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RESEARCH ARTICLE

Differential performance of two forage species, Medicago truncatula and Sulla carnosa, under water-deficit stress and recovery

Aida Rouached A B , Inès Slama A C , Walid Zorrig A , Asma Jdey A , Caroline Cukier B , Mokded Rabhi A , Ons Talbi A , Anis Mohamed Limami B and Chedly Abdelly A
+ Author Affiliations
- Author Affiliations

A Laboratoire des Plantes Extrêmophiles, BP 901, Centre de Biotechnologie de Borj Cédria, Hammam-Lif 2050, Tunisia.

B University of Angers, UMR 1345 Research Institute of Horticulture and Seeds (INRA, Agrocampus-Ouest, University of Angers), SFR 4207 Quasav, 2 Bd Lavoisier, 49045 Angers Cedex, France.

C Corresponding author. Email: slama_ines@hotmail.fr

Crop and Pasture Science 64(3) 254-264 https://doi.org/10.1071/CP13049
Submitted: 6 February 2013  Accepted: 4 June 2013   Published: 30 July 2013

Abstract

The response patterns during water deficit stress and subsequent recovery of two forage species, Medicago truncatula and Sulla carnosa, were studied. After germination and pre-treatment, seedlings were individually cultivated for two months under two irrigation modes: 100% and 33% of field capacity. Measured parameters were plant growth, water relations, leaf osmotic potential, lipid peroxidation, and leaf inorganic (Na+ and K+) and organic (proline and soluble sugars) solute contents, as well as delta-1-pyrroline-5-carboxylate synthase (P5CS) and proline dehydrogenase (PDH) activities. Our results showed that under control conditions, and in contrast to roots, no significant differences were observed in shoot biomass production between the two species. However, when subjected to water-deficit stress, M. truncatula appeared to be more tolerant than S. carnosa (reduction by 50 and 70%, respectively). In the two studied species, water-deficit stress led to an increase in root/shoot ratio and leaf proline and soluble sugar contents, and a decrease in leaf osmotic potential. Enzymatic assay revealed that in the two species, P5CS activity was stimulated whereas that of PDH was inhibited under stress conditions. Despite greater accumulation of proline, sugar, and potassium in leaves of S. carnosa, M. truncatula was more tolerant to water deficit. This was essentially due to its capacity to control tissue hydration and water-use efficiency, in addition to its greater ability to protect membrane integrity. Following stress relief, M. truncatula and S. carnosa showed partial re-establishment of growth capacity.

Additional keywords: legume species, osmolytes, rehydration, tolerance, water relations.


References

Anjum SA, Xie X, Wang L, Saleem MF, Man C, Lei W (2011a) Morphological, physiological and biochemical responses of plants to drought stress. African Journal of Agricultural Research 9, 2026–2032.

Anjum SA, Wang LC, Farooq M, Khan I, Xue LL (2011b) Methyl jasmonate-induced alteration in lipid peroxidation, antioxidative defense system and yield in soybean under drought. Journal of Agronomy & Crop Science 197, 296–301.
Methyl jasmonate-induced alteration in lipid peroxidation, antioxidative defense system and yield in soybean under drought.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhtFCrurfL&md5=2cfc01a25f2979cf7372af4470c3ce94CAS |

Ashraf M (2009) Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotechnology Advances 27, 84–93.
Biotechnological approach of improving plant salt tolerance using antioxidants as markers.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhsV2nsrvP&md5=ba43ccc38bacd5b534e951145ff90a20CAS | 18950697PubMed |

Azcon-Bieto J (1983) Inhibition of photosynthesis by carbohydrates in wheat leaves. Plant Physiology 73, 681–686.
Inhibition of photosynthesis by carbohydrates in wheat leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2cXitVKntg%3D%3D&md5=f8ac5f4eca3d160dc096a766e99c4c87CAS | 16663282PubMed |

Bahrani MJ, Bahrami H, Haghighi AAK (2010) Effect of water stress on ten forage grasses native or introduced to Iran. Grassland Science 56, 1–5.
Effect of water stress on ten forage grasses native or introduced to Iran.Crossref | GoogleScholarGoogle Scholar |

Ben Amor N, Jimenez A, Megdiche W, Lundqvist M, Sevilla F, Abdelly C (2006) Response of antioxidant systems to NaCl stress in the halophyte Cakile maritima. Physiologia Plantarum 126, 446–457.
Response of antioxidant systems to NaCl stress in the halophyte Cakile maritima.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XjtVehur8%3D&md5=cac6b3ddb3fbd72ebbd310abf26245d9CAS |

Bouyoucos (1983) Les propriétés physiques du sol dépendent de sa texture et de sa structure. In’les bases de la production végétale’. Tome 1. Collection Sciences et Technique agricoles, pp. 67-87.

Chaves MM (1991) Effect of water deficits on carbon assimilation. Journal of Experimental Botany 42, 1–16.
Effect of water deficits on carbon assimilation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXhtFyntrw%3D&md5=99355be124509b52bd293df75c90bd98CAS |

Chaves MM, Maroco JP, Pareira JS (2003) Understanding plant responses to drought from genes to the whole plant. Functional Plant Biology 30, 239–264.
Understanding plant responses to drought from genes to the whole plant.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXjtVKlt7o%3D&md5=aee0bac31d0589f54dd0c73cc73561f1CAS |

Choi HB, Ohashi H (2003) Generic criteria and an infrageneric system for Hedysarum and related genera (Papilionoidea-Luguminosea). Taxon 52, 567–576.
Generic criteria and an infrageneric system for Hedysarum and related genera (Papilionoidea-Luguminosea).Crossref | GoogleScholarGoogle Scholar |

Cornic G, Fresneau C (2002) Photosynthetic carbon reduction and carbon oxidation cycles are the main electron sinks for photosystem II activity during a mild drought. Annals of Botany 89, 887–894.
Photosynthetic carbon reduction and carbon oxidation cycles are the main electron sinks for photosystem II activity during a mild drought.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlsVeitLY%3D&md5=dbd4b127740828c20a8f6820fca516b5CAS | 12102514PubMed |

Draper HH, Hadley M (1990) Malondialdehyde determination as index of lipid peroxidation. Methods in Enzymology 186, 421–431.
Malondialdehyde determination as index of lipid peroxidation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXksVGhtLo%3D&md5=8c8f949923420939c512e38363b50999CAS | 2233309PubMed |

Erice G, Louahlia S, Irigoyen JJ, Sanchez-Diaz M, Avice JC (2010) Biomass partitioning, morphology and water status of four alfalfa genotypes submitted to progressive drought and subsequent recovery. Journal of Plant Physiology 167, 114–120.
Biomass partitioning, morphology and water status of four alfalfa genotypes submitted to progressive drought and subsequent recovery.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXisFymtrw%3D&md5=93c9b6b38c72a0bb21eb40dff3de6b66CAS | 19744745PubMed |

Gorai M, Hachef A, Neffati M (2010) Differential responses in growth and water relationship of Medicago sativa (L.) cv. Gabès and Astragalus gombiformis (Pom.) under water-limited conditions. Emirates Journal of Food and Agriculture 22, 1–12.

Hamilton EW, Heckathorn SA (2001) Mitochondrial adaptation to NaCl. complex I is protected by antioxidant and small heat shock proteins, whereas complex II is protected by proline and betaine. Plant Physiology 126, 1266–1274.
Mitochondrial adaptation to NaCl. complex I is protected by antioxidant and small heat shock proteins, whereas complex II is protected by proline and betaine.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXlsFemsbk%3D&md5=af51677e352657467976eadff782797aCAS | 11457977PubMed |

Hawkins HJ, Lewis OAM (1993) Effect of NaCI salinity, nitrogen form, calcium and potassium concentration on nitrogen uptake and kinetics in Triticum aestivum L. cv. Gamtoos. New Phytologist 124, 171–177.
Effect of NaCI salinity, nitrogen form, calcium and potassium concentration on nitrogen uptake and kinetics in Triticum aestivum L. cv. Gamtoos.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3sXmsVKjurw%3D&md5=80ed2ecb5ea11b25c4cf7bcca62ce8c2CAS |

Hernández JA, Ferrer MA, Jiménez A, Barcelo AR, Sevilla F (2001) Antioxidant systems and O2 –/H2O2 production in the apoplast of pea leaves, its relation with salt-induced necrotic lesions in minor veins. Plant Physiology 127, 817–831.
Antioxidant systems and O2 /H2O2 production in the apoplast of pea leaves, its relation with salt-induced necrotic lesions in minor veins.Crossref | GoogleScholarGoogle Scholar | 11706165PubMed |

Hessini K, Gandour M, Albouchi A, Soltani A, Koyro HW, Abdelly C (2008) Biomass production, photosynthesis, and leaf water relations of Spartina alterniflora under moderate water stress. Journal of Plant Research 121, 311–318.
Biomass production, photosynthesis, and leaf water relations of Spartina alterniflora under moderate water stress.Crossref | GoogleScholarGoogle Scholar | 18389173PubMed |

Hester MW, Mendelsohn IA, Mckee KL (2001) Species and population variation to salinity stress in Panicum hemitomon, Spartina patens, and Spartina alterniflora: morphological and physiological constraints. Environmental and Experimental Botany 46, 277–297.

Hewitt EJ (1966) Sand and water culture methods used in the study of plant nutrition. Commonwealth Bureau of Horticulture, Technical Communication 22, 431–446.

Jones MM, Osmond CB, Turner NC (1980) Accumulation of solutes in leaves of sorghum and sunflower in reponse to water deficits. Australian Journal of Plant Physiology 7, 193–205.
Accumulation of solutes in leaves of sorghum and sunflower in reponse to water deficits.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXktVCisLs%3D&md5=b27a5133ea89a62d9453533ac3f9ebdeCAS |

Kameli A, Lösel DM (1995) Contribution of carbohydrates and other solutes to osmotic adjustment in wheat leaves under water stress. Journal of Plant Physiology 145, 363–366.
Contribution of carbohydrates and other solutes to osmotic adjustment in wheat leaves under water stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXjs1ars7g%3D&md5=aac14c1d79c2a8dc1a0b7ba65be0330cCAS |

Koch KE (1996) Carbohydrate modulated gene expression in plants. Annual Review of Plant Physiology and Plant Molecular Biology 47, 509–540.
Carbohydrate modulated gene expression in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XjtlWgtrY%3D&md5=dac6e9166dfdd1adb8cba6b8761eb0c1CAS | 15012299PubMed |

Kumar UD, Saraswathy R, Das VSR (1984) Differential performance of Cleome gynandra L. (C4) and C. speciosa L. (C3) under water stress and recovery. Environmental and Experimental Botany 24, 305–310.
Differential performance of Cleome gynandra L. (C4) and C. speciosa L. (C3) under water stress and recovery.Crossref | GoogleScholarGoogle Scholar |

Loreto F, Centritto M, Chartzoulakis K (2003) Photosynthetic limitations in olive cultivars with different sensitivity to salt stress. Plant Cell and Environment 26, 595–604.

Martínez-Ballesta MC, Martínez V, Carvajal M (2004) Osmotic adjustment, water relations and gaz exchange in pepper plants grown under NaCl or KCl. Environmental and Experimental Botany 52, 161–174.
Osmotic adjustment, water relations and gaz exchange in pepper plants grown under NaCl or KCl.Crossref | GoogleScholarGoogle Scholar |

McCann S, Huang B (2008) Drought responses of Kentucky bluegrass and creeping bentgrass as affected by abscisic acid and trinexapac-ethyl. Journal of the American Society for Horticultural Science 133, 20–26.

Morgan JM (1984) Osmoregulation and water stress in higher plants. Annual Review of Plant Physiology 35, 299–319.
Osmoregulation and water stress in higher plants.Crossref | GoogleScholarGoogle Scholar |

Noreen Z, Ashraf M, Akram NA (2010) Salt-induced regulation of some key antioxidant enzymes and physio-biochemical phenomena in five diverse cultivars of turnip (Brassica rapa L.). Journal of Agronomy & Crop Science 196, 273–285.

Pei F, Li X, Liu X, Lao C (2013) Assessing the impacts of droughts on net primary productivity in China. Journal of Environmental Management 114, 362–371.
Assessing the impacts of droughts on net primary productivity in China.Crossref | GoogleScholarGoogle Scholar | 23164540PubMed |

Planchet E, Rannou O, Ricoult C, Mercey SB, Grondard AM, Limami AM (2011) Nitrogen metabolism responses to water deficit act through both abscisic acid (ABA)-dependent and independent pathways in M. truncatula during post-germination. Journal of Experimental Botany 62, 605–615.
Nitrogen metabolism responses to water deficit act through both abscisic acid (ABA)-dependent and independent pathways in M. truncatula during post-germination.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsFyrsbzN&md5=525e57cd94203da886ae0719a8b444cfCAS | 20943826PubMed |

Rathinasabapathi B (2000) Metabolic engineering for stress tolerance, installing osmoprotectant synthesis pathways. Annals of Botany 86, 709–716.
Metabolic engineering for stress tolerance, installing osmoprotectant synthesis pathways.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXmsFKmu70%3D&md5=cfba4573828a73f632669cc20dc65cf7CAS |

Roberts SK (1998) Regulation of K+ channels in maize roots by water stress and abscisic acid. Plant Physiology 116, 145–153.
Regulation of K+ channels in maize roots by water stress and abscisic acid.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXkslCrtQ%3D%3D&md5=be89bbe1c6cec7915e05691550dd3394CAS |

Ruiz JM, Sánchez E, Garcia PC, Lόpez-Lefebre LR, Rivero RM, Romero L (2002) Proline metabolism and NAD kinase activity in green bean plants subjected to cold-shock. Phytochemistry 59, 473–478.
Proline metabolism and NAD kinase activity in green bean plants subjected to cold-shock.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XhtlCqs7w%3D&md5=692f070fa883b5dc24ad44701bdf1a1eCAS | 11853741PubMed |

Schonfeld MA, Johnson RC, Carver BF, Mornhinweg DW (1988) Water relations in winter wheat as drought resistance indicator. Crop Science 28, 526–531.

Slama I, Messedi D, Ghnaya T, Savouré A, Abdelly C (2006) Effects of water-deficit on growth and proline metabolism in Sesuvium portulacastrum. Environmental and Experimental Botany 56, 231–238.
Effects of water-deficit on growth and proline metabolism in Sesuvium portulacastrum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XktVyisLo%3D&md5=99b2f95ab56dfcfca9b94766ee2b2022CAS |

Slama I, Ghnaya T, Messedi D, Hessini K, Labidi N, Savouré A, Abdelly C (2007) Effect of sodium chloride on the response of the halophyte species Sesuvium portulacastrum grown in mannitol-induced water stress. Journal of Plant Research 120, 291–299.
Effect of sodium chloride on the response of the halophyte species Sesuvium portulacastrum grown in mannitol-induced water stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXivVSht7w%3D&md5=203b60497b7d2fbf7dae6d14685ac32cCAS | 17219010PubMed |

Slama I, Tayachi S, Jdey A, Rouached A, Abdelly C (2011) Differential response to water deficit stress in alfalfa (Medicago sativa) cultivars, Growth, water relations, osmolyte accumulation and lipid peroxidation. African Journal of Biotechnology 72, 16 250–16 259.

Song S, Chen Y, Zhao M, Zhang WH (2012) A novel M. truncatula HD-Zip gene, MtHB2, is involved in abiotic stress responses. Environmental and Experimental Botany 80, 1–9.
A novel M. truncatula HD-Zip gene, MtHB2, is involved in abiotic stress responses.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XksFalsbc%3D&md5=5265b3b3c5a6104890a42449ee6f0f8aCAS |

Sperdouli I, Moustakas M (2012) Interaction of proline, sugars, and anthocyanins during photosynthetic acclimation of Arabidopsis thaliana to drought stress. Journal of Plant Physiology 169, 577–585.
Interaction of proline, sugars, and anthocyanins during photosynthetic acclimation of Arabidopsis thaliana to drought stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhvVGntrY%3D&md5=8cd10af0a9fc0ade144d94b2ea72873fCAS | 22305050PubMed |

Steudle E, Peterson CA (1998) How does water get through roots. Journal of Experimental Botany 49, 775–788.

Trifi-Farah N, Marrakchi M (2002) Intra- and interspecific genetic variability in Hedysarum revealed by rDNAeRFLP markers. Journal of Genetics & Breeding 56, 1–9.

Trifi-Farah N, Baatout H, Boussaid M, Combes D, Figier J, Hannachi-Salhi A, Marrakchi M (2002) Evaluation des ressources génétiques des espèces du genre Hedysarum dans le bassin méditerranéen. Plant Genetic Resources Newsletter 130, 1–6.

Valentovic P, Luxova M, Kolarovic L, Gasparikova O (2006) Effect of osmotic stress on compatible solutes content, membrane stability and water relations in two maize cultivars. Plant, Soil and Environment 52, 186–191.

Vijn I, Smeekens S (1999) Fructan, more than a reserve carbohydrate. Plant Physiology 120, 351–360.
Fructan, more than a reserve carbohydrate.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXktFWrurc%3D&md5=e02c3d6ea4074b5bbc09456dbc3769d0CAS | 10364386PubMed |

Yang F, Miao LF (2010) Adaptive responses to progressive drought stress in two poplar species originating from different altitudes. Silva Fennica 44, 23–37.

Zhang J, Kirkham MB (1996) Antioxidant response to drought in sunflower and sorghum seedlings. New Phytologist 132, 361–373.
Antioxidant response to drought in sunflower and sorghum seedlings.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XislOisbs%3D&md5=f201666f077b6d591b6001b347de9272CAS |