Report of Biscogniauxia nummularia as pathogenic agent of charcoal canker disease of beech (Fagus orientalis) from Iran

Document Type : Short paper

Authors

1 Assistant Professor, Research Institute of Forests and Rangeland, Agricultural Research, Education and Extension Organization (AREEO), Tehran, Iran.

2 Researcher, Research Institute of Forests and Rangelands, Agricultural Research Education and Extension Organization (AREEO), Tehran, Iran

3 MSc, Natural Resources and Watershed Management Organization, Tehran, Iran

4 Prof., Iranian Research Institute of Plant Protection, Agricultural Research Education and Extension Organization (AREEO), Tehran, Iran

10.22092/ijfrpr.2024.364708.1611

Abstract

Background and objectives:     Beech trees (Oriental beech: Fagus orientalis Lipsky.), native to Hyrcanian forests of Iran, are considered as one of the most valuable forest tree species in the north of the Iran. Biscogniauxia nummularia (Bull.) Kuntze is an endophytic fungus which acts as a pathogenic fungus under favorable conditions and causes strip-cankers (commonly known as charcoal canker) in Fagus species. The disease occurs in tree hosts affected by stress. High temperatures and summer droughts are favorable conditions for causing and distributing this disease in the forest.
Methodology: During the field surveys across the beech forests of Sangdeh region in Mazandaran province, beech trees with severe symptoms of charcoal canker were observed. The most visible symptoms of the disease in the form of round spots to black stripes on the trunk and branches, as well as dieback of the beech tree branches in the area. Several samples were collected from infected parts of oriental beech trees and transferred to the plant pathology laboratory. Microscopic slides of the fungal stroma were prepared from infected tree bark and subjected to microscopic observation based on valid identification keys. Furthermore, the samples were cultured on Potato Dextrose Agar (PDA) culture medium and the pathogenic agent was identified after purification by hyphal tip and single spore techniques, using microscopic examination and morphological characteristics.
Results: Results showed that Biscogniauxia nummularia is the agent of disease, which causes severe damage to beech trees and has already been identified as cause of beech charcoal canker in many European countries. This fungal species has some special morphological characteristics, including applanate stroma, ostioles are slightly papillate to nearly at the same level as the stromatal surface, ascus apical apparatus blue in iodine and Melzer's reagents, so it is separated from other species. This is the first report of identification of B. nummularia as the causal agent of beech canker disease from Iran. This fungus spends most of its life cycle as an endophyte, and under unfavorable environmental conditions, especially drought stress. B. nummularia takes advantage to alter host physiology, invading host tissue and causing black bark cankers on trunk and branches, known as strip cankers, and wood decay in mature trees.  
Conclusion: The direct relationship between the consequences of climate change, especially water and temperature stress in the host and the development of forest pathogens in the case of several important and key pathogenic fungi, including B. nummularia, has been reported by various researchers in the world, and it has been determined that environmental stress plays an important role in the development of this disease on beech trees in different parts of the world. Meanwhile, as one of the requirements of disease management, it is important to identify the phenotypic and genotypic characteristics of the populations of this fungus in Iran and to identify the distribution and frequency of the disease, which can be very useful in choosing its management strategies. On the other hand, due to the prediction of progressive adverse climate changes in the future, which are an important factor in the development of the disease, continuous monitoring of current changes in beech natural habitats should be included in forest ecosystem monitoring programs to predict future changes, possible ecosystem consequences, and as a vital part of sustainable forest management.

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  • Daneshpazhuh, B. 1980. Identification of some species of Daldinia, Hypoxylon and Xylaria in Iran. Iranian Journal of Plant Pathology, 16: 44-55.
  • Dulamsuren, C., Hauck, M., Kopp, G., Ruff, M., and Leuschner, C., 2016. European beech responds to climate change with growth decline at lower, and growth increase at higher elevations in the center of its distribution range (SW Germany). Trees, 31: 673-686.
  • Granata, G., Sidoti, A. 2004. Biscogniauxia nummularia: Pathogenic agent of a beech decline. The Journal of Pathology, 34: 363-367.
  • Granata, G., and Whalley, A. 1994. Decline of beech associated to Biscogniauxia nummularia in Italy. Petria, 4: 111-116.
  • Hendry, S.J., Boddy, L., and Lonsdale, D., 2002. Abiotic variables effect differential expression of latent infections in beech (Fagus sylvatica). New Phytologist. 155: 449-460.
  • Henriques, J., Nóbrega, F., Sousa, E., and Lima, A., 2015. Morphological and genetic diversity of Biscogniauxia mediterranea associated to Quercus suber in the Mediterranean Basin. Revista Brasileirade Ciencias Agrarias. 38: 166-175.
  • La Porta, N., Capretti, P., Thomsen, I. M., Kasanen, R., Hietala, A.M., and Von Weissenberg, K., 2008. Forest pathogens with higher damage potential due to climate change in Europe. Canadian Journal of Plant Pathology. 30: 177-195.
  • Læssøe, T., Granmo, A., and Scheuer, C., 1999. Biscogniauxia granmoi (Xylariaceae) in Europe. Österreichische Zeitschrift für Pilzkunde, 8: 139-147.
  • Lakatos, F., and Molnár, M., 2009. Mass Mortality of Beech (Fagus sylvatica) in South-West Hungary. Acta Silvatica et Lignaria Hungarica. 5: 75-82.
  • Leuschner, C., Hertel, D., Schmid, I., Koch, O., Muhs, A., and Holscher, D., 2004. Stand fine root biomass and fine root morphology in old-growth beech forests as a function of precipitation and soil fertility. Plant and Soil, 258: 43-56.
  • Lindner, M., Fitzgerald, J.B., Zimmermann, N.E., Reyer, C., Delzon, S., van der Maaten, E., Schelhaas, M. J., Lasch, P., Eggers, J., van der Maaten-Theunissen, M., 2014. Climate change and European forests: What do we know, what are the uncertainties, and what are theimplications for forest management? Journal of Environmental Management, 146: 69-83.
  • Luchi, N., Capretti, P., Feducci, M., Vannini, A., Ceccarelli, B., and Vettraino, A.M., 2015. Latent infection of Biscogniauxia nummularia in Fagus sylvatica: a possible bioindicator of beech health conditions. iForest, 9: 49-54.
  • Luchi, N., Capretti, P., Vettraino, A.M., Vannini, A., Pinzani, P., and Pazzagli, M., 2006. Early detection of Biscogniauxia nummularia in symptomless European beech (Fagus sylvatica) by TaqMan™ real-time PCR. Letters in Applied Microbiology, 43: 33-38.
  • Mirabolfathy, M. 2013. Outbreak of charcoal disease on Quercus and Zelkova carpinifolia trees in forests of Zagros and Alborz mountains in Iran. Journal of Plant Pathology, 49: 257-263.
  • Mirabolfathy, M., Groenewald, J. Z., and Crous, P. W. 2011., The Occurrence of charcoal disease caused by Biscogniauxia mediterranea on chestnut- leaved oak (Quercus castaneifolia) in the Golestan forests of Iran. Plant Disease, 95: 876.
  • Nugent, L.K., Sihanonth, P., Thienhirun, S., and Whalley, A.J.S., 2005. Biscogniauxia: A genus of latent in-vaders. Mycologist, 2005, 19: 40-43.
  • Osono, T., Tateno, O., and Masuya, H., 2013. Diversity and ubiquity of xylariaceous endophytes in live and dead leaves of temperate forest trees. Mycoscience, 2013: 54, 54-61.
  • Paoletti, E., Goggioli, V., Maresi, G. and Reperti, D., 1996. nummularia su faggio in Italia. [Biscogniauxia nummularia on beech in Italy]. Italian Journal of Mycology, 1: 27-35 (In Italian)
  • Patejuk, K., Baturo-Cieśniewska, A., Pusz, W., and Kaczmarek-Pieńczewska, A., 2022. Biscogniauxia Charcoal Canker—A New Potential Threat for Mid-European Forests as an Effect of Climate Change. Forests, 13(1): 89.
  • Patejuk, K., Baturo-Cieśniewska, A., Kaczmarek-Pieńczewska, A. and Pusz, W., 2021. Mycobiota of peat-bog pine (Pinus × rhaetica) needles in the Stołowe Mountains National Park, Poland. Nova Hedwigia, 112: 253-265.
  • Petrini, L., and Petrini, O., 1985. Xylariaceous fungi as endophytes. Sydowia, 38: 216-234.
  • Ragazzi, A., Ginetti, B., and Moricca, S. 2012. First report of Biscogniauxia mediterranea on english ash in Italy. Plant Disease, 96: 1694.
  • Rostamian, M., Kavosi, M. R., Bazgir, E., and Babanezhad, M., 2016. First report of Biscogniauxia mediterranea causing canker on wild almond (Amygdalus scoparia). Australas. Plant Disease Notes, 11: 30.
  • Vujanovic, V., Kim, S.H., Latinovic, J., and Latinovic, N., 2020. Natural fungicolous regulators of Biscogniauxia destructiva nov. That Causes Beech Bark Tarcrust in Southern European (Fagus sylvatica) Forests. Microorganisms, 8: 1999.
  • Yangui, I., Zouaoui Boutiti, M., Vettraino, A.M., Bruni, N., Vannini, A., Ben Jamaâ, M.L., Boussaid, M., and Messaoud, C., 2019. Biscogniauxia mediterranea associated with cork oak (Quercus suber) in Tunisia: Relationships between phenotypic variation, genetic diversity and ecological factors. Fungal Ecology, 41: 224-233.
  • Zabalgogeazcoa, I., Pedro, J., and Canals, R.M., 2015. Biscogniauxia nummularia infecting beech (Fagus sylvatica) trees and sympatric plants of the sedge Carex brevicollis. The Journal of Pathology, 45: 346-348.
  • Zíbarová, L., and Kout, J. 2017. Xylariaceous pyrenomycetes from Bohemia: Species of Biscogniauxia and Hypoxylon new to the Czech Republic, and notes on other rare species. Czech Mycology, 69: 77-108.