Abstract
Recent progress in nanotechnology-enabled sensors that can be placed inside of living plants has shown that it is possible to relay and record real-time chemical signaling stimulated by various abiotic and biotic stresses. The mathematical form of the resulting local reactive oxygen species (ROS) wave released upon mechanical perturbation of plant leaves appears to be conserved across a large number of species, and produces a distinct waveform from other stresses including light, heat and pathogen-associated molecular pattern (PAMP)-induced stresses. Herein, we develop a quantitative theory of the local ROS signaling waveform resulting from mechanical stress in planta. We show that nonlinear, autocatalytic production and Fickian diffusion of H2O2 followed by first order decay well describes the spatial and temporal properties of the waveform. The reaction–diffusion system is analyzed in terms of a new approximate solution that we introduce for such problems based on a single term logistic function ansatz. The theory is able to describe experimental ROS waveforms and degradation dynamics such that species-dependent dimensionless wave velocities are revealed, corresponding to subtle changes in higher moments of the waveform through an apparently conserved signaling mechanism overall. This theory has utility in potentially decoding other stress signaling waveforms for light, heat and PAMP-induced stresses that are similarly under investigation. The approximate solution may also find use in applied agricultural sensing, facilitating the connection between measured waveform and plant physiology.
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References
Abrahamson JT, Strano MS (2010) Analytical solution to coupled chemical reaction and thermally diffusing systems: applicability to self-propagating thermopower waves. J Phys Chem Lett 1:3514–3519. https://doi.org/10.1021/JZ101381M
Ani Akpinar B, Avsar B, Lucas SJ, Budak H (2012) Plant abiotic stress signaling. Plant Signal Behav 7:1–6. https://doi.org/10.4161/PSB.21894
Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55:373–399. https://doi.org/10.1146/ANNUREV.ARPLANT.55.031903.141701
Choi WG, Miller G, Wallace I, Harper J, Mittler R, Gilroy S (2017) Orchestrating rapid long-distance signaling in plants with Ca2+. ROS Electr Signals Plant J 90:698–707. https://doi.org/10.1111/TPJ.13492
Fichman Y, Mittler R (2020) Rapid systemic signaling during abiotic and biotic stresses: is the ROS wave master of all trades? Plant J 102:887–896. https://doi.org/10.1111/TPJ.14685
Gilroy S, Suzuki N, Miller G, Choi WG, Toyota M, Devireddy AR, Mittler R (2014) A tidal wave of signals: calcium and ROS at the forefront of rapid systemic signaling. Trends Plant Sci 19:623–630. https://doi.org/10.1016/J.TPLANTS.2014.06.013
Han GZ (2019) Origin and evolution of the plant immune system. New Phytol 222:70–83. https://doi.org/10.1111/NPH.15596
Huang H, Ullah F, Zhou DX, Yi M, Zhao Y (2019) Mechanisms of ROS regulation of plant development and stress responses. Front Plant Sci 10:800. https://doi.org/10.3389/FPLS.2019.00800
Johns S, Hagihara T, Toyota M, Gilroy S (2021) The fast and the furious: rapid long-range signaling in plants. Plant Physiol 185:694–706. https://doi.org/10.1093/PLPHYS/KIAA098
Källén A (1984) Thresholds and travelling waves in an epidemic model for rabies. Nonlinear Anal Theory Methods Appl 8:851–856. https://doi.org/10.1016/0362-546X(84)90107-X
Källén A, Arcuri P, Murray JD (1985) A simple model for the spatial spread and control of rabies. J Theor Biol 116:377–393. https://doi.org/10.1016/s0022-5193(85)80276-9
Klug D, Rabani J, Fridovich I (1972) A direct demonstration of the catalytic action of superoxide dismutase through the use of pulse radiolysis. J Biol Chem 247:4839–4842. https://doi.org/10.1016/S0021-9258(19)44987-9
Kot M (2001) Elements of mathematical ecology. Cambridge University Press, Cambridge. https://doi.org/10.1017/CBO9780511608520
Kudryashov NA (2015) Logistic function as solution of many nonlinear differential equations. Appl Math Model 39:5733–5742. https://doi.org/10.1016/J.APM.2015.01.048
Lew TTS, Wong MH, Kwak S-Y, Sinclair R, Koman VB, Strano MS (2018) Rational design principles for the transport and subcellular distribution of nanomaterials into plant protoplasts. Small 14:1802086. https://doi.org/10.1002/SMLL.201802086
Lew TTS, Koman VB, Silmore KS, Seo JS, Gordiichuk P, Kwak SY, Park M, Ang MCY, Khong DT, Lee MA, Chan-Park MB, Chua NH, Strano MS (2020) Real-time detection of wound-induced H2O2 signalling waves in plants with optical nanosensors. Nat Plants 6:404–415. https://doi.org/10.1038/s41477-020-0632-4
Lomdahl PS (1984) What Is a soliton? Los Alamos Sci 10:27–31
Mittler R, Vanderauwera S, Suzuki N, Miller G, Tognetti VB, Vandepoele K, Gollery M, Shulaev V, Van Breusegem F (2011) ROS signaling: the new wave? Trends Plant Sci 16:300–309. https://doi.org/10.1016/J.TPLANTS.2011.03.007
Navarro L, Dunoyer P, Jay F, Arnold B, Dharmasiri N, Estelle M, Voinnet O, Jones JDG (2006) A plant miRNA contributes to antibacterial resistance by repressing auxin signaling. Science 312:436–439. https://doi.org/10.1126/science.1126088
Petrov VD, Van Breusegem F (2012) Hydrogen peroxide—a central hub for information flow in plant cells. AoB Plants 2012:14. https://doi.org/10.1093/AOBPLA/PLS014
Pieterse CMJ, Van Der Does D, Zamioudis C, Leon-Reyes A, Van Wees SCM (2012) Hormonal modulation of plant immunity. Annu Rev Cell Dev Biol 28:489–521. https://doi.org/10.1146/ANNUREV-CELLBIO-092910-154055
Pinar Z, Rezazadeh H, Eslami M (2020) Generalized logistic equation method for Kerr law and dual power law Schrödinger equations. Opt Quantum Electron 52:1–16. https://doi.org/10.1007/S11082-020-02611-2
Spoel SH, Dong X (2008) Making sense of hormone crosstalk during plant immune responses. Cell Host Microbe 3:348–351. https://doi.org/10.1016/J.CHOM.2008.05.009
Thaler JS, Humphrey PT, Whiteman NK (2012) Evolution of jasmonate and salicylate signal crosstalk. Trends Plant Sci 17:260–270. https://doi.org/10.1016/J.TPLANTS.2012.02.010
Truman W, Bennet MH, Kubigsteltig I, Turnbull C, Grant M (2007) Arabidopsis systemic immunity uses conserved defense signaling pathways and is mediated by jasmonates. Proc Natl Acad Sci USA 104:1075–1080. https://doi.org/10.1073/PNAS.0605423104
Van Breusegem F, Bailey-Serres J, Mittler R (2008) Unraveling the tapestry of networks involving reactive oxygen species in plants. Plant Physiol 147:978–984. https://doi.org/10.1104/PP.108.122325
Vega-Muñoz I, Duran-Flores D, Fernández-Fernández ÁD, Heyman J, Ritter A, Stael S (2020) Breaking bad news: dynamic molecular mechanisms of wound response in plants. Front Plant Sci 11:1959. https://doi.org/10.3389/FPLS.2020.610445
Vestergaard CL, Flyvbjerg H, Møller IM (2012) Intracellular signaling by diffusion: can waves of hydrogen peroxide transmit intracellular information in plant cells? Front Plant Sci 3:295. https://doi.org/10.3389/FPLS.2012.00295
Wong MH, Misra RP, Giraldo JP, Kwak S-Y, Son Y, Landry MP, Swan JW, Blankschtein D, Strano MS (2016) Lipid exchange envelope penetration (LEEP) of nanoparticles for plant engineering: a universal localization mechanism. Nano Lett 16:1161–1172. https://doi.org/10.1021/ACS.NANOLETT.5B04467
Zandalinas SI, Mittler R (2018) ROS-induced ROS release in plant and animal cells. Free Radic Biol Med 122:21–27. https://doi.org/10.1016/J.FREERADBIOMED.2017.11.028
Acknowledgements
The mathematical and analytical work is supported by Nanotechnology for Agricultural and Food Systems (A1511) [Grant No. 2021-67021-33999/Project Accession No. 1025638] from the USDA National Institute of Food and Agriculture. The extension of the theory to plant signaling data was supported by the National Research Foundation (NRF), Prime Minister’s Office, Singapore under its Campus for Research Excellence and Technological Enterprise (CREATE) program. The Disruptive & Sustainable Technology for Agricultural Precision (DiSTAP) is an interdisciplinary research group of the Singapore MIT Alliance for Research and Technology (SMART) Centre. DJL and TKP are grateful for support from the National Science Foundation Graduate Research Fellowship Program under Grant No. 1745302. TTSL acknowledges a graduate fellowship by the Agency of Science, Research and Technology, Singapore. KSS was supported by the Department of Energy Computational Science Graduate Fellowship program under Grant DE-FG02-97ER25308. Professor Per-Olof Persson is acknowledged for helpful insights during the development of the approximate solutions.
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TKP: Data Curation, Formal analysis, Methodology, Software, Visualization, Writing—Original Draft (main text), Writing—Review & Editing. MNH: Formal analysis, Methodology, Software, Writing—Original Draft (Supplementary Information), Writing—Review & Editing. DJL: Formal analysis, Methodology, Writing—Review & Editing. AMB: Formal analysis, Methodology, Writing—Review & Editing. TTSL: Data Curation, Formal analysis, Investigation, Methodology, Software, Writing—Review & Editing. KSS: Formal analysis, Methodology, Software, Writing—Review & Editing. VBK: Formal analysis, Methodology, Writing—Review & Editing. MCYA: Investigation, Validation, Writing—Review & Editing. DTK: Investigation, Validation, Writing—Review & Editing. GPS: Conceptualization, Funding acquisition, Supervision, Writing—Review & Editing. JWS: Conceptualization, Formal analysis, Methodology, Supervision. RS: Conceptualization, Funding acquisition, Supervision, Writing—Reviewing & Editing. NHC: Conceptualization, Funding acquisition, Supervision, Writing—Review & Editing. MSS: Conceptualization, Formal analysis, Funding acquisition, Methodology, Supervision, Writing—Review & Editing.
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This paper is dedicated, with appreciation, to our colleague and co-author Professor James W. Swan, who died suddenly on Nov. 5th, 2021.
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Porter, T.K., Heinz, M.N., Lundberg, D.J. et al. A theory of mechanical stress-induced H2O2 signaling waveforms in Planta. J. Math. Biol. 86, 11 (2023). https://doi.org/10.1007/s00285-022-01835-y
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DOI: https://doi.org/10.1007/s00285-022-01835-y
Keywords
- Plant systemic stress signaling
- Plant wounding response
- ROS wave
- Reaction–diffusion
- Solitons
Mathematics Subject Classification
- 35
- 92