Sugarcane mosaic virus - Long history but still a threat to industry

Crop Protection

Volumn 42, Issue , 2012, Pages 74-78

  Wu, Liuji ^a,b   Zu, Xiaofeng ^a   Wang, Shunxi ^a   Chen, Yanhui ^a,b  

^a HENAN AGRICULTURAL UNIVERSITY   (China)

^b Key Laboratory of Physiology   (China)

Author keywords

Co infection; Control; Genetic variability; Resistance breeding; SCMV

Indexed keywords

APHID; CROP PRODUCTION; CULTIVATION; DISEASE CONTROL; DISEASE RESISTANCE; DISEASE TRANSMISSION; GENETIC VARIATION; GEOGRAPHICAL DISTRIBUTION; INFECTIVITY; MAIZE; PATHOGEN; SORGHUM; SUGAR CANE; VIRUS;

CHINA; EUROPE;

APHIDIDAE; RNA VIRUSES; SUGARCANE MOSAIC VIRUS; ZEA MAYS;

EID: 84867115594     PISSN: 02612194     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cropro.2012.07.005     Document Type: Review

References (64)

1. Adams M.J., Antoniw J.F., Beaudoin F. Overview and analysis of the polyprotein cleavage sites in the family Potyviridae. Mol. Plant Pathol. 2005, 6:471-487.
2. Agindotan B.O., Ahonsi M.O., Domier L.L., Gray M.E., Bradley C.A. Application of sequence-independent amplification (SIA) for the identification of RNA viruses in bioenergy crops. J. Virol. Methods 2010, 169:119-128.
3. Alegria O.M., Royer M., Bousalem M., Chatenet M., Peterschmitt M., Girard J.C., Rott P. Genetic diversity in the coat protein coding region of eighty-six sugarcane mosaic virus isolates from eight countries, particularly from Cameroon and Congo. Arch. Virol. 2003, 148:357-372.
4. Baulcombe D. RNA silencing in plants. Nature 2004, 431:356-363.
5. Bernstein E., Caudy A.A., Hammond S.M., Hannon G.J. Role for a bidentate ribonuclease in the initiation step of RNA interference. Nature 2001, 409:363-366.
6. Blackman L.M., Boevink P., Cruz S.S., Palukaitis P., Oparka K.J. The movement protein of cucumber mosaic virus traffics into sieve elements in minor veins of Nicotiana clevelandii. Plant Cell 1998, 10:525-538.
7. Brandes E.W. The mosaic disease of sugarcane and other grasses. Tech. Bull. US Dept. Agr. 1919, 829:1-26.
8. Carrington J.C., Jensen P.E., Schaad M.C. Genetic evidence for an essential role for Potyvirus CI protein in cell-to-cell movement. Plant J. 1998, 14:393-400.
9. Chare E.R., Holmes E.C. A phylogenetic survey of recombination frequency in plant RNA viruses. Arch. Virol. 2006, 151:933-946.
10. Chaves-Bedoya G., Espejel F., Alcalá-Briseño R.I., Hernández-Vela J., Silva-Rosales L. Short distance movement of genomic negative strands in a host and nonhost for Sugarcane mosaic virus (SCMV). Virol. J. 2011, 8:15.
11. Chung B.Y., Miller W.A., Atkins J.F., Firth A.E. An overlapping essential gene in the Potyviridae. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:5897-5902.
12. Cilia M.L., Jackson D. Plasmodesmata form and function. Curr. Opin. Cell. Biol. 2004, 16:500-506.
13. Dorsett Y., Tuschl T. siRNAs: applications in functional genomics and potential as therapeutics. Nat. Rev. Drug Discov. 2004, 3:318-329.
14. Dussle C.M., Quint M., Xu M.L., Melchinger A.E., Lübberstedt T. Conversion of AFLP fragments tightly linked to SCMV resistance genes Scmv1 and Scmv2 into simple PCR-based markers. Theor. Appl. Genet. 2002, 105:1190-1195.
15. Dussle C.M., Quint M., Melchinger A.E., Xu M.L., Lübberstedt T. Saturation of two chromosome regions conferring resistance to SCMV with SSR and AFLP markers by targeted BSA. Theor. Appl. Genet. 2003, 106:485-493.
16. Edwardson J.R., Christie R.G. Use of virus-induced inclusions in classification and diagnosis. Annu. Rev. Phytopathol. 1978, 16:31-55.
17. Edwardson J.R. Electron microscopy of cytoplasmic inclusions in cells infected with rod-shaped viruses. Am. J. Bot. 1966, 53:359-364.
18. Gan D.F., Zhang J., Jiang H.B., Jiang T., Zhu S.W., Cheng B.J. Bacterially expressed dsRNA protects maize against SCMV infection. Plant Cell. Rep. 2010, 29:1261-1268.
19. Gao B., Cui X.W., Li X.D., Zhang C.Q., Miao H.Q. Complete genomic sequence analysis of a highly virulent isolate revealed a novel strain of sugarcane mosaic virus. Virus Genes 2011, 43:390-397.
20. Gilbertson R.L., Lucas W.J. How do viruses traffic on the 'vascular highway'?. Trends Plant Sci. 1996, 1:260-268.
21. Gómez M., Rago A.M., Serino G. Rapid identification of viruses causing sugarcane mosaic by direct sequencing of RT-PCR products from crude extracts: a method for large scale virus surveys. J. Virol. Methods 2009, 157:188-194.
22. Govier D.A., Woods R.D. Changes induced by magnesium ions in the morphology of some plant viruses with filamentous particles. J. Gen. Virol. 1971, 13:127-132.
23. Grisham M.P., Pan Y.B. A genetic shift in the virus strains that cause mosaic in Louisiana sugarcane. Plant Dis. 2007, 91:453-458.
24. Gygi S.P., Rochon Y., Franza B.R., Aebersold R. Correlation between protein and mRNA abundance in yeast. Mol. Cell. Biol. 1999, 19:1720-1730.
25. Ha C., Revill P., Harding R.M., Vu M., Dale J.L. Identification and sequence analysis of potyviruses infecting crops in Vietnam. Arch. Virol. 2008, 153:45-60.
26. Handley J.A., Smith G.R., Dale J.L., Harding R.M. Sequence diversity in the NIb coding region of eight sugarcane mosaic potyvirus isolates infecting sugarcane in Australia. Arch. Virol. 1996, 141:2289-2300.
27. Handley J.A., Smith G.R., Dale J.L., Harding R.M. Sequence diversity in the coat protein coding region of twelve sugarcane mosaic potyvirus isolates from Australia, USA and South Africa. Arch. Virol. 1998, 143:1145-1153.
28. Harrison B.D., Finch J.T., Gibbs A.J., Hollings M., Shepherd R.J., Valenta V., Wetter C. Sixteen groups of plant viruses. Virology 1971, 45:356-363.
29. Ingvardsen C.R., Xing Y.Z., Frei U.K., Lübberstedt T. Genetic and physical Wne mapping of Scmv2, a potyvirus resistance gene in maize. Theor. Appl. Genet. 2010, 120:1621-1634.
30. Janson B.F., Ellett C.W. A new corn disease in Ohio. Plant Dis. Rep. 1963, 47:1107-1108.
31. Jensen O.N. Interpreting the protein language using proteomics. Nat. Rev. Mol. Cell. Biol. 2006, 7:391-403.
32. Jones M.W., Boyd E.C., Redinbaugh M.G. Responses of maize (Zea mays L.) near isogenic lines carrying Wsm1, Wsm2, and Wsm3 to three viruses in the Potyviridae. Theor. Appl. Genet. 2011, 123:729-740.
33. Kasschau K.D., Cronin S., Carrington J.C. Genome amplification and longdistance movement functions associated with the central domain of tobacco etch potyvirus helper component-proteinase. Virology 1997, 228:251-262.
34. Kuntze L., Fuchs E., Grüntzig M., Schulz B., Klein D., Melchinger A.E. Resistance of early-maturing European maize germplasm to sugarcane mosaic virus (SCMV) and maize dwarf mosaic virus (MDMV). Plant Breed. 1997, 116:499-501.
35. Lesemann D.E., Shukla D.D., Tosic M., Huth W. Differentiation of the four viruses of the sugarcane mosaic virus subgroup based on cytopathology. Arch. Virol. Suppl. 1992, 5:353-361.
36. Louie R., Knoke J.K. Strains of maize dwarf mosaic virus. Plant Dis. Rep. 1975, 59:518-522.
37. Lucas W.J. Plant viral movement proteins: agents for cell-to-cell trafficking of viral genomes. Virology 2006, 344:169-184.
38. Matthews R.E.F. Classification and nomenclature of viruses. Fourth report of the international committee on classification of viruses. Intervirology 1982, 17:1-199.
39. Mehta A., Magalhães B.S., Souza D.S., Vasconcelos E.A., Silva L.P., Grossi-de-Sa M.F., Franco O.L., da Costa P.H., Rocha T.L. Rooteomics: the challenge of discovering plant defense-related proteins in roots. Curr. Protein Pept. Sci. 2008, 9:108-116.
40. Oertel U., Schubert J., Fuchs E. Sequence comparison of the 3'-terminal parts of the RNA of four German isolates of sugarcane mosaic potyvirus (SCMV). Arch. Virol. 1997, 142:675-687.
41. Padhi A., Ramu K. Genomic evidence of intraspecific recombination in sugarcane mosaic virus. Virus Genes 2011, 42:282-285.
42. Pallas A., García J.A. How do plant viruses induce disease? Interactions and interference with host components. J. Gen. Virol. 2011, 92:2691-2705.
43. Pandey A., Mann M. Proteomics to study genes and genomes. Nature 2000, 405:837-846.
44. Perera M.F., Filippone M.P., Ramallo C.J., Cuenya M.I., García M.L., Ploper L.D., Castagnaro A.P. Genetic diversity among viruses associated with sugarcane mosaic disease in Tucumán, Argentina. Phytopathology 2009, 99:38-49.
45. Quint M., Mihaljevic R., Dussle C.M., Xu M.L., Melchinger A.E., Lübberstedt T. Development of RGA-CAPS markers and genetic mapping of candidate genes for sugarcane mosaic virus resistance in maize. Theor. Appl. Genet. 2002, 105:355-363.
46. Reddy C.V., Sreenivasulu P., Sekhar G. Duplex-immunocapture-RT-PCR for detection and discrimination of two distinct potyviruses naturally infecting sugarcane (Saccharum spp. hybrid). Indian J. Exp. Biol. 2011, 49:68-73.
47. Revers F., Le Gall O., Candresse T., Maule A. New advances in understanding the molecular biology of plant/potyvirus interactions. Mol. Plant Microbe. Interact. 1999, 12:367-376.
48. Roossinck M.J. Mechanisms of plant virus evolution. Annu. Rev. Phytopathol. 1997, 35:191-209.
49. Safarnejad M.R., Jouzani G.S., Tabatabaie M., Twyman R.M., Schillberg S. Antibody-mediated resistance against plant pathogens. Biotechnol. Adv. 2011, 29:961-971.
50. Shi C., Ingvardsen C., Thummler F., Melchinger A.E., Wenzel G., Lübberstedt T. Identification by suppression subtractive hybridization of genes that are differentially expressed between near-isogenic maize lines in association with sugarcane mosaic virus resistance. Mol. Genet. Genomics 2005, 273:450-461.
51. Shi C., Thummler F., Melchinger A.E., Wenzel G., Lübberstedt T. Comparison of transcript profiles between near-isogenic maize lines in association with SCMV resistance based on unigene-microarrays. Plant Sci. 2006, 170:159-169.
52. Shukla D.D., Strike P.M., Tracy S.L., Gough K.H., Ward C.W. The N and C termini of the coat proteins of potyviruses are surface- located and the N terminus contains the major virus-specific epitopes. J. Gen. Virol. 1988, 69:1497-1508.
53. Shukla D.D., Tosic M., Jilka J., Ford R.E., Toler R.W., Langham M.A.C. Taxonomy of potyviruses infecting maize, sorghum, and sugarcane in Australia and the United States as determined by reactivities of polyclonal antibodies directed towards virus-specific N-termini of coat proteins. Phytopathology 1989, 79:223-229.
54. Stange C. Plant-virus interactions during the infective process. Cien. Inv. Agr. 2006, 33:1-18.
55. Tenllado F., Martínez-García B., Vargas M., Díaz-Ruíz J.R. Crude extracts of bacterially expressed dsRNA can be used to protect plants against virus infections. BMC Biotechnol. 2003, 3:3.
56. Uzarowska A., Dionisio G., Sarholz B., Piepho H.P., Xu M.L., Ingvardsen C.R., Wenzel G., Lübberstedt T. Validation of candidate genes putatively associated with resistance to SCMV and MDMV in maize (Zea mays L.) by expression profiling. BMC Plant Biol. 2009, 9:15.
57. Viswanathan R., Karuppaiah R., Balamuralikrishnan M. Identification of new variants of SCMV causing sugarcane mosaic in India and assessing their genetic diversity in relation to SCMV type strains. Virus Genes 2009, 39:375-386.
58. Wei T.Y., Zhang C.W., Hong J., Xiong R.Y., Kasschau K.D., Zhou X.P., Carrington J.C., Wang A.M. Formation of complexes at plasmodesmata for potyvirus intercellular movement is mediated by the viral protein P3N-PIPO. PlosOne Pathog. 2010, 6:e1000962.
59. Xia X.C., Melchinger A.E., Kuntze L., Lübberstedt T. Quantitative trait loci mapping of resistance to sugarcane mosaic virus in maize. Phytopathology 1999, 89:660-667.
60. Xiao X.W., Frenkel M.J., Teakle D.S., Ward C.W., Shukla D.D. Sequence diversity in the surface-exposed amino-terminal region of the coat proteins of seven strains of sugarcane mosaic virus correlates with their host range. Arch. Virol. 1993, 132:399-408.
61. Xu M.L., Melchinger A.E., Xia X.C., Lübberstedt T. High-resolution mapping of loci conferring resistance to sugarcane mosaic virus in maize using RFLP, SSR, and AFLP markers. Mol. Gen. Genet. 1999, 261:574-581.
62. Xu D.L., Park J.W., Mirkov T.E., Zhou G.H. Viruses causing mosaic disease in sugarcane and their genetic diversity in southern. China. Arch. Virol. 2008, 153:1031-1039.
63. Yang Z.N., Mirkov T.E. Sequence and relationships of sugarcane mosaic and sorghum mosaic virus strains and development of RT-PCR-based RFLPs for strain discrimination. Phytopathology 1997, 87:932-939.
64. Yin G.H., Sun Z.N., Liu N., Zhang L., Song Y.Z., Zhu C.X., Wen F.J. Production of double-stranded RNA for interference with TMV infection utilizing a bacterial prokaryotic expression system. Appl. Microbiol. Biotechnol. 2009, 84:323-333.