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Drought stress had a predominant effect over heat stress on three tomato cultivars subjected to combined stress

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Zhou, Rong, Yu, Xiaqing, Ottosen, Carl-Otto, Rosenqvist, Eva, Zhao, Liping, Wang, Yinlei, Yu, Wengui, Zhao, Tongmin, Wu, Zhen·2017·BMC Plant Biology

Abstract

Abiotic stresses due to environmental factors could adversely affect the growth and development of crops. Among the abiotic stresses, drought and heat stress are two critical threats to crop growth and sustainable agriculture worldwide. Considering global climate change, incidence of combined drought and heat stress is likely to increase. The aim of this study was to shed light on plant growth performance and leaf physiology of three tomatoes cultivars (‘Arvento’, ‘LA1994’ and ‘LA2093’) under control, drought, heat and combined stress. Shoot fresh and dry weight, leaf area and relative water content of all cultivars significantly decreased under drought and combined stress as compared to control. The net photosynthesis and starch content were significantly lower under drought and combined stress than control in the three cultivars. Stomata and pore length of the three cultivars significantly decreased under drought and combined stress as compared to control. The tomato ‘Arvento’ was more affected by heat stress than ‘LA1994’ and ‘LA2093’ due to significant decreases in shoot dry weight, chlorophyll a and carotenoid content, starch content and NPQ (non-photochemical quenching) only in ‘Arvento’ under heat treatment. By comparison, the two heat-tolerant tomatoes were more affected by drought stress compared to ‘Arvento’ as shown by small stomatal and pore area, decreased sucrose content, Φ PSII (quantum yield of photosystem II), ETR (electron transport rate) and q L (fraction of open PSII centers) in ‘LA1994’ and ‘LA2093’. The three cultivars showed similar response when subjected to the combination of drought and heat stress as shown by most physiological parameters, even though only ‘LA1994’ and ‘LA2093’ showed decreased F v /F m (maximum potential quantum efficiency of photosystem II), Φ PSII , ETR and q L under combined stress. The cultivars differing in heat sensitivity did not show difference in the combined stress sensitivity, indicating that selection for tomatoes with combined stress tolerance might not be correlated with the single stress tolerance. In this study, drought stress had a predominant effect on tomato over heat stress, which explained why simultaneous application of heat and drought revealed similar physiological responses to the drought stress. These results will uncover the difference and linkage between the physiological response of tomatoes to drought, heat and combined stress and be important for the selection and breeding of tolerant tomato cultivars under single and combine stress.

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Research works printed but not linked: 51

  1. Mittler R. Abiotic stress, the field environment and stress combination. Trends Plant Sci. 2006;11:15–9. · DOI · Paper page
  2. Aprile A, Havlickova L, Panna R, Marè C, Borrelli GM, Marone D, et al. Different stress responsive strategies to drought and heat in two durum wheat cultivars with contrasting water use efficiency. BMC Genomics. 2013;14:821–38. · DOI
  3. Siddiqui MH, Al-Khaishany MY, Al-Qutami MA, Al-Whaibi MH, Grover A, Ali HM, et al. Morphological and physiological characterization of different genotypes of faba bean under heat stress. Saudi J Biol Sci. 2015;22:656–63. · DOI
  4. Zhou R, Yu X, Kjær KH, Rosenqvist E, Ottosen CO, Wu Z. Screening and validation of tomato genotypes under heat stress using Fv/Fm to reveal the physiological mechanism of heat tolerance. Environ Exp Bot. 2015;118:1–11. · DOI · Paper page
  5. Chew YH, Halliday KJ. A stress-free walk from Arabidopsis to crops. Curr Opin Biotech. 2011;22:281–6. · doi:10.1016/j.copbio.2010.11.011
  6. Suzuki N, Rivero RM, Shulaev V, Blumwald E, Mittler R. Abiotic and biotic stress combinations. New Phytol. 2014;203:32–43. · DOI · Paper page
  7. Lipiec J, Doussan C, Nosalewicz A, Kondracka K. Effect of drought and heat stresses on plant growth and yield: a review. Int Agrophys. 2013;27:463–77. · DOI · Paper page
  8. Awasthi R, Kaushal N, Vadez V, Turner NC, Berger J, Siddique KHM, et al. Individual and combined effects of transient drought and heat stress on carbon assimilation and seed filling in chickpea. Funct Plant Biol. 2014;41:1148–67. · DOI · Paper page
  9. Seki M, Umezawa T, Urano K, Shinozaki K. Regulatory metabolic networks in drought stress responses. Curr Opin Plant Bio. 2007;10:296–302. · DOI · Paper page
  10. Vadez V, Berger JD, Warkentin T, Asseng S, Ratnakumar P, Rao KPC, et al. Adaptation of grain legumes to climate change: a review. Agron Sustain Dev. 2012;32:31–44. · doi:10.1007/s13593-011-0020-6
  11. Hall AE. In: Janick J, editor. Breeding for heat tolerance: plant breeding reviews. USA: Wiley; 1992. p. 129–68. · DOI · Paper page
  12. Ahuja I, de Vos RC, Bones AM, Hall RD. Plant molecular stress responses face climate change. Trends Plant Sci. 2010;15:664–74. · DOI · Paper page
  13. Camejo D, Rodríguez P, Morales MA, Dell'Amico JM, Torrecillas A, Alarcón JJ. High temperature effects on photosynthetic activity of two tomato cultivars with different heat susceptibility. J Plant Physiol. 2005;162:281–9. · DOI · Paper page
  14. Camejo D, Jiménez A, Alarcón JJ, Torres W, Gómez JM, Sevilla F. Changes in photosynthetic parameters and antioxidant activities following heat-shock treatment in tomato plants. Funct Plant Biol. 2006;33:177–87. · DOI · Paper page
  15. Patanè C. Leaf area index, leaf transpiration and stomatal conductance as affected by soil water deficit and VPD in processing tomato in semi arid mediterranean climate. J Agron Crop Sci. 2011;197:165–76. · doi:10.1111/j.1439-037x.2010.00454.x
  16. Mishra KB, Iannacone R, Petrozza A, Mishra A, Armentano N, Vecchia GL, et al. Engineered drought tolerance in tomato plants is reflected in chlorophyll fluorescence emission. Plant Sci. 2012;182:79–86. · DOI · Paper page
  17. Rizhsky L, Liang H, Mittler R. The combined effect of drought stress and heat shock on gene expression in tobacco. Plant Physiol. 2002;130:1143–51. · DOI · Paper page
  18. Rizhsky L, Liang H, Shuman J, Shulaev V, Davletova S, Mittler R. When defense pathways collide: the response of Arabidopsis to a combination of drought and heat stress. Plant Physiol. 2004;134:1683–96. · DOI · Paper page
  19. Prasch CM, Sonnewald U. Simultaneous application of heat, drought, and virus to Arabidopsis plants reveals significant shifts in signaling networks. Plant Physiol. 2013;162:1849–66. · DOI · Paper page
  20. Grigorova B, Vasevam II, Demirevska K, Feller U. Expression of selected heat shock proteins after individually applied and combined drought and heat stress. Acta Physiol Plant. 2011;33:2041–9. · DOI
  21. Rivero RM, Mestre TC, Mittler RON, Rubio F, Garcia-Sanchez F, Martinez V. The combined effect of salinity and heat reveals a specific physiological, biochemical and molecular response in tomato plants. Plant Cell Environ. 2014;37:1059–73. · DOI · Paper page
  22. Ashoub A, Baeumlisberger M, Neupaertl M, Karas M, Brüggemann W. Characterization of common and distinctive adjustments of wild barley leaf proteome under drought acclimation, heat stress and their combination. Plant Mol Biol. 2015;87:459–71. · DOI
  23. Chaves MM, Flexas J, Pinheiro C. Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot. 2009;103:551–60. · DOI · Paper page
  24. Havaux I. Rapid photosynthetic adaptation to heat stress triggered in potato leaves by moderately elevated temperatures. Plant Cell Environ. 1993;16:461–7. · DOI · Paper page
  25. Allakhverdiev SI, Hayashi H, Nishiyama Y, Ivanov AG, Aliev JA, Klimov VV, et al. Glycinebetaine protects the D1/D2/Cytb559 complex of photosystem II against photo-induced and heat-induced inactivation. J Plant Physiol. 2003;160:41–9. · DOI
  26. Sharma DK, Andersen SB, Ottosen CO, Rosenqvist E. Wheat cultivars selected for high Fv/Fm under heat stress maintain high photosynthesis, total chlorophyll, stomatal conductance, transpiration and dry matter. Physiol Plant. 2015;153:284–98. · DOI · Paper page
  27. Cajánek M, Štroch M, Lachetová I, Kalina J, Spunda V. Characterization of the photosystem II inactivation of heat-stressed barley leaves as monitored by the various parameters of chlorophyll a fluorescence and delayed fluorescence. J Photochem Photobiol B. 1998;47:39–45. · DOI
  28. Baker NR, Rosenqvist E. Applications of chlorophyll fluorescence can improve crop production strategies: an examination of future possibilities. J Exp Bot. 2004;55:1607–21. · DOI · Paper page
  29. Sharma DK, Andersen SB, Ottosen CO, Rosenqvist E. Phenotyping of wheat cultivars for heat tolerance using chlorophyll a fluorescence. Funct Plant Biol. 2012;39:936–47. · DOI
  30. Wintermans J, De Mots A. Spectrophotometric characteristics of chlorophylls a and b and their phenophytins in ethanol. Biochim Biophys Acta. 1965;109:448–53. · DOI · Paper page
  31. Giday H, Kjaer KH, Fanourakis D, Ottosen CO. Smaller stomata require less severe leaf drying to close: a case study in Rosa hydrida. J Plant Physiol. 2013;170:1309–16. · DOI
  32. Lobell DB, Schlenker W, Costa-Roberts J. Climate trends and global crop production since 1980. Science. 2011;333:616–20. · DOI · Paper page
  33. Chen J, Xu W, Velten J, Xin Z, Stout J. Characterization of maize inbred lines for drought and heat tolerance. J Soil Water Conserv. 2012;67:354–64. · DOI · Paper page
  34. Dreesen FE, de Boeck HJ, Janssens IA, Nijs I. Summer heat and drought extremes trigger unexpected changes in productivity of a temperate annual/biannual plant community. Environ Exp Bot. 2012;79:21–30. · DOI · Paper page
  35. Rollins JA, Habte E, Templer SE, Colby T, Schmidt J, von Korff M. Leaf proteome alterations in the context of physiological and morphological responses to drought and heat stress in barley (Hordeum vulgare L.). J Exp Bot. 2013;64:3201–12. · DOI · Paper page
  36. Pandey P, Ramegowda V, Senthilkumar M. Shared and unique responses of plants to multiple individual stresses and stress combinations: physiological and molecular mechanisms. Front Plant Sci. 2015;6:723–36. · DOI · Paper page
  37. Nankishore A, Farrell AD. The response of contrasting tomato genotypes to combined heat and drought stress. J Plant Physiol. 2016;202:75–82. · DOI
  38. Vile D, Pervent M, Belluau M, Vasseur F, Bresson J, Muller B, et al. Arabidopsis growth under prolonged high temperature and water deficit: independent or interactive effects? Plant Cell Environ. 2012;35:702–18. · DOI · Paper page
  39. Von Caemmerer SV, Farquhar GD. Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta. 1981;153:376–87. · DOI · Paper page
  40. Lalonde S, Boles E, Hellmann H, Barker L, Patrick JW, Frommer WB, et al. The dual function of sugar carriers: transport and sugar sensing. Plant Cell. 1999;11:707–26. · DOI · Paper page
  41. Iii WWA, Muller O, Cohu CM, Demmig-Adams B. Photosystem II efficiency and non-photochemical fluorescence quenching in the context of source-sink balance: non-photochemical quenching and energy dissipation in plants, algae and cyanobacteria. Netherlands: Springer; 2014. p. 503–29.
  42. Cairns JE, Crossa J, Zaidi PH, Grudloyma P, Sanchez C, Araus JL, et al. Identification of drought, heat, and combined drought and heat tolerant donors in maize. Crop Sci. 2013;53:1335–46. · DOI · Paper page
  43. Albacete AA, Martínez-Andújar C, Pérez-Alfocea F. Hormonal and metabolic regulation of source-sink relations under salinity and drought: from plant survival to crop yield stability. Biotechnol Adv. 2014;32:12–30. · DOI · Paper page
  44. Pérez-Alfocea F, Albacete A, Ghanem ME, Dodd LC. Hormonal regulation of source-sink relations to maintain crop productivity under salinity: a case study of root-to-root signalling in tomato. Funct Plant Bio. 2010;37:592–603. · DOI
  45. Hana M, Marie H, Jana D, Veronika T, Ondřej N, Zuzana L, et al. Enhanced drought and heat stress tolerance of tobacco plants with ectopically enhanced cytokinin oxidase/dehydrogenase gene expression. J Exp Bot. 2013;64:2805–15. · doi:10.1093/jxb/ert131
  46. Stoddard FL, Balko C, Erskine W, Khan HR, Link W, Sarker A. Screening techniques and sources of resistance to abiotic stresses in cool-season food legumes. Euphytica. 2006;147:167–86. · DOI · Paper page
  47. Sekmen AH, Ozgur R, Uzilday B, Turkan I. Reactive oxygen species scavenging capacities of cotton (Gossypium hirsutum) cultivars under combined drought and heat induced oxidative stress. Environ Exp Bot. 2014;99:141–9. · DOI · Paper page
  48. Alexieva V, Sergiev I, Mapelli S, Karanov E. The effect of drought and ultraviolet radiation on growth and stress markers in pea and wheat. Plant Cell Environ. 2001;24:1337–44. · DOI · Paper page
  49. Upreti KK, Murti GSR, Bhatt RM. Response of pea cultivars to water stress: changes in morpho-physiological characters, endogenous hormones and yield. Veg Sci. 2000;27:57–61.
  50. Castonguay Y, Markhart AH. Saturated rates of photosynthesis in waterstressed leaves of common bean and tepary bean. Crop Sci. 1991;31:1605–11. · DOI
  51. Ort DR, Baker NR. A photoprotective role for O2 as an alternative electron sink in photosynthesis? Curr Opin Plant Biol. 2002;5:193–8. · DOI · Paper page

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Metadata

Authors
Zhou, R., Yu, X., Ottosen, C.-O., Rosenqvist, E., Zhao, L., Wang, Y., Yu, W., Zhao, T., & Wu, Z.
Venue
BMC Plant Biology
Published
2017-01-25
Volume
17
Issue
1
Pages
24-24
ISSN
1471-2229 (ISSN-L)
OpenAlex
W2580379435
Cited by
427
References
2
FWCI
23.68
Type
journal article
Language
en
Open access
gold
Funders
  • Natural Science Foundation of Youth in Jiangsu Province (BK20160579, BK20140739)
  • National Natural Science Foundation of China (31601745)
  • Basic Scientific Research project in Jiangsu Academy of Agricultural Science (ZX(15)2003)

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Zhou, R., Yu, X., Ottosen, C.-O., Rosenqvist, E., Zhao, L., Wang, Y., Yu, W., Zhao, T., & Wu, Z. (2017). Drought stress had a predominant effect over heat stress on three tomato cultivars subjected to combined stress. BMC Plant Biology. https://doi.org/10.1186/s12870-017-0974-x

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