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1. Fusarium and allied fusarioid taxa (FUSA). 1

Author

Crous, P. W., Sandoval-Denis, M., Costa, M. M., Groenewald, J. Z., Iperen, A. L. van, Starink-Willemse, M., Hernández-Restrepo, Margarita, Kandemir, H., Ulaszewski, B., Boer, W. de, Abdel-Azeem, A. M., Abdollahzadeh, J., Akulov, A., Bakhshi, Mounes, Bezerra, J. D. P., Bhunjun, C.S., Câmara, M. P. S., Chaverri, Priscila, Vieira, Willie A. S., Decock, Cony A., Gaya, Ester, Gené, J., Guarro, J., Gramaje, David, Grube, Martin, Gupta, Vijai Kumar, Guarnaccia, Vladimiro, Hill, R., Hirooka, Y., Hyde, K. D., Jayawardena, R. S., Jeewon, Rajesh, Jurjević, Željko, Korsten, L., Lamprecht, Sandra Christina, Lombard, L., Maharachchikumbura, Sajeewa S. N., Polizzi, Giancarlo, Rajeshkumar, Kunhiraman C., Salgado-Salazar, Catalina, Shang, Q. J., Shivas, R. G., Summerbell, Richard C., Sun, G. Y., Swart, Wijnand J., Tan, Y. P., Vizzini, Alfredo, Xia, J. W., Zare, Rasoul, Crous, P. W., Sandoval-Denis, M., Costa, M. M., Groenewald, J. Z., Iperen, A. L. van, Starink-Willemse, M., Hernández-Restrepo, Margarita, Kandemir, H., Ulaszewski, B., Boer, W. de, Abdel-Azeem, A. M., Abdollahzadeh, J., Akulov, A., Bakhshi, Mounes, Bezerra, J. D. P., Bhunjun, C.S., Câmara, M. P. S., Chaverri, Priscila, Vieira, Willie A. S., Decock, Cony A., Gaya, Ester, Gené, J., Guarro, J., Gramaje, David, Grube, Martin, Gupta, Vijai Kumar, Guarnaccia, Vladimiro, Hill, R., Hirooka, Y., Hyde, K. D., Jayawardena, R. S., Jeewon, Rajesh, Jurjević, Željko, Korsten, L., Lamprecht, Sandra Christina, Lombard, L., Maharachchikumbura, Sajeewa S. N., Polizzi, Giancarlo, Rajeshkumar, Kunhiraman C., Salgado-Salazar, Catalina, Shang, Q. J., Shivas, R. G., Summerbell, Richard C., Sun, G. Y., Swart, Wijnand J., Tan, Y. P., Vizzini, Alfredo, Xia, J. W., and Zare, Rasoul

Abstract

Seven Fusarium species complexes are treated, namely F. aywerte species complex (FASC) (two species), F. buharicum species complex (FBSC) (five species), F. burgessii species complex (FBURSC) (three species), F. camptoceras species complex (FCAMSC) (three species), F. chlamydosporum species complex (FCSC) (eight species), F. citricola species complex (FCCSC) (five species) and the F. concolor species complex (FCOSC) (four species). New species include Fusicolla elongata from soil (Zimbabwe), and Neocosmospora geoasparagicola from soil associated with Asparagus officinalis (Netherlands). New combinations include Neocosmospora akasia, N. awan, N. drepaniformis, N. duplosperma, N. geoasparagicola, N. mekan, N. papillata, N. variasi and N. warna. Newly validated taxa include Longinectria gen. nov., L. lagenoides, L. verticilliforme, Fusicolla gigas and Fusicolla guangxiensis. Furthermore, Fusarium rosicola is reduced to synonymy under N. brevis. Finally, the genome assemblies of Fusarium secorum (CBS 175.32), Microcera coccophila (CBS 310.34), Rectifusarium robinianum (CBS 430.91), Rugonectria rugulosa (CBS 126565), and Thelonectria blattea (CBS 952.68) are also announced here

Published
2022

3. Fusarium: more than a node or a foot-shaped basal cell

Author

Crous, P. W., Lombard, L., Sandoval-Denis, M., Seifert, K. A., Schroers, H. J., Chaverri, P., Gené, 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., Araújo, J. P. M., Ariyawansa, H. A., Bakhshi, M., Bendiksby, M., Ben Hadj Amor, A., Bezerra, J. D. P., Boekhout, T., Câmara, M. P. S., Carbia, M., Cardinali, G., Castañeda-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., Fernández, N. B., Gaya, E., González, 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., Hernández-Restrepo, M., Houbraken, J., Hubka, V., Hyde, K. D., Iturriaga, T., Jeewon, R., Johnston, P. R., Jurjević, Ž, Karalti, İ, Korsten, L., Kuramae, E. E., Kušan, 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., Matočec, N., McTaggart, A. R., Mlčoch, 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, Yu Pei, Taylor, J. E., Taylor, P. W. J., Tiago, P. V., Váczy, 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., Yáñez-Morales, M. J., Yurkov, A., Zamora, J. C., Zare, R., Zhang, C. L., Thines, M., Crous, P. W., Lombard, L., Sandoval-Denis, M., Seifert, K. A., Schroers, H. J., Chaverri, P., Gené, 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., Araújo, J. P. M., Ariyawansa, H. A., Bakhshi, M., Bendiksby, M., Ben Hadj Amor, A., Bezerra, J. D. P., Boekhout, T., Câmara, M. P. S., Carbia, M., Cardinali, G., Castañeda-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., Fernández, N. B., Gaya, E., González, 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., Hernández-Restrepo, M., Houbraken, J., Hubka, V., Hyde, K. D., Iturriaga, T., Jeewon, R., Johnston, P. R., Jurjević, Ž, Karalti, İ, Korsten, L., Kuramae, E. E., Kušan, 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., Matočec, N., McTaggart, A. R., Mlčoch, 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, Yu Pei, Taylor, J. E., Taylor, P. W. J., Tiago, P. V., Váczy, 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., Yáñez-Morales, M. J., Yurkov, A., Zamora, J. C., Zare, R., Zhang, C. L., and Thines, M.

Abstract

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 th

Published
2021

4. Fungal Planet description sheets: 1284-1382

Author

Ministry of Business, Innovation, and Employment (New Zealand), Ministry of Health of the Czech Republic, Japan Society for the Promotion of Science, Charles University (Czech Republic), European Commission, Fundação para a Ciência e a Tecnologia (Portugal), Ministério da Ciência, Tecnologia e Ensino Superior (Portugal), Research Foundation - Flanders, Russian Science Foundation, Lomonosov Moscow State University, Kerala State Council for Science, Technology and Environment, Universidad de Alcalá, Ministry of Innovation and Technology (Hungary), National Research, Development and Innovation Office (Hungary), Hungarian Academy of Sciences, Agencia Nacional de Investigación y Desarrollo (Chile), Ministerio de Ciencia, Tecnología, Conocimiento e Innovación (Chile), Fondo Nacional de Desarrollo Científico y Tecnológico (Chile), Estonian Research Council, Conselho Nacional de Desenvolvimento Científico e Tecnológico (Brasil), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brasil), Ministerio de Ciencia, Innovación y Universidades (España), Agencia Estatal de Investigación (España), Swedish Taxonomy Initiative, Australian Biological Resources Study, Croatian Science Foundation, Fundación Séneca, National Science Foundation (US), New York Botanical Garden, National Science Centre (Poland), Russian Academy of Sciences, Crous, P. W., Osieck, E. R., Jurjević, Željko, Boers, J., Iperen, A. L. van, Starink-Willemse, M., Dima, B., Balashov, S., Bulgakov, T. S., Johnston, P. R., Morozova, O. V., Barreto, R. W., Baseia, I. G., Miller, A. N., Bellanger, J.-M., Berraf-Tebbal, Akila, Biketova, A. Yu., Malysheva, V. F, Bukharova, N. V., Burgess, T. I., Cabero, J., Navarro-Ródenas, A., Câmara, M. P. S., Cano-Lira, J. F., Ceryngier, P., Mironova, P., Chávez, R., Cowan, D. A., Lima, A. F. de, Oliveira, R. L., Martín, B., Denman, S., Nel, W. J., Dang, Q. N., Dovana, F., Duarte, I. G., Eichmeier, Ales, Pinruan, U., Erhard, A., Esteve-Raventós, F., Fellin, A., Ferisin, G., Ferreira, Renato Juciano, Zhao, L., Martín, María P., Ferrer, A., Finy, P., Gaya, E., Geering, A. D. W., Moreau, Pierre-Arthur, Gil-Durán, C., Glässnerová, K., Glushakova, A. M., Gramaje, David, Nguyen, T. H., Guard, F. E., Guarnizo, A.L., Matočec, N., Haelewaters, D., Halling, R. E., Hill, R., Morte, A., Hirooka, Y., Hubka, V., Iliushin, V. A., Nóbrega, T. F., Ivanova, D. D., Ivanushkina, N. E., Jangsantear, P., Justo, A., McTaggart, Alistair R., Kachalkin, A.V., Kato, S., Müller, K., Khamsuntorn, P., Kirtsideli, I. Y., Noordeloos, M. E., Knapp, D. G., Kochkina, G. A., Koukol, O., Kovács, G. M., Kruse, J., Kumar, T. K. A., Mehrabi-Koushki, M., Kušan, I., Nagy, L. G., Læssøe, T., Sommai, S., Larsson, E., Lebeuf, R., Levicán, G., Loizides, M., Marinho, P., Luangsa-Ard, J. J., Lukina, E. G., Magaña-Dueñas, V., Mešić, A., Nanu, S., Olariaga, I., Maggs-Kölling, G., Overton, B. E., Ozerskaya, S. M., Angelini, C., Palani, P., Pancorbo, F., Papp, V., Abdollahzadeh, J., Pawłowska, J., Pham, T. Q., Phosri, C., Popov, E. S., Alvarado, P., Portugal, A., Antonín, V., Pošta, A., Reschke, K., Reul, M., Ricci, G. M., Abrinbana, M., Rodríguez, A., Romanowski, J., Ruchikachorn, N., Saar, I., Safi, A., Malysheva, E. F., Decock, Cony A., Sakolrak, B., Salzmann, F., Sandoval-Denis, M., Sangwichein, E., Ageev, D. V., Sanhueza, L., Sato, T., Sastoque, A., Senn-Irlet, B., Arenas, F., Shibata, A., Siepe, K., Lebel, T., Somrithipol, S., Spetik, M., Sridhar, P., Akhmetova, G., Stchigel, A. M., Stuskova, Katerina, Suwannasai, N., Asselman, P., Tan, Y. P., Thangavel, R., Tiago, I., Tiwari, S., McMullan-Fisher, S., Tkalčec, Z., Tomashevskaya, M. A., Alexandrova, A. V., Tonegawa, C., Tran, H. X., Badali, F., Tran, N. T., Trovão, J., Trubitsyn, V. E., Wyk, J. van, Vieira, Willie A. S., Vila, J., Moreno, G., Visagie, C. M., Altés, A., Vizzini, Alfredo, Baghela, A., Volobuev, S. W., Vu, D. T., Wangsawat, N., Yaguchi, T., Ercole, E., Ferreira, B. W., Souza, A. P. de, Vieira, B. S., Shivas, R. G., Amaral, A. G. G., Bañares, Ángel, Groenewald, J. Z., Ministry of Business, Innovation, and Employment (New Zealand), Ministry of Health of the Czech Republic, Japan Society for the Promotion of Science, Charles University (Czech Republic), European Commission, Fundação para a Ciência e a Tecnologia (Portugal), Ministério da Ciência, Tecnologia e Ensino Superior (Portugal), Research Foundation - Flanders, Russian Science Foundation, Lomonosov Moscow State University, Kerala State Council for Science, Technology and Environment, Universidad de Alcalá, Ministry of Innovation and Technology (Hungary), National Research, Development and Innovation Office (Hungary), Hungarian Academy of Sciences, Agencia Nacional de Investigación y Desarrollo (Chile), Ministerio de Ciencia, Tecnología, Conocimiento e Innovación (Chile), Fondo Nacional de Desarrollo Científico y Tecnológico (Chile), Estonian Research Council, Conselho Nacional de Desenvolvimento Científico e Tecnológico (Brasil), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brasil), Ministerio de Ciencia, Innovación y Universidades (España), Agencia Estatal de Investigación (España), Swedish Taxonomy Initiative, Australian Biological Resources Study, Croatian Science Foundation, Fundación Séneca, National Science Foundation (US), New York Botanical Garden, National Science Centre (Poland), Russian Academy of Sciences, Crous, P. W., Osieck, E. R., Jurjević, Željko, Boers, J., Iperen, A. L. van, Starink-Willemse, M., Dima, B., Balashov, S., Bulgakov, T. S., Johnston, P. R., Morozova, O. V., Barreto, R. W., Baseia, I. G., Miller, A. N., Bellanger, J.-M., Berraf-Tebbal, Akila, Biketova, A. Yu., Malysheva, V. F, Bukharova, N. V., Burgess, T. I., Cabero, J., Navarro-Ródenas, A., Câmara, M. P. S., Cano-Lira, J. F., Ceryngier, P., Mironova, P., Chávez, R., Cowan, D. A., Lima, A. F. de, Oliveira, R. L., Martín, B., Denman, S., Nel, W. J., Dang, Q. N., Dovana, F., Duarte, I. G., Eichmeier, Ales, Pinruan, U., Erhard, A., Esteve-Raventós, F., Fellin, A., Ferisin, G., Ferreira, Renato Juciano, Zhao, L., Martín, María P., Ferrer, A., Finy, P., Gaya, E., Geering, A. D. W., Moreau, Pierre-Arthur, Gil-Durán, C., Glässnerová, K., Glushakova, A. M., Gramaje, David, Nguyen, T. H., Guard, F. E., Guarnizo, A.L., Matočec, N., Haelewaters, D., Halling, R. E., Hill, R., Morte, A., Hirooka, Y., Hubka, V., Iliushin, V. A., Nóbrega, T. F., Ivanova, D. D., Ivanushkina, N. E., Jangsantear, P., Justo, A., McTaggart, Alistair R., Kachalkin, A.V., Kato, S., Müller, K., Khamsuntorn, P., Kirtsideli, I. Y., Noordeloos, M. E., Knapp, D. G., Kochkina, G. A., Koukol, O., Kovács, G. M., Kruse, J., Kumar, T. K. A., Mehrabi-Koushki, M., Kušan, I., Nagy, L. G., Læssøe, T., Sommai, S., Larsson, E., Lebeuf, R., Levicán, G., Loizides, M., Marinho, P., Luangsa-Ard, J. J., Lukina, E. G., Magaña-Dueñas, V., Mešić, A., Nanu, S., Olariaga, I., Maggs-Kölling, G., Overton, B. E., Ozerskaya, S. M., Angelini, C., Palani, P., Pancorbo, F., Papp, V., Abdollahzadeh, J., Pawłowska, J., Pham, T. Q., Phosri, C., Popov, E. S., Alvarado, P., Portugal, A., Antonín, V., Pošta, A., Reschke, K., Reul, M., Ricci, G. M., Abrinbana, M., Rodríguez, A., Romanowski, J., Ruchikachorn, N., Saar, I., Safi, A., Malysheva, E. F., Decock, Cony A., Sakolrak, B., Salzmann, F., Sandoval-Denis, M., Sangwichein, E., Ageev, D. V., Sanhueza, L., Sato, T., Sastoque, A., Senn-Irlet, B., Arenas, F., Shibata, A., Siepe, K., Lebel, T., Somrithipol, S., Spetik, M., Sridhar, P., Akhmetova, G., Stchigel, A. M., Stuskova, Katerina, Suwannasai, N., Asselman, P., Tan, Y. P., Thangavel, R., Tiago, I., Tiwari, S., McMullan-Fisher, S., Tkalčec, Z., Tomashevskaya, M. A., Alexandrova, A. V., Tonegawa, C., Tran, H. X., Badali, F., Tran, N. T., Trovão, J., Trubitsyn, V. E., Wyk, J. van, Vieira, Willie A. S., Vila, J., Moreno, G., Visagie, C. M., Altés, A., Vizzini, Alfredo, Baghela, A., Volobuev, S. W., Vu, D. T., Wangsawat, N., Yaguchi, T., Ercole, E., Ferreira, B. W., Souza, A. P. de, Vieira, B. S., Shivas, R. G., Amaral, A. G. G., Bañares, Ángel, and Groenewald, J. Z.

Abstract

Novel species of fungi described in this study include those from various countries as follows: Antartica, Cladosporium austrolitorale from coastal sea sand. Australia, Austroboletus yourkae on soil, Crepidotus innuopurpureus on dead wood, Curvularia stenotaphri from roots and leaves of Stenotaphrum secundatum and Thecaphora stajsicii from capsules of Oxalis radicosa. Belgium, Paraxerochrysium coryli (incl. Paraxerochrysium gen. nov.) from Corylus avellana. Brazil, Calvatia nordestina on soil, Didymella tabebuiicola from leaf spots on Tabebuia aurea, Fusarium subflagellisporum from hypertrophied floral and vegetative branches of Mangifera indica and Microdochium maculosum from living leaves of Digitaria insularis. Canada, Cuphophyllus bondii fromagrassland. Croatia, Mollisia inferiseptata from a rotten Laurus nobilis trunk. Cyprus, Amanita exilis oncalcareoussoil. Czech Republic, Cytospora hippophaicola from wood of symptomatic Vaccinium corymbosum. Denmark, Lasiosphaeria deviata on pieces of wood and herbaceousdebris. Dominican Republic, Calocybella goethei among grass on a lawn. France (Corsica) , Inocybe corsica onwetground. France (French Guiana) , Trechispora patawaensis on decayed branch of unknown angiosperm tree and Trechispora subregularis on decayed log of unknown angiosperm tree. [...]

Published
2021

10. First Report of a Member of the Fusarium oxysporum Species Complex Causing Cladode Rot in Nopalea cochenillifera in Brazil

Author

Santiago, M. F., primary, Santos, A. M. G., additional, Inácio, C. P., additional, Neves, R. P., additional, Andrade, D. E. G. T., additional, Santos, D. C., additional, Assis, T. C., additional, Doyle, V. P., additional, Vieira, W. A. S., additional, Veloso, J. S., additional, Câmara, M. P. S., additional, and Laranjeira, D., additional

Published
2018
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12. Analysis of phylogeny, distribution, and pathogenicity of Botryosphaeriaceae species associated with gummosis of Anacardium in Brazil, with a new species of Lasiodiplodia

Author

BRITO NETTO, M. S., LIMA, W. G., CORREIA, K. C., SILVA, C. de F. B. da, THON, M., MARTINS, R. B., MILLER, R. N. G., MICHEREFF, S. J., CÂMARA, M. P. S., MARIOTE dos SANTOS BRITO NETTO, Departamento de Agronomia, Universidade Federal Rural de Pernambuco., WALERIA G. LIMA, Departamento de Agronomia, Universidade Federal Rural de Pernambuco., KAMILA C. CORREIA, Centro de Ciências Agrárias e Biodiversidade, Universidade Federal do Cariri., CHRISTIANA DE FATIMA BRUCE DA SILVA, CNPAT, MICHAEL THON, Centro Hispano Luso de Investigaciones Agrarias (CIALE), Universidad de Salamanca, Villamayor, Espanha., RICARDO B. MARTINS, Campus Arapiraca, Universidade Federal de Alagoas., ROBERT N. G. MILLER, Departamento de Biologia Celular, Universidade de Brasília., SAMI J. MICHEREFF, Departamento de Agronomia, Universidade Federal Rural de Pernambuco., and MARCOS P. S. CÂMARA, Departamento de Agronomia, Universidade Federal Rural de Pernambuco.

Subjects
Agressiveness, Tropical fruit, Caju, Cashew, ITS, Agressividade, Fruta Tropical
Abstract

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Published
2017

18. Genetic diversity and population structure of Lasiodiplodia theobromae from different hosts in northeastern Brazil and Mexico.

Author

Rêgo, T. J. S., Câmara, M. P. S., Elena, G., Armengol, J., Berbegal, M., Correia, K. C., Michereff, S. J., and Tovar‐Pedraza, J. M.

Subjects
*BOTRYODIPLODIA theobromae, *FUNGAL remediation, *PATHOGENIC fungi, *AGRICULTURE, FRUIT genetics
Abstract

Lasiodiplodia theobromae is one of the most frequent fungal pathogens associated with dieback, gummosis, leaf spot, stem‐end rot and fruit rot symptoms in cashew, mango, papaya and grapevine. In this study, the variation in the genetic diversity of 117 L. theobromae isolates from northeastern Brazil (n = 100) and Mexico (n = 17), which were collected from these four crops, was analysed using microsatellite markers. The results revealed low genetic diversity among L. theobromae populations and the existence of two genetic groups. All Mexican isolates were grouped with Brazilian isolates, suggesting a low level of differentiation between these populations. Furthermore, no evident host or climate‐based population differentiation was observed for L. theobromae in Brazil. The populations studied were mostly clonal, but additional studies are needed to better understand the mode of reproduction of the pathogen. The low genetic diversity of L. theobromae populations in northeastern Brazil suggests that resistant cultivars could be used as a durable management strategy to reduce the impact of the diseases caused by this pathogen. [ABSTRACT FROM AUTHOR]

Published
2019
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31. Fusarium and allied fusarioid taxa (FUSA). 1.

Author

Crous PW, Sandoval-Denis M, Costa MM, Groenewald JZ, van Iperen AL, Starink-Willemse M, Hernández-Restrepo M, Kandemir H, Ulaszewski B, de Boer W, Abdel-Azeem AM, Abdollahzadeh J, Akulov A, Bakhshi M, Bezerra JDP, Bhunjun CS, Câmara MPS, Chaverri P, Vieira WAS, Decock CA, Gaya E, Gené J, Guarro J, Gramaje D, Grube M, Gupta VK, Guarnaccia V, Hill R, Hirooka Y, Hyde KD, Jayawardena RS, Jeewon R, Jurjević Ž, Korsten L, Lamprecht SC, Lombard L, Maharachchikumbura SSN, Polizzi G, Rajeshkumar KC, Salgado-Salazar C, Shang QJ, Shivas RG, Summerbell RC, Sun GY, Swart WJ, Tan YP, Vizzini A, Xia JW, Zare R, González CD, Iturriaga T, Savary O, Coton M, Coton E, Jany JL, Liu C, Zeng ZQ, Zhuang WY, Yu ZH, and Thines M

Abstract

Seven Fusarium species complexes are treated, namely F. aywerte species complex (FASC) (two species), F. buharicum species complex (FBSC) (five species), F. burgessii species complex (FBURSC) (three species), F. camptoceras species complex (FCAMSC) (three species), F. chlamydosporum species complex (FCSC) (eight species), F. citricola species complex (FCCSC) (five species) and the F. concolor species complex (FCOSC) (four species). New species include Fusicolla elongata from soil (Zimbabwe), and Neocosmospora geoasparagicola from soil associated with Asparagus officinalis (Netherlands). New combinations include Neocosmospora akasia, N. awan, N. drepaniformis, N. duplosperma, N. geoasparagicola, N. mekan, N. papillata, N. variasi and N. warna. Newly validated taxa include Longinectria gen. nov. , L. lagenoides , L. verticilliforme , Fusicolla gigas and Fusicolla guangxiensis . Furthermore, Fusarium rosicola is reduced to synonymy under N. brevis. Finally, the genome assemblies of Fusarium secorum (CBS 175.32) , Microcera coccophila (CBS 310.34), Rectifusarium robinianum (CBS 430.91), Rugonectria rugulosa (CBS 126565), and Thelonectria blattea (CBS 952.68) are also announced here. Citation: Crous PW, Sandoval-Denis M, Costa MM, Groenewald JZ, van Iperen AL, Starink-Willemse M, Hernández-Restrepo M, Kandemir H, Ulaszewski B, de Boer W, Abdel-Azeem AM, Abdollahzadeh J, Akulov A, Bakhshi M, Bezerra JDP, Bhunjun CS, Câmara MPS, Chaverri P, Vieira WAS, Decock CA, Gaya E, Gené J, Guarro J, Gramaje D, Grube M, Gupta VK, Guarnaccia V, Hill R, Hirooka Y, Hyde KD, Jayawardena RS, Jeewon R, Jurjević Ž, Korsten L, Lamprecht SC, Lombard L, Maharachchikumbura SSN, Polizzi G, Rajeshkumar KC, Salgado-Salazar C, Shang Q-J, Shivas RG, Summerbell RC, Sun GY, Swart WJ, Tan YP, Vizzini A, Xia JW, Zare R, González CD, Iturriaga T, Savary O, Coton M, Coton E, Jany J-L, Liu C, Zeng Z-Q, Zhuang W-Y, Yu Z-H, Thines M (2022). Fusarium and allied fusarioid taxa (FUSA). 1. Fungal Systematics and Evolution 9 : 161-200. doi: 10.3114/fuse.2022.09.08., Competing Interests: Conflict of interest: The authors declare that there is no conflict of interest., (© 2022 Westerdijk Fungal Biodiversity Institute.)

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2022
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32. Fungal Planet description sheets: 1284-1382.

Author

Crous PW, Osieck ER, Jurjević Ž, Boers J, van Iperen AL, Starink-Willemse M, Dima B, Balashov S, Bulgakov TS, Johnston PR, Morozova OV, Pinruan U, Sommai S, Alvarado P, Decock CA, Lebel T, McMullan-Fisher S, Moreno G, Shivas RG, Zhao L, Abdollahzadeh J, Abrinbana M, Ageev DV, Akhmetova G, Alexandrova AV, Altés A, Amaral AGG, Angelini C, Antonín V, Arenas F, Asselman P, Badali F, Baghela A, Bañares A, Barreto RW, Baseia IG, Bellanger JM, Berraf-Tebbal A, Biketova AY, Bukharova NV, Burgess TI, Cabero J, Câmara MPS, Cano-Lira JF, Ceryngier P, Chávez R, Cowan DA, de Lima AF, Oliveira RL, Denman S, Dang QN, Dovana F, Duarte IG, Eichmeier A, Erhard A, Esteve-Raventós F, Fellin A, Ferisin G, Ferreira RJ, Ferrer A, Finy P, Gaya E, Geering ADW, Gil-Durán C, Glässnerová K, Glushakova AM, Gramaje D, Guard FE, Guarnizo AL, Haelewaters D, Halling RE, Hill R, Hirooka Y, Hubka V, Iliushin VA, Ivanova DD, Ivanushkina NE, Jangsantear P, Justo A, Kachalkin AV, Kato S, Khamsuntorn P, Kirtsideli IY, Knapp DG, Kochkina GA, Koukol O, Kovács GM, Kruse J, Kumar TKA, Kušan I, Læssøe T, Larsson E, Lebeuf R, Levicán G, Loizides M, Marinho P, Luangsa-Ard JJ, Lukina EG, Magaña-Dueñas V, Maggs-Kölling G, Malysheva EF, Malysheva VF, Martín B, Martín MP, Matočec N, McTaggart AR, Mehrabi-Koushki M, Mešić A, Miller AN, Mironova P, Moreau PA, Morte A, Müller K, Nagy LG, Nanu S, Navarro-Ródenas A, Nel WJ, Nguyen TH, Nóbrega TF, Noordeloos ME, Olariaga I, Overton BE, Ozerskaya SM, Palani P, Pancorbo F, Papp V, Pawłowska J, Pham TQ, Phosri C, Popov ES, Portugal A, Pošta A, Reschke K, Reul M, Ricci GM, Rodríguez 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 AM, Stuskova K, Suwannasai N, Tan YP, Thangavel R, Tiago I, Tiwari S, Tkalčec Z, Tomashevskaya MA, Tonegawa C, Tran HX, Tran NT, Trovão J, Trubitsyn VE, Van Wyk J, Vieira WAS, Vila J, Visagie CM, Vizzini A, Volobuev SV, Vu DT, Wangsawat N, Yaguchi T, Ercole E, Ferreira BW, de Souza AP, Vieira BS, and Groenewald JZ

Abstract

Novel species of fungi described in this study include those from various countries as follows: Antartica , Cladosporium austrolitorale from coastal sea sand. Australia , Austroboletus yourkae on soil, Crepidotus innuopurpureus on dead wood, Curvularia stenotaphri from roots and leaves of Stenotaphrum secundatum and Thecaphora stajsicii from capsules of Oxalis radicosa. Belgium , Paraxerochrysium coryli (incl. Paraxerochrysium gen. nov.) from Corylus avellana. Brazil , Calvatia nordestina on soil, Didymella tabebuiicola from leaf spots on Tabebuia aurea, Fusarium subflagellisporum from hypertrophied floral and vegetative branches of Mangifera indica and Microdochium maculosum from living leaves of Digitaria insularis. Canada , Cuphophyllus bondii from a grassland. Croatia , Mollisia inferiseptata from a rotten Laurus nobilis trunk. Cyprus , Amanita exilis on calcareous soil. Czech Republic , Cytospora hippophaicola from wood of symptomatic Vaccinium corymbosum. Denmark , Lasiosphaeria deviata on pieces of wood and herbaceous debris. Dominican Republic , Calocybella goethei among grass on a lawn. France (Corsica) , Inocybe corsica on wet ground. France (French Guiana) , Trechispora patawaensis on decayed branch of unknown angiosperm tree and Trechispora subregularis on decayed log of unknown angiosperm tree. Germany , Paramicrothecium sambuci (incl. Paramicrothecium gen. nov.) on dead stems of Sambucus nigra. India , Aureobasidium microtermitis from the gut of a Microtermes sp. termite, Laccaria diospyricola on soil and Phylloporia tamilnadensis on branches of Catunaregam spinosa . Iran , Pythium serotinoosporum from soil under Prunus dulcis. Italy , Pluteus brunneovenosus on twigs of broadleaved trees on the ground. Japan , Heterophoma rehmanniae on leaves of Rehmannia glutinosa f. hueichingensis. Kazakhstan , Murispora kazachstanica from healthy roots of Triticum aestivum. Namibia , Caespitomonium euphorbiae (incl. Caespitomonium gen. nov.) from stems of an Euphorbia sp. Netherlands , Alfaria junci, Myrmecridium junci, Myrmecridium juncicola, Myrmecridium juncigenum, Ophioceras junci, Paradinemasporium junci (incl. Paradinemasporium gen. nov.), Phialoseptomonium junci, Sporidesmiella juncicola, Xenopyricularia junci and Zaanenomyces quadripartis (incl. Zaanenomyces gen. nov.), from dead culms of Juncus effusus, Cylindromonium everniae and Rhodoveronaea everniae from Evernia prunastri, Cyphellophora sambuci and Myrmecridium sambuci from Sambucus nigra, Kiflimonium junci, Sarocladium junci, Zaanenomyces moderatricis-academiae and Zaanenomyces versatilis from dead culms of Juncus inflexus, Microcera physciae from Physcia tenella, Myrmecridium dactylidis from dead culms of Dactylis glomerata, Neochalara spiraeae and Sporidesmium spiraeae from leaves of Spiraea japonica, Neofabraea salicina from Salix sp., Paradissoconium narthecii (incl. Paradissoconium gen. nov.) from dead leaves of Narthecium ossifragum, Polyscytalum vaccinii from Vaccinium myrtillus, Pseudosoloacrosporiella cryptomeriae (incl. Pseudosoloacrosporiella gen. nov.) from leaves of Cryptomeria japonica, Ramularia pararhabdospora from Plantago lanceolata, Sporidesmiella pini from needles of Pinus sylvestris and Xenoacrodontium juglandis (incl. Xenoacrodontium gen. nov. and Xenoacrodontiaceae fam. nov.) from Juglans regia . New Zealand , Cryptometrion metrosideri from twigs of Metrosideros sp., Coccomyces pycnophyllocladi from dead leaves of Phyllocladus alpinus, Hypoderma aliforme from fallen leaves Fuscopora solandri and Hypoderma subiculatum from dead leaves Phormium tenax. Norway , Neodevriesia kalakoutskii from permafrost and Variabilispora viridis from driftwood of Picea abies. Portugal , Entomortierella hereditatis from a biofilm covering a deteriorated limestone wall. Russia , Colpoma junipericola from needles of Juniperus sabina, Entoloma cinnamomeum on soil in grasslands, Entoloma verae on soil in grasslands, Hyphodermella pallidostraminea on a dry dead branch of Actinidia sp., Lepiota sayanensis on litter in a mixed forest, Papiliotrema horticola from Malus communis , Paramacroventuria ribis (incl. Paramacroventuria gen. nov.) from leaves of Ribes aureum and Paramyrothecium lathyri from leaves of Lathyrus tuberosus. South Africa , Harzia combreti from leaf litter of Combretum collinum ssp. sulvense, Penicillium xyleborini from Xyleborinus saxesenii , Phaeoisaria dalbergiae from bark of Dalbergia armata, Protocreopsis euphorbiae from leaf litter of Euphorbia ingens and Roigiella syzygii from twigs of Syzygium chordatum . Spain , Genea zamorana on sandy soil, Gymnopus nigrescens on Scleropodium touretii, Hesperomyces parexochomi on Parexochomus quadriplagiatus, Paraphoma variabilis from dung, Phaeococcomyces kinklidomatophilus from air in men's locker room and Tuber suaveolens in soil under Quercus faginea. Svalbard and Jan Mayen , Inocybe nivea associated with Salix polaris. Thailand , Biscogniauxia whalleyi on corticated wood. UK , Parasitella quercicola from Quercus robur. USA , Aspergillus arizonicus from indoor air in a hospital, Caeliomyces tampanus (incl. Caeliomyces gen. nov.) from office dust, Cippumomyces mortalis (incl. Cippumomyces gen. nov.) from a tombstone, Cylindrium desperesense from air in a store, Tetracoccosporium pseudoaerium from air sample in house, Toxicocladosporium glendoranum from air in a brick room, Toxicocladosporium losalamitosense from air in a classroom, Valsonectria portsmouthensis from air in men's locker room and Varicosporellopsis americana from sludge in a water reservoir. Vietnam , Entoloma kovalenkoi on rotten wood, Fusarium chuoi inside seed of Musa itinerans , Micropsalliota albofelina on soil in tropical evergreen mixed forests and Phytophthora docyniae from soil and roots of Docynia indica. Morphological and culture characteristics are supported by DNA barcodes. Citation : Crous PW, Osieck ER, Jurjević Ž, et al. 2021. Fungal Planet description sheets: 1284-1382. Persoonia 47: 178-374. https://doi.org/10.3767/persoonia.2021.47.06., (© 2021 Naturalis Biodiversity Center & Westerdijk Fungal Biodiversity Institute.)

Published
2021
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33. Fusarium : more than a node or a foot-shaped basal cell.

Author

Crous PW, Lombard L, Sandoval-Denis M, Seifert KA, Schroers HJ, Chaverri P, Gené J, Guarro J, Hirooka Y, Bensch K, Kema GHJ, Lamprecht SC, Cai L, Rossman AY, Stadler M, Summerbell RC, Taylor JW, Ploch S, Visagie CM, Yilmaz N, Frisvad JC, Abdel-Azeem AM, Abdollahzadeh J, Abdolrasouli A, Akulov A, Alberts JF, Araújo JPM, Ariyawansa HA, Bakhshi M, Bendiksby M, Ben Hadj Amor A, Bezerra JDP, Boekhout T, Câmara MPS, Carbia M, Cardinali G, Castañeda-Ruiz RF, Celis A, Chaturvedi V, Collemare J, Croll D, Damm U, Decock CA, de Vries RP, Ezekiel CN, Fan XL, Fernández NB, Gaya E, González CD, Gramaje D, Groenewald JZ, Grube M, Guevara-Suarez M, Gupta VK, Guarnaccia V, Haddaji A, Hagen F, Haelewaters D, Hansen K, Hashimoto A, Hernández-Restrepo M, Houbraken J, Hubka V, Hyde KD, Iturriaga T, Jeewon R, Johnston PR, Jurjević Ž, Karalti I, Korsten L, Kuramae EE, Kušan I, Labuda R, Lawrence DP, Lee HB, Lechat C, Li HY, Litovka YA, Maharachchikumbura SSN, Marin-Felix Y, Matio Kemkuignou B, Matočec N, McTaggart AR, Mlčoch P, Mugnai L, Nakashima C, Nilsson RH, Noumeur SR, Pavlov IN, Peralta MP, Phillips AJL, Pitt JI, Polizzi G, Quaedvlieg W, Rajeshkumar KC, Restrepo S, Rhaiem A, Robert J, Robert V, Rodrigues AM, Salgado-Salazar C, Samson RA, Santos ACS, Shivas RG, Souza-Motta CM, Sun GY, Swart WJ, Szoke S, Tan YP, Taylor JE, Taylor PWJ, Tiago PV, Váczy KZ, van de Wiele N, van der Merwe NA, Verkley GJM, Vieira WAS, Vizzini A, Weir BS, Wijayawardene NN, Xia JW, Yáñez-Morales MJ, Yurkov A, Zamora JC, Zare R, Zhang CL, and Thines M

Abstract

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. Production and hosting by ELSEVIER B.V.)

Published
2021
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