4 is thus the only capping enzyme in the family for which RTase, GTase and both MTase activities have all been formally demonstrated. This enzyme is unique in combining four capping enzyme activities into a single protein.
Recently, the atomic structure of the protein has revealed how a single protein orchestrates all of these activities (Sutton et al., 2007). To date, almost all structural studies of enzymes associated with cap formation have involved proteins with only one of the activities needed for cap formation. The possible exception to this is reovirus, for which a crystal structure of the core is available. In the 3.6 Å resolution structure of the orthoreovirus core, two methyltransferase domains were identified in the 2 protein (Reinisch et al., 2000; Bujnicki & Rychlewski, 2001). However, as discussed above, the pentameric turret structures that form the orthoreovirus capping complex are missing in the BTV core.
The 2.5 Å resolution crystal structure of recombinant BTV VP4 has revealed how VP4 achieves a series of catalytic activities in the absence of any other core proteins (Sutton et al., 2007). Surprisingly, there is no structural evidence that the capping machinery of BTV and orthoreovirus share a single common ancestor, which may have implications for the evolution of the family Reoviridae. The atomic structure reveals an elongated molecule with four discrete domains that are arranged in linear fashion (Fig. 6). The GTase and possibly the RTase active sites are located as a discrete domain in the C-terminal 135 residues and form a compact stack of six helices, while the N7MTase domain (underneath the GTase domain) and the 2'OMTase domain (aa 155–377) are located at the centre of the polypeptide. The N7MTase domain is split into two sections (residues 110–154 and 378–509), in between which the 2'OMTase is inserted. Interestingly, an additional domain was identified in the first 108 aa of the protein, a kinase-like (KL) domain with architecture similar to other KL folds. KL domains are named after guanylate kinase because they are structurally similar to this enzyme, but lack any catalytic activity. However, they have been shown to participate in protein–protein interactions. The KL domain of VP4 may be the site where the VP1 interacts.
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). The GTase and N7MTase domains are closely associated, while the KL domain is reasonably strongly associated with both of these domains. In contrast, the 2'OMT domain is more isolated and only flexibly attached to the remainder of the molecule, but it is structurally similar to the catalytic domains of class I AdoMet-dependent methyltransferases. Superimpositions of the VP4 2'OMT domain on other capping structures show most similarity with the vaccinia virus VP39 structure (Fig. 7), including the signature ‘KDKE’ active site (Bujnicki & Rychlewski, 2001; Egloff et al., 2002), the only RNA 2'OMTase structure to be reported with a bound RNA substrate and cofactor (Hodel et al., 1998). Many of the residues identified as AdoMet/AdoHcy (S-adenosyl-L-homocysteine) ligands in vaccinia virus VP39 are structurally conserved in BTV VP4 and all other orbivirus VP4 molecules. Further confirmation of the identification of the domains was obtained from analysis of various substrates (GTP, 7mGDP, 5'GpppG5') and product complexes. Interestingly, both the cap and AdoHcy moieties bound in a very similar fashion to that observed for vaccinia virus VP39, indicating the high conservative nature of the overall structure of this enzyme (Li et al., 2004). Indeed, the 2'OMTase domain appears to be relatively well conserved across many organisms. Unlike the RNA 2'OMTase, very few RNA N7MTases have been determined structurally and the chemistry of the guanine-N7 methylation is distinct from 2'OMTase. Assignment of the N7MTase was based on similarity to the one other N7MT structure (Ecm1) currently in the database and the putative reovirus 2 N7MT. The overall structure of this domain of VP4 is most similar to Ecm1 of protozoan parasite Encephalitozoon cuniculi mRNA cap (guanine-N7) methyltransferase (Fig. 7), a structure of which is available (Fabrega et al., 2004). Modelling of the Ecm1 cap ligand onto the VP4 structure by superimposition of the protein chains suggests that a group of conserved residues form a pocket for the cap G0, analogous to that observed in Ecm1, confirming further that this is the N7MTase active site of VP4 (Sutton et al., 2007).
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) and Candida albicans (Fabrega et al., 2004) show similarity to DNA and RNA ligases and consist of an N-terminal nucleotidyl transferase domain. The structure of the GTase domain of orthoreovirus (Reinisch et al., 2000) is quite different, suggesting that there is more than one family of such enzymes, utilizing different structural motifs to perform a common reaction pathway. None of these structures could be identified in the GT domain of VP4 and no similar structures could be detected in the protein database. This domain is most probably responsible for the remaining two activities of VP4, RNA-triphosphatase (RTPase) and/or guanylyltransferase (GTase) activity. Indeed, by radiolabelled GTP-binding assay followed by analysis of trypsin digested peptides, it has been shown that these two catalytic activities are associated with this domain (Sutton et al., 2007). The overall layout of active sites in a largely linear fashion along the molecule and the nature of the molecular surface between active sites are consistent with substrate channelling. The efficiency of the process must be optimized by a tight protein–protein interaction with the polymerase enzyme, such that the emerging chain is capped almost immediately. Attachment of the KL domain to the polymerase would facilitate this, since it is closest to the GT domain that is likely to perform the first two capping reactions on the emerging transcript. However, this possibility will only be confirmed by co-crystallizing the VP1–VP4 complex, which is currently under investigation. Thus, the combinations of molecular and structural studies have revealed how a single protein can achieve all the catalytic activities required to form the cap 1 structure at the 5'-terminus of a de novo BTV RNA transcript.
In summary, each of the three minor proteins of BTV core has the ability to function on its own, and together they constitute a molecular motor that can unwind RNAs, synthesize ssRNAs of both polarities and modify the 5' termini of the newly synthesized mRNA molecules. Much less is known about the in vivo RNA replication mechanisms of BTV. It is believed that, like other members of the family, the packaged plus-strand RNA serves as a template for synthesis of a minus-strand, and, once the minus-strand is synthesized, the dsRNA remains within the nascent progeny particle. As discussed, VP1 acts as the replicase enzyme, but the roles of other proteins in minus-strand synthesis remain undefined.
Due to the unique characteristics of BTV VP4 (combining all four capping activities in a single protein), the availability of the atomic structure of this protein represents an important opportunity to completely understand the molecular basis of an mRNA capping mechanism.
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BTV transcripts alone in the absence of any proteins can generate infectious virus |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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). The ability to recover infectious BTV wholly from ssRNA also suggested a means for establishing a helper virus-independent reverse genetics system for BTV. This was assessed by further extending the manipulation of BTV genes by the addition of one or more plasmid-derived T7 transcripts. Initially, as a proof of concept, it was demonstrated that cells transfected with a mixture of viral mRNAs from two serotypes of BTV could generate reassortant progeny genomes that contain genome segments derived from both parental sets of mRNA (Fig. 8). Further, in vitro-synthesized T7 transcripts (either wild-type or mutant variants) derived from cDNA clones were introduced into the genome of BTV using the same system (Boyce et al., 2008). The ability to recover specific mutations in the genome of BTV for the first time not only provides a novel tool for the molecular dissection of BTV and related orbiviruses, but also the opportunity to develop specifically attenuated vaccines from these viruses. More recently, recovery of infectious virus has been shown from transcripts that were generated entirely from ten cDNA clones of the complete genome of BTV serotype (Boyce et al., 2008). The recovered infectious virus showed no difference from either the native virus or the infectious virus recovered from in vitro core-derived transcripts.
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; Komoto et al., 2006; Kobayashi et al., 2007). The first reverse genetics system was a helper virus system for the mammalian orthoreoviruses (Roner & Joklik, 2001). This approach combined reovirus infection of permissive cells and transfection with viral dsRNA, viral mRNA, a T7 transcript and in vitro-translated viral mRNA. Another helper virus approach has allowed the replacement of a rotavirus outer capsid protein with the corresponding protein from another serotype (Komoto et al., 2006). The expression of the introduced genome segment was driven in vivo by the recombinant T7 vaccinia virus system, and selective pressure against the equivalent helper virus protein was provided by the use of antibody selection. Most recently, mammalian orthoreovirus has been recovered using a plasmid-based system similar to the T7 driven systems first used with negative-strand viruses (Kobayashi et al., 2007) and, in this case, expression of all ten genome segments was driven in vivo by a recombinant T7 vaccinia virus system.
Successful reverse genetics strategies to date all have several notable features in common: 1) the genome segments derived from cDNA clones are provided as message-sense transcripts in the transfected cell, 2) the cDNA-derived transcripts have the same 5' end and 3' end sequences as the corresponding viral transcript (5' ends are generated through the use of a T7 promoter with the appropriate sequence, and 3' ends are generated through the use of the hepatitis delta ribozyme in vivo or a restriction enzyme site in vitro), and 3) like authentic viral transcripts, the cDNA-derived transcripts are capped, either in vitro with a cap analogue or in vivo through the cross-capping activity associated with the vaccinia T7 RNA polymerase recombinant (Fuerst et al., 1989). As has been amply demonstrated for other viruses, a reverse genetics system for BTV should contribute to the further understanding of the virus in several research areas. The molecular dissection of BTV protein function to date has mainly been based on recombinant proteins. The ability to introduce specific mutations into the genes of BTV will further our understanding of the functions of these viral proteins in replicating virus and allow the corroboration of the enzymic or structural functions already assigned. The cis-acting RNA sequences that control the replication, packaging, and expression of orbivirus genomes remain unmapped, and are poorly understood. Reverse genetics will allow the mapping of these regulatory sequences and an investigation of their functions. The replacement of outer capsid proteins can be used to generate vaccine strains with different serotypes based on a common genetic background, and it may be possible to identify the determinants of pathogenicity of BTV and related orbiviruses such that strains with varying levels of attenuation could be generated.
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Future perspectives |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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Current understanding is that the polymerase complex contacts the template RNA and the dsRNA is used to produce transcripts. How does the polymerase make a copy-choice between the plus- and minus-strand RNAs? The only physical feature that differs between these strands as they are found in the viral genomic RNA is that only the plus-strand RNA has a cap structure. Does VP1 also possesses a cap-binding domain, and is it the recognition of the cap structure juxtaposed with the 3' end of the viral minus-strand that positions the start of the minus-strand for transcription activity? The purified VP1, VP4 and VP6 have RdRp, capping and helicase activities, respectively, in vitro, but what is the precise order of contacts between proteins that allows formation of this complex, and how does this relate to efficient enzyme function and processivity as a whole?
In addition, the ability to introduce specific mutations into BTV genes, particularly in the polymerase or helicase genes in replicating virus, will allow the corroboration of the enzymic or structural functions already assigned. Such studies will also reveal if mutations in polymerase or helicase proteins have any significance in virus replication and pathogenesis in the variety of hosts that BTV infects as appears to be the case for influenza virus (Finkelstein et al., 2007).
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ACKNOWLEDGEMENTS |
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REFERENCES |
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TOPABSTRACTBackgroundOverview of BTV replicationThe architecture of BTV...Dissecting the enzymic...VP6 as a RNA...The largest protein VP1...The second largest minor...BTV transcripts alone in...Future perspectivesREFERENCES |
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