Variations in chemical constituents of the rhizosphere of bread wheat genotypes and their significance for using as markers for heat and drought tolerance

References

• Ahlawat, O. P., T. Chugh, K. Venkatesh, R. Tiwari, P. Sharma, S. Sheoran, R. Singh, H. M. Mamrutha, N. K. Arora, G. Singh, et al. 2021. Response of contrasting bread wheat genotypes for heat and drought stress tolerance for rhizospheric soil properties. Journal of Environmental Biology 42 (5):1298–306. doi:10.22438/jeb/42/5/MRN-1777.
   Web of Science ®Google Scholar
• Akter, N., and M. Rafiqul Islam. 2017. Heat stress effects and management in wheat. A review. Agronomy for Sustainable Development 37 (5):37. doi:10.1007/s13593-017-0443-9.
   Web of Science ®Google Scholar
• Ali, M. M., M. Waleed Shafique, S. Gull, W. Afzal Naveed, T. Javed, A. F. Yousef, and R. P. Mauro. 2021. Alleviation of heat stress in tomato by exogenous application of sulfur. Horticulturae 7 (2):21. doi:10.3390/horticulturae7020021.
   Web of Science ®Google Scholar
• Al-Shwaiman, H. A., M. Shahid, A. M. Elgorban, K. H. M. Siddique, and A. Syed. 2022. Beijerinckia fluminensis BFC-33, a novel multi-stress-tolerant soil bacterium: Deciphering the stress amelioration, phytopathogenic inhibition and growth promotion in Triticum aestivum (L.). Chemosphere 295:133843. doi:10.1016/j.chemosphere.2022.133843.
   PubMed Web of Science ®Google Scholar
• Bais, H. P., T. L. Weir, L. G. Perry, S. Gilroy, and J. M. Vivanco. 2006. The role of root exudates in rhizosphere interactions with plants and other organisms. Annual Review of Plant Biology 57:233–66. doi:10.1146/annurev.arplant.57.032905.105159.
   PubMed Web of Science ®Google Scholar
• Bechtaoui, N., M. K. Rabiu, A. Raklami, K. Oufdou, M. Hafidi, and M. Jemo. 2021. Phosphate-dependent regulation of growth and stresses management in plants. Frontiers in Plant Science 12:679916. doi:10.3389/fpls.2021.679916.
   PubMed Web of Science ®Google Scholar
• Bhargava, G. P. 2003. Training manual for undertaking studies on genesis of sodic/alkali soils. Division of Soil and Crop Management, ICAR-CSSRI, Karnal, India.
   Google Scholar
• Bhat, B. A., L. Tariq, S. Nissar, S. T. Islam, S. U. Islam, Z. Mangral, N. Ilyas, R. Z. Sayyed, G. Muthusamy, W. Kim, et al. 2022. The role of plant-associated rhizobacteria in plant growth, bio-control and abiotic stress management. Journal of Applied Microbiology 133 (5):2717–41. doi:10.1111/jam.15796.
   PubMed Web of Science ®Google Scholar
• Brasil, E. C., V. M. C. Alves, I. E. Marriel, G. V. E. Pitta, and J. G. de Carvalho. 2011. Rhizosphere properties of maize genotypes with contrasting phosphorus efficiency. Revista Brasileira de Ciência Do Solo 35 (1):171–81. doi:10.1590/S0100-06832011000100016.
   Web of Science ®Google Scholar
• Carvalhais, L. C., P. G. Dennis, D. Fedoseyenko, M. R. Hajirezaei, R. Borriss, and N. von Wiren. 2011. Root exudation of sugars, amino acids, and organic acids by maize as affected by nitrogen, phosphorus, K, and iron deficiency. Journal of Plant Nutrition and Soil Science 174 (1):3–11. doi:10.1002/jpln.201000085.
   Google Scholar
• Gee, G. W., and J. W. Bauder. 1986. Particle-size analysis. In Methods of soil analysis, Part 1, Physical and mineralogical methods. edA. Klute, Agronomy monograph no. 9, 2nd ed., 383–411. Madison, WI: American Society of Agronomy/Soil Science Society of America.
   Google Scholar
• Gransee, A., and H. Führs. 2013. Magnesium mobility in soils as a challenge for soil and plant analysis, magnesium fertilization and root uptake under adverse growth conditions. Plant and Soil 368 (1-2):5–21. doi:10.1007/s11104-012-1567-y.
   Web of Science ®Google Scholar
• Gupta, A., C. Singh, V. Kumar, V. Kumar, R. Chatrath, and G. P. Singh. 2018b. An inventory of registered wheat and barley genetic stocks in India. Karnal, India: ICAR-Indian Institute of Wheat & Barley Research.
   Google Scholar
• Gupta, A., C. Singh, V. Kumar, B. S. Tyagi, V. Tiwari, R. Chatrath, and G. P. Singh. 2018a. Wheat varieties notified in India since 1965. Karnal, India: ICAR-Indian Institute of Wheat and Barley Research.
   Google Scholar
• Hao, W. Y., L. X. Ren, W. Ran, and Q. R. Shen. 2010. Allelopathic effects of root exudates from watermelon and rice plants on Fusarium oxysporum f. sp. niveum. Plant and Soil 336 (1-2):485–97. doi:10.1007/s11104-010-0505-0.
   Web of Science ®Google Scholar
• Hassan, S., and U. Mathesius. 2012. The role of flavonoids in root–rhizosphere signaling: Opportunities and challenges for improving plant–microbe interactions. Journal of Experimental Botany 63 (9):3429–44. doi:10.1093/jxb/err430.
   PubMed Web of Science ®Google Scholar
• Henry, A., W. Doucette, J. Norton, and B. Bugbee. 2007. Changes in crested wheatgrass root exudation caused by flood, drought, and nutrient stress. Journal of Environmental Quality 36 (3):904–12. doi:10.1016/j.rhisph.2017.04.012.
   PubMed Web of Science ®Google Scholar
• Hummel, I., F. Pantin, R. Sulpice, M. Piques, G. Rolland, M. Dauzat, A. Christophe, M. Pervent, M. Bouteillé, M. Stitt, et al. 2010. Arabidopsis plants acclimate to water deficit at low cost through changes of carbon usage: An integrated perspective using growth, metabolite, enzyme, and gene expression analysis. Plant Physiology 154 (1):357–72. doi:10.1104/pp.110.157008.
   PubMed Web of Science ®Google Scholar
• Jackson, M. L. 1973. Soil chemical analysis. New Delhi: Prentice Hall of India Pvt. Ltd.
   Google Scholar
• Jones, D. L., C. Nguyen, and R. D. Finlay. 2009. Carbon flow in the rhizosphere: Carbon trading at the soil-root interface. Plant and Soil 321 (1-2):5–33. doi:10.1007/s11104-009-9925-0.
   Web of Science ®Google Scholar
• Kaushal, M., and S. P. Wani. 2016. Plant growth-promoting rhizobacteria: Drought stress alleviators to ameliorate crop production in dry lands. Annals of Microbiology 66 (1):35–42. doi:10.1007/s13213-015-1112-3.
   Web of Science ®Google Scholar
• Kawasaki, A., S. Donn, P. R. Ryan, U. Mathesius, R. Devilla, A. Jones, and M. Watt. 2016. Microbiome and exudates of the root and rhizosphere of Brachypodium distachyon, a model for wheat. PloS One 11 (10):e0164533. doi:10.1371/journal.pone.0164533.
   PubMed Web of Science ®Google Scholar
• Khalil, U., S. Ali, M. Rizwan, K. U. Rahman, S. T. Ata-Ul-Karim, U. Najeeb, M. N. Ahmad, M. Adrees, M. S. Sarwar, and S. M. Hussain. 2018. Role of mineral nutrients in plant growth under extreme temperatures. In Plant nutrients and abiotic stress tolerance, ed. M. Hasanuzzaman, M. Fujita, H. Oku, K. Nahar, and B. Hawrylak-Nowak, 499–524. Singapore: Springer, Nature, Pte Ltd.
   Google Scholar
• Khan, A., and A. V. Singh. 2021. Multifarious effect of ACC deaminase and EPS producing Pseudomonas sp. and Serratia marcescens to augment drought stress tolerance and nutrient status of wheat. World Journal of Microbiology & Biotechnology 37 (12):198. doi:10.1007/s11274-021-03166-4.
   PubMed Web of Science ®Google Scholar
• Kuo, S. 1996. Phosphorus. In Methods of soil analysis, ed. D. L. Sparks, A. L. Page, P. A. Helmke, R. H. Loeppert, P. N. Soltanpour, M. A. Tabatabai, C. T. Johnston, and M. E. Sumner, Part 3-Chemical methods, 869–919. Madison, WI: American Society of Agronomy/Soil Science Society of America.
   Google Scholar
• Lindsay, W. L., and W. A. Norvell. 1978. Development of DTPA soil test for zinc, iron, manganese and copper. Soil Science Society of America Journal 42 (3):421–8. doi:10.2136/sssaj1978.03615995004200030009x.
   Web of Science ®Google Scholar
• Ling, N., Q. W. Huang, S. W. Guo, and Q. R. Shen. 2011. Paenibacillus polymyxa SQR-21 systemically affects root exudates of watermelon to decrease the conidial germination of Fusarium oxysporum f sp. niveum. Plant and Soil 341 (1-2):485–93. doi:10.1007/s11104-010-0660-3.
   Web of Science ®Google Scholar
• Liu, H., M. Y. Khan, L. C. Carvalhais, M. Delgado-Baquerizo, L. Yan, M. Crawford, P. G. Dennis, B. Singh, and P. M. Schenk. 2019. Soil amendments with ethylene precursor alleviate negative impacts of salinity on soil microbial properties and productivity. Scientific Reports 9 (1):6892. doi:10.1038/s41598-019-43305-4.
   PubMedGoogle Scholar
• Mendoza-Mendoza, A., R. Zaid, R. Lawry, R. Hermosa, E. Monte, B. A. Horwitz, and P. K. Mukherjee. 2018. Molecular dialogues between Trichoderma and roots: Role of the fungal secretome. Fungal Biology Reviews 32 (2):62–85. doi:10.1016/j.fbr.2017.12.001.
   Web of Science ®Google Scholar
• Nadeem, S. M., Z. A. Zahir, M. Naveed, M. Arshad, and M. Shahid. 2014. Rhizobacteria containing ACC-deaminase confer salt tolerance in maize grown on salt-affected fields. Canadian Journal of Microbiology 60 (2):89–96.
   Google Scholar
• Ndour, P. M. S., T. Heulin, W. Achouak, L. Laplaze, and L. Cournac. 2020. The rhizosheath: From desert plants adaptation to crop breeding. Plant and Soil 456 (1-2):1–13. doi:10.1007/s11104-020-04700-3.
   Web of Science ®Google Scholar
• Nelson, D. W., and L. E. Sommers. 1996. Total carbon, organic carbon, and organic matter. In Methods of soil analysis, ed. D. L. Sparks, A. L. Page, P. A. Helmke, R. H. Loeppert, P. N. Soltanpour, M. A. Tabatabai, C. T. Johnston, and M. E. Sumner, Part 3-Chemical methods, 961–1010. Madison, WI: American Society of Agronomy/Soil Science Society of America.
   Google Scholar
• Panchal, P., A. J. Miller, and J. Giri. 2021. Organic acids: Versatile stress-response roles in plants. Journal of Experimental Botany 72 (11):4038–52. doi:10.1093/jxb/erab019.
   PubMed Web of Science ®Google Scholar
• Pandey, P., V. Irulappan, M. V. Bagavathiannan, and M. Senthil-Kumar. 2017. Impact of combined abiotic and biotic stresses on plant growth and avenues for crop improvement by exploiting physio-morphological traits. Frontiers in Plant Science 8:537. doi:10.3389/fpls.2017.00537.
   PubMed Web of Science ®Google Scholar
• Rengel, Z. 2005. Breeding crops for adaptation to environments with low nutrient availability. In Abiotic stresses: Plant resistance through breeding and molecular approaches, ed. M. Ashraf, and P. J. C. Harris, 239–76. New York: The Haworth Press.
   Google Scholar
• Richards, L. A. 1954. Diagnosis and improvement of saline-alkali soils. Agriculture hand book 60. Washington D.C.: USDA.
   Google Scholar
• Sairam, R. K. 1994. Effect of moisture stress on physiological activities of two contrasting wheat genotypes. Indian Journal of Experimental Biology 32:594–7.
   Google Scholar
• Sallam, A., A. M. Alqudah, M. F. A. Dawood, P. S. Baenziger, and A. Börner. 2019. Drought stress tolerance in wheat and barley: Advances in physiology, breeding and genetics research. International Journal of Molecular Sciences 20 (13):3137. doi:10.3390/ijms20133137.
   PubMed Web of Science ®Google Scholar
• Sarkar, J., U. Chakraborty, and B. Chakraborty. 2021. High‐temperature resilience in Bacillus safensis primed wheat plants: A study of dynamic response associated with modulation of antioxidant machinery, differential expression of HSPs and osmolyte biosynthesis. Environmental and Experimental Botany 182:104315. doi:10.1016/j.envexpbot.2020.104315.
   Web of Science ®Google Scholar
• Sarwar, M., M. F. Saleem, N. Ullah, S. Ali, M. Rizwan, M. R. Shahid, M. N. Alyemeni, S. A. Alamri, and P. Ahmad. 2019. Role of mineral nutrition in alleviation of heat stress in cotton plants grown in glasshouse and field conditions. Scientific Reports 9 (1):13022. doi:10.1038/s41598-019-49404-6.
   PubMedGoogle Scholar
• SAS Institute Inc 2012. SAS/STAT® 12.1 User’s guide. Cary, NC: SAS Institute Inc.
   Google Scholar
• Singh, S. K., V. R. Reddy, D. H. Fleisher, and D. J. Timlin. 2018. Phosphorus nutrition affects temperature response of soybean growth and canopy photosynthesis. Frontiers in Plant Science 9:1116. doi:10.3389/fpls.2018.01116.
   PubMed Web of Science ®Google Scholar
• Tariq, A., K. Pan, O. A. Olatunji, C. Graciano, Z. Li, F. Sun, X. Sun, D. Song, W. Chen, A. Zhang, et al. 2017. Phosphorous application improves drought tolerance of Phoebe zhennan. Frontiers in Plant Science 8:1561. doi:10.3389/fpls.2017.01561.
   PubMed Web of Science ®Google Scholar
• Tawaraya, K., R. Horie, A. Saito, T. Shinano, T. Wagatsuma, K. Saito, and A. Oikawa. 2013. Metabolite profiling of shoot extracts, root extracts, and root exudates of rice plant under phosphorus deficiency. Journal of Plant Nutrition 36 (7):1138–59. doi:10.1080/01904167.2013.780613.
   Web of Science ®Google Scholar
• Tawaraya, K., R. Horie, T. Shinano, T. Wagatsuma, K. Saito, and A. Oikawa. 2014. Metabolite profiling of soybean root exudates under phosphorus deficiency. Soil Science and Plant Nutrition 60 (5):679–94. doi:10.1080/00380768.2014.945390.
   Web of Science ®Google Scholar
• Ulrich, D. E. M., S. Sevanto, M. Ryan, M. B. N. Albright, R. B. Johansen, and J. M. Dunbar. 2019. Plant-microbe interactions before drought influence plant physiological responses to subsequent severe drought. Scientific Reports 9 (1):249. doi:10.1038/s41598-018-36971-3.
   PubMedGoogle Scholar
• UN News 2022. World ‘at a crossroads’ as droughts increase nearly a third in a generation. UN News Global perspective Human stories, United Nations. Accessed 7th June 2023 https://news.un.org/en/story/2022/05/1118142.
   Google Scholar
• Vílchez, S., L. Molina, C. Ramos, and J. L. Ramos. 2000. Proline catabolism by Pseudomonas putida: Cloning, characterization, and expression of the put genes in the presence of root exudates. Journal of Bacteriology 182 (1):91–9. doi:10.1128/JB.182.1.91-99.2000.
   PubMed Web of Science ®Google Scholar
• Vishwakarma, K., M. Mishra, S. Jain, J. Singh, N. Upadhyay, R. K. Verma, P. Verma, D. K. Tripathi, V. Kumar, and R. Mishra. 2017a. Exploring the role of plant-microbe interactions in improving soil structure and function through root exudation: A key to sustainable agriculture. In Plant microbe interactions in agro-ecological perspectives, ed. D. P. Singh, H. B. Singh, and R. Prabha, 467–87. Singapore: Springer. doi:10.1007/978-981-10-5813-4_23.
   Google Scholar
• Vishwakarma, K., S. Sharma, V. Kumar, N. Upadhyay, N. Kumar, R. Mishra, G. Yadav, R. K. Verma, and D. K. Tripathi. 2017b. Current scenario of root exudate-mediated plant-microbe interaction and promotion of plant growth. In Probiotics in agroecosystem, ed. V. Kumar, M. Kumar, S. Sharma, and R. Prasad, 349–69. Singapore: Springer. doi:10.1007/978-981-10-4059-7_18.
   Google Scholar
• Vives-Peris, V., C. de Ollas, A. Gómez-Cadenas, and R. M. Pérez-Clemente. 2020. Root exudates: From plant to rhizosphere and beyond. Plant Cell Reports 39 (1):3–17. doi:10.1007/s00299-019-02447-5.
   PubMed Web of Science ®Google Scholar
• Vives-Peris, V., L. Molina, A. Segura, A. Gómez-Cadenas, and R. M. Pérez-Clemente. 2018. Root exudates from citrus plants subjected to abiotic stress conditions have a positive effect on rhizobacteria. Journal of Plant Physiology 228:208–17. doi:10.1016/j.jplph.2018.06.003.
   PubMed Web of Science ®Google Scholar
• Walkley, A., and I. A. Black. 1934. An examination of the Degtjareff method for determining soil organic matter, and a proposed modification of the chromic acid titration method. Soil Science 37 (1):29–38. doi:10.1097/00010694-193401000-00003.
   Google Scholar
• Waraich, E. A., R. Ahmad, A. Halim, and T. Aziz. 2012. Alleviation of temperature stress by nutrient management in crop plants: A review. Journal of Soil Science and Plant Nutrition 12 (2):221–44. doi:10.4067/S0718-95162012000200003.
   Web of Science ®Google Scholar
• Williams, C. H., and A. Steinbergs. 1959. Soil sulphur fractions as chemical indices of available sulphur in some Australian soils. Australian Journal of Agricultural Research 10 (3):340–52. doi:10.1071/AR9590340.
   Google Scholar
• Zhang, F., Z. Zhu, X. Yang, W. Ran, and Q. Shen. 2013. Trichoderma harzianum T-E5 significantly affects cucumber root exudates and fungal community in the cucumber rhizosphere. Applied Soil Ecology 72:41–8. doi:10.1016/j.apsoil.2013.05.016.
   Web of Science ®Google Scholar