Gene expression and biochemical changes of carbohydrate metabolism in invitro micro-propagated apple plantlets infected by 'Candidatus Phytoplasma mali'

Plant Physiology and Biochemistry

Volumn 70, Issue , 2013, Pages 311-317

  Giorno, Filomena ^a   Guerriero, Gea ^a,c   Biagetti, Matteo ^a   Ciccotti, Anna Maria ^b   Baric, Sanja ^a  

^a Laimburg Research Centre for Agriculture and Forestry   (Italy)

^b RESEARCH AND INNOVATION CENTRE   (Italy)

^c Centre de Recherche Public   (Luxembourg)

Author keywords

APP; Apple proliferation; Carbohydrate metabolism; Gene expression; Hsp70; Malus x domestica; PR; PS II; QRT PCR; Stress response

Indexed keywords

HEAT SHOCK PROTEIN 70; HEXOSE; STARCH; SUCROSE; VEGETABLE PROTEIN;

APP; APPLE PROLIFERATION; APPLE PROLIFERATION PHYTOPLASMA; ARTICLE; CARBOHYDRATE METABOLISM; GENE EXPRESSION; GENE EXPRESSION REGULATION; GENETICS; HOST PATHOGEN INTERACTION; HSP70; MALUS; MALUS DOMESTICA; METABOLISM; MICROBIOLOGY; PATHOGENESIS RELATED; PHOTOSYSTEM II; PHYSIOLOGICAL STRESS; PHYTOPLASMA; PLANT DISEASE; PLANT GENE; PR; PS II; QRT-PCR; QUANTITATIVE REVERSE TRANSCRIPTASE REAL-TIME PCR; REAL TIME POLYMERASE CHAIN REACTION; STRESS;

APP; APPLE PROLIFERATION; APPLE PROLIFERATION PHYTOPLASMA; CARBOHYDRATE METABOLISM; GENE EXPRESSION; HEAT SHOCK PROTEIN 70; HSP70; MALUS X DOMESTICA; PATHOGENESIS RELATED; PHOTOSYSTEM II; PR; PS II; QRT-PCR; QUANTITATIVE REVERSE TRANSCRIPTASE REAL-TIME PCR; STRESS RESPONSE;

CARBOHYDRATE METABOLISM; GENE EXPRESSION; GENE EXPRESSION REGULATION, PLANT; GENES, PLANT; HEXOSES; HOST-PATHOGEN INTERACTIONS; HSP70 HEAT-SHOCK PROTEINS; MALUS; PHYTOPLASMA; PLANT DISEASES; PLANT PROTEINS; REAL-TIME POLYMERASE CHAIN REACTION; STARCH; STRESS, PHYSIOLOGICAL; SUCROSE;

CANDIDATUS PHYTOPLASMA; CANDIDATUS PHYTOPLASMA MALI; MALUS X DOMESTICA;

EID: 84879830484     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2013.05.040     Document Type: Article

References (33)

1. Sugio A., MacLean A.M., Kingdom H.N., Grieve V.M., Manimekalai R., Hogenhout S.A. Diverse targets of phytoplasma effectors: from plant development to defense against insects. Annu. Rev. Phytopathol 2011, 49:175-195.
2. Musetti R., Paolacci A., Ciaffi M., Tanzarella O.A., Polizzotto R., Tubaro F., Mizzau M., Ermacora P., Badiani M., Osler R. Phloem cytochemical modification and gene expression following the recovery of apple plants from apple proliferation disease. Phytopathology 2010, 4:390-399.
3. Matteoni J.A., Sinclair W.A. Stomatal closure in plants infected with mycoplasma like organisms. Phytopathology 1983, 73:398-402.
4. Leon R., Santamaria J.M., Alpizar L., Escamilla J.A., Oropeza C. Physiological and biochemical changes in shoots of coconut palms affected by lethal yellowing. New Phytol. 1996, 134:227-234.
5. Jagoueix-Eveillard S., Tarendeau F., Guolter K., Danet J.L., Bové J.M., Garnier M. Catharanthus roseus genes regulated differentially by mollicute infections. Mol. Plant Microbe Interact. 2001, 14:225-233.
6. Albertazzi G., Caffagni A., Milc J.A., Francia E., Roncaglia E., Ferrari F., Tagliafico E., Stefani E., Secchioni N. Gene expression in grapevine cultivars in response to Bois Noir phytoplasma infection. Plant Sci. 2009, 176:792-804.
7. Carginale V., Maria G., Capasso C., Ionata E., La Cara F., Pastore M., Bertaccini A., Capasso A. Identification of genes expressed in response to phytoplasma infection in leaves of Prunus armeniaca by messenger RNA differential display. Gene 2004, 332:29-34.
8. Hren M., Nikolić P., Rotter A., Blejec A., Terrier N., Ravnikar M., Dermastia M., Gruden K. 'Bois noir' phytoplasma induces significant reprogramming of the leaf transcriptome in the field grown grapevine. BMC Genomics 2009, 10:460.
9. Landi L., Romanazzi G. Seasonal variation of defense-related gene expression in leaves from Bois noir affected and recovered grapevines. J.Agric. Food Chem. 2011, 59:6628-6637.
10. Guerriero G., Giorno F., Ciccotti A.M., Schmidt S., Baric S. Agene expression analysis of cell wall biosynthetic genes in Malus x domestica infected by 'Candidatus Phytoplasma mali'. Tree Physiol. 2012, 32:1365-1377.
11. Lepka P., Stitt M., Moll E., Seemüller E. Effect of phytoplasmal infection on concentration and translocation of carbohydrates and amino acids in periwinkle and tobacco. Physiol. Mol. Plant Pathol. 1999, 55:59-68.
12. Maust B.E., Espadas F., Talavera C., Aguilar M., Santamaría J.M., Oropeza C. Changes in carbohydrate metabolism in coconut palms infected with the lethal yellowing phytoplasma. Phytopathology 2003, 93:976-981.
13. Ji X., Gai Y., Zheng C., Mu Z. Comparative proteomic analysis provides new insights into mulberry dwarf responses in mulberry (Morus alba L.). Proteomics 2009, 9:5328-5339.
14. Machenaud J., Raphaël H., Dieuaide-Noubhani M., Pracros P., Renaudin J., Eveillard S. Gene expression and enzymatic activity of invertases and sucrose synthase in Spiroplasma citri or stolbur phytoplasma infected plants. B.Insectol 2007, 60:219-220.
15. Baric S., Berger J., Cainelli C., Kerschbamer C., Dalla Via J. Molecular typing of 'Candidatus Phytoplasma mali' and epidemic history tracing by a combined T-RFLP/VNTR analysis approach. Eur. J. Plant Pathol. 2011, 131:573-584.
16. Rekab D., Pirajno G., Cettul E., De Salvador F.R., Firrao G. On the apple proliferation symptom display and the canopy colonization pattern of 'Candidatus Phytoplasma mali' in apple trees. Eur. J. Plant Pathol. 2010, 127:7-12.
17. Santi S., Grisan S., Pierasco A., De Marco F., Musetti R. Laser microdissection of grapevine leaf phloem infected by stolbur reveals site-specific gene responses associated to sucrose transport and metabolism. Plant Cell Environ. 2013, 36:343-355.
18. Bonasera J.M., Kim J.F., Beer S.V. PR genes of apple: identification and expression in response to elicitors and inoculation with Erwinia amylovora. BMC Plant Biol. 2006, 6:23.
19. Zhang J., Du X., Wang Q., Chen X., Lv D., Xu K., Qu S., Zhang Z. Expression of pathogenesis related genes in response to salicylic acid, methyl jasmonate and 1-aminocyclopropane-1-carboxylic acid in Malus hupehensis (Pamp.) Rehd. BMC Res. Notes 2010, 3:208.
20. Wang W., Vinocur B., Shoseyov O., Altman A. Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 2004, 9:244-252.
21. Rosa M., Prado C., Podazza G., Interdonato R., González J.A., Hilal M., Prado F.E. Soluble sugars-metabolism, sensing and abiotic stress: a complex network in the life of plants. Plant Signaling Behav. 2009, 4:388-393.
22. Rolland F., Baena-Gonzalez E., Sheen J. Sugar sensing and signaling in plants: conserved and novel mechanisms. Annu. Rev. Plant Biol. 2006, 57:675-709.
23. Li M., Feng F., Cheng L. Expression patterns of genes involved in sugar metabolism and accumulation during apple fruit development. PLoS One 2012, 7:e33055.
24. Bolouri Moghaddam M.R., Van den Ende W. Sugars and plant innate immunity. J.Exp. Bot. 2012, 63:3989-3998.
25. Gómez-Ariza J., Campo S., Rufat M., Estopà M., Messeguer J., San Segundo B., Coca M. Sucrose-mediated priming of plant defense responses and broad-spectrum disease resistance by overexpression of the maize pathogenesis-related PRms protein in rice plants. Mol. Plant Microbe Interact 2007, 20:832-842.
26. Li T.H., Li S.H. Leaf responses of micropropagated apple plants to water stress: nonstructural carbohydrate composition and regulatory role of metabolic enzymes. Tree Physiol. 2005, 25:495-504.
27. Jang J.C., Leon P., Zhou L., Sheen J. Hexokinase as a sugar sensor in higher plants. Plant Cell 1997, 9:5-19.
28. Cheng J., Khan M.A., Qiu W.M., Li J., Zhou H., Zhang Q., Guo W., Zhu T., Peng J., Sun F., Li S., Korban S.S., Han Y. Diversification of genes encoding granule-bound starch synthase in monocots and dicots is marked by multiple genome-wide duplication events. PLoS One 2012, 7:e30088.
29. Geigenberger P., Muller-Rober B., Stitt M. Contribution of adenosine 5'-diphosphoglucose pyrophosphorylase to the control of starch synthesis is decreased by water stress in growing potato tubers. Planta 1999, 209:338-345.
30. Asaoka M., Kazutoshi O., Fuwa H. Effect of environmental temperature at the milky stage on amylose content and fine structure of amylopectin of waxy and nonwaxy endosperm starches of rice (Oryza sativa L.). Agric. Biol. Chem. 1985, 49:373-379.
31. Hirano H.Y., Sano Y. Enhancement of Wx gene expression and the accumulation of amylose in response to cool temperatures during seed development in rice. Plant Cell Physiol. 1998, 39:807-812.
32. Wang S.J., Liu L.F., Chen C.K., Chen L.W. Regulations of granule-bound starch synthase I gene expression in rice leaves by temperature and drought stress. Biol. Plant. 2006, 50:537-541.
33. Giorno F., Guerriero G., Baric S., Mariani C. Heat shock transcriptional factors in Malus domestica: identification, classification and expression analysis. BMC Genomics 2012, 13:639.