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Developmental Interactions Between Clavicipitaleans and Their Host Plants

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Plant Surface Microbiology

Clavicipitalean fungi have evolved to survive as saprophytes, degrading organic material, as well as biotrophs of plants, fungi, nematodes, and insects. They have become particularly successful as epibionts and endophytes of grasses. We believe that the associations between clavicipitalean fungi and their hosts constitute unique biotrophic symbioses where the stages of physiological adaptation to the plant host may be examined to gain an understanding of how evolution among these fungi has progressed.

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References and Selected Reading

  • Alexopoulos CJ, Mims CW, Blackwell M (1996) Introductory mycology. Wiley, New York

    Google Scholar 

  • Apel PC, Panaccione DG, Holden FR, Walton JD (1993) Cloning and targeted gene dis-ruption of XYL1, a 1, 4-xylanase gene from the maize pathogen Cochliobolus car-bonum. Mol Plant-Microbe Interact 6:457-473

    Google Scholar 

  • Bacon CW, White JF Jr (1994) Stains, media, and procedures for analyzing endophytes. In: Bacon CW, White JF Jr (eds) Biotechnology of endophytic fungi of grasses. CRC Press, Boca Raton, Florida, pp 47-58

    Google Scholar 

  • Bacon CW, White JF Jr (2000) Microbial endophytes. Marcel-Dekker, New York, pp 341-388

    Google Scholar 

  • Bartnicki-Garcia S (1973) Fundamental aspects of hyphal morphogenesis. In: Ashworth JM, Smith JE (eds) Microbial differentiation. Cambridge University Press, Cambridge

    Google Scholar 

  • Bonants PJM, Fitters PFL, Thijs H, den Belder E, Waalwijk C, Henfling JWDM (1995) A basic serine protease from Paecilomyces lilacinus with biological activity against Meloidogyne hapla eggs. Microbiology 141:775-784

    Article  CAS  PubMed  Google Scholar 

  • Bowen JK, Templeton MD, Sharrock KR, Crowhurst RN, Rikkerink EHA (1995) Gene inactivation in the plant pathogen Glomerella cingulata: three strategies for the dis-ruption of the pectin lyase gene pnlA. Mol Gen Genet 246:196-205

    Article  CAS  PubMed  Google Scholar 

  • Bultman TL, White JF Jr, Bowdish TI, Welch AM, Johnston J (1995) Mutualistic transfer of Epichloë spermatia by Phorbia flies. Mycologia 87:182-189

    Article  Google Scholar 

  • Cabral D, Cafaro M, Saidman B, Lugo M, Reddy PV, White JF Jr (1999) Evidence support-ing the occurrence of a new species of endophyte in some South American grasses. Mycologia 91:315-325

    Article  Google Scholar 

  • Chet I (1987) Trichoderma - application, mode of action, and potential as a biocontrol agent of soil borne plant pathogenic fungi. In: Chet I (ed) Innovative approaches to plant disease control. Wiley, New York

    Google Scholar 

  • Chung KR, Schardl CL (1997) Sexual cycle and horizontal transmission of the grass sym-biont, Epichloë typhina. Mycological Res 101:295-301

    Article  Google Scholar 

  • Clarke BB, White, JF Jr, Funk CR Jr, Sun S, Huff DR, Hurley RH (2003) Enhanced resistance to dollar spot in endophyte-infected fine fescues. Plant Dis (in press)

    Google Scholar 

  • Clay K (1988) Clavicipitaceous fungal endophytes of grasses: coevolution and the change from parasitism to mutualism. In: Pirozynski KA, Hawksworth DL (eds) Coevolution of fungi with plants and animals. Academic Press, London, pp 79-105

    Google Scholar 

  • Diehl (1950) Balansia and Balansiae in America, USDA Monograph, US Govt Printing Office, Washington, DC, 99 pp

    Google Scholar 

  • Faeth S, Sullivan H, Hamilton CE (2000) What maintains high levels of Neotyphodium endophytes in native grasses? A dissenting view and alternative hypotheses, In: Paul VH, Krohn K, Dapprich PD, Gutter B (eds) Proceedings Fourth International Neoty-phodium/Grass Interactions Symposium. The University of Paderborn, Soest, p 14

    Google Scholar 

  • Garcia I, Lora JM, de la Cruz J, Benitez T, Llobell A, Pintor-Toro JA (1994) Cloning and characterization of a chitinase (CHIT42) cDNA from the mycoparasitic fungus Tri-choderma harzianum. Curr Genet 27:83-89

    Article  CAS  PubMed  Google Scholar 

  • Geremia RA, Goldman GH, Jacobs D, Ardiles W, Vila SB, Van Montagu M, Herrera-Estrella (1993) A. Molecular characterization of the proteinase-encoding gene, prb1, related to mycoparasitism by Trichoderma harzianum. Mol Microbiol 8:603-613

    Article  CAS  PubMed  Google Scholar 

  • Gooday GW, Gow NAR (1990) Enzymology of tip growth in fungi. In: Heath IB (ed) Tip growth in plant and fungal cells. Academic Press, New York, pp 31-58

    Google Scholar 

  • Grant V (1977) Organismic Evolution. WH Freeman, San Francisco

    Google Scholar 

  • Gwinn KD, Gavin AM (1992) Relationship between endophyte infestation level of tall fescue seed lots and Rhizoctonia zeae seedling disease. Plant Dis 76:911-914

    Google Scholar 

  • Gwinn KD, Blank CA, Cole AM, Pless CD (1991) Resistance of endophyte-infected tall fescue seedlings to pathogens and pests. Tenn Farm Home Sci 160:72

    Google Scholar 

  • Hammond-Kosack KE, Jones JDG (1996) Resistance gene-dependent plant defense responses. Plant Cell 8:1773-1791

    Article  CAS  PubMed  Google Scholar 

  • Hywel-Jones NL, Samuels GJ (1998) Three species of Hypocrella with large stromata pathogenic on scale insects. Mycologia 90:36-46

    Article  Google Scholar 

  • Kirby EJM (1961) Host-parasite relations in the choke disease of grasses. Trans Br Mycol Soc 44:493-503

    Article  Google Scholar 

  • Lam CK, Belanger FC, White JF Jr, Daie J (1995) Invertase activity in Epichloë/Acremo-nium fungal endophytes and its possible role in choke disease. Mycol Res 99:867-873

    Article  CAS  Google Scholar 

  • Lane GA, Christensen MJ, Miles CO (2000) Coevolution of fungal endophytes with grasses: the significance of secondary metabolites. In: Bacon CW, White JF Jr (eds) Microbial Endophytes. Marcel-Dekker, New York, pp 341-388

    Google Scholar 

  • Leuchtmann A, Clay K (1990) Isozyme variation in the Acremonium/Epichloë fungal endophyte complex. Phytopathology 80:1133-1139

    Article  CAS  Google Scholar 

  • Lewis GC, White JF Jr, Bonnefont J (1993) Evaluation of grasses infected with fungal endophytes against locusts. Ann Appl Biol; Tests Agrochem Cultivars 14:142-143

    Google Scholar 

  • Lindstrom JT, Belanger FC (1994) A novel fungal protease expressed in endophytic infec-tion of Poa species. Plant Physiol 102:645-650

    Google Scholar 

  • Lora JM, de la Cruz J, Llobell A, Benitez T, Pintor-Toro JA (1995) Molecular characteriza-tion and heterologous expression of an endo-b-1, 6-glucanase gene from the myco-parasitic fungus Trichoderma harzianum. Mol Gen Genet 247:639-645

    Article  CAS  PubMed  Google Scholar 

  • Mauseth JD (2003) Botany: An introduction to plant biology. Jones and Bartlett, Boston

    Google Scholar 

  • Mendgen K, Hahn M, Deising H (1996) Morphogenesis and mechanisms of penetration by plant pathogenic fungi. Ann Rev Phytopathol 34:367-386

    Article  CAS  Google Scholar 

  • Miller CO (1961) A kinetin-like compound in maize. Proc Natl Acad Sci USA 47:170-174

    Article  CAS  PubMed  Google Scholar 

  • Moon CD, Scott B, Schardl CL, Christensen MJ (2000) The evolutionary origins of Epichloë endophytes from annual ryegrasses. Mycologia 92:1103-1118

    Article  Google Scholar 

  • Moubarak AS, Piper EL, West CP, Johnson ZB (1993) Interaction of purified ergovaline from endophyte-infected tall fescue with synaptosomal ATPase enzyme system. J Agric Food Chem 41:407-409

    Article  CAS  Google Scholar 

  • Moy M, Belanger F, Duncan R, Freehof A, Leary C, Meyer W, Sullivan R, White JF Jr (2000) Identification of epiphyllous mycelial nets on leaves of grasses infected by clavicipita-ceous endophytes. Symbiosis 28:291-302

    Google Scholar 

  • Oliver R, Osbourn A (1995) Molecular dissection of fungal phytopathogenicity. Microbi-ology 141:1-9

    Article  CAS  Google Scholar 

  • Papavizas GC (1985) Trichoderma and Gliocladium: biology, ecology, and potential for biocontrol. Annu Rev Phytopathol 23:23-54

    Article  Google Scholar 

  • Peberdy JF (1990) Fungal cell walls - a review. In: Kuhn PJ, Trinci APJ, Jung MJ, Goosey MW, Copping LG (eds) Biochemistry of cell walls and membranes in fungi. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Porter JK, Bacon CW, Cutler HG, Arrendale RF, Robbins JD (1985) In vitro auxin produc-tion by Balansia epichloë. Phytochemistry 24:1429-1431

    Article  CAS  Google Scholar 

  • Reddy PV, Lam CK, Belanger FC (1996) Mutualistic fungal endophytes express a proteinase which is homologous to proteases suspected to be important in fungal pathogenicity. Plant Physiol 111:1209-1218

    Article  CAS  PubMed  Google Scholar 

  • Rykard DM, Bacon CW, Luttrell ES (1985) Host relations of Myriogenospora atramentosa and Balansia epichloë (Clavicipitaceae). Phytopathology 75:950-956

    Article  Google Scholar 

  • Schaeffer JH, Leykam J, Walton JD (1994) Cloning and targeted gene disruption of EXG1, encoding exo-1, 3-glucanase, in the phytopathogenic fungus Cochliobolus carbonum. Appl Environ Microbiol 60:594-598

    CAS  PubMed  Google Scholar 

  • Schardl CL, Wilkinson HH (2000) Hybridization and cospeciation hypotheses for the evolution of grass endophytes. In: Bacon CW, White JF Jr (eds) Microbial endophytes. Marcel-Dekker, New York, pp 63-83

    Google Scholar 

  • Scott-Craig JS, Panaccione DG, Cervone F, Walton JD (1990) Endopolygalacturonase is not required for pathogenicity of Cochliobolus carbonum on maize. Plant Cell 2:1191-1200

    Article  CAS  PubMed  Google Scholar 

  • Sposato P, Ahn J-H, Walton JD (1995) Characterization and disruption of a gene in the maize pathogen Cochliobolus carbonum encoding a cellulose binding domain and hinge region. Mol Plant-Microbe Interact 8:602-609

    CAS  PubMed  Google Scholar 

  • St. Leger RJ (1995) The role of cuticle-degrading proteases in fungal pathogenesis of insects. Can J Bot 73:1119-1125

    Article  Google Scholar 

  • Sullivan RF, Bills GF, Hywel-Jones NL, White JF Jr (2000) Hyperdermium: a new clavicip-italean genus for some tropical epibionts of dicotyledonous plants. Mycologia 92:908-919

    Article  Google Scholar 

  • Tenberge KB, Homann V, Oeser B, Tudzynski P (1996) Structure and expression of two polygalacturonase genes of Claviceps purpurea oriented in tandem and cytological evidence for pectinolytic enzyme activity during infection of rye. Phytopathology 86:1084-1097

    Article  CAS  Google Scholar 

  • Tsai H-F, Liu J-S, Staben C, Christensen MJ, Latch GCM, Siegel MR, Schardl CL (1994) Evolutionary diversification of fungal endophytes of tall fescue grass by hybridiza-tion with Epichloë species. Proc Natl Acad Sci USA 91:2542-2546

    Article  CAS  PubMed  Google Scholar 

  • Tzean SS, Hsieh LS, Wu WJ (1997) Atlas of entomopathogenic fungi from taiwan. Coun-cil of Agriculture, Yuan, Taiwan, Republic of China

    Google Scholar 

  • White JF Jr (1987) Widespread distribution of endophytes in the Poaceae. Plant Dis 71:340-342

    Article  Google Scholar 

  • White JF Jr (1988) Endophyte-host associations in forage grasses. XI. A proposal con-cerning origin and evolution. Mycologia 80:442-446

    Article  Google Scholar 

  • White JF Jr, Cole GT (1986) Endophyte-host associations in forage grasses. IV. The endo-phyte of Festuca versuta. Mycologia 78:102-107

    Google Scholar 

  • White JF Jr, Bultman TL (1987) Endophyte-host associations in forage grasses. VIII. Het-erothallism in Epichloë typhina. Am J Bot 74:1716-1721

    Google Scholar 

  • White JF Jr, Chambless DA (1991) Endophyte-host associations in forage grasses. XV. Clustering of stromata-bearing individuals of Agrostis hiemalis infected by Epichloë typhina. Am J Bot 78:527-533

    Article  CAS  Google Scholar 

  • White JF Jr, Owens JR (1992) Stromal development and mating system of Balansia epichloë, a leaf-colonizing endophyte of warm-season grasses. Appl Environ Micro-biol 58:513-519

    Google Scholar 

  • White JF Jr, Glenn AE (1994) A study of two fungal epibionts of grasses: structural fea-tures, host relationships, and classification in genus Myriogenospora Atk. (Clavicipi-tales). Am J Bot 81:216-223

    Article  Google Scholar 

  • White JF Jr, Camp CR (1996) A study of water relations of Epichloë amarillans White, an endophyte of the grass Agrostis hiemalis (Walt.) B. S. P. Symbiosis 18:15-25

    Google Scholar 

  • White JF Jr, Breen JP, Morgan-Jones G (1991) Substrate utilization in selected Acremo-nium, Atkinsonella, and Balansia species. Mycologia 83:601-610

    Article  CAS  Google Scholar 

  • White JF Jr, Morrow AC, Morgan-Jones G, Chambless DA (1991) Endophyte-host associ-ations in forage grasses. XIV. Primary stromata formation and seed transmission in Epichloë typhina: developmental and regulatory aspects. Mycologia 83:72-81

    Article  Google Scholar 

  • White JF Jr, Martin TI, Cabral D (1996) Endophyte-host associations in grasses. XXIII. Conidia formation by Acremonium endophytes in the phylloplanes of Agrostis hiemalis and Poa rigidifolia. Mycologia 88:174-178

    Article  Google Scholar 

  • White JF Jr, Bacon CW, Hinton DM (1997) Modifications of host cells and tissues by the biotrophic endophyte Epichloë amarillans (Clavicipitaceae;Ascomycotina). Canadian J Bot 75:1061-1069

    Article  Google Scholar 

  • Yue C, Miller CJ, White JF, Richardson M (2000) Isolation and characterization of fungal inhibitors from Epichloë festucae. J Agric Food Chem 48:4687-4692

    Article  CAS  PubMed  Google Scholar 

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White, J.F. et al. (2008). Developmental Interactions Between Clavicipitaleans and Their Host Plants. In: Varma, A., Abbott, L., Werner, D., Hampp, R. (eds) Plant Surface Microbiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-74051-3_10

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  • DOI: https://doi.org/10.1007/978-3-540-74051-3_10

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