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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Main Congress Theme II: SYSTEMATICS, PHYLOGENY AND EVOLUTION Posters<br />

texture and color <strong>of</strong> mycelial mats and in fruitage ability.<br />

Some <strong>of</strong> the Lentinellus hyphal structures like clamps,<br />

gloeocystidiaes, chlamydospores, conidias, hyphal<br />

swellings, rings and incrustations were species-specific.<br />

Strains <strong>of</strong> all studied species could produce laccase,<br />

whereas tyrosinase was determined only for L. micheneri,<br />

L. ursinus and L. castoreus.<br />

755 - Group I intron evolution as mobile and nonmobile<br />

elements within the lichen-forming fungal<br />

family Acarosporaceae<br />

V. Reeb 1* , P. Haugen 2 , D. Bhattacharya 2 & F. Lutzoni 1<br />

1 Duke University - Biology, Box 90338, Durham NC<br />

27705, U.S.A. - 2 University <strong>of</strong> Iowa - Biological Sciences,<br />

Iowa City IOWA 52242, U.S.A. - E-mail: vreeb@duke.edu<br />

Autocatalytic group I introns in the nucleus are found only<br />

in ribosomal DNA genes. These genetic elements are most<br />

commonly inherited vertically although their widespread<br />

and <strong>of</strong>ten sporadic distribution suggests their ability to<br />

integrate in novel rDNA sites. Two models exist for group<br />

I intron spread: 1) intron homing facilitated by an<br />

endonuclease encoded in the intron, and 2) reversesplicing.<br />

It seems that many organellar group I introns rely<br />

primarily on homing for spread, whereas virtually none <strong>of</strong><br />

the rDNA introns contain endonucleases. To date only<br />

eight endonucleases have been reported in algae, nonlichenized<br />

ascomycetes, and amoeb<strong>of</strong>lagellates. In this<br />

paper, we study the evolution <strong>of</strong> group I introns within the<br />

lichenized ascomycete family Acarosporaceae. Group I<br />

introns are well known in the ascomycetes and are<br />

particularly abundant in the Acarosporaceae (128 in 2.5 Kb<br />

<strong>of</strong> rDNA in 35 taxa). The family Acarosporaceae appears<br />

to be one <strong>of</strong> the most basal divergences within the<br />

lichenized ascomycetes, therefore, the study <strong>of</strong> its introns is<br />

<strong>of</strong> particular interest to better understand the evolution <strong>of</strong><br />

lichen introns. We provide evidence for both relatively<br />

ancient and recently acquired group I intron lineages within<br />

the Acarosporaceae. Furthermore, we report for the first<br />

time in lichenized ascomycetes, the presence <strong>of</strong> a homing<br />

endonuclease in members <strong>of</strong> the Acarosporaceae. These<br />

endonucleases may facilitate the lateral transfer <strong>of</strong> some<br />

ascomycete group I introns.<br />

756 - The rust genus Hemileia - Monograph and<br />

collection <strong>of</strong> the characteristics in a DeltaAccess<br />

database<br />

A. Ritschel * , R. Berndt & F. Oberwinkler<br />

Chair <strong>of</strong> Special Botany/Mycology, University <strong>of</strong> Tübingen,<br />

Auf der Morgenstelle 1, D-72076 Tübingen, Germany. - Email:<br />

anja.ritschel@uni-tuebingen.de<br />

The genus Hemileia is phytoparasitic mainly on hosts<br />

belonging to the families Rubiaceae, Apocynaceae and<br />

Asclepiadaceae. The species are distributed tropically to<br />

228<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong><br />

subtropically, probably originally in Africa and Asia. By<br />

the cultivation <strong>of</strong> c<strong>of</strong>fee, however, members <strong>of</strong> the genus<br />

occur nowadays pantropically. Regarding the life cycle, so<br />

far only those for uredinia and telia are known. Hitherto, 53<br />

species <strong>of</strong> Hemileia have been described. Some <strong>of</strong> these<br />

species were described upon the uredinial stage and require<br />

nomenclatural revision. The type species Hemileia<br />

vastatrix represents one <strong>of</strong> the most important pathogens<br />

world-wide in the cultivation <strong>of</strong> c<strong>of</strong>fee and thus has great<br />

economical importance. Although there have been<br />

numerous studies on the morphology and the parasitism <strong>of</strong><br />

several Hemileia species, no monograph <strong>of</strong> the genus exists<br />

up to now. Therefore, an investigation <strong>of</strong> all Hemileia<br />

species is carried out by means <strong>of</strong> light and electron<br />

microscopy. The work is based on extensive herbarium<br />

material. The morphological data gathered are entered into<br />

a database. This database was developed within the<br />

framework <strong>of</strong> the GLOPP-project and is designed to<br />

register rust fungus biodiversity, morphological features<br />

and to allow the identification <strong>of</strong> the pathogens. Our final<br />

aim is to make this database available on the internet.<br />

757 - Molecular identification <strong>of</strong> Taphrina species<br />

parasitic on Prunus<br />

M.G. Rodrigues * & A. Fonseca<br />

CREM, SABT, Universidade Nova de Lisboa, Quinta da<br />

Torre, 2829-516 Caparica, Portugal. - E-mail:<br />

manuel.jg.rodrigues@clix.pt<br />

The dimorphic ascomycete genus Taphrina comprises ca.<br />

100 species recognised by their filamentous parasitic stage<br />

on several vascular plants. Infection symptoms may<br />

develop on leaves, fruits, shoots and flowers. Most species<br />

parasitise a single host and/or cause a specific infection<br />

symptom. The best known species is Taphrina deformans,<br />

causal agent <strong>of</strong> peach leaf curl, a disease with a pronounced<br />

impact on peach growing areas worldwide. Other<br />

economically important species <strong>of</strong> the genus Prunus are<br />

also potential Taphrina hosts, such as almond, cherry and<br />

plum trees. The present work focuses on the<br />

characterisation <strong>of</strong> Taphrina spp. on Prunus using<br />

molecular techniques: PCR-fingerprinting (MSP-PCR),<br />

sequencing <strong>of</strong> rDNA (ITS and D1/D2 regions) and DNA-<br />

DNA hybridizations. MSP-PCR proved to be a quick and<br />

reproducible method for species differentiation, allowing<br />

the selection <strong>of</strong> strains for sequencing. The D1/D2 region<br />

was too conserved to differentiate the Taphrina studied.<br />

The ITS regions were more useful for this purpose, and<br />

phylogenetic clustering <strong>of</strong> Taphrina spp. correlated with<br />

the host, geographic origin and/or the type <strong>of</strong> infection<br />

symptom. Intraspecific variability in the ITS regions was<br />

evaluated by comparison with the results <strong>of</strong> MSP-PCR and<br />

hybridization experiments. The conventional identification<br />

<strong>of</strong> the Taphrina species studied was re-evaluated in the<br />

light <strong>of</strong> the results <strong>of</strong> the molecular techniques employed.

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