Book of Abstracts (PDF) - International Mycological Association
Book of Abstracts (PDF) - International Mycological Association
Book of Abstracts (PDF) - International Mycological Association
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IMC7 Main Congress Theme II: SYSTEMATICS, PHYLOGENY AND EVOLUTION Posters<br />
745 - Characterization <strong>of</strong> Laetiporus sulphureus<br />
complex in Japan using phylogenetic analyses,<br />
morphological study and incompatibility tests<br />
Y. Ota * & T. Hattori<br />
Forestry and Forest Products Research Institute, Tsukuba,<br />
305-8687, Japan. - E-mail: yuota@ffpri.affrc.go.jp<br />
Phylogenetic analyses, morphological studies and<br />
incompatibility tests were conducted to define intra-generic<br />
taxa <strong>of</strong> Japanese Laetiporus sulphureus complex.<br />
Phylogenetic analyses based on the nucleotide sequences <strong>of</strong><br />
the ITS regions <strong>of</strong> the ribosomal DNA and beta-tubulin<br />
gene suggest that Japanese Laetiporus spp. are divided into<br />
four distinct groups (groups A-D). European population <strong>of</strong><br />
L. sulphureus is clearly distinct from all Japanese groups.<br />
Each group shares similar morphological characteristics<br />
and host range (conifers vs. hardwoods). Group A has a<br />
white pore layer, pinkish orange pileus surface, and<br />
imbricated pilei. This group is distributed in the cooltemperate<br />
area and associated with hardwoods. Group B<br />
has lemon yellow pore layer, pinkish orange pileus surface,<br />
and imbricated pilei. This group is associated with conifers.<br />
Group C has a lemon yellow pore layer, yellow pileus<br />
surface and non-imbricated pilei. Sometimes it produces<br />
semi-globose basidiocarps with abundant chlamydospores<br />
in the context. Group C is distributed in the warmtemperate<br />
area <strong>of</strong> central parts <strong>of</strong> Japan. Group D has a<br />
lemon yellow pore layer and pinkish orange to yellow<br />
pileus surface. This group also produces semi-globose<br />
form. This group is distributed in the warm-temperate to<br />
subtropical areas <strong>of</strong> southern part <strong>of</strong> Japan. Single spore<br />
isolates from groups A, B and C were incompatible each<br />
other, which revealed that L. sulphureus complex in Japan<br />
is composed <strong>of</strong> at least three species.<br />
746 - Penicillium tulipae and P. carotae, two new species<br />
belonging to the series Corymbifera<br />
D.P. Overy * & J.C. Frisvad<br />
Mycology Group, Bio-Centrum, DTU, Building 221,<br />
Danish Technical University, DK-2800, Kgs. Lyngby,<br />
Denmark. - E-mail: do@biocentrum.dtu.dk<br />
Taxa <strong>of</strong> the Penicillium series Corymbifera are known for<br />
their synnemata and association with the rhizosphere <strong>of</strong><br />
vegetables, most commonly with bulbs. The known species<br />
P. allii, causing a storage rot <strong>of</strong> garlic, P. hordei, associated<br />
with cereals, and P. hirsutum associated with a variety <strong>of</strong><br />
vegetables can easily be separated based on colony<br />
morphology. The concepts <strong>of</strong> P. albocoremium and P.<br />
venetum, reported to cause a severe bulb rot on a variety <strong>of</strong><br />
commercially grown flower and Allium species, later<br />
evolved from P. hirustum senso lato as a response to<br />
apparent differences in secondary metabolism. Further<br />
secondary metabolite investigations involving P.<br />
albocoremium indicated the potential presence <strong>of</strong> two or<br />
more taxa. Described here using micromorphology, colony<br />
characteristics on various media and chemotaxonomic<br />
pr<strong>of</strong>iling are P. albocoremium sensu stricto and two new<br />
species, P. tulipae and P. carotae, which were resolved<br />
during a taxonomic survey <strong>of</strong> P. albocoremium isolates<br />
contained within the IBT culture collection. Although these<br />
novel taxa are micromorphologically quite similar, their<br />
unique secondary metabolite pr<strong>of</strong>iles individually<br />
distinguish them from isolates <strong>of</strong> P. albocoremium.<br />
Moreover, these bulb associated species produce the<br />
following mycotoxins: citrinin, penicillic acid and terrestric<br />
acid by P. carotae and penitrem A and terrestric acid by P.<br />
tulipae.<br />
747 - Cladistic biogeography <strong>of</strong> Lignincola laevis<br />
(Halosphaeriales, Ascomycota)<br />
K.L. Pang 1* , E.B.G. Jones 2 , L.L.P. Vrijmoed 3 & R.Y.C.<br />
Kong 3<br />
1 School <strong>of</strong> Biological Sciences, University <strong>of</strong> Portsmouth,<br />
King Henry Building, King Henry I Street, Portsmouth<br />
PO1 2DY, England, U.K. - 2 BIOTEC, National Centre for<br />
Genetic Engineering and Biotechnology, 113, Thailand<br />
Science Park, Paholyothin Road, Klong 1, Klong Luang,<br />
Pathumthani, 12120, Thailand. - 3 Department <strong>of</strong> Biology<br />
and Chemistry, City University <strong>of</strong> Hong Kong, 83 Tat Chee<br />
Avenue, Kowloon Tong, Hong Kong, China. - E-mail: kalai.pang@port.ac.uk<br />
Partial large subunit and the ITS regions <strong>of</strong> the ribosomal<br />
DNA <strong>of</strong> ten Lignincola laevis strains, which were isolated<br />
from different geographical locations, substrata and habitat,<br />
were sequenced and subjected to phylogenetic analysis to<br />
determine their genetic difference. These strains do not<br />
form distinct geographical groupings. No correlation was<br />
discovered between strains and habitat as freshwater and<br />
marine water isolates <strong>of</strong> L. laevis form a coherent and wellsupported<br />
group. Strains isolated from mangroves form a<br />
robust clade while isolates from other substrata constitute<br />
others. Different genes infer different phylogeny for two L.<br />
laevis strains. These results suggest that ascospores (asci)<br />
<strong>of</strong> L. laevis may be able to disperse over long distances.<br />
More strains from wider geographical locations, different<br />
habitats (freshwater, brackish water and marine water) and<br />
different substrata should be explored to explain the current<br />
distribution pattern and evolution <strong>of</strong> aquatic fungi.<br />
748 - Phylogenetic relationships <strong>of</strong> Hydnodon Banker<br />
V. Patiño-Conde 1* , D. González 2 , J. Cifuentes 1 , M.<br />
Villegas 1 & R. García-Sandoval 1<br />
1 FCME Herbario, UNAM., PO Box 70-399, Cd.<br />
Universitaria, CP 04510, DF., Mexico. - 2 Sistemática<br />
Vegetal, Instituto de Ecología AC, PO Box 63, Xalapa, CP<br />
91000, Veracruz, Mexico. - E-mail:<br />
viole_pconde@correo.unam.mx<br />
<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 225