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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Tuesday August 13th Lectures<br />

contain both lichenized and non-lichenized species. Here<br />

we report a phylogenetic-comparative analysis <strong>of</strong> RPB2,<br />

and the small and large subunit <strong>of</strong> the nuclear rRNA genes<br />

from about 60 species representing about 75% <strong>of</strong> the<br />

species diversity <strong>of</strong> the Ascomycota, a phylum that<br />

includes > 98% <strong>of</strong> known lichenized fungal species. Using<br />

a Bayesian phylogenetic tree sampling methodology,<br />

combined with a statistical model <strong>of</strong> trait evolution, we<br />

take into account uncertainty about the phylogenetic tree<br />

and ancestral state reconstructions. Our results, based upon<br />

a sample <strong>of</strong> 19,900 phylogenetic trees, show that lichens<br />

evolved earlier than believed, and that gains <strong>of</strong><br />

lichenization have been infrequent during Ascomycota<br />

evolution, but have been followed by multiple independent<br />

losses <strong>of</strong> the lichen symbiosis. As a consequence, major<br />

Ascomycota lineages (Ascosphaerales, Eurotiales,<br />

Onygenales and Chaetothyriales) <strong>of</strong> exclusively nonlichen-forming<br />

species are derived from lichen-forming<br />

ancestors.<br />

108 - Evolution <strong>of</strong> interkingdom host-jumping <strong>of</strong><br />

Cordyceps and the Clavicipitaceae<br />

J.W. Spatafora * & G.-H. Sung<br />

Oregon State University, Dept. <strong>of</strong> Botany and Plant<br />

Pathology, 2082 Cordley Hall, Corvallis, OR 97331-2902,<br />

U.S.A. - E-mail: spatafoj@bcc.orst.edu<br />

The genus Cordyceps includes over 300 described species<br />

<strong>of</strong> fungi that are pathogens <strong>of</strong> arthropods and fungi. It is a<br />

member <strong>of</strong> the Clavicipitaceae (Ascomycota, Hypocreales)<br />

which also includes symbionts <strong>of</strong> plants, mainly <strong>of</strong> the<br />

Poaceae. Current subfamilial classification <strong>of</strong> the<br />

Clavicipitaceae comprises the Clavicipitoideae, which<br />

includes all <strong>of</strong> the grass symbionts, and the<br />

Cordycipitoideae, which includes all <strong>of</strong> the pathogens <strong>of</strong><br />

arthropods and fungi. This represents an evolutionary<br />

hypothesis that implicitly assumes inter-Kingdom host<br />

jumps are rare and irreversible. To test this hypothesis we<br />

initiated a molecular phylogenetic study <strong>of</strong> the<br />

Clavicipitaceae with a particular emphasis on Cordyceps.<br />

We have assembled a four-gene region dataset that<br />

includes data from the nuclear SSU and LSU rDNA, betatubulin,<br />

and elongation factor 1-alpha for 75 taxa.<br />

Phylogenetic analyses reject the monophyly <strong>of</strong> Cordyceps<br />

and the Cordycipitoideae and do not support host jumps as<br />

being rare and irreversible. Three clades <strong>of</strong> clavicipitaceous<br />

fungi, which all contained pathogens <strong>of</strong> animals and fungi,<br />

were resolved in these analyses. Pathogen <strong>of</strong> animals is<br />

resolved as the primitive symbiosis for the Clavicipitaceae<br />

with a single jump to the Poaceae that was most likely<br />

followed by a reversal to animals. Multiple jumps have<br />

occurred from animals to fungi with at least one reversal to<br />

animals. Character coding <strong>of</strong> host affiliation and testing<br />

character state reconstructions will be discussed.<br />

36<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong><br />

109 - Molecular phylogenetics and breeding systems in<br />

the ascomycete fungi<br />

M.L. Berbee<br />

Department <strong>of</strong> Botany, University <strong>of</strong> British Columbia,<br />

Vancouver BC V6T 1Z4, Canada. - E-mail:<br />

berbee@interchange.ubc.ca<br />

By a combination <strong>of</strong> phylogenetic approaches, we are<br />

studying the evolution <strong>of</strong> breeding systems among fungi in<br />

the Ascomycota. Within the family Pleosporaceae,<br />

combined data from the glyceraldehyde-3-phosphate<br />

dehydrogenase gene and ribosomal ITS regions provide<br />

good resolution. Our phylogenetic analysis shows that the<br />

'asexual' species and the selfing species are nested among<br />

outcrossing sexual species, indicating that outcrossing<br />

sexuality was the ancestral condition for the family. In<br />

sexual filamentous ascomycetes, opposite mating type<br />

information at the MAT1 locus regulates mating and the<br />

opposite mating type genes each have a clonal, nonrecombining<br />

phylogenetic history. Many species in the<br />

Pleosporaceae have no known sexual states, but where<br />

tested, these supposedly asexual fungi have intact,<br />

functional mating type genes. We used PCR to amplify and<br />

sequence fragments <strong>of</strong> the opposite mating type genes from<br />

supposedly asexual species in the genus Alternaria, in the<br />

Pleosporaceae. Each haploid fungal isolate had just one<br />

mating type, but both mating types were present in each<br />

species. We sequenced the ribosomal ITS regions for<br />

isolates <strong>of</strong> opposite mating types, for three asexual species<br />

and four known related sexual species. Analysis <strong>of</strong> the<br />

probability <strong>of</strong> substitution patterns indicated that, if<br />

sexuality had been lost, it was lost after the most recent ITS<br />

substitutions had evolved in each species.<br />

110 - Trends in morphological evolution in<br />

homobasidiomycetes<br />

D.S. Hibbett * & M. Binder<br />

Biology Department, Clark University, Worcester MA<br />

01610, U.S.A. - E-mail: dhibbett@black.clarku.edu<br />

Homobasidiomycetes display an incredible diversity <strong>of</strong><br />

fruiting body forms, ranging from simple corticioid forms,<br />

which lie flat on their substrates, to elaborate,<br />

developmentally integrated forms, such as stinkhorns.<br />

More than half <strong>of</strong> all described homobasidiomycetes have<br />

pileate-stipitate fruiting bodies, with gills or other<br />

configurations <strong>of</strong> the hymenophore. A functional (if not<br />

phylogenetic) distinction can be made between<br />

gasteromycetes, which lack ballistospory and produce<br />

spores internally, and hymenomycetes, which retain<br />

ballistospory and produce spores externally. Much <strong>of</strong> the<br />

research in higher-level homobasidiomycete systematics in<br />

the last century has focused on tracing patterns <strong>of</strong> evolution<br />

in fruiting body forms, and has revealed extensive<br />

convergence. Our recent analyses concern trends in the<br />

evolution <strong>of</strong> fruiting body morphology. Examples <strong>of</strong> the

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