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 />
Ishiguri, Maki*, Arima, Toshihide and Morinaga, Tsutomu. <strong>56</strong>2 Nanatsukacho,<br />
Shobara-city, Hiroshima 727-0023, Japan. tmorina@bio.hiroshima-pu.ac.jp.<br />
Mechanism <strong>of</strong> fruiting body formation in Polyporus arcularius.<br />
Polyporus arcularius is basidiomycetous fungus and there are many papers<br />
inrespect to photo-induction <strong>of</strong> fruiting and nutritional aspects <strong>of</strong> mycelium. But,<br />
there are no studies about the mechanism <strong>of</strong> fruiting body formation <strong>of</strong> this fungus.<br />
Since Leonard (1971) showed that phenoloxidase (PO) was related to form<br />
the fruiting body in Schizophyllum commune, there had been many papers about<br />
PO <strong>of</strong> another mushrooms. But, it was not clear yet. We already reported about<br />
the mutants that had not PO activity in Polyporus arcularius. These mutants were<br />
called PO-TA-1 and PO-TA-2, respectively. PO-TA-1 and PO-TA-2 were<br />
homokaryon and had the opposite mating type against to each other. Also, these<br />
mutants were crossed with wild type homokaryon having an opposite mating type<br />
and could make the fruiting body. But, after the crossing between these we could<br />
not find. Namely, these homozygous PO-less dikaryon could not produce fruiting<br />
body. Therefore, we did the cloning <strong>of</strong> this P.O. gene and sequenced. And,<br />
now by using this clone, we tried northern analysis and RT-PCR after light irradiation.<br />
poster<br />
Jackson, Kimberland, Bashir, M.E. and Gunasekaran, M.* Dept. <strong>of</strong> Biology, Fisk<br />
University, Nashville, TN 37208, USA. mguna@fisk.edu. An in situ assay for<br />
glutathione reductase from permeabilized cells <strong>of</strong> Candida albicans.<br />
A procedure is described which allows the rapid permeabilization <strong>of</strong> yeast<br />
cells, Candida albicans for quantitative in situ assay <strong>of</strong> glutathione reductase<br />
(GSSGR, EC 1.6.4.2) activity. GSSGR is a flavoprotein that catalyzes the reduction<br />
<strong>of</strong> GSSG to reduced GSH using NADPH as an electron donor. It is a key enzyme<br />
in the GSH-ascorbate cycle, which provides protection against oxidation<br />
stress. Candida cells are permeabilized by incubation in buffer containing different<br />
solvents: toluene, xylene, diethyl ether, ethanol and their combinations to examine<br />
their effect on membrane permeability. In addition the effect <strong>of</strong> various<br />
temperatures and time on permeablization was investigated. The results obtained<br />
by in situ assay were compared with standard GSSGR assay carried out with cellfree<br />
extracts. Based on the results we feel that the permeation method <strong>of</strong> in situ<br />
assay is highly sensitive, specific and less time consuming. This procedure is<br />
equally applicable to fresh and frozen samples. poster<br />
Jacobson, David 1,3 *, Cornelia Boesl 2 , Shahana Sultana 2 , Till Roenneberg 2 ,<br />
Martha Merrow 2 , Rachel Adams 3 , Jeremy Dettman 3 , Margarida Duarte 4 , Isabel<br />
Marques 4 , Alexandra Ushakova 4 Patricia Carneiro 4 , Arnaldo Videira 4 , Laura<br />
Navarro-Sampedro 5 , Maria Olmedo 5 , Luis M. Chorrochano 5 , Natvig, Donald O. 6 ,<br />
and John Taylor 3 . 1 Dept. <strong>of</strong> Biological Sciences, Stanford University, Stanford,<br />
California, USA, 2 Institute for Medical Psychology, University <strong>of</strong> Munich, Germany,<br />
3 Dept. <strong>of</strong> Plant and Microbial Biology, University <strong>of</strong> California, Berkeley<br />
94720, USA, 4 Instituto de Biologia Molecular e Celular, Porto, Portugal, 5 Departamento<br />
de Genetica, Universidad de Sevilla, Spain, 6 Dept. <strong>of</strong> Biology, University<br />
<strong>of</strong> New Mexico, Albuquerque NM, USA. djjacob@stanford.edu. New findings<br />
<strong>of</strong> Neurospora in Europe and comparisons <strong>of</strong> diversity in temperate<br />
climates on continental scales.<br />
Neurospora was previously considered primarily a tropical or subtropical<br />
genus. However, recent field surveys found Neurospora occupying an entirely<br />
new ecological niche under the bark <strong>of</strong> fire-damaged trees in dry and cold habitats<br />
within a new geographic range, western North <strong>America</strong>, from New Mexico<br />
(34°N) to Alaska (64°N) (Jacobson et al. 2004 Mycologia 96:55-74). Isolates<br />
from these sites were composed predominantly (95%) <strong>of</strong> a single species, N. discreta,<br />
heret<strong>of</strong>ore the least common species <strong>of</strong> Neurospora collected. In 2003 and<br />
2004, a multinational effort surveyed southern Europe for Neurospora after unusually<br />
devastating wildfires. Neurospora was found from southern Portugal and<br />
Spain (37°N) to Switzerland (46°N). Species collected included N. crassa, N.<br />
discreta, N. sitophila, and N. tetrasperma. Although the latitude, climate and vegetation<br />
are similar to western North <strong>America</strong>, species distribution and spatial dynamics<br />
were quite different. Rather, these characteristics are more similar between<br />
southern Europe and semitropical Florida, where four different species are<br />
also present over very small spatial scales (Powell et al. 2003 Mycologia 95:809-<br />
819). These differences in regional diversity will form the basis <strong>of</strong> testable hypotheses,<br />
furthering the value <strong>of</strong> this model organism as a subject for studying<br />
fungal ecology. poster<br />
James, Timothy Y. 1 *, Vilgalys, Rytas J. 1 , Longcore, Joyce E. 2 , Mozley-Standridge,<br />
Sharon E. 3 , and the Assembling the Fungal Tree <strong>of</strong> Life Working Group.<br />
1 Dept. <strong>of</strong> Biology, Duke University, Durham, NC 27708 USA, 2 Dept. <strong>of</strong> Biol.<br />
Sciences, U. Maine, Orono, ME 04469 USA, 3 Dept. <strong>of</strong> Plant Sciences, U. Georgia,<br />
Athens, GA 30602 USA. tyj2@duke.edu. Early diverging lineages on the<br />
fungal tree <strong>of</strong> life: novel endoparasitic clades <strong>of</strong> Chytridiomycota.<br />
The basal branches on the fungal tree consist <strong>of</strong> a heterogeneous mix <strong>of</strong> taxa<br />
possessing ancestral characters such as coenocytic hyphae, reproduction through<br />
sporangia, and motile spores. How these basal taxa are related to each other and<br />
to the major radiation <strong>of</strong> the terrestrial fungi (Dikary<strong>of</strong>ungi) is unclear. Among<br />
these basal lineages are endoparasitic Chytridiomycetes with extremely reduced<br />
morphology, such as Olpidium and Rozella. In this study we address the phylogenetic<br />
arrangement <strong>of</strong> the basal lineages <strong>of</strong> Fungi and address the phylogenetic<br />
28 <strong>Inoculum</strong> <strong>56</strong>(4), August 2005<br />
position <strong>of</strong> Olpidium and Rozella using molecular sequence data from six gene regions<br />
(nuclear 18S and 28S rRNA genes, ATP6, EF1-alpha, RPB1, and RPB2).<br />
Both the Zygomycota and Chytridiomycota appear paraphyletic in most analyses.<br />
The Blastocladiales are highly diverged from the other four orders <strong>of</strong> Chytridiomycetes.<br />
Olpidium and Rozella were recovered as separate lineages in the fungal<br />
phylogeny, both distinct from previously sampled clades <strong>of</strong> chytrids. Rozella<br />
spp. are well supported as the earliest diverging lineage in rDNA and<br />
RPB1+RPB2 phylogenies. This placement <strong>of</strong> Rozella renders the Chytridiomycetes<br />
paraphyletic. contributed presentation<br />
Jeewon, Rajesh*, Yeung, Quin SY and Hyde, Kevin D. Dept. Ecology & Biodiversity,<br />
University <strong>of</strong> Hong Kong, Pokfulam Road, Hong Kong SAR, China.<br />
rrjeewon@hku.hk. Molecular pr<strong>of</strong>iling and phylogenetic diversity <strong>of</strong> fungal<br />
communities associated with pine needles.<br />
Fungal communities undoubtedly contribute immensely to plants ecosystem.<br />
This study investigates fungal diversity and succession from Pine needles<br />
(Keteleeria fortunei, Pinus elliottii and Pinus massoniana) based on morphological<br />
comparison coupled with a molecular approach based on DGGE and phylogenetics.<br />
Morphological and culture dependent studies showed that about 80% <strong>of</strong><br />
fungi were anamorphic, with Trichoderma and Cladosporium being dominant.<br />
Others include Bostrichonema, Gliocladium, Gliocephalotrichum and Paecilomyces.<br />
Two hyphomycetes, Cancellidium pinicola and Thozetella pinicola,<br />
new to science were also recorded. 40 different fungal operational taxonomic<br />
units (OTU) recovered from DGGE bands were sequenced and analysed. Phylogenies<br />
based on partial 18S rDNA sequences indicate that 32 are bitunicate ascomycetes,<br />
4 are phylogenetically related to mitosporic Letiomycetes, 2 are members<br />
<strong>of</strong> Trichocomaceae and another 2 belong to the Hypocreales and Lecanorales<br />
(lichens) respectively. Most <strong>of</strong> these fungi have not been recovered from morphological<br />
and cultural methodologies as well as from previous endophytic studies<br />
reported elsewhere. It is highly possible that many <strong>of</strong> them are very important<br />
in the decomposition process but are morphologically and culturally undetected.<br />
These findings have important scientific implications in biodiversity and ecological<br />
studies. poster<br />
Jewell, Kelsea A.* and Volk, Thomas J. Department <strong>of</strong> Biology, University <strong>of</strong><br />
Wisconsin-La Crosse, La Crosse, WI 54601, USA.<br />
jewell.kels@students.uwlax.edu. The possible biocontrol <strong>of</strong> pathogenic Candida<br />
albicans using the killer yeast Candida glabrata Y55.<br />
Candida albicans is responsible for both minor and serious mycoses, commonly<br />
termed candidiasis. These infections are difficult to treat due both to the ineffective<br />
nature <strong>of</strong> antifungal drugs and the emergence <strong>of</strong> resistant strains. It is increasingly<br />
important to identify novel antifungal therapies. One area <strong>of</strong> possible<br />
exploitation is killer yeasts. The term “killer yeasts” includes fungi in Ascomycota,<br />
Basidiomycota, or deuteromycetes that produce extracellular fungicidal or<br />
fungistatic toxins due to internal viral infections. We have performed a series <strong>of</strong><br />
competition experiments between several clinical isolates <strong>of</strong> C. albicans against a<br />
killer strain <strong>of</strong> Candida glabrata. These experiments have been aimed at determining<br />
the fungicidal and dimorphism-inhibiting ability <strong>of</strong> a killer Candida strain<br />
against C. albicans. Killing activity was determined by plating killer strains in<br />
lawns <strong>of</strong> C. albicans on media containing methylene blue dye. This dye is taken<br />
up by the yeast and released upon cell death; killing activity is indicated by areas<br />
<strong>of</strong> increased pigmentation. Killing activity was verified using the LIVE/DEAD<br />
stain under epifluoresence microscopy. Inhibition <strong>of</strong> dimorphism is determined<br />
by the changing total protein ratios <strong>of</strong> yeast and hyphal growth forms. Results indicate<br />
that there is antagonism between various strains <strong>of</strong> C. albicans and C.<br />
glabrata. contributed presentation<br />
Johnson, Desirée*, Sung, Gi-Ho and Spatafora, Joseph W. Oregon State University,<br />
Dept. <strong>of</strong> Botany & Plant Pathology, Corvallis, OR 97331, USA. johnsode@onid.orst.edu.<br />
Systematics <strong>of</strong> the genus Torrubiella.<br />
Torrubiella is a genus <strong>of</strong> ~60 species <strong>of</strong> arthropod pathogenic fungi that primarily<br />
includes pathogens <strong>of</strong> spiders and scale insects. It is characterized by the<br />
production <strong>of</strong> superficial perithecia and the absence <strong>of</strong> a stroma. Like much <strong>of</strong> the<br />
Clavcipitaceae, Torrubiella’s asci are cylindrical with thickened apices and ascospores<br />
are filiform and either remain intact or disarticulate into partspores according<br />
to species. The most common anamorphs linked to the genus include<br />
Akanthomyces, Gibellula, Paecilomyces and Verticillium. The phylogenetic relationship<br />
<strong>of</strong> Torrubiella to the rest <strong>of</strong> the Clavicipitaceae is poorly understood with<br />
leading hypotheses suggesting a link between Torrubiella and species <strong>of</strong> Cordyceps<br />
that produce superficial perithecia on poorly formed stroma (e.g., C. tuberculata).<br />
Phylogenetic placement <strong>of</strong> Torrubiella and its relationship to other members<br />
<strong>of</strong> the Clavicipitaceae were investigated via multigene phylogenetic analysis<br />
<strong>of</strong> five gene regions including SSU nrDNA, LSU nrDNA, RPB1, RPB2 and tef<br />
1-alpha. Taxon sampling included teleomorphic and anamorphic isolates and a<br />
broad representation <strong>of</strong> the Clavicipitaceae. The monophyly <strong>of</strong> Torrubiella was<br />
rejected with three main groups inferred by these analyses. The relationships <strong>of</strong><br />
Torrubiella, and its anamorphs, to Cordyceps and the Clavicipitaceae will be discussed.<br />
poster<br />
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