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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Friday August 16th Lectures<br />

artificial inoculation and were identified as A. laevigatum.<br />

Isolates from the basidiocarps and the mycangia <strong>of</strong><br />

horntails had similar ITS and peroxidase A sequences. The<br />

wood <strong>of</strong> all inoculated trees showed discoloration, with no<br />

difference in shape and pattern <strong>of</strong> discoloration among the<br />

two isolates from the basidiocarps <strong>of</strong> A. laevigatum and<br />

two from the mycangia <strong>of</strong> horntails. The inoculated fungi<br />

were reisolated from the areas <strong>of</strong> discoloration in the<br />

inoculated trees. This is the first report on wood<br />

discoloration <strong>of</strong> hinoki and sugi caused by the horntails and<br />

A. laevigatum.<br />

430 - Relationships amongst the fungal symbionts <strong>of</strong><br />

Siricid woodwasps and their spread in the Southern<br />

Hemisphere<br />

B. Slippers 1* , T.A. Coutinho 1 , B.D. Wingfield 2 & M.J.<br />

Wingfield 1<br />

1<br />

Forestry and Agricultural Biotechnology Institute (FABI),<br />

Dept <strong>of</strong> Microbiology and Plant Pathology, University <strong>of</strong><br />

2<br />

Pretoria, Pretoria, South Africa. - Forestry and<br />

Agricultural Biotechnology Insititute (FABI), Dept <strong>of</strong><br />

Genetics, University <strong>of</strong> Pretoria, Pretoria, South Africa. -<br />

E-mail: bernard.slippers@fabi.up.ac.za<br />

The Basidiomycetes genus Amylostereum is best known for<br />

its symbiosis with siricid wood wasps. In this study, the<br />

phylogenetic relationships between Amylostereum spp. and<br />

other Basidiomycetes were investigated, using sequence<br />

data <strong>of</strong> the nuc-IGS and mt-SSU rDNA regions. A.<br />

areolatum was more distantly related to the three other<br />

species <strong>of</strong> Amylostereum, than they were to each other. A.<br />

ferreum and A. laevigatum were the most closely related<br />

species. These data support hypotheses relating to the<br />

mating behaviour and ecology <strong>of</strong> Amylostereum spp.<br />

Furthermore, contrary to previous suggestions, the<br />

Amylostereum spp. were more closely related to<br />

Echinodontium tinctorium (Echinodontiaceae) than to the<br />

Stereaceae. Apart from phylogenetic studies, vegetative<br />

compatibility and PCR-RFLP analyses were also used to<br />

study the spread <strong>of</strong> the introduced S. noctilio-A. areolatum<br />

complex in the Southern Hemisphere. Isolates <strong>of</strong> A.<br />

areolatum from South Africa and South America were<br />

found to represent a single VCG. PCR-RFLP pr<strong>of</strong>iles from<br />

nuc-IGS region showed that all isolates from the Southern<br />

Hemisphere shared the same pr<strong>of</strong>ile, which differed from<br />

that <strong>of</strong> other populations. This genetically uniform<br />

population <strong>of</strong> A. areolatum has emerged from its obligate<br />

relationship with S. noctilio, which disperses only asexual<br />

fungal propagules. These results suggest a single or limited<br />

introduction <strong>of</strong> the A. areolatum-S. noctilio into the<br />

Southern Hemisphere.<br />

431 - Interspecific combative interactions - an overview<br />

L. Boddy * & D.P. Donnelly<br />

Cardiff School <strong>of</strong> Biosciences, Cardiff University, PO Box<br />

915, Cardiff CF10 3TL, U.K. - E-mail:<br />

boddyl@cardiff.ac.uk<br />

Competition by fungi for nutrients in dead organic<br />

resources is effectively brought about by competition for<br />

space. Such competition can be divided into primary<br />

resource capture (obtaining uncolonized resources) and<br />

secondary resource capture (combat to obtain resources<br />

already colonized by other fungi). Combat occurs not only<br />

in organic resources but also when mycelia grow out <strong>of</strong> the<br />

resource, e.g.into soil, in search <strong>of</strong> new resources.<br />

Combative mechanisms include antagonism at a distance,<br />

mycoparasitism, hyphal interference and gross mycelial<br />

contact. Outcome <strong>of</strong> interactions can be deadlock, where<br />

neither species gains territory from the other, or<br />

replacement, where one mycelium partially or completely<br />

wrests territory from the other. A hierarchy <strong>of</strong> combative<br />

abitlity can be discerned amongst fungi that inhabit a<br />

particular resource, but within this hierarchy there is<br />

intransitivity and outcomes can vary depending on abioic<br />

variables and the presence <strong>of</strong> other organisms. Interactions<br />

can dramatically alter mycelial function even when the<br />

outcome is deadlock. The review will be illustrated largely<br />

with examples <strong>of</strong> wood decay fungi and <strong>of</strong> wood decay<br />

fungi interacting with ectomycorrhizal mycelium.<br />

432 - Interactions among wood-inhabiting fungi:<br />

implications for fungal succession and biocontrol<br />

J. Stenlid * , L. Holmer & A. Iakovlev<br />

Dept Forest Mycology and Pathology, Swedish University<br />

<strong>of</strong> Agricultural Sciences, Box 7026, S- 750 07 Uppsala,<br />

Sweden. - E-mail: Jan.Stenlid@mykopat.slu.se<br />

Interactions among wood inhabiting fungi are important for<br />

succession and have also implications for biocontrol. Early<br />

establishment secures resources for the mycelium while<br />

late arrival to a substrate necessitates strategies for entering<br />

an already established decay community. Mycelial<br />

parasitism and replacement in wood has proven to be one<br />

important driving force in succession in wood.<br />

Replacement involves developmental changes in the<br />

mycelia and can <strong>of</strong>ten be facilitated by production <strong>of</strong><br />

antimicrobial secondary substances. Other key factors for<br />

succession include differences in ability to handle<br />

recalcitrant compounds, differences in growth rate,<br />

differences in responses to gaseous regime and water<br />

potential etc. We will describe experiments indicating both<br />

species specific and general replacement patterns,<br />

metabolite production, and gene expression during<br />

interaction between various wood inhabiting fungi. Special<br />

reference will be given to the possibilities to find<br />

biocontrol against economically important root rot fungi<br />

such as Heterobasidion annosum.<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 133

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