Abstract
Foliar endophytes of white pine were isolated from trees at a site in New Brunswick (Canada) and grown in liquid culture. Oxford disk bioassays of the resulting extracts against yeast showed that, of the 86 strains tested, 22 produced antifungal extracts. The resulting extracts were screened by LC-MS and showed variability in metabolite production, but the majority produced pyrenophorol and a number of related derivatives, all of which are known to be antifungal. DNA sequencing of these strains determined that the majority were Lophodermium nitens. A strain of white pine blister rust was isolated in liquid culture from young seedlings infected with the pathogen for toxicity testing. Bioassays performed with 5 μM pyrenophorol showed that it significantly reduced the cell dry weight of the pathogen compared to controls. These data support the hypothesis that pyrenophorol-producing L. nitens endophytes may increase the tolerance of the host tree to white pine blister rust.
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References
Miller JD (2011) Foliar endophytes of spruce species found in the Acadian forest: basis and potential for improving the tolerance of the forest to spruce budworm. In: Pirttil AM, Frank AC (eds) Endophytes of forest trees: biology and applications, forestry sciences, vol 80. Springer, Berlin, pp 237–249
Allen EA, Humble LM (2002) Nonindigenous species introductions: a threat to Canada’s forests and forest economy. Canad J Plant Pathol 24:103–110
Hunt RS (2009) History of western white pine and blister rust in British Columbia. For Chronicle 85:516–520
Geils BW, Hummer KE, Hunt RS (2010) White pines, Ribes, and blister rust: a review and synthesis. For Pathol 40:147–185
Meagher MD, Hunt RS (1996) Heritability and gain of reduced spotting vs blister rust on western white pine in British Columbia, Canada. Silvae Genetica 45:75–81
Ganley RJ, Sniezko RA, Newcombe G (2008) Endophyte-mediated resistance against white pine blister rust in Pinus monticola. For Ecol Manage 255:2751–2760
Kearns HJS, Jacobi WJ (2007) The distribution and incidence of white pine blister rust in central and southeastern Wyoming and Northern Colorado. Can J Forest Res 37:462–472
Kinloch BB Jr, Davis DA, Burton D (2008) Resistance and virulence interactions between two white pine species and blister rust in a 30-year field trial. Tree Genet Genome 4:65–74
Sumarah MW, Miller JD (2009) Anti-insect secondary metabolites from fungal endophytes of conifer trees. Nat Prod Commun 4:1497–1504
Sumarah MW, Puniani E, Blackwell BA, Miller JD (2008) Characterization of polyketide metabolites from foliar endophytes of Picea glauca. J Nat Prod 71:1393–1398
Sumarah MW, Puniani E, Sørensen D, Blackwell BA, Miller JD (2010) Secondary metabolites from anti-insect extracts of endophytic fungi isolated from Picea rubens. Phytochemistry 71:760–765
Kuldau G, Bacon C (2008) Clavicipitaceous endophytes: their ability to enhance resistance of grasses to multiple stresses. Biol Control 46:57–71
Christensen MJ (1996) Antifungal activity in grasses infected with Acremonium and Epichloë endophytes. Australias Plant Path 25:186–191
Clay K, Schardl C (2002) Evolutionary origins and ecological consequences of endophyte symbiosis with grasses. Am Nat 160:S99–S127
Clay K (1989) Clavicipitaceous endophytes of grasses: their potential as biocontrol agents. Mycol Res 92:1–12
Li C-J, Gao J-H, Nan Z-B (2007) Interactions of Neotyphodium gansuense, Achnatherum inebrians and plant-pathogenic fungi. Mycol Res 111:1220–1227
Siegel MR, Latch GCM (1991) Expression of antifungal activity in agar culture by isolates of grass endophytes. Mycologia 83:529–537
Sumarah MW, Kesting JR, Sørensen D, Miller JD (2011) Antifungal metabolites from fungal endophytes of Pinus strobus. Phytochemistry 72:1833–1837
Zhang W, Krohn K, Egold H, Draeger S, Schulz B (2008) Diversity of antimicrobial pyrenophorol derivatives from an endophytic fungus, Phoma sp. Eur J Org Chem 25:4320–4328
Schoch CL, Seifert KA, Huhndorf S, Robert V, Spouge JL, Levesque CA, Chen W (2012) Fungal barcoding consortium. Proc Natl Acad Sci U S A 109:6241–6246
Guindon S, Gascuel O (2003) A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 52:696–704
Schmitt I, Barker FK (2009) Phylogenetic methods in natural product research. Nat Prod Rep 26:1585–1602
Kinloch BB, Dupper GE (1996) Genetics of Cronartium ribicola 1. Axenic culture of haploid clones. Can J Bot 74:456–460
Gresshoff PM, Doy CH (1972) Development and differentiation of haploid Lycopersicon esculentum (tomato). Planta 107:161–170
Deckert RJ, Hsiang T, Peterson RL (2002) Genetic relationships of endophytic Lophodermium nitens isolates from needles of Pinus strobus. Mycol Res 106:305–313
Minter DW (1981) Lophodermium on pines. Mycological Papers 147:1–75
Ortiz-García S, Gernandt DS, Stone JK, Johnston PR, Chapela IH, Salas-Lizana R, Alvarez-Buylla ER (2003) Phylogenetics of Lophodermium from pine. Mycologia 95:846–859
Salas-Lizana R, Santini NS, Miranda-Pérez A, Piñero DI (2012) The Pleistocene glacial cycles shaped the historical demography and phylogeography of a pine fungal endophyte. Mycol Prog 11:569–581
Müller MM, Valjakka R, Hantula J (2007) Genetic diversity of Lophodermium piceae in South Finland. For Pathol 37:329–337
Chrysayi-Tokousbalides M, Machera K, Kyriakopoulou K, Aliferis KA, Schrader KK, Tsoutsanis I, Anastasiadou P (2007) Comparative toxicity of the phytotoxins (8R,16R)-(-)-pyrenophorin and (5S,8R,13S,16R)-(-)-pyrenophorol on aquatic organisms. Bull Environ Contam Toxicol 79:499–503
Shiomi K, Omura S (2004) Antiparasitic agents produced by microorganisms. Proc Jpn Acad Ser B Phys Biol Sci 80:245–258
Alonso MA, Vázquez D, Carrasco L (1979) Compounds affecting membranes that inhibit protein synthesis in yeast. Antimicrob Agents Chemother 16:750–756
Tulloch AP, Ledingham GA (1962) The component fatty acids of oils found in spores of plant rusts and other fungi. Part II Canad J Microbiol 8:379–387
Weete JD, Abril M, Blackwell M (2010) Phylogenetic distribution of fungal sterols. PLoS One 5(5), e10899
Miller JD, Cherid H, Sumarah MW, Adams GW (2009) Horizontal transmission of the Picea glauca foliar endophyte Phialocephala scopiformis CBS 120377. Fungal Ecol 2:98–101
Frasz SL, Walker AK, Nsiama TK, Adams GA, Miller JD (2014) Distribution of the foliar fungal endophyte Phialocephala scopiformis and its toxin in the crown of a mature white spruce tree as revealed by chemical and qPCR analyses. Can J Forest Res 44:1138–1143
Frasz SL (2014) The development and comparison of quantitative PCR assays and enzyme-linked immunosorbent assays as rapid detection methods for specific foliar endophytes. Department of Biology, Carleton University, Ottawa, Ontario, MSc thesis
Richardson SN, Walker AK, Nsiama TK, McFarlane J, Sumarah MW, Ibrahim A, Miller JD (2014) Griseofulvin-producing Xylaria endophytes of Pinus strobus and Vaccinium angustifolium: evidence for a conifer-understory species endophyte ecology. Fungal Ecol 11:107–113
Acknowledgments
This study was supported by J.D. Irving, Limited, the National Research Council Industrial Research Assistance Program, and the Natural Science and Engineering Research Council of Canada. Dr. Andrew McCartney (J.D. Irving) collected the needle samples and made the primary isolations of the endophytes. We thank Dr. P. Tanguay (Laurentian Forestry Centre), G. Dupper (USDA Forest Service) for assistance with the isolation of the C. ribicola strain, and Dr. Dan Sørensen (Merck/McMaster University) for assistance with metabolite identification.
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Sumarah, M.W., Walker, A.K., Seifert, K.A., Todorov, A., Miller, J.D. (2015). Screening of Fungal Endophytes Isolated from Eastern White Pine Needles. In: Jetter, R. (eds) The Formation, Structure and Activity of Phytochemicals. Recent Advances in Phytochemistry, vol 45. Springer, Cham. https://doi.org/10.1007/978-3-319-20397-3_8
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DOI: https://doi.org/10.1007/978-3-319-20397-3_8
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