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 />
at least a year. While the works in Dominican Republic and Puerto Rico have provided<br />
good information on the discomycetes <strong>of</strong> the region, more studies should be<br />
conducted on other islands, habitats and substrates. symposium presentation<br />
Carpenter, Margaret A.*, Stringer, Alison, Stewart, Alison and Ridgway, Hayley.<br />
National Centre for Advanced Bio-Protection Technologies, Lincoln University,<br />
Canterbury, New Zealand. carpentm@lincoln.ac.nz. Mycoparasitism by Trichoderma<br />
hamatum involves expression <strong>of</strong> a novel FAD-dependent<br />
monooxygenase.<br />
Biological control <strong>of</strong> fungal plant diseases by the mycoparasite Trichoderma<br />
hamatum is facilitated by the actions <strong>of</strong> a range <strong>of</strong> cell wall degrading enzymes.<br />
As mycoparasitism is a complex process, it is likely that T. hamatumuses<br />
additional mechanisms to attack its hosts. Any unknown genes involved in mycoparasitism<br />
may show changes in expression when T. hamatum makes contact<br />
with a host fungus. Subtractive hybridization was used to target T. hamatum genes<br />
up-regulated during mycoparasitism <strong>of</strong> the plant pathogen Sclerotinia sclerotiorum.<br />
One <strong>of</strong> the genes identified encoded an FAD-dependent monooxygenease.<br />
The gene product was 66 % identical to an Aspergillus flavus monooxygenase<br />
which is encoded by a gene that lies adjacent to, and may be part <strong>of</strong>, a gene cluster<br />
involved in synthesis <strong>of</strong> a mycotoxin. The T. hamatum monooxygenase gene<br />
was not expressed when T. hamatum was growing alone, nor in dual culture with<br />
itself. However when T. hamatum was grown in dual culture with S. sclerotiorum,<br />
expression <strong>of</strong> the gene was detected when the two colonies overlapped, but not<br />
prior to contact. Analysis <strong>of</strong> the promoter region <strong>of</strong> the gene revealed motifs suggesting<br />
that expression <strong>of</strong> the gene may be affected by carbon and nitrogen repression,<br />
and by pH. Gene expression in response to these factors has been investigated<br />
by northern blotting. poster<br />
Carris, Lori M. 1 * and Castlebury, Lisa A. 2 . 1 Dept. <strong>of</strong> Plant Pathology, Washington<br />
State University, Pullman WA 99164, USA, 2 USDA ARS Systematic Botany<br />
and Mycology Lab, 10300 Baltimore Ave., Beltsville, MD 20705, USA. carris@wsu.edu.<br />
Identification <strong>of</strong> species <strong>of</strong> Tilletia in U.S. wheat and grass seed<br />
exports.<br />
Tilletia controversa (dwarf bunt <strong>of</strong> wheat) is a quarantine pest with major<br />
impact on the worldwide movement <strong>of</strong> wheat and grass seed. Commonly used<br />
identification methods rely on morphological features <strong>of</strong> teliospores found in seed<br />
washes. However, teliospores <strong>of</strong> closely related species are difficult to identify<br />
based only on morphological features, and the source <strong>of</strong> spores in wheat and grass<br />
seed may be contaminating weeds. For example, in 2004 teliospores <strong>of</strong> T. bromi<br />
from Bromus tectorum (downy brome, cheatgrass), misidentified as T. controversa,<br />
were present in sufficiently high levels in some fields in the Pacific Northwest<br />
to prevent the export <strong>of</strong> that wheat to China. Similarly, shipments <strong>of</strong> Kentucky<br />
bluegrass seed (Poa pratensis) have been refused for import to China because<br />
they are contaminated with spores <strong>of</strong> T. bromi. In contrast, two putative new<br />
species <strong>of</strong> Tilletia have recently been intercepted by Chinese quarantine <strong>of</strong>ficials,<br />
one in seed <strong>of</strong> Puccinellia distans (alkali grass) from the U.S., and a second in<br />
Festuca rubra (fine fescue) from the U.S. and Lolium perenne (perennial ryegrass)<br />
from Australia. Species <strong>of</strong> Tilletia commonly encountered in wheat or grass<br />
seed shipments, including the new species from Puccinellia and Festuca/Lolium,<br />
are morphologically characterized and relationships among the weedy grass-infecting<br />
bunts and wheat bunt species are presented. poster<br />
Castlebury, Lisa A. USDA ARS SBML, 10300 Baltimore Ave, Beltsville, MD<br />
20705, USA. castlebury@nt.ars-grin.gov. The Diaporthe vaccinii complex <strong>of</strong><br />
fruit pathogens.<br />
Diaporthe vaccinii (anamorph Phomopsis vaccinii) causes twig blight and<br />
upright dieback <strong>of</strong> Vaccinium corymbosum (blueberry) and V. macrocarpon<br />
(cranberry). However, other species <strong>of</strong> Diaporthe/Phomopsis have also been reported<br />
on Vaccinium spp. In addition, isolates from a variety <strong>of</strong> hosts are reported<br />
to be closely related to D. vaccinii. Relationships among this complex <strong>of</strong> fungi<br />
were characterized with the ITS regions <strong>of</strong> the nuclear rDNA and intron regions<br />
in the actin and translation elongation factor-1 alpha genes. Four species were resolved:<br />
D. vaccinii, P. fukushii, D. allegheniensis and an as-yet unidentified<br />
species with a broad host range. In this analysis, only D. vaccinii was host specific<br />
and limited to species <strong>of</strong> Vaccinium. Authentic isolates <strong>of</strong> P. fukushii, a<br />
pathogen <strong>of</strong> Pyrus, grouped with isolates from Vaccinium, Chamaecyparis and<br />
Ulmus. Diaporthe allegheniensis from Betula was most closely related to D. vaccinii.<br />
A large group <strong>of</strong> isolates from a variety <strong>of</strong> hosts including Vaccinium, Acer,<br />
Rubus, Malus, Corylus, Glycine, Viburnum and Vitis form a separate and wellsupported<br />
species in this complex. Several isolates in this group are from specimens<br />
identified as D. eres, the type species <strong>of</strong> the genus, which has been reported<br />
to have a broad host range and variable morphology. Results <strong>of</strong> this study<br />
suggest that although certain pathogenic species in Diaporthe/Phomopsis may be<br />
host specific, many taxa in this genus will have a broad host range. poster<br />
Celio, Gail J. 1 *, Padamsee, Mahajabeen 1 , Detinger, Bryn C. 1 , McLaughlin, David<br />
J. 1 , Hibbett, David S. 2 , Lutzoni, François 3 , Spatafora, Joseph W. 4 , and Vilgalys,<br />
Rytas J. 3 . 1 Dept. <strong>of</strong> Plant Biology, Univ. <strong>of</strong> Minnesota, St. Paul, MN 55018, USA,<br />
2 Biology Department, Clark University, Worcester, MA 01610, USA, 3 Dept. <strong>of</strong><br />
Biology, Duke University, Durham, NC 27708, USA, 4 Dept. <strong>of</strong> Botany and Plant<br />
12 <strong>Inoculum</strong> <strong>56</strong>(4), August 2005<br />
Pathology, Oregon State University, Corvallis, OR 97331, USA.<br />
celio001@umn.edu. The Nucleus in the AFTOL Non-Molecular Database.<br />
Subcellular characters relating to polar structures and nuclear division have<br />
been useful for inferring evolutionary relationships since the 1960s. Nuclear division<br />
features are shared by all eukaryotes. The long evolutionary history <strong>of</strong> the<br />
Fungi has permitted diversification <strong>of</strong> nuclear division and related processes. In<br />
motile fungal cells polar structures include centrioles, while in other fungi they appear<br />
as electron-opaque spindle pole bodies (SPBs). SPBs vary among taxa in<br />
shape, position relative to the nuclear envelope, and timing <strong>of</strong> replication, migration,<br />
and spindle initiation. The nuclear envelope may remain intact, become disrupted,<br />
or disperse completely and reappear at various times during nuclear division.<br />
Several patterns <strong>of</strong> nucleolus behavior are observed during the cell cycle.<br />
Perinuclear endoplasmic reticulum and/or spindle pole body caps may be associated<br />
with dividing nuclei. The database currently contains 17 characters and 67<br />
character states from 81 species <strong>of</strong> the estimated 85,000 species <strong>of</strong> fungi. Compilation<br />
<strong>of</strong> data from published nuclear division studies reveals the need for comprehensive<br />
examination <strong>of</strong> representative species. poster<br />
Charlton, Nikki D. 1 , Carbone, Ignazio 1 , Tavantzis, Stellos M. 2 and Cubeta, Marc<br />
A. 1 *. 1 Dept. <strong>of</strong> Plant Pathology, North Carolina State University, Raleigh, NC<br />
27695-7616, USA, 2 Dept. <strong>of</strong> Biological Sciences, University <strong>of</strong> Maine, Orono,<br />
ME 04469-5722, USA. marc_cubeta@ncsu.edu. Genetic diversity and genealogical<br />
history <strong>of</strong> the M2 dsRNA mycovirus in a field population <strong>of</strong> Rhizoctonia<br />
solani anastomosis group 3.<br />
Populations <strong>of</strong> the soil fungus Rhizoctonia solani anastomosis group 3 (AG-<br />
3) (teleomorph= Thanatephorus cucumeris are genetically diverse and can harbor<br />
double stranded RNA (dsRNA) mycoviruses. Recently, Tavantzis and colleagues<br />
have demonstrated that isogenic strains <strong>of</strong> R. solani AG-3 that possess the 3.6 kb<br />
dsRNA (M2) exhibited reduced virulence on potato stems. In this study, a sample<br />
<strong>of</strong> 115 isolates from a field population <strong>of</strong> R. solani AG-3 was examined for the<br />
M2 dsRNA with reverse transcription PCR (RT-PCR). The M2 dsRNA was detected<br />
in approximately 48% <strong>of</strong> the sample. Three regions consisting <strong>of</strong> 3248 bp<br />
<strong>of</strong> the M2 dsRNA from a subsample <strong>of</strong> 11 isolates were sequenced to examine<br />
the genetic diversity and to reconstruct the genealogical history <strong>of</strong> the M2 dsRNA.<br />
Ten haplotypes were inferred for each <strong>of</strong> the three regions and mutation rates were<br />
not significantly different between these three regions. A preliminary site compatibility<br />
analysis performed using SNAP Workbench for all putative clades in<br />
the M2 mycovirus strict consensus tree identified recombination events among<br />
the clades. M2 dsRNA haplotypes and clades will be examined further to determine<br />
their relationship with phenotypic characteristics <strong>of</strong> the fungus and to design<br />
transmission experiments. contributed presentation<br />
Chatasiri, Sinchai 1 * and Ono, Yoshitaka 2 . 1 Graduate School <strong>of</strong> Science and Engineering,<br />
Ibaraki University, 2 College <strong>of</strong> Education, Ibaraki University, 2-1-1<br />
Bunkyo, Mito, Ibaraki 310-8512, Japan. herb-iba@mx.ibaraki.ac.jp. Taxonomy<br />
and phylogeny <strong>of</strong> the Puccinia hemerocallidis species complex.<br />
Puccinia hemerocallidis is a pathogen <strong>of</strong> daylily rust native <strong>of</strong> East Asia;<br />
and it has recently invaded and established in North <strong>America</strong> and Australia. The<br />
fungus has long been believed to cause plantainlily rust as well. However, P.<br />
hemerocallidis and a pathogen <strong>of</strong> plantainlily rust, once named as P. funkiae, are<br />
found distinct in host specificity in their macrocyclic life cycle and urediniospore<br />
morphology; thus, the two fungi are taxonomically separated. Puccinia patriniae<br />
and P. melanoplaca are microcylic, producing only telia/teliospores on different<br />
species <strong>of</strong> Patrinia, a spermogonial- aecial host genus <strong>of</strong> P. hemerocallidis and P.<br />
funkiae. Puccinia patriniae and P. melanoplaca are similar to P. hemerocallids<br />
and P. funkiae in teliospore morphology. These suggest monophyly <strong>of</strong> the four<br />
species and evolutionary derivation <strong>of</strong> either one <strong>of</strong> the two or both microcyclic<br />
species from either P. hemerocallids or P. funkiae. To determine possible phylogenetic<br />
relationships <strong>of</strong> the four species, ITS regions including 5.8S gene <strong>of</strong> small<br />
subunit rDNA were amplified by a PCR method, sequenced and analyzed. During<br />
the course <strong>of</strong> the study, P. melanoplaca was deleted from the consideration<br />
due to failure <strong>of</strong> rDNA amplification. The results show that the three species are<br />
monophyletic as indicated by their host specificity and teliospore morphology and<br />
indicate that P. hemerocallidis and P. funkiae had derived from a hypothetical<br />
common ancestor and P. patriniae had branched <strong>of</strong>f from a hypothetical common<br />
ancestor shared by P. hemerocallidis. symposium presentation<br />
Chavarria, Allan* and González, Maria C. Departamento de Botanica, Instituto de<br />
Biologia, UNAM, Mexico. acchs2002@yahoo.com.mx. Some freshwater mitosporic<br />
fungi from Xochimilco, Mexico City.<br />
New records <strong>of</strong> freshwater mitosporic fungi from Xochimilco, Mexico City,<br />
are described and illustrated. Sixty wood blocks (Pinus sp.) were submerged during<br />
2 months in two canals and one lagoon. All the samples were placed in plastic<br />
bags and returned to the laboratory. Collected material was washed in tap water<br />
and placed in sterile plastic boxes containing paper towels and the samples were<br />
incubated at laboratory conditions. Woody substrates were examinated periodically<br />
for the presence <strong>of</strong> fungal structures. The common recorded genera were<br />
Arthrobotrys, Phoma, Taeniollela, and Trichocladium. The present study is the<br />
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