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Multiple aromatic amino acids are involved in potyvirus movement by forming π-stackings to maintain coat protein accumulation
Phytopathology Research volume 3, Article number: 10 (2021)
Coat protein (CP) is required for potyviruses to move and establish a systemic infection in plants. π-stackings formed by aromatic residues play critical roles in maintaining protein stability and functions. As we know, many aromatic residues located in the core region of potyvirus CPs are conserved. However, their roles in potyvirus infection remain largely unknown. Here, through analysis of the three-dimensional model of the tobacco vein banding mosaic virus (TVBMV; genus Potyvirus) CP, 16 aromatic residues were predicated to form π-stackings. The results of transient expression experiments demonstrated that deletion of any of these 16 aromatic residues reduced CP accumulation. Infectivity assays showed that deletion of any of these aromatic residues in the TVBMV infectious clone abolished cell-to-cell movement and reduced replication of the virus. Substitution of Y105 and Y147 individually with non-aromatic residues alanine or glycine reduced CP accumulation, virus replication, and abolished the ability of TVBMV to move intercellularly, while substitution of these two residues individually with aromatic residues phenylalanine or tryptophan, had no or little effect on CP accumulation and TVBMV systemic movement and replication. Similar results were obtained from the CP mutants of watermelon mosaic virus (WMV, genus Potyvirus). Taken together, our results demonstrate that multiple aromatic residues in CP are involved in potyvirus movement by forming π-stackings to maintain CP accumulation.
Potyviral CP is a multifunctional protein involved in encapsidation, aphid transmission, viral replication and movement (Weber and Bujarski 2015). It is divided into three regions: the N-terminal, the C-terminal and the conserved core regions (Shukla et al. 1988). The three-dimensional (3D) structures of CPs from three potyviruses, i.e., watermelon mosaic virus (WMV), potato virus Y (PVY) and turnip mosaic virus (TuMV), show that the N- and C-terminal regions of CP are flexible and lack secondary structure, while the core region contains eight to ten α-helices and two β-sheet structures (Zamora et al. 2017; Cuesta et al. 2019; Kežar et al. 2019). The N- and C-terminal regions of CP are responsible for long-distance movement of tobacco etch virus (TEV) (Dolja et al. 1994, 1995). Maintaining the net charge of the N-terminal region is essential for cell-to-cell movement of zucchini yellow mosaic virus (ZYMV) (Kimalov et al. 2004). Substitutions of the charged residues in the C-terminal region of CP affect cell-to-cell movement of soybean mosaic virus (SMV) (Seo et al. 2013). Deletion of residues 6–50 in the CP N-terminus of TuMV has no obvious effect on its cell-to-cell and long-distance movement; while deletion of residues 265–274 in the CP C-terminus abolishes TuMV intercellular movement (Dai et al. 2020). Mutation of any of the conserved residues serine, arginine and aspartic acid at positions 122, 154 and 198, respectively (named as S122, R154 and D198) in the core region of CP abolishes cell-to-cell movement of TEV (Dolja et al. 1994, 1995). Mutations of residues corresponding to R154 and D198 of TEV CP in CPs of TuMV and wheat streak mosaic virus (WSMV, genus Tritimovirus, family Potyviridae) also abolish cell-to-cell movement of these two viruses (Tatineni et al. 2014; Dai et al. 2020). The residues at positions 192 and 225 (R192 and K225) located in the RNA binding pocket of CP are involved in cell-to-cell movement of TVBMV and WMV (Yan et al. 2021b). Recently, we have found that the conserved aromatic residue tryptophan at position 122 (W122) in the core region of CP plays an important role in CP stability and cell-to-cell movement of TVBMV, PVY and WMV (Yan et al. 2021a).
Previous studies have shown that aromatic residues, including tyrosine (Y), phenylalanine (F) and tryptophan (W), are involved in protein stability and functions (Salonen et al. 2011; Chatterjee et al. 2019). The sidechains of aromatic residues in the core of a protein play essential roles in paired interactions (Burley and Petsko 1985). Mutation of the conserved aromatic residue F in the LFEYQ motif at the C-terminus of the readthrough protein of potato leafroll virus reduces long-distance movement of the virus and symptom expression (Xu et al. 2018). Changing the aromatic residue Y398 in the nonstructural protein S (NSs) of watermelon silver mottle virus reduces the strength of self-interaction and stability of the protein, and also virus pathogenicity on squash plants (Huang et al. 2015). Two rings of aromatic residues with a centroid distance less than 10.0 Å can form π-stacking (Burley and Petsko 1985). π-stacking is involved in recognizing the mRNA cap-binding protein (eukaryotic initiation factor 4E) (Marcotrigiano et al. 1997; Matsuo et al. 1997). π-stacking plays essential roles in maintaining the stability of several proteins, including small ribonuclease barnase in Bacillus amyloliquefaciens, the outer membrane protein and the cold shock protein in Escherichia coli (Serrano et al. 1991; Hillier et al. 1998; Hong et al. 2007). The aromatic residue pair Y51-F64 in small ubiquitin-like modifier (SUMO) protein forms a specific edge-to-face conformation, which is vital for SUMO fold and stability (Chatterjee et al. 2019). The carp parvalbumin protein contains a cluster of seven F residues that can form a stereotypic aromatic ring network, which is essential for maintaining functional structure (Burley and Petsko 1985). To date, little is known about the function of π-stackings in regulating virus infection.
Here, we found that multiple conserved aromatic residues in the CPs of TVBMV and WMV could form π-stackings, which are essential for maintaining CP accumulation and virus movement. Our finding provides new insight into the role of evolutionarily conserved aromatic residues of CP in potyvirus infection.
Sixteen aromatic residues in TVBMV CP are predicted to form π-stackings
It has been demonstrated that the π-stacking structure can be formed with a centroid distance less than 10.0 Å between two rings of aromatic residues (Burley and Petsko 1985). Here, sequence analysis showed there were 18 aromatic residues in TVBMV CP in addition to the previous reported W122 (Yan et al. 2021a). All the 19 aromatic residues were located in the core region of CP. To determine whether these aromatic residues could form π-stacking, we measured the centroid distance between aromatic residue rings based on the predicted 3D model of TVBMV CP. The results showed that residues F46, Y77 or F237 could not form π-stacking with any other aromatic residues within TVBMV CP, but other 16 aromatic residues, including F94, W97, Y98, Y105, W122, W136, Y147, F160, F167, Y174, Y184, Y188, Y202, F204, F206 and Y207, could form π-stackings (Fig. 1 and Additional file 1: Table S1). Residues Y105 and W122 could form one π-stacking with Y147 and W136, respectively; residues Y98, Y147 and Y184 could form two π-stackings with other aromatic residues; residues F94, W136, Y174 and Y202 could form three π-stackings with other aromatic residues; residues W97, F160, F167, Y188 and Y207 could form four π-stackings with other aromatic residues; residues F204 and F206 could form six π-stackings with other aromatic residues (Fig. 1 and Additional file 1: Table S1).
The π-stackings are essential for maintaining CP accumulation
To determine the role of π-stackings in TVBMV CP accumulation, we individually deleted each of the above-mentioned 16 aromatic residues that could form π-stacking in the transient expression construct pCamGFP-TVBMVCP (the expressed protein was named as GFP-TVBMVCP) to produce their corresponding mutant plasmids, including pCamGFP-TVBMVCP (ΔF94), pCamGFP-TVBMVCP (ΔW97), pCamGFP-TVBMVCP (ΔY98), pCamGFP-TVBMVCP (ΔY105), pCamGFP-TVBMVCP (ΔW122), pCamGFP-TVBMVCP (ΔW136), pCamGFP-TVBMVCP (ΔY147), pCamGFP-TVBMVCP (ΔF160), pCamGFP-TVBMVCP (ΔF167), pCamGFP-TVBMVCP (ΔY174), pCamGFP-TVBMVCP (ΔY184), pCamGFP-TVBMVCP (ΔY188), pCamGFP-TVBMVCP (ΔY202), pCamGFP-TVBMVCP (ΔF204), pCamGFP-TVBMVCP (ΔF206) and pCamGFP-TVBMVCP (ΔY207). Meanwhile, deletions were also introduced into codons coding for F46, Y77 and F237 that could not form π-stacking, and the resultant mutants were named pCamGFP-TVBMVCP (ΔF46), pCamGFP-TVBMVCP (ΔY77) and pCamGFP-TVBMVCP (ΔF237), respectively. Agrobacterium (OD600 = 0.4) carrying plasmid pCamGFP-TVBMVCP or one of the 19 mutant plasmids was infiltrated into fully expanded leaves of N. benthamiana. At 5 days post-agro-infiltration (dpai), the expression level of GFP-TVBMVCP (ΔF46) was similar to that of GFP-TVBMVCP, and those of GFP-TVBMVCP (ΔY77) and GFP-TVBMVCP (ΔF237) were reduced to 60 and 80% of that of GFP-TVBMVCP, respectively, while those of the rest 16 mutant proteins were less than 20% of that of GFP-TVBMVCP (Fig. 2a, b). These results indicate that π-stackings are essential for maintaining TVBMV CP accumulation.
The π-stackings are required for cell-to-cell movement and replication of TVBMV
To determine the role of π-stackings in TVBMV infection of N. benthamiana plants, we individually introduced each deleted mutation of aromatic residues that could form π-stacking into a GFP-expressing TVBMV infectious clone pCamTVBMV-GFP (the produced virus was named as TVBMV-GFP) to produce mutant plasmids, including pCamTVBMV-GFP (ΔF94), pCamTVBMV-GFP (ΔW97), pCamTVBMV-GFP (ΔY98), pCamTVBMV-GFP (ΔY105), pCamTVBMV-GFP (ΔW122), pCamTVBMV-GFP (ΔW136), pCamTVBMV-GFP (ΔY147), pCamTVBMV-GFP (ΔF160), pCamTVBMV-GFP (ΔF167), pCamTVBMV-GFP (ΔY174), pCamTVBMV-GFP (ΔY184), pCamTVBMV-GFP (ΔY188), pCamTVBMV-GFP (ΔY202), pCamTVBMV-GFP (ΔF204), pCamTVBMV-GFP(Δ F206) and pCamTVBMV-GFP (ΔY207). We also deleted the codon coding for F46, which could not form π-stacking with other aromatic residues within CP, in the pCamTVBMV-GFP to produce pCamTVBMV-GFP (ΔF46) and used it as a control. Agrobacterium (OD600 = 0.2) carrying pCamTVBMV-GFP or one of the mutant plasmids was infiltrated into leaves of N. benthamiana plants. At 7 dpai, GFP fluorescence was observed not only in the infiltrated leaves but also in the systemic leaves of N. benthamiana plants when agrobacterium carrying TVBMV-GFP or TVBMV-GFP (ΔF46). However, GFP fluorescence was observed only in the infiltrated leaves of N. benthamiana plants when agrobacterium carrying each of the16 mutants, as illustrated by TVBMV-GFP (ΔY105) and TVBMV-GFP (ΔY147) (Fig. 3a). Enzyme-linked immunosorbent assay (ELISA) results also showed that the virus was detected in the systemic leaves of plants when agrobacterium carrying TVBMV-GFP or TVBMV-GFP (ΔF46), rather than other mutant viruses was infiltrated (Fig. 3b).
To examine cell-to-cell movement of these systemic movement-defective mutants, we infiltrated the agrobacterium (OD600 = 0.0001) carrying one of these 16 mutant plasmids into N. benthamiana leaves. At 5 dpai, the leaves inoculated were observed under a confocal microscope. We analyzed 30 fluorescent foci for each mutant. The results showed that GFP fluorescence produced by the 16 mutant viruses was confined only to single cells (Fig. 3c), as illustrated by TVBMV-GFP (ΔY105) and TVBMV-GFP (ΔY147), whereas the fluorescence signal produced by TVBMV-GFP was observed to spread to many neighboring cells (Fig. 3d).
We further determined the viral RNA accumulation levels of these 16 mutant viruses. Agrobacterium (OD600 = 0.2) carrying pCamTVBMV-GFP or one of the 16 mutant plasmids was infiltrated into N. benthamiana leaves. The replication-defective mutants pCamTVBMV-GFP (NIbΔGDD) and pCamTVBMV-GFP (CPSTOP), in which the codon encoding residues GDD in NIb was deleted, or a stop codon was inserted between the first and second codon of CP-encoding sequence in pCamTVBMV-GFP, were used as controls (Geng et al. 2017; Yan et al. 2021a). At 60 h post-agro-infiltration (hpai), the viral minus (−)RNA accumulating levels were detected by using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). It was showed that viral (−)RNA accumulating levels of these 16 mutants amounted to 30–40% of that of TVBMV-GFP, while those of TVBMV-GFP (NIbΔGDD) and TVBMV-GFP (CPSTOP) were ~ 20% of that of TVBMV-GFP (Fig. 3e). There was no significant difference in (−)RNA accumulating level among mutant viruses derived from these 16 aromatic residues (Fig. 3e). These results indicate that π-stackings are critical for cell-to-cell movement and replication of TVBMV.
Mutations retaining π-stackings can maintain CP accumulation, replication and movement of TVBMV
To test whether the mutations retaining π-stackings could maintain TVBMV CP accumulation, we selected two aromatic residues Y105 and Y147, which could form π-stacking, for non-aromatic or aromatic substitution experiments. We individually substituted the codon for Y105 or Y147 in pCamGFP-TVBMVCP with that for non-aromatic residues A and G, or aromatic residues F and W to produce pCamGFP-TVBMVCP(Y105A), pCamGFP-TVBMVCP(Y105G), pCamGFP-TVBMVCP(Y147A), pCamGFP-TVBMVCP(Y147G), pCamGFP-TVBMVCP(Y105F), pCamGFP-TVBMVCP(Y105W), pCamGFP-TVBMVCP(Y147F) and pCamGFP-TVBMVCP(Y147W). N. benthamiana leaves were infiltrated with agrobacterium (OD600 = 0.4) harboring pCamGFP-TVBMVCP or one of the above eight mutant plasmids. At 5 dpai, the GFP fluorescence intensity in the patches expressing GFP-TVBMVCP(Y105A), GFP-TVBMVCP(Y105G), GFP-TVBMVCP(Y147A) or GFP-TVBMVCP(Y147G) was similar to that expressing GFP-TVBMVCP (ΔY105) or GFP-TVBMVCP (ΔY147), less than 20% of that of GFP-TVBMVCP. In contrast, GFP fluorescence intensity in the patches expressing GFP-TVBMVCP(Y105F), GFP-TVBMVCP(Y147F) or GFP-TVBMVCP(Y147W) was similar to that expressing GFP-TVBMVCP. We also noted that GFP fluorescence intensity produced by GFP-TVBMVCP(Y105W) was approximately 75% of that by GFP-TVBMVCP (Fig. 4a, b). To exclude the effect of GFP on CP accumulation, we substituted the codon for Y105 or Y147 to that for A and G in pCamTVBMVCP, which could express TVBMV CP, to produce pCamTVBMVCP(Y105A), pCamTVBMVCP(Y105G), pCamTVBMVCP(Y147A) and pCamTVBMVCP(Y147G). The CP accumulation was detected by western blotting at 5 dpai. The results showed that the CP accumulation levels of these four mutants was significantly lower than that of TVBMVCP (Additional file 2: Figure S1). These results indicate that π-stacking formed by Y105 and Y147 is critical for TVBMV CP accumulation.
To determine whether the mutations retaining π-stackings can maintain TVBMV systemic movement, we individually introduced mutations of Y105A, Y105G, Y147A, Y147G, Y105F, Y105W, Y147F and Y147W into pCamTVBMV-GFP to produce pCamTVBMV-GFP(Y105A), pCamTVBMV-GFP(Y105G), pCamTVBMV-GFP(Y147A), pCamTVBMV-GFP(Y147G), pCamTVBMV-GFP(Y105F), pCamTVBMV-GFP(Y105W), pCamTVBMV-GFP(Y147F) and pCamTVBMV-GFP(Y147W), respectively. Agrobacterium (OD600 = 0.2) harboring pCamTVBMV-GFP or one of these eight mutant plasmids was infiltrated into N. benthamiana plants. At 7 dpai, TVBMV-GFP, TVBMV-GFP(Y105F), TVBMV-GFP(Y105W), TVBMV-GFP(Y147F) and TVBMV-GFP(Y147W) could, whereas TVBMV-GFP(Y105A), TVBMV-GFP(Y105G), TVBMV-GFP(Y147A) and TVBMV-GFP(Y147G) could not move systemically in N. benthamiana plants (Fig. 4c). The RT-qPCR results showed that no viral RNA of TVBMV-GFP(Y105A), TVBMV-GFP(Y105G), TVBMV-GFP(Y147A) and TVBMV-GFP(Y147G) was detected in the systemic leaves of the assayed plants. TVBMV-GFP(Y105F) and TVBMV-GFP(Y147F) accumulated to a similar level of viral RNA compared with TVBMV-GFP. TVBMV-GFP(Y105W) and TVBMV-GFP(Y147W) accumulated to ~ 50% level of viral RNA of TVBMV-GFP (Fig. 4d).
To further confirm the role of π-stacking formed by Y105 and Y147 in viral cell-to-cell movement, we infiltrated the agrobacterium (OD600 = 0.0001) carrying pCamTVBMV-GFP or one of the eight mutant plasmids into N. benthamiana leaves. At 5 dpai, TVBMV-GFP, TVBMV-GFP(Y105F), TVBMV-GFP(Y105W), TVBMV-GFP(Y147F) and TVBMV-GFP(Y147W) were observed to spread to many cells, but TVBMV-GFP(Y105A), TVBMV-GFP(Y105G), TVBMV-GFP(Y147A) and TVBMV-GFP(Y147G) could not move intercellularly (Fig. 4e–g).
We further detected the viral RNA accumulation in the infiltrated leaves at 60 hpai. RT-qPCR results showed that the (−)RNA accumulation levels of TVBMV-GFP(Y105A), TVBMV-GFP(Y105G), TVBMV-GFP(Y147A) and TVBMV-GFP(Y147G) were approximately 40% of that of TVBMV-GFP (Fig. 4h). The (−)RNA accumulation levels of TVBMV-GFP(Y105F), TVBMV-GFP(Y147F) and TVBMV-GFP(Y147W) were similar to that of TVBMV-GFP, and it was 80% of that of TVBMV-GFP for TVBMV-GFP(Y105W) (Fig. 4h).
These results indicate that mutations retaining π-stackings can maintain CP accumulation, replication and movement of TVBMV.
Disrupting π-stackings reduces virus particle number
To determine the effect of π-stackings on virus particle assembly and yield, we purified virus particles from the agroinfiltrated leaves. The extracts were negatively stained and then observed under transmission electron microscopy. The results showed that typical virus particles were easily observed in leave samples treated with TVBMV-GFP, TVBMV-GFP(Y105F), TVBMV-GFP(Y105W), TVBMV-GFP(Y147F) and TVBMV-GFP(Y147W). However, virus particles in leave samples treated with TVBMV-GFP(Y105A), TVBMV-GFP(Y105G), TVBMV-GFP(Y147A) and TVBMV-GFP(Y147G) were barely detected (Fig. 5a, b). These results indicate that destroying the π-stackings does not completely abolish the ability of mutant viruses to assemble virus particles, but significantly reduces the number of virus particles.
The π-stackings play essential roles in CP accumulation and cell-to-cell movement of WMV
Sequence analysis of 234 potyvirus CP sequences showed that among the 16 aromatic residues in TVBMV CP that could form π-stackings, 11 residues were completely conserved, and the rest five were incompletely conserved (Additional file 2: Figure S2), indicating that π-stackings were conserved in potyvirus CPs.
We compared the predicted 3D model of TVBMV CP with those of PVY, WMV and TuMV CPs (Zamora et al. 2017; Cuesta et al. 2019; Kežar et al. 2019), and found that they shared structural similarities (Additional file 2: Figure S3). The same as in TVBMV CP, there were 19 aromatic residues in WMV CP, and all of them were located in the core region of WMV CP. Sixteen of them, including F105, W108, Y109, Y116, F130, W133, W147, Y158, F178, Y185, Y195, Y199, Y213, F215, F217 and Y218, were predicted to form π-stackings, whereas the rest three aromatic residues, including Y88, F96 and F248, could not form this structure (Fig. 6 and Additional file 1: Table S2). Sequence analysis showed that 15 of these 16 aromatic residues in WMV CP were identical to that in the corresponding positions in TVBMV CP (Additional file 2: Figure S4).
We individually deleted the codon for these 19 aromatic residues from pCamGFP-WMVCP that express GFP-WMVCP, a fusion protein of GFP and wild-type WMV CP, to produce 19 mutant plasmids. The N. benthamiana leaves were infiltrated with agrobacterium carrying pCamGFP-WMVCP or one of these 19 mutants. At 5 dpai, GFP fluorescence intensity in the leaf patches expressing one of 16 mutants decreased to 20–40% of that of GFP-WMVCP, and it was 60% of that of GFP-WMVCP for GFP-WMVCP (ΔF96). For GFP-WMVCP (ΔY88) and GFP-WMVCP (ΔF248), the same level of fluorescence intensities with that of GFP-WMVCP were observed (Fig. 7a, b). These results indicate that mutations disrupting any π-stackings compromise the accumulation of WMV CP.
To investigate the effects of π-stacking on WMV movement, we individually deleted the codons for the 16 aromatic residues that could form π-stackings from the WMV infectious clone pCBWMV-GFP (WMV-GFP) to produce the corresponding virus mutants. N. benthamiana leaves were infiltrated with agrobacterium (OD600 = 0.0001) harboring pCBWMV-GFP or one of these 16 mutant plasmids. At 5 dpai, WMV-GFP was found to have spread to many cells in the infiltrated leaf patches. In contrast, GFP fluorescence in the WMV-GFP (ΔF105)-, WMV-GFP (ΔW108)-, WMV-GFP (ΔY109)-, WMV-GFP (ΔY116)-, WMV-GFP (ΔF130)-, WMV-GFP (ΔW133)-, WMV-GFP (ΔW147)-, WMV-GFP (ΔY158)-, WMV-GFP (ΔF178)-, WMV-GFP (ΔY185)-, WMV-GFP (ΔY195)-, WMV-GFP (ΔY199)-, WMV-GFP (ΔY213)-, WMV-GFP (ΔF215)-, WMV-GFP (ΔF217)- and WMV-GFP (ΔY218)-inoculated leaf patches was only confined to single cells (Fig. 7c).
These results indicate that π-stackings play critical roles in maintaining the CP accumulation and cell-to-cell movement of WMV.
Previous studies have shown that π-stacking formed by aromatic residues is involved in maintaining protein stability via stabilizing α-helixes and β-sheets (Butterfield et al. 2002; Budyak et al. 2013). Recently, we have found that the aromatic rings of W122 (residue numbered according to the full length of TVBMV CP) in CPs of several potyvirus are critical for CP stability (Yan et al. 2021a). However, the mechanism of the ring of W122 in maintaining CP stability is unclear. In this study, we found that all 19 aromatic residues are located at the core region of TVBMV CP. Our prediction results showed that W122 and other 15 aromatic residues in the core regions of both TVBMV and WMV CPs could form π-stackings (Figs. 1 and 6; Additional file 1: Tables S1and S2). Deletion of the aromatic residues that could form π-stackings significantly reduced CP accumulation to 20% of that of wild-type TVBMV CP. Furthermore, we found that substitutions of Y105 and Y147 individually with non-aromatic residues A or G significantly reduced TVBMV CP accumulation, while substitutions of Y105 and Y147 with aromatic residues F or W had little effect on TVBMV CP accumulation (Fig. 4a, b). Deletion of the aromatic residues that could form π-stackings also significantly reduced CP accumulation of WMV (Fig. 7a, b). These results imply that disturbing π-stacking in potyvirus CPs reduce the stability of the proteins, as a consequence, reduce their accumulation. We also found that the accumulation of GFP-TVBMVCP(Y105W) was lower than that of GFP-TVBMVCP(Y105F). The similar phenotype has been reported previously, which showed that a specific edge-to-face conformation between the Y51-F64 pair of interacting aromatics is important for the fold and stability of SUMO, and substitution of Y51 with F51 could perturb the edge-to-face conformation and reduce SUMO stability (Chatterjee et al. 2019). It is also possible that Y51F substitution can create major distortions in the network of interactions between the pair and other residues at the buried environment of SUMO1 and then reduce protein stability (Chatterjee et al. 2019).
Our previous study has shown that mutation of W122 to non-aromatic residues remarkably reduces CP accumulation, virus replication and abolishes intercellular movement of TVBMV (Yan et al. 2021a). In consistent with these results, we further found that deletion mutation of any of the 16 aromatic residues, including W122 that could form π-stacking within CP, abolished TVBMV and WMV cell-to-cell movement (Figs. 3c and 7c). These mutations also significantly reduced CP accumulation and TVBMV replication (Figs. 2 and 3e). As efficient replication is the prerequisite step for potyviral cell-to-cell movement (Deng et al. 2015; Chai et al. 2020), the low accumulation of CP and viral RNA might be responsible for the abolishment of cell-to-cell movement of TVBMV mutants.
Previous study has shown that TEV mutants derived from S122, R154 and D198 fail to move between cells and to form virus particles to a detectable level. Similar results are obtained in the corresponding point mutants of TuMV and WSMV (Tatineni et al. 2014; Dai et al. 2020). We have found that movement-defective TVBMV mutants derived from W122 form fewer virus particles compared with wild-type TVBMV (Yan et al. 2021a). Here, we also found that movement-defective TVBMV mutants, including TVBMV-GFP(Y105A), TVBMV-GFP(Y105G), TVBMV-GFP(Y147A) and TVBMV-GFP(Y147G), produced fewer virus particles compared with wild-type TVBMV-GFP and the movement-competent mutants including TVBMV-GFP(Y105F), TVBMV-GFP(Y105W), TVBMV-GFP(Y147F) and TVBMV-GFP(Y147W) (Fig. 5). Combined with the results in Additional file 2: Figure S1, it was showed that disrupting π-stackings formed by those aromatic amino acid residues reduced the accumulation level of CP (Additional file 2: Figure S1) and subsequently the number of virus particles. CP is an essential viral protein for cell-to-cell movement of potyviruses, which is transported through plasmodesmata in the form of virus particles or vRNA/CP interaction complex (Wang 2021). Our results suggest that π-stackings formed by those aromatic amino acid residues are important for the accumulation level of CP, and this can further affect virus movement.
Aromatic residues are usually essential for maintaining both protein structure and function. An aromatic residue in the readthrough protein may regulate systemic infection of potato leafroll virus together with an α-helix structural motif (Xu et al. 2018). Mutations of aromatic residues buried at the core of SUMO affect its conformation and therefore reduce interface affinity with SUMO interacting motifs of promyelocytic leukemia protein (Chatterjee et al. 2019). There is a possibility that mutations of aromatic residues affect CP conformation and impair interactions of CP with viral/host proteins.
The conserved residues are discontinuously distributed in the primary sequence and have a relationship in the 3D structure, which is critical for specific function of proteins. The conserved residues S140, R172 and D216 are located in the RNA-binding pocket of CP of WMV, PVY and TuMV, respectively (Zamora et al. 2017; Cuesta et al. 2019; Kežar et al. 20192017). Residues R192 and K225 in RNA-binding pocket of TVBMV CP control virus cell-to-cell movement and replication (Yan et al. 2021b). Our results presented here further reveal the role of discontinuous conserved aromatic residues in the potyvirus CP core region in forming π-stacking and maintaining CP stability and virus movement.
In this paper, we showed that the conserved aromatic residues in the core regions of TVBMV and WMV CPs were predicted to form π-stackings, which are critical for CP accumulation, potyvirus replication and viral cell-to-cell movement. These results support the conclusion that multiple evolutionarily conserved aromatic residues of CP are involved in potyvirus movement by forming π-stackings to maintain CP accumulation. This research provides novel insight into the role of evolutionarily conserved aromatic residues of CP in potyvirus infection.
The three-dimensional modeling and π-stacking analysis
Three-dimensional (3D) models in this study were predicted using the I-TASSER software (Yang et al. 2014). The centroid distance between two aromatic rings was measured using the PyMOL Molecular Graphics System (https://pymol.org).
The infectious clones pCamTVBMV-GFP (GenBank accession no: JQ407082) and pCBWMV-GFP (MN910314) were constructed previously by our laboratory (Gao et al. 2012; Ji 2020). The CP-encoding sequences of TVBMV and WMV were PCR-amplified from the above clones and individually ligated into the pCam35S::GFP vector to generate pCamGFP-TVBMVCP and pCamGFP-WMVCP to express different GFP-CP fusion proteins in N. benthamiana leaves. The mutant plasmids of pCamTVBMV-GFP, pCamWMV-GFP, pCamGFP-TVBMVCP and pCamGFP-WMVCP were produced using a site-directed mutagenesis technology as described previously (Liu and Naismith 2008). Primers used in this study were listed in Additional file 1: Table S3.
Plant growth and vector inoculation
N. benthamiana plants were grown in a greenhouse under controlled conditions (25 °C, 16/8 h light/dark photoperiod). Agrobacterium carrying infectious clone was cultured and diluted to an OD600 of 0.2 for viral infectivity assay, and 0.0001 for viral cell-to-cell movement assay. For transient protein expression assay, agrobacterium (OD600 = 0.4) carrying one of the expressing vectors was mixed at a ratio of 1:1 with agrobacterium (OD600 = 0.4) carrying the pBinP19 vector expressing the RNA silencing suppressor P19 of tomato bushy stunt virus. The mixed agrobacterial cultures were infiltrated into leaves of 4–6 weeks old N. benthamiana plants. The inoculation tests were repeated three times independently.
Confocal microscopy and GFP imaging
To examine virus cell-to-cell movement, agroinfiltrated N. benthamiana leaves were harvested at 5 dpai and examined under a confocal microscope (Leica, Wetzlar, Germany) for viral cell-to-cell movement. The excitation wavelength was set at 488 nm and the emission wavelength was set at 520–540 nm. To record GFP fluorescence loci in the agroinfiltrated leaves, the leaves were photographed at 5 dpai using a digital camera (Canon 80D, Tokyo, Japan) under a hand-held UV lamp (LUYOR, Shanghai, China).
Measurement of GFP fluorescence intensity
Leaf discs of 5 mm in diameter were cut from agroinfiltrated leaves with a cork borer and individually placed in wells of 96-well microtiter plates. The intensity of GFP fluorescence for each disc was measured using a multi-function microplate reader (BioTek, Synergy™ Mx, Winooski, VT, USA) set at the 485/10 nm excitation wavelength and the 535/10 nm emission wavelength.
Western blotting assay was performed as described previously (Yan et al. 2021a). Total protein was extracted from N. benthamiana leaf tissues with extraction buffer (100 mM Tris-HCl, 150 mM NaCl, 1 mM EDTA, 5% sucrose and 1 mM phenylmethanesulfonyl fluoride). TVBMV CP antibody and horseradish peroxidase-conjugated goat anti-rabbit IgG (Sigma-Aldrich, St. Louis, MO, USA) were used as the primary and the secondary antibodies, respectively. After the addition of the SuperSignal™ West Dura Extended Duration Substrate solution (Thermo Fisher Scientific), the detection signal was visualized using a Chemiluminescent Imaging and Analysis System (Sage, Beijing, China).
Tissues of 0.2 g in weight were collected from systemic leaves of the assayed N. benthamiana plants and individually homogenized in 400 μL coating buffer (15 mM Na2CO3 and 35 mM NaHCO3, pH 9.6). One hundred microliters of crude leaf extract were loaded into one well of a 96-well microtiter plate, with three wells used for each sample. The plate was incubated overnight at 4 °C. After four rinses with PBST buffer (80 mM Na2HPO4, 1.5 M NaCl, 20 mM KH2PO4, 30 mM KCl and 0.5% Tween-20 in distilled water, pH 7.4), an antibody solution specific for TVBMV CP was loaded into the wells followed by 4 h incubation at 37 °C. After four rinses with PBST buffer, an alkaline phosphatase-conjugated goat anti-rabbit IgG solution was added to each well and the plate was incubated at 37 °C for 4 h. Detection signal was developed by the addition of 100 μL p-Nitrophenyl phosphate substrate (Sigma-Aldrich, St. Louis, MO, USA) solution into each well and the optical density at 405 nm (OD405) of each well was read using a multi-function microplate reader.
RNA isolation and RT-qPCR
Systemic leaf tissues (0.2 g per sample) were collected from leaves of the assayed N. benthamiana plants and used for total RNA isolation using TransZol reagent (TransGen Biotech, Beijing, China). Genomic DNA was removed from samples using a gDNA removal enzyme as instructed (Vazyme, Nanjing, China). Reverse transcription was performed in a reaction volume of 10 μL containing 500 ng total RNA, 0.5 μL HiScript II reverse transcriptase (200 U/μL, Vazyme), 0.5 μL random primer (50 ng/μL) for detecting viral accumulation in system leaves, or 0.5 μL specific primers qTVBMVCP-F (10 μM) and EF1A-R (10 μM) for detecting TVBMV (−)RNA accumulation. For RT-qPCR, 0.3 μL cDNA was used in each 20 μL reaction with virus-specific primers and a ChamQ SYBR qPCR master mix (Vazyme) on an LC96 qPCR system (Roche, Basel, Switzerland). In this study, the expression level of the NbEF1A gene was used as an internal control. The primers used in this study were listed in Additional file 1: Table S3. The RT-qPCR was performed with three biological replicates.
Virus particle purification
Six grams of infiltrated leaves were ground in liquid nitrogen and then homogenized in 12 mL extract buffer (0.2 M phosphate buffer, 0.15% β-mercaptoethanol and 0.01 M EDTA, pH = 8). The homogenate was centrifuged at 11,000×g for 20 min and then filtered through four layers of Miracloth (Millipore, Billerica, MA, USA). The supernatant was loaded on a 20% sucrose cushion at a ratio of 2:5 (vol/vol) and centrifuged for 1 h at 100,000×g, 4 °C (CP100WX, Hitachi, Tokyo, Japan). The pellets were resuspended overnight in 100 μL of 0.02 M phosphate buffer (pH = 8) at 4 °C. The undissolved parts were removed by centrifugation at 8000×g for 20 min at 4 °C. The supernatant was loaded onto 230-mesh carbon-coated copper grids, washed with 2 drops of 0.02 M phosphate buffer (pH = 8), negatively stained with 2% phosphotungstic acid (PTA) (pH = 7), and then observed under a transmission electron microscope (JEM-1200Ex, Joel, Tokyo, Japan).
Statistical differences (P < 0.05) between the treatments were determined using Duncan’s multiple range test in the SPSS (version 19) statistical software.
Availability of data and materials
Enzyme-linked immunosorbent assay
Potato virus Y
Reverse transcription-quantitative polymerase chain reaction
Soybean mosaic virus
Small ubiquitin-like modifier
Tobacco etch virus
Turnip mosaic virus
Tobacco vein banding mosaic virus
Watermelon mosaic virus
Zucchini yellow mosaic virus
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We are grateful to Dr. Ping Qian from the College of Chemistry and Material Science, Shandong Agricultural University, China, and Dr. Hong Guo from the University of Tennessee, USA, for their valuable suggestions and discussions.
This study was supported by grants from the National Natural Science Foundation of China (NSFC; 31720103912, 31871933), ‘Taishan Scholar’ Construction Project (TS201712023) and Funds of Shandong ‘Double Tops’ Program (SYL2017XTTD11).
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The authors declare that they have no competing interests.
. Centroid distances between rings of aromatic residues in TVBMV CP. Table S2. Centroid distances between rings of aromatic residues in WMV CP. Table S3. Primers used in this study.
. CP accumulation in the N. benthamiana leaf patches expressing TVBMVCP, TVBMV(Y105A), TVBMV(Y105G), TVBMV(Y147A) or TVBMV(Y147G) at 5 dpai. Ponceau red-stained nitrocellulose membrane-bound RuBisCO large subunit protein (Rubi) was used to show sample loadings. Figure S2. Alignment of 234 full-length CP sequences representing 127 potyviruses. The color scheme of residues shows different hydrophobicity. Blue indicates hydrophilic residues, green indicates neutral residues and black indicates hydrophobic residues. Positions of aromatic residues predicted to form π-stacking in TVBMV CP are indicated by arrowheads. The positions labeled with red and blue arrowheads indicate the completely and incompletely conserved residues for aromatic residues, respectively. Figure S3. Comparison of the predicted 3D model of TVBMV, WMV, PVY and TuMV CPs. Protein Data Bank (PDB) code: 6HXX for PVY CP, 5ODV for WMV CP and 6T34 for TuMV CP. The 3D model of TVBMV CP was predicted using the I-TASSER server. Figure S4. Alignment of TVBMV and WMV CP aromatic residues forming π-stackings.
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Yan, ZY., Xu, XJ., Fang, L. et al. Multiple aromatic amino acids are involved in potyvirus movement by forming π-stackings to maintain coat protein accumulation. Phytopathol Res 3, 10 (2021). https://doi.org/10.1186/s42483-021-00088-9
- Coat protein
- Tobacco vein banding mosaic virus
- Watermelon mosaic virus