Cocksfoot mottle virus coat protein is dispensable for the systemic infection
© Olspert et al.; licensee BioMed Central Ltd. 2014
Received: 17 November 2013
Accepted: 27 January 2014
Published: 4 February 2014
The Sobemovirus genome consists of polycistronic single-stranded positive-sense RNA. The first ORF encodes P1, a suppressor of RNA silencing required for virus movement. The coat protein (CP) is expressed from the 3′ proximal ORF3 via subgenomic RNA. In addition to its structural role, the CP of some sobemoviruses has been reported to be required for systemic movement and to interact with P1. The aim of this study was to analyse the role of Cocksfoot mottle virus (CfMV) CP in the suppression of RNA silencing and virus movement.
Agrobacterium-mediated transient expression method was used for testing CfMV CP capacity to suppress RNA silencing. CP substitution and deletion mutants were generated to examine the role of this protein in CfMV infection, using three host plants (oat, barley and wheat). The viral movement was characterised with CfMV expressing EGFP fused to the C-terminus of CP.
In the current study we show that CfMV CP is an additional RNA silencing suppressor. Interestingly, we observed that all CP mutant viruses were able to infect the three tested host plants systemically, although usually with reduced accumulation. CfMV expressing EGFP was detected in epidermal and mesophyll cells of inoculated leaves. Although EGFP fluorescence was not detected in upper leaves, some plants displayed CfMV symptoms. Analysis of the upper leaves revealed that the viruses had lost the EGFP sequence and sometimes also most of the CP gene.
The present study demonstrates that CfMV CP suppresses RNA silencing but, surprisingly, is dispensable for systemic movement. Thus, CfMV does not move as virion in the tested host plants. The composition of the movement RNP complex remains to be elucidated.
KeywordsSobemovirus Virus movement RNA silencing suppressor Coat protein
Sobemovirus is a small genus of plant viruses with single-stranded positive-sense RNA genome (for review ). Sobemoviruses have a viral protein genome linked (VPg) covalently attached to the 5′ end of genomic and subgenomic RNA. The 5′ proximal open reading frame 1 (ORF1) encodes the P1 protein, while the viral capsid or coat protein (CP) is expressed from the 3′ proximal ORF3 via subgenomic RNA. The central part of the genome encodes the viral polyproteins P2a and P2ab, the latter is translated through a-1 programmed frameshift mechanism .
Sobemoviral proteins, and CP among them, are multifunctional. CPs primary function is structural, being the building block for the virion. Virions of sobemoviruses have an icosahedral structure according to T = 3 symmetry comprising of 180 CP monomers . Though the primary sequences of sobemoviral CPs are poorly conserved, their three-dimensional structures are highly similar. Sobemoviral CPs contain two domains–the N-terminal R (random) and C-terminal S (shell) domain which is responsible for subunit-subunit contacts in the virion [3–8]. The N-terminal part of all sobemoviral CPs is rich in basic amino acids and contains an arginine-rich region, which is necessary for CP-RNA interactions and RNA encapsidation [9–11]. It has also been shown that the N-terminal part of Southern cowpea mosaic virus (SCPMV) CP interacts with membranes  and that the N-terminus of Cocksfoot mottle virus (CfMV) CP contains functional nuclear localisation signals . CPs have also been reported to be involved in virus movement. For instance, CPs of Rice yellow mottle virus (RYMV) and SCPMV are required for cell-to-cell movement, but are not necessary for virus replication [14, 15]. Moreover, long distance movement of RYMV and SCPMV has been proposed to be dependent on viral particle formation [16, 17]. The CP of Sesbania mosaic virus (SeMV) has been shown to interact with P1, which is a suppressor of RNA silencing and has been implicated in virus movement [18–20].
In this study we analyse the role of CfMV CP in suppression of RNA silencing and virus movement. We show that the CP of CfMV acts as an RNA silencing suppressor and that CP is dispensable for cell-to-cell as well as systemic movement of CfMV in oats, wheat and barley.
CP and RNA silencing
Viruses can encode more than one RNA silencing suppressor and the P1 protein has been shown to interact with CP . Therefore we decided to test if CP affects RNA silencing. Using the Agrobacterium-mediated transient expression method we infiltrated N. benthamiana 16c line, expressing GFP, with Agrobacterium carrying the RNA silencing inducer GFP gene together with Agrobacterium containing CfMV CP gene. GFP together with the empty vector or with CfMV P1 were used as controls. The CP’s potential influence on the P1 suppression activity was also assessed by infiltrating a mixture of Agrobacterium carrying both genes together with GFP.
Infectivity of CP mutants
Mechanical transmission of CP mutants
As CP is essential for the formation of virus particles, it was interesting to see whether the mutant viruses would be transmissible by mechanical inoculation. Oat plants were inoculated with sap obtained from the upper leaves of plants infected with the mutants and analysed for CfMV infection as described above (Figure 4B). Mechanical transmission of mutant R3L occurred in a similar way to wild type (wt) virus, infection was detected in both inoculated and upper leaves. In the case of mutant R5X the transmission was also successful as the virus was detected in the inoculated leaves, but the mutant was unable to infect the plants systemically. For both mutants the presence of the mutations in the viral RNA was verified by sequencing (data not shown). Interestingly, we were unable to detect infection in plants inoculated with noCP.
Infectivity of mutant noCP in other hosts
Movement of CP-EGFP and CPdelta-EGFP viruses
In the case of CPdelta-EGFP the fluorescence was considerably weaker of what was observed with CP-EGFP. The fluorescence appeared strongest around the 3rd to the 4th dpi with CPdelta-EGFP (Figure 7). Weak fluorescence was detected in single epidermal cells after 2 dpi, which sometimes spread to neighbouring epidermal cells the following days. EGFP was not detected in mesophyll cells. The signal from epidermal cells usually disappeared around the 5th day (Figure 7). No distinguishable EGFP signal was detected in the upper leaves with either of the EGFP containing viruses.
Detection of CfMV recombination mutants
It was previously reported that P1 of CfMV is indispensable for virus movement and accumulation in oats  and that it is a suppressor of RNA silencing . However, it still remains unclear whether P1 facilitates virus spread as an RNA silencing suppressor or as a member of the movement RNP complex. Here we demonstrate that CP is also an RNA silencing suppressor in 16c N. benthamiana. It is not a surprise that CfMV encodes two suppressors of RNA silencing, since more than one suppressor has been identified for other viruses as well [21, 22]. Both suppressors, P1 and CP, are able to interfere with the RNA silencing mechanism independently and a strong synergistic effect was not observed. It seems plausible that CfMV CP contributes to virus spread through enhancement of accumulation. Such claim is supported by experiments with RYMV, which accumulated to higher levels in transgenic plants expressing RYMV CP compared to control plants, indicating that transgenic CP further enhanced virus infection and accumulation . The authors speculated that CP may enhance viral accumulation by influencing replication or host susceptibility or, alternatively, by suppressing RNA silencing.
The arginine-rich region of the CP of sobemoviruses has been studied before. The CP of mutants R3L and R5X localises to cytoplasm and nucleus whereas the wt CP localises almost exclusively to the nucleus . Results obtained here, with viruses containing the same mutations in CP, demonstrate that these mutations have no deleterious effect on virus cell-to-cell and systemic movement as well as on mechanical transmission in oats. The majority of CP-EGFP fusion protein localises to the cell nucleus when expressed independently from the rest of the virus genome . Here we observed that when CP-EGFP was expressed together with the rest of the viral proteins, the fluorescence did not accumulate in the nucleus, but remained evenly distributed between cytoplasm and nucleus. Most probably the CP was interacting with other viral and/or host proteins or with full-length genomic RNA and therefore was not accumulating in the nucleus any more.
Despite these possible interactions, CfMV CP null mutant (noCP) was capable of cell-to-cell as well as systemic movement in all three tested hosts. The fact that CfMV CP is not strictly needed for the infection was further demonstrated by experiments with viruses expressing CP-EGFP and CPdelta-EGFP. As expected, the virus replicated in single epidermal cells and migrated to the mesophyll, beneath these epidermal cells, from where it presumably entered vascular tissue. Spontaneous CfMV recombination mutants detected in plants inoculated with mutants CP-EGFP/CPdelta-EGFP that lacked most of the CP cistron (group I, deleted nt 3254-3864), produced systemic infection as well as symptoms, again demonstrating the dispensability of CfMV CP for cell-to-cell and systemic movement.
In contrast, it has been previously documented that sobemoviruses require P1 as well as CP for systemic movement [14–17]. An RYMV CP mutant failed to infect rice plants systemically, but accumulated in the inoculated leaves, indicating cell-to-cell movement , whereas SCPMV CP initiation codon mutant, analogous to CfMV noCP, was undetectable even in inoculated leaves, but replicated in protoplasts . The CP of Turnip rosette virus, another sobemovirus, has been reported to facilitate long distance movement of red clover necrotic mosaic dianthovirus . Based on protein interaction studies of P1 with either CP or native virions of SeMV, closely related to SCPMV, Chowdhury and Savithri  have proposed a model for CP involvement in SeMV movement. We conclude that CfMV in general utilises a different movement strategy from SCPMV and RYMV.
Interestingly, we were unable to transmit noCP mechanically, whereas R3L and R5X were transmittable. This demonstrates that CP is necessary for an efficient sap-transmission and that mutations in the arginine-rich region do not affect the viral RNA-CP complex involved in this transmission. The mutant noCP should be, in theory, transmissible as well, since viral RNA is all what is needed for initiating the infection. Nevertheless, we have observed that mechanical inoculation with in vitro synthesised CfMV RNA is less efficient than biolistic inoculation with the same RNA (our unpublished observations). When compared to the R3L and R5X (that were transmissible), mutant noCP did not have significantly lower viral RNA levels in the systemically infected leaves which were used as the source for sap-inoculation (data not shown). Most likely the formation of virus particles is necessary for the efficient CfMV transmission.
Mutant R5X failed to produce systemic infection in mechanically inoculated plants. We propose that this deficiency is due to the mutation in RdRp yielding a less fit virus.
CPdelta-EGFP produced a considerably weaker EGFP signal in infected cells than CP-EGFP. It is possible that the EGFP sequence was just lost more rapidly than in case of CP-EGFP or that CPdelta-EGFP had considerably lower accumulation. It seems that, if available, the virus usually maintains as much of the CP sequence as possible. Foreign EGFP sequence seems to be the trigger for recombination because we have not encountered recombinant viruses in plants infected with mutant noCP or with the wt virus.
It is interesting that the mutants, which had lost the EGFP and CP coding sequences, all contained almost the entire 3′ UTR. The 3′ UTR starts at nt 3858 and the recombinant mutants had retained the sequence starting from nt 3865 or 3869. This leads us to speculate that the 3′ UTR might contain sequences or structural elements important for the transport, as the full-length 3′ UTR is not needed for replication, translation and accumulation in oats (Olspert, unpublished results). Another explanation is that nt 3865-3869 simply contain a hot-spot for recombination. These two hypotheses are, of course, not mutually exclusive.
Sobemoviral P1 is known to be a suppressor of RNA silencing. This study demonstrates that, at least for CfMV, CP is a second suppressor.
The viral RNA genome is usually transported from cell-to-cell and systemically through the vasculature either as virions or as some other form of RNP complex. Trafficking as virions can be now ruled out for CfMV, at least in the tested host plants, since all the experiments reported here indicate that CP is not needed for cell-to-cell and systemic movement.
Altogether we have demonstrated that in different pathosystems individual sobemoviruses can exploit alternative cell-to-cell and long distance movement strategies. It would be interesting to determine whether the CfMV P1 RNA silencing suppressor activity can be uncoupled from the movement function and to determine the composition of the movement RNP complex. The RNA silencing suppression mechanism by which CP contributes to higher virus accumulation of CfMV deserves further investigation as well.
Construction of CfMV mutants
Base numbering of constructs generated for this study corresponds to CfMV Norwegian isolate . All CfMV cDNA clones were created by modifying the original cDNA clone . It was decided to simplify plant inoculation by removing the necessity for in vitro RNA synthesis before plant inoculation. To achieve this, the CfMV genome was cloned downstream of CaMV 35S promoter and Hepatitis delta virus ribozyme together with nopaline synthetase terminator were introduced after the genome in order to maintain the exact 3′ end of the genome after transcription. The exchange of the promoter and the addition of the ribozyme coupled with a terminator were carried out using overlap-extension-PCR with appropriate primers and standard cloning techniques.
cDNA clones of CfMV containing mutations were also generated using overlap-PCR. Mutations of R5X and R3L were introduced by primers described in Olspert et al.  and in mutant noCP the CP initiation sequence ATGATG was mutated to ACGACG. Using primers containing the mutations, the CfMV fragments containing nt 3096-3853 and 1604-3162 were produced and merged in a following round of PCR, so that a fragment corresponding to CfMV nt 1604-3853 was obtained. The latter fragment was used to introduce the mutations to the CfMV cDNA by employing NcoI sites at positions 2508 and 3619. In the case of virus mutant noCP, in addition to the CP initiation codon mutation a stop codon was introduced to CP reading frame after the overlap with RdRp gene (Figure 3B). This was achieved by cleaving the plasmid with XmaJI restriction endonuclease at CfMV position 3311, filling in the termini and re-ligating the plasmid. This produced a reading frame switch starting from position 3311 and an in frame stop codon at position 3343.
Virus clones expressing CP-EGFP fusions were generated by replacing the CfMV sequence between XmaJI and PstI restriction sites at positions 3311 and 3869, respectively. In the case of CP-EGFP, the fusion sequence was obtained by PCR using a plasmid expressing the fusion protein  as the template. For CPdelta-EGFP EGFP primers with aforementioned restriction sites were used to generate the appropriate fragment.
All DNA constructs used in this work were verified by sequencing.
Plant inoculation and virus detection
12-14 days old oat (cv. Jaak) plants were inoculated biolistically (Helios, BioRad) with CfMV constructs according to manufacturer’s instructions. Samples from the inoculated leaves were collected at 14 dpi and from upper leaves at 21 dpi. Each experiment was repeated at least twice and with a minimum of 8 plants per construct. Follow-up analysis in wheat (cv. Zebra) and barley (cv. Kymppi) were conducted once with 16 plants per construct. Plant tissue was homogenised with TissueLyzer (QIAGEN) and total RNA was extracted from samples according to Logemann et al. . The analysis of RNA by RT-PCR was carried out with primers detecting nt 2749-4082 of the positive strand of viral RNA. The obtained RT-PCR fragments were purified from the agarose gel and the region containing the mutations was sequenced. Protein samples from the same material were obtained in parallel from the cell debris collected after the first centrifugation of RNA extraction. The pellet was suspended in PBS-Tween buffer and total protein was precipitated from the supernatant with trichloroacetic acid. Subsequently, the protein extract was analysed on 12.5% SDS-PAGE, blotted onto Hybond C membrane (GE Healthcare) and probed with rabbit polyclonal anti-CP antiserum . Goat anti-rabbit HRP conjugate was used for detection. Ribulose-1,5-bisphosphate carboxylase oxygenase large subunit was visualised with Ponceau S (Sigma) stain for calibration.
For the analysis of mechanical transmission, the upper leaves of infected plants were ground in liquid nitrogen and the homogenate suspended in 10 volumes (w/v) of 100 mM potassium phosphate buffer (pH 7.0) containing 0.5% Celite. This suspension was used to mechanically inoculate plants and the following analysis of virus infection was done as in the case of bombarded plants.
Agroinfiltration assay and siRNA analysis
CfMV CP coding sequence nt 3096–4082 was amplified with primers containing the appropriate restriction sites, excised with BamHI and FspAI and cloned into pBin61  between the 35S promoter and Nos terminator to give pBin61-CP. 35S-CP refers to Agrobacterium tumefaciens containing pBin61-CP.
The recombinant A. tumefaciens strain used throughout the experiment was C58C1 harbouring pCH32 . Equal volumes of 35S-CP and 35S-GFP (A. tumefaciens carrying GFP, kindly provided by D. Baulcombe), as well as of 35S-P1 (A. tumefaciens containing CfMV P1 ) and 35S-GFP or 35S-P1 and 35S-CP together with 35S-GFP (total volume divided in three parts) were mixed and co-infiltrated (OD600 = 1) to N. benthamiana line 16c (kind gift of D. Baulcombe) leaves of 4-week-old plants, as described previously . As a control, A. tumefaciens carrying the empty binary vector pBin61 was infiltrated together with 35S-GFP. Three independent experiments were carried out, each including 5-8 infiltrated plants for each mixture (35S-GFP + 35S-CP, 35S-GFP + 35S-P1, 35S-GFP + 35S-CP + 35S-P1 and 35S-GFP + pBin61). Infiltrated plants were kept in a plant chamber at 22°C under a 16-h photoperiod. GFP fluorescence was monitored using a hand-held 100 W, long-wave UV lamp (Black-Ray B-100AP, Ultraviolet Products) until 28 dpi. Plants were photographed with Pentax K200D digital camera and pictures were processed with Adobe Photoshop CS2 (version 9.0.2).
Total RNA was extracted from the infiltrated patches 7 dpi using TRIzol reagent (Invitrogen) according to the manufacturer’s instructions. For the analysis of GFP siRNA 20 μg of total RNA were denatured and loaded on 15% polyacrylamide gel (19:1 ratio of acrylamide to bis-acrylamide, 8 M urea). The gel was run at 400 V for 3.5 h and then cut in the middle. The lower half of the gel was transferred to Hybond N + -membrane by electroblotting in 0.5 X TBE buffer at 10 V overnight. ULTRAhyb-Oligo buffer (Ambion) was used for overnight hybridisation at 42°C. As a radioactive probe DNA oligo containing a sequence complementary to GFP (5′-CTCTTGAAGAAGTCGTGCCGCTTCATATGA-3′) was end-labeled with 32P by T4 polynucleotide kinase (Fermentas) and purified through NICK Sephadex G-50 columns (GE Healthcare) according to manufacturers’ protocols. The membrane was finally washed twice with 2X SSC, 0.1% SDS for 30 min at 42°C. As a reference marker we used a 30-nt [32P]-end labelled DNA oligo. As loading control we detected U6 snRNA in the same membrane with a [32P]-end labelled oligo according to Akbergenov et al. . The Northern blot analysis of GFP mRNA was done as described above but using 5 μg of total RNA and 8% polyacrylamide gel. The hybridisation was carried out according to Szittya et al.  using as probe [32P]-labelled in vitro transcript corresponding to the anti-sense strand of GFP. The membrane was washed with greater stringency. Radioactive signals were detected using Personal Molecular Imager FX (BioRad) after 20 h (for siRNA detection) or 1 h exposure (for mRNA detection).
We wish to thank Signe Nõu for excellent plant care, Heiti Paves for his assistance in microscopy and Jaanus Suurväli for his earlier efforts with EGFP containing CfMV. We thank David Baulcombe for N. benthamiana 16c line, pBin61 and GFP in pBin61, supplied by PBL. This work was supported by the EU through the European Regional Development Fund (Centre of Excellence ENVIRON) and Estonian Science Foundation grant no. 7363.
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