FULL POSTER SESSION ABSTRACTSDurham, NC; 2) Department of Plant Pathology, North Carolina State University, Raleigh NC; 3) School of Plant Sciences, University of Arizona, Tucson AZ;4) Department of Ecology, Evolution, and Behavior, University of Minnesota, St. Paul, MN.Many foliar fungal endophytes are transferred horizontally among plant hosts and exhibit various degrees of host specificity. For example, endophyticLophodermium species (Rhytismatales) are commonly found in needles of certain pine species but infrequently in broad leaves of angiosperm hosts. Suchendophytes may have populations or subspecies that are genetically structured according to their host preference, climate regimes or geographic ranges,which might be associated with increased fitness for plants hosting specific mutualistic endophytic fungi. Hence, we set out to explore the populationstructure of Lophodermium spp. within mature foliage of loblolly (Pinus taeda) and Virginia pine (Pinus virginiana) in southeastern U.S., covering hostranges from the mountains of Appalachia to the coasts of the Atlantic. We analyzed the nuclear ribosomal internal transcribed spacer (ITS1/5.8S/ITS2) andthe intragenic spacer (IGS) regions as well as three protein-coding genes (actin, calmodulin, chitin synthase I) of the isolated Lophodermium strains. Thesein-depth population genetic analyses of endophyte species provide insight into the capacity of multilocus genetic markers that resolve on differentevolutionary time scales to capture sub-species level structure and to identify criteria for species delimitation. This multilocus analysis identified a rarecryptic species, which possibly explains the high genetic diversity of the Lophodermium spp. Genetic and geographic distance were correlated in the rarecryptic species, but not in the common species. We found no evidence for host species preference for the cryptic species vs. the common species. Ourfindings suggest that genetic exchange and recombination can be limited by dispersal if the species is rare.686. <strong>Fungal</strong> pathogen and endophyte genetics within the context of forest community dynamics. M.-S. Benitez 1 , M. H. Hersh 2 , L. Becker 1 , R. Vilgalys 3 , J. S.Clark 1,3 . 1) Nicholas School of the Environment, Duke University, Durham, NC; 2) Department of Biology, Eastern Michigan University, Ypsilanti, MI; 3)Department of Biology, Duke University, Durham, NC.<strong>Fungal</strong> pathogens play important roles in forest community dynamics, particularly through negative-density dependent regulation. Negative-densitydependence regulation is hypothesized to be regulated by the presence of host-specific pathogens. Studies on forest pathogens, however, indicate thepredominance of generalist seedling pathogens, capable of infecting more than one host species. To understand the mechanisms through which“generalist” pathogens contribute to forest-community dynamics we conducted extensive surveys of seedling pathogens in temperate hardwood forestsof the eastern U.S.A. Species in the genera Colletotrichum and Ilyonectria were among the most commonly isolated and recovered amplicon sequencefrom seedlings of multiple host species showing disease symptoms. Further, co-infection by both Colletotrichum and Ilyonectria species decreases hostsurvival, as quantified by posterior model probabilities. To investigate molecular mechanisms associated with multi-host generalism and co-infection, andto determine whether these “generalist” pathogens are distinct species or species-complexes, the genomes of three common species in our dataset (e.g.C. fioriniae, C. gloesporoides and Ilyonectria europea) were sequenced. The largest genome of the three belonged to Ilyonectria at 63.66 Mb, which alsocontained the highest number (22,250) of genes. The smallest genome belonged to C. fioriniae with 50.04 Mb and 15,777 genes. Genome size and numberof predicted genes appears expanded, confirming their role as seedling pathogens. For instance, three out of four polysaccharide lyase (PL) enzymedomains found in fungal genomes, are enriched in these three species. PL enzymes are relevant in plant pathogenicity since they may contribute to initialstages of host penetration. The genome sequence of these fungal groups will serve as a reference set for population level studies to address hostspecificityand local adaptation within our isolate database.687. Discovery of Sexual Reproduction in the Black Aspergilli. Heather L. Darbyshir 1 , Peter JI. van de Vondervoort 2 , Paul S. Dyer 1 . 1) School of Biology,University of Nottingham, Nottingham, NG7 2RD United Kingdom; 2) DSM Biotechnology Center, PO Box 1, 2600 MA Delft, The Netherlands.The black aspergilli are members of the genus Aspergillus that are typically characterized by the production of dark or black asexual conidia (classified assection Nigri). The group includes Aspergillus niger, which is of particular industrial importance because of its safe use status and ability to produce a widerange of enzymes and organic acids. All members of the black aspergilli have previously only been known to reproduce by asexual means. However, as aresult of combined molecular and cultural experimental studies it can now be revealed that at least one member of the black aspergilli, Aspergillussclerotiicarbonarius, is able to complete a sexual cycle. Wild type isolates of A. sclerotiicarbonarius were found to retain the ability to form sclerotia,structures associated with both dormancy and sexual reproduction, and strains of complementary MAT1-1 and MAT1-2 could be identified based on thepresence of mating-type genes. Crossing strains of opposite mating type, and an extended period of incubation, resulted in the production of sclerotiacontaining multiple ascocarps, with asci and viable ascospores, within the matrix of a sclerotium. This is consistent with past studies of phylogeneticallyrelated species in the Aspergillus section Flavi (teleomorph genus Petromyces). Progeny analysis is being undertaken based on data arising fromcomparative genome sequencing of parental isolates, mating-type distribution and phylogenetic analysis. The discovery of a heterothallic sexual cycle in A.sclerotiicarbonarius provides insights into the evolution of asexuality in the black aspergilli. It is hoped that ongoing molecular genetic studies into theearly sexual morphogenesis may provide an insight into the regulation of sexual reproduction in the black aspergilli.688. Culture-based survey of soil fungi from bat hibernacula. Jeffrey M. Lorch 1 , Daniel L. Lindner 2 , Andrea Gargas 3 , Laura K. Muller 4 , Andrew M. Minnis 2 ,David S. Blehert 4 . 1) University of Wisconsin - Madison, Madison, WI, USA; 2) US Forest Service, Northern Research Station, Center for Forest MycologyResearch, One Gifford Pinchot Drive, Madison, WI, USA; 3) Symbiology LLC, Middleton, WI, 53562, USA; 4) US Geological Survey - National Wildlife HealthCenter, Madison, WI, USA.Bat white-nose syndrome (WNS), a fungal disease now spreading in eastern North America, is causing unprecedented mortality among hibernating bats.To investigate fungal communities present in bat hibernacula, we identified culturable fungi present in soil samples from 24 bat hibernation sites in theeastern United States. Isolates were characterized by sequencing regions of ribosomal DNA (internal transcribed spacer and partial intergenic spacer). Weisolated Geomyces destructans from soil samples collected in hibernacula within the known range of WNS, and we found a wide diversity of Geomycesspecies, comprising around one third of all isolates. Many of these Geomyces species, along with numerous potentially novel lineages, appear to beundescribed.Other Topics689. Understanding the cellular basis of Azole resistance in Aspergillus fumigatus. Michael J. Bromley, Marcin Fraczek, Rebecca Collins, Emma Davies,Paul Bowyer. Translational Med, Univ Manchester, Manchester, United Kingdom.Resistance of Aspergillus fumigatus to the azole class of antifungals is becoming a major problem in Europe and is being driven by two factors, theprolonged exposure (several months to several years) of patients to azoles and the extensive use of agricultural azoles driving environmental resistance.Our understanding of the mechanisms that govern azole resistance in filamentous fungi is limited. While some clinical resistant isolates harbor mutations290
FULL POSTER SESSION ABSTRACTSin the azole target, lanosterol 14 a-demethylase (cyp51A), more than 50% do not. We have used a combination of whole genome sequencing,transcriptomics, transposon based mutagenesis and high throughput directed mutagenesis to identify novel mechanisms that may explain the resistanceobserved in these strains. I will summarize and discuss our progress to date and present a worrying mechanism that results in both pan-azole andamphotericinB resistance.690. Chemically Induced Haploinsufficiency Screens to Identify Drug Mechanism of Action in Aspergillus Fumigatus. D. A. Macdonald 1 , A. E. Johns 1 , M.Eberle 2 , P. Bowyer 1 , D. Denning 1 , M. J. Bromley 1 . 1) Institute of Inflammation and Repair, Respiratory & Allergy Centre, University of Manchester,Manchester, United Kingdom; 2) Applied Microbiology, Institute for Applied Life Sciences, University of Karlsruhe, Hertzstrae 16, 76187 Karlsruhe,Germany.Current drugs used to treat Aspergillus infections are limited and suffer from a variety of shortcomings including low efficacy, toxicity and increasingresistance. Despite the discovery of numerous promising drug targets, few lead compounds have been discovered by target based approaches. This can beexplained, in part, by the ‘druggability’ of a target as some compounds which demonstrate promising activity against an enzyme are not active against thewhole cell or are toxic to humans. Consequently most of the antimicrobials presently on the market were originally discovered by random screening ofcompounds against whole cell screens. A solution to this problem is to identify gene targets utilizing compounds that already show antifungal activity andhave clean toxicity profiles.Chemical genetic profiling aids identification of drug mechanism of action as a diploid strain lacking a single copy of a drug’s target is hypersensitive tothat drug. Heterozygote S. cerevisiae and C. albicans libraries have been used to identify the mechanism of action of several promising compounds;however, this has been hindered in A. fumigatus by the complexity in generating an adequate set of heterozygous strains. A high-throughput targetedgene KO method for A. fumigatus has been established by employing fusion-PCR to generate targeted gene disruption cassettes, optimizing the commontransformation protocol for A. fumigatus high-throughput gene disruption, and utilising a diploid Ku80 - /Ku80 - mutant to facilitate more reliablehomologous recombination. Preliminary efforts have produced 46 heterozygous KO strains and subsequently, the feasibility of chemical genetichaploinsufficiency studies in filamentous fungi has been demonstrated with several compounds. High-throughput methods of chemical genetic profiling bypooling multiple heterozygous KO strains into a single culture is currently being validated and preliminary data is promising. This will enable highthroughputmethods for surveying the genome of A. fumigatus for new drug targets and supports unveiling the mechanisms of action of antifungal drugs.691. Antifungal Pisum sativum defensin 1 Induces a non-Apoptotic Death in Aspergillus nidulans. Caroline M Fernandes 1 , Luciano N Medeiros 1 , Landi VGCostilla 1 , Hilda Petrs-Silva 1 , Patrícia A de Castro 2 , Gustavo H Goldman 2 , Eleonora Kurtenbach 1 . 1) Federal University of Rio de Janeiro, Rio de Janeiro, Rio deJaneiro, Brazil; 2) Sao Paulo University, Ribeirao Preto, Sao Paulo, Brazil.Psd1 is a basic, cysteine-rich plant defensin isolated from Pisum sativum seeds which inhibits the growth of a broad range fungi species. Defensins arealso non-toxic to mammalian cells, highlighting their potential as antifungal drugs. We have shown that FITC-labelled Psd1 was internalized in F. solanihyphae, interacting with cyclin F and leading to fungal cell cycle arrest. This internalization seemed to be dependent of glucosylceramide (CMH, ofcerebroside monohexoside), once C. albicans cells lacking the ceramide synthase are 25 % less susceptible to Psd1 than the parental strain. <strong>Fungal</strong> andmammalian CMH are structurally divergent, as the former presents a C8-unsaturation and C9-methylation on the sphingoid base, which could possiblydrive Psd1 selectivity. In this work, we investigated the cell death mechanisms triggered by Psd1 in Aspergillus nidulans and the contribution of CMHstructure to Psd1-induced fungal death. We characterized, through fluorescence microscopy, several apoptotic events, such as intense formation ofreactive oxygen species (ROS), metacaspase activation and DNA strand breaks. Although A. nidulans hyphae treated with 20 mM Psd1 for 24 hoursexhibited severe cell injury, no apoptosis-phenotype was observed. We also investigated whether Psd1 incubation would lead to membranepermeabilization typical of a necrotic death. To this, A. nidulans cells were maintained in the presence or absence of the peptide and the membranedamage was evaluated through Propidium Iodide (PI) staining. We observed 15 % PI positive cells in the suspension treated with Psd1, in contrast to 2 % incontrol culture. To investigate the role of fungal CMH and its structural modifications to Psd1-induced cell death, we constructed strains lacking theglucosylceramide synthase (ANID_08806), sphingolipid DD8-desaturase (ANID_04592) and sphingolipid C9-methylase (ANID_05688 and ANID_07375)genes. Phenotype analysis showed impaired growth of strains deficient in ANID_08806 and ANID_04592 in comparison to the parental strain. Furtherinvestigation will be conducted to characterize Psd1 antifungal activity and apoptosis or necrosis induction in the mutant strains. Unraveling themechanisms of cell death induced by antifungal peptides may lead to the identification of new targets that drive antimycotic selectivity.692. Is fungal secondary metabolism regulated by competing insects? Annika Regulin 1 , Nancy Keller 2 , Frank Kempken 1 . 1) Department of Botany,Christian-Albrechts University, Kiel, Germany; 2) Department Medical Microbiology and Immunology, Dept of Bacteriology, UW-Madison, USA.Fungi synthesize an astonishing variety of secondary metabolites, some of which belong to the most toxic compounds in the living world. Even thoughlittle is known about the benefit of these metabolites, the ability to regulate the secondary metabolism might be seen as an evolutionary adaptation.Presumably fungi regulate secondary metabolites (e.g. mycotoxin) in response to confrontation with natural competitors like insects to guarantee efficientexploitation of environmental resources (1-3). Admittedly it should be mentioned that secondary metabolites are not the only defence mechanisms offungi (4). In order to enlighten the biological function of these secondary metabolites with reference to chemical defence reactions of insect-fungalinteractions, we utilized complementary approaches of experimental ecology and functional genomic techniques. The vinegar fly Drosophila melanogasterand its natural antagonist Aspergillus nidulans are used as an ecology model system. To analyse fungal up- or down regulated target genes in theinteraction of A. nidulans with Drosophila larvae microarray analysis was performed. This led to the identification of secondary metabolite genes up- ordown-regulated under these conditions. Quantitative RT-PCR was employed to analyze secondary metabolite gene expression at different time points.<strong>Fungal</strong> single, double and triple mutations of identified up-regulated genes are currently analyzed in confrontation assays to identify potentialmodifications in gene expression and the survival rate of larvae concerning to chemical defense reaction of fungus-insect interaction compared to wildtype. This could reveal insights about the biological function of secondary metabolite genes and clusters such as stc and mdp.(1.) Rohlfs, M., Albert, M., Keller, N. P., and Kempken, F. (2007) Biol Lett 3, 523-25. (2.) Kempken, F., and Rohlfs, M. (2010) <strong>Fungal</strong> Ecol 3, 107-14. (3.)Rohlfs, M., Trienens, M., Fohgrub, U., and Kempken, F. (2009) in "The Mycota XV. (Anke, T., Ed.), Springer Heidelberg, New York, Tokyo, pp. 131-51 (4.)Kempken, F. (2011) Mol Ecol 20, 2876-77.693. Eisosome distribution and localization in the meiotic progeny of Aspergillus nidulans. A. Athanasopoulos 1 , H. Boleti 2 , C. Scazzocchio 3 , V.Sophianopoulou 1 . 1) Institute of Biosciences and Applications, Microbial Molecular <strong>Genetics</strong> Laboratory, National Center for Scientific Research,Demokritos (NCSRD), Athens, Greece; 2) Intracellular Parasitism Group, Molecular Parasitology Laboratory, Department of Microbiology and Light<strong>27th</strong> <strong>Fungal</strong> <strong>Genetics</strong> <strong>Conference</strong> | 291
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