Handbook Part 2 - International Mycological Association
Handbook Part 2 - International Mycological Association
Handbook Part 2 - International Mycological Association
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PS5-575-0841<br />
Comparisons between the rust flora of Tibetan East Himalaya and the rust floras of India, Nepal and<br />
Pakistan<br />
J.Y. Zhuang<br />
Institute of Microbiology, Academia Sinica, Beijing, China<br />
The rust flora of Tibetan East Himalaya is characterized by the predominance of eastern Asian species. One hundred<br />
twenty-nine species, amounting to 55.4% of the total known species in the region, are in common with the rust species<br />
of Japan.<br />
Tibetan East Himalaya adjoins Indian subcontinent and geologically is situated at the suture line connecting Indian<br />
plate with Eurasian plate. The penetration of Indian-Malaysian floristic component to the Tibetan Himalaya is<br />
unavoidable. The southern slope of East Himalaya has a climate effected deeply by the monsoon from Indian Ocean<br />
and an abundant rainfall and a rich vegetation presenting sight of tropical rain forest are suitable for survival of rust<br />
fungi from India. Seventy-four rust species, amounting to 31.8% of the total known species in Tibetan East Himalaya,<br />
are in common with the rust species of India. It is worth mentioning that the primeval forest in the south to Medog<br />
adjacent to India is still inadequately explored. The Indian rust flora is exceedingly luxuriant, containing a number of<br />
phylogenetically primitive monotypic and small genera such as Arthuria, Chrysocelis, Hiratsukamyces, Masseeëlla,<br />
Phragmidiella, etc. which are still not known in Tibetan East Himalaya. The distribution of their host plants suggests that<br />
they are probably present in the tropical forest of the region and yet await the collectors.<br />
Situated in Central Himalaya, Nepal is relatively similar to East Himalaya in forest vegetation. Comparison between the<br />
rust flora of Tibetan East Himalaya and that of Napalese Himalaya shows some similarities. There are 61 species in<br />
common, amounting to 26.2% of Tibetan East Himalayan total. The abundance of East Asian species suggests that the<br />
Nepalese rust flora is a continuation of the East Himalayan rust flora.<br />
Pakistan is of generally typical climate of subtropical steppe and desert. The Himalayas, Karakoram Mts. and Pamir<br />
Plateau occupy the northern part of the country. The rust flora is quite different from that of the other parts of Himalaya.<br />
There are about 200 known species belonging to some 20 genera. Only 36 rust species in Tibetan East Himalaya,<br />
amounting to 15.5% of the total, are in common with the rusts of Pakistan. The tropical genera commonly found in East<br />
Himalaya such as Gerwasia, Hamaspora, Maravalia and Ravenelia are rare or not found in the vast areas of Pakistan<br />
inland. The connexion between the rust flora of Tibetan East Himalaya and that of Pakistan seems very weak.<br />
PS5-576-0861<br />
Metabolic and molecular biodiversity – evidence from a survey of New Caldedonian Fungi and New<br />
Zealand Xylariaceae<br />
M Stadler 1, JM Seng 3, S Buchet 2, HG Wetzstein 4<br />
1 InterMed Discovery GmbH, BioMedizinZentrum, 44227 Dortmund, Germany, 2 BIOtransfer, 41 rue Emile Zola, -, 93100<br />
Montreuil, France, 3 Laboratoire de Phytopathologie Moléculaire, Université de Paris-Sud , centre d’Orsay, Institut de<br />
Biotechnologie des Plantes ( IBP ), 91405 Orsay Cedex, France, 4 Bayer HealthCare AG, Div. Animal Health, Research<br />
& Development, 51368 Leverkusen, Germany<br />
Much work has been dedicated to fungal biodiversity inventories, using traditional morphology, and meanwhile even<br />
molecular approaches. The “innovative potential” of tropical fungi with respect to the discovery of novel secondary<br />
metabolites and other innovative products for application in the Biotech industry was advertised repeatedly. However,<br />
most of the lead compounds ever derived from fungi have been originally discovered from temperate species! There<br />
are only few exceptions, such as nodulisporic acid from a group of pantropically distributed endophytes [1]. We have<br />
attempted to correlate molecular and morphological data on species abundance vs. diversity of secondary<br />
metabolite production in fungi from tropical and temperate climates and wish to present results of two different<br />
projects.<br />
a) A study on the xylariaceous genus Hypoxylon based on HPLC profiling [2] revealed an essentially redundant<br />
secondary metabolism in many of their species, independent from differences in molecular and morphological traits.<br />
In contrast, several apparently rare or endemic Hypoxylon spp. from New Zealand and the temperate Northern<br />
hemisphere were found to contain unprecedented metabolites. Most of the New Zealand fungi studied that produce<br />
specific metabolites were found from islands or other isolated areas.<br />
b) During a survey of New Caledonian fungi from different habitats, carried out by a combination of molecular and<br />
chemical methodology (comparison of ITS nrDNA and dereplication by HPLC profiling), we found that about 35 % of<br />
the isolates contained several metabolites whose spectral data did not match with the entries of commercial<br />
secondary metabolite databases, and with a proprietary HPLC-MS library. The ITS nrDNA and HPLC data correlated<br />
very well; groups of strains with redundant DNA sequences generally showed similar HPLC profiles. It was occasionally<br />
even possible to predict metabolite production by the molecular data and chemotaxonomic information. Some<br />
strains from public collections whose sequences were retrieved from GenBank by BLAST searches showed similar HPLC<br />
profiles as the wild type isolates.<br />
=> Attaining quality assurance by molecular phylogeny appears ideal to identify redundancies prior to screening,<br />
especially if and when microscopic/cultural characters do not allow for an effective morphological dereplication.<br />
[1] J. Polishook et al. (2001) Mycologia 93: 1125–1137.<br />
[2] V. Hellwig et al. (2005) Mycol Progr 4: 39–54.<br />
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