Oligo-carrageenans induce a long-term and broad-range protection against pathogens in tobacco plants (var. Xanthi)

Physiological and Molecular Plant Pathology

Volumn 79, Issue , 2012, Pages 31-39

  Vera, Jeannette ^a   Castro, Jorge ^a   Contreras, Rodrigo A ^a   González, Alberto ^a   Moenne, Alejandra ^a  

^a UNIVERSIDAD DE SANTIAGO DE CHILE   (Chile)

Author keywords

B. cinerea; Botrytis cinerea; Defense responses; LOX; Nicotiana tabacum; Oligo carrageenans; P. carotovorum; PAL; Pectobacterium carotovorum; Tobacco mosaic virus

Indexed keywords

BOTRYOTINIA FUCKELIANA; NICOTIANA OBTUSIFOLIA; NICOTIANA TABACUM; PECTOBACTERIUM CAROTOVORUM; TOBACCO MOSAIC VIRUS;

EID: 84859805039     PISSN: 08855765     EISSN: 10961178     Source Type: Journal    
DOI: 10.1016/j.pmpp.2012.03.005     Document Type: Article

References (49)

1. Darvill A., Bergmann C., Servone F., De Lorenzo G., Ham K.S., Spiro M.D., et al. Oligosaccharins involved in plant growth and host-pathogen interactions. Biochem Soc Symp 1994, 60:89-94.
2. Silipo A., Erbs G., Shinya T., Dow J.M., Parilli M., Lanzetta R., et al. Glyco-conjugates as elicitors or suppressors of plant innate immunity. Glycobiology 2010, 20:406-419.
3. Aziz A., Heyraud A., Lambert B. Oligogalacturonide signal transduction, induction of defense-related responses and protection of grapevine against Botrytis cinerea. Planta 2004, 218:767-774.
4. Denoux C., Galetti R., Mamarella L., Gopalan S., Werck D., De Lorenzo G., et al. Activation of defense response pathways by OGs and Flg22 elicitors in Arabidopsis seedlings. Mol Plant 2008, 1:423-445.
5. Silipo A., Molinaro A., Sturiale L., Dow J.M., Erbs G., Lanzetta R., et al. The elicitation of plant innate immunity by lipooligosaccharide from Xanthomona campestris. J Biol Chem 2005, 280:33660-33668.
6. Varnier A.L., Sánchez L., Vatsa P., Boudesocque L., Garcia-Brugger A., Rabenoelina F., et al. Bacterial rhamnolipids are novel MAMPs conferring resistance to Botrytis cinerea in grapevine. Plant Cell Environ 2009, 32:178-193.
7. Aziz A., Gauthier A., Bézier A., Poinssot B., Joubert J.M., Pugin A., et al. Elicitor and resistance-inducing activities of 1,4 cellodextrins in grapevine, comparison with beta-1,3 glucans and alpha-1,4 oligogalacturonides. J Exp Bot 2007, 58:1463-1472.
8. Wang F., Feng G., Chen K. Burdock fructooligosaccharide induces resistance to tobacco mosaic virus in tobacco seedlings. Physiol Mol Plant Pathol 2009, 74:34-40.
9. Ferrari S., Galetti R., Pontiggia D., Manfredini C., Lionetti V., Bellicampi D., et al. Transgenic expression of a fungal endo-polygalacturonase increases plant resistance to pathogens and reduces auxin sensitivity. Plant Physiol 2008, 146:669-681.
10. Galetti R., Ferrari S., De Lorenzo G. Arabidopsis MPK3 and MPK6 play diffrent roles in basal and oligogalacturonide- or flagellin-induced resistance against Botrytis cinerea. Plant Physiol 2011, 157:804-814.
11. Fliegman J., Mithofer A., Wanner G., Ebel J. An ancient enzyme domain hidden in the putative beta-glucan elicitor receptor of soybean may play an active part in the perception of pathogen-associated molecular patterns during broad host resistance. J Biol Chem 2004, 279:1132-1140.
12. Kaku H., Nishizawa Y., Ishii-Minami N., Akimoto-Tomiya C., Dohmae N., Takio K., et al. Plant cells recognize chitin fragments for defense signaling through a plasma membrane receptor. Proc Natl Acad Sci USA 2006, 103:11086-11091.
13. Madsen E.B., Madsen L.H., Radutoiu S., Olbryt M., Rakwalska M., Szczglowsky K., et al. A receptor kinase gene of the LysM type is involved in legume perception of rhizobial signals. Nature 2003, 425:637-640.
14. Petutschnig E.K., Jones A.M., Serazetdinova L., Lipka U., Lipka V. The LysM-RLK CERK1 is a major chitin binding protein in Arabidopsis thaliana and subject to chinin-induced phosphorylation. J Biol Chem 2010, 285:28902-28911.
15. Decreux A., Thomas A., Spies E., Brasseur R., Van Cutsem P., Messiaen J. In vitro characterization of the homogalacturonan binding domain of the wall-associated kinase WAK1 using site-directed mutagenesis. Phytochemistry 2006, 67:1068-1079.
16. Brutus A., Sicilia F., Maccone A., Cervone F., De Lorenzo G. A domain swap approach reveals a role of the plant wall-associated kinase 1 (WAK1) as a receptor of oligogalacturonides. Proc Natl Acad Sci USA 2010, 107:9452-9457.
17. De Lorenzo G., Brutus A., Savatin D.V., Sicilia F., Cervone F. Engineering plant resistance by constructing chimeric receptors that recognize Damage-Associated Molecular Pattern (DAMPs). FEBS Lett 2011, 585:1521-1526.
18. Klarzynski O., Plesse B., Joubert J., Yvin J.C., Kopp M., Kloareg B., et al. Linear β-1,3 glucans are elicitors of defense responses in tobacco. Plant Physiol 2000, 124:1027-1037.
19. Aziz A., Poinssot B., Daire X., Adrian M., Bézier A., Lambert B., et al. Laminarin elicits defense responses in grapevine and induces protection against Botrytis cinerea and Plasmopara viticola. Mol Plant Microbe Interact 2003, 16:1118-1128.
20. Ménard R., Alban S., De Ruffray P., Jamois F., Franz G., Fritig B., et al. β-1,3 glucan sulfate, but not β-1,3 glucan, induces salycilic acid signaling pathway in tobacco and Arabidopsis. Plant Cell 2004, 16:3020-3032.
21. Trouvelot S., Varnier A.L., Allègre M., Mercier L., Baillieul L., Arnould C., et al. A β-1,3 laminarin sulphate induces resistance in grapevine against Plasmopara viticola through priming of defense responses, including HR-like cell death. Mol Plant Microbe Interact 2008, 21:232-243.
22. Klarzynski O., Descamps V., Plesse B., Yvin J.C., Kloareg B., Fritig B. Sulfated fucan oligosaccharides elicit defense responses in tobacco and local and systemic resistance against Tobacco Mosaic Virus. Mol Plant Microbe Interact 2003, 16:115-122.
23. Mercier L., Lafitte C., Borderies G., Briand X., Esquerré-Tugayé M.T., Fournier J. The algal polysaccharide carrageenans can act as an elicitor of plant defence. New Phytol 2001, 149:43-51.
24. Patier P., Potin P., Rochas C., Kloareg B., Yvin J.C., Liénart Y. Free or silica-bound oligokappa-carrageenans elicits laminarase activity in Rubus cells and protoplast. Plant Sci 1995, 110:27-35.
25. Laporte D., Vera J., Chandía N.P., Zúñiga E., Matsuhiro B., Moenne A. Structurally unrelated algal oligosaccharides differentially stimulate growth and defense against tobacco mosaic virus in tobacco plants. J Appl Phycol 2007, 19:79-88.
26. Vera J., Castro J., González A., Barrientos H., Matsuhiro B., Arce P., et al. Long-term protection against tobacco mosaic virus induced by the marine alga oligo-sulphated-galactan Poly-Ga in tobacco plants. Mol Plant Pathol 2011, 12:437-447.
27. Moenne A. Composition and method to stimulate plant growth and defense against pathogens in plants. 2009, United State Patent Application No 12,666,700.
28. Branca C., De Lorenzo G., Cervone F. Competitive inhibition of the auxin-induced elongation by α-D-oligogalacturonides in pea stem segments. Physiol Plant 1988, 72:499-504.
29. Bilisics L., Vojtassák J., Capek P., Kolárová K., Lisková D. Change in glycosidase activities during galactoglucomannan oligosaccharide inhibition of auxin induced growth. Phytochemistry 2004, 65:19034-21909.
30. Castro J., Vera J., González A., Moenne A. Oligo-carrageenans stimulate growth by enhancing photosynthesis, basal metabolism and cell cycle in tobacco plants (var. Burley). J Plant Growth Regul 2011, 10.1007/s00344-011-9229-5.
31. -ΔΔCT method. Methods 2001, 25:402-408.
32. Bradford M.M. A rapid and sensitive method for the quantification of microgram quantities of proteins utilizing the principle of protein-dye binding. Anal Biochem 1976, 72:248-254.
33. Zar J. Biostatistical analysis 1999, UK. E. Cliffs (Ed.).
34. x types in addition to the sulphate N-glycans of lutropin. J Exp Med 2000, 191:1117-1126.
35. Su Y., Bakker T., Harris J., Tsang C., Brown G.D., Wormald M.R., et al. Glycosilation influences the lectin activities of the macrophage mannose receptor. J Biol Chem 2005, 280:32811-32820.
36. Decreux A., Messiaen J. Wall-associated kinase WAK1 interacts with cell wall pectins in a calcium-induced conformation. Plant Cell Physiol 2005, 46:268-278.
37. Yuan H., Song J., Li X., Li N., Dai J. Immunomodulation and antitumor activity of kappa-carrageenan oligosaccharides. Cancer Lett 2006, 243:228-234.
38. Leiro J.M., Castro R., Arranz J.A., Lamas J. Immunomodulating activities of acididc sulphated polysaccharides obtained from the seaweed Ulva rigida C. Agardh Int Immunopharmacol 2007, 7:879-888.
39. Ahl-Goy P., Signer H., Reitz R., Aicholtz W., Blum W., Schmidt E., et al. Accumulation of scopoletin associated with the high disease resistance of the hybrid Nicotiana glutinosa x Nicotiana debneyi. Planta 1993, 19:200-2006.
40. Chong J., Baitz R., Schmitt C., Beffa R., Fritig B., Saindrenan P. Down regulation of a pathogen-responsive tobacco UDP-glc phenylpropanoid glucosyltransferase reduces scopoletin glucoside accumulation, enhance oxidative stress and weakens virus resistance. Plant Cell 2002, 145:1093-1107.
41. NN and to increase resistance against infection with potato virus Y. Plant Cell Environ 2006, 29:126-137.
42. Wu Z.J., Ouyang M.A., Wang C.Z., Zhang Z.K. Shen JG Anti-tobacco mosai virus (TMV) triterpenoid saponins from the leaves of Ilex oblonga. J Agric Food Chem 2007, 55:1712-17171.
43. Zhang Z.K., Ouyang M.A., Wu Z.J., Lin Q.Y., Xie L.H. Structure activity relationship of triterpenes and triterpenoid glycosides against tobacco mosaic virus. Planta Med 2007, 73:1457-1463.
44. Yan H.H., Chen J., Di Y.T., Fang X., Dong J.H., Sang P., et al. Hao XJ Anti-tobacco mosaic virus (TMV) quassinoids from Brucea javanica (L.) Merr. J Agric Food Chem 2010, 58:1572-1577.
45. Sels J., Mathys J., De Conink B.M.A., Cammue B.P.A., De Bolle M.F.C. Plant pathogenesis-related proteins: a focus on PR peptides. Plant Physiol Biochem 2008, 46:941-950.
46. Bailey J.A., Vincent G.G., Burden R.S. The antifungal activity of of glutinosone and capsidiol and their accumulation in virus-infected tobacco species. Physiol Plant Pathol 1976, 8:35-41.
47. Bollina V., Kuwarasyamy G.K., Kushalappa A.C., Shoo T.M., Dion Y., Rioux S., et al. Mass spectrometry-based metabolomics application to identify quantitative resistance-related metabolites in barley against Fusarium head blight. Mol Pant Pathol 2010, 11:769-782.
48. Carpinella M.C., Giorda L.M., Farrayol C.G., Palacios S.M. Antifungal effects of different organic extracts from Media azedarach L. on phytopathogenic fungi and their isolated active components. J Agric Food Chem 2003, 51:2506-2511.
49. Maddox C.E., Laur L.M., Tian L. Antibacterial activity of phenolic compounds against the phytopathogen. Xillela Fastidiosa Curr Microbiol 2010, 60:53-58.