Drought stress responses in maize are diminished by Piriformospora indica

References

• Fang Y, Xiong L. General mechanisms of drought response and their application in drought resistance improvement in plants. Cell Mol Life Sci: CMLS. 2015;72:673–89. doi:10.1007/s00018-014-1767-0.
   PubMed Web of Science ®Google Scholar
• Lopes MS, Araus JL, van Heerden PD, Foyer CH. Enhancing drought tolerance in C(4) crops. J Exp Bot. 2011;62:3135–53. doi:10.1093/jxb/err105.
   PubMed Web of Science ®Google Scholar
• Sahay NS, Varma A. Piriformospora indica: a new biological hardening tool for micropropagated plants. FEMS Microbiol Lett. 1999;181:297–302 doi:10.1111/j.1574-6968.1999.tb08858.x.
   PubMed Web of Science ®Google Scholar
• Lou B, Sun C, Cai D. Piriformaspora indica with multiple functions and its application prospects. Acta Phytophylacica Sinica. 2007;34:653–6
   Google Scholar
• Nautiyal C, Chauhan P, DasGupta S, Seem K, Varma A, Staddon W. Tripartite interactions among Paenibacillus lentimorbus NRRL B-30488, Piriformospora indica DSM 11827, and Cicer arietinum L. J Microbiol Biotech. 2010;26:1393–99. doi:10.1007/s11274-010-0312-z.
   Google Scholar
• Anith KN, Faseela KM, Archana PA, Prathapan KD. Compatibility of Piriformospora indica and Trichoderma harzianum as dual inoculants in black pepper (Piper nigrum L.). Symbiosis. 2011;55:11–7. doi:10.1007/s13199-011-0143-1.
   Web of Science ®Google Scholar
• Yadav V, Kumar M, Deep DK, Kumar H, Sharma R, Tripathi T, Tuteja N, Saxena AK, Johri AK. A phosphate transporter from the root endophytic fungus Piriformospora indica plays a role in phosphate transport to the host plant. J Biol Chem. 2010;285:26532–44. doi:10.1074/jbc.M110.111021.
   PubMed Web of Science ®Google Scholar
• Baltruschat H, Fodor J, Harrach BD, Niemczyk E, Barna B, Gullner G, Janeczko A, Kogel KH, Schafer P, Schwarczinger I, Zuccaro A, Skoczowski A. Salt tolerance of barley induced by the root endophyte Piriformospora indica is associated with a strong increase in antioxidants. The New Phytologist. 2008;180:501–10. doi:10.1111/j.1469-8137.2008.02583.x.
   PubMed Web of Science ®Google Scholar
• Waller F, Achatz B, Baltruschat H, Fodor J, Becker K, Fischer M, Heier T, Huckelhoven R, Neumann C, von Wettstein D, Franken P, Kogel KH. The endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield. Proc Natl Acad Sci USA. 2005;102:13386–91. doi:10.1073/pnas.0504423102.
   PubMed Web of Science ®Google Scholar
• Waller F, Achatz B, Baltruschat H, Fodor J, Becker K, Fischer M, Heier T, Huckelhoven R, Neumann C, von Wettstein D, Franken P, Kogel KH. The endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield. Proc Natl Acad Sci USA. 2005;102:13386–91. doi:10.1073/pnas.0504423102.
   PubMed Web of Science ®Google Scholar
• Sun C, Johnson J M, Cai D, Sherameti I, Oelmüller R, Lou B. Piriformospora indica confers drought tolerance in Chinese cabbage leaves by stimulating antioxidant enzymes, the expression of drought-related genes and the plastid-localized CAS protein. Plant Physiol. 2010;167:1009–17. doi:10.1016/j.jplph.2010.02.013.
   Google Scholar
• Jogawat A, Saha S, Bakshi M, Dayaman V, Kumar M, Dua M, Varma A, Oelmüller R, Tuteja N, Johri AK. Piriformospora indica rescues growth diminution of rice seedlings during high salt stress. Plant Signal Behav. 2013;8(10):e2689. doi:10.4161/psb.26891.
   PubMedGoogle Scholar
• Fathi A, Tari D B. Effect of drought stress and its mechanism in plants. Int J Life Sci. 2016;10(1):1. doi:10.3126/ijls.v10i1.14509.
   Google Scholar
• Bartels D, Sunkar R. Drought and salt tolerance in plants. Crit Rev Plant Sci. 2005;24:23–58 doi:10.1080/07352680590910410.
   Web of Science ®Google Scholar
• Valliyodan B, Nguyen HAT. Understanding regulatory networks and engineering for enhanced drought tolerance in plants. Curr Opin Plant Biol. 2006;9:189–95. doi:10.1016/j.pbi.2006.01.019.
   PubMed Web of Science ®Google Scholar
• Krasensky J, Jonak C. Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks. J Exp Bot. 2012;63:1593–608. doi:10.1093/jxb/err460.
   PubMed Web of Science ®Google Scholar
• Shinozaki K, Yamaguchi-Shinozaki K. Gene networks involved in drought stress response and tolerance. J Exp Bot. 2007;58:221–7. doi:10.1093/jxb/erl164.
   PubMed Web of Science ®Google Scholar
• Tuteja N, Sopory SK. Chemical signaling under abiotic stress environment in plants. Plant Signal Behav. 2008;3:525–36 doi:10.4161/psb.3.8.6186.
   PubMedGoogle Scholar
• Wolters H, Jurgens G. Survival of the flexible: hormonal growth control and adaptation in plant development. Nat Rev Genet. 2009;10:305–17. doi:10.1038/nrg2558.
   PubMed Web of Science ®Google Scholar
• Yamaguchi-Shinozaki K, Shinozaki K. Organization of cis-acting regulatory elements in osmotic- and cold-stress-responsive promoters. Trends Plant Sci. 2005;10:88–94. doi:10.1016/j.tplants.2004.12.012.
   PubMed Web of Science ®Google Scholar
• de Ollas C, Hernando B, Arbona V, Gomez-Cadenas A. Jasmonic acid transient accumulation is needed for abscisic acid increase in citrus roots under drought stress conditions. Physiol Plantarum. 2013;147:296–306. doi:10.1111/j.1399-3054.2012.01659.x.
   PubMed Web of Science ®Google Scholar
• Liu F, Xing S, Ma H, Du Z, Ma B, Cytokinin-producing, plant growth-promoting rhizobacteria that confer resistance to drought stress in Platycladus orientalis container seedlings. Appl Microbiol Biotech. 2013;97:9155–64. doi:10.1007/s00253-013-5193-2.
   PubMed Web of Science ®Google Scholar
• Farooq M, Hussain M, Wahid A, Siddique KHM. Drought stress in plants: an overview. In: Aroca R (ed) Plant responses to drought stress. Springer Berlin Heidelberg, 2012; pp 1–33. doi:10.1007/978-3-642-32653-0_1
   Google Scholar
• Shi H, Chen L, Ye T, Liu X, Ding K, Chan Z. Modulation of auxin content in Arabidopsis confers improved drought stress resistance. Plant Physiol and Biochem: PPB / Societe Francaise de Physiologie Vegetale 2014;82:209–17. doi:10.1016/j.plaphy.2014.06.008 doi:10.1016/j.plaphy.2014.06.008.
   PubMed Web of Science ®Google Scholar
• Tamiru M, Undan JR, Takagi H, Abe A, Yoshida K, Undan JQ, Natsume S, Uemura A, Saitoh H, Matsumura H, Urasaki N, Yokota T, Terauchi R. A cytochrome P450, OsDSS1, is involved in growth and drought stress responses in rice (Oryza sativa L.). Plant Mol Biol. 2015;88:85–99. doi:10.1007/s11103-015-0310-5.
   PubMed Web of Science ®Google Scholar
• Sherameti I, Tripathi S, Varma A, Oelmuller R. The root-colonizing endophyte Pirifomospora indica confers drought tolerance in Arabidopsis by stimulating the expression of drought stress-related genes in leaves. Mol Plant-Microbe Interact: MPMI. 2008a;21:799–807. doi:10.1094/MPMI-21-6-0799.
   PubMed Web of Science ®Google Scholar
• Xu L, Wang A, Wang J, et al. Piriformospora indica confers drought tolerance on Zea mays L.through enhancement of antioxidant activity and expression of drought-related genes. Crop J. 2017;5:251–58. doi:10.1016/j.cj.2016.10.002.
   Google Scholar
• Zheng J, Zhao J, Tao Y, Wang J, Liu Y, Fu J, Jin Y, Gao P, Zhang J, Bai Y, Wang G. Isolation and analysis of water stress induced genes in maize seedlings by subtractive PCR and cDNA macroarray. Plant Mol Biol. 2004;55:807–23. doi:10.1007/s11103-005-1969-9.
   PubMed Web of Science ®Google Scholar
• Tiwari SB, Wang XJ, Hagen G, Guilfoyle TJ. AUX/IAA proteins are active repressors, and their stability and activity are modulated by auxin. Plant Cell. 2001;13:2809–22. doi:10.1105/tpc.13.12.2809.
   PubMed Web of Science ®Google Scholar
• Boudsocq M, Barbier-Brygoo H, Lauriere C. Identification of nine sucrose nonfermenting 1-related protein kinases 2 activated by hyperosmotic and saline stresses in Arabidopsis thaliana. J Biol Chem. 2004;279:41758–66. doi:10.1074/jbc.M405259200 doi:10.1074/jbc.M405259200.
   PubMed Web of Science ®Google Scholar
• Breviario D, Gianì S, Morello L. Multiple tubulins: evolutionary aspects and biological implications. Plant Journal. 2013;75:202–18. doi:10.1111/tpj.12243.
   PubMed Web of Science ®Google Scholar
• Komis G, Luptovčiak I, Doskočilová A, Šamaj J. Biotechnological aspects of cytoskeletal regulation in plants. Biotech Advances. 2015;33:1043–1062. doi:10.1016/j.biotechadv.2015.03.008.
   Web of Science ®Google Scholar
• Ganguly A, Dixit R. Mechanisms for regulation of plant kinesins. Curr Opin Plant Biol. 2013;16:704–9. doi:10.1016/j.pbi.2013.09.003.
   PubMed Web of Science ®Google Scholar
• Nick P. Microtubules, signalling and abiotic stress. Plant J. 2013;75:309–23. doi:10.1111/tpj.12102.
   PubMed Web of Science ®Google Scholar
• Wallace JG, Zhang X, Beyene Y, Semagn K, Olsen M, Prasanna BM, Buckler ES. Genome-wide association for plant height and flowering time across 15 tropical maize populations under managed drought stress and well-watered conditions in Sub-Saharan Africa. Crop Sci. 2016;56:1–14. doi:10.2135/cropsci2015.10.0632.
   Web of Science ®Google Scholar
• Chan KX, Wirtz M, Phua SY, Estavillo GM, Pogson BJ. Balancing metabolites in drought: the sulfur assimilation conundrum. Trends Plant Sci. 2013;18:18–29. doi:10.1016/j.tplants.2012.07.005.
   PubMed Web of Science ®Google Scholar
• Pinheiro C, Chaves MM. Photosynthesis and drought: can we make metabolic connections from available data? J Exp Bot. 2011;62 (3):869–82. doi:10.1093/jxb/erq340.
   PubMed Web of Science ®Google Scholar
• Sadok W, Naudin P, Boussuge B, Muller B, Welcker C, Tardieu F. Leaf growth rate per unit thermal time follows QTL-dependent daily patterns in hundreds of maize lines under naturally fluctuating conditions. Plant Cell Environ. 2007;30:135–46. doi:10.1111/j.1365-3040.2006.01611.x.
   PubMed Web of Science ®Google Scholar
• Tardieu F, Reymond M, Hamard P, Granier C, Muller B. Spatial distributions of expansion rate, cell division rate and cell size in maize leaves: a synthesis of the effects of soil water status, evaporative demand and temperature. J Exp Bot. 2000;51:1505–14. doi:10.1093/jexbot/51.350.1505.
   PubMed Web of Science ®Google Scholar
• Hummel I, Pantin F, Sulpice R, Piques M, Rolland G, Dauzat M, Christophe A, Pervent M, Bouteille M, Stitt M, Gibon Y, Muller B. 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 Physiol. 2010;154:357–72. doi:10.1104/pp.110.157008.
   PubMed Web of Science ®Google Scholar
• McDowell NG. Mechanisms linking drought, hydraulics, carbon metabolism, and vegetation mortality. Plant Physiol. 2011;155:1051–59. doi:10.1104/pp.110.170704.
   PubMed Web of Science ®Google Scholar
• Ernst L, Goodger JQ, Alvarez S, Marsh EL, Berla B, Lockhart E, Jung J, Li P, Bohnert HJ, Schachtman DP. Sulphate as a xylem-borne chemical signal precedes the expression of ABA biosynthetic genes in maize roots. J Exp Bot. 2010;61:3395–405. doi:10.1093/jxb/erq160.
   PubMed Web of Science ®Google Scholar
• Garber AJ, Karl IE, Kipnis DM. Alanine and glutamine synthesis and release from skeletal muscle. II. The precursor role of amino acids in alanine and glutamine synthesis. J Biol Chem. 1976;251:836–43
   PubMed Web of Science ®Google Scholar
• Hasanuzzaman M, Nahar K, Anee TI, Fujita M. Glutathione in plants: biosynthesis and physiological role in environmental stress tolerance. Physiol Mol Biol Plants. 2017:23;249. doi:10.1007/s12298-017-0422-2.
   PubMed Web of Science ®Google Scholar
• Foyer CH, Noctor G. Ascorbate and glutathione: the heart of the redox hub. Plant Physiology. 2011, 155:2–18. doi:10.1104/pp.110.167569.
   PubMed Web of Science ®Google Scholar
• Shearer HL, Cheng YT, Wang L, Liu J, Boyle P, Despres C, Zhang Y, Li X, Fobert PR. Arabidopsis clade I TGA transcription factors regulate plant defenses in an NPR1-independent fashion. Mol Plant-Microbe Interact MPMI. 2012;25:1459–68. doi:10.1094/MPMI-09-11-0256.
   PubMed Web of Science ®Google Scholar
• Ohri P, Bhardwaj R, Bali S, Kaur R, Jasrotia S, Khajuria A, Parihar RD. The common molecular players in plant hormone crosstalk and signaling. Curr Protein Pept Sci. 2015;16:369–88. doi:10.2174/1389203716666150330141922.
   PubMed Web of Science ®Google Scholar
• Rai M, Acharya D, Singh A, Varma A. Positive growth responses of the medicinal plants Spilanthes calva and Withania somnifera to inoculation by Piriformospora indica in a field trial. Mycorrhiza. 2001;11:123–8. doi:10.1007/s005720100115.
   PubMed Web of Science ®Google Scholar
• Kumar M, Yadav V, Tuteja N, Johri AK. Antioxidant enzyme activities in maize plants colonized with Piriformospora indica. Microbiology. 2009;155:780–90. doi:10.1099/mic.0.019869-0.
   PubMed Web of Science ®Google Scholar
• Du Z, Zhou X, Ling Y, Zhang Z, Su Z. agriGO: a GO analysis toolkit for the agricultural community. Nucleic Acids Res. 2010;38:W64–70. doi:10.1093/nar/gkq310.
   PubMed Web of Science ®Google Scholar