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Increased Silicon Acquisition in Bananas Colonized by Rhizophagus irregularis MUCL 41833 Reduces the Incidence of Pseudocercospora fijiensis

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  1. Abadie Catherine, Zapater Marie-Françoise, Pignolet Luc, Carlier Jean, Mourichon Xavier, Artificial inoculation on plants and banana leaf pieces withMycosphaerellaspp., responsible for Sigatoka leaf spot diseases, 10.1051/fruits:2008030
  2. Ahuja Ishita, Borgen Birgit Hafeld, Hansen Magnor, Honne Bjørn Ivar, Müller Caroline, Rohloff Jens, Rossiter John Trevor, Bones Atle Magnar, Oilseed rape seeds with ablated defence cells of the glucosinolate–myrosinase system. Production and characteristics of double haploid MINELESS plants of Brassica napus L., 10.1093/jxb/err195
  3. Anene Abla, Declerck Stéphane, Combination of Crotalaria spectabilis with Rhizophagus irregularis MUCL41833 decreases the impact of Radopholus similis in banana, 10.1016/j.apsoil.2016.04.017
  4. Bélanger R. R., Benhamou Nicole, Menzies J. G., Cytological Evidence of an Active Role of Silicon in Wheat Resistance to Powdery Mildew (Blumeria graminisf. sp.tritici), 10.1094/phyto.2003.93.4.402
  5. Brundrett Mark C., Mycorrhizal associations and other means of nutrition of vascular plants: understanding the global diversity of host plants by resolving conflicting information and developing reliable means of diagnosis, 10.1007/s11104-008-9877-9
  6. Camara, Caractérisation des Parasites Fongiques Foliaires et Telluriques en Côte d’Ivoire chez les Bananiers (Musa sp.) et Recherche De Méthodes de Lutte. (2011)
  7. Campbell, Introduction to Plant Disease Epidemiology. (1990)
  8. Carlier, Mycosphaerella Leaf Spot Diseases of Bananas: Present Status and Outlook. Proceedings of the Workshop on Mycosphaerella Leaf Spot Diseases, 123 (2003)
  9. Chao T.T., Sanzolone R.F., Decomposition techniques, 10.1016/0375-6742(92)90048-d
  10. CHURCHILL ALICE C. L., Mycosphaerella fijiensis, the black leaf streak pathogen of banana: progress towards understanding pathogen biology and detection, disease development, and the challenges of control : M. fijiensis, BLS pathogen of banana, 10.1111/j.1364-3703.2010.00672.x
  11. Datnoff, Mineral Nutrition and Plant Disease. (2007)
  12. Declerck S., Plenchette C., Strullu D. G., Mycorrhizal dependency of banana (Musa acuminata, AAA group) cultivar, 10.1007/bf00017688
  13. Declerck S., Risede J. M., Rufyikiri G., Delvaux B., Effects of arbuscular mycorrhizal fungi on severity of root rot of bananas caused byCylindrocladium spathiphylli, 10.1046/j.0032-0862.2001.656.x
  14. Elsen A., Declerck S., De Waele D., Use of Root Organ Cultures To Investigate the Interaction between Glomus intraradices and Pratylenchus coffeae, 10.1128/aem.69.7.4308-4311.2003
  15. Epstein, Silicon, 50, 641 (1999)
  16. Erwin, Phytophthora Diseases World Wide. (1996)
  17. Faurie Bertrand, Cluzet Stéphanie, Mérillon Jean-Michel, Implication of signaling pathways involving calcium, phosphorylation and active oxygen species in methyl jasmonate-induced defense responses in grapevine cell cultures, 10.1016/j.jplph.2009.05.015
  18. Fawe A., Abou-Zaid M., Menzies J. G., Bélanger R. R., Silicon-Mediated Accumulation of Flavonoid Phytoalexins in Cucumber, 10.1094/phyto.1998.88.5.396
  19. Fauteux François, Rémus-Borel Wilfried, Menzies James G., Bélanger Richard R., Silicon and plant disease resistance against pathogenic fungi, 10.1016/j.femsle.2005.06.034
  20. Fawe Anne, Menzies James G., Chérif Mohamed, Bélanger Richard R., Chapter 9 Silicon and disease resistance in dicotyledons, Silicon in Agriculture (2001) ISBN:9780444502629 p.159-169, 10.1016/s0928-3420(01)80013-6
  21. Fortunato Alessandro Antonio, Rodrigues Fabrício Ávila, Baroni Júlio Cezar Parpaiola, Soares Gustavo César Barbosa, Rodriguez Miguel Angel Dita, Pereira Olinto Liparini, Silicon Suppresses Fusarium Wilt Development in Banana Plants, 10.1111/jph.12005
  22. Frew Adam, Allsopp Peter G., Gherlenda Andrew N., Johnson Scott N., Increased root herbivory under elevated atmospheric carbon dioxide concentrations is reversed by silicon-based plant defences, 10.1111/1365-2664.12822
  23. Garg Neera, Bhandari Purnima, Silicon nutrition and mycorrhizal inoculations improve growth, nutrient status, K+/Na+ ratio and yield of Cicer arietinum L. genotypes under salinity stress, 10.1007/s10725-015-0099-x
  24. Gauhl, Diseases of Banana, Abacá and Enset, 56 (2000)
  25. Harrison Maria J., Isoflavonoid Accumulation and Expression of Defense Gene Transcripts During the Establishment of Vesicular-Arbuscular Mycorrhizal Associations in Roots ofMedicago truncatula, 10.1094/mpmi-6-643
  26. Heine G., Tikum G., Horst W. J., The effect of silicon on the infection by and spread of Pythium aphanidermatum in single roots of tomato and bitter gourd, 10.1093/jxb/erl232
  27. Henriet C., Bodarwé L., Dorel M., Draye X., Delvaux B., Leaf silicon content in banana (Musa spp.) reveals the weathering stage of volcanic ash soils in Guadeloupe, 10.1007/s11104-008-9680-7
  28. Hewitt, Sand and Water Culture Methods Used in the Study of Plant Nutrition (1966)
  29. Hidalgo William, Chandran Jima N., Menezes Riya C., Otálvaro Felipe, Schneider Bernd, Phenylphenalenones protect banana plants from infection by Mycosphaerella fijiensis and are deactivated by metabolic conversion : Phenylphenalenones deactivated by metabolism, 10.1111/pce.12630
  30. Holderness, Organic Banana: towards an Organic Banana initiative in the Carribean, 133 (2000)
  31. Inanaga Shunji, Okasaka Ayumi, Calcium and silicon binding compounds in cell walls of rice shoots, 10.1080/00380768.1995.10419563
  32. Jaizme-Vega M.C., Tenoury P., Pinochet J., Jaumot M., 10.1023/a:1004236310644
  33. Jung Sabine C., Martinez-Medina Ainhoa, Lopez-Raez Juan A., Pozo Maria J., Mycorrhiza-Induced Resistance and Priming of Plant Defenses, 10.1007/s10886-012-0134-6
  34. Kablan L., Lagauche A., Delvaux B., Legr`ve A., Silicon Reduces Black Sigatoka Development in Banana, 10.1094/pdis-04-11-0274
  35. Keeping M.G., Reynolds O.L., Silicon in agriculture: new insights, new significance and growing application, 10.1111/j.1744-7348.2009.00358.x
  36. Keymer Andreas, Pimprikar Priya, Wewer Vera, Huber Claudia, Brands Mathias, Bucerius Simone L, Delaux Pierre-Marc, Klingl Verena, Röpenack-Lahaye Edda von, Wang Trevor L, Eisenreich Wolfgang, Dörmann Peter, Parniske Martin, Gutjahr Caroline, Lipid transfer from plants to arbuscular mycorrhiza fungi, 10.7554/elife.29107
  37. Koffi Marie Chantal, Vos Christine, Draye Xavier, Declerck Stéphane, Effects of Rhizophagus irregularis MUCL 41833 on the reproduction of Radopholus similis in banana plantlets grown under in vitro culture conditions, 10.1007/s00572-012-0467-6
  38. Kumakech A, Lyngs Jørgensen HJ, Edema R, Okori P, Efficient screening procedure for black sigatoka disease of banana, 10.4314/acsj.v23i4.8
  39. Laliberté Etienne, Lambers Hans, Burgess Treena I., Wright S. Joseph, Phosphorus limitation, soil-borne pathogens and the coexistence of plant species in hyperdiverse forests and shrublands, 10.1111/nph.13203
  40. Li, Int. J. Agric. Biol., 15, 342 (2013)
  41. Liang Yongchao, Nikolic Miroslav, Bélanger Richard, Gong Haijun, Song Alin, Silicon in Agriculture, ISBN:9789401799775, 10.1007/978-94-017-9978-2
  42. Liu Jinyuan, Maldonado-Mendoza Ignacio, Lopez-Meyer Melina, Cheung Foo, Town Christopher D., Harrison Maria J., Arbuscular mycorrhizal symbiosis is accompanied by local and systemic alterations in gene expression and an increase in disease resistance in the shoots : Local and systemic alterations in transcript profiles in AM symbiosis, 10.1111/j.1365-313x.2007.03069.x
  43. Ma Jian Feng, Yamaji Naoki, Silicon uptake and accumulation in higher plants, 10.1016/j.tplants.2006.06.007
  44. Ma J. F., Yamaji N., Functions and transport of silicon in plants, 10.1007/s00018-008-7580-x
  45. Ma Jian Feng, Yamaji Naoki, A cooperative system of silicon transport in plants, 10.1016/j.tplants.2015.04.007
  46. Mali Manju, Aery N. C., Influence of Silicon on Growth, Relative Water Contents and Uptake of Silicon, Calcium and Potassium in Wheat Grown in Nutrient Solution, 10.1080/01904160802402666
  47. McGONIGLE T. P., MILLER M. H., EVANS D. G., FAIRCHILD G. L., SWAN J. A., A new method which gives an objective measure of colonization of roots by vesicular-arbuscular mycorrhizal fungi, 10.1111/j.1469-8137.1990.tb00476.x
  48. Mohiuddin, Agriculture, 12, 148 (2014)
  49. Murashige Toshio, Skoog Folke, A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures, 10.1111/j.1399-3054.1962.tb08052.x
  50. Navazio Lorella, Mariani Paola, Calcium opens the dialogue between plants and arbuscular mycorrhizal fungi, 10.4161/psb.3.4.5093
  51. Oye Anda Corinne Coretta, Dupré de Boulois Hervé, Declerck Stéphane, The arbuscular mycorrhiza fungusRhizophagus irregularisMUCL 41833 decreases disease severity of Black Sigatoka on banana c.v. Grande naine, underin vitroculture conditions, 10.1051/fruits/2014041
  52. Oye Anda Corinne Coretta, Opfergelt Sophie, Declerck Stéphane, Silicon acquisition by bananas (c.V. Grande Naine) is increased in presence of the arbuscular mycorrhizal fungus Rhizophagus irregularis MUCL 41833, 10.1007/s11104-016-2954-6
  53. Phelps R. H., Shand C. R., Brown leaf spot disease and fertilizer interaction in irrigated rice growing on different soil types, Nitrogen Economy in Tropical Soils (1995) ISBN:9789401072649 p.117-121, 10.1007/978-94-009-1706-4_11
  54. Plouznikoff Katia, Declerck Stéphane, Calonne-Salmon Maryline, Mitigating Abiotic Stresses in Crop Plants by Arbuscular Mycorrhizal Fungi, Belowground Defence Strategies in Plants (2016) ISBN:9783319423173 p.341-400, 10.1007/978-3-319-42319-7_15
  55. Pozo Marı́a J., Azcón-Aguilar Concepción, Dumas-Gaudot Eliane, Barea José M., β-1,3-Glucanase activities in tomato roots inoculated with arbuscular mycorrhizal fungi and/or Phytophthora parasitica and their possible involvement in bioprotection, 10.1016/s0168-9452(98)00243-x
  56. Silicon and Plant Diseases, ISBN:9783319229294, 10.1007/978-3-319-22930-0
  57. Rufyikiri, Fruits, 55, 367 (2000)
  58. Schouteden Nele, De Waele Dirk, Panis Bart, Vos Christine M., Arbuscular Mycorrhizal Fungi for the Biocontrol of Plant-Parasitic Nematodes: A Review of the Mechanisms Involved, 10.3389/fmicb.2015.01280
  59. Seydou Tuo, Elisee Amari Ler-N`ogn Dade, Brahima Camara, Sibirina Soro, Fatogoma Sorho, Kouabenan Abo, Leonard Ouedraogo Somgnogdin, Daouda Kone, Assessment of Banana and Plantain Behavior under Natural Infestation by Mycosphaerella fijiensis, Morelet in Southern Côte d'Ivoire, 10.3923/ja.2016.151.164
  60. Van Bockhaven Jonas, De Vleesschauwer David, Höfte Monica, Towards establishing broad-spectrum disease resistance in plants: silicon leads the way, 10.1093/jxb/ers329
  61. Vermeire Marie-Liesse, Kablan Lucie, Dorel Marc, Delvaux Bruno, Risède Jean-Michel, Legrève Anne, Protective role of silicon in the banana-Cylindrocladium spathiphylli pathosystem, 10.1007/s10658-011-9835-x
  62. Whipps John M, Prospects and limitations for mycorrhizas in biocontrol of root pathogens, 10.1139/b04-082
  63. Wu Qiang-Sheng, Xia Ren-Xue, Arbuscular mycorrhizal fungi influence growth, osmotic adjustment and photosynthesis of citrus under well-watered and water stress conditions, 10.1016/j.jplph.2005.04.024
Bibliographic reference Gbongue, Louis-Raymond ; Lalaymia, Ismahen ; Zeze, Adolphe ; Delvaux, Bruno ; Declerck, Stephan. Increased Silicon Acquisition in Bananas Colonized by Rhizophagus irregularis MUCL 41833 Reduces the Incidence of Pseudocercospora fijiensis. In: Frontiers in Plant Science, Vol. 9, no.1977, p. 1-11 (2019)
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