Investigations concerning the role of Chalara fraxinea in declining Fraxinus excelsior

A study was carried out to clarify the role of the fungus Chalara fraxinea in decline of Fraxinus excelsior , which is observed on a large scale in central and northern Europe with high incidence of tree mortality. The aims of this work were: (i) to check for the presence of C. fraxinea in various tissues of declining F. excelsior by agar culture isolations and by direct analysis of plant tissues using molecular techniques (DNA extraction, ITS-PCR, cloning, ITS sequencing and T-RFLP); (ii) to study fungal communities inhabiting tissues with symptoms; and (iii) to test the pathogenicity of C. fraxinea to F. excelsior . Chalara fraxinea was isolated from 93% of stem cankers, 91% of necrotic leaf stalks, 27‐28% of bark wounds and 30% of visually healthy leaf stalks. Molecular analyses of necrotic leaves, leaf stalks and bark revealed the presence of 25 different fungal taxa, 14 of which were detected in all three types of tissue sample. Chalara fraxinea was the second most common species (61% of samples), and only Cryptococcus foliicola occurred more often (70%). All eight of the tested C. fraxinea isolates induced necroses in bark and cambium on each of 86 inoculated trees, and all controls remained healthy. Average length of necroses caused by different C. fraxinea strains varied from 4·2 to 8·9 cm, but the differences were statistically insignificant. Instead, differences in resistance of individual trees to C. fraxinea were observed.

[1]  A. Magurran Ecological Diversity and Its Measurement , 1988, Springer Netherlands.

[2]  T. Nakase Expanding world of ballistosporous yeasts: Distribution in the phyllosphere, systematics and phylogeny. , 2000, The Journal of general and applied microbiology.

[3]  K. Larsson,et al.  Wood-inhabiting fungi in stems of Fraxinus excelsior in declining ash stands of northern Lithuania, with particular reference to Armillaria cepistipes , 2005 .

[4]  T. Kowalski,et al.  Chalara fraxinea sp. nov. associated with dieback of ash (Fraxinus excelsior) in Poland , 2006 .

[5]  Rytas Vilgalys,et al.  Fungal Community Analysis by Large-Scale Sequencing of Environmental Samples , 2005, Applied and Environmental Microbiology.

[6]  R. Koide,et al.  Vertical niche differentiation of ectomycorrhizal hyphae in soil as shown by T-RFLP analysis. , 2002, The New phytologist.

[7]  Laura Aldrich-Wolfe Distinct mycorrhizal communities on new and established hosts in a transitional tropical plant community. , 2007, Ecology.

[8]  P. Barklund,et al.  Endophytic fungi in branches of Norway spruce with particular reference to Tryblidiopsis pinastri , 1996 .

[9]  O. Claisse,et al.  Inventory and monitoring of wine microbial consortia , 2007, Applied Microbiology and Biotechnology.

[10]  K. Przybył Fungi associated with necrotic apical parts of Fraxinus excelsior shoots , 2002 .

[11]  T. Kirisits,et al.  First report of the ash dieback pathogen Chalara fraxinea on Fraxinus excelsior in Austria , 2008 .

[12]  T. Kuyper,et al.  Molecular Identification of Ectomycorrhizal Mycelium in Soil Horizons , 2003, Applied and Environmental Microbiology.

[13]  F. Buscot,et al.  Diversity of Cryptococcus and Dioszegia yeasts (Basidiomycota) inhabiting arbuscular mycorrhizal roots or spores. , 2004, FEMS yeast research.

[14]  S. Trumbore,et al.  Spatial separation of litter decomposition and mycorrhizal nitrogen uptake in a boreal forest. , 2007, The New phytologist.

[15]  J. P. Skovsgaard,et al.  Associations among symptoms of dieback in even-aged stands of ash (Fraxinus excelsior L.) , 2010 .

[16]  R. Blanchette,et al.  Fungal diversity in soils and historic wood from the Ross Sea Region of Antarctica , 2006 .

[17]  R. Shattock Diseases of Trees and Shrubs, 2nd edn ‐ Wayne A. Sinclair and Howard H. Lyon , 2006 .

[18]  K. Przybył Effect of Pseudomonas spp. on inoculation of young plants of Fraxinus excelsior stem with Diplodia mutila , 2003 .