12 results on '"Abdollahzadeh, J"'
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2. Massarilactones D and H, phytotoxins produced by Kalmusia variispora , associated with grapevine trunk diseases (GTDs) in Iran.
- Author
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Cimmino A, Bahmani Z, Masi M, Di Lecce R, Amini J, Abdollahzadeh J, Tuzi A, and Evidente A
- Subjects
- Iran, Plant Diseases, Ascomycota, Vitis
- Abstract
A strain of Kalmusia variispora associated with grapevine trunk diseases (GTDs) was identified in Iran and induced disease symptoms on the host in greenhouse conditions. The grapevine pathogens are able to produce a plethora of toxic metabolites belonging to different classes of naturally occurring compounds. Two homogeneous compounds were isolated from the organic extract of K. variispora culture filtrates. They were identified by physic (specific optical rotation), and spectroscopic (essentially 1D
1 H and13 C NMR and HR ESIMS) methods as the fungal polyketides massarilactones D and H ( 1 and 2 ). The unassigned absolute configuration of massarilactone D was unambiguously determined by X-ray diffractometric analysis. Massarilactones D and H showed phytotoxic activity on Vitis vinifera L. at two concentrations used and depending from the days of inoculation. Phytotoxicity is also increased when the 3,4,7- O,O',O"- triacetyl derivative of massarilactone D ( 3 ) was assayed on the host plant. This is the first report on the investigation of phytotoxic metabolites produced by K. variispora isolated from infected grapevine in Iran and they seem to be involved in the development of disease symptoms.- Published
- 2021
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3. Phytotoxins Produced by Two Biscogniauxia rosacearum Strains, Causal Agents of Grapevine Trunk Diseases, and Charcoal Canker of Oak Trees in Iran.
- Author
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Masi M, Bashiri S, Cimmino A, Bahmani Z, Abdollahzadeh J, and Evidente A
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- Ascomycota metabolism, Charcoal, Iran, Mycotoxins chemistry, Mycotoxins isolation & purification, Quercus microbiology, Structure-Activity Relationship, Vitis microbiology, Ascomycota pathogenicity, Mycotoxins toxicity, Plant Diseases microbiology
- Abstract
Biscogniauxia rosacearum, recognized for the first time as a pathogen involved in grapevine trunk diseases in Paveh (west of Iran) vineyards, produced meso -2,3-butanediol ( 1 ) as the only phytotoxin. Nectriapyrone ( 2 ), (3 R )-5-methylmellein ( 3 ), (3 R )-5-methyl-6-methoxymellein ( 4 ), and tyrosol ( 5 ) were instead produced as phytotoxins from a strain of the same fungus isolated from oak trees in Zagros forests of Gilan-e Gharb, Kermanshah Province. They were identified comparing their
1 H and13 C NMR, ESIMS, and specific optical rotation data with those already reported in the literature. The phytotoxicity of metabolites ( 1-5 ) was estimated by leaf puncture assay on Quercus ilex L. and Hedera helix L., and by leaf absorption assay on grapevine ( Vitis vinifera L.) at a concentration of 5 × 10-3 and 10-3 M. Tested on grapevine, meso -2,3-butanediol ( 1 ) and (3 R )-5-methyl-6-methoxymellein ( 4 ) resulted to be the most phytotoxic compounds. On Q. ilex , nectriapyrone ( 2 ) and tyrosol ( 5 ) showed severe necrosis at the highest concentration while none of the compounds ( 1 - 5 ) was active on H. helix . Furthermore, the phytotoxicity of compounds 3 and 4 was also compared with that of some related natural melleins to perform a structure-activity relationship (SAR) study. The results of this study were also discussed.- Published
- 2021
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4. Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata , a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran.
- Author
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Cimmino A, Bahmani Z, Castaldi S, Masi M, Isticato R, Abdollahzadeh J, Amini J, and Evidente A
- Subjects
- Antifungal Agents pharmacology, Basidiomycota, Iran, Phenazines, Plant Diseases, Ascomycota, Vitis
- Abstract
The phytopathogenic fungus Truncatella angustata , associated with grapevine trunk diseases (GTDs) in Iran, produces the well-known secondary metabolite isocoumumarin (+)-6-hyroxyramulosin and surprisingly also phenazine-1-carboxylic acid (PCA). PCA, identified by spectroscopic (essentially
1 H NMR and ESI MS) spectra, is a bacterial metabolite well known for its antifungal activity and was found for the first time in T. angustata culture filtrates. The antifungal activity of PCA was assayed against four different fungi responsible for GTDs, Phaeoacremonium minimum , Phaeoacremonium italicum , Fomitiporia mediterranea , involved in grapevine esca disease, and Neofusicoccum parvum , responsible for Botryosphaeria dieback. The activity was compared with that of the known commercial fungicide, pentachloronitrobenzene, and the close phenazine. PCA and phenazine exhibited strong antifungal activity against all phytopathogenic fungi, inhibiting the fungal growth by about 90-100% and 80-100%, respectively. These results suggested that T. angustata could use PCA to compete with other phytopathogenic fungi that attack grapevine and thus PCA could be proposed as a biofungicide against the fungi responsible for grapevine esca and Botryosphaeria dieback diseases.- Published
- 2021
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5. Biscogniauxia rosacearum the charcoal canker agent as a pathogen associated with grapevine trunk diseases in Zagros region of Iran.
- Author
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Bahmani Z, Abdollahzadeh J, Amini J, and Evidente A
- Subjects
- Ascomycota genetics, Ascomycota isolation & purification, DNA, Intergenic genetics, Geography, Iran, Phylogeny, Ascomycota pathogenicity, Plant Diseases microbiology, Vitis microbiology
- Abstract
Grapevine trunk diseases (GTDs) are well-known and significant fungal diseases of Vitis vinifera with a worldwide distribution. During August to November 2016 in a survey to characterize fungi associated with grapevine trunk diseases in Kermanshah Province (west of Iran) vineyards, 286 fungal isolates were obtained. Based on morphology and DNA sequences data eight species were identified, of which Biscogniauxia rosacearum, Neoscytalidium hyalinum and Phaeoacremonium minimum were the most aggressive fungal pathogenic species characterized in this research. N. hyalinum was the most prevalent species. N. hyalinum and Ph. minimum have previously been reported from Vitis vinifera. Thus far, there are two records of Biscogniauxia mediterranea and Biscogniauxia capnodes on grapevine in the world with no data on pathology aspects. To our knowledge, it is the first time B. rosacearum is reported from grapevine across the globe. Pathogenicity test with three strains of B. rosacearum on 2-year-old potted grapevines confirmed the pathogenicity of B. rosacearum on grapevine. The proximity of vineyards to the oak trees in Zagros forests as one of the plant hosts of Biscogniauxia spp. further highlights the need for extensive studies on B. rosacearum as a new fungal pathogen.
- Published
- 2021
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6. Development of an efficient Tef-1α RNA hairpin structure to efficient management of Lasiodiplodia theobromae and Neofusicoccum parvum.
- Author
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Nili O, Azizi A, and Abdollahzadeh J
- Subjects
- Disease Resistance, Fragaria microbiology, Vitis microbiology, Ascomycota, Fragaria genetics, Plant Diseases microbiology, RNA, Small Interfering, Vitis genetics
- Abstract
Lasiodiplodia theobromae and Neofusicoccum parvum are serious worldwide-distributed plant pathogenic fungi with a wide host range in tropical and temperate climates. They cause fruit rot, canker, and dieback of twigs in various woody plants. Protection of pruning wounds using fungicides is the prevalent strategy for the management of the diseases caused by these fungi. Chemical control of plant diseases is not environmentally safe and the residues of fungicides are a threat to nature. Furthermore, genetic resources of resistance to plant diseases in woody plants are limited. The aim of this study was to investigate the efficiency of RNA silencing using an efficient hairpin structure based on Tef-1α gene for the management of L. theobromae and N. parvum. Hairpin structure of Tef-1α was cloned in pFGC5941 binary vector and the recombinant construct was named pFGC-TEF-d. Transient expression of pFGC-TEF-d using Agrobacterium LBA4404 in grapevine (Bidaneh Sefid cv.) and strawberry cultivars (Camarosa and Ventana) led to a reduction in disease progress of L. theobromae. The disease reduction in grapevine was estimated by 55% and in strawberries cultivars Camarosa and Ventana by 58% and 93%, respectively. Further analysis of transient expression of pFGC-TEF-d in strawberry (Camarosa) shown disease reduction using Neofusicoccum parvum. Here we introduce RNAi silencing using pFGC-TEF-d construct as an efficient strategy to the management of L. theobromae and N. parvum for the first time.
- Published
- 2021
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7. Families, genera, and species of Botryosphaeriales.
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Yang T, Groenewald JZ, Cheewangkoon R, Jami F, Abdollahzadeh J, Lombard L, and Crous PW
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- Cluster Analysis, DNA, Fungal chemistry, DNA, Fungal genetics, Genes, rRNA, Phylogeny, RNA Polymerase II genetics, RNA, Fungal genetics, RNA, Ribosomal genetics, Sequence Analysis, DNA, Ascomycota classification, Ascomycota genetics, Plant Diseases microbiology, Plants microbiology
- Abstract
Members of Botryosphaeriales are ecologically diverse, but most commonly associated with leaf spots, fruit and root rots, die-back or cankers of diverse woody hosts. Based on morphology and DNA sequence data, the Botryosphaeriales have to date been shown to contain eight families, with an additional two, Endomelanconiopsisaceae (Endomelanconiopsis) and Pseudofusicoccumaceae (Pseudofusicoccum) being newly described in this study. Furthermore, Oblongocollomyces is introduced as new genus, while Spencermartinsia is reduced to synonymy under Dothiorella. Novel species include Diplodia pyri (Pyrus sp., the Netherlands), Diplodia citricarpa (Citrus sp., Iran), Lasiodiplodia vitis (Vitis vinifera, Italy), L. sterculiae (Sterculia oblonga, Germany), Neofusicoccum pistaciarum (Pistacia vera, USA), N. buxi (Buxus sempervirens, France), N. stellenboschiana (Vitis vinifera, South Africa), and Saccharata hawaiiensis (Protea laurifolia, Hawaii). New combinations are also proposed for Camarosporium pistaciae (associated with fruit rot of Pistacia vera) in Neofusicoccum, and Sphaeria gallae (associated with galls of Quercus) in Diplodia. The combination of large subunit of the nuclear ribosomal RNA gene (LSU)-rpb2 proved effective at delineating taxa at family and generic level. Furthermore, rpb2 also added additional resolution for species delimitation, in combination with ITS, tef1 and tub2. In this study we analysed 499 isolates, and produce an expanded phylogenetic backbone for Botryosphaeriales, which will help to delimit novelties at species, genus and family level in future., (Copyright © 2016 British Mycological Society. Published by Elsevier Ltd. All rights reserved.)
- Published
- 2017
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8. Efficiency of rep-PCR fingerprinting as a useful technique for molecular typing of plant pathogenic fungal species: Botryosphaeriaceae species as a case study.
- Author
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Abdollahzadeh J and Zolfaghari S
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- Ascomycota classification, Ascomycota genetics, DNA Primers genetics, Plants microbiology, Ascomycota isolation & purification, DNA Fingerprinting methods, Molecular Typing methods, Mycological Typing Techniques methods, Plant Diseases microbiology, Polymerase Chain Reaction methods
- Abstract
Progress in molecular biology and the advent of rapid and accurate molecular techniques have contributed to precise and rapid detection and differentiation of microbial pathogens. Identification of the Botryosphaeriaceae species based on morphology has been problematic over time. In this study, we used rep-PCR technique as a molecular tool for typing and differentiation of the Botryosphaeriaceae species, well-known and cosmopolitan fungal pathogens on woody plants. Three primer sets BOX, ERIC and REP were used to differentiate 27 species belong to eight genera. The majority of them were examined in terms of typing and differentiation using molecular methods for the first time. All the primer sets were able to generate species-specific DNA fingerprints from all the tested strains, with two exceptions in the genera Diplodia and Spencermartinsia. Despite the deficiency of each primer sets to separate a few species, cluster analysis of combined data sets indicated the ability of rep-PCR technique to separate 26 out of 27 examined species in highly supported clusters corresponded to the species recognized based on DNA sequence data. Our findings revealed the efficiency of rep-PCR for detection and differentiation of the Botryosphaeriaceae species, especially cryptic species with the same ITS sequences and similar morphology., (© 2014 Federation of European Microbiological Societies. Published by John Wiley & Sons Ltd. All rights reserved.)
- Published
- 2014
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9. Phylogeny and taxonomy of Botryosphaeria and Neofusicoccum species in Iran, with description of Botryosphaeria scharifii sp. nov.
- Author
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Abdollahzadeh J, Zare R, and Phillips AJ
- Subjects
- Ascomycota genetics, Ascomycota growth & development, DNA, Fungal genetics, DNA, Ribosomal Spacer genetics, Iran, Molecular Sequence Data, Spores, Fungal classification, Spores, Fungal genetics, Spores, Fungal growth & development, Spores, Fungal isolation & purification, Ascomycota classification, Ascomycota isolation & purification, Mangifera microbiology, Phylogeny, Plant Diseases microbiology
- Abstract
Species of Botryosphaeriaceae are important pathogens and endophytes associated with woody plants. Botryosphaeria and Neofusicoccum are two well known genera of the family. In this study 125 isolates morphologically resembling members of this family were collected from about 20 different fruit and forest trees in Iran. Based on morphology, MSP-PCR profile and DNA sequence data (ITS and tef1-a), four species were identified. Of these, Botryosphaeria dothidea, Neofusicoccum mediterraneum and N. parvum are known while Botryosphaeria scharifii is described here as new. N. mediterraneum is a new record for Iran and is reported here for the first time on mango trees. High diversity within Iranian population of N. parvum suggests the need to revise and reassess the morphological species description of N. parvum and closely related species.
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- 2013
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10. Fusarium chuoi R. Hill, Gaya, D.T. Vu, Sand.-Den. & Crous, R. Hill, Gaya, D.T. Vu, Sand.-Den. & Crous sp. nov
- Author
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Crous, P.W., Osieck, E.R., Jurjevi, ��, Boers, J., Van Iperen, A.L., Starink-Willemse, M., Dima, B., Balashov, S., Bulgakov, T.S., Johnston, P.R., Morozova, O.V., Pinruan, U., Sommai, S., Alvarado, P., Decock, C.A., Lebel, T., McMullan-Fisher, S., Moreno, G., Shivas, R.G., Zhao, L., Abdollahzadeh, J., Abrinbana, M., Ageev, D.V., Akhmetova, G., Alexandrova, A.V., Alt��s, A., Amaral, A.G.G., Angelini, C., Anton��n, V., Arenas, F., Asselman, P., Badali, F., Baghela, A., Ba��ares, A., Barreto, R.W., Baseia, I.G., Bellanger, J.-M., Berraf-Tebbal, A., Biketova, A. Yu., Bukharova, N.V., Burgess, T.I., Cabero, J., C��mara, M.P.S., Cano-Lira, J.F., Ceryngier, P., Ch��vez, R., Cowan, D.A., de Lima, A.F., Oliveira, R.L., Denman, S., Dang, Q.N., Dovana, F., Duarte, I.G., Eichmeier, A., Erhard, A., Esteve-Ravent��s, F., Fellin, A., Ferisin, G., Ferreira, R.J., Ferrer, A., Finy, P., Gaya, E., Geering, A.D.W., Gil-Dur��n, C., Gl��ssnerov��, K., Glushakova, A.M., Gramaje, D., Guard, F.E., Guarnizo, A.L., Haelewaters, D., Halling, R.E., Hill, R., Hirooka, Y., Hubka, V., Iliushin, V.A., Ivanova, D.D., Ivanushkina, N.E., Jangsantear, P., Justo, A., Kachalkin, A.V., Kato, S., Khamsuntorn, P., Kirtsideli, I.Y., Knapp, D.G., Kochkina, G.A., Koukol, O., Kov��cs, G.M., Kruse, J., Kumar, T.K.A., Ku��an, I., L��ss��e, T., Larsson, E., Lebeuf, R., Levic��n, G., Loizides, M., Marinho, P., Luangsa-ard, J.J., Lukina, E.G., Maga��a-Due��as, V., Maggs-K��lling, G., Malysheva, E.F., Malysheva, V.F., Mart��n, B., Mart��n, M.P., Mato��ec, N., McTaggart, A.R., Mehrabi-Koushki, M., Me��i��, A., Miller, A.N., Mironova, P., Moreau, P.-A., Morte, A., M��ller, K., Nagy, L.G., Nanu, S., Navarro-R��denas, A., Nel, W.J., Nguyen, T.H., N��brega, T.F., Noordeloos, M.E., Olariaga, I., Overton, B.E., Ozerskaya, S.M., Palani, P., Pancorbo, F., Papp, V., Paw��owska, J., Pham, T.Q., Phosri, C., Popov, E.S., Portugal, A., Po��ta, A., Reschke, K., Reul, M., Ricci, G.M., Rodr��guez, A., Romanowski, J., Ruchikachorn, N., Saar, I., Safi, A., Sakolrak, B., Salzmann, F., Sandoval-Denis, M., Sangwichein, E., Sanhueza, L., Sato, T., Sastoque, A., Senn-Irlet, B., Shibata, A., Siepe, K., Somrithipol, S., Spetik, M., Sridhar, P., Stchigel, A.M., Stuskova, K., Suwannasai, N., Tan, Y.P., Thangavel, R., Tiago, I., Tiwari, S., Tkal��ec, Z., Tomashevskaya, M.A., Tonegawa, C., Tran, H.X., Tran, N.T., Trov��o, J., Trubitsyn, V.E., Van Wyk, J., Vieira, W.A.S., Vila, J., Visagie, C.M., Vizzini, A., Volobuev, S.V., Vu, D.T., Wangsawat, N., Yaguchi, T., Ercole, E., Ferreira, B.W., de Souza, A.P., Vieira, B.S., and Groenewald, J.Z.
- Subjects
Ascomycota ,Sordariomycetes ,Hypocreales ,Fungi ,Nectriaceae ,Biodiversity ,Taxonomy - Abstract
Crous, P.W., Osieck, E.R., Jurjevi, ��, Boers, J., Van Iperen, A.L., Starink-Willemse, M., Dima, B., Balashov, S., Bulgakov, T.S., Johnston, P.R., Morozova, O.V., Pinruan, U., Sommai, S., Alvarado, P., Decock, C.A., Lebel, T., McMullan-Fisher, S., Moreno, G., Shivas, R.G., Zhao, L., Abdollahzadeh, J., Abrinbana, M., Ageev, D.V., Akhmetova, G., Alexandrova, A.V., Alt��s, A., Amaral, A.G.G., Angelini, C., Anton��n, V., Arenas, F., Asselman, P., Badali, F., Baghela, A., Ba��ares, A., Barreto, R.W., Baseia, I.G., Bellanger, J.-M., Berraf-Tebbal, A., Biketova, A. Yu., Bukharova, N.V., Burgess, T.I., Cabero, J., C��mara, M.P.S., Cano-Lira, J.F., Ceryngier, P., Ch��vez, R., Cowan, D.A., de Lima, A.F., Oliveira, R.L., Denman, S., Dang, Q.N., Dovana, F., Duarte, I.G., Eichmeier, A., Erhard, A., Esteve-Ravent��s, F., Fellin, A., Ferisin, G., Ferreira, R.J., Ferrer, A., Finy, P., Gaya, E., Geering, A.D.W., Gil-Dur��n, C., Gl��ssnerov��, K., Glushakova, A.M., Gramaje, D., Guard, F.E., Guarnizo, A.L., Haelewaters, D., Halling, R.E., Hill, R., Hirooka, Y., Hubka, V., Iliushin, V.A., Ivanova, D.D., Ivanushkina, N.E., Jangsantear, P., Justo, A., Kachalkin, A.V., Kato, S., Khamsuntorn, P., Kirtsideli, I.Y., Knapp, D.G., Kochkina, G.A., Koukol, O., Kov��cs, G.M., Kruse, J., Kumar, T.K.A., Ku��an, I., L��ss��e, T., Larsson, E., Lebeuf, R., Levic��n, G., Loizides, M., Marinho, P., Luangsa-ard, J.J., Lukina, E.G., Maga��a-Due��as, V., Maggs-K��lling, G., Malysheva, E.F., Malysheva, V.F., Mart��n, B., Mart��n, M.P., Mato��ec, N., McTaggart, A.R., Mehrabi-Koushki, M., Me��i��, A., Miller, A.N., Mironova, P., Moreau, P.-A., Morte, A., M��ller, K., Nagy, L.G., Nanu, S., Navarro-R��denas, A., Nel, W.J., Nguyen, T.H., N��brega, T.F., Noordeloos, M.E., Olariaga, I., Overton, B.E., Ozerskaya, S.M., Palani, P., Pancorbo, F., Papp, V., Paw��owska, J., Pham, T.Q., Phosri, C., Popov, E.S., Portugal, A., Po��ta, A., Reschke, K., Reul, M., Ricci, G.M., Rodr��guez, A., Romanowski, J., Ruchikachorn, N., Saar, I., Safi, A., Sakolrak, B., Salzmann, F., Sandoval-Denis, M., Sangwichein, E., Sanhueza, L., Sato, T., Sastoque, A., Senn-Irlet, B., Shibata, A., Siepe, K., Somrithipol, S., Spetik, M., Sridhar, P., Stchigel, A.M., Stuskova, K., Suwannasai, N., Tan, Y.P., Thangavel, R., Tiago, I., Tiwari, S., Tkal��ec, Z., Tomashevskaya, M.A., Tonegawa, C., Tran, H.X., Tran, N.T., Trov��o, J., Trubitsyn, V.E., Van Wyk, J., Vieira, W.A.S., Vila, J., Visagie, C.M., Vizzini, A., Volobuev, S.V., Vu, D.T., Wangsawat, N., Yaguchi, T., Ercole, E., Ferreira, B.W., de Souza, A.P., Vieira, B.S., Groenewald, J.Z. (2021): Fusarium chuoi R. Hill, Gaya, D.T. Vu, Sand.-Den. & Crous, R. Hill, Gaya, D.T. Vu, Sand.-Den. & Crous sp. nov. Fungal Planet 47 (1): 310-311, DOI: http://doi.org/10.5281/zenodo.5856199, URL: http://dx.doi.org/10.3767/persoonia.2021.47.06, {"references": ["Abad ZG, Burgess TI,Bienapfl JC,et al.2019.IDphy:Molecular and morphological identification of Phytophthora based on the types.USDAAPHIS PPQ S&T Beltsville Lab, USDA APHIS PPQ S&T ITP, Centre for Phytophthora Science and Management, and World Phytophthora Collection.", "Abdollahzadeh J, Groenewald JZ, Coetzee MPA, et al. 2020. Evolution of lifestyles in Capnodiales. Studies in Mycology 95: 381-414.", "Alvarado P, Cabero J, Moreno G, et al. 2014. Species diversity of Genea (Ascomycota, Pezizales) in Europe. Ascomycete.org 6: 41-51.", "Alvarado P, Cabero J, Moreno G, et al. 2016. Phylogenetic overview of the genus Genea (Pezizales, Ascomycota) with an emphasis on European taxa. Mycologia 108: 441-456.", "Alvarado P, Perez J-B, Van Vooren N, et al. 2020. Genea coronata (Pyronemataceae, Pezizales), a cryptic new species in a highly polymorphic genus. Sydowia 72: 231-242.", "Anonymous. 1969. Flora of British Fungi - Colour Identification Chart. Her Majesty's Stationery Office, Edinburgh.", "Antonin V, Noordeloos M. 2010. A monograph of marasmioid and collybioid fungi in Europe. IHW Verlag.", "Arzanlou A, Groenewald JZ, Gams W, et al. 2007. Phylogenetic and morphotaxonomic revision of Ramichloridium and allied genera. Studies in Mycology 58: 57-93.", "Aveskamp MM, Verkley GJM, De Gruyter J, et al. 2009. DNA phylogeny reveals polyphyly of Phoma section Peyronellaea and multiple taxonomic novelties. Mycologia 101: 363-382.", "Bandini D, Oertel B, Ploch S, et al. 2019.Revision of some central European species of Inocybe (Fr.: Fr.) Fr. subgenus Inocybe, with description of five new species. Mycological Progress 18: 247-294.", "Bandini D, Sesli E, Oertel B, et al. 2020.Inocybe antoniniana,a new species of Inocybe section Marginatae with nodulose spores.Sydowia 72: 95-106.", "Bao DF, Wanasinghe DN, Luo ZL, et al. 2019. Murispora aquatica sp. nov. and Murispora fagicola, a new record from freshwater habitat in China. Phytotaxa 416: 1-13.", "Baral H-O.1987.Lugol's solution / IKI versus Melzer's reagent:hemiamyloidity, a universal feature of the ascus wall. Mycotaxon 29: 399-450.", "Bates ST, Roberson RW, Desjardin DE. 2009. Arizona gasteroid fungi I: Lycoperdaceae (Agaricales,Basidiomycota).Fungal Diversity 37:153-207.", "Bensch K, Groenewald JZ, Braun U, et al. 2015. Common but different: The expanding realm of Cladosporium. Studies in Mycology 82: 23-74.", "Bensch K, Groenewald JZ, Meijer M, et al. 2018. Cladosporium species in indoor environments. Studies in Mycology 89: 177-301.", "Berkeley,MJ.1845.Decades of Fungi:Australian Fungi.The London Journal of Botany 4: 42-73.", "Bertault R. 1965. Amanites du Maroc. Bulletin trimestriel de la Societe mycologique de France 81: 345-371.", "Bezerra JDP, Sandoval-Denis M, Paiva LM, et al. 2017. New endophytic Toxicocladosporium species from cacti in Brazil, and description of Neocladosporium gen. nov. IMA Fungus 8: 77-97.", "Bien S, Kraus C, Damm U. 2020. Novel collophorina-like genera and species from Prunus trees and vineyards in Germany. Persoonia 45: 46-67.", "Boerema GH,De Gruyer J, Noordeloos ME,et al. 2004.Phoma identification manual. Differentiation of specific and intra-specific and intra-specific taxa in culture. CABI Publishing, Wallingford, UK.", "Bose T, Wingfield MJ, Roux J, et al. 2021. Phytophthora species associated with roots of native and non-native trees in natural and managed forests Microbial Ecology 81: 122-133.", "Braun U. 1998.A monograph of Cercosporella,Ramularia and allied genera (phytopathogenic hyphomycetes), Vol. 2, IHW-Verlag, Eching, Munich, Germany.", "Buisman CJ. 1927. Root rots caused by Phycomycetes. Mededelingen uit het Phytopathologisch laboratorium Willie Commelin Scholten 11: 1-65.", "Bukharova NV, Zmitrovich IV. 2014. Aphyllophoroid fungi of the Bastak Reserve. Mikologiya i fitopatologiya 48: 343-354.", "Castaneda-Ruiz RF.1984.Nuevos taxones de Deuteromycotina:Arnoldiella robusta gen. et sp. nov.; Roigiella lignicola gen. et sp. nov.; Sporidesmium pseudolmediae sp.nov.y Thozetella havanensis sp.nov.Revista del Jardin Botanico Nacional Universidad de la Habana 5: 57-87.", "Castaneda-Ruiz RF, Gams W, Saikawa M. 1997. Three new conidial fungi (hyphomycetes) from Cuba. Nova Hedwigia 64: 473-483.", "Chen C, Verkley GJM, Sun G, et al. 2016. Redefining common endophytes and plant pathogens in Neofabraea, Pezicula, and related genera.Fungal Biology 120: 1291-1322.", "Chen Q, Hou LW, Duan WJ, et al. 2017. Didymellaceae revisited. Studies in Mycology 87: 105-159.", "Chen Q, Jiang JR, Zhang GZ, et al. 2015. Resolving the Phoma enigma. Studies in Mycology 82: 137-217.", "Chernomor O, von Haeseler A, Minh BQ. 2016. Terrace aware data structure for phylogenomic inference from supermatrices. Systematic Biology 65: 997-1008.", "Contu M. 1985a '1984'. Novitates (2). Documents Mycologiques 14: 26.", "Contu M. 1985b.Amanita mairei Foley sensu Foley.A.mairei sensu Bertault: Nome nuovo per la specie di Bertault:Amanita bertaultii sp. nov. Funghie Ambiente 1: 11-13.", "Contu M.2000.Chiave per la determinazione delle specie europee del genere Amanita sez. Vaginatae. Bollettino del gruppo micologico G. Bresadola 43: 233-240.", "Contu M, Pacioni G. 1998.Amanita cistetorum and Psathyrella liciosae, two new Mediterranean species. Mycotaxon 69: 437-446.", "Corriol G. 2003. Pluteus diverticulatus sp. nov., une espece nouvelle de la sous-section Mixtini. Bulletin Trimestriel de la Societe Mycologique de France 119: 231-244.", "Corriol G, Moreau PA,Bellanger JM. 2017.Calocybe hymenoderma sp. nov., Calocybella juncicola comb.nov. et les contours taxinomiques de la section Rugosomyces. Errotari 14: 35-46.", "Crandall BS. 1947.A new Phytophthora causing root and collar rot of cinchona in Peru. Mycologia 39: 218-223.", "Crous PW, Braun U, McDonald BA, et al.2020a.Redefining genera of cereal pathogens: Oculimacula, Rhynchosporium and Spermospora. Fungal Systematics and Evolution 7: 67-98.", "Crous PW, Braun U, Wingfield MJ, et al. 2009. Phylogeny and taxonomy of obscure genera of microfungi. Persoonia 22: 139-161.", "Crous PW, Carnegie AJ,Wingfield MJ,et al. 2019a.Fungal Planet description sheets: 868-950. Persoonia 42: 291-473.", "Crous PW, Cowan DA, Maggs-Kolling G, et al.2021a.Fungal Planet description sheets: 1182-1283. Persoonia 46: 313-528.", "Crous PW, Groenewald JZ,Mansilla JP, et al. 2004. Phylogenetic reassessment of Mycosphaerella spp. and their anamorphs occurring on Eucalyptus. Studies in Mycology 50: 195-214.", "Crous PW, Lombard L, Sandoval-Denis M, et al. 2021b. Fusarium: more than a node or a foot-shaped basal cell. Studies in Mycology 98: 100116.", "Crous PW, Luangsa-ard JJ, Wingfield MJ, et al. 2018a. Fungal Planet description sheets: 785-867. Persoonia 41: 238-417.", "Crous PW, Schumacher RK, Akulov A, et al. 2019b. New and Interesting Fungi. 2. Fungal Systematics and Evolution 3: 57-134.", "Crous PW, Schumacher RK,Wingfield MJ, et al. 2018b.New and interesting fungi. 1. Fungal Systematics and Evolution 1: 169-215.", "Crous PW, Shivas RG,Quaedvlieg W,et al. 2014a.Fungal Planet description sheets: 214-280. Persoonia 32: 184-306.", "Crous PW, Summerell BA,Shivas RG, et al. 2011. Fungal Planet description sheets: 92-106. Persoonia 27: 130-162.", "Crous PW, Verkley GJM, Christensen M, et al. 2012. How important are conidial appendages? Persoonia 28:126-137.", "Crous PW, Wingfield MJ, Burgess TI, et al. 2017. Fungal Planet description sheets: 625-715. Persoonia 39: 270-467.", "Crous PW, Wingfield MJ, Cheewangkoon R, et al. 2019c. Foliar pathogens of eucalypts. Studies in Mycology 94: 125-298.", "Crous PW, Wingfield MJ, Chooi Y-H,et al. 2020b. Fungal Planet description sheets: 1042-1111. Persoonia 44: 301-459.", "Crous PW, Wingfield MJ, le Roux JJ, et al. 2015. Fungal Planet description sheets: 371-399. Persoonia 35: 264-327.", "Crous PW, Wingfield MJ,Lombard L, et al.2019d. Fungal Planet description sheets: 951-1041. Persoonia 43: 223-425.", "Crous PW, Wingfield MJ,Richardson DM, et al.2016.Fungal Planet description sheets: 400-468. Persoonia 36: 316-458.", "Crous PW, Wingfield MJ, Schumacher RK, et al. 2014b. Fungal Planet description sheets 281-319. Persoonia 33: 212-289.", "Crous PW, Wingfield MJ, Schumacher RK,et al. 2020c.New and interesting fungi 3. Fungal Systematics and Evolution 6: 157-231.", "Darriba D, Taboada GL, Doallo R, et al. 2012. jModelTest 2: more models, new heuristics and parallel computing. Nature Methods 9: 772.", "De Gruyter J, Noordeloos ME. 1992. Contributions towards a monograph of Phoma (Coelomycetes) - I. 1. Section Phoma:Taxa with very small conidia in vitro. Persoonia 15: 71-92.", "De Gruyter J, Noordeloos ME, Boerema GH. 1993. Contributions towards a monograph of Phoma (Coelomycetes) - I. 2. Section Phoma:Additional taxa with very small conidia and taxa with conidia up to 7 \u00b5m long. Persoonia 15: 369-400.", "De Hoog GS. 1977. Rhinocladiella and allied genera. Studies in Mycology 15: 1-140.", "De Hoog GS, Mayser P, Haase G, et al. 2000.A new species, Phialophora europaea,causing superficial infections in humans.Mycoses 43:409-416.", "Denk T, Grimm GW. 2010. The oaks of western Eurasia: Traditional classifications and evidence from two nuclear markers. Taxon 59: 351-366.", "Diederich P,Braun U. 2009.First lichenicolous record of Acremonium hypholomatis (anamorphic Ascomycota). Bulletin de la Societe des naturalistes luxembourgeois 110: 97-99.", "Domsch KH, Gams W, Anderson TH. 1993. Compendium of soil fungi. Reprinted by IHW-Verlag with supplement.", "Domsch KH, Gams W,Anderson T-H. 2007. Compendium of soil fungi. 2nd ed. IHW-Verlag, Eching, Germany.", "Dong W, Hyde KD, Jeewon R, et al. 2021. Towards a natural classification of annulatascaceae-like taxa II: introducing five new genera and eighteen new species from freshwater. Mycosphere 12: 1-88.", "Drummond AJ, Suchard MA, Xie D, et al. 2012. Bayesian phylogenetics with BEAUti and the BEAST 1.7. Molecoluar Biology and Evolution 29: 1969-1973.", "Duan JX, Wu WP, Liu XZ. 2007. Dinemasporium (coelomycetes). Fungal Diversity 26: 205-218.", "Edler D, Klein J, Antonelli A, et al. 2020. raxmlGUI 2.0: a graphical interface and toolkit for phylogenetic analyses using RAxML. Methods in Ecology and Evolution 12: 373-377.", "Egidi E, De Hoog GS, Isola D, et al. 2014. Phylogeny and taxonomy of meristematic rock-inhabiting black fungi in the Dothideomycetes based on multi-locus phylogenies. Fungal Diversity 65: 127-165.", "Ekanayaka AH, Hyde KD,Gentekaki E, et al. 2019. Preliminary classification of Leotiomycetes. Mycosphere 10: 310-489.", "Esteve-Raventos F, Moreno G, Bizio E, et al. 2015. Inocybe flavobrunnescens, a new species in section Marginatae. Mycological Progress 14: 14.", "Farr DF, Rossman AY. Fungal Databases, U.S. National Fungus Collections, ARS, USDA. Retrieved October 14, 2021, from https://nt.ars-grin. gov/fungaldatabases/.", "Fassatiova O. 1986.Moulds and filamentous fungi in technical microbiology. Elsevier, Amsterdam.", "Fechner N, Bonito G,Bougher NL,et al. 2017.New species of Austroboletus (Boletaceae) in Australia. Mycological Progress 16: 769-775.", "Feng P, Lu Q, Najafzadeh MJ, et al. 2014. Cyphellophora and its relatives in Phialophora biodiversity and possible role in human infection. Fungal Diversity 65: 17-45.", "Fries E. 1821. Systema mycologicum 1. Ex officina Berlingiana, Lund, Sweden.", "Gams W. 1971. Cephalosporium-artige Schimmelpilze (Hyphomycetes), Fischer, Stuttgart, Germany.", "Gams W. 1975. Cephalosporium-like Hyphomycetes:Some tropical species. Transactions of the British Mycological Society 64: 389-404.", "Gams W. 1976. Some new or noteworthy species of Mortierella. Persoonia 9: 111-140.", "Giraldo A,Gene J, Sutton DA, et al. 2015. Phylogeny of Sarocladium (Hypocreales). Persoonia 34: 10-24.", "Goncalves MFM, Santos L, Silva BMV,et al. 2019.Biodiversity of Penicillium species from marine environments in Portugal and description of Penicillium lusitanum sp. nov., a novel species isolated from sea water. International Journal of Systematic and Evolutionary Microbiology 69: 3014-3021.", "Gouy M, Guindon S, Gascuel O. 2010. SeaView version 4: A multiplatform graphical user interface for sequence alignment and phylogenetic tree building. Molecular Biology and Evolution 27: 221-224.", "Grafenhan T, Schroers H-J, Nirenberg HI, et al. 2011. An overview of the taxonomy,phylogeny,and typification of nectriaceous fungi in Cosmospora, Acremonium, Fusarium, Stilbella, and Volutella. Studies in Mycology 68: 79-113.", "Gryzenhout M, Tarigan M, Clegg PA,et al.2010. Cryptometrion aestuescens gen. sp. nov. (Cryphonectriaceae) pathogenic to Eucalyptus in Indonesia. Australasian Plant Pathology 39: 161-169.", "Guindon S, Lethiec F, Duroux P et al. 2010. PHYML Online - a web server for fast maximum likelihood-based phylogenetic inference. Nucleic Acids Research 33: W557-W559.", "Guzman-Davalos L, Pradeep CK, Vrinda KB, et al. 2017. A new stipitate species of Crepidotus from India and Thailand,with notes on other tropical species. Mycologia 109: 804-814.", "Haelewaters D, De Kesel A. 2020. Checklist of thallus-forming Laboulbeniomycetes from Belgium and the Netherlands, including Hesperomyces halyziae and Laboulbenia quarantenae spp. nov. MycoKeys 71: 23-86.", "Haelewaters D, De Kesel A, Pfister DH. 2018. Integrative taxonomy reveals hidden species within a common fungal parasite of ladybirds. Scientific Reports 8: 15966.", "Hall TA. 1999. BioEdit:A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41: 95-98.", "Halling RE. 1996. Notes on Collybia V. Gymnopus section Levipedes in tropical South America, with comments on Collybia.Brittonia 48: 487-494.", "Hanss J-M, Moreau P-A. 2020. Une Revision des Amanites \"vaginees\" (Amanita sect. Vaginatae) en Europe, 1re partie: quelques Amanites argentees. Bulletin de la Societe mycologique de France 133: 67-141.", "Hashimoto A, Sato G, Matsuda T, et al. 2015. Taxonomic revision of Pseudolachnea and Pseudolachnella and establishment of Neopseudolachnella and Pseudodinemasporium gen. nov. Mycologia 107: 383-408.", "Hawksworth DL. 1972. A large-spored species of Acremonium sect. Nectrioidea. Transactions of the British Mycological Society 58: 510-512.", "Hawksworth DL. 1979. The lichenicolous hyphomycetes. Bulletin of the British Museum for Natural History 6: 183-300.", "He M-Q, Hyde KD, Ratchadawan C, et al. 2020. Two new species of Micropsalliota (Agaricaceae/Agaricales) from Thailand.Phytotaxa 453:140-141.", "Heinemann P, Leelavathy KM.1991.The genus Micropsalliota (Agaricaceae) in Kerala State, India. Mycological Research 95: 343-344.", "Heinemann P, Little Flower S. 1983.Micropsalliota de Kerala (Inde). Bulletin du Jardin Botanique National de Belgique 53: 75-84.", "Hernandez-Restrepo M, Groenewald JZ,Crous PW,et al.2016a.Taxonomic and phylogenetic re-evaluation of Microdochium,Monographella and Idriella. Persoonia 36: 57-82.", "Hernandez-Restrepo M, Groenewald JZ, Elliott ML, et al. 2016b. Take-all or nothing. Studies in Mycology 83: 19-48.", "Hipp AL, Manos PS, Hahn M, et al. 2020. Genomic landscape of the global oak phylogeny. New Phytologist 226: 1198-1212.", "Hjortstam K, Ryvarden L. 2007. Checklist of corticioid fungi (Basidiomycotina) from the tropics, subtropics and the southern hemisphere. Synopsis Fungorum 22: 27-146.", "Hoang DT, Chernomor O, von Haeseler A, et al. 2018. UFBoot2: Improving the ultrafast bootstrap approximation. Molecular Biology and Evolution 35: 518-522.", "Holubova-Jechova V. 1974. A revision of the genus Olpitrichum Atk. Folia Geobotanica et Phytotaxonomica 9: 425-432.", "Hongo T. 1971. Notulae mycologicae. Mem Shiga University 21: 62-68.", "Horak E.1976.On cuboid spored species of Entoloma.Sydowia 28:171-236.", "Horak E. 1977.Additions to 'On cuboid spored species of Entoloma'.Sydowia 29: 289-299.", "Horak E. 1978 '1977'. Crepidotus episphaeria and related species from the Southern Hemisphere. Berichte der Schweizerischen Botanischen Gesellschaft 87: 227-235.", "Horak E. 2018 Agaricales (Basidiomycota) of New Zealand 2. Brown spored genera p.p. Crepidotus, Flammulaster, Inocybe, Phaeocollybia, Phaeomarasmius, Pleuroflammula, Pyrrhoglossum, Simocybe, Tubaria and Tympanella. Fungi of New Zealand Nga Hekaheka o Aotearoa Volume 6. Westerdijk Biodiversity Series 16: 1-205. Westerdijk Fungal Biodiversity Institute, Utrecht, the Netherlands.", "Hou C-L,Lin Y-R,Piepenbring M. 2005.Species of Rhytismataceae on needles of Juniperus spp. from China. Canadian Journal of Botany 83: 37-46.", "Hou LW,Groenewald JZ,Pfenning LH, et al. 2020a.The phoma-like dilemma. Studies in Mycology 96: 309-396.", "Hou LW, Hernandez-Restrepo M, Groenewald JZ, et al. 2020b. Citizen science project reveals high diversity in Didymellaceae (Pleosporales, Dothideomycetes). MycoKeys 65: 49-99.", "Houbraken J, Kocsube S, Visagie CM,et al. 2020. Classification of Aspergillus,Penicillium,Talaromyces and related genera (Eurotiales):an overview of families, genera, subgenera, sections, series and species. Studies in Mycology 95: 5-169.", "Huang S,Xia J, Zhang X, et al. 2020.Two new species of Microdochium from Indocalamus longiauritus in south-western China. MycoKeys 72: 93-108.", "Hubka V, Dudova Z, Kubatova A, et al. 2017.Taxonomic novelties in Aspergillus section Fumigati: A. tasmanicus sp. nov., induction of sexual state in A. turcosus and overview of related species. Plant Systematics and Evolution 303: 787-806.", "Hubka V, Peterson SW, Frisvad JC, et al. 2013. Aspergillus waksmanii sp. nov. and Aspergillus marvanovae sp. nov., two closely related species in section Fumigati. International Journal of Systematic and Evolutionary Microbiology 63: 783-789.", "Huelsenbeck JP, Ronquist F. 2001. MrBayes: Bayesian inference of phylogenetic trees. Bioinformatics 17: 754-755.", "Huson DH, Kloepper TH 2005. Computing recombination networks from binary sequences. Bioinformatics, 21: ii159-ii165.", "Hyde KD, Dong Y, Phookamsak R, et al. 2020. Fungal diversity notes 1151-1276: taxonomic and phylogenetic contributions on genera and species of fungal taxa. Fungal Diversity 100: 5-277.", "Hyde KD, Norphanphoun C, Abreu VP, et al. 2017. Fungal diversity notes 603-708: taxonomic and phylogenetic notes on genera and species. Fungal Diversity 87: 1-235.", "Hyde KD, Tennakoon DS, Jeewon R. et al. 2019. Fungal diversity notes 1036-1150: taxonomic and phylogenetic contributions on genera and species of fungal taxa. Fungal Diversity 96: 1-242.", "Hymphries Z, Seifert KA, Hirooka Y, et al. 2017. A new family and genus in Dothideales for Aureobasidium-like species isolated from house dust. IMA Fungus 8: 299-315.", "Irwin JAG. 1991. Phytophthora macrochlamydospora, a new species from Australia. Mycologia 83: 517-519.", "Jiang H-B, Hyde KD,Yang E-F, et al. 2021. Morphological and phylogenetic appraisal of Ophioceras (Ophioceraceae, Magnaporthales). PLoS ONE 16: e0253853.", "Jiang N,Fan X,Tian C,et al.2020.Reevaluating Cryphonectriaceae and allied families in Diaporthales. Mycologia 112: 267-292.", "Johnston PR. 1986. Rhytismataceae in New Zealand 1. Some foliicolous species of Coccomyces de Notaris and Propolis (Fries) Corda.New Zealand Journal of Botany 24: 89-124.", "Johnston PR. 1994.Ascospore sheaths of some Coccomyces,Hypoderma, and Lophodermium species (Rhytismataceae). Mycotaxon 52: 221-239.", "Johnston PR, Gamundi IJ. 2000. Torrendiella (Ascomycota, Helotiales) on Nothofagus. New Zealand Journal of Botany 38: 493-513.", "Ju Y-M, Rogers JD. 2001. New and interesting Biscogniauxia taxa, with a key to the world species. Mycological Research 9: 1123-1133.", "Kalyaanamoorthy S, Minh BQ, Wong TFK, et al. 2017. ModelFinder: fast model selection for accurate phylogenetic estimates. Nature Methods 14: 587-589.", "Karstedt F,Baroni TJ,Largent DL, et al. 2019.Phylogenetic and morphological analyses of species of the Entolomataceae (Agaricales,Basidiomycota) with cuboid basi
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11. Fusarium chuoi Crous, Osieck, Jurjevi, Boers, Iperen, Starink-Willemse, Dima, Balashov, Bulgakov, Johnston, Morozova, Pinruan, Sommai, Alvarado, Decock, Lebel, McMullan-Fisher, Moreno, Shivas, Zhao, Abdollahzadeh, Abrinbana, Ageev, Akhmetova, Alexandrova, Altés, Amaral, Angelini, Antonín, Arenas, Asselman, Badali, Baghela, Bañares, Barreto, Baseia, Bellanger, Berraf-Tebbal, Biketova, Bukharova, Burgess, Cabero, Câmara, Cano-Lira, Ceryngier, Chávez, Cowan, Lima, Oliveira, Denman, Dang, Dovana, Duarte, Eichmeier, Erhard, Esteve-Raventós, Fellin, Ferisin, Ferreira, Ferrer, Finy, Gaya, Geering, Gil-Durán, Glässnerová, Glushakova, Gramaje, Guard, Guarnizo, Haelewaters, Halling, Hill, Hirooka, Hubka, Iliushin, Ivanova, Ivanushkina, Jangsantear, Justo, Kachalkin, Kato, Khamsuntorn, Kirtsideli, Knapp, Kochkina, Koukol, Kovács, Kruse, Kumar, Kušan, Læssøe, Larsson, Lebeuf, Levicán, Loizides, Marinho, Luangsa-ard, Lukina, Magaña-Dueñas, Maggs-Kölling, Malysheva, Malysheva, Martín, Martín, Matočec, McTaggart, Mehrabi-Koushki, Mešić, Miller, Mironova, Moreau, Morte, Müller, Nagy, Nanu, Navarro-Ródenas, Nel, Nguyen, Nóbrega, Noordeloos, Olariaga, Overton, Ozerskaya, Palani, Pancorbo, Papp, Pawłowska, Pham, Phosri, Popov, Portugal, Pošta, Reschke, Reul, Ricci, Rodríguez, Romanowski, Ruchikachorn, Saar, Safi, Sakolrak, Salzmann, Sandoval-Denis, Sangwichein, Sanhueza, Sato, Sastoque, Senn-Irlet, Shibata, Siepe, Somrithipol, Spetik, Sridhar, Stchigel, Stuskova, Suwannasai, Tan, Thangavel, Tiago, Tiwari, Tkalčec, Tomashevskaya, Tonegawa, Tran, Tran, Trovão, Trubitsyn, Wyk, Vieira, Vila, Visagie, Vizzini, Volobuev, Vu, Wangsawat, Yaguchi, Ercole, Ferreira, Souza, Vieira & Groenewald, 2021, sp. nov
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Crous, P. W., Osieck, E. R., Jurjevi, ��, Boers, J., Van Iperen, A. L., Starink-Willemse, M., Dima, B., Balashov, S., Bulgakov, T. S., Johnston, P. R., Morozova, O. V., Pinruan, U., Sommai, S., Alvarado, P., Decock, C. A., Lebel, T., McMullan-Fisher, S., Moreno, G., Shivas, R. G., Zhao, L., Abdollahzadeh, J., Abrinbana, M., Ageev, D. V., Akhmetova, G., Alexandrova, A. V., Alt��s, A., Amaral, A. G. G., Angelini, C., Anton��n, V., Arenas, F., Asselman, P., Badali, F., Baghela, A., Ba��ares, A., Barreto, R. W., Baseia, I. G., Bellanger, J. - M., Berraf-Tebbal, A., Biketova, A. Yu., Bukharova, N. V., Burgess, T. I., Cabero, J., C��mara, M. P. S., Cano-Lira, J. F., Ceryngier, P., Ch��vez, R., Cowan, D. A., de Lima, A. F., Oliveira, R. L., Denman, S., Dang, Q. N., Dovana, F., Duarte, I. G., Eichmeier, A., Erhard, A., Esteve-Ravent��s, F., Fellin, A., Ferisin, G., Ferreira, R. J., Ferrer, A., Finy, P., Gaya, E., Geering, A. D. W., Gil-Dur��n, C., Gl��ssnerov��, K., Glushakova, A. M., Gramaje, D., Guard, F. E., Guarnizo, A. L., Haelewaters, D., Halling, R. E., Hill, R., Hirooka, Y., Hubka, V., Iliushin, V. A., Ivanova, D. D., Ivanushkina, N. E., Jangsantear, P., Justo, A., Kachalkin, A. V., Kato, S., Khamsuntorn, P., Kirtsideli, I. Y., Knapp, D. G., Kochkina, G. A., Koukol, O., Kov��cs, G. M., Kruse, J., Kumar, T. K. A., Ku��an, I., L��ss��e, T., Larsson, E., Lebeuf, R., Levic��n, G., Loizides, M., Marinho, P., Luangsa-ard, J. J., Lukina, E. G., Maga��a-Due��as, V., Maggs-K��lling, G., Malysheva, E. F., Malysheva, V. F., Mart��n, B., Mart��n, M. P., Mato��ec, N., McTaggart, A. R., Mehrabi-Koushki, M., Me��i��, A., Miller, A. N., Mironova, P., Moreau, P. - A., Morte, A., M��ller, K., Nagy, L. G., Nanu, S., Navarro-R��denas, A., Nel, W. J., Nguyen, T. H., N��brega, T. F., Noordeloos, M. E., Olariaga, I., Overton, B. E., Ozerskaya, S. M., Palani, P., Pancorbo, F., Papp, V., Paw��owska, J., Pham, T. Q., Phosri, C., Popov, E. S., Portugal, A., Po��ta, A., Reschke, K., Reul, M., Ricci, G. M., Rodr��guez, A., Romanowski, J., Ruchikachorn, N., Saar, I., Safi, A., Sakolrak, B., Salzmann, F., Sandoval-Denis, M., Sangwichein, E., Sanhueza, L., Sato, T., Sastoque, A., Senn-Irlet, B., Shibata, A., Siepe, K., Somrithipol, S., Spetik, M., Sridhar, P., Stchigel, A. M., Stuskova, K., Suwannasai, N., Tan, Y. P., Thangavel, R., Tiago, I., Tiwari, S., Tkal��ec, Z., Tomashevskaya, M. A., Tonegawa, C., Tran, H. X., Tran, N. T., Trov��o, J., Trubitsyn, V. E., Van Wyk, J., Vieira, W. A. S., Vila, J., Visagie, C. M., Vizzini, A., Volobuev, S. V., Vu, D. T., Wangsawat, N., Yaguchi, T., Ercole, E., Ferreira, B. W., de Souza, A. P., Vieira, B. S., and Groenewald, J. Z.
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Ascomycota ,Fusarium ,Sordariomycetes ,Hypocreales ,Fungi ,Nectriaceae ,Biodiversity ,Fusarium chuoi ,Taxonomy - Abstract
Fusarium chuoi R. Hill, Gaya, D.T. Vu, Sand.-Den. & Crous, sp. nov. Etymology. From chu���i, Vietnamese vernacular name for Musa spp., from which the ex-type strain was isolated. Classification ��� Nectriaceae, Hypocreales, Sordariomycetes. On SNA and CLA, sporulation abundant from aerial conidiophores and sporodochia. Aerial conidiophores erect or prostrate, copiously branching laterally and sympodially, giving rise to macro-, and rarely, microconidia; aerial conidiogenous cells mono- and polyphialidic, subulate to subcylindrical, smooth- and thin-walled, proliferating sympodially, 6.5���40.5 �� 2.5���4 ��m, with apical flared collarette and periclinal thickening; aerial conidia of two types: microconidia often produced on prostrate conidiophores, rarely on aerial mycelium, aggregating in false heads, ellipsoidal, subcylindrical to slightly falcate, 0 ���1-septate, 8���15 �� 2���29.5 ��m; macroconidia fusiform to falcate, straight to apically dorsiventrally curved, apex curved to pointed, base obtuse to papillate, 1���3-septate, smooth- and thin-walled; 1-septate conidia: (14���)18���27.5(���29.5) �� (2.5���)3���4 ��m (av. 22.8 �� 3.2 ��m); 2-septate conidia: 26���28.5 �� 3���4 ��m (av. 27.4 �� 3.6 ��m); 3-septate conidia: (28���)31.5���43(���50.5) �� 3���4 ��m (av. 37.3 �� 3.5 ��m). Sporodochia saffron, luteous to ochreous coloured (Rayner 1970), formed abundantly on the agar surface and carnation leaves under nuv. Conidiophores in sporodochia, densely and irregularly branched, bearing apical whorls of 2 ��� 4 monophialides; sporodochial monophialides subcylindrical, 10���26 �� 2.5���4.5 ��m, smooth- and thin-walled, with a distinct apical collarette. Sporodochial conidia (macroconidia) falcate, almost straight to gently curved, tapering at both ends, apex curved to blunt, base poorly- to well-developed foot-shaped, 1���6-septate, hyaline, smooth- and thin-walled; 1-septate conidia: (14.5���)15���20.5(���24) �� 3���4.5 ��m (av. 17.9 �� 3.9 ��m); 2-septate conidia: 21.5���32 �� 3���4.5 ��m (av. 26.4 �� 3.5 ��m); 3-septate conidia: (33���)43���61(���71.5) �� (3���)4���5 ��m (av. 51.8 �� 4.2 ��m); 4-septate conidia: (50.5���)55���69(���74.5) �� 3.5���5 ��m (av. 62.3 �� 4.2 ��m); 5-septate conidia: 54 �� 4.5 ��m (rare); 6-septate conidia: (49.5���)56.5���71(���73) �� (3.5���)4���4.5(���5) ��m (av. 63.8 �� 4.3 ��m). Chlamydospores not observed. Culture characteristics ��� Colonies on potato dextrose agar (PDA) and oatmeal agar (OA) growing in the dark at 24 �� C covering and entire 9 cm Petri dish in 7 d. Colony surface peach to vinaceous, flat, velvety to felty with abundant floccose aerial mycelium forming concentric rings; colony margins undulate. Reverse flesh to salmon with diffuse coral to brick pigment throughout the medium. Typus. VIETNAM, H�� Tĩnh Province, H����ng S��n District,S��n Kim commune, N18��25'37.38" E105��12'53.95", inside seed of Musa itinerans (Musaceae), 9 Nov. 2014, D.M. Thu, L.T. Phong & T.T. Duong, isol. R. Hill (holotype CBS H-24901,culture ex-type CBS 148464; ITS, LSU, cmdA, rpb1, rpb2, tef1 and tub2 sequences GenBank OK586454, OK586452, OK626304, OK626306, OK626302, OK626308 and OK626310, MycoBank MB 841865). Colour illustrations. Flowers, fruits, leaves and seeds of Musa itinerans (background photo by D. T. Vu); from top to bottom and left to right: colony on PDA after 14 d at 24 �� C in darkness (left = obverse,right = reverse), sporodochia formed on CLA,aerial conidiophore,aerial conidiogenous cells,aerial conidia, sporodochial conidia. Scale bars: black = 20 ��m, white = 10 ��m. Additional material examined. VIETNAM, Ngh��� An Province, Con Cu��ng District, Ch��u Kh�� commune, N19��1'48.73" E104��43'31.97", inside seed of M. itinerans, 18 Nov. 2014, L.T. Phong, V.V. Tung & T.T. Duong, isol. R. Hill (culture CBS 148465; ITS, LSU, cmdA, rpb1, rpb2, tef1 and tub2 sequences GenBank OK586455, OK586453, OK626305, OK626307, OK626303, OK626309 and OK626311). Notes ��� Fusarium chuoi resides in the Asian clade of the Fusarium fujikuroi species complex (FFSC: O���Donnell et al. 1998, Yilmaz et al. 2021, Crous et al. 2021b). Based on nucleotide searches using the Fusarium Pairwise ID engine on the Fusarioid-ID database (www.fusarium.org, Crous et al. 2021) the closest hit using the ITS sequence was Fusarium siculi (strain CBS 142422; identities = 449/450 (99 %), no gaps). The closest hit using the LSU sequence was F. siculi (strain CBS 142422; identities = 804/805 (99 %), no gaps). Closest hit using the cmdA sequence was Fusarium fractiflexum (strain NRRL 28852; identities = 426/434 (98 %), no gaps). Closest hit using the rpb1 sequence was F. fujikuroi (strain NRRL 13566; identities = 687/702 (98 %), no gaps). Closest hit using the rpb2 sequence was Fusarium globosum (strain CBS 428.97; identities = 856/867 (98 %), no gaps). Closest hit using the tef1 sequence was F. fractiflexum (strain NRRL 28852; identities = 619/643 (96 %), 2 gaps (0.3 %)). The phylogenetic results, however, showed that F. chuoi is not directly related to any of the previously described species of FFSC (see Suppl. material FP1353), clustering as the second basal-most species of that clade after F. sacchari. Asian Fusarium spp. in the FFSC are characterised by mono-and polyphialides producing oval to ellipsoid, rarely pyriform to globose (i.e., F. annulatum, F. fujikuroi and F. globosum) microconidia organized in chains or false heads; 3���5-septate sporodochial conidia and lacking chlamydospores. The elaborate, profusely branched aerial conidiophores of F. chuoi are comparable to those of F. concentricum, F. lumajangense, F. mangiferae and F. sacchari, all the latter species producing oval, ellipsoidal to allantoid microconidia on false heads.Aerial conidiophores of F. chuoi, however, mostly produce macroconidia, while microconidia grouped on false heads are restricted to short, mostly unbranched and prostrate conidiophores formed on the surface on the culture media. Several Asian species of the FFSC have been reported from Musa spp. i.e., F. annulatum, F. concentricum, F. fujikuroi, F. lumajangense and F. sacchari (Leslie & Summerell 2006, Maryani et al. 2019, Farr & Rossman 2021). The two strains representing F. chuoi were isolated as endophytes from asymptomatic seeds of wild banana (Musa itinerans), which had been collected predispersal and stored in the Millennium Seed Bank for ~2.5 years at -20 �� C prior to isolation. Supplementary material FP1353 Phylogenetic tree., Published as part of Crous, P. W., Osieck, E. R., Jurjevi, ��, Boers, J., Van Iperen, A. L., Starink-Willemse, M., Dima, B., Balashov, S., Bulgakov, T. S., Johnston, P. R., Morozova, O. V., Pinruan, U., Sommai, S., Alvarado, P., Decock, C. A., Lebel, T., McMullan-Fisher, S., Moreno, G., Shivas, R. G., Zhao, L., Abdollahzadeh, J., Abrinbana, M., Ageev, D. V., Akhmetova, G., Alexandrova, A. V., Alt��s, A., Amaral, A. G. G., Angelini, C., Anton��n, V., Arenas, F., Asselman, P., Badali, F., Baghela, A., Ba��ares, A., Barreto, R. W., Baseia, I. G., Bellanger, J. - M., Berraf-Tebbal, A., Biketova, A. Yu., Bukharova, N. V., Burgess, T. I., Cabero, J., C��mara, M. P. S., Cano-Lira, J. F., Ceryngier, P., Ch��vez, R., Cowan, D. A., de Lima, A. F., Oliveira, R. L., Denman, S., Dang, Q. N., Dovana, F., Duarte, I. G., Eichmeier, A., Erhard, A., Esteve-Ravent��s, F., Fellin, A., Ferisin, G., Ferreira, R. J., Ferrer, A., Finy, P., Gaya, E., Geering, A. D. W., Gil-Dur��n, C., Gl��ssnerov��, K., Glushakova, A. M., Gramaje, D., Guard, F. E., Guarnizo, A. L., Haelewaters, D., Halling, R. E., Hill, R., Hirooka, Y., Hubka, V., Iliushin, V. A., Ivanova, D. D., Ivanushkina, N. E., Jangsantear, P., Justo, A., Kachalkin, A. V., Kato, S., Khamsuntorn, P., Kirtsideli, I. Y., Knapp, D. G., Kochkina, G. A., Koukol, O., Kov��cs, G. M., Kruse, J., Kumar, T. K. A., Ku��an, I., L��ss��e, T., Larsson, E., Lebeuf, R., Levic��n, G., Loizides, M., Marinho, P., Luangsa-ard, J. J., Lukina, E. G., Maga��a-Due��as, V., Maggs-K��lling, G., Malysheva, E. F., Malysheva, V. F., Mart��n, B., Mart��n, M. P., Mato��ec, N., McTaggart, A. R., Mehrabi-Koushki, M., Me��i��, A., Miller, A. N., Mironova, P., Moreau, P. - A., Morte, A., M��ller, K., Nagy, L. G., Nanu, S., Navarro-R��denas, A., Nel, W. J., Nguyen, T. H., N��brega, T. F., Noordeloos, M. E., Olariaga, I., Overton, B. E., Ozerskaya, S. M., Palani, P., Pancorbo, F., Papp, V., Paw��owska, J., Pham, T. Q., Phosri, C., Popov, E. S., Portugal, A., Po��ta, A., Reschke, K., Reul, M., Ricci, G. M., Rodr��guez, A., Romanowski, J., Ruchikachorn, N., Saar, I., Safi, A., Sakolrak, B., Salzmann, F., Sandoval-Denis, M., Sangwichein, E., Sanhueza, L., Sato, T., Sastoque, A., Senn-Irlet, B., Shibata, A., Siepe, K., Somrithipol, S., Spetik, M., Sridhar, P., Stchigel, A. M., Stuskova, K., Suwannasai, N., Tan, Y. P., Thangavel, R., Tiago, I., Tiwari, S., Tkal��ec, Z., Tomashevskaya, M. A., Tonegawa, C., Tran, H. X., Tran, N. T., Trov��o, J., Trubitsyn, V. E., Van Wyk, J., Vieira, W. A. S., Vila, J., Visagie, C. M., Vizzini, A., Volobuev, S. V., Vu, D. T., Wangsawat, N., Yaguchi, T., Ercole, E., Ferreira, B. W., de Souza, A. P., Vieira, B. S. & Groenewald, J. Z., 2021, Fusarium chuoi R. Hill, Gaya, D. T. Vu, Sand. - Den. & Crous, R. Hill, Gaya, D. T. Vu, Sand. - Den. & Crous sp. nov., pp. 310-311 in Fungal Planet 47 (1) on page 311, DOI: 10.5281/zenodo.5856199, {"references":["Rayner RW. 1970. A Mycological Colour Chart. Commonwealth Mycological Institute, Kew and British Mycological Society.","O'Donnell K, Cigelnik E, Nirenberg H. 1998. Molecular systematics and phylogeography of the Gibberella fujikuroi species complex. Mycologia 90: 465 - 493.","Yilmaz N, Sandoval-Denis M, Lombard L, et al. 2021. Redefining species limits in the Fusarium fujikuroi species complex. Persoonia 46: 129 - 162.","Crous PW, Lombard L, Sandoval-Denis M, et al. 2021 b. Fusarium: more than a node or a foot-shaped basal cell. Studies in Mycology 98: 100116.","Crous PW, Cowan DA, Maggs-Kolling G, et al. 2021 a. Fungal Planet descrip- tion sheets: 1182 - 1283. Persoonia 46: 313 - 528.","Leslie JF, Summerell BA. 2006. The Fusarium laboratory manual. Blackwell Publishing, Ames.","Maryani N, Sandoval-Denis M, Lombard L, et al. 2019. New endemic Fusarium species hitch-hiking with pathogenic Fusarium strains causing Panama disease in small-holder banana plots in Indonesia. Persoonia 43: 48 - 69."]}
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- 2021
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12. Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran
- Author
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Stefany Castaldi, Alessio Cimmino, Jafar Abdollahzadeh, Jahanshir Amini, Rachele Isticato, Zeinab Bahmani, Marco Masi, Antonio Evidente, Cimmino, A., Bahmani, Z., Castaldi, S., Masi, M., Isticato, R., Abdollahzadeh, J., Amini, J., and Evidente, A.
- Subjects
Fomitiporia mediterranea ,Metabolite ,Phenazine ,Plant Disease ,biological control ,Fungus ,Iran ,Secondary metabolite ,Truncatella angustata ,chemistry.chemical_compound ,Ascomycota ,Botany ,medicine ,Antifungal Agent ,Vitis ,Botryosphaeria ,biology ,biology.plant_disease_cause ,phenazine ,Basidiomycota ,antifungal activity ,phenazine-1-carboxylic acid (PCA) ,Pentachloronitrobenzene ,General Chemistry ,biology.organism_classification ,Fungicide ,chemistry ,General Agricultural and Biological Sciences ,medicine.drug - Abstract
The phytopathogenic fungus Truncatella angustata, associated with grapevine trunk diseases (GTDs) in Iran, produces the well-known secondary metabolite isocoumumarin (+)-6-hyroxyramulosin and surprisingly also phenazine-1-carboxylic acid (PCA). PCA, identified by spectroscopic (essentially 1H NMR and ESI MS) spectra, is a bacterial metabolite well known for its antifungal activity and was found for the first time in T. angustata culture filtrates. The antifungal activity of PCA was assayed against four different fungi responsible for GTDs, Phaeoacremonium minimum, Phaeoacremonium italicum, Fomitiporia mediterranea, involved in grapevine esca disease, and Neofusicoccum parvum, responsible for Botryosphaeria dieback. The activity was compared with that of the known commercial fungicide, pentachloronitrobenzene, and the close phenazine. PCA and phenazine exhibited strong antifungal activity against all phytopathogenic fungi, inhibiting the fungal growth by about 90-100% and 80-100%, respectively. These results suggested that T. angustata could use PCA to compete with other phytopathogenic fungi that attack grapevine and thus PCA could be proposed as a biofungicide against the fungi responsible for grapevine esca and Botryosphaeria dieback diseases.
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- 2021
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