Труды сотрудников ИЛ им. В.Н. Сукачева СО РАН

[Text] / G. G. Polyakova, V. V. Stasova, N. V. Pashenova // Russ. J. Plant Physiol. - 2011. - Vol. 58, Is. 5. - P819-827, DOI 10.1134/S1021443711050177. - Cited References: 23. - This work was supported by the Russian Foundation for Basic Research, project no. 09-04-09030. . - 9. - ISSN 1021-4437РУБ Plant Sciences

Аннотация: Ophiostomatoid fungi colonize the conducting tissues of conifer stems, the phloem and the xylem. These pathogenic fungi penetrate into the stem through injuries made by xylophagous insects vectoring these pathogens. In this study the response of the phloem of Scotch pine (Pinus sylvestris L.) to wounding (treatment 1) was compared with the response to wounding combined with application of high-molecular-weight compounds isolated from the mycelium of the ophiostomatoid fungus Ceratocystis laricicola Redfern & Minter (treatment 2). Both treatments induced the appearance of necrosis in the inner bark, the formation of periderm separating living and dead tissues, and formation of the callus alongside the wound perimeter. In addition, the bark accumulated lignin, bound proanthocyanidins, and resins, with a parallel decrease in the content of free proanthocyanidins, low-molecular-weight carbohydrates, and non-lignin components of the cell wall (P > 0.95). The size of necrotic spots, as well as changes in the content of most substances, were significantly higher in the treatment 2 than in the treatment 1 (P > 0.95). The accumulation of lignin in cell walls of phloem sieve cells was delayed in the treatment 2 as compared with that in the treatment 1. This suggested that the mycelial extract temporarily inhibited lignification at the early stage of the wound response. This disturbance of the cell wall protective transformation led to the hypothesis that the fungal suppressors retard the repair of inner bark injured by insects, thereby favoring the invasion of conifer tissues by ophiostomatoid fungi.

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[Polyakova, G. G.
Stasova, V. V.
Pashenova, N. V.] Russian Acad Sci, Sukachev Inst Forest, Siberian Branch, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Polyakova, G.G.; Stasova, V.V.; Pashenova, N.V.

[Text] / G. F. Antonova, V. V. Stasova // Russ. J. Dev. Biol. - 2008. - Vol. 39, Is. 4. - P207-218, DOI 10.1134/S1062360408040024. - Cited References: 82 . - 12. - ISSN 1062-3604РУБ Developmental Biology

Аннотация: The seasonal development of phloem in the stems of Siberian larch (Larix sibirica Ldb.) was studied over two seasons on 50-60-year-old trees growing in a natural stand in the Siberian forest-steppe zone. Trees at the age of 20-25 years were used to study metabolites in differentiating and mature phloem elements, cambial zone, and radially growing xylem cells in the periods of early and late wood formation. The development of the current-year phloem in the stems of 50-60-year-old trees started, depending on climatic conditions, in the second-third decades of May, 10-20 days before the xylem formation, and ended together with the shoot growth cessation in late July. Monitoring of the seasonal activity of cambium producing phloem sieve cells and the duration of their differentiation compared to the xylem derivatives in the cambium demonstrated that the top production of phloem and xylem cells could coincide or not coincide during the season, while their differentiation activity was always in antiphase. Sieve cells in the early phloem are separated from those in the late phloem by a layer of tannin-containing cells, which are formed in the period when late xylem formation starts. The starch content in the structural elements of phloem depends on the state of annual xylem layer development. The content of low molecular weight carbohydrates, amino acids, organic acids, and phenols in phloem cells, cambial zone, and xylem derivatives of the cambium depends on the cell type and developmental stage as well as on the type of forming wood (early or late) differing by the cell wall parameters and, hence, by the requirement for assimilates. Significant differences in the dynamics of substances per dry weight and cell were observed during cell development.

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Держатели документа:
[Antonova, G. F.
Stasova, V. V.] Russian Acad Sci, Sukachev Inst Forest, Siberian Branch, Krasnoyarsk 660036, Russia

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Antonova, G.F.; Stasova, V.V.

[Text] / G. G. Polyakova [et al.] // Russ. J. Plant Physiol. - 2008. - Vol. 55, Is. 4. - P496-502, DOI 10.1134/S1021443708040109. - Cited References: 25 . - 7. - ISSN 1021-4437РУБ Plant Sciences

Аннотация: The elicitor activity of compounds extracted from the mycelia of six species of phytopathogenic fungi was assessed from the sizes of necrotic lesions on the external surface of the living trunk phloem of five coniferous species inhabiting Siberia: Siberian larch (Larix sibirica L.), Scotch pine (Pinus sylvestris L.), Siberian spruce (Picea obovata Ledeb.), Siberian fir (Abies sibirica L.), and cedar pine (Pinus sibirica (Rupr.) Mayr.). The compounds for inoculation were extracted from the mycelium of ascomycetes imperfect, and basidium fungi; the living mycelia of these fungi were also used. The fungal extract or mycelium was placed into the hollows 7 mm in diameter in the trunk bark. Infection triggered the formation of hypersensitivity necrotic lesions in the inner bark exceeding in size those appeared after control wounding of four tree species (larch, pine, spruce, and cedar); fir was an exclusion. In experiments with tree trunks and conifer calluses, a dependence of immune response parameters (the sizes of necrotic lesions and the content of lignin and bound proanthocyanidins) on the quantity of the fungal preparation was elucidated. The largest necrotic lesions appeared after injection of 500 mu g of the fungal preparation into the hollow in the trunk, and its higher quantities did not increase the indices measured. The size of the necrotic lesion on the trunk bark is supposed to be used as a promising index characterizing the level of tree immunity and tolerance under various ecological conditions.

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Держатели документа:
[Polyakova, G. G.
Pashenova, N. V.
Polyakov, V. I.
Zrazhevskaya, G. K.] Russian Acad Sci, Sukachev Inst Forestry, Siberian Div, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Polyakova, G.G.; Pashenova, N.V.; Polyakov, V.I.; Zrazhevskaya, G.K.

[Text] / I. D. Grodnitskaya, N. D. Sorokin // Eurasian Soil Sci. - 2007. - Vol. 40, Is. 3. - P329-334, DOI 10.1134/S106422930703012X. - Cited References: 22 . - 6. - ISSN 1064-2293РУБ Soil Science

Аннотация: The introduction of Trichoderma viride spores (10(8) CFU per 1 cm(2)) essentially changed the structure of micromycetes in the soils of tree nurseries in Krasnoyarsk region. During the first 20 days, in the variants with dark gray forest soils and podzolized chernozems, the total number of fungi decreased by 3-4 and 1.5 times, respectively, as compared to that in the control plots. During the intense development of the introduced microbes, the species composition of the soil fungi changed considerably. The treatment of Scots pine seeds with metabolites of Trichoderma fungi, as well as Pseudomonas and Bacillus bacteria, in the form of water suspensions, biopreparations, and dry spores promoted an increase in the yield of seedlings and improve their morphometric parameters. At the end of the growing period, the treatment with Trichoderma and the biopreparation on its basis increased these parameters, on average, by 18-70%, and the treatment with bacteria increased the same parameters by 13-15%. The application of microbial preparations improved the phytosanitary state of the soils in the studied tree nurseries. The use of the strains of indigenous microorganisms might be feasible for solving bioremediation problems more successfully in particular regions.

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Держатели документа:
Russian Acad Sci, Siberian Div, Sukachev Inst Forestry, Krasnoyarsk 660036, Russia

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Grodnitskaya, I.D.; Sorokin, N.D.

[Text] / V. I. Polyakov [et al.] // Biol. Bull. - 2005. - Vol. 32, Is. 4. - P419-424, DOI 10.1007/s10525-005-0119-x. - Cited References: 16 . - 6. - ISSN 1062-3590РУБ Biology

Аннотация: Two methods for evaluation of pine stand vigor were tested on permanent sample plots near Krasnoyarsk City: visual evaluation and exposure to fungal metabolites. In the first case, forest vigor was estimated using the six-point system of the Sanitary Regulations of the Russian Federation as the mean score for 200 trees on the sample plots. In the second case, the vigor was evaluated from the size of the necrotic spot on inner bark of the tree after inoculation of 22-25 randomly chosen pines with the extract of fungus Ceratocystis laricicola Redfern and Minter. The necrotic spot size was significantly larger in pines from polluted forest as compared to background one. This points to the decrease in infection protection of trees affected by pollution, although visual evaluation of the stand vigor could not distinguish the polluted and background stands.

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Держатели документа:
Russian Acad Sci, VN Sukachev Inst Forest, Siberian Div, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Polyakov, V.I.; Polyakova, G.G.; Pashenova, N.V.; Stasova, V.V.

[Text] / J. . SUOMELA, V. . OSSIPOV, E. . HAUKIOJA // J. Chem. Ecol. - 1995. - Vol. 21, Is. 10. - P1421-1446, DOI 10.1007/BF02035143. - Cited References: 81 . - 26. - ISSN 0098-0331РУБ Biochemistry & Molecular Biology + Ecology

Аннотация: Leaf quality of the mountain birch (Betula pubescens ssp. tortuosa) for herbivores was studied at several hierarchical levels: among trees, among ramets within trees, among branches within ramets, and among short shoots within branches. The experimental units at each level were chosen randomly. The indices of leaf quality were the growth rate of the larvae of a geometrid, Epirrita autumnata, and certain biochemical traits of the leaves (total phenolics and individual phenolic compounds, total carbohydrates and individual sugars, free and protein-bound amino acids). We also discuss relationships between larval growth rate and biochemical foliage traits. Larval growth rates during two successive years correlated positively at the level of tree, the ramet, and the branch, indicating that the relationships in leaf quality remained constant between seasons both among and within trees. The distribution of variation at different hierarchical levels depended on the trait in question. In the case of larval growth rate, ramets and short shoots accounted for most of the explained variation. In the case of biochemical compounds, trees accounted for most of the variance in the content of total phenolics and individual low-molecular-weight phenolics. In the content of carbohydrates (total carbohydrates, starch, fructose, glucose, and sucrose) and amino acids, variation among branches was generally larger than variation among trees. Variation among ramets was low for most compounds. No single leaf trait played a paramount role in larval growth. Secondary compounds, represented by phenolic compounds, or primary metabolites, particularly sugars, may both be important in determining the suitability of birch leaves for larvae. If phenols are causally more important, genet-specific analyses of foliage chemistry are needed. If sugars are of primary importance, within-genet sampling and analysis of foliage chemistry are necessary.

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TURKU UNIV,KEVO SUBARCTIC RES STN,SF-20500 TURKU,FINLAND
INST FOREST,KRASNOYARSK 660036,RUSSIA

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SUOMELA, J...; OSSIPOV, V...; HAUKIOJA, E...

/ N. -S. Cho [et al.] // Journal of the Faculty of Agriculture, Kyushu University. - 2008. - Vol. 53, Is. 2. - P395-398 . - ISSN 0023-6152
Аннотация: A method for estimation of tree's condition on activity of defence response in phloem was checked in Pinus sylvestris L. stands located near Krasnoyarsk (Siberia, Russia). The length of necrosis caused by inoculation of phloem of living tree by Ceratocystis laricicola Redf. et Minter was used as the parameter being measured. The field experiments were carried out in two even-aged (about 60 years) pine stands that were approximately equal on structure, productivity, density and recreation loading, but differentiated on degree of industrial pollution. The two permanent sample plots (SP) were founded in the severely polluted stand. The other two SP were placed in the unpolluted pine forest. The amount of pine trees within each SP varied from 200 to 250. From 22 up to 37 pine-trees selected randomly within every SP were inoculated with C. laricicola mycelium (test 1) and its extract (test 2). One inoculation hole per one tree (diameter 7 mm) was made in stem at a height of 1.3 m. Application of the both agents caused necrosis in phloem around the place of inoculation. In the case of fungal inoculation (test 1), the average length of necrosis in the unpolluted forest exceeded significantly the same parameter in the polluted stand: 51.7-79.4mm and 39.4-41.3mm, correspondingly. The action of the fungal metabolites caused the opposite results: in the unpolluted stand the average size of necroses was smaller in comparison with this parameter in the polluted stands 44.5-15.3 mm and 57.9-61.8 mm. The reasons of this difference are discussed. The both agents (C. laricicola mycelium and its extract) were suitable to reveal the difference of tree's condition in polluted and unpolluted pine stands. The application of fungal extract is more preferable in comparison with fungal mycelium because of smaller variability of necrosis size. Besides, the application of extract allows controlling inoculum dose and excludes the dangerous of spreading infection in forests.

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Держатели документа:
Department of Forest and Forest Products Sciences, Laboratory of Forest Resources Management, Division of Forest Ecosphere Management, Sasaguri, Fukuoka 811-2415, Japan
Wood and Paper Science, Chungbuk National University, Cheongju 361-763, South Korea
Department of Physical and Chemical Biology and Biotechnology of Woody Plants, V. N. Sukachev Institute of Forest SB RAS, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Cho, N.-S.; Pashenova, N.V.; Choi, T.-H.; Ohga, S.

/ G. F. Antonova, V. V. Stasova // Russian Journal of Developmental Biology. - 2006. - Vol. 37, Is. 5. - P306-320, DOI 10.1134/S1062360406050043 . - ISSN 1062-3604
Аннотация: The formation of phloem was studied for two years in stems of 50 to 60 year old trees of Scots pine (Pinus sylvestris L.) growing in nature. The development of phloem of the current year begins 10 to 20 days before the xylem formation and is completed with the termination of shoot growth in the end of June. Observations over the seasonal activity of cambium producing sieve cells of phloem and duration of their differentiation as compared to the xylem derivatives of cambium have shown that the maxima of formation of phloem and xylem cells could coincide or not coincide by season, while the activities of their differentiation were always in antiphase. The sieve cells of early phloem were separated from those of late phloem by a layer of tannin-containing cells, which are formed simultaneously with the formation of late xylem cells by the cambium. Seasonal dynamics of accumulation of starch grain in structural elements of the phloem is related to the xylem development. The content of metabolites in differentiating and mature phloem elements, in the cambium zone, and in the xylem cells growing in the radial direction depended on cell specificity, stage of their development, and type of forming wood, early or late, which differ in the cell wall parameters and, hence, requirement of assimilates. Significant differences were described between the content of low molecular weigh carbohydrates, amino acids, organic acids, and phenol compounds using two methods of calculation: per dry weight and per cell. В© Nauka/Interperiodica 2006.

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Держатели документа:
Sukachev Institute of Forest, Siberian Branch, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Antonova, G.F.; Stasova, V.V.

/ T. M. Kharpukhaeva, L. V. Mukhortova // Contemp. Probl. Ecol. - 2016. - Vol. 9, Is. 1. - P125-139, DOI 10.1134/S1995425516010066 . - ISSN 1995-4255
Аннотация: Successional stages of epixylic lichens in conjunction with fallen deadwood decomposition were studied in the eastern Baikal region. It was found that lichens passed through four stages of epixylic succession: from the epiphytic and epixylic stages to the epigeic stage. It was also determined that lichens could inhibit the decomposition of the higher layer of fallen deadwood, which served as a substrate to them. © 2016, Pleiades Publishing, Ltd.

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Держатели документа:
Institute of General and Experimental Biology, Russian Academy of Sciences, ul. Sakh’yanovoi 6, Ulan-Ude, Russian Federation
Sukhachev Institute of Forest, Russian Academy of Sciences, Akademgorodok 50/28, Krasnoyarsk, Russian Federation

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Kharpukhaeva, T. M.; Mukhortova, L. V.

/ V. P. Zhelifonova [et al.] // Appl. Biochem. Microbiol. - 2019. - Vol. 55, Is. 3. - P277-283, DOI 10.1134/S0003683819030153. - Cited References:18 . - ISSN 0003-6838. - ISSN 1608-3024РУБ Biotechnology & Applied Microbiology + Microbiology

Аннотация: Secondary metabolites of the basidiomycetes of Armillaria borealis Marxm. and Korhonen, A.cepistipes Velen., A. gallica Marxm., A. ostoyae (Romagn.) Herink, and A. sinapina Berube and Dessur isolated in Southern Siberia (Krasnoyarsk region and Tyva Republic) and in the Far East (Sikhote-Alin) were studied. Metabolites belonging to the class of protoilludene sesquiterpene aryl esters of the melleolides group have been identified in the species A. borealis, A. cepistipes, and A. sinapina. The strains differ in the spectrum of synthesized melleolides. A. borealis strain 74g synthesized a wider range of melleolides than other strains of the species: melleolides B, C, D and H, melledonals B and C, 5'-O-methylmelledonal, 13-hydroxy-5'-O-methylmelledonal, and armillarinin. It was shown that the composition of the medium influenced the amount of synthesized metabolites. All of the studied strains synthesizing melleolides exhibited a toxicogenic and phytopathogenic effect on seeds and seedlings of Picea abies (L.) H. Karst. and Abies sibirica Ledeb. A significant decrease in seed germination energy, laboratory and ground seed germination, the development of the root system of conifer seedlings was revealed. The maximum inhibitory effect was shown by the culture fluid of A. borealis 74g with the greatest amounts and variety of melleolides in the metabolome profile.

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Держатели документа:
Russian Acad Sci, Skryabin Inst Biochem & Physiol Microorganisms, Pushchino 142290, Russia.
Russian Acad Sci, Siberian Branch, Sukachev Inst Forest, Krasnoyarsk 660036, Russia.
Reshetnev Siberian State Univ Sci & Technol, Krasnoyarsk 660049, Russia.

Доп.точки доступа:
Zhelifonova, V. P.; Antipova, T. V.; Litvinova, E. A.; Baskunov, B. P.; Litovka, Yu. A.; Pavlov, I. N.; Kozlovsky, A. G.

/ T. V. Antipova, V. P. Zhelifonova, Y. A. Litovka [et al.] // Appl. Biochem. Microbiol. - 2020. - Vol. 56, Is. 2. - P185-193, DOI 10.1134/S0003683820020039. - Cited References:30 . - ISSN 0003-6838. - ISSN 1608-3024РУБ Biotechnology & Applied Microbiology + Microbiology

Аннотация: The composition of secondary metabolites from strains Heterobasidion genus isolated in central and western Siberia and in South Korea were studied. Morphological-cultural and molecular-genetic methods were used to assign the cultures to the species of H. annosum (Fr.) Bref. (five strains), H. abietinum Niemela & Korhonen (four strains), and H. ecrustosum Tokuda, T. Hatt. & Y.C. Give (one strain). Fomannoxin predominated in the metabolome profiles of three H. annosum strains and all H. abietinum strains. Two strains of H. annosum synthesized fomannoxin-related compounds: 2-(2-hydroxypropan-2-yl)-2,3-dihydrobenzofuran-5-carbaldehyde and 2-(2-hydroxypropan-2-yl)benzofuran-5-carbaldehyde. Fomannosin and its precursors were identified in H. annosum 45-2. It was shown that the composition of the fermentation medium affected the number and range of the synthesized metabolites. Under in vitro conditions, all H. annosum and H. abietinum strains exhibited phytopathogenic effects on Pinus sylvestris L. seedlings, causing necrotic damage to stems of various degrees and plant death. Higher phytopathogenicity is characteristic of H. annosum strains: maximal aggressiveness was observed in H. annosum 45-2 with the greatest diversity of compounds in the metabolome profile and active fomannoxin production.

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Держатели документа:
Russian Acad Sci, Pushchino Sci Ctr, Biol Res Fed Res Ctr, Skryabin Inst Biochem & Physiol Microorganisms, Pushchino 142290, Russia.
Russian Acad Sci, Siberian Branch, Sukachev Forest Inst, Krasnoyarsk 660036, Russia.
Reshetnev Siberian State Univ Sci & Technol, Krasnoyarsk 660049, Russia.
RAS, SB, FRC Krasnoyarsk Sci Ctr, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Antipova, T. V.; Zhelifonova, V. P.; Litovka, Yu. A.; Pavlov, I. N.; Baskunov, B. P.; Timofeev, A. A.; Kozlovsky, A. G.; Timofeev, Anton

/ P. W. Crous, L. Lombard, M. Sandoval-Denis [et al.] // Stud. Mycol. - 2021. - Vol. 98. - Ст. 100116, DOI 10.1016/j.simyco.2021.100116. - Cited By :2 . - ISSN 0166-0616
Аннотация: Recent publications have argued that there are potentially serious consequences for researchers in recognising distinct genera in the terminal fusarioid clade of the family Nectriaceae. Thus, an alternate hypothesis, namely a very broad concept of the genus Fusarium was proposed. In doing so, however, a significant body of data that supports distinct genera in Nectriaceae based on morphology, biology, and phylogeny is disregarded. A DNA phylogeny based on 19 orthologous protein-coding genes was presented to support a very broad concept of Fusarium at the F1 node in Nectriaceae. Here, we demonstrate that re-analyses of this dataset show that all 19 genes support the F3 node that represents Fusarium sensu stricto as defined by F. sambucinum (sexual morph synonym Gibberella pulicaris). The backbone of the phylogeny is resolved by the concatenated alignment, but only six of the 19 genes fully support the F1 node, representing the broad circumscription of Fusarium. Furthermore, a re-analysis of the concatenated dataset revealed alternate topologies in different phylogenetic algorithms, highlighting the deep divergence and unresolved placement of various Nectriaceae lineages proposed as members of Fusarium. Species of Fusarium s. str. are characterised by Gibberella sexual morphs, asexual morphs with thin- or thick-walled macroconidia that have variously shaped apical and basal cells, and trichothecene mycotoxin production, which separates them from other fusarioid genera. Here we show that the Wollenweber concept of Fusarium presently accounts for 20 segregate genera with clear-cut synapomorphic traits, and that fusarioid macroconidia represent a character that has been gained or lost multiple times throughout Nectriaceae. Thus, the very broad circumscription of Fusarium is blurry and without apparent synapomorphies, and does not include all genera with fusarium-like macroconidia, which are spread throughout Nectriaceae (e.g., Cosmosporella, Macroconia, Microcera). In this study four new genera are introduced, along with 18 new species and 16 new combinations. These names convey information about relationships, morphology, and ecological preference that would otherwise be lost in a broader definition of Fusarium. To assist users to correctly identify fusarioid genera and species, we introduce a new online identification database, Fusarioid-ID, accessible at www.fusarium.org. The database comprises partial sequences from multiple genes commonly used to identify fusarioid taxa (act1, CaM, his3, rpb1, rpb2, tef1, tub2, ITS, and LSU). In this paper, we also present a nomenclator of names that have been introduced in Fusarium up to January 2021 as well as their current status, types, and diagnostic DNA barcode data. In this study, researchers from 46 countries, representing taxonomists, plant pathologists, medical mycologists, quarantine officials, regulatory agencies, and students, strongly support the application and use of a more precisely delimited Fusarium (= Gibberella) concept to accommodate taxa from the robust monophyletic node F3 on the basis of a well-defined and unique combination of morphological and biochemical features. This F3 node includes, among others, species of the F. fujikuroi, F. incarnatum-equiseti, F. oxysporum, and F. sambucinum species complexes, but not species of Bisifusarium [F. dimerum species complex (SC)], Cyanonectria (F. buxicola SC), Geejayessia (F. staphyleae SC), Neocosmospora (F. solani SC) or Rectifusarium (F. ventricosum SC). The present study represents the first step to generating a new online monograph of Fusarium and allied fusarioid genera (www.fusarium.org). © 2021 Westerdijk Fungal Biodiversity Institute

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Держатели документа:
Westerdijk Fungal Biodiversity Institute, Utrecht, 3508 AD, Netherlands
Wageningen University and Research Centre (WUR), Laboratory of Phytopathology, Droevendaalsesteeg 1, Wageningen, 6708 PB, Netherlands
Netherlands Institute of Ecology (NIOO-KNAW), Department of Microbial Ecology, Droevendaalsesteeg 10, Wageningen, 6708 PB, Netherlands
Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, ON K1S 5B6, Canada
Plant Protection Department, Agricultural Institute of Slovenia, Hacquetova ulica 17, Ljubljana, 1000, Slovenia
Department of Plant Science and Landscape Architecture, University of Maryland, College Park, MD, United States
Escuela de Biologia and Centro de Investigaciones en Productos Naturales, Universidad de Costa Rica, San Pedro, Costa Rica
Unitat de Micologia, Facultat de Medicina i Ciencies de la Salut i Institut d'Investigacio Sanitaria Pere Virgili (IISPV), Universitat Rovira i Virgili, Reus, 43201, Spain
Department of Clinical Plant Science, Faculty of Bioscience, Hosei University, 3-7-2 Kajino-cho, Koganei, Tokyo, 184-8584, Japan
ARC-Plant Health and Protection, Private Bag X5017, Stellenbosch, Western Cape 7599, South Africa
State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China
University of Chinese Academy of Sciences, Beijing, 100049, China
Department of Botany & Plant Pathology, Oregon State University, Corvallis, OR 97330, United States
Department of Microbial Drugs, Helmholtz Centre for Infection Research GmbH (HZI), Inhoffenstrasse 7, Braunschweig, 38124, Germany
Sporometrics, Toronto, ON, Canada
Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada
Plant and Microbial Biology, 111 Koshland Hall, University of California, Berkeley, CA 94720-3102, United States
Senckenberg Biodiversity and Climate Research Center, Senckenberganlage 25, Frankfurt am Main, D-60325, Germany
Department of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), Faculty of Natural and Agricultural Sciences, University of Pretoria, P. Bag X20, Hatfield, Pretoria, 0028, South Africa
Department of Biotechnology and Biomedicine, DTU-Bioengineering, Technical University of Denmark, Kongens Lyngby, 2800, Denmark
Systematic Mycology Lab., Botany and Microbiology Department, Faculty of Science, Suez Canal University, Ismailia, 41522, Egypt
Department of Plant Protection, Faculty of Agriculture, University of Kurdistan, P.O. Box 416, Sanandaj, Iran
Department of Medical Microbiology, King's College Hospital, London, UK, United Kingdom
Department of Infectious Diseases, Imperial College London, London, UK, United Kingdom
Department of Mycology and Plant Resistance, V. N. Karazin Kharkiv National University, Maidan Svobody 4, Kharkiv, 61022, Ukraine
Department of Food Science and Technology, Cape Peninsula University of Technology, P.O. Box 1906, Bellville, 7535, South Africa
School of Forest Resources and Conservation, University of Florida, Gainesville, FL, United States
Department of Plant Pathology and Microbiology, College of Bio-Resources and Agriculture, National Taiwan University, No.1, Sec.4, Roosevelt Road, Taipei, 106, Taiwan
Iranian Research Institute of Plant Protection, Agricultural Research, Education and Extension Organization (AREEO), P.O. Box 19395-1454, Tehran, Iran
Natural History Museum, University of Oslo, Norway
Department of Natural History, NTNU University Museum, Trondheim, Norway
Setor de Micologia/Departamento de Biociencias e Tecnologia, Instituto de Patologia Tropical e Saude Publica, Universidade Federal de Goias/Federal University of Goias, Rua 235 - s/n – Setor Universitario - CEP: 74605-050, Goiania, Brazil
Departamento de Agronomia, Universidade Federal Rural de Pernambuco, Recife, PE 52171-900, Brazil
Departamento de Parasitologia y Micologia, Instituto de Higiene, Facultad de Medicina – Universidad de la Republica, Av. A. Navarro 3051, Montevideo, Uruguay
Department of Pharmaceutical Science, University of Perugia, Via Borgo 20 Giugno, Perugia, 74, Italy
Instituto de Investigaciones Fundamentales en Agricultura Tropical Alejandro de Humboldt (INIFAT), Academico Titular de la Academia de Ciencias de, Cuba
Grupo de Investigacion Celular y Molecular de Microorganismos Patogenos (CeMoP), Departamento de Ciencias Biologicas, Universidad de Los Andes, Bogota, 111711, Colombia
Mycology Laboratory, New York State Department of Health Wadsworth Center, Albany, NY, United States
Laboratory of Evolutionary Genetics, Institute of Biology, University of Neuchatel, Neuchatel, CH-2000, Switzerland
Senckenberg Museum of Natural History Gorlitz, PF 300 154, Gorlitz, 02806, Germany
Mycotheque de l'Universite catholique de Louvain (MUCL, BCCMTM), Earth and Life Institute – ELIM – Mycology, Universite catholique de Louvain, Croix du Sud 2 bte L7.05.06, Louvain-la-Neuve, B-1348, Belgium
Department of Microbiology, Babcock University, Ilishan Remo, Ogun State, Nigeria
The Key Laboratory for Silviculture and Conservation of Ministry of Education, Beijing Forestry University, Beijing, 100083, China
Laboratorio de Micologia Clinica, Hospital de Clinicas, Universidad de Buenos Aires, Buenos Aires, Argentina
Facultad de Farmacia y Bioquimica, Universidad de Buenos Aires, Buenos Aires, Argentina
Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, United Kingdom
Laboratorio de Salud de Bosques y Ecosistemas, Instituto de Conservacion, Biodiversidad y Territorio, Facultad de Ciencias Forestales y Recursos Naturales, Universidad Austral de Chile, casilla 567, Valdivia, Chile
Institute of Grapevine and Wine Sciences (ICVV), Spanish National Research Council (CSIC)-University of La Rioja-Government of La Rioja, Logrono, 26007, Spain
Institut fur Biologie, Karl-Franzens-Universitat Graz, Holteigasse 6, Graz, 8010, Austria
Applied genomics research group, Universidad de los Andes, Cr 1 # 18 a 12, Bogota, Colombia
Center for Safe and Improved Food, Scotland's Rural College (SRUC), Kings Buildings, West Mains Road, Edinburgh, EH9 3JG, United Kingdom
Biorefining and Advanced Materials Research Center, Scotland's Rural College (SRUC), Kings Buildings, West Mains Road, Edinburgh, EH9 3JG, United Kingdom
Department of Agricultural, Forestry and Food Sciences (DISAFA), University of Torino, Largo P. Braccini 2, Grugliasco, TO 10095, Italy
BioAware, Hannut, Belgium
Research Group Mycology, Department of Biology, Ghent University, 35 K.L. Ledeganckstraat, Ghent, 9000, Belgium
Faculty of Science, University of South Bohemia, Branisovska 31, Ceske Budejovice, 370 05, Czech Republic
Department of Botany, Swedish Museum of Natural History, P.O. Box 50007, Stockholm, SE-104 05, Sweden
Microbe Division/Japan Collection of Microorganisms RIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki, 305-0074, Japan
Department of Botany, Charles University in Prague, Prague, Czech Republic
Center of Excellence in Fungal Research, Mae Fah Luang University, Chaing Rai, 57100, Thailand
Cornell University, 334 Plant Science Building, Ithaca, NY 14850, United States
Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Reduit, Mauritius
Manaaki Whenua Landcare Research, Private Bag 92170, Auckland, 1142, New Zealand
EMSL Analytical, Inc., 200 Route 130 North, Cinnaminson, NJ 08077, United States
Department of Nutrition and Dietetics, Faculty of Health Sciences, Yeditepe University, Turkey
Department of Plant and Soil Sciences, University of Pretoria, P. Bag X20 Hatfield, Pretoria, 0002, South Africa
Institute of Environmental Biology, Ecology and Biodiversity, Utrecht University, Utrecht, 3584 CH, Netherlands
Laboratory for Biological Diversity, Ruder Boskovic Institute, Bijenicka cesta 54, Zagreb, HR-10000, Croatia
University of Veterinary Medicine, Vienna (VetMed), Institute of Food Safety, Food Technology and Veterinary Public Health, Veterinaerplatz 1, 1210 Vienna and BiMM – Bioactive Microbial Metabolites group, Tulln a.d. Donau, 3430, Austria
University of California, Davis, One Shields Ave., Davis, CA 95616, United States
Department of Agricultural Biological Chemistry, College of Agriculture & Life Sciences, Chonnam National University, Yongbong-Dong 300, Buk-Gu, Gwangju, 61186, South Korea
Ascofrance, 64 route de Chize, Villiers-en-Bois, 79360, France
The Key Laboratory of Molecular Biology of Crop Pathogens and Insects of Ministry of Agriculture, The Key Laboratory of Biology of Crop Pathogens and Insects of Zhejiang Province, Institute of Biotechnology, Zhejiang University, 866 Yuhangtang Road, Hangzhou, 310058, China
V.N. Sukachev Institute of Forest SB RAS, Laboratory of Reforestation, Mycology and Plant Pathology, Krasnoyarsk, 660036, Russian Federation
Reshetnev Siberian State University of Science and Technology, Department of Chemical Technology of Wood and Biotechnology, Krasnoyarsk, 660037, Russian Federation
School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 611731, China
Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, Ecosciences Precinct, G.P.O. Box 267, Brisbane, 4001, Australia
Department of Botany, Faculty of Science, Palacky University Olomouc, Slechtitelu 27, Olomouc, CZ-783 71, Czech Republic
Department of Agricultural, Food, Environmental and Forestry Science and Technology (DAGRI), Plant Pathology and Entomology section, University of Florence, P.le delle Cascine 28, Firenze, 50144, Italy
Graduate school of Bioresources, Mie University, Kurima-machiya 1577, Tsu, Mie 514-8507, Japan
Gothenburg Global Biodiversity Center at the Department of Biological and Environmental Sciences, University of Gothenburg, Box 461, Gothenburg, 405 30, Sweden
Department of Microbiology and Biochemistry, Faculty of Natural and Life Sciences, University of Batna 2, Batna, 05000, Algeria
Laboratorio de Micodiversidad y Micoprospeccion, PROIMI-CONICET, Av. Belgrano y Pje. Caseros, Argentina
Universidade de Lisboa, Faculdade de Ciencias, Biosystems and Integrative Sciences Institute (BioISI), Campo Grande, Lisbon, 1749-016, Portugal
Microbial Screening Technologies, 28 Percival Rd, Smithfield, NSW 2164, Australia
Dipartimento di Agricoltura, Alimentazione e Ambiente, sez. Patologia vegetale, University of Catania, Via S. Sofia 100, Catania, 95123, Italy
Phytopathology, Van Zanten Breeding B.V., Lavendelweg 15, Rijsenhout, 1435 EW, Netherlands
National Fungal Culture Collection of India (NFCCI), Biodiversity and Palaeobiology (Fungi) Group, Agharkar Research Institute, Pune, Maharashtra 411 004, India
Laboratory of Mycology and Phytopathology – (LAMFU), Department of Chemical and Food Engineering, Universidad de los Andes, Cr 1 # 18 a 12, Bogota, Colombia
Plant Pathology and Population Genetics, Laboratory of Microorganisms, National Gene Bank, Tunisia
Laboratory of Emerging Fungal Pathogens, Department of Microbiology, Immunology, and Parasitology, Discipline of Cellular Biology, Federal University of Sao Paulo (UNIFESP), Sao Paulo, 04023062, Brazil
USDA-ARS Mycology & Nematology Genetic Diversity & Biology Laboratory, Bldg. 010A, Rm. 212, BARC-West, 10300 Baltimore Ave, Beltsville, MD 20705, United States
Departamento de Micologia Prof. Chaves Batista, Universidade Federal de Pernambuco, Centro de Biociencias, Cidade Universitaria, Av. Prof. Moraes Rego, s/n, Recife, PE CEP: 50670-901, Brazil
Centre for Crop Health, University of Southern Queensland, Toowoomba, Queensland 4350, Australia
College of Plant Protection, Northwest A&F University, Yangling, Shaanxi, China
Faculty of Natural and Agricultural Sciences, Department of Plant Sciences, University of the Free State, P.O. Box 339, Bloemfontein, 9300, South Africa
Queensland Plant Pathology Herbarium, Department of Agriculture and Fisheries, Dutton Park, Queensland 4102, Australia
Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh, EH3 5LR, United Kingdom
Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC 3010, Australia
Food and Wine Research Institute, Eszterhazy Karoly University, 6 Leanyka Street, Eger, H-3300, Hungary
Department of Life Sciences and Systems Biology, University of Torino and Institute for Sustainable Plant Protection (IPSP-SS Turin), C.N.R, Viale P.A. Mattioli, 25, Torino, I-10125, Italy
Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biological Resource and Food Engineering, Qujing Normal University, Qujing, Yunnan 655011, China
Shandong Provincial Key Laboratory for Biology of Vegetable Diseases and Insect Pests, College of Plant Protection, Shandong Agricultural University, Taian, 271018, China
Fitosanidad, Colegio de Postgraduados-Campus Montecillo, Montecillo-Texcoco, Edo. de Mexico 56230, Mexico
Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbH, Inhoffenstrasse 7 B, Braunschweig, 38124, Germany
Museum of Evolution, Uppsala University, Norbyvagen 16, Uppsala, SE-752 36, Sweden
Ministry of Agriculture Key Laboratory of Molecular Biology of Crop Pathogens and Insects, Institute of Biotechnology, College of Agriculture and Biotechnology, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou, 310058, China
Goethe-University Frankfurt am Main, Department of Biological Sciences, Institute of Ecology, Evolution and Diversity, Max-von-Laue Str. 13, Frankfurt am Main, D-60438, Germany
LOEWE Centre for Translational Biodiversity Genomics, Georg-Voigt-Str. 14-16, Frankfurt am Main, D-60325, Germany

Доп.точки доступа:
Crous, P. W.; Lombard, L.; Sandoval-Denis, M.; Seifert, K. A.; Schroers, H. -J.; Chaverri, P.; Gene, J.; Guarro, J.; Hirooka, Y.; Bensch, K.; Kema, G. H.J.; Lamprecht, S. C.; Cai, L.; Rossman, A. Y.; Stadler, M.; Summerbell, R. C.; Taylor, J. W.; Ploch, S.; Visagie, C. M.; Yilmaz, N.; Frisvad, J. C.; Abdel-Azeem, A. M.; Abdollahzadeh, J.; Abdolrasouli, A.; Akulov, A.; Alberts, J. F.; Araujo, J. P.M.; Ariyawansa, H. A.; Bakhshi, M.; Bendiksby, M.; Ben Hadj Amor, A.; Bezerra, J. D.P.; Boekhout, T.; Camara, M. P.S.; Carbia, M.; Cardinali, G.; Castaneda-Ruiz, R. F.; Celis, A.; Chaturvedi, V.; Collemare, J.; Croll, D.; Damm, U.; Decock, C. A.; de Vries, R. P.; Ezekiel, C. N.; Fan, X. L.; Fernandez, N. B.; Gaya, E.; Gonzalez, C. D.; Gramaje, D.; Groenewald, J. Z.; Grube, M.; Guevara-Suarez, M.; Gupta, V. K.; Guarnaccia, V.; Haddaji, A.; Hagen, F.; Haelewaters, D.; Hansen, K.; Hashimoto, A.; Hernandez-Restrepo, M.; Houbraken, J.; Hubka, V.; Hyde, K. D.; Iturriaga, T.; Jeewon, R.; Johnston, P. R.; Jurjevic, Z.; Karalti, I.; Korsten, L.; Kuramae, E. E.; Kusan, I.; Labuda, R.; Lawrence, D. P.; Lee, H. B.; Lechat, C.; Li, H. Y.; Litovka, Y. A.; Maharachchikumbura, S. S.N.; Marin-Felix, Y.; Matio Kemkuignou, B.; Matocec, N.; McTaggart, A. R.; Mlcoch, P.; Mugnai, L.; Nakashima, C.; Nilsson, R. H.; Noumeur, S. R.; Pavlov, I. N.; Peralta, M. P.; Phillips, A. J.L.; Pitt, J. I.; Polizzi, G.; Quaedvlieg, W.; Rajeshkumar, K. C.; Restrepo, S.; Rhaiem, A.; Robert, J.; Robert, V.; Rodrigues, A. M.; Salgado-Salazar, C.; Samson, R. A.; Santos, A. C.S.; Shivas, R. G.; Souza-Motta, C. M.; Sun, G. Y.; Swart, W. J.; Szoke, S.; Tan, Y. P.; Taylor, J. E.; Taylor, P. W.J.; Tiago, P. V.; Vaczy, K. Z.; van de Wiele, N.; van der Merwe, N. A.; Verkley, G. J.M.; Vieira, W. A.S.; Vizzini, A.; Weir, B. S.; Wijayawardene, N. N.; Xia, J. W.; Yanez-Morales, M. J.; Yurkov, A.; Zamora, J. C.; Zare, R.; Zhang, C. L.; Thines, M.

/ Y. A. Litovka, P. V. Makolova, A. A. Leonenko [et al.] // IOP Conference Series: Earth and Environmental Science : IOP Publishing Ltd, 2021. - Vol. 848: 5th International Workshop on Innovations in Agro and Food Technologies, WIAFT-V 2021 (17 June 2021 through 18 June 2021, ) Conference code: 172027, Is. 1. - Ст. 012163, DOI 10.1088/1755-1315/848/1/012163 . -
Аннотация: A phytopathogenic complex of the genus Fusarium, common on 19 wheat varieties cultivated in Siberia, was investigated. It was found eleven fungal species in wheat grain (Fusarium avenaceum, F. culmorum, F. diversisporum, F. heterosporum, F. oxysporum, F.poae, F. sambucinum, F. incarnatum, F. sporotrichioides, F. tricinctum, Neocosmospora solani), with the dominant one being F. sporotrichioides (from 23 to 68 % of the total number of species). Seven species were found in the rhizosphere of wheat (F. avenaceum, F.incarnatum, F. oxysporum, F. sambucinum, F. sporotrichioides, F. tricinctum, N. solani), with the most common being F. oxysporum (up to 39 %) and F. sporotrichioides (up to 35%). Biotesting a mixture of metabolites in wheat seeds and seedlings revealed highly toxic species, namely F. sporotrichioides and F. oxysporum (a decrease of in vitro seed germination by more than 55 % and a prolonged inhibitory effect on seedling development). F. avenaceum, N.solani and F. culmorum are moderately toxic species. The greatest danger for the development of wheat fusariosis in Siberia in terms of the total frequency of occurrence, phytotoxic and phytopathogenic properties is represented by F. sporotrichioides. © Published under licence by IOP Publishing Ltd.

Scopus

Держатели документа:
Sukachev Institute of Forest, Siberian Branch, Russian Academy of Sciences, 50/28 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Reshetnev Siberian State University of Science and Technology, 31, Krasnoyarsky rabochy prospect, Krasnoyarsk, 660037, Russian Federation

Доп.точки доступа:
Litovka, Y. A.; Makolova, P. V.; Leonenko, A. A.; Vasilieva, A. A.; Kokorin, A. N.; Pavlov, I. N.

/ P. W. Crous, L. Lombard, M. Sandoval-Denis [et al.] // Stud. Mycol. - 2021. - Is. 98. - Ст. 100116, DOI 10.1016/j.simyco.2021.100116. - Cited References:403 . - ISSN 0166-0616. - ISSN 1872-9797РУБ Mycology

Аннотация: Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), Faculty of Natural and Agricultural Sciences, University of Pretoria, P. Bag X20, Hatfield, 0028, Pretoria, South Africa; 20Department of Biotechnology and Biomedicine, DTU-Bioengineering, Technical University of Denmark, 2800, Kongens Lyngby, Denmark; 21Systematic Mycology Lab., Botany and Microbiology Department, Faculty of Science, Suez Canal University, Ismailia, 41522, Egypt; 22Department of Plant Protection, Faculty of Agriculture, University of Kurdistan, P.O. Box 416, Sanandaj, Iran; 23Department of Medical Microbiology, King's College Hospital, London, UK;24Department of Infectious Diseases, Imperial College London, London, UK;25Department of Mycology and Plant Resistance, V. N. Karazin Kharkiv National University, Maidan Svobody 4, 61022, Kharkiv, Ukraine; 26Department of Food Science and Technology, Cape Peninsula University of Technology, P.O. Box 1906, Bellville, 7535, South Africa; 27School of Forest Resources and Conservation, University of Florida, Gainesville, FL, USA; 28Department of Plant Pathology and Microbiology, College of Bio-Resources and Agriculture, National Taiwan University, No.1, Sec.4, Roosevelt Road, Taipei, 106, Taiwan, ROC;

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Westerdijk Fungal Biodivers Inst, NL-3508 AD Utrecht, Netherlands.
Wageningen Univ & Res Ctr WUR, Lab Phytopathol, Droevendaalsesteeg 1, NL-6708 PB Wageningen, Netherlands.
Netherlands Inst Ecol NIOO KNAW, Dept Microbial Ecol, Droevendaalsesteeg 10, NL-6708 PB Wageningen, Netherlands.
Carleton Univ, Dept Biol, 1125 Colonel By Dr, Ottawa, ON K1S 5B6, Canada.
Agr Inst Slovenia, Plant Protect Dept, Hacquetova Ulica 17, Ljubljana 1000, Slovenia.
Univ Maryland, Dept Plant Sci & Landscape Architecture, College Pk, MD 20742 USA.
Univ Costa Rica, Escuela Biol, San Pedro, Costa Rica.
Univ Costa Rica, Ctr Invest Prod Nat, San Pedro, Costa Rica.
Univ Rovira & Virgili, Fac Med & Ciencies Salut, Unitat Micol, Reus 43201, Spain.
Univ Rovira & Virgili, Inst Invest Sanitaria Pere Virgili IISPV, Reus 43201, Spain.
Hosei Univ, Fac Biosci, Dept Clin Plant Sci, 3-7-2 Kajino Cho, Koganei, Tokyo 1848584, Japan.
Arc Plant Hlth & Protect, Private Bag X5017, ZA-7599 Stellenbosch, Western Cape, South Africa.
Chinese Acad Sci, Inst Microbiol, State Key Lab Mycol, Beijing 100101, Peoples R China.
Univ Chinese Acad Sci, Beijing 100049, Peoples R China.
Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97330 USA.
Helmholtz Ctr Infect Res GmbH HZI, Dept Microbial Drugs, Inhoffenstr 7, D-38124 Braunschweig, Germany.
Sporometrics, Toronto, ON, Canada.
Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada.
Univ Calif Berkeley, Plant & Microbial Biol, 111 Koshland Hall, Berkeley, CA 94720 USA.
Senckenberg Biodivers & Climate Res Ctr, Senckenberganlage 25, D-60325 Frankfurt, Germany.
Univ Pretoria, Fac Nat & Agr Sci, Forestry & Agr Biotechnol Inst FABI, Dept Biochem Genet & Microbiol, P Bag X20, ZA-0028 Pretoria, South Africa.
Tech Univ Denmark, Dept Biotechnol & Biomed, DTU Bioengn, DK-2800 Lyngby, Denmark.
Suez Canal Univ, Fac Sci, Bot & Microbiol Dept, Systemat Mycol Lab, Ismailia 41522, Egypt.
Univ Kurdistan, Fac Agr, Dept Plant Protect, POB 416, Sanandaj, Iran.
Kings Coll Hosp London, Dept Med Microbiol, London, England.
Imperial Coll London, Dept Infect Dis, London, England.
VN Karazin KharkivNatl Univ, Dept Mycol & Plant Resistance, Maidan Svobody 4, UA-61022 Kharkiv, Ukraine.
Cape Peninsula Univ Technol, Dept Food Sci & Technol, POB 1906, ZA-7535 Bellville, South Africa.
Univ Florida, Sch Forest Resources & Conservat, Gainesville, FL 32611 USA.
Natl Taiwan Univ, Coll Bioresources & Agr, Dept PlantPathol & Microbiol, 1,Sec 4,Roosevelt Rd, Taipei 106, Taiwan.
Agr Res Educ & Extens Org AREEO, Iranian Res Inst Plant Protect, POB 19395-1454, Tehran, Iran.
Univ Oslo, Nat Hist Museum, Oslo, Norway.
NTNU Univ Museum, Dept Nat Hist, Trondheim, Norway.
Univ Fed Goias, Inst Patol Trop & Saude PUbl, Dept Biociencias & Tecnol, Setor Micol, Rua 235 S-N Setor Univ, BR-74605050 Goiania, Go, Brazil.
Univ Fed Rural Pernambuco, Dept Agron, BR-52171900 Recife, PE, Brazil.
Univ Republica, Inst Higiene, Dept Parasitol & Micol, Fac Med, Av A Navarro 3051, Montevideo, Uruguay.
Univ Perugia, Dept Pharmaceut Sci, Via Borgo 20 Giugno, I-74 Perugia, Italy.
Inst Invest Fundamentales Agr Trop Alejandro de H, Acad Ciencias, Havana, Cuba.
Univ Los Andes, Dept Ciencias Biol, Grp Invest Celular & Mol Microorganismos Patogeno, Bogota 111711, Colombia.
NewYork State Dept Hlth, Mycol Lab, Wadsworth Ctr, Albany, NY USA.
Univ Neuchatel, Inst Biol, Lab Evolutionary Genet, CH-2000 Neuchatel, Switzerland.
Senckenberg Museum Nat Hist Gorlitz, PF 300 154, D-02806 Gorlitz, Germany.
Catholic Univ Louvain, Earth & Life Inst ELIM Mycol, BCCMTM, Mycotheque Univ Catholique Louvain MUCL, Croix Sud 2 Bte L7-05-06, B-1348 Louvain La Neuve, Belgium.
Babcock Univ, Dept Microbiol, Ilishan Remo, Ogun State, Nigeria.
Beijing Forestry Univ, Key Lab Silviculture & Conservat, Minist Educ, Beijing 100083, Peoples R China.
Univ Buenos Aires, Hosp Clin, Lab Micol Clin, Buenos Aires, DF, Argentina.
Univ Buenos Aires, Fac Farm & Bioquim, Buenos Aires, DF, Argentina.
Royal Bot Gardens, Richmond TW9 3DS, Surrey, England.
Univ Austral Chile, Fac Ciencias Forestales & Recursos Nat, Inst Conservac Biodiversidad & Terr, Lab Salud Bosques & Ecosistemas, Casilla 567, Valdivia, Chile.
Univ La Rioja, Govt La Rioja, Spanish Natl Res Council CSIC, Inst Grapevine & Wine Sci ICVV, Logrono 26007, Spain.
Karl Franzens Univ Graz, Inst Biol, Holteigasse 6, A-8010 Graz, Austria.
Univ Los Andes, Appl Genom Res Grp, Cr 1 18 A 12, Bogota, Colombia.
Scotlands Rural Coll SRUC, Ctr Safe & Improved Food, Kings Bldg,West Mains Rd, Edinburgh EH9 3JG, Midlothian, Scotland.
Scotlands Rural Coll SRUC, Biorefining & Adv Mat Res Ctr, Kings Bldg,West Mains Rd, Edinburgh EH9 3JG, Midlothian, Scotland.
Univ Torino, Dept Agr Forestry & Food Sci DISAFA, Largo P Braccini 2, I-10095 Grugliasco, TO, Italy.
BioAware, Hannut, Belgium.
Univ Ghent, Dept Biol, Res Grp Mycol, 35 KL Ledeganckstr, B-9000 Ghent, Belgium.
Univ South Bohemia, Fac Sci, Branisovska 31, Ceske Budejovice 37005, Czech Republic.
Swedish Museum Nat Hist, Dept Bot, POB 50007, S-10405 Stockholm, Sweden.
Japan Collect Microorganisms RIKEN, Microbe Div, BioResource Res Ctr, 3-1-1 Koyadai, Tsukuba, Ibaraki 3050074, Japan.
Charles Univ Prague, Dept Bot, Prague, Czech Republic.
Mae Fah Luang Univ, Ctr Excellence Fungal Res, Chaing Rai 57100, Thailand.
Cornell Univ, 334 Plant Sci Bldg, Ithaca, NY 14850 USA.
Univ Mauritius, Fac Med & Hlth Sci, Dept Hlth Sci, Reduit, Mauritius.
Manaaki Whenua Landcare Res, Private Bag 92170, Auckland 1142, New Zealand.
EMSL Analyt Inc, 200 Route 130 North, Cinnaminson, NJ 08077 USA.
Yeditepe Univ, Fac Hlth Sci, Dept Nutr & Dietet, Istanbul, Turkey.
Univ Pretoria, Dept Plant & Soil Sci, PBag X20 Hatfield, ZA-0002 Pretoria, South Africa.
Univ Utrecht, Inst Environm Biol Ecol & Biodivers, NL-3584 CH Utrecht, Netherlands.
Rudjer Boskovic Inst, Lab Biol Divers, Bijenicka Cesta 54, HR-10000 Zagreb, Croatia.
Univ Vet Med Vienna VetMed, Inst Food Safety Food Technol & Vet Publ Hlth, Vet Pl 1, A-1210 Vienna, Austria.
BiMM Bioact Microbial Metabolites Grp, A-3430 Tulin Aa Donau, Austria.
Univ Calif Davis, One Shields Ave, Davis, CA 95616 USA.
Chonnam Natl Univ, Coll Agr & Life Sci, Dept Agr Biol Chem, Yongbong Dong 300, Gwangju 61186, South Korea.
Ascofrance, 64 Route Chize, F-79360 Villiers En Bois, France.
Zhejiang Univ, Inst Biotechnol, Key Lab Biol Crop Pathogens & Insects Zhejiang Pr, Key Lab Mol Biol Crop Pathogens & Insects,Minist, 866 Yuhangtang Rd, Hangzhou 310058, Peoples R China.
VN Sukachev Inst Forest SB RAS, Lab Reforestat Mycol & Plant Pathol, Krasnoyarsk 660036, Russia.
Reshetnev Siberian StateUniv Sci & Technol, Dept Chem Technol Wood & Biotechnol, Krasnoyarsk 660037, Russia.
Univ Elect Sci & Technol China, Sch Life Sci AndTechnol, Chengdu 611731, Peoples R China.
Univ Queensland, Ecosci Precinct, Queensland Alliance Agr & Food Innovat, GPO Box 267, Brisbane, Qld 4001, Australia.
Palack Univ, Fac Sci, Dept Bot, Slechtitelu 27, CZ-78371 Olomouc, Czech Republic.
Univ Florence, Dept Agr Food Environm & Forestry Sci & Technol D, Plant Pathol & Entomol Sect, Ple Cascine 28, I-50144 Florence, Italy.
Mie Univ, Grad Sch Bioresources, Kurima Machiya 1577, Tsu, Mie 5148507, Japan.
Universityof Gothenburg, Gothenburg Global Biodivers Ctr, Dept Biol & Environm Sci, Box 461, S-40530 Gothenburg, Sweden.
Univ Batna 2, Fac Nat & Life Sci, Dept Microbiol & Biochem, Batna 05000, Algeria.
PROIMI CONICET, Lab Micodiversidad & Micoprospecc, Av Belgrano & Pje Caseros, San Miguel De Tucuman, Tucuman, Argentina.
Univ Lisbon, Fac Ciencias, Biosyst & Integrat Sci Inst BioISI, P-1749016 Lisbon, Portugal.
Microbial Screening Technol, 28 Percival Rd, Smithfield, NSW 2164, Australia.
Univ Catania, Sez Patol Vegetale, Dipartimento Agr Alimentaz & Ambiente, Via S Sofia 100, I-95123 Catania, Italy.
Van Zanten Breeding BV, Phytopathol, Lavendelweg 15, NL-1435 EW Rijsenhout, Netherlands.
NationalFungal Culture Collect India NFCCI, Biodivers & Palaeobiol Fungi Grp, Agharkar Res Inst, Pune 411004, Maharashtra, India.
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Natl Gene Bank, Lab Microorganisms, Plant Pathol & Populat Genet, Tunis, Tunisia.
Fed Univ Sao Paulo UNIFESP, Dept Microbiol Immunol & Parasitol, Lab Emerging Fungal Pathogens, Discipline Cellular Biol, BR-04023062 Sao Paulo, Brazil.
USDA ARS, Mycol & Nematol Genet Divers & Biol Lab, Bldg 010A,Rm 212,BARC West,10300 Baltimore Ave, Beltsville, MD 20705 USA.
Univ Fed Pernambuco, Ctr Biociencias, Dept Micol Prof Chaves Batista, Cidade Univ,Av Prof Moraes Rego S-N, BR-50670901 Recife, PE, Brazil.
Univ Southern Queensland, Ctr Crop Hlth, Toowoomba, Qld 4350, Australia.
Northwest A&F Univ, Coll Plant Protect, Yangling, Shaanxi, Peoples R China.
Univ Free State, Fac Nat & Agr Sci, Dept Plant Sci, POB 339, ZA-9300 Bloemfontein, South Africa.
Dept Agr & Fisheries, Queensland Plant Pathol Herbarium, Dutton Pk, Qld 4102, Australia.
Royal Bot Garden Edinburgh, 20A Inverleith Row, Edinburgh EH3 5LR, Midlothian, Scotland.
Univ Melbourne, Fac Vet & Agr Sci, Parkville, Vic 3010, Australia.
Eszterhazy Karoly Univ, Food & Wine Res Inst, 6 Leanyka St, H-3300 Eger, Hungary.
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CNR, Inst Sustainable Plant Protect IPSP SS Turin, Viale PA Mattioli 25, I-10125 Turin, Italy.
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Colegio Postgrad, Fitosanidad, Campus Montecillo, Texcoco 56230, Edo De Mexico, Mexico.
Leibniz Inst DSMZ German Collect Microorganisms &, Inhoffenstr 7 B, D-38124 Braunschweig, Germany.
Uppsala Univ, Museum Evolut, Norbyvagen 16, SE-75236 Uppsala, Sweden.
Zhejiang Univ, Coll Agr & Biotechnol, Inst Biotechnol, Minist Agr,Key Lab Mol Biol Crop Pathogens & Inse, 866 Yuhangtang Rd, Hangzhou 310058, Peoples R China.
Goethe Univ Frankfurt Main, Inst Ecol Evolut & Divers, Dept Biol Sci, Max von Laue Str 13, D-60438 Frankfurt, Germany.
LOEWE Ctr Translat Biodivers Genom, Georg Voigt Str 14-16, D-60325 Frankfurt, Germany.

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Crous, P. W.; Lombard, L.; Sandoval-Denis, M.; Seifert, K. A.; Schroers, H-J; Chaverri, P.; Gene, J.; Guarro, J.; Hirooka, Y.; Bensch, K.; Kema, G. H. J.; Lamprecht, S. C.; Cai, A. Y.; Rossman, A. Y.; Stadler, R. C.; Summerbell, R. C.; Taylor, J. W.; Ploch, C. M.; Visagie, C. M.; Yilmaz, J. C.; Frisvad, J. C.; Abdel-Azeem, A. M.; Abdollahzadeh, A.; Abdolrasouli, A.; Akulov, J. F.; Alberts, J. F.; Araujo, J. P. M.; Ariyawansa, H. A.; Bakhshi, A. B.; Bendiksby, T.; Amor, A. Ben Hadj; Bezerra, J. D. P.; Boekhout, R. F.; Camara, M. P. S.; Carbia, V.; Cardinali, J.; Castaneda-Ruiz, R. F.; Celis, U.; Chaturvedi, C. A.; Collemare, R. P.; Croll, C. N.; Damm, X. L.; Decock, C. A.; de Vries, R. P.; Ezekiel, C. N.; Fan, X. L.; Fernandez, N. B.; Gaya, M.; Gonzalez, C. D.; Gramaje, V. K.; Groenewald, J. Z.; Grube, A.; Guevara-Suarez, F.; Gupta, V. K.; Guarnaccia, K.; Haddaji, A.; Hagen, M.; Haelewaters, J.; Hansen, V.; Hashimoto, K. D.; Hernandez-Restrepo, T.; Houbraken, R.; Hubka, P. R.; Hyde, K. D.; Iturriaga, I.; Jeewon, L.; Johnston, P. R.; Jurjevic, I.; Karalti, R.; Korsten, D. P.; Kuramae, E. E.; Kusan, C.; Labuda, H. Y.; Lawrence, D. P.; Lee, H. B.; Lechat, B. M.; Li, H. Y.; Litovka, Y. A.; Maharachchikumbura, S. S. N.; Marin-Felix, L.; Kemkuignou, B. Matio; Matocec, R. H.; McTaggart, A. R.; Mlcoch, I. N.; Mugnai, M. P.; Nakashima, J. I.; Nilsson, R. H.; Noumeur, S. R.; Pavlov, I. N.; Peralta, M. P.; Phillips, A. J. L.; Pitt, J., I; Polizzi, V.; Quaedvlieg, A. M.; Rajeshkumar, K. C.; Restrepo, R. A.; Rhaiem, R. G.; Robert, C. M.; Robert, G. Y.; Rodrigues, A. M.; Salgado-Salazar, S.; Samson, R. A.; Santos, A. C. S.; Shivas, R. G.; Souza-Motta, C. M.; Sun, G. Y.; Swart, W. J.; Szoke, A.; Tan, Y. P.; Taylor, P. W. J.; Tiago, P., V; Vaczy, K. Z.; van de Wiele, J. C.; van der Merwe, N. A.; Verkley, G. J. M.; Vieira, W. A. S.; Vizzini, A.; Weir, B. S.; Wijayawardene, N. N.; Xia, J. W.; Yanez-Morales, M. J.; Yurkov, A.; Zamora, J. C.; Zare, R.; Zhang, C. L.; Thines, M.; Yilmaz, Neriman; da, Ana Carla; bakhshi, mounes; Rodrigues, Anderson M.; Ruiz, Rafael F. Castaneda; Sandoval-Denis, Marcelo; Frisvad, Jens; Stadler, Marc; Abdel-Azeem, Ahmed; Chaturvedi, Vishnu; Pavlov, Igor; Haelewaters, Danny; Zamora, Juan Carlos; Souza-Motta, Cristina

/ T. V. Antipova, V. P. Zhelifonova, Y. A. Litovka [et al.] // iForest. - 2022. - Vol. 15. - P38-46, DOI 10.103832/ifor3840014. - Cited References:28 . - ISSN 1971-7458РУБ Forestry

Аннотация: Basidiomycetes Armillaria infect deciduous, coniferous and fruit trees, causing enormous economic damage. The role of secondary metabolites (tricyclic sesquiterpene aryl esters - melleolides) in the life cycle and pathogenesis of Armillaria is under active investigation. To date, not all species of Armillaria have been tested for the biosynthesis of melleolides. We investigated the secondary metabolite profiles of six root-pathogenic species of the genus Armillaria (A. borealis Marxmuller & Korhonen, A. cepistipes Velenovsky, A. gallica Marxm, A. mellea (Vahl) P. Kummer, A. sinapina Berube & Dessur, A. ostoyae (Romagn.) Herink) distributed in Siberia (South Krasnoyarsk Krai, Republic of Tyva, Republic of Khakassia, Taimyr Peninsula), Russian Far East (Sikhote-Alin) and Crimea (Krymsky National Park, Chatyr-Dag Mountain Lower Plateau). A total of 15 compounds were identified in the metabolome profile. Two compounds (melleolide D and melledonal C) are synthesized by all investigated strains irrespective of their geographic location and host plant. The maximum spectrum of melleolides (7-8 compounds) was found in isolates of A. borealis, A. gallica, A. sinapina, A. ostoyae. In submerged culture, the maximum accumulation of melleolides varied from 2 up to 239 mg l(-1). A mixture of melleolide D and melledonal C (1:1) synthesized by the most productive strain A. mellea Cr2-17 was first found to have a phytotoxic action on the growth parameters of the callus culture Populus balsamifera and 10-day-old conifer seedlings. A 0.5% concentration of melleolides caused a credible decrease of P. balsamifera callus raw biomass; a decrease of the viability of Larix sibirica and, which is especially significant, Pinus sylvestris seedlings; inhibition of stem and root growth processes; dechromation of foliage; loss of turgor. The occurrence of a broad range of melleolides in the metabolome profile and two common compounds in all investigated strains, with a phytotoxic action at their sufficiently high concentration, enables considering the synthesis of melleolides by Armillaria fungi as one of the possible mechanisms of their pathogenicity efficiently realized in strains characterized by overproduction of melleolides under natural conditions.

WOS

Держатели документа:
Russian Acad Sci, GK Skryabin Inst Biochem & Physiol Microorganisms, FRC Pushchino Ctr Biol Res, 5 Prosp Nauki, Pushchino 142290, Moscow Region, Russia.
Russian Acad Sci, VN Sukachev Inst Forest, FRC KSC, Siberian Branch, 50 Akad Gorodok Str, Krasnoyarsk 660036, Russia.
FSBEIHE MF Reshetnev Siberian State Univ Sci & Te, 82 Prosp Mira, Krasnoyarsk 660037, Russia.
FSBEIHE Krasnoyarsk State Agr Univ, 90 Prosp Mira, Krasnoyarsk 660049, Russia.

Доп.точки доступа:
Antipova, Tatyana, V; Zhelifonova, Valentina P.; Litovka, Yulia A.; Pavlov, Igor N.; Baskunov, Boris P.; Kokh, Zhanna A.; Makolova, Polina, V; Timofeev, Anton A.; Kozlovsky, Anatoly G.