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Inoculum 56(4) - Mycological Society of America

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MSA ABSTRACTS<br />

quences were generated from three ribosomal loci (large nuclear subunit, small<br />

nuclear subunit, small mitochondrial subunit) and three protein-coding genes<br />

(RNA polymerase II largest and second largest subunits, translation elongation<br />

factor-1 alpha). Taxon sampling included representatives for all major Ascomycota<br />

classes with an emphasis on the filamentous fungi <strong>of</strong> the Pezizomycotina and<br />

non-lichenized lineages. Several comparative analyses utilizing parsimony and<br />

Bayesian methodologies were performed. The final data set includes more than<br />

5000 molecular characters and more than 150 taxa. A total <strong>of</strong> 10 higher nodes,<br />

corresponding to classes, were recovered with strong support as measured by concurrent<br />

parsimony bootstrapping and Bayesian posterior probabilities. The inclusion<br />

<strong>of</strong> data from all genes in simultaneous analyses improved both the resolution<br />

<strong>of</strong> the phylogenies and overall nodal support as compared to analyses <strong>of</strong> individual<br />

loci. This study provides strong support for the majority <strong>of</strong> the Ascomycota<br />

classes as currently defined by Eriksson, but certain groups were not recovered as<br />

monophyletic (e.g. Leotiomycetes). The combination <strong>of</strong> protein and ribosomal<br />

data in simultaneous analyses provided increased resolution <strong>of</strong> class level clades,<br />

advancing the resolution <strong>of</strong> deep nodes in the Ascomycota phylogeny. As such,<br />

these results provide a more accurate phylogenetic foundation for comparative<br />

studies <strong>of</strong> the Ascomycota ranging from ecology to genomics. contributed presentation<br />

Schoch, Conrad L.*, Spatafora, Joseph W. and the AFTOL consortium. Dept.<br />

Botany and Plant Pathology, Oregon State University, Corvallis, OR 97330,<br />

USA. schochc@science.oregonstate.edu. Deep relationships in the non-lichenized<br />

Ascomycota - the poster<br />

See the Oral Presentation Abstract. poster<br />

Scholler, Markus 1 * and Boellmann, Joerg 2 . 1 Staatliches Museum f. Naturkunde,<br />

Erbprinzenstr. 13, D-76133 Karlsruhe, Germany, 2 Brandenburgische Technische<br />

Universität, Lehrstuhl für Bodenschutz und Rekultivierung, P. O Box 101344, D-<br />

03013 Cottbus, Germany. scholler@naturkundeka-bw.de. Puccinia glechomatis<br />

and P. lagenophorae in North <strong>America</strong>: invasion patterns, life cycle and life<br />

strategies.<br />

Puccinia glechomatis and P. lagenophorae are taxonomically distinct autoecious<br />

rust species native to Eurasia and Australia which were recently introduced<br />

to the United States. Although their life cycle (microcyclic versus autodemicyclic)<br />

and host range differ (monophageous on Glechoma hederacea s. l.,<br />

Lamiaceae versus polyphagous on numerous Asteraceae) there are common characters<br />

with respect to their invasion pattern in North <strong>America</strong>. Both species have<br />

spread throughout the U.S. (not restricted to a certain geographical or climatical<br />

area), both species appeared first on the East Coast and the West Coast before establishing<br />

in Central U.S. and both species seem not to progress continuously but<br />

patchy. In order to explain these invasion patterns detailed lab, field and literature<br />

studies on the life cycle and life strategies <strong>of</strong> P. glechomatis and its host were carried<br />

out and compared with those <strong>of</strong> P. lagenophorae. Results indicate that the invasive<br />

capacity <strong>of</strong> rust fungi is supported by several factors, three <strong>of</strong> which are the<br />

production <strong>of</strong> several generations per year, a predominance <strong>of</strong> an asexual mode <strong>of</strong><br />

reproduction, and ruderal host plants occurring in man-made habitats. symposium<br />

presentation<br />

Seifert, Keith A.*, Hughes, Stanley J., Boulay, Hillary and Louis-Seize, Gerry.<br />

Biodiversity Theme (Mycology & Botany), Agriculture & Agri-Food Canada,<br />

960 Carling Ave., Ottawa, Ontario K1A 0C6, Canada. seifertk@agr.gc.ca. What<br />

should we call the jet fuel fungus?<br />

The jet fuel fungus, Hormoconis resinae (also widely known as Cladosporium<br />

resinae), grows in fuel contaminated with small amounts <strong>of</strong> water, and its<br />

growth can clog fuel lines and corrode metal parts. Consequently, fuel tanks in airports<br />

and on jets are carefully monitored for this fungus. Around the world, several<br />

private companies make their fortunes detecting and identifying this fungus<br />

using a variety <strong>of</strong> technologies. Unfortunately, when the anamorph genus Hormoconis<br />

was proposed (1973), an error was perpetuated that originated when the<br />

teleomorph Amorphotheca resinae was described (1969). Various nomenclatural<br />

options for stabilizing the name <strong>of</strong> the jet-fuel fungus will be discussed. Using<br />

morphological, cultural and molecular data, we will consider the taxonomy and<br />

phylogenetic relationships <strong>of</strong> several cladosporium-like fungi, including A.<br />

resinae, and the synnematous fungi Sorocybe resinae and Pycnostysanus azalea.<br />

The precise phylogenetic relationships <strong>of</strong> A. resinae, which sits alone in its own<br />

family Amorphothecaceae, are difficult to determine with certainty with existing<br />

data. contributed presentation<br />

Setoguchi, Masanobu*, Yamada, Akiyoshi and Kuga, Yukari. Faculty <strong>of</strong> Agriculture,<br />

Shinshu University, Minami-minowa, Nagano 399-4598, Japan.<br />

akiyosh@gipmc.shinshu-u.ac.jp. Fungal colonization occurs at the seed germination<br />

<strong>of</strong> achlorophylous monotropoid plants, Monotropa hypopithys and<br />

Monotropastrum humile.<br />

Monotropaceae consists <strong>of</strong> achlorophylous plants that develop monotropoid<br />

mycorrhizas in the root system <strong>of</strong> adult individuals. However, little is known<br />

about their fungal association at the seed germination and the early developmental<br />

stage. We buried seeds <strong>of</strong> Monotropa hypopithys and Monotropastrum humile<br />

in Pinus densiflora forests, where both the monotropoid plants are naturally dis-<br />

52 <strong>Inoculum</strong> <strong>56</strong>(4), August 2005<br />

tributed. Three to five months after the sowing, seed germination was observed,<br />

which was determined by the increase <strong>of</strong> seed size and the budding <strong>of</strong> root-like<br />

organ that possess vascular structure in the central. In addition, fungi epigeously<br />

colonized to most <strong>of</strong> such seeds, which <strong>of</strong>ten developed the fungal sheath as well<br />

as that <strong>of</strong> monotropoid mycorhizas. In M. humile, cystidia were observed on the<br />

fungal sheath, and fungal penetration pegs were also observed in the epigeous cell<br />

<strong>of</strong> seed. In M. hypopithys, clamp connections were <strong>of</strong>ten observed on the hyphae<br />

<strong>of</strong> colonized mycelium. poster<br />

Shefferson, Richard P. 1 * and Taylor, D. Lee 2 . 1 Forestry and Forest Products Research<br />

Institute, Tsukuba, Japan, 2 Institute <strong>of</strong> Arctic Biology, University <strong>of</strong> Alaska<br />

Fairbanks, Fairbanks, Alaska, USA. dormancy@gmail.com. Lady-slipper orchid<br />

mycorrhizal associations reveal specificity suggestive <strong>of</strong> resource<br />

fragmentation and resource tracking.<br />

Generalism in biotic interactions, measured at one level <strong>of</strong> study, <strong>of</strong>ten<br />

masks specialization at finer scales. Here, we examine mycorrhizal specificity <strong>of</strong><br />

temperate terrestrial lady∞fs slipper orchids (Cypripedium spp.) in northern California,<br />

USA, to assess if high mycorrhizal specificity at the fungal family level<br />

masks low specificity to fungi within the Tulasnellaceae, the primary family <strong>of</strong><br />

Cypripedium-mycorrhizal fungi. First, we hypothesized that if Cypripedium<br />

species are highly specialized to fungi within family Tulasnellaceae, then sympatric<br />

Cypripedium populations will associate with divergent tulasnelloid symbionts,<br />

while allopatric populations may not. Second, we hypothesized that within-Tulasnellaceae<br />

specificity may correspond to host abundance, leading to<br />

greater specialization in areas with lower diversity <strong>of</strong> potential host fungal families.<br />

We observed no evidence <strong>of</strong> ecological divergence in mycorrhizal association<br />

in sympatric populations. However, we observed evidence that within-Tulasnellaceae<br />

specificity varied inversely with among-family specificity. We suggest<br />

that in areas where potential host families are less abundant, Cypripedium species<br />

must compensate for a lower chance <strong>of</strong> mycorrhizal colonization by widening the<br />

breadth <strong>of</strong> association with fungi within remaining host families. Cypripedium<br />

species appear to be resource-trackers, specializing on resources provided by a<br />

range <strong>of</strong> host fungi. This implies that Cypripedium rarity may indeed be due to<br />

mycorrhizal specialization. poster<br />

Shi, Ainong and Mmbaga, Margaret T. Tennessee State University, Nursery Crop<br />

Research Center, 472 Cadillac Lane, McMinnville, TN 37110, USA. mmmbaga@tnstate.edu.<br />

Molecular identification <strong>of</strong> the powdery mildew pathogen <strong>of</strong><br />

crape myrtle (Lagerstroemia indica) using internal transcribed spacers or<br />

rDNA. The fungus, Erysiphe lagerstroemiae, has been reported to be the causal<br />

agent <strong>of</strong> powdery mildew in crape myrtle in the United States since 1933. However,<br />

in 1979, the powdery mildew pathogen <strong>of</strong> crape myrtle in China, Japan and<br />

Australia was reported to be caused by Uncinuliella australiana. Certain features<br />

<strong>of</strong> the teliomorph <strong>of</strong> powdery mildew pathogens are used for identification. However,<br />

these structures are rarely observed on crape myrtle in Tennessee (USA). In<br />

this study, DNA analysis <strong>of</strong> the internal transcribed spacer (ITS) region <strong>of</strong> rDNA<br />

was used for the identification <strong>of</strong> the powdery mildew pathogen in crape myrtle.<br />

Polymorphic band <strong>of</strong> 666 bp amplified using primer pair ITS1/ITS4 and a band<br />

<strong>of</strong> 704 bp amplified using primer pair ITS1-F/ITS4 were obtained and sequenced.<br />

The sequence <strong>of</strong> the ITS region <strong>of</strong> 16 Tennessee isolates was identical to the sequence<br />

reported for U. australiana clearly showing that the Tennessee isolates<br />

were the same as those reported in Asia. For this work, ITS-specific primers were<br />

developed to provide pathogen diagnosis tool using the anamorphic stage which<br />

is prominent during spring and autumn. Four primer pairs and four double primer<br />

pairs were highly specific to the crape myrtle powdery mildew and did not amplify<br />

E. pulchra found on dogwoods or Microsphaera syringae-japonicae on the<br />

common lilac. Recently, the genus Uncinuliella has been changed to Uncinula<br />

and presently to Erysiphe. This study provides conclusive evidence that that E.<br />

lagerstroemiae and U. australiana are the same. Because <strong>of</strong> international nomenclature<br />

rules, the name E. lagerstroemiae take priority over U. australiana. Thus,<br />

E. lagerstroemiae (syn. U. australiana) reported in the USA is the causal agent <strong>of</strong><br />

powdery mildew pathogen in crape myrtle in mid-Tennessee and in China, Japan<br />

and Australia. poster<br />

Shirasaka, Norifumi. Laboratory <strong>of</strong> Food Microbiological Science and Biotechnology,<br />

Faculty <strong>of</strong> Agriculture, Kin-ki University, 3327-204, Nakamachi, Nara<br />

631-8505, Japan. sirasaka@nara.kindai.ac.jp. Effect <strong>of</strong> cyanocobalamin and ptoluic<br />

acid on the fatty acid composition <strong>of</strong> Schizochytrium limacinum SR21.<br />

DHA (22:6n-3), which is one <strong>of</strong> most abundant components <strong>of</strong> the brain’s<br />

structural lipids, has attracted great interest recently owing to its specific function<br />

in the brain and retina. It was reported that Schizochytrium limacinum SR21 was<br />

potent producer <strong>of</strong> DHA and the suitable conditions for DHA production was reported.<br />

Although the conditions <strong>of</strong> production <strong>of</strong> DHA were well investigated,<br />

the metabolic specificities <strong>of</strong> PUFAs are still unclear. In this study, we searched<br />

the compounds which affected fatty acid composition <strong>of</strong> Schizocytrium limacinum<br />

SR21. The structural analysis <strong>of</strong> newly detected fatty acids in the case <strong>of</strong> inhibitor<br />

addition was described putative biosynthetic pathway <strong>of</strong> fatty acid in this<br />

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