Chinese Journal of Applied Ecology ›› 2017, Vol. 28 ›› Issue (9): 3099-3110.doi: 10.13287/j.1001-9332.201709.013
HUANG Hua-gang1, LYU Li-xin2, ZHANG Yan-ming2, JIANG Zhuang2, SHEN Yan1, AN Qian-li2*
Received:
2017-01-04
Online:
2017-09-18
Published:
2017-09-18
Contact:
* E-mail: an@zju.edu.cn
Supported by:
This work was supported by the Bijie Tobacco Company of Guizhou Province (BJYC-201309) and Natural Science Foundation of Zhejiang Province, China (LY14C010002).
HUANG Hua-gang, LYU Li-xin, ZHANG Yan-ming, JIANG Zhuang, SHEN Yan, AN Qian-li. Microbe-assisted drought resistance for tobacco plants: Mechanisms and applications.[J]. Chinese Journal of Applied Ecology, 2017, 28(9): 3099-3110.
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URL: https://www.cjae.net/EN/10.13287/j.1001-9332.201709.013
[1] Hu H, Xiong L. Genetic engineering and breeding of drought-resistant crops. Annual Review of Plant Biology, 2014, 65: 715-741 [2] He J-L (何俊龙), Zhao S-Q (赵世钦), Wang Y-N (王彦楠), et al. Response of endogenous hormones of tobacco to drought stress. Chinese Agricultural Science Bulletin (中国农学通报), 2015, 31(30): 205-209 (in Chinese) [3] Hirayama T, Shinozaki K. Perception and transduction of abscisic acid signals: Keys to the function of the versatile plant hormone ABA. Trends in Plant Sciences, 2007, 12: 343-351 [4] Song L, Huang SC, Wise A, et al. A transcription factor hierarchy defines an environmental stress response network. Science, 2016, 354: 1550 [5] Berendsen RL, Pieterse CM, Bakker PA. The rhizosphere microbiome and plant health. Trends in Plant Science, 2012, 17: 478-486 [6] Willis A, Rodrigues BF, Harris PJC. The ecology of arbuscular mycorrhizal fungi. Critical Reviews in Plant Sciences, 2013, 32: 1-20 [7] Strullu-Derrien C, Strullu DG. Mycorrhization of fossil and living plants. Comptes Rendus Palevol, 2007, 6: 483-494 [8] Augé RM. Water relations, drought and vesicular mycorrhizal fungi symbiosis. Mycorrhiza, 2001, 11: 3-42 [9] Solaiman ZM, Abbott LK, Varma A. Mycorrhizal Fungi: Use in Sustainable Agriculture and Land Restoration. Soil Biology, Volume 41. Berlin: Springer-Verlag, 2014 [10] Zhu Y (祝 英), Xiong J-L (熊俊兰), Lyu G-C (吕广超), et al. Effects of arbuscular mycorrhizal fungi and plant symbiosis on plant water relation and its mechanism. Acta Ecologica Sinica (生态学报), 2015, 35(8): 2419-2427 (in Chinese) [11] Smith SE, Smith FA. Roles of arbuscular mycorrhizas in plant nutrition and growth: New paradigms from cellular to ecosystem scales. Annual Review of Plant Biology, 2011, 62: 227-250 [12] Li T, Hu YJ, Hao ZP, et al. First cloning and characterization of two functional aquaporin genes from an arbuscular mycorrhizal fungus Glomus intraradices. New Phytologist, 2013, 197: 617-630 [13] Sánchez-Romera B, Ruiz-Lozano JM, Zamarreño ÁM, et al. Arbuscular mycorrhizal symbiosis and methyl jasmonate avoid the inhibition of root hydraulic conductivity caused by drought. Mycorrhiza, 2016, 26: 111-122 [14] Bárzana G, Aroca R, Bienert GP, et al. 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, 2014, 27: 349-363 [15] Li A-R (李爱荣), Guan K-Y (管开云). Research history and recent advances in nutrient absorption and transport mechanisms of arbuscular mycorrhizae. Journal of Microbiology (微生物学杂志), 2006, 26(4): 72-76 (in Chinese) [16] Subramanian KS, Santhanakrishnan P, Balasubramanian P. Responses of field grown tomato plants to arbuscular mycorrhizal fungal colonization under varying intensities of drought stress. Scientia Horticulturae, 2006, 107: 245-253 [17] Ruiz-Lozano JM, Collados C, Barea JM, et al. Clonig of cDNAs enconding SODs from lettuce plants which show differential regulation by arbuscular mycorhizal symbiosis and by drought stress. Journal of Experimental Botany, 2001, 52: 2241-2242 [18] Baslam M, Goicoechea N. Water deficit improved the capacity of arbuscular mycorrhizal fungi (AMF) for inducing the accumulation of antioxidant compounds in lettuce leaves. Mycorrhiza, 2012, 22: 347-359 [19] Porcel R, Azcón R, Ruiz-Lozano JM. Evaluation of the role of genes encoding for △1-pyrroline-5-carboxylate synthetase (P5CS) during drought stress in arbuscular mycorrhizal Glycine max and Lactuca sativa plants. Phy-siological & Molecular Plant Pathology, 2004, 65: 211-221 [20] Ábrahám E, RigÓ G, Székely G, et al. Light-dependent induction of proline biosynthesis by abscisic acid and salt stress is inhibited by brassinosteroid inArabidopsis. Plant Molecular Biology, 2003, 51: 363-372 [21] Huang Z (黄 志), Zou Z-R (邹志荣), Huang H-H (黄焕焕), et al. Cloning, analysis and expression of a drought-related gene MeP5CS from melon. Acta Horticulturae Sinica (园艺学报), 2010, 37(8): 1279-1286 (in Chinese) [22] Shaul-Keinan O, Gadkar V, Ginzberg I, et al. Hormone concentrations in tobacco roots change during arbuscular mycorrhizal colonization with Glomus intraradices. New Phytologist, 2002, 154: 501-507 [23] Fester T, Hause B. Drought and symbiosis: Why is abscisic acid necessary for arbuscular mycorrhiza? New Phytologist, 2007, 175: 383-386 [24] Hause B, Mrosk C, Isayenkov S, et al. Jasmonates in arbuscular mycorrhizal interactions. Phytochemistry, 2007, 68: 101-110 [25] LÓpez-Raez JA, Pozo MJ, García-Garrido JM. Strigolactones: A cry for help in the rhizosphere. Botany, 2011, 89: 513-522 [26] Niu Z-Q (牛志强), Liu G-S (刘国顺), Shi T-T (师婷婷), et al. Cloning of NCED3 gene in Nicotiana tabacum and analysis of its drought stress-induced expression. Acta Tabacaria Sinica (中国烟草学报), 2015, 21(3): 100-106 (in Chinese) [27] Thompson AJ, Jackson AC, Parker RA, et al. Abscisic acid biosynthesis in tomato: Regulation of zeaxanthin epoxidase and 9-cis-epoxycarotenoid dioxygenase mRNAs by light/dark cycles, water stress and abscisic acid. Plant Molecular Biology, 2000, 42: 833-845 [28] Aroca R, del Mar Alguacil M, Vernieri P, et al. Plant responses to drought stress and exogenous ABA application are modulated differently by mycorrhization in tomato and an ABA-deficient mutant (Sitiens). Microbial Ecology, 2008, 56: 704-719 [29] Herrera-Medina MJ, Steinkellner S, Vierheilig H, et al. Abscisic acid determines arbuscule development and functionality in the tomato arbuscular mycorrhiza. New Phytologist, 2007, 175: 554-564 [30] Martín-Rodríguez JA, LeÓ n-Morcillo R, Vierheilig H, et al. Ethylene-dependent/ethylene-independent ABA regu-lation of tomato plants colonized by arbuscular mycorrhiza fungi. New Phytologist, 2011, 190: 193-205 [31] Daynes CN, Field DJ, Saleeba JA, et al. Development and stabilisation of soil structure via interactions between organic matter, arbuscular mycorrhizal fungi and plant roots. Soil Biology & Biochemistry, 2013, 57: 683-694 [32] Wang Q (王 茜), Wang Q (王 强), Wang X-J (王晓娟), et al. Research progress on ecological function of arbuscular mycorrhizal network. Chinese Journal of Applied Ecology (应用生态学报), 2015, 26(7): 2192-2202 (in Chinese) [33] Hallet PD, Feeney DS, Bengough AG, et al. Disentangling the impact of AM fungi versus roots on soil structure and water transport. Plant and Soil, 2009, 314: 183-196 [34] Wang J (王 建), Zhou Z-Y (周紫燕), Ling W-T (凌婉婷). Distribution and environmental function of glomalin-related soil protein: A review. Chinese Journal of Applied Ecology (应用生态学报), 2016, 27(2): 634-642 (in Chinese) [35] Toljander JF, Lindahl BD, Paul LR, et al. Influence of arbuscular mycorrhizal mycelial exudates on soil bacterial growth and community structure. FEMS Microbiology Ecology, 2007, 61: 295-304 [36] Augé RM, Toler HD, Moore JL, et al. Comparing contributions of soil versus root colonization to variations in stomatal behavior and soil drying in mycorrhizal Sorghum bicolor and Cucurbita pepo. Journal of Plant Phy-siology, 2007, 164: 1289-1299 [37] Augé RM, Sylvia DM, Park SJ, et al. Partitioning mycorrhizal influence on water relations of Phaseolus vulgaris into soil and plant components. Canadian Journal of Botany, 2004, 82: 503-514 [38] Liu Y-R (刘延荣), Fang Y-C (方宇澄). The selection of effective VAM fungi forming mycorrhizae on tobacco roots. Journal of Shandong Agricultural University (Natural Science)(山东农业大学学报:自然科学版), 1997, 28(3): 269-274 (in Chinese) [39] Zhao F-G (赵方贵), Chen L-P (陈丽平), He X-L (贺学礼). Effects of AM fungi on late growth of tobacco leaf under different phosphate levels. Acta Botanica Boreali-Occidentalia Sinica (西北植物学报), 2004, 24(11): 2122-2125 (in Chinese) [40] Jiang L (江 龙), Huang J-G (黄建国), Yuan L (袁玲). Effects of different arbuscular mycorrhizal fungus on growth, nutrition and physiological activity of tobacco seedlings. Guizhou Agricultural Sciences (贵州农业科学), 2009, 37(12): 53-57 (in Chinese) [41] Wang M-S (王茂胜), Zhang C-H (张长华), Chen X-M (陈晓明), et al. Effect of arbuscular mycorrhiza fungi on drought tolerance of tobacco seedlings. Journal of Mountain Agriculture and Biology (山地农业生物学报), 2012, 31(6): 501-505 (in Chinese) [42] Zhou X (周 霞), Liang Y-J (梁永江), Zhang C-H (张长华), et al. Effects of arbuscular mycorrhizal fungi on growth, nutrition and drought resistance of fluecured tobacco seedlings. Acta Agriculturae Boreali-Sinica (华北农学报), 2012, 27(3): 181-185 (in Chinese) [43] Xie L (谢 莉), Wei Y-W (韦业旺), Cai M (蔡敏), et al. Influences of fungicides on growth and resis-tance of arbuscular mycorrhizal tobacco seedlings. Guang-xi Agricultural Sciences (广西农业科学), 2010, 41(4): 319-322 (in Chinese) [44] Sheng P-P (盛萍萍), Li M (李 敏), Liu R-J (刘润进). Effects of agricultural practices on community structure of arbuscular mycorrhizal fungi in agricultural ecosystem: A review. Chinese Journal of Applied Microbiology (应用生态学报), 2011, 22(6): 1639-1645 (in Chinese) [45] Li J-W (李建伟), Jiang L (江 龙), Yuan L (袁 玲), et al. Influences of arbuscular mycorrhizal fungi on growth and nutrition of tobacco seedlings under different fertilizer levels. Plant Nutrition and Fertilizer Science (植物营养与肥料学报), 2010, 16(5): 1190-1195 (in Chinese) [46] IJdo M, Cranenbrouck S, Declerck S. Methods for large-scale production of AM fungi: Past, present, and future. Mycorrhiza, 2011, 21: 1-16 [47] Wilson D. Endophyte: The evolution of a term, and clarification of its use and definition. Oikos, 1995, 73: 274-276 [48] Xing Y (邢 颖), Zhang X (张 莘), Hao Z-P (郝志鹏), et al. Biodiversity of endophytes in tobacco plants and their potential application: A mini review. Microbiology China (微生物学通报), 2015, 42(2): 411-419 (in Chinese) [49] Weiβ M, Sýkorová Z, Garnica S, et al. Sebacinales everywhere: Previously overlooked ubiquitous fungal endophytes. PLoS One, 2011, 6(2): e16793 [50] Verma S, Varma A, Rexer KH, et al. Piriformospora indica, gen. et sp. nov. a new root-colonizing fungus. Mycologia, 1998, 90: 896-903 [51] Lou B-G (楼兵干), Sun C (孙 超), Cai D-G (蔡大广). Piriformospora indica with multiple functions and its application prospects. Acta Phytophylacia Sinica (植物保护学报), 2007, 34(6): 653-656 (in Chinese) [52] Oelmüller R, Sherameti I, Tripathi S, et al. Piriformospora indica, a cultivable root endophyte with multiple biotechnological applications. Symbiosis, 2009, 49: 1-17 [53] Varma A, Kost G, Oelmüller R. Piriformospora indica: Sebacinales and their biotechnological applications. Soil Biology, Volume 33. Berlin: Springer-Verlag, 2013 [54] Franken P. The plant strengthening root endophyte Piriformospora indica: Potential application and the biology behind. Applied Microbiology and Biotechnology, 2012, 96: 1455-1464 [55] Barazani O, Benderoth M, Groten K, et al. Piriformospora indica and Sebacina vermifera increase growth performance at the expense of herbivore resistance in Nicotiana attenuata. Oecologia, 2005, 146: 234-243 [56] Sherameti I, Shahollari B, Venus Y, et al. The endophytic fungus Piriformospora indica stimulates the expression of nitrate reductase and the starch-degrading enzyme glucan-water dikinase in tobacco and Arabidopsis roots through a homeodomain transcription factor which binds to a conserved motif in their promoters. Journal of Biological Chemistry, 2005, 280: 2641-2647 [57] Sahay N, Varma A. Piriformospora indica, a new biological hardening tool for micropropagated plants. FEMS Microbiology Letters, 1999, 181: 297-302 [58] Ghabooli M, Khatabi B, Ahmadi FS, et al. Proteomics study reveals the molecular mechanisms underlying water stress tolerance induced by Piriformospora indica in barley. Journal of Proteomics, 2013, 94: 289-301 [59] Sun C, Johnson JM, Cai D, et al. 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. Journal of Plant Physiology, 2010, 167: 1009-1017 [60] Hui F-Q (惠非琼), Ma J (马 杰), Liu J (刘 剑), et al. Disease resistance analysis of Nicotiana tabacum induced by Piriformospora indica. Tobacco Science & Technology (烟草科技), 2014 (11): 74-79 (in Chinese) [61] Fakhro A, Andrade-Linares DR, von Bargen S, et al. Impact of Piriformospora indica on tomato growth and on interaction with fungal and viral pathogens. Mycorrhiza, 2010, 20: 191-200 [62] Deshmukh S, Hückelhoven R, Schäfer P, et al. The root endophytic fungus Piriformospora indica requires host cell death for proliferation during mutualistic symbio-sis with barley. Proceedings of the National Academy of Sciences of the United States of America, 2006, 103: 18450-18457 [63] Qiang X, Weiss M, Kogel K, et al. Piriformospora indica: A mutualistic basidiomycete with an exceptionally large plant host range. Molecular Plant Pathology, 2011, 13: 508-518 [64] Jacobs S, Zechmann B, Molitor A, et al. Broad-spectrum suppression of innate immunity is required for colonization of Arabidopsis roots by the fungus Piriformospora indica. Plant Physiology, 2011, 156: 726-740 [65] Schäfer P, Pfiffi S, Voll LM, et al. Phytohormones in plant root-Piriformospora indica mutualism. Plant Signaling & Behavior, 2009, 4: 669-671 [66] Schäfer P, Pfiffi S, Voll LM, et al. Manipulation of plant innate immunity and gibberellin as factor of compatibility in the mutualistic association of barley roots with Piriformospora indica. Plant Journal, 2009, 59: 461-474 [67] Camehl I, Sherameti I, Venus Y, et al. Ethylene signalling and ethylene-targeted transcription factors are required to balance beneficial and nonbeneficial traits in the symbiosis between the endophytic fungus Piriformospora indica and Arabidopsis thaliana. New Phytologist, 2010, 185: 1062-1073 [68] Johnson JM, Alex T, Oelmüller R. Piriformospora indica: The versatile and multifunctional root endophytic fungus for enhanced yield and tolerance to biotic and abiotic stress in crop plants. Journal of Tropical Agriculture, 2014, 52: 103-122 [69] Vadassery J, Ritter C, Venus Y, et al. The role of au-xins and cytokinins in the mutualistic interaction between Arabidopsis and Piriformospora indica. Molecular Plant-Microbe Interactions, 2008, 21: 1371-1383 [70] Malla R, Prasad R, Kumari R, et al. Phosphorus solubilizing symbiotic fungus: Piriformospora indica. Endocytobiosis & Cell Research, 2004, 15: 579-600 [71] Yadav V, Kumar M, Deep DK, et al. A phosphate transporter from a root endophytic fungus Piriformospora indica plays a role in the phosphate transfer to the plants. Journal of Biological Chemistry, 2010, 285: 26532-26544 [72] Kumar M, Yadav V, Kumar H, et al. Piriformospora indica enhances plant growth by transferring phosphate. Plant Signaling & Behavior, 2011, 6: 723-725 [73] Vahabi K, Dorcheh SK, Monajembashi S, et al. Stress promotes Arabidopsis-Piriformospora indica interaction. Plant Signaling & Behavior, 2016, 11: e1136763 [74] Sarma MVRK, Kumar V, Saharan K, et al. Application of inorganic carrier-based formulations of fluorescent pseudomonads and Piriformospora indica on tomato plants and evaluation of their efficacy. Journal of Applied Microbiology, 2011, 111: 456-466 [75] Anith KN, Faseela KM, Archana PA, et al. Compatibi-lity of Piriformospora indica and Trichoderma harzianum as dual inoculants in black pepper (Piper nigrum L.). Symbiosis, 2011, 55: 11-17 [76] Yang J, Kloepper JW, Ryu CM. Rhizosphere bacteria help plants tolerate abiotic stress. Trends in Plant Scien-ce, 2009, 14: 1-4 [77] Vurukonda SSKP, Vardharajula S, Shrivastava M, et al. Enhancement of drought stress tolerance in crops by plant growth promoting rhizobacteria. Microbiological Research, 2015, 184: 13-24 [78] Duca D, Lorv J, Patten CL, et al. Indole-3-acetic acid in plant-microbe interactions. Antonie van Leeuwenhoek, 2014, 106: 85-125 [79] Glick BR, Penrose DM, Li J. A model for the lowering of plant ethylene concentrations by plant growth promoting bacteria. Journal of Theoretical Biology, 1998, 190: 63-68 [80] Correa-Aragunde N, Graziano M, Lamattina L. Nitric oxide plays a central role in determining lateral root development in tomato. Planta, 2004, 218: 900-905 [81] Molina-Favero C, Creus CM, Simontacchi M, et al. Aerobic nitric oxide production by Azospirillum brasilense Sp245 and its influence on root architecture in tomato. Molecular Plant-Microbe Interactions, 2008, 21: 1001-1009 [82] Glick BR, Todorovic B, Czarny J, et al. Promotion of plant growth by bacterial ACC deaminase. Critical Reviews in Plant Sciences, 2007, 26: 227-242 [83] Mayak S, Tirosh T, Glick BR. Plant growth-promoting bacteria that confer resistance to water stress in tomatoes and peppers. Plant Science, 2004, 166: 525-530 [84] Pieterse CMJ, Zamioudis C, Berendsen RL, et al. Induced systemic resistance by beneficial microbes. Annual Review of Phytopathology, 2014, 52: 347-375 [85] Ryu CM, Farag MA, Hu CH, et al. Bacterial volatiles induce systemic resistance in Arabidopsis. Plant Physio-logy, 2004, 134: 1017-1026 [86] Cho SM, Kang BR, Han SH, et al. 2R, 3R-butaneidol, a bacterial volatile produced by Pseudomonas chlororaphis O6, is involved in induction of systemic tolerance to drought in Arabidopsis thaliana. Molecular Plant-Microbe Interactions, 2008, 21: 1067-1075 [87] Miller SH, Browne P, Prigentcombaret C, et al. Biochemical and genomic comparison of inorganic phosphate solubilization in pseudomonas species. Environmental Microbiology Reports, 2010, 2: 403-411 [88] Sandhya V, Ali SKZ, Grover M, et al. Alleviation of drought stress effects in sunflower seedlings by the exo-polysaccharides producing Pseudomonas putida strain GAP-P45. Biology and Fertility of Soils, 2009, 46: 17-26 [89] Grichko VP, Glick BR. Amelioration of flooding stress by ACC deaminase-containing plant growth-promoting bacteria. Plant Physiology & Biochemistry, 2001, 39: 11-17 [90] Li Z, Chang S, Lin L, et al. A colorimetric assay of 1-aminocyclopropane-1-carboxylate (ACC) based on ninhydrin reaction for rapid screening of bacteria containing ACC deaminase. Letters in Applied Microbiology, 2011, 53: 178-185 [91] Li Z, Chang S, Ye S, et al. Differentiation of 1-aminocyclopropane-1-carboxylate (ACC) deaminase from its homologs is the key for identifying bacteria containing ACC deaminase. FEMS Microbiology Ecology, 2015, 91: fiv112, doi: 10.1093/femsec/fiv112 [92] Marasco R, Rolli E, Ettoumi B, et al. A drought resis-tance-promoting microbiome is selected by root system under desert farming. PLoS One, 2012, 7(10): e48479 [93] Bruto M, Prigent-Combaret C, Muller D, et al. Analysis of genes contributing to plant-beneficial functions in plant growth-promoting rhizobacteria and related Proteobacteria. Scientific Reports, 2014, 4: 6261, doi: 10.1038/srep06261 [94] Penrose DM, Glick BR. Methods for isolating and characterizing ACC deaminase-containing plant growth-promoting rhizobacteria. Physiologia Plantarum, 2003, 118: 10-15 [95] Smyth EM, McCarthy J, Nevin R, et al. In vitro analyses are not reliable predictors of the plant growth promotion capability of bacteria: A Pseudomonas fluorescens strain that promotes the growth and yield of wheat. Journal of Applied Microbiology, 2011, 111: 683-692 [96] Jain M. Function genomics of abiotic stress tolerance in plants: A CRISPR approach. Frontiers in Plant Science, 2015, 6: 375, doi: 10.3389/fpls.2015.00375 [97] Gao J, Wang G, Ma S, et al. CRISPR/Cas9-mediated targeted mutagenesis in Nicotiana tabacum. Plant Mole-cular Biology, 2015, 87: 99-110 |
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