Inoculum 56(4) - Mycological Society of America
Inoculum 56(4) - Mycological Society of America
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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