期刊论文详细信息
Virology Journal
iTRAQ-based quantitative proteomics analysis of rice leaves infected by Rice stripe virus reveals several proteins involved in symptom formation
Xifeng Wang2  Chuantao Lu1  Yingdang Ren1  Jamal-U-Ddin Hajano2  Biao Wang2 
[1] Institute of Plant Protection, Henan Academy of Agricultural Sciences, Zhengzhou, 450002, China;State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China
关键词: Plant defense;    Peptidase;    Magnesium chelatase;    iTRAQ;    Proteome;    Rice;   
Others  :  1224915
DOI  :  10.1186/s12985-015-0328-y
 received in 2015-05-01, accepted in 2015-06-18,  发布年份 2015
PDF
【 摘 要 】

Background

Rice plants infected by Rice stripe virus (RSV) usually leads to chlorosis and death of newly emerged leaves. However, the mechanism of RSV-induced these symptoms was not clear.

Methods

We used an iTRAQ approach for a quantitative proteomics comparison of non-infected and infected rice leaves. RT-qPCR and Northern blot analyses were performed for assessing the transcription of candidate genes.

Results

As a whole, 681 (65.8 % downregulated, 34.2 % upregulated infected vs. non-infected) differentially accumulated proteins were identified. A bioinformatics analysis indicated that ten of these regulated proteins are involved in chlorophyll biosynthesis and three in cell death processes. Subsequent RT-qPCR results showed that downregulation of magnesium chelatase was due to reduced expression levels of the genes encoding subunits CHLI and CHLD, which resulted in chlorophyll reduction involved in leaf chlorosis. Three aspartic proteases expressed higher in RSV-infected leaves than those in the control leaves, which were also implicated in RSV-induced cell death. Northern blot analyses of CHLI and p0026h03.19 confirmed the RT-qPCR results.

Conclusions

The magnesium chelatase and aspartic proteases may be associated with RSV-induced leaf chlorosis and cell death, respectively. The findings may yield new insights into mechanisms underlying rice stripe disease symptom formation.

【 授权许可】

   
2015 Wang et al.

【 预 览 】
附件列表
Files Size Format View
20150915100320918.pdf 1702KB PDF download
Fig. 7. 29KB Image download
Fig. 6. 25KB Image download
Fig. 5. 49KB Image download
Fig. 4. 101KB Image download
Fig. 3. 80KB Image download
Fig. 2. 27KB Image download
Fig. 1. 77KB Image download
【 图 表 】

Fig. 1.

Fig. 2.

Fig. 3.

Fig. 4.

Fig. 5.

Fig. 6.

Fig. 7.

【 参考文献 】
  • [1]Hibino H. Biology and epidemiology of rice viruses. Annu Rev Phytopathol. 1996; 34:249-74.
  • [2]Zhu FM, Xiao QP, Wang FM, Chen YL. Several new diseases occurring in rice south of the Yangtze River. Plant Protection. 1964; 2:100-2.
  • [3]Zhou Y, Li S, Cheng Z, Zhou T, Fan Y. Research advances in rice stripe disease in China. Jiangsu J Agr Sci. 2012; 28:1007-15.
  • [4]Zhang HM, Sun HR, Wang HD, Chen JP. Advances in the studies of molecular biology of Rice stripe virus. Acta Phytophyilacica Sinica. 2007; 34:436-40.
  • [5]Toriyama S. Rice stripe virus: prototype of a new group of viruses that replicate in plants and insects. Microbiol Sci. 1986; 3:347-51.
  • [6]Huo Y, Liu W, Zhang F, Chen X, Li L, Liu Q et al.. Transovarial transmission of a plant virus is mediated by vitellogenin of its insect vector. PLoS Path. 2014; 10:e1003949.
  • [7]Zhu Y, Hayakawa T, Toriyama S, Takahashi M. Complete nucleotide sequence of RNA 3 of rice stripe virus: an ambisense coding strategy. J Gen Virol. 1991; 72:763-7.
  • [8]Zhu Y, Hayakawa T, Toriyama S. Complete nucleotide sequence of RNA 4 of rice stripe virus isolate T, and comparison with another isolate and with maize stripe virus. J Gen Virol. 1992; 73:1309-12.
  • [9]Knudson LL, Tibbitts TW, Edwards GE. Measurement of ozone injury by determination of leaf chlorophyll concentration. Plant Physiol. 1977; 60:606-8.
  • [10]McNulty IB, Newman DW. Mechanism (s) of fluoride induced chlorosis. Plant Physiol. 1961; 36:385-8.
  • [11]Dawson WO. Tobamovirus-plant interactions. Virology. 1992; 186:359-67.
  • [12]Smith NA, Eamens AL, Wang M-B. Viral small interfering RNAs target host genes to mediate disease symptoms in plants. PLoS Path. 2011; 7:e1002022.
  • [13]Shimura H, Pantaleo V, Ishihara T, Myojo N, Inaba J-i, Sueda K et al.. A viral satellite RNA induces yellow symptoms on tobacco by targeting a gene involved in chlorophyll biosynthesis using the RNA silencing machinery. PLoS Path. 2011; 7:e1002021.
  • [14]Liu J, Yang J, Bi H, Zhang P. Why mosaic? Gene expression profiling of African cassava mosaic virus-infected cassava reveals the effect of chlorophyll degradation on symptom development. J Integr Plant Biol. 2014; 56:122-32.
  • [15]Lehto K, Tikkanen M, Hiriart JB, Paakkarinen V, Aro EM. Depletion of the photosystem II core complex in mature tobacco leaves infected by the flavum strain of tobacco mosaic virus. Mol Plant Microbe In. 2003; 16:1135-44.
  • [16]Kong L, Wu J, Lu L, Xu Y, Zhou X. Interaction between Rice stripe virus disease-specific protein and host PsbP enhances virus symptoms. Mol Plant. 2014; 7:691-708.
  • [17]Hatsugai N, Kuroyanagi M, Yamada K, Meshi T, Tsuda S, Kondo M et al.. A plant vacuolar protease, VPE, mediates virus-induced hypersensitive cell death. Science. 2004; 305:855-8.
  • [18]Niu NN, Liang WQ, Yang XJ, Jin WL, Wilson ZA, Hu JP et al.. EAT1 promotes tapetal cell death by regulating aspartic proteases during male reproductive development in rice. Nat Commun. 2013; 4:1445.
  • [19]Mar T, Liu WW, Wang XF. Proteomic analysis of interaction between P7-1 of Southern rice black-streaked dwarf virus and the insect vector reveals diverse insect proteins involved in successful transmission. J Proteomics. 2014; 102:83-97.
  • [20]Qin FL, Liu WW, Li L, Wang XF. Screening of putative proteins in vector Laodelphax striatellus which are interacted with disease-specific protein of Rice stripe virus by yeast two-hybrid based on the split-ubiquitin. Scientia Agricultura Sinica. 2014; 47:2784-94.
  • [21]Scofield SR, Tobias CM, Rathjen JP, Chang JH, Lavelle DT, Michelmore RW et al.. Molecular basis of gene-for-gene specificity in bacterial speck disease of tomato. Science. 1996; 274:2063-5.
  • [22]Nomura K, Debroy S, Lee YH, Pumplin N, Jones J, He SY. A bacterial virulence protein suppresses host innate immunity to cause plant disease. Science. 2006; 313:220-3.
  • [23]Feng F, Yang F, Rong W, Wu X, Zhang J, Chen S et al.. A Xanthomonas uridine 5′-monophosphate transferase inhibits plant immune kinases. Nature. 2012; 485:114-8.
  • [24]Wang Y, Mao Q, Liu W, Mar T, Wei T, Liu Y et al.. Localization and distribution of Wheat dwarf virus in its vector leafhopper, Psammotettix alienus. Phytopathology. 2014; 104:897-904.
  • [25]Digonnet C, Martinez Y, Denance N, Chasseray M, Dabos P, Ranocha P et al.. Deciphering the route of Ralstonia solanacearum colonization in Arabidopsis thaliana roots during a compatible interaction: focus at the plant cell wall. Planta. 2012; 236:1419-31.
  • [26]Kim ST, Kim SG, Agrawal GK, Kikuchi S, Rakwal R. Rice proteomics: a model system for crop improvement and food security. Proteomics. 2014; 14:593-610.
  • [27]Agrawal GK, Rakwal R. Rice proteomics: A move toward expanded proteome coverage to comparative and functional proteomics uncovers the mysteries of rice and plant biology. Proteomics. 2011; 11:1630-49.
  • [28]Marsh E, Alvarez S, Hicks LM, Barbazuk WB, Qiu W, Kovacs L et al.. Changes in protein abundance during powdery mildew infection of leaf tissues of Cabernet Sauvignon grapevine (Vitis vinifera L.). Proteomics. 2010; 10:2057-64.
  • [29]Ross PL, Huang YLN, Marchese JN, Williamson B, Parker K, Hattan S et al.. Multiplexed protein quantitation in Saccharomyces cerevisiae using amine-reactive isobaric tagging reagents. Mol Cell Proteomics. 2004; 3:1154-69.
  • [30]Karp NA, Huber W, Sadowski PG, Charles PD, Hester SV, Lilley KS. Addressing accuracy and precision issues in iTRAQ quantitation. Mol Cell Proteomics. 2010; 9:1885-97.
  • [31]Gross W, Lenze D, Nowitzki U, Weiske J, Schnarrenberger C. Characterization, cloning, and evolutionary history of the chloroplast and cytosolic class I aldolases of the red alga Galdieria sulphuraria. Gene. 1999; 230:7-14.
  • [32]Lai MM. Cellular factors in the transcription and replication of viral RNA genomes: a parallel to DNA-dependent RNA transcription. Virology. 1998; 244:1-12.
  • [33]Hara MR, Agrawal N, Kim SF, Cascio MB, Fujimuro M, Ozeki Y et al.. S-nitrosylated GAPDH initiates apoptotic cell death by nuclear translocation following Siah1 binding. Nat Cell Biol. 2005; 7:665-74.
  • [34]Wang RY-L, Nagy PD. Tomato bushy stunt virus co-opts the RNA-binding function of a host metabolic enzyme for viral genomic RNA synthesis. Cell Host Microbe. 2008; 3:178-87.
  • [35]Prasanth KR, Huang Y-W, Liou M-R, Wang RY-L, Hu C-C, Tsai C-H et al.. Glyceraldehyde 3-phosphate dehydrogenase negatively regulates the replication of Bamboo mosaic virus and its associated satellite RNA. J Virol. 2011; 85:8829-40.
  • [36]Zaffagnini M, Fermani S, Costa A, Lemaire SD, Trost P. Plant cytoplasmic GAPDH: redox post-translational modifications and moonlighting properties. Front Plant Sci. 2013; 4:450.
  • [37]Kaido M, Abe K, Mine A, Hyodo K, Taniguchi T, Taniguchi H et al.. GAPDH-a recruits a plant virus movement protein to cortical virus replication complexes to facilitate viral cell-to-cell movement. PLoS Pathog. 2014; 10:e1004505.
  • [38]Han S, Wang Y, Zheng X, Jia Q, Zhao J, Bai F et al.. Cytoplastic glyceraldehyde-3-phosphate dehydrogenases interact with ATG3 to negatively regulate autophagy and immunity in Nicotiana benthamiana. Plant Cell. 2015; 27:1316-31.
  • [39]Aranda MA, Escaler M, Wang DW, Maule AJ. Induction of HSP70 and polyubiquitin expression associated with plant virus replication. Proc Natl Acad Sci U S A. 1996; 93:15289-93.
  • [40]Whitham SA, Yang CL, Goodin MM. Global impact: Elucidating plant responses to viral infection. Mol Plant Microbe In. 2006; 19:1207-15.
  • [41]Wang S, Blumwald E. Stress-induced chloroplast degradation in Arabidopsis is regulated via a process independent of autophagy and senescence-associated vacuoles. Plant Cell. 2014; 26:4875-88.
  • [42]Schelbert S, Aubry S, Burla B, Agne B, Kessler F, Krupinska K et al.. Pheophytin Pheophorbide Hydrolase (Pheophytinase) is involved in chlorophyll breakdown during leaf senescence in Arabidopsis. Plant Cell. 2009; 21:767-85.
  • [43]Moulin M, McCormac AC, Terry MJ, Smith AG. Tetrapyrrole profiling in Arabidopsis seedlings reveals that retrograde plastid nuclear signaling is not due to Mg-protoporphyrin IX accumulation. Proc Natl Acad Sci U S A. 2008; 105:15178-83.
  • [44]Lundqvist J, Elmlund H, Wulff RP, Berglund L, Elmlund D, Emanuelsson C et al.. ATP-induced conformational dynamics in the AAA+ motor unit of magnesium chelatase. Structure. 2010; 18:354-65.
  • [45]Sawicki A, Willows RD. Kinetic analyses of the magnesium chelatase provide insights into the mechanism, structure, and formation of the complex. J Biol Chem. 2008; 283:31294-302.
  • [46]Kuwata S, Masuta C, Takanami Y. Reciprocal phenotype alterations between two satellite RNAs of cucumber mosaic virus. J Gen Virol. 1991; 72:2385-9.
  • [47]Masuta C, Takanami Y. Determination of sequence and structural requirements for pathogenicity of a cucumber mosaic virus satellite RNA (Y-satRNA). Plant Cell. 1989; 1:1165-73.
  • [48]Vierstra RD. The ubiquitin-26S proteasome system at the nexus of plant biology. Nat Rev Mol Cell Bio. 2009; 10:385-97.
  • [49]Smalle J, Vierstra RD. The ubiquitin 26S proteasome proteolytic pathway. Annu Rev Plant Biol. 2004; 55:555-90.
  • [50]Dudler R. Manipulation of host proteasomes as a virulence mechanism of plant pathogens. Annu Rev Phytopathol. 2013; 51:521-42.
  • [51]Dielen AS, Badaoui S, Candresse T, German-Retana S. The ubiquitin/26S proteasome system in plant-pathogen interactions: a never-ending hide-and-seek game. Mol Plant Pathol. 2010; 11:293-308.
  • [52]Vierstra RD. Proteolysis in plants: mechanisms and functions. Plant Mol Biol. 1996; 32:275-302.
  • [53]van Loon LC, Rep M, Pieterse CMJ. Significance of inducible defense-related proteins in infected plants. Annu Rev Phytopathol. 2006; 44:135-62.
  • [54]Marković-Housley Z, Degano M, Lamba D, von Roepenack-Lahaye E, Clemens S, Susani M et al.. Crystal structure of a hypoallergenic isoform of the major birch pollen allergen Bet v 1 and its likely biological function as a plant steroid carrier. J Mol Biol. 2003; 325:123-33.
  • [55]Liu JJ, Ekramoddoullah AKM. The family 10 of plant pathogenesis-related proteins: Their structure, regulation, and function in response to biotic and abiotic stresses. Physiol Mol Plant P. 2006; 68:3-13.
  • [56]Park CJ, Kim KJ, Shin R, Park JM, Shin YC, Paek KH. Pathogenesis-related protein 10 isolated from hot pepper functions as a ribonuclease in an antiviral pathway. Plant J. 2004; 37:186-98.
  • [57]Casado-Vela J, Selles S, Martinez RB. Proteomic analysis of tobacco mosaic virus-infected tomato (Lycopersicon esculentum M.) fruits and detection of viral coat protein. Proteomics. 2006; 6:S196-206.
  • [58]Wu L, Han Z, Wang S, Wang X, Sun A, Zu X et al.. Comparative proteomic analysis of the plant–virus interaction in resistant and susceptible ecotypes of maize infected with sugarcane mosaic virus. J Proteomics. 2013; 89:124-40.
  • [59]Ventelon-Debout M, Delalande F, Brizard JP, Diemer H, Van Dorsselaer A, Brugidou C. Proteome analysis of cultivar-specific deregulations of Oryza sativa indica and O. sativa japonica cellular suspensions undergoing Rice yellow mottle virus infection. Proteomics. 2004; 4:216-25.
  • [60]Zhang X, Wang X, Zhou G. A one-step real time RT-PCR assay for quantifying rice stripe virus in rice and in the small brown planthopper (Laodelphax striatellus Fallen). J Virol Methods. 2008; 151:181-7.
  • [61]Huang DW, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009; 4:44-57.
  • [62]Kanehisa M, Goto S, Sato Y, Kawashima M, Furumichi M, Tanabe M. Data, information, knowledge and principle: back to metabolism in KEGG. Nucleic Acids Res. 2014; 42:D199-205.
  • [63]Franceschini A, Szklarczyk D, Frankild S, Kuhn M, Simonovic M, Roth A et al.. STRING v9.1: protein-protein interaction networks, with increased coverage and integration. Nucleic Acids Res. 2013; 41:D808-15.
  • [64]Liu B, Chen Z, Song X, Liu C, Cui X, Zhao X et al.. Oryza sativa Dicer-like4 reveals a key role for small interfering RNA silencing in plant development. Plant Cell. 2007; 19:2705-18.
  • [65]Zhang P, Mar TT, Liu WW, Li L, Wang XF. Simultaneous detection and differentiation of Rice black streaked dwarf virus (RBSDV) and Southern rice black streaked dwarf virus (SRBSDV) by duplex real time RT-PCR. Virol J. 2013; 10:24. BioMed Central Full Text
  • [66]Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2 −ΔΔCT Method. Methods. 2001; 25:402-8.
  • [67]Russell DW, Sambrook J. Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press. 2001.
  文献评价指标  
  下载次数:0次 浏览次数:6次