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March 2008 - Mycological Society of America

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Everhart, Sydney E.*, Keller, Harold W. and Ely, Joseph S. Department<br />

<strong>of</strong> Biology, University <strong>of</strong> Central Missouri, Warrensburg, MO<br />

64093, USA. everhart@ucmo.edu. Quantitative analysis <strong>of</strong> bark<br />

characteristics and epiphyte cover on distribution patterns <strong>of</strong> corticolous<br />

myxomycetes (true slime molds) in the tree canopy. Corticolous<br />

myxomycetes form plasmodia and fruiting bodies on the bark <strong>of</strong><br />

living trees and vines. Bark was sampled from 30 trees and 30<br />

grapevines along a vertical transect up to 15 m, to examine the relationship<br />

between bark characteristics (pH, water absorption, and thickness),<br />

epiphyte cover, geographic location, and myxomycete species.<br />

Moist chamber culture technique was used to induce myxomycete<br />

fruiting and bark pH was measured after 24 hours using an Orion 610<br />

pH flat probe. Plates were scanned for presence <strong>of</strong> myxomycetes after<br />

4, 16, and 32 days, and percent cover data was collected in a stratified<br />

random design on day 32. Different species <strong>of</strong> trees and grapevines had<br />

significantly different bark characteristics, however, the only tree<br />

which had a significant difference in the vertical variation <strong>of</strong> any bark<br />

characteristic was P. occidentalis. Accordingly, P. occidentalis also<br />

had a significant decrease in richness <strong>of</strong> myxomycete species with increasing<br />

height in the canopy. Non-metric multi-dimensional scaling<br />

and multi-response permutation procedure were performed; distinct<br />

species assemblages correspond to each tree and grapevine species and<br />

were differentiated by pH, DBH, and elevation. Financially supported<br />

by NSF Award DEB-0343447, National Geographic Research and Exploration<br />

Award-7272-02, and Discover Life in <strong>America</strong> Awards<br />

2001-26 and 2002-17. Poster<br />

Exeter, Ronald L. 1 and Norvell, Lorelei L. 2 * 1 USDI Bureau <strong>of</strong> Land<br />

Management, 1717 Fabry Road SE, Salem, OR 97306-1720, USA,<br />

2 Pacific Northwest Mycology Service, Portland, OR 97229-1309.<br />

USA. llnorvell@pnw-ms.com. Ramarias <strong>of</strong> Pacific Northwest. The<br />

colorful coral fungi are among the loveliest denizens <strong>of</strong> the vast temperate<br />

rainforests <strong>of</strong> western North <strong>America</strong>. The US government’s<br />

Northwest Forest Plan targeted 28 rare or uncommon taxa <strong>of</strong> Ramaria<br />

(Basidiomycota, Gomphales) as worthy <strong>of</strong> survey and management<br />

within the range <strong>of</strong> the endangered northern spotted owl. Examination<br />

<strong>of</strong> both type and recent collections and reference to classic papers by<br />

Marr & Stuntz, Petersen, and others led to the development <strong>of</strong> a single<br />

key identifying all species in the region and the discovery <strong>of</strong> a new<br />

species, Ramaria rasilisporoides. A recent 157-page USDI-BLM publication,<br />

Ramaria <strong>of</strong> the Pacific Northwestern United States (Exeter,<br />

Norvell & Cazares, 2006), treats all four subgenera: Lentoramaria,<br />

Echinoramaria, Ramaria, and Laeticolora. The lavishly illustrated<br />

monograph contains 193 color photos and covers all 90 <strong>of</strong> the region’s<br />

known species and varieties. Each one- to two-page taxonomic treatment<br />

presents synonyms, field descriptions, summary technical descriptions<br />

from hard-to-find publications, ecological and distributional<br />

data, diagnostic characters, additional comments, and references.<br />

Known phylogenetic relationships, taxonomic characters, tables, a new<br />

glossary, complete bibliography, and previously published microscopic<br />

keys are also provided. Poster<br />

Fedorova, Natalie 1 , McDonagh, Andrew 2 , Yu, Yan 1 , Armstrong-<br />

James, Darius 2 , Haynes, Ken 2 , Bignell, Elaine 2 and Nierman, William<br />

C. 1 * 1 J. Craig Venter Institute, Rockville, MD, USA, 2 Department <strong>of</strong><br />

Molecular Microbiology and Infection, Imperial College London, London<br />

SW7 2AZ, UK. wnierman@jcvi.org. Transcriptome analysis <strong>of</strong><br />

Aspergillus fumigatus during early stage mammalian lung infection.<br />

Aspergillus fumigatus is a particularly virulent fungus whose<br />

spores infect human hosts having compromised immunity. Its success<br />

as a pathogen is unique among close phylogenetic relatives and thought<br />

to depend upon concerted control over multiple functions including nutrient<br />

acquisition, metabolic plasticity and immunotoxin production. A.<br />

fumigatus virulence, and that <strong>of</strong> other opportunistic fungal pathogens,<br />

has escaped definition at the molecular level promoting scepticism regarding<br />

the existence <strong>of</strong> ‘true’ virulence factors in such species. Newly<br />

published genomes for several fungal pathogens and emerging evidence<br />

for epigenetic control <strong>of</strong> fungal virulence mechanisms support<br />

the view that hierarchical co-ordination <strong>of</strong> multiple processes may un-<br />

16 Inoculum 59(2), <strong>March</strong> <strong>2008</strong><br />

derpin fungal pathogenicity. Comparative genomics analysis has raised<br />

suspicions that niche adaptation genes may reside in lineage-specific<br />

regions <strong>of</strong> the Aspergillus genomes. To assess transcriptional co-ordination<br />

during host niche-adaptation we have characterised A. fumigatus<br />

gene expression during initiation <strong>of</strong> mammalian infection, using laboratory<br />

cultured germlings as a comparator. We show that during the<br />

early phase <strong>of</strong> infection A. fumigatus co-ordinately regulates expression<br />

<strong>of</strong> gene clusters encoding biosynthesis <strong>of</strong> gliotoxin, iron siderophore,<br />

and five other putative secondary metabolites. In addition our analyses<br />

identify multiple clusters <strong>of</strong> physically linked, co-regulated genes,<br />

which are likely to share a concerted function, which cannot be predicted<br />

from genomic analyses alone. The analysis demonstrated a<br />

genome-wide transcriptional reprogramming favoring subtelomeric<br />

and lineage-specific genes. Taken together these observations reveal a<br />

pattern <strong>of</strong> co-ordinated gene regulation thus far undiscovered from in<br />

vitro analyses, and provides the first transcriptional snapshot <strong>of</strong> a fungal<br />

genome during initiation <strong>of</strong> mammalian infection. Symposium<br />

Presentation<br />

Ferreira, Renato B. 1 , Inácio, Carlos A. 2 and Dianese, José C. 21 Centro<br />

Universitário de Brasília, UNICEUB, Asa Norte, Brasília, DF, Brazil,<br />

2 Dep. de Fitopatologia, Universidade de Brasília, 70910-900, Brasília,<br />

DF, Brazil. jcarmine@unb.br. New Ascomycota on petioles <strong>of</strong> Mauritia<br />

flexuosa (Palmae) from Central Brazil. Mauritia flexuosa (Burití)<br />

is a palm tree found endemically on swampy areas (“veredas”) <strong>of</strong><br />

the cerrado. In 2006 leaf samples were collected from the State <strong>of</strong><br />

Goiás in Central Brazil. Two new Ascomycota were detected on leaf<br />

petioles and are now described, as follows: 1. a new xylariaceous ascomycete,<br />

forming lesions that are darkened and irregular; ascomata 50<br />

– 213 × 105 - 300 µm, black, partially erumpent, irregular in shape with<br />

a convoluted internal lining, and 26 – 13 µm thick black outer wall; paraphyses:<br />

1 µm diam., hyaline, septate, branched; asci: 30 - 50 × 7 - 15<br />

µm, cylindrical, unitunicate, 7-8 ascospores, J+; ascospores: 11 – 17 ×<br />

5 - 10 µm, ellipsoidal, guttulate when young becoming light-brown to<br />

brown, uniseriate, aseptate, with mucilaginous sheath and a clear germ<br />

slit. 2. a new Saccardiaceae (Dothideomycetidae) forming colonies 8-<br />

21 mm diam., dark, circular, confluent; greyish, containing dark ascomata;<br />

ascomata 75 – 103 × 225 - 475 µm, superficial, black, circular,<br />

discoid, non-ostiolate; upper wall 13 – 24 µm; paraphyses: 40 – 60 × 1<br />

– 2 µm diam., hyaline, filiform, simple; asci: 20 – 45 × 16 - 34 µm, globose<br />

to ovoid, bitunicate; ascospores: 17 – 30 × 8 - 14 µm, hyaline, ellipsoidal,<br />

6 - 8 transversal septa and rare longitudinal septa, covered by<br />

a mucilaginous sheath. Poster<br />

Ferrer, A. 1 *, Sarmiento, C. 2 and Shearer, C.A. 1 1 Plant Biology, University<br />

<strong>of</strong> Illinois, 505 S. Goodwin Ave., Urbana, Il 61801, USA, 2 Universidad<br />

de Los Andes, Bogota, Colombia. aferrer@life.uiuc.edu. Distribution<br />

<strong>of</strong> ascomycete diversity in Costa Rican freshwater<br />

habitats. Diversity patterns <strong>of</strong> freshwater ascomycetes in the tropics<br />

are undescribed. As part <strong>of</strong> an ongoing study <strong>of</strong> the distribution <strong>of</strong><br />

freshwater ascomycetes along latitudinal gradients, we undertook a<br />

comparative survey <strong>of</strong> three lowland sites and one lower montane site<br />

in Costa Rica. Submerged wood was collected from streams at La<br />

Selva, Barra del Colorado and Las Cruces National Park and from<br />

lentic habitats in Caño Negro. At each site, 30 samples <strong>of</strong> submerged,<br />

partially decomposed woody debris were collected. Wood samples<br />

were incubated in moist chambers and examined periodically for fruiting<br />

body production. Species richness was higher than that reported<br />

from temperate areas and included new species discovered at each site.<br />

No one genus or family dominated any site. We recorded very few<br />

species that were shared between sites indicating high alpha and beta<br />

diversity in this fungal community. Numerous species collected from<br />

Costa Rica also have been reported from similar habitats in the paleotropics,<br />

suggesting a global distribution for some tropical freshwater<br />

species. Our results highlight the importance <strong>of</strong> sampling multiple sites<br />

to capture freshwater fungal diversity, and indicate that many freshwater<br />

taxa remain to be discovered. Poster<br />

Continued on following page

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