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Improvement of plant performance under water deficit with the employment of biological and chemical priming agents

  • R. Balestrini (a1), W. Chitarra (a1) (a2), C. Antoniou (a3), M. Ruocco (a1) and V. Fotopoulos (a3)...


Drought represents one of the major constraints on agricultural productivity and food security and in future is destined to spread widely as a consequence of climate change. Research efforts are focused on developing strategies to make crops more resilient and to mitigate the effects of stress on crop production. In this context, the use of root-associated microbial communities and chemical priming strategies able to improve plant tolerance to abiotic stresses, including drought, have attracted increasing attention in recent years. The current review offers an overview of recent research aimed at verifying the role of arbuscular mycorrhizal fungi and chemical agents to improve plant tolerance to drought and to highlight the mechanisms involved in this improvement. Attention will be devoted mainly to current knowledge on the mechanisms involved in water transport.

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Author for correspondence: R. Balestrini, E-mail:


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Abbaspour, H, Saeidi-Sar, S, Afshari, H and Abdel-Wahhab, MA (2012) Tolerance of mycorrhiza infected pistachio (Pistacia vera L.) seedling to drought stress under glasshouse conditions. Journal of Plant Physiology 169, 704709.
Antoniou, C, Chatzimichail, G, Kashfi, K and Fotopoulos, V (2014) P77: exploring the potential of NOSH-aspirin as a plant priming agent against abiotic stress factors. Nitric Oxide 39(suppl.), S39.
Antoniou, C, Savvides, A, Christou, A and Fotopoulos, V (2016) Unravelling chemical priming machinery in plants: the role of reactive oxygen–nitrogen–sulfur species in abiotic stress tolerance enhancement. Current Opinion in Plant Biology 33, 101107.
Antoniou, C, Chatzimichail, G, Xenofontos, R, Pavlou, G, Panagiotou, E, Christou, A and Fotopoulos, V (2017) Melatonin systemically ameliorates drought stress-induced damage in Medicago sativa plants by modulating nitro-oxidative homeostasis and proline metabolism. Journal of Pineal Research 62, e12401.
Aroca, R, Porcel, R and Ruiz-Lozano, JM (2007) How does arbuscular mycorrhizal symbiosis regulate root hydraulic properties and plasma membrane aquaporins in Phaseolus vulgaris under drought, cold or salinity stresses? New Phytologist 173, 808816.
Aroca, R, Bago, A, Sutka, M, Paz, JA, Cano, C, Amodeo, G and Ruiz-Lozano, JM (2009) Expression analysis of the first arbuscular mycorrhizal fungi aquaporin described reveals concerted gene expression between salt-stressed and nonstressed mycelium. Molecular Plant-Microbe Interactions 22, 11691178.
Aroca, R, Porcel, R and Ruiz-Lozano, JM (2011) Plant drought tolerance enhancement by arbuscular mycorrhizal symbiosis. In Fulton, SM (ed.). Mycorrhizal Fungi: Soil, Agriculture and Environmental Implications, New York: Nova Science Publishers, Inc, pp. 229240.
Aroca, R, Ruiz-Lozano, JM, Zamarreño, AM, Paz, JA, Garcia-Mina, JM, Pozo, MJ and Lopez-Raez, JA (2013) Arbuscular mycorrhizal symbiosis influences strigolactone production under salinity and alleviates salt stress in lettuce plants. Journal of Plant Physiology 170, 4755.
Augé, RM (2001) Water relations, drought and vesicular-arbuscular mycorrhizal symbiosis. Mycorrhiza 11, 342.
Augé, RM (2004) Arbuscular mycorrhizae and soil/plant water relations. Canadian Journal of Soil Science 84, 373381.
Augé, RM, Toler, HD and Saxton, AM (2015) Arbuscular mycorrhizal symbiosis alters stomatal conductance of host plants more under drought than under amply watered conditions: a meta-analysis. Mycorrhiza 25, 1324.
Balestrini, R, Chitarra, W, Fotopoulos, V and Ruocco, M (2017) Potential role of beneficial soil microorganisms in plant tolerance to abiotic stress. In Lukac, M, Gamboni, M and Grenni, P (eds). Soil Biological Communities and Ecosystem Resilience. Sustainability in Plant and Crop Protection Series. Cham, Switzerland: Springer International Publishing AG, pp. 191207.
Balmer, A, Pastor, V, Gamir, J, Flors, V and Mauch-Mani, B (2015) The ‘prime-ome’: towards a holistic approach to priming. Trends in Plant Science 20, 443452.
Bárzana, G, Aroca, R, Paz, JA, Chaumont, F, Martinez-Ballesta, MC, Carvajal, M and Ruiz-Lozano, JM (2012) Arbuscular mycorrhizal symbiosis increases relative apoplastic water flow in roots of the host plant under both well-watered and drought stress conditions. Annals of Botany 109, 10091017.
Bárzana, G, Aroca, R, Bienert, P, Chaumont, F and Ruiz-Lozano, JM (2014) New insights into the regulation of aquaporins by the arbuscular mycorrhizal symbiosis in maize plants under drought stress and possible implications for plant performance. Molecular Plant-Microbe Interactions 27, 349363.
Bárzana, G, Aroca, R and Ruiz-Lozano, JM (2015) Localized and non-localized effects of arbuscular mycorrhizal symbiosis on accumulation of osmolytes and aquaporins and on antioxidant systems in maize plants subjected to total or partial root drying. Plant, Cell & Environment 38, 16131627.
Berruti, A, Lumini, E, Balestrini, R and Bianciotto, V (2015) Arbuscular mycorrhizal fungi as natural biofertilizers: let's benefit from past successes. Frontiers in Microbiology 6, 1559. doi: 10.3389/fmicb.2015.01559.
Boyer, JS, Byrne, P, Cassman, KG, Cooper, M, Delmer, D, Greene, T, Gruis, F, Habben, J, Hausmann, N, Kenny, N, Lafitte, R, Paszkiewicz, S, Porter, D, Schlegel, A, Schussler, J, Setterh, T, Shanahan, J, Sharp, RE, Vyn, TJ, Warner, D and Gaffney, J (2013) The U.S. Drought of 2012 in perspective: a call to action. Global Food Security 2, 139143.
Bucher, M, Hause, B, Krajinski, F and Küster, H (2014) Through the doors of perception to function in arbuscular mycorrhizal symbioses. New Phytologist 204, 833840.
Calvo-Polanco, M, Sánchez-Castro, I, Cantos, M, García, JL, Azcón, R, Ruiz-Lozano, JM, Beuzón, CR and Aroca, R (2016) Effects of different arbuscular mycorrhizal fungal backgrounds and soils on olive plants growth and water relation properties under well-watered and drought conditions. Plant, Cell & Environment 39, 24982514.
Casenave, EC and Toselli, ME (2007) Hydropriming as a pre-treatment for cotton germination under thermal and water stress conditions. Seed Science and Technology 35, 8898.
Cattivelli, L, Rizza, F, Badeck, FW, Mazzucotelli, E, Mastrangelo, AM, Francia, E, Marè, C, Tondelli, A and Stanca, AM (2008) Drought tolerance improvement in crop plants: an integrated view from breeding to genomics. Field Crops Research 105, 114.
Chatzidaki, E and Ventura, F (2010) Adaptation to climate change and mitigation strategies in cultivated and natural environments. A review. Italian Journal of Agrometeorology 3, 2142.
Chen, J, Wu, FH, Wang, WH, Zheng, CJ, Lin, GH, Dong, XJ, He, JX, Pei, ZM and Zheng, HL (2011) Hydrogen sulphide enhances photosynthesis through promoting chloroplast biogenesis, photosynthetic enzyme expression, and thiol redox modification in spinacia oleracea seedlings. Journal of Experimental Botany 62, 44814493.
Chen, J, Shang, Y-T, Wang, W-H, Chen, X-Y, He, E-M, Zheng, H-L and Shangguan, Z (2016) Hydrogen sulfide-mediated polyamines and sugar changes are involved in hydrogen sulfide-induced drought tolerance in Spinacia oleracea seedlings. Frontiers in Plant Science 7, 1173. doi: 10.3389/fpls.2016.01173.
Chen, K, Fessehaie, A and Arora, R (2012) Dehydrin metabolism is altered during seed osmopriming and subsequent germination under chilling and desiccation in Spinacia oleracea L. cv. Bloomsdale: possible role in stress tolerance. Plant Science 183, 2736.
Chen, K, Fessehaie, A and Arora, R (2013) Aquaporin expression during seed osmopriming and post-priming germination in spinach. Biologia Plantarum 57, 193198.
Chitarra, W, Pagliarani, C, Maserti, B, Lumini, E, Siciliano, I, Cascone, P, Schubert, A, Gambino, G, Balestrini, R and Guerrieri, E (2016) Insights on the impact of arbuscular mycorrhizal symbiosis on tomato tolerance to water stress. Plant Physiology 171, 10091023.
Cho, SM, Kang, BR, Han, SH, Anderson, AJ, Park, JY, Lee, YH, Cho, BH, Yang, KY, Ryu, CM and Kim, YC (2008) 2R,3R-butanediol, a bacterial volatile produced by Pseudomonas chlororaphis o6, is involved in induction of systemic tolerance to drought in Arabidopsis thaliana. Molecular Plant-Microbe Interactions 21, 10671075.
Christou, A, Manganaris, G, Papadopoulos, I and Fotopoulos, V (2013) Hydrogen sulfide induces systemic tolerance to salinity and non-ionic osmotic stress in strawberry plants through modification of reactive species biosynthesis and transcriptional regulation of multiple defence pathways. Journal of Experimental Botany 64, 19531966.
Christou, A, Manganaris, G and Fotopoulos, V (2014) Systemic mitigation of salt stress by hydrogen peroxide and sodium nitroprusside in strawberry plants via transcriptional regulation of enzymatic and non-enzymatic antioxidants. Environmental and Experimental Botany 107, 4654.
Daryanto, S, Wang, L and Jacinthe, PA (2017) Global synthesis of drought effects on cereal, legume, tuber and root crops production: a review. Agricultural Water Management 179, 1833.
Da Silva, EC, Nogueira, RJMC, Da Silva, MA and de Albuquerque, M (2011) Drought stress and plant nutrition. In Anjum, NA and Lopez-Lauri, F (eds). Plant Nutrition and Abiotic Stress Tolerance III. Plant Stress 5 (Special Issue 1). Ikenobe, Japan: Global Science Books, pp. 3241.
Doubková, P, Vlasáková, E and Sudová, R (2013) Arbuscular mycorrhizal symbiosis alleviates drought stress imposed on Knautia arvensis plants in serpentine soil. Plant and Soil 370, 149161.
Dubey, RS and Pessarakli, M (2001) Physiological mechanisms of nitrogen absorption and assimilation in plants under stressful conditions. In Pessarakli, M (ed.). Handbook of Plant and Crop Physiology, 2nd edn., Revised and Expanded. New York: Marcel Dekker, Inc, pp. 637655.
El-Mesbahi, MN, Azcón, R, Ruiz-Lozano, JM and Aroca, R (2012) Plant potassium content modifies the effects of arbuscular mycorrhizal symbiosis on root hydraulic properties in maize plants. Mycorrhiza 22, 555564.
Eulenstein, F, Tauschke, M, Behrendt, A, Monk, J, Schindler, U, Lana, MA and Monk, S (2017) The application of mycorrhizal fungi and organic fertilisers in horticultural potting soils to improve water use efficiency of crops. Horticulturae 3, 8. doi: 10.3390/horticulturae3010008.
Fan, QJ and Liu, JH (2012) Nitric oxide is involved in dehydration/drought tolerance in Poncirus trifoliata seedlings through regulation of antioxidant systems and stomatal response. Plant Cell Reports 31, 145154.
Farooq, M, Hussain, M, Wahid, A and Siddique, KHM (2012) Drought stress in plants: an overview. In Aroca, R (ed.). Plant Responses to Drought Stress: From Morphological to Molecular Features. Belin, Germany: Springer-Verlag, pp. 133.
Filippou, P, Antoniou, C, Obata, T, Harokopos, E, Van Der Kelen, K, Kanetis, L, Aidinis, V, Van Breusegem, F, Fernie, AR and Fotopoulos, V (2016) Kresoxim-methyl primes Medicago truncatula plants against abiotic stress factors via altered reactive oxygen and nitrogen species signalling leading to downstream transcriptional and metabolic readjustment. Journal of Experimental Botany 67, 12591274.
Fotopoulos, V, Antoniou, C, Filippou, P, Mylona, P, Fasoula, D, Ioannides, I and Polidoros, A (2014) Application of sodium nitroprusside results in distinct antioxidant gene expression patterns in leaves of mature and senescing Medicago truncatula plants. Protoplasma 251, 973978.
García-Mata, C and Lamattina, L (2001) Nitric oxide induces stomatal closure and enhances the adaptive plant responses against drought stress. Plant Physiology 126, 11961204.
Gilbert, ME and Medina, V (2016) Drought adaptation mechanisms should guide experimental design. Trends in Plant Science 21, 639647.
Gill, SS and Tuteja, N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry 48, 909930.
Giovannetti, M, Balestrini, R, Volpe, V, Guether, M, Straub, D, Costa, A, Ludewig, U and Bonfante, P (2012) Two putative-aquaporin genes are differentially expressed during arbuscular mycorrhizal symbiosis in Lotus japonicus. BMC Plant Biology 12, 186.
Hancock, JT and Whiteman, M (2016) Alone NO longer: interactions of nitric oxide with reactive oxygen species and hydrogen sulfide. Advances in Botanical Research 77, 114.
Hazzoumi, Z, Moustakime, Y, Elharchli, E and Amrani Joutei, K (2015) Effect of arbuscular mycorrhizal fungi (AMF) and water stress on growth, phenolic compounds, glandular hairs, and yield of essential oil in basil (Ocimum gratissimum L.). Chemical and Biological Technologies in Agriculture 2, 10.
He, F, Zhang, H and Tang, M (2016) Aquaporin gene expression and physiological responses of robinia pseudoacacia L. to the mycorrhizal fungus rhizophagus irregularis and drought stress. Mycorrhiza 26, 311323.
He, F, Sheng, M and Tang, M (2017) Effects of rhizophagus irregularis on photosynthesis and antioxidative enzymatic system in Robinia pseudoacacia L. Under drought stress. Frontiers in Plant Science 8, 183. doi: 10.3389/fpls.2017.00183.
Hu, H and Xiong, L (2014) Genetic engineering and breeding of drought-resistant crops. Annual Review of Plant Biology 65, 715741.
Huang, Y-M, Zou, Y-N and Wu, Q-S (2017) Alleviation of drought stress by mycorrhizas is related to increased root H2O2 efflux in trifoliate orange. Scientific Reports 7, Article number: 42335. doi: 10.1038/srep42335.
Ishibashi, Y, Yamaguchi, H, Yuasa, T, Iwaya-Inoue, M, Arima, S and Zheng, SH (2011) Hydrogen peroxide spraying alleviates drought stress in soybean plants. Journal of Plant Physiology 168, 15621567.
Islam, MM, Hoque, MA, Okuma, E, Banu, MN, Shimoishi, Y, Nakamura, Y and Murata, Y (2009) Exogenous proline and glycinebetaine increase antioxidant enzyme activities and confer tolerance to cadmium stress in cultured tobacco cells. Journal of Plant Physiology 166, 15871597.
Kashfi, K and Fotopoulos, V (2015) Patent: Method of Priming Plants Against Abiotic Stress Factors and Promoting Growth, WO2015123273 A1. Research Foundation of the City University of New York, Cyprus University of Technology. Geneva, Switzerland: World Intellectual Property Organization.
Khalvati, MA, Hu, Y, Mozafar, A and Schmidhalter, U (2005) Quantification of water uptake by arbuscular mycorrhizal hyphae and its significance for leaf growth, water relations, and gas exchange of barley subjected to drought stress. Plant Biology 7, 706712.
Khattab, HI, Emam, MA, Emam, MM, Helal, NM and Mohamed, MR (2014) Effect of selenium and silicon on transcription factors NAC5 and DREB2A involved in drought-responsive gene expression in rice. Biologia Plantarum 58, 265273.
Lai, D, Mao, Y, Zhou, H, Li, F, Wu, M, Zhang, J, He, Z, Cui, W and Xie, Y (2014) Endogenous hydrogen sulfide enhances salt tolerance by coupling the reestablishment of redox homeostasis and preventing salt-induced K + loss in seedlings of Medicago sativa. Plant Science 225, 117129.
Lenoir, I, Fontaine, J and Sahraoui, ALH (2016) Arbuscular mycorrhizal fungal responses to abiotic stresses: a review. Phytochemistry 123, 415.
Li, T, Hu, YJ, Hao, ZP, Li, H, Wang, YS and Chen, BD (2013a) First cloning and characterization of two functional aquaporin genes from an arbuscular mycorrhizal fungus glomus intraradices. New Phytologist 197, 617630.
Li, T, Hu, YJ, Hao, ZP, Li, H and Chen, BD (2013b) Aquaporin genes GintAQPF1 and GintAQPF2 from glomus intraradices contribute to plant drought tolerance. Plant Signal & Behavior 8, e24030. doi: 10.4161/psb.24030.
Li, T, Hu, Y, Du, X, Tang, H, Shen, C and Wu, J (2014) Salicylic acid alleviates the adverse effects of salt stress in torreya grandis cv. Merrillii seedlings by activating photosynthesis and enhancing antioxidant systems. PLoS ONE 9, e109492. doi: 10.1371/journal.pone.0109492.
Li, T, Sun, Y, Ruan, Y, Xu, L, Hu, Y, Hao, Z, Zhang, X, Li, H, Wang, Y, Yang, L and Chen, B (2016) Potential role of D-myo-inositol-3-phosphate synthase and 14-3-3 genes in the crosstalk between Zea mays and Rhizophagus intraradices under drought stress. Mycorrhiza 26, 879893.
Li, T, Zhang, X and Chen, B (2017) Crosstalk between Arbuscular Mycorrhizal Fungi and Host Plants under Drought Stress. Atlas of Science online resource. Available at (Accessed 24 January 2017).
Li, Z, Jing, W, Peng, Y, Zhang, XQ, Ma, X, Huang, LK and Yan, YH (2015) Spermine alleviates drought stress in white clover with different resistance by influencing carbohydrate metabolism and dehydrins synthesis. PLoS ONE 10, e0120708.
Liu, T, Li, Z, Hui, C, Tang, M and Zhang, H (2016) Effect of rhizophagus irregularis on osmotic adjustment, antioxidation and aquaporin PIP genes expression of Populus × canadensis ‘Neva’ under drought stress. Acta Physiologiae Plantarum 38, 191.
López-Ráez, JA (2016) How drought and salinity affect arbuscular mycorrhizal symbiosis and strigolactone biosynthesis? Planta 243, 13751385.
Marulanda, A, Azcón, R and Ruiz-Lozano, JM (2003) Contribution of six arbuscular mycorrhizal fungal isolates to water uptake by Lactuca sativa plants under drought stress. Physiologia Plantarum 119, 526533.
Maurel, C, Boursiac, Y, Luu, DT, Santoni, V, Shahzad, Z and Verdoucq, L (2015) Aquaporins in plants. Physiology Review 95, 13211358.
McAdam, SAM, Brodribb, TJ and Ross, JJ (2016) Shoot-derived abscisic acid promotes root growth. Plant, Cell and Environment 39, 652659.
Merewitz, E (2016) Chemical priming-induced drought stress tolerance in plants. In Hossain, MA, Wani, SH, Bhattacharjee, S, Burritt, DJ and Tran, LSP (eds). Drought Stress Tolerance in Plants, vol. 1. Cham, Switzerland: Springer International Publishing, pp. 77103.
Mo, Y, Wang, Y, Yang, R, Zheng, J, Liu, C, Li, H, Ma, J, Zhang, Y, Wei, C and Zhang, X (2016) Regulation of plant growth, photosynthesis, antioxidation and osmosis by an arbuscular mycorrhizal fungus in watermelon seedlings under well-watered and drought conditions. Frontiers in Plant Science 7, 644. doi: 10.3389/fpls.2016.00644.
Molassiotis, A and Fotopoulos, V (2011) Oxidative and nitrosative signaling in plants: two branches in the same tree? Plant Signaling & Behavior 6, 210214.
Müller, DB, Vogel, C, Bai, Y and Vorholt, JA (2016) The plant microbiota: systems-level insights and perspectives. Annual Review of Genetics 50, 211234.
Nakashima, K and Yamaguchi-Shinozaki, K (2013) ABA signaling in stress-response and seed development. Plant Cell Reports 32, 959970.
Nakashima, K, Yamaguchi-Shinozaki, K and Shinozaki, K (2014) The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat. Frontiers in Plant Science 5, 170. doi: 10.3389/fpls.2014.00170.
Osakabe, Y, Osakabe, K, Shinozaki, K and Tran, LSP (2014) Response of plants to water stress. Frontiers in Plant Science 5, Article 86. doi: 10.3389/fpls.2014.00086.
Pandey, V, Ansari, MW, Tula, S, Sahoo, RK, Bains, G, Kumar, J, Tuteja, N and Shukla, A (2016) Ocimum sanctum leaf extract induces drought stress tolerance in rice. Plant Signaling & Behavior 11, e1150400. doi: 10.1080/15592324.2016.1150400.
Paparella, S, Araújo, SS, Rossi, G, Wijayasinghe, M, Carbonera, D and Balestrazzi, A (2015) Seed priming: state of the art and new perspectives. Plant Cell Reports 34, 12811293.
Pedranzani, H, Rodríguez-Rivera, M, Gutiérrez, M, Porcel, R, Hause, B and Ruiz-Lozano, JM (2016) Arbucular mycorrhizal symbiosis regulates physiology and performance of Digitaria eriantha plants subjected to abiotic stresses by modulating antioxidant and jasmonate levels. Mycorrhiza 26, 141152.
Perez, IB and Brown, PJ (2014) The role of ROS signaling in cross-tolerance: from model to crop. Frontiers in Plant Science 5, Article number 754. doi: 10.3389/fpls.2014.00754.
Porcel, R, Aroca, R, Azcón, R and Ruiz-Lozano, JM (2006) PIP aquaporin gene expression in arbuscular mycorrhizal glycine max and lactuca sativa plants in relation to drought stress tolerance. Plant Molecular Biology 60, 389404.
Porcel, R, Aroca, R and Ruíz-Lozano, JM (2012) Salinity stress alleviation using arbuscular mycorrhizal fungi. A review. Agronomy for Sustainable Development 32, 181200.
Rapparini, F and Peñuelas, J (2014) Mycorrhizal fungi to alleviate drought stress on plant growth. In Miransari, M (ed.) Use of Microbes for the Alleviation of Soil Stresses, vol. 1. New York: Springer, pp. 2142.
Reuscher, S, Akiyama, M, Mori, C, Aoki, K, Shibata, D and Shiratake, K (2013) Genome-wide identification and expression analysis of aquaporins in tomato. PLoS ONE 8, e79052. doi: 10.1371/journal.pone.0079052.
Rolli, E, Marasco, R, Vigani, G, Ettoumi, B, Mapelli, F, Deangelis, ML, Gandolfi, C, Casati, E, Previtali, F, Gerbino, R, Pierotti Cei, F, Borin, S, Sorlini, C, Zocchi, G and Daffonchio, D (2015) Improved plant resistance to drought is promoted by the root-associated microbiome as a water stress-dependent trait. Environmental Microbiology 17, 316331.
Ruiz-Lozano, JM (2003) Arbuscular mycorrhizal symbiosis and alleviation of osmotic stress. New perspectives for molecular studies. Mycorrhiza 13, 309317.
Ruiz-Lozano, JM and Aroca, R (2017) Plant aquaporins and mycorrhizae: their regulation and involvement in plant physiology and performance. In Chaumont, F and Tyerman, SD (eds). Plant Aquaporins: From Transport to Signaling. Cham, Switzerland: Springer International Publishing, pp. 333353.
Ruiz-Lozano, JM and Azcón, R (1995) Hyphal contribution to water uptake in mycorrhizal plants as affected by the fungal species and water status. Physiologia Plantarum 95, 472478.
Ruiz-Lozano, JM, Gómez, M and Azcón, R (1995) Influence of different Glomus species on the time-course of physiological plant-responses of lettuce to progressive drought stress periods. Plant Science 110, 3744.
Ruiz-Lozano, JM, Porcel, R and Aroca, R (2006) Does the enhanced tolerance of arbuscular mycorrhizal plants to water deficit involve modulation of drought-induced plant genes? New Phytologist 171, 693698.
Ruiz-Lozano, JM, Alguacil, MM, Bárzana, G, Vernieri, P and Aroca, R (2009) Exogenous ABA accentuates the differences in root hydraulic properties between mycorrhizal and non mycorrhizal maize plants through regulation of PIP aquaporins. Plant Molecular Biology, 70, 565579.
Ruiz-Lozano, JM, Aroca, R, Zamarreño, AM, Molina, S, Andreo-Jiménez, B, Porcel, R, García-Mina, JM, Ruyter-Spira, C and López-Ráez, JA (2016) Arbuscular mycorrhizal symbiosis induces strigolactone biosynthesis under drought and improves drought tolerance in lettuce and tomato. Plant, Cell and Environment 39, 441452.
Ruth, B, Khalvati, M and Schmidhalter, U (2011) Quantification of mycorrhizal water uptake via high-resolution on-line water content sensors. Plant and Soil 342, 459468.
Sánchez-Romera, B, Ruiz-Lozano, JM, Zamarreño, ÁM, García-Mina, JM and Aroca, R (2016) Arbuscular mycorrhizal symbiosis and methyl jasmonate avoid the inhibition of root hydraulic conductivity caused by drought. Mycorrhiza 26, 111122.
Savvides, A, Ali, S, Tester, M and Fotopoulos, V (2016) Chemical priming of plants against multiple abiotic stresses: mission possible? Trends in Plant Science 21, 329340.
Schmidt, JE and Gaudin, ACM (2017) Toward an integrated root ideotype for irrigated systems. Trends in Plant Science 22, 433443.
Shakirova, F, Allagulova, C, Maslennikova, D, Fedorova, K, Yuldashev, R, Lubyanova, A, Bezrukova, M and Avalbaev, A (2016) Involvement of dehydrins in 24-epibrassinolide-induced protection of wheat plants against drought stress. Plant Physiology and Biochemistry 108, 539548.
Sheffield, J, Wood, EF and Roderick, ML (2012) Little change in global drought over the past 60 years. Nature 491, 435438.
Shi, H, Jiang, C, Ye, T, Tan, D-X, Reiter, RJ, Zhang, H, Liu, R and Chan, Z (2015) Comparative physiological, metabolomic, and transcriptomic analyses reveal mechanisms of improved abiotic stress resistance in bermudagrass [Cynodon dactylon (L) Pers.] by exogenous melatonin. Journal of Experimental Botany 66, 681694.
Shi, Y, Zhang, Y, Han, W, Feng, R, Hu, Y, Guo, J and Gong, H (2016) Silicon enhances water stress tolerance by improving root hydraulic conductance in Solanum lycopersicum L. Frontiers in Plant Science 7, 196. doi: 10.3389/fpls.2016.00196.
Tanou, G, Fotopoulos, V and Molassiotis, A (2012 a) Priming against environmental challenges and proteomics in plants: update and agricultural perspectives. Frontiers in Plant Science 3, 216. doi: 10.3389/fpls.2012.00216.
Tanou, G, Filippou, P, Belghazi, M, Job, D, Diamantidis, G, Fotopoulos, V and Molassiotis, A (2012 b) Oxidative and nitrosative-based signaling and associated post-translational modifications orchestrate the acclimation of citrus plants to salinity stress. Plant Journal 72, 585599.
Tanou, G, Ziogas, V, Belghazi, M, Christou, A, Filippou, P, Job, D, Fotopoulos, V and Molassiotis, Α (2014) Polyamines reprogram oxidative and nitrosative status and the proteome of citrus plants exposed to salinity stress. Plant, Cell and Environment 37, 864885.
Tombesi, S, Nardini, A, Frioni, T, Soccolini, M, Zadra, C, Farinelli, D, Poni, S and Palliotti, A (2015) Stomatal closure is induced by hydraulic signals and maintained by ABA in drought-stressed grapevine. Scientific Reports 5, 12449. doi: 10.1038/srep12449.
Uehlein, N, Fileschi, K, Eckert, M, Bienert, G, Bertl, A and Kaldenhoff, R (2007) Arbuscular mycorrhizal symbiosis and plant aquaporin expression. Phytochemistry 68, 122129.
Vannier, N, Mony, C, Bittebière, AK and Vandenkoornhuyse, P (2015) Epigenetic mechanisms and microbiota as a toolbox for plant phenotypic adjustment to environment. Frontiers in Plant Science 6, 1159. doi: 10.3389/fpls.2015.01159.
Vishwakarma, K, Upadhyay, N, Kumar, N, Yadav, G, Singh, J, Mishra, RK, Kumar, V, Verma, R, Upadhyay, RG, Pandey, M and Sharma, S (2017) Abscisic acid signaling and abiotic stress tolerance in plants: a review on current knowledge and future prospects. Frontiers in Plant Science 8, 161. doi: 10.3389/fpls.2017.00161.
Wang, W, Vinocur, B and Altman, A (2003) Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance. Planta 218, 114.
Wei, W, Li, QT, Chu, YN, Reiter, RJ, Yu, XM, Zhu, DH, Zhang, WK, Ma, B, Lin, Q, Zhang, JS and Chen, SY (2015) Melatonin enhances plant growth and abiotic stress tolerance in soybean plants. Journal of Experimental Botany 66, 695707.
Wojtyla, L, Lechowska, K, Kubala, S and Garnczarska, M (2016) Molecular processes induced in primed seeds increasing the potential to stabilize crop yields under drought conditions. Journal of Plant Physiology 203, 116126.
Wu, H-H, Zou, Y-N, Rahman, MM, Ni, Q-D and Wu, Q-S (2017) Mycorrhizas alter sucrose and proline metabolism in trifoliate orange exposed to drought stress. Scientific Reports 7, Article number: 42389. doi: 10.1038/srep42389.
Wu, Q-S, Srivastava, AK and Zou, Y-N (2013) AMF-induced tolerance to drought stress in citrus: a review. Scientia Horticulture 164, 7787.
Yamaguchi-Shinozaki, Y and Shinozaki, K (2006) Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. Annual Review of Plant Biology 57, 781803.
Zhou, Q, Ravnskov, S, Jiang, D and Wollenweber, B (2015) Changes in carbon and nitrogen allocation, growth and grain yield induced by arbuscular mycorrhizal fungi in wheat (Triticum aestivum L.) subjected to a period of water deficit. Plant Growth Regulation 75, 751760.
Ziogas, V, Tanou, G, Belghazi, M, Filippou, P, Fotopoulos, V, Grigorios, D and Molassiotis, A (2015) Roles of sodium hydrosulfide and sodium nitroprusside as priming molecules during drought acclimation in citrus plants. Plant Molecular Biology 89, 433450.
Zou, Y-N, Wang, P, Liu, C-Y, Ni, Q-D, Zhang, D-J and Wu, Q-S (2017) Mycorrhizal trifoliate orange has greater root adaptation of morphology and phytohormones in response to drought stress. Scientific Reports 7, Article number: 41134. doi: 10.1038/srep41134.


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Improvement of plant performance under water deficit with the employment of biological and chemical priming agents

  • R. Balestrini (a1), W. Chitarra (a1) (a2), C. Antoniou (a3), M. Ruocco (a1) and V. Fotopoulos (a3)...


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