Erratum to "Impact of sugarcane yellow leaf virus (ScYLV) on the carbohydrate status of sugarcane: Comparison of virus-free plants with symptomatic and asymptomatic virus-infected plants". [Physiological and Molecular Plant Pathology 70 (2007) 180-188] (DOI:10.1016/j.pmpp.2007.09.005);Impact of sugarcane yellow leaf virus (ScYLV) on the carbohydrate status of sugarcane: Comparison of virus-free plants with symptomatic and asymptomatic virus-infected plants

Physiological and Molecular Plant Pathology

Volumn 70, Issue 4-6, 2007, Pages 180-188

  Lehrer, Axel T ^a,b   Moore, Paul H ^c   Komor, Ewald ^a  

^a UNIVERSITY OF BAYREUTH   (Germany)

^b HAWAII AGRICULTURE RESEARCH CENTER   (United States)

^c AGRICULTURAL RESEARCH SERVICE   (United States)

Author keywords

Assimilate export; Carbon assimilation; Hexoses; Saccharum spec.; Starch; Sucrose

Indexed keywords

SACCHARUM; SUGARCANE YELLOW LEAF VIRUS;

EID: 36148968037     PISSN: 08855765     EISSN: 10961178     Source Type: Journal    
DOI: 10.1016/j.pmpp.2008.04.001     Document Type: Erratum

References (31)

1. Schenck S. Yellow leaf syndrome-a new sugarcane disease. Hawaiian Sugar Planters Association: annual report;1990. p. 38.
2. Vega J., Scagliusi S.M., and Ulian E.C. Sugarcane yellow leaf disease in Brazil: evidence for association with a Luteovirus. Plant Dis 81 (1997) 21-26
3. Comstock J.C., Irvine J.E., and Miller J.D. Yellow leaf syndrome appears on the United States mainland. Sugar J March (1994) 33-35
4. Moutia J.F.Y., and Saumtally S. Symptomology of yellow leaf syndrome and detection and distribution of sugarcane yellow leaf virus in Mauritius. Proc Int Soc Sugar Cane Technol 23 (1999) 355-364
5. Smith G.R., Borg Z., Lockhart B.E.L., Braithwaite K.S., and Gibbs M.J. Sugarcane yellow leaf virus: a novel member of the Luteoviridae that probably arose by interspecies recombination. J Gen Virol 81 (2000) 1865-1869
6. Moonan F., Molina J., and Mirkov T.E. Sugarcane yellow leaf virus: an emerging virus that has evolved by recombination between luteoviral and poleroviral ancestors. Virology 269 (2000) 156-171
7. Maia L.G., Goncalves M.C., Arruda P., and Vega J. Molecular evidence that sugarcane yellow leaf virus (ScYLV) is a member of the Luteoviridae family. Arch Virol 45 (2000) 1009-1019
8. Scagliusi S.M., and Lockhart B.E.L. Transmission, characterization and serology of a luteovirus associated with yellow leaf syndrome of sugarcane. Phytopathology 90 (2000) 120-124
9. Miller W.A., and Rasochova L. Barley yellow dwarf virus. Annu Rev Phytopathol 35 (1997) 167-190
10. Jensen S.G. Composition and metabolism of barley leaves infected with barley yellow dwarf virus. Phytopathology 59 (1996) 1694-1698
11. Esau K. Phloem degeneration in gramineae affected by the barley yellow dwarf virus. Am J Bot 44 (1957) 245-251
12. Krapp A., Quick W.P., and Stitt M. Ribulose-1,5-bisphosphate carboxylase-oxygenase, other photosynthetic enzymes and chlorophyll decrease when glucose is supplied to mature spinach leaves via the transpiration stream. Planta 186 (1991) 58-69
13. Krapp A., and Stitt M. An evaluation of direct and indirect mechanisms for the "sink-regulation" of photosynthesis in spinach: changes in gas exchange, carbohydrates, metabolites, enzyme activities and steady-state transcript levels after cold-girdling source leaves. Planta 195 (1995) 313-323
14. Izaguirre-Mayoral M.L., Carballo O., Alceste C., Romano M., and Nass H.A. Physiological performance of asymptomatic and yellow leaf syndrome-affected sugarcanes in Venezuela. J Phytopathol 150 (2002) 13-19
15. Fontaniella B., Vicente C., Legaz M.E., de Armas R., Rodriguez C.W., Martinez M., et al. Yellow leaf syndrome modifies the composition of sugarcane juices in polysaccharides, phenols and polyamines. Plant Physiol Biochem 41 (2003) 1027-1036
16. Schenck S., and Lehrer A.T. Factors affecting the transmission and spread of sugarcane yellow leaf virus. Plant Dis 84 (2000) 1085-1088
17. Lehrer A, Meinzer R, Moore P, Komor E. Physiological consequences of sugarcane yellow leaf virus infection on the sugarcane plant. In: Hogarth DM, editor. International Society of Sugar Cane Technologists. Proceedings of the XXIV congress, vol. II. Australia: ASSCT Mackay; 2001. p. 657-9.
18. Rassaby L., Girard J.-C., Letourmy P., Chaume J., Irey M.S., Lockhart B.E.L., et al. Impact of Sugarcane yellow leaf virus on sugarcane yield and juice quality in Réunion Island. Eur J Plant Pathol 109 (2003) 459-466
19. Fitch M.M.M., Lehrer A.T., Komor E., and Moore P.H. Elimination of sugarcane yellow leaf virus from infected sugarcane plants by meristem tip culture visualized by tissue blot immunoassay. Plant Pathol 50 (2001) 676-680
20. Schenck S., Hu J.S., and Lockhart B.E.L. Use of a tissue blot immunoassay to determine the distribution of sugarcane yellow leaf virus in Hawaii. Sugar Cane 4 (1997) 5-8
21. Fondy B.R., and Geiger D.R. Diurnal pattern of translocation and carbohydrate metabolism in source leaves of Beta vulgaris L. Plant Physiol 70 (1982) 671-676
22. Hendrix D.L., and Huber S.C. Diurnal fluctuations in cotton leaf carbon export, carbohydrate content, and sucrose synthesizing enzymes. Plant Physiol 81 (1986) 584-586
23. Kalt-Torres W., and Huber S.C. Diurnal changes in maize leaf photosynthesis. III. Leaf elongation rate in relation to carbohydrates and activities of sucrose metabolizing enzymes in elongating leaf tissue. Plant Physiol 83 (1987) 294-298
24. Lucas W.J., Ding B., and van der Schoot C. Plasmodesmata and the supracellular nature of plants. New Phytol 125 (1993) 435-476
25. Shalitin D., and Wolf S. Cucumber Mosaic Virus infection affects sugar transport in melon plants. Plant Physiol 123 (2000) 597-604
26. Herbers K., Takahata Y., Melzer M., Mock H.-P., Hajirezaei M., and Sonnewald U. Regulation of carbohydrate partitioning during the interaction of Potato Virus Y with tobacco. Mol Plant Pathol 1 (2000) 51-59
27. Kobayashi K., Cabral S., Calamante G., Maldonado S., and Mentaberry A. Transgenic tobacco plants expressing the Potato virus X open reading frame 3 gene develop specific resistance and necrotic ring symptoms after infection with the homologous virus. Mol Plant-Microbe Interact 14 (2001) 1274-1285
28. Herbers K., Tacke E., Hazirezaei M., Krause K.P., Melzer M., Rohde W., et al. Expression of a luteoviral movement protein in transgenic plants leads to carbohydrate accumulation and reduced photosynthetic capacity in source leaves. Plant J 12 (1997) 1045-1056
29. Olesinski A.A., Almon E., Navot N., Perl A., Galun E., et al. Tissue-specific expression of the Tobacco Mosaic Virus movement protein in transgenic potato plants alters plasmodesmal function and carbohydrate partitioning. Plant Physiol 111 (1996) 541-550
30. Gonçalves M.C., Vega J., Oliveira J.G., and Gomes M.M.A. Sugarcane yellow leaf virus infection leads to alterations in photosynthetic efficiency and carbohydrate accumulation in sugarcane leaves. Fitopatologia Brasileira 30 (2005) 10-16
31. Grime J.P., and Hunt R. Relative growth rate: its range and adaptive significance in a local flora. J Ecol 63 (1975) 393-422