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Inoculum 56(4) - Mycological Society of America

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Upadhyay, Srijana, Long, Melissa and Shaw, Brian D.* Program for the Biology<br />

<strong>of</strong> Filamentous Fungi, Department <strong>of</strong> Plant Pathology and Microbiology, Texas<br />

A&M University, College Station, Texas 77803, USA. bdshaw@tamu.edu. Protein<br />

glycosylation is essential for maintenance <strong>of</strong> hyphal growth in Aspergillus<br />

nidulans.<br />

Two temperature sensitive developmental mutants <strong>of</strong> A. nidulans have been<br />

isolated and characterized. The swoM1 mutant extends a primary germ tube that<br />

quickly losses polarity and swells to a uniform cell <strong>of</strong> approximately 20 micrometer<br />

diameter, while the swoN1 mutant is roughly wild type, with the exception <strong>of</strong><br />

numerous periodic swellings along the hyphae that give rise to multiple germ<br />

tubes leading to a hyper-branched appearance. The swoM1 mutant is fully complemented<br />

by a gene encoding a homolog <strong>of</strong> a phosphoglucose isomerase. This<br />

enzyme interconverts glucose-6-phosphate and fructose-6-phosphate. The swoN1<br />

mutant is fully restored to wild type growth when transformed with a gene encoding<br />

a GDP-mannose pyrophosphorylase. This enzyme synthesizes GDP-mannose<br />

from GTP and mannose-1-phosphate. These two enzymes are both upstream<br />

<strong>of</strong> production <strong>of</strong> Dol-P-Mannose and thus are important for protein glycosylation.<br />

Previous work with the swoA mutant defective in a protein mannosyl transferase<br />

also implicated mannoprotein synthesis in cell morphogenesis (Shaw and Momany,<br />

2002). We hypothesize that a mannosylated protein(s) is critical for proper<br />

cell wall assembly that leads to maintenance <strong>of</strong> polar growth. symposium presentation<br />

van der Merwe, Marlien M. 1 *, Maier, Wolfgang, Burdon, Jeremy J. 2 , Thrall, Peter<br />

H. 2 , Ericson, Lars 3 and Walker, John 2 . 1 CSIRO Plant Industry, Canberra, Australia,<br />

2 FABI, University <strong>of</strong> Pretoria, Pretoria, South Africa, 3 University <strong>of</strong> Umea,<br />

Umea, Sweden. marlien.vandermerwe@csiro.au. Phylogenetic relationships<br />

within the family Pucciniaceae with emphasis on Puccinia and Uromyces.<br />

The family Pucciniaceae is by far the most speciose family in the Uredinales.<br />

Within this family species numbers per genus vary dramatically among the<br />

genera with Puccinia and Uromyces having between 3000 and 4000 and over 600<br />

described species respectively with less than 8 species in most <strong>of</strong> the other genera.<br />

Thus species diversity within the family can be attributed almost exclusively<br />

to Puccinia and Uromyces. As with most rusts morphological characters do not<br />

always shed light on evolutionary relationships among the species within this<br />

family. The aim <strong>of</strong> our study is to get a deeper understanding <strong>of</strong> the evolutionary<br />

relationships among the species within this family by integrating DNA sequence<br />

data with what is known regarding host plant specificity and morphological characters.<br />

Here we use the results from two separate studies to discuss phylogenetic<br />

patterns found mainly within Puccinia and Uromyces. Sequence data from three<br />

genes, the nuc lsu rDNA, beta-tub 1 and EF 1-alpha, was generated. As has been<br />

hinted at before neither Uromyces nor Puccinia were supported as monophyletic<br />

genera with the molecular data. However all three data sets supported the division<br />

<strong>of</strong> the sampled taxa into two clades. The host plant specificities <strong>of</strong> the telial stage<br />

seem to mirror the evolutionary split <strong>of</strong> these two clades. symposium presentation<br />

Van der Nest, Magrieta A 1 , Slippers, Bernard 2 , Wingfield, Brenda D. 1 * and<br />

Wingfield, Michael J 1 . 1 Dept. <strong>of</strong> Genetics, Forestry and Agricultural Biotechnology<br />

Institute (FABI), University <strong>of</strong> Pretoria, Pretoria 0002, South Africa, 2 Dept.<br />

<strong>of</strong> Forest Mycology and Pathology, Swedish University <strong>of</strong> Agricultural Sciences,<br />

Uppsala, Sweden. brenda.wingfield@fabi.up.ac.za. Vegetative incompatibility<br />

in Amylostereum areolatum.<br />

The wood wasp, Sirex noctilio and its fungal symbiont, Amylostereum areolatum,<br />

seriously threaten pine plantations in the southern hemisphere. The genetic<br />

diversity <strong>of</strong> A. areolatum, as expressed in vegetative incompatibility (VC)<br />

groups, is limited. This is most pronounced in areas where the fungus is introduced,<br />

but also in some native environments. To explore the potential impact <strong>of</strong><br />

the introduction <strong>of</strong> new VC groups into Southern Hemisphere countries and to<br />

promote our understanding <strong>of</strong> VC in this fungus, we are investigating the genetics<br />

<strong>of</strong> vegetative incompatibility in A. areolatum. Basidiomata were collected<br />

from native European locations and single basidiospore cultures were made.<br />

These monokaryons were subjected to mating-type compatibility tests, where sexual<br />

compatibility was reflected in the formation <strong>of</strong> clamp connections. Sexually<br />

compatible monokaryons from one parent sporocarp were paired to produce sibling<br />

dikaryons. Sib-related dikaryons were also generated by pairing<br />

monokaryons from the first parent with those <strong>of</strong> a second, unrelated parent. The<br />

results <strong>of</strong> the sexual compatibility tests confirmed that A. areolatum has a typical<br />

tetrapolar mating system. VC interactions were either compatible, weakly incompatible<br />

or strongly incompatible. Approximately 25% <strong>of</strong> the interactions among<br />

the sib-related dikaryons were compatible, which indicates that a minimum <strong>of</strong> two<br />

hetloci control VC in A. areolatum. Such low numbers <strong>of</strong> VC loci are also present<br />

in other basidiomycetes (e.g. Armilaria ostoyae, Phellinus weirii and Heterobasidion<br />

annosum). Our findings also suggest that VC tests may result in an underestimation<br />

<strong>of</strong> the true genetic diversity as compatible isolates may differ<br />

genetically. poster<br />

Van Wyk, Marelize*, Roux, Jolanda, Barnes, Irene, Wingfield, Brenda D. and<br />

Wingfield, Michael J. Department <strong>of</strong> Genetics, Forestry and Agricultural Biotechnology<br />

Institute (FABI), University <strong>of</strong> Pretoria, Pretoria 0002, South Africa.<br />

marelize.vanwyk@fabi.up.ac.za. Ceratocystis tribiliformis prov. nom. a new<br />

MSA ABSTRACTS<br />

species from Sumatra, Indonesia.<br />

Two recently described Ceratocystis spp. (C. bhutanensis and C. moniliformopis)<br />

are morphologically almost indistinguishable from C. moniliformis. This<br />

similarity in morphology has led us to consider previous suggestions that C.<br />

moniliformis could represent a species complex. The aim <strong>of</strong> this study was to consider<br />

the phylogenetic relationships between isolates identified as C. moniliformis<br />

from various hosts and origins, based on comparisons <strong>of</strong> DNA sequences for three<br />

gene regions. Results showed that most <strong>of</strong> the isolates <strong>of</strong> C. moniliformis used in<br />

this study represent a well-resolved monophyletic group. However, a collection <strong>of</strong><br />

isolates initially identified as C. moniliformis, from Pinus merkusii in Sumatra<br />

resided in a distinct clade. These isolates can also be distinguished from C. moniliformis<br />

based on minor morphological features and the fungus is being described<br />

as Ceratocystis tribiliformis prov. nom. Recognition <strong>of</strong> this new species adds credence<br />

to the view that C. moniliformis includes many cryptic species and we expect<br />

that more will be identified in the future. poster<br />

Vellinga, Else C.* and Bruns, Thomas D. Department <strong>of</strong> Plant and Microbial Biology,<br />

University <strong>of</strong> California, Berkeley, Berkeley CA 94720-3102, USA. vellinga@berkeley.edu.<br />

Lepiotaceous fungi in California - diversity and phylogenetics.<br />

California is recognized as a biodiversity hotspot and lepiotaceous fungi<br />

(Agaricaceae) bear this out. Stands <strong>of</strong> endemic Sequoia sempervirens and Cupressus<br />

macrocarpa harbor an exceptional variety <strong>of</strong> this group, notably 26<br />

species in one small cypress grove south <strong>of</strong> San Francisco. Inventories during the<br />

last six years in the northern coastal part <strong>of</strong> the state have revealed approx. 70<br />

species, <strong>of</strong> which about a third are endemic, and at least 20 are new to science.<br />

The species are distinguished by morphological and molecular characters; ITS<br />

and EF1alpha have proven especially useful. Phylogenies <strong>of</strong> the family Agaricaceae<br />

as a whole with representatives from all over the world have been constructed<br />

using a variety <strong>of</strong> loci and several analytical methods. The Leucoagaricus/Leucocoprinus<br />

clade, which contains many species that fruit with the first<br />

rains at the end <strong>of</strong> the long dry summer, is the most diverse with around 40<br />

species. The Lepiota clade, with approx. 25 species, has its peak fruiting later<br />

when temperatures are lower. This reflects a universal biogeographic pattern, in<br />

which species in the Leucoagaricus/Leucocoprinus clade occur at lower latitudes<br />

and altitudes than Lepiota species. In addition, the few Chlorophyllum species in<br />

California are cosmopolitan cultivation followers, whereas the genus Macrolepiota<br />

occupies natural habitats but occurs very rarely. poster<br />

Vilgalys, Rytas J. 1 *, Moncalvo, Jean-Marc 2 , Parrent, Jerri L. 1 , O’Brien, Heath 1 ,<br />

Richter, Daniel D. 1 and Jackson, Jason L 1 . 1 Dept. <strong>of</strong> Biology and Nicholas<br />

School <strong>of</strong> the Environment and Earth and Ocean Sciences, Duke University,<br />

Durham, NC 27708, USA, 2 Royal Ontario Museum, and Department <strong>of</strong> Botany,<br />

University <strong>of</strong> Toronto, Toronto, Canada. fungi@duke.edu. Probing fungal diversity<br />

using sequence libraries: lessons from the Duke Forest <strong>Mycological</strong><br />

Observatory (DFMO).<br />

This talk will summarize results from recent culture-independent studies <strong>of</strong><br />

fungal diversity in southeastern USA Piedmont forests based in the Duke Forest<br />

(Durham, NC) and the Calhoun Experimental Forest (Sumter National Forest,<br />

SC). Analysis <strong>of</strong> ribosomal DNA sequences from soil clone-libraries reveals a<br />

diverse community <strong>of</strong> eukaryotic microorganisms dominated by fungi, and also<br />

including protistan, chlorophyte and metazoan lineages. Phylogenetic analysis <strong>of</strong><br />

ITS sequences from basidiome surveys and environmental sources, combined<br />

with data available in public databases, permits the identification to the species<br />

level for many common saprobic and mycorrhizal groups (Russula, Suillus,<br />

Mycena, Gymnopus and others). As a taxonomic reference database, the DFMO<br />

sequence collection used to study how fungal communities respond to global<br />

change. Examples include study <strong>of</strong> community shifts in response to CO 2 enrichment<br />

(FACE study), and community response to long-term land-use histories<br />

with different recovery histories (Calhoun Forest). The development <strong>of</strong> DFMO<br />

protocols also identified a number <strong>of</strong> technical problems (chimeric sequences,<br />

PCR-bias, etc.); these will be discussed. Development <strong>of</strong> new screening technologies,<br />

including RT-PCR and the use <strong>of</strong> taxon-specific primers will also be discussed.<br />

symposium presentation<br />

Voth, Peter D. 1 *, Lockhart, Ben 2 and May, Georgiana 3 . 1 Plant Biological Sciences<br />

Graduate Group, 2 Dept. <strong>of</strong> Plant Pathology, and 3 Dept. <strong>of</strong> Ecology, Evolution, and<br />

Behavior; University <strong>of</strong> Minnesota, St. Paul, MN, USA. voth0016@umn.edu.<br />

Population dynamics <strong>of</strong> a fungal virus across the <strong>America</strong>s.<br />

Fungal viruses appear to be ubiquitous throughout Fungi, <strong>of</strong>ten persisting<br />

with no detriment to the host. All mycoviruses have no extracellular stage and are<br />

transmitted only through cytoplasmic fusion <strong>of</strong> host cells. Symbiotic interactions<br />

strongly affect the evolutionary trajectory <strong>of</strong> each other and are important in structuring<br />

communities. One such symbiosis is that <strong>of</strong> Ustilago maydis, Ustilago<br />

maydis Virus H1 (UMV- H1), and Zea mays. Ustilago maydis, commonly known<br />

as corn smut, causes infections on vegetative and reproductive tissues <strong>of</strong> corn.<br />

UMV- H1 is vertically transmitted during mating <strong>of</strong> U. maydis individuals and,<br />

thus, the population dynamics <strong>of</strong> U. maydis can affect the population structure <strong>of</strong><br />

Continued on following page<br />

<strong>Inoculum</strong> <strong>56</strong>(4), November 2005 61

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