Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1995 Dec;109(4):1259–1266. doi: 10.1104/pp.109.4.1259

Evidence for a Mechanically Induced Oxidative Burst.

T Yahraus 1, S Chandra 1, L Legendre 1, P S Low 1
PMCID: PMC157658  PMID: 12228667

Abstract

Rapid release of H2O2 may constitute an initial defense response mounted by a plant. Inauguration of this oxidative burst is known to occur upon stimulation with chemical elicitors, but the possibility of mechanical elicitation arising from pathogen penetration/weakening of the cell wall has never been examined. To introduce an adjustable mechanical stress on the plasma membrane, cultured soybean (Glycine max Merr. cv Kent) cells were subjected to defined changes in medium osmolarity. Dilution of the medium with water or resuspension of cells in sucrose solutions of reduced osmolarity yielded an oxidative burst similar to those stimulated by chemical elicitors. Furthermore, the magnitude of oxidant biosynthesis and osmotic stress correlated directly. Upon return of the cells to normal tonicity, the oxidative burst abruptly halted, indicating that its expression depended on maintenance of the osmotic stress and not on any external chemical signal. To confirm the ability of soybean cells to respond to a mechanical stimulus with induction of an oxidative burst, cells were subjected to direct physical pressure. Application of pressure yielded a characteristic oxidative burst. Because neither these cells nor those subjected to osmotic pressure were damaged by their treatments, we conclude that plant cells can detect mechanical disturbances and initiate a classical defense reaction in response.

Full Text

The Full Text of this article is available as a PDF (1.2 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alexandre J., Lassalles J. P. Hydrostatic and osmotic pressure activated channel in plant vacuole. Biophys J. 1991 Dec;60(6):1326–1336. doi: 10.1016/S0006-3495(91)82170-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Apostol I., Heinstein P. F., Low P. S. Rapid Stimulation of an Oxidative Burst during Elicitation of Cultured Plant Cells : Role in Defense and Signal Transduction. Plant Physiol. 1989 May;90(1):109–116. doi: 10.1104/pp.90.1.109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Apostol I., Low P. S., Heinstein P., Stipanovic R. D., Altman D. W. Inhibition of elicitor-induced phytoalexin formation in cotton and soybean cells by citrate. Plant Physiol. 1987 Aug;84(4):1276–1280. doi: 10.1104/pp.84.4.1276. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Baker C. J., Orlandi E. W., Mock N. M. Harpin, An Elicitor of the Hypersensitive Response in Tobacco Caused by Erwinia amylovora, Elicits Active Oxygen Production in Suspension Cells. Plant Physiol. 1993 Aug;102(4):1341–1344. doi: 10.1104/pp.102.4.1341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bishop P. D., Pearce G., Bryant J. E., Ryan C. A. Isolation and characterization of the proteinase inhibitor-inducing factor from tomato leaves. Identity and activity of poly- and oligogalacturonide fragments. J Biol Chem. 1984 Nov 10;259(21):13172–13177. [PubMed] [Google Scholar]
  6. Blumenkrantz N., Asboe-Hansen G. New method for quantitative determination of uronic acids. Anal Biochem. 1973 Aug;54(2):484–489. doi: 10.1016/0003-2697(73)90377-1. [DOI] [PubMed] [Google Scholar]
  7. Bradley D. J., Kjellbom P., Lamb C. J. Elicitor- and wound-induced oxidative cross-linking of a proline-rich plant cell wall protein: a novel, rapid defense response. Cell. 1992 Jul 10;70(1):21–30. doi: 10.1016/0092-8674(92)90530-p. [DOI] [PubMed] [Google Scholar]
  8. Chandra S., Low P. S. Role of phosphorylation in elicitation of the oxidative burst in cultured soybean cells. Proc Natl Acad Sci U S A. 1995 May 9;92(10):4120–4123. doi: 10.1073/pnas.92.10.4120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Chen Z., Silva H., Klessig D. F. Active oxygen species in the induction of plant systemic acquired resistance by salicylic acid. Science. 1993 Dec 17;262(5141):1883–1886. doi: 10.1126/science.8266079. [DOI] [PubMed] [Google Scholar]
  10. Degousee N., Triantaphylides C., Montillet J. L. Involvement of Oxidative Processes in the Signaling Mechanisms Leading to the Activation of Glyceollin Synthesis in Soybean (Glycine max). Plant Physiol. 1994 Mar;104(3):945–952. doi: 10.1104/pp.104.3.945. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dempsey D. A., Klessig D. F. Salicylic acid, active oxygen species and systemic acquired resistance in plants. Trends Cell Biol. 1994 Sep;4(9):334–338. doi: 10.1016/0962-8924(94)90235-6. [DOI] [PubMed] [Google Scholar]
  12. Ding J. P., Pickard B. G. Mechanosensory calcium-selective cation channels in epidermal cells. Plant J. 1993 Jan;3(1):83–110. [PubMed] [Google Scholar]
  13. Falke L. C., Edwards K. L., Pickard B. G., Misler S. A stretch-activated anion channel in tobacco protoplasts. FEBS Lett. 1988 Sep 12;237(1-2):141–144. doi: 10.1016/0014-5793(88)80188-1. [DOI] [PubMed] [Google Scholar]
  14. Horn M. A., Meadows R. P., Apostol I., Jones C. R., Gorenstein D. G., Heinstein P. F., Low P. S. Effect of Elicitation and Changes in Extracellular pH on the Cytoplasmic and Vacuolar pH of Suspension-Cultured Soybean Cells. Plant Physiol. 1992 Feb;98(2):680–686. doi: 10.1104/pp.98.2.680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Howard R. J., Ferrari M. A., Roach D. H., Money N. P. Penetration of hard substrates by a fungus employing enormous turgor pressures. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11281–11284. doi: 10.1073/pnas.88.24.11281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Legendre L., Yueh Y. G., Crain R., Haddock N., Heinstein P. F., Low P. S. Phospholipase C activation during elicitation of the oxidative burst in cultured plant cells. J Biol Chem. 1993 Nov 25;268(33):24559–24563. [PubMed] [Google Scholar]
  17. Levine A., Tenhaken R., Dixon R., Lamb C. H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell. 1994 Nov 18;79(4):583–593. doi: 10.1016/0092-8674(94)90544-4. [DOI] [PubMed] [Google Scholar]
  18. Low P. S., Heinstein P. F. Elicitor stimulation of the defense response in cultured plant cells monitored by fluorescent dyes. Arch Biochem Biophys. 1986 Sep;249(2):472–479. doi: 10.1016/0003-9861(86)90024-x. [DOI] [PubMed] [Google Scholar]
  19. Mehdy M. C. Active Oxygen Species in Plant Defense against Pathogens. Plant Physiol. 1994 Jun;105(2):467–472. doi: 10.1104/pp.105.2.467. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Schroeder J. I., Hedrich R. Involvement of ion channels and active transport in osmoregulation and signaling of higher plant cells. Trends Biochem Sci. 1989 May;14(5):187–192. doi: 10.1016/0968-0004(89)90272-7. [DOI] [PubMed] [Google Scholar]
  21. Trewavas A., Knight M. Mechanical signalling, calcium and plant form. Plant Mol Biol. 1994 Dec;26(5):1329–1341. doi: 10.1007/BF00016478. [DOI] [PubMed] [Google Scholar]
  22. Vera-Estrella R., Blumwald E., Higgins V. J. Effect of Specific Elicitors of Cladosporium fulvum on Tomato Suspension Cells : Evidence for the Involvement of Active Oxygen Species. Plant Physiol. 1992 Jul;99(3):1208–1215. doi: 10.1104/pp.99.3.1208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Yang X. C., Sachs F. Block of stretch-activated ion channels in Xenopus oocytes by gadolinium and calcium ions. Science. 1989 Feb 24;243(4894 Pt 1):1068–1071. doi: 10.1126/science.2466333. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES