S. M. Badalyan, R. A. Hovsepyan, M. Iotti & A. Zambonelli

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S. M. Badalyan, R. A. Hovsepyan, M. Iotti & A. Zambonelli On the presence of truffles in Armenia Abstract Badalyan, S. M., Hovsepyan, R. A., Iotti, M. & Zambonelli, A.: On the presence of truffles in Armenia. Fl. Medit. 15: 683-692. 2005. ISSN 1120-4052. This study reports the finding of Tuber rufum, T. rapaeodorum and T. scruposum in Armenia. The morphological characters of the ascomata together with the climate, vegetation and soil features of the areas where the truffles grow are described. The ascomata were also molecularly characterized by sequence analyses from the ITS region of ribosomal DNA. Introduction The Republic of Armenia occupies an area of 29800 km 2 and is situated in the mountainous region of the South Caucasus and it is part of a region conventionally called the Armenian Highland. This is a wedge shaped portion of land between the Iranian and Minor Asiatic mountains which covers more than 300.000 km 2 and has a mean altitude of 1700 m above sea level. The neighbouring countries of Armenia are Georgia, Azerbaijan, Turkey and Iran. The climate of Armenia is characterized by the northern humid area and the southern dry area. Six climate zones are recognized: dry subtropical, dry continental, warm dry temperate, cool forest temperate, cold-mountain and sever high-mountain (Baghdasaryan 1962). The highest value of air temperature is from the Arax river valley (+ 42 C) whereas in the higher mountainous region the temperature does not rise above + 20 C with a minimum temperature of 46 C and up to 2 m of snow. The main soil types are: mountainous meadows, meadow-steppes, grey sylvan, turf carbonate sylvan, brown sylvan, black, black soils of meadows, brown, grey soils of semideserts, grey soils of irrigated meadows, flood-land - terraces soils, saline-alkaline and palaeohydromorphe cemented alkaline ground soils and ground soils near lake Sevan (Edilyan 1990). Armenia has a rich and heterogeneous flora. Approximately 3200 species of vascular plants have been described. Vegetation types include: desert, semi-desert, phryganoid (xerophyte), mountain steppes (1500-2200 m asl), subalpine meadow (2200-2800 m asl), alpine meadow (2700-4000 m asl), wetlands and forests (6-9 % of north-eastern 1900-2000 m asl) and south (2200-2400 m asl) parts of the country. The main forest-forming trees are Quercus (35 %), Fagus (32 %), Carpinus (18 %), Pinus, as well as Fraxinus and Acer (15 %) (Takhtajyan 1936).

684 Badalyan & al.: On the presence of Truffles... Studies on truffles have scientific and practical significance because of their role as the fungal partner in ectomycorrhizal associations primarily with species of the genera Quercus, Fagus, Corylus, Carpinus, Populus, Salix, Tilia and Pinus. Some of them, such as Tuber melanosporum Vittad. and T. magnatum Pico, are also economically important because of the very high prices paid for their fruiting bodies whilst T. mesentericum Vittad., T. brumale Vittad., T. aestivum Vittad., Choiromyces meandriformis Vittad. and Terfezia arenaria (Moris) Trappe, are recognized as medicinal mushrooms (Garibova 1976; Denisova 1998; Tardif 2000; Pegler & al. 1993; Pegler 2002). Up to now the only record of truffles from Armenia is Tuber aestivum Vittad. (Taslakhchyan & Nanagulyan 1988) although Armenia s geographic position, eastward the Mediterranean and northward the Middle East, would suggest that other species truffles could be present in this region. The study reported here attempts to increase the knowledge on Armenian truffles. The biotic, climatic and edaphic environmental details where truffles were found were also recorded by several Authors and such data are very important to support field investigations (Lawrynowicz 1988; Tibiletti & Zambonelli 1999; Bencivenga 2001). Material and Methods Sample collection Ascomata of truffles were collected in Armenian forests characterized by more than 10 years old trees and not less than 5 cm of humus layer. The field trips were carried out from April to October in the years 2002-2004 near Dilijan (July, 2003; August, 2004), Vanadzor (June, 2003; July, 2004), Kapan (August, 2003; June, 2004), Ijevan (August, 2004) and Megri (April, 2002) towns (Fig. 1). According to literature data (Garibova 1976; Prokhorov 1976; Pegler & al. 1993) hypogeous fungi grow commonly in sylvan ecosystems. Ascomata were sought in moist forested areas with sylvan soils, close to the possible host plants (species of Quercus, Fagus, Carpinus, Tilia, Populus, Salix, etc.). The ascomata were found by digging in soil 1-1.5 m around the trunks. The soil was dug to 30-50 cm and afterwards replaced and covered with leaf-litter. Morphological characterization Fresh samples of Tuber ascomata were preliminary described (colour, surface, smell, etc.), numbered using the first letter of location plus an accession number (e.g. K 20 ), dried and stored both in the herbarium of Laboratory of Fungal Biology and Biotechnology (FBBL), Yerevan State University (Armenia) and in the herbarium of Dipartimento di Protezione e Valorizzazione Agroalimentare (CMI-Unibo), University of Bologna (Italy). The micro-morphological characteristics of both fresh and dry ascomata were described. Part of the asomata were embedded in Tissue Tek OCT (Sakura, Zoeterwounde, Netherlands) compound and then cut with a rotary cryomicrotome (Tissue Tek II, Miles, Elkhart, IN, USA) (8-10 μm thickness). Serial sections were

Flora Mediterranea 15 2005 685 Fig. 1. Map of flora regions of Armenia (Takhtajyan 1978): 1. Upper-Akhuryan; 2. Shirak; 3. Aragats; 4. Lori; 5. Ijevan; 6. Aparan; 7. Sevan; 8. Geghama; 9. Yerevan; 10. Daralagez; 11. Zangezour; 12. Meghri. The favourable regions for growth of truffles in Armenia marked in grey: Tuber scruposum, Tuber rufum, Tuber rapaeodorum. mounted in lactic acid and observed under a microscope ECLIPSE TE 2000-E (Nikon, Tokyo, Japan). Main dimensions of the peridium cells, asci and spores were determined using Axio Vision 2.05 software (Carl Zeiss Vision GmbH, Hallbergmoos, Germany) from images captured with a DXM1200F digital camera (Nikon, Tokyo, Japan).

686 Badalyan & al.: On the presence of Truffles... Molecular analyses Molecular analysis was performed using sequence data of the ITS regions of the ribosomal DNA. Total genomic DNA was isolated from 100 μg of dehydrated ascomata tissue by DNeasy â Plant Mini Kit (QIAGEN, Hilden, Germany) according to the manufacturer s instructions. DNA was then eluted in 50 μl of sterile water. ITS-1, 5.8S and ITS-2 regions were amplified in a 50 μl volume reaction containing 1-10 ng of genomic DNA, using the primers pair ITS1 and ITS4 (White & al. 1990) in a T gradient Thermal Cycler (BIOME- TRA, Göttingen, Germany) according to Amicucci & al. (1996). PCRs were performed using 1.5 U of TaKaRa TM Taq DNA polymerase (Takara, Otsu, Japan). The amplified products were first purified by Gene Clean II kit (BIO 101, Vista, CA, USA) and then sequenced using both the primers mentioned above. Sequence reaction was performed using the ABI PRISM 3700 DNA Analyzer (Applied Biosystem, Foster City, CA, USA) with Big Dye terminator v. 3.1 chemistry. The obtained ITS sequences of ascomata were compared to those of GenBank database (http://www.ncbi.nlm.nih.gov/blast/) using the BLASTN search (Altschul & al. 1997). Ru1 species-specific primer and ITS4 were used to identify T. rufum ascomas (Iotti & al. 2005). Results Truffles were found on the northern and north-eastern slopes of mountains covered by woods of Fagus orientalis Lipsky, Carpinus betulus L., Tilia cordata Mill., Corylus avellana L., Pinus sp. In particular Fagus and Carpinus woods were investigated near to mountain streams and small rivers (Table 1). Generally the truffles were usually found in the humus-layer of sandy-clayish soils (Hovsepyan 2004). Currently, the following species of truffles have been firstly identified in Armenia: Tuber scruposum R. Hesse (Herbarium samples n. [FBBL-YSU / CMI-Unibo]: D 7 / 2192; D 3 / 2197; D 11 / 2201; D 13 / 2194; D 19 / 2207). The ascomata were found in oak-hornbeam forest (near the town of Dilijan) where the main trees are C. betulus, T. cordata and F. orientalis. Morphology of ascoma - subglobose or globose, orifice or cavity absent, 0.3-0.6 cm in diameter, yellow or ochre, smooth, peridium slightly warty, finely pubescent, colour of spore-bearing tissue brown, veins wide and sparse (Fig. 2a). Peridium 150-400 μm, pseudoparenchimatous formed of small cells 8-17 4-12 μm (Fig. 2b). External cystidia present with septa. Morphology of asci and spores - Asci globose, 50-75 45-65 μm, 2-4 irregularly clustered spores per ascus. Spores ellipsoid or subglobose, 25-40 20-25 μm, pale brown or medium brown, reticulated (Fig. 2c). Tuber rufum Pico (Herbarium samples n. [FBBL-YSU / CMI-Unibo]: K 20 / 2203). Asomata were found in hornbeam forest, in the environment of the town of Kapan, in hornbeam forest on C. avellana. Morphology of ascoma - globose, orifice or cavity absent, 0.5 cm in diameter, reddishbrown. Peridium 300-450 μm, scabrous; spore-bearing tissue brown, veins wide and

Flora Mediterranea 15 2005 687 Table 1. Favourable conditions for growth of truffles in Armenia. Fig. 2. Ascomata (a), peridium (b) and spores (c) of Tuber scruposum (Bars = 10 μm).

688 Badalyan & al.: On the presence of Truffles... Fig. 3. Ascomata (a), asci and spores (b) of Tuber rufum (Bar = 10 μm). sparse (Fig. 3a). External cystidia absent. Morphology of asci and spores - Asci saccate or globose with a short or sometimes enlonged stalk, 60-70 45-50 μm. Spores irregularly clusted, 1-5 per ascus, ellipsoid or subglobose, spiny, 25-30 20-25 μm length, with pale brown or medium brown colour (Fig. 3b). Tuber rapaeodorum Tul. (Herbarium samples n. [FBBL-YSU / CMI-Unibo]: K 24 / 2483; K 27 / 2481). Ascomata were collected in the environment of the town of Kapan, under C. betulus. Morphology of ascoma - subglobose or globose, orifice or cavity absent, 0.5-1 cm in diameter, dingy yellow and smooth (Fig. 4a). Peridium approximately 90-230 μm thick, externally pseudoparenchimatous with rounded cells 9-20 7-17 μm (Fig. 4b). External cystidia absent. Spore-bearing tissue brown, veins numerous and dense. Morphology of asci and spores - Asci globose, sometimes oval, 38-57 37-53 μm, (1)3(4) irregularly clustered spores (1)3(4). Spores ellipsoidal, 18-47 18-30 μm, pale brown or medium brown, reticulated (Fig. 4c). The accession numbers of the obtained ITS1 / ITS4 sequences of the ribosomal DNA

Flora Mediterranea 15 2005 689 Fig. 4. Ascomata (a), peridium (b) and spores (c) of Tuber rapaeodorum (Bars = 7 μm). and the results of the Blast searches are listed in Table 2. A specific 568 bp amplicon was obtained by the amplification of the ascoma K 20 / 2203 by Ru1 and ITS4 primers confirming the morphological T. rufum identification. Discussion Tuber scruposum, T. rapaeodorum and T. rufum were found associated with F. orientalis, C. betulus, T. cordata, C. avellana and Pinus sp. in northern region of Ijevan (1400 2000 m asl) and southern region of Zangezur (850 950 m asl) towns on sylvan grey, sylvan brown and sylvan turf-carbonate soils. They were most abundant in moist areas on northern and north-eastern slopes of ravines, gullies, and on the banks of small mountain rivers and streams (Fig. 1, Table 1). The ascomata of truffles recorded were always very small even when ripe. Such char-

690 Badalyan & al.: On the presence of Truffles... Table 2. Results of molecular identification of Armenian truffles. Identified species Herbarium Region, Collection Sequence Best Blast identities number town data accession YSU FBBL- CMI- Unibo number Tuber scruposum D11 2201 Dilijan 9.07.2003 DQ011845 Tuber sp., B-1667. AJ557539, identity 99.1% Tuber scruposum D7 2192 Dilijan 9.07.2003 DQ011846 Tuber sp., B-1667. AJ557539, identity 99.1% Tuber scruposum D19 2207 Dilijan 10.07.2003 DQ011847 Tuber sp., B-1667. AJ557539, identity 99.1% Tuber scruposum D13 2194 Dilijan 9.07.2003 DQ011848 Uncultured ectomycorrhiza of Tuber sp. AY634175, identity 97.4% Tuber rapaeodorum K24 2483 Kapan 13.06.2004 DQ011849 Tuber rapaeodorum, AJ557521, identity 99.6% Tuber rapaeodorum K27 2481 Kapan 13.06.2004 DQ011850 Tuber rapaeodorum, AJ557521, identity 99.6% Notes: FBBL - YSU: Fungal Biology and Biotechnology Lab, Yerevan State University; CMI-Unibo: Herbarium of the Mycological Centre of the Bologna University, Dipartimento di Protezione e Valorizzazione Agroalimentare. acter is probably due to which to the relatively dry conditions in the areas where they were collected. Besides the tendency to be immature made difficult the morphological characterization of some ascomata (D 7 / 2192, D 19 / 2207 and K27 / 2481). For the reasons stated above the use of molecular techniques is essential and the identification of these Tuber species was possible comparing their ITS sequences with those of morphologically identified ripe ascomata (D 11 / 2201, K27 / 2483). The morphological characters of the specimens D 3 / 2197, D 11 / 2201, D 13 / 2194 correspond to Hesse (1894), Ceruti & al. s (2003) and Gross s (1987) descriptions of T. scruposum. The pseudoparenchimatous peridium formed by small roundish cells is also different from Pegler & al. s (1993) description of T. rapaeodorum. The specimens identified as T. rapaeodorum and T. scruposum are morphologically different from other species of the T. borchii group (T. puberulum Berk. & Broome, T. maculatum Vittad., T. foetidum Vittad. and T. borchii Vittad.) held in the CMI-Unibo herbarium and described by

Flora Mediterranea 15 2005 691 Zambonelli & al. (2000). T. scruposum has an almost pseudoparenchimatic peridium with small cells which is different from those of T. borchii, T. dryophilum, T. foetidum, T. puberulum and T. maculatum. The ellipsoid or subglobose spores also differs from those of T. puberulum which are typically spherical. T. rapaeodorum has a very thin peridium, thinner than T. borchii, T. foetidum, T. puberulum and T. maculatum and similar to T. dryophilum. However, the external pseudoparenchimatic and internal plectenchimatic appearance does not resemble T. dryophilum which is predominantly pseudoparenchimatous. Identification of T. rapaeodorum was confirmed by comparing the ITS sequences of ribosomal DNA with those in the GenBank database (Tab. 2). Molecular identification of T. scuposum was not possible because its ITS sequence is lacking in GenBank database. ITS sequences of T. scruposum showed a high level of similarity (99.1 % of identity) only with a Tuber unidentified species. The discovery of T. scruposum in Armenia confirms Ceruti & al. s (2003) conclusions that the distribution area of this species is limited to north and central Europe. Acknowledgements SM Badalyan s participation in this work was partially supported by NATO (#FEL. RIG. 980764) and DAAD (#548. 104401.174) grants. We would like to thank Dr Ian Hall for assistance in writing the paper. References Altschul, S. F., Madden, T. L., Schaffer, A. A., Zhang, J. H., Zhang, Z., Miller, W. & Lipman, G. J. 1997: Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25: 3389-3402. Amicucci, A., Rossi, I., Potenza, L., Zambonelli, A., Agostini, D., Palma, F. & Stocchi, V. 1996: Identification of ectomycorrhizas from Tuber species by RFLP analysis of the ITS region. Biotechnol. Lett. 18: 821-826. Baghdasaryan, A. B. 1962: Brief characteristics of natural conditions of Armenia. Pp. 23-53 in: Geology of Armenian SSR, Vol. 1, Geomorphology. Yerevan. Bencivenga, M. 2001: La tartuficoltura in Italia: problematiche e prospettive. Pp. 27-29 in: Actes du V e Congrès International: Science et Culture de la Truffe, Fédération Française des Trufficulteurs. Paris. Ceruti, A., Fontana, A. & Nosenzo, C. 2003: Le specie europee del genere Tuber. Una revisione storica. Torino. Denisova, N. P. 1998: Medicinal properties of mushrooms. St. Petersburg. Edilyan, R. A. (ed.) 1990: Map of Soils of the Republic of Armenia. Yerevan. Garibova, L. V. 1976: Fungi. Pp. 316-338 in: Life of plants, 2. Moscow. Gross, G. 1987: Zu den europäischen Sippen der Gattung Tuber. Pp. 79-100 in: Derbsch, H. & Schmitt, J. A. (eds.), Atlas der Pilze des Saarlandes, 2. Saarbrucken. Hesse, R. 1894: Die hypogaeen Deutschlands. 2 Die Tuberaceen und Elaphomyceten. Halle a. S. Hovsepyan, R. A. 2004: Analyses of Armenian nature conditions favourable for growth of hypogeal fungi. Pp. 69-70 in: Proceeding of VIII Conference of Young Botanists. St. Petersburg. Iotti, M., Amicucci, A., Bonuso, E., Cerigini, E., Zambonelli, A. & Stocchi, V. 2005: Selection of specific primers for Tuber rufum ectomycorrhiza identification. Abstract in: VII Congresso Nazionale di Biotecnologie, 7-9 settembre. Siena.

692 Badalyan & al.: On the presence of Truffles... Lawrynowicz, M. 1988: Fungi (Mycota, Ascomycetes, Elaphomycetales, Tuberales). Flora Polska. Warsaw-Krakow. Pegler, D. N. 2002: Useful Fungi of the World: the Poor man s truffles of Arabia and Manna of the Israelites. Mycologist 16(1): 8-9., Spooner, B. M. & Young, T. W. K. 1993: British Truffles. A revision of British hypogeous fungi. London. Prokhorov, V. P. 1976: Fungi Pp. 201-205 in: Life of plants, 2. Moscow. Takhtajyan, A. L. 1936: Review of vegetation of Armenia. Bull. St. Geogr. Soc. 68 (3): 367-390. 1978: Earth floristic regions. Leningrad. Tardif, A. 2000: La Mycothérapie ou les propriétés médicinales des champignons. Paris. Taslakhchyan, M. G. & Nanagulyan, S. G. 1988: New for Armenian SSR taxa of ascomycetes mushrooms. Biol. J. Armenia 41: 821-827. Tibiletti, E. & Zambonelli, A. 1999: I tartufi della provincia di Forlì-Cesena. Bologna. White, T. J., Bruns, T., Lee, S. & Taylor, J. 1990: Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. Pp. 315-322 in: Innis, M. A., Gelfand, D. H., Sninsky, J. J. & White, T. J. (eds.), PCR protocol: a guide to methods and applications. San Diego. Zambonelli, A., Rivetti, C., Percudani, R. & Ottonello, S. 2000: TuberKey: a DELTA-based tool for the description and interactive identification of truffles. Mycotaxon 74: 57-76. Addresses of the authors: S. M. Badalyan, Laboratory of Fungal Biology and Biotechnology, Yerevan State University, 1 Aleg Manoogian St., 375025 Yerevan, Armenia. R. A. Hovsepyan, Laboratory of Fungal Biology and Biotechnology, Yerevan State University, 1 Aleg Manoogian St., 375025 Yerevan, Armenia. M. Iotti, Dipartimento di Protezione e Valorizzazione Agroalimentare, Università degli Studi di Bologna, via Fanin 46, 40127 Bologna, Italy. A. Zambonelli, Dipartimento di Protezione e Valorizzazione Agroalimentare, Università degli Studi di Bologna, via Fanin 46, 40127 Bologna, Italy. E-mail: zambonel@agrsci.unibo.it