- -

Genetic and virulence diversity, and mating type distribution of Togninia minima causing grapevine trunk diseases in Spain

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Compartir/Enviar a

Citas

Estadísticas

  • Estadisticas de Uso

Genetic and virulence diversity, and mating type distribution of Togninia minima causing grapevine trunk diseases in Spain

Mostrar el registro sencillo del ítem

Ficheros en el ítem

dc.contributor.author Gramaje Pérez, David es_ES
dc.contributor.author Armengol Fortí, Josep es_ES
dc.contributor.author Ridgway, H. J. es_ES
dc.date.accessioned 2016-07-07T09:57:55Z
dc.date.available 2016-07-07T09:57:55Z
dc.date.issued 2013-04
dc.identifier.issn 0929-1873
dc.identifier.uri http://hdl.handle.net/10251/67304
dc.description.abstract [EN] Fifty eight single-spore Togninia minima (anamorph Phaeoacremonium aleophilum) isolates were recovered from grape rootstock wood of plants that showed symptoms of Petri disease and esca from 2001 to 2008 in Spain. These isolates were studied by means of mating type distribution, UP-PCR analysis, and virulence assays. Analysis of clone-corrected data sets showed equal frequencies of both mating types in the entire Spanish population, in the Ciudad Real region, at inter-vineyard and intra-vine spatial scales; while unequal mating type distribution was detected in Valencia and Zaragoza regions, at intra-vineyard and intra-vine spatial scales. This is the first study on distribution of T. minima mating types on spatial scales varying from vineyards to regions. A total of 49 polymorphic UP-PCR markers were obtained using seven UP-PCR primers. Four optimal clusters were inferred with Bayesian structure and multivariate analyses from the UP-PCR data. The high number of unique genotypes observed within the Spanish population, combined with a near-equal distribution of mating types, suggested that sexual reproduction probably does occur. However, based on allele distribution and frequency, each of the three subpopulations appeared to be evolving independently. Gene and genotype diversities across the subpopulations were similar and ranged from 0.24 to 0.27 and from 0.27 to 0.37, respectively. The detection of genetically identical isolates within and among subpopulations indicates that an asexual reproductive component should not be excluded. Contrast analysis among groups defined by UP-PCR analyses showed no significant differences in the virulence of T. minima isolates. es_ES
dc.description.sponsorship We thank M. G. Milgroom (Department of Plant Pathology and Plant-Microbe Biology, Cornell University) and M. Berbegal (Instituto Agroforestal Mediterraneo, UPV) for providing valuable advice on the writing of this manuscript. The authors gratefully acknowledge M. Leon (Instituto Agroforestal Mediterraneo, UPV) for technical assistance, and B. B. Landa, R. Pineda and J. A. Navas (Institute of Sustainable Agriculture, CSIC) for assistance with cluster analyses. Financial support by the 'Programa de Apoyo a la Investigacion y Desarrollo (PAID-00-09) de la Universidad Politecnica de Valencia for D. Gramaje during his three months stay in New Zealand is gratefully acknowledged. This research was financially supported by the projects RTA2007-00023-C04-03 and RTA2010-00009-C03-03 (Instituto Nacional de Investigacion y Tecnologia Agraria y Alimentaria, INIA, Spain) and the European Regional Development Fund (ERDF). en_EN
dc.language Inglés es_ES
dc.publisher Springer Verlag (Germany) es_ES
dc.relation.ispartof European Journal of Plant Pathology es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject Esca es_ES
dc.subject Petri disease es_ES
dc.subject Phaeoacremonium aleophilum es_ES
dc.subject Population structure es_ES
dc.subject Vitis vinifera es_ES
dc.subject.classification PRODUCCION VEGETAL es_ES
dc.title Genetic and virulence diversity, and mating type distribution of Togninia minima causing grapevine trunk diseases in Spain es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1007/s10658-012-0110-6
dc.relation.projectID info:eu-repo/grantAgreement/UPV//PAID-00-09/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/MEC//RTA2007-00023-C04-03/ES/Biología y desarrollo de métodos de control de hongos de madera de la vid en planta joven./ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/MICINN//RTA2010-00009-C03-03/ES/RTA2010-00009-C03-03/ es_ES
dc.rights.accessRights Cerrado es_ES
dc.contributor.affiliation Universitat Politècnica de València. Instituto Agroforestal Mediterráneo - Institut Agroforestal Mediterrani es_ES
dc.contributor.affiliation Universitat Politècnica de València. Departamento de Ecosistemas Agroforestales - Departament d'Ecosistemes Agroforestals es_ES
dc.description.bibliographicCitation Gramaje Pérez, D.; Armengol Fortí, J.; Ridgway, HJ. (2013). Genetic and virulence diversity, and mating type distribution of Togninia minima causing grapevine trunk diseases in Spain. European Journal of Plant Pathology. 135(4):727-743. https://doi.org/10.1007/s10658-012-0110-6 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://dx.doi.org/10.1007/s10658-012-0110-6 es_ES
dc.description.upvformatpinicio 727 es_ES
dc.description.upvformatpfin 743 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 135 es_ES
dc.description.issue 4 es_ES
dc.relation.senia 236013 es_ES
dc.contributor.funder Ministerio de Educación y Ciencia es_ES
dc.contributor.funder Ministerio de Ciencia e Innovación es_ES
dc.contributor.funder Universitat Politècnica de València es_ES
dc.contributor.funder European Regional Development Fund es_ES
dc.description.references Adalat, K., Whiting, C., Rooney, S., & Gubler, W. D. (2000). Pathogenicity of three species of Phaeoacremonium spp. on grapevine in California. Phytopathologia Mediterranea, 39, 92–99. es_ES
dc.description.references Ajello, L., Georg, L. K., Steigbigel, R. T., & Wang, C. J. K. (1974). A case of phaeohyphomycosis caused by a new species of Phialophora. Mycologia, 66, 490–498. es_ES
dc.description.references Aroca, A., & Raposo, R. (2009). Pathogenicity of Phaeoacremonium species on grapevines. Journal of Phytopathology, 157, 413–419. es_ES
dc.description.references Borie, B., Jacquiot, L., Jamaux-Despréaux, I., Larignon, P., & Péros, J. P. (2002). Genetic diversity in populations of the fungi Phaeomoniella chlamydospora and Phaeoacremonium aleophilum on grapevine in France. Plant Pathology, 51, 85–96. es_ES
dc.description.references Bulat, S. A., Mironenko, N. V., Lapteva, M. N., & Strelchenko, P. P. (1994). Polymerase chain reaction with universal primers (UP-PCR) and its application to plant genome analysis. In R. P. Adams, J. S. Miller, E. M. Goldenberg, & J. E. Adams (Eds.), Conservation of plant genes II: utilization of ancient and modern DNA (pp. 113–129). St Louis: Missouri Botanical Garden. es_ES
dc.description.references Bulat, S. A., Lübeck, M., Mironenko, N., Jensen, D. F., & Lübeck, P. S. (1998). UPPCR analysis and ITS1 ribotyping of strains of Trichoderma and Gliocladium. Mycological Research, 102, 933–943. es_ES
dc.description.references Comont, G., Corio-Costet, M.-F., Larignon, P., & Delmotte, F. (2010). AFLP markers reveal two genetic groups in the French population of the grapevine fungal pathogen Phaeomoniella chlamydospora. European Journal of Plant Pathology, 127, 451–454. es_ES
dc.description.references Corander, J., Waldmann, P., Marttinen, P., & Sillanpää, M. J. (2004). BAPS 2: enhanced possibilities for the analysis of genetic population structure. Bioinformatics, 20, 2363–2369. es_ES
dc.description.references Cottral, E., Ridgway, H. J., Pascoe, I., Edwards, J., & Taylor, P. (2001). UP-PCR analysis of Australian isolates of Phaeomoniella chlamydospora and Phaeoacremonium aleophilum. Phytopathologia Mediterranea, 40, S479. es_ES
dc.description.references Cumagun, C. J. R., Hockenhull, J., & Lübeck, M. (2000). Characterization of Trichoderma isolates from Philippine rice fields by UP-PCR and rDNA-ITS1 analysis: identification of UP-PCR markers. Journal of Phytopathology, 14, 109–115. es_ES
dc.description.references Damm, U., Mostert, L., Crous, P. W., & Fourie, P. H. (2008). Novel Phaeoacremonium species associated with necrotic wood of Prunus trees. Persoonia, 20, 87–102. es_ES
dc.description.references Dhingra, O. D., & Sinclair, J. B. (1995). Basic plant pathology methods (2nd ed., p. 434). Boca Raton: CRC Press. es_ES
dc.description.references Eskalen, A., & Gubler, W. D. (2001). Association of spores of Phaeomoniella chlamydospora, Phaeoacremonium inflatipes, and Pm. aleophilum with grapevine cordons in California. Phytopathologia Mediterranea, 40, S429–S432. es_ES
dc.description.references Essakhi, S., Mugnai, L., Crous, P. W., Groenewald, J. Z., & Surico, G. (2008). Molecular and phenotypic characterization of novel Phaeoacremonium species associated with Petri disease and esca of grapevine. Persoonia, 21, 119–134. es_ES
dc.description.references Evanno, G., Regnaut, S., & Goudet, J. (2005). Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. Molecular Ecology, 14(8), 2611–2620. es_ES
dc.description.references Excoffier, L., Laval, G., & Schneider, S. (2005). Arlequin ver. 3.0: An integrated software package for population genetics data analysis. Evolutionary Bioinformatics Online, 1, 47–50. es_ES
dc.description.references Falush, D., Stephens, M., & Pritchard, J. K. (2007). Inference of population structure using multilocus genotype data: dominant markers and null alleles. Molecular Ecology Notes, 7(4), 574–578. es_ES
dc.description.references Feliciano, A. J., & Gubler, W. D. (2001). Histological investigations on infection of grape roots and shoots by Phaeoacremonium spp. Phytopathologia Mediterranea, 40, S387–S393. es_ES
dc.description.references Fincham, J. R. S., & Day, P. R. (1963). Fungal genetics (3rd ed.). Oxford: Blackwell Scientific Publication. es_ES
dc.description.references Glass, N. L., & Donaldson, G. C. (1995). Development of primer sets designed for use with the PCR to amplify conserved genes from filamentous infection due to Phaeoacremonium spp. Journal of Clinical Microbiology, 41, 1332–1336. es_ES
dc.description.references Graham, A. B., Johnston, P. R., & Weir, B. S. (2009). Three new Phaeoacremonium species on grapevines in New Zealand. Australasian Plant Pathology, 38, 505–513. es_ES
dc.description.references Gramaje, D., & Armengol, J. (2011). Fungal trunk pathogens in the grapevine propagation process: potential inoculum sources, detection, identification and management strategies. Plant Disease, 95, 1040–1055. es_ES
dc.description.references Gramaje, D., Armengol, J., Mohammadi, H., Banihashemi, Z., & Mostert, L. (2009). Novel Phaeoacremonium species associated with Petri disease and esca of grapevine in Iran and Spain. Mycologia, 101, 920–929. es_ES
dc.description.references Gramaje, D., Armengol, J., Salazar, D., López-Cortés, I., & García-Jiménez, J. (2009). Effect of hot-water treatments above 50 °C on grapevine viability and survival of Petri disease pathogens. Crop Protection, 28, 280–285. es_ES
dc.description.references Gramaje, D., García-Jiménez, J., & Armengol, J. (2010). Grapevine rootstock susceptibility to fungi associated with Petri disease and esca under field conditions. American Journal of Enology and Viticulture, 61, 512–520. es_ES
dc.description.references Guarro, J., Alves, S. H., Gené, J., Grazziotin, N. A., Muzzuco, R., Dalmagro, C., et al. (2003). Two cases of subcutaneous infection due to Phaeoacremonium spp. Journal of Clinical Microbiology, 41, 1332–1336. es_ES
dc.description.references Halleen, F., Mostert, L., & Crous, P. W. (2007). Pathogenicity testing of lesser-known vascular fungi of grapevines. Australasian Plant Pathology, 36, 277–285. es_ES
dc.description.references Hausner, G., Eyjólfsdóttir, G. G., Reid, J., & Klassen, G. R. (1992). Two additional species of the genus Togninia. Canadian Journal of Botany, 70, 724–732. es_ES
dc.description.references Jombart, T. (2008). Adegenet: a R package for the multivariate analysis of genetic markers. Bioinformatics, 24, 1403–1405. es_ES
dc.description.references Jombart, T., Devillard, S., & Balloux, F. (2010). Discriminant analysis of principal components: a new method for the analysis of genetically structured populations. BMC Genetics, 11, 94. es_ES
dc.description.references Larignon, P., & Dubos, B. (1997). Fungi associated with esca disease in grapevine. European Journal of Plant Pathology, 103, 147–157. es_ES
dc.description.references Lübeck, P. S., Alekhina, I. A., Lübeck, M., & Bulat, S. A. (1998). UP-PCR genotyping and rDNA analysis of Ascochyta pisi Lib. Journal of Phytopathology, 146, 51–55. es_ES
dc.description.references Lübeck, M., Alekhina, I. A., Lübeck, P. S., Jensen, D. F., & Bulat, S. A. (1999). Delineation of Trichoderma harzianum into two genotypic groups by a highly robust fingerprinting method, UP-PCR, and UP-PCR product crosshybridization. Mycological Research, 103, 289–298. es_ES
dc.description.references Marco, S. D. I., Calzarano, F., Osti, F., & Mazzullo, A. (2004). Pathogenicity of fungi associated with a decay of kiwifruit. Australasian Plant Pathology, 33, 337–342. es_ES
dc.description.references Martín, L., & Martín, M. T. (2010). Molecular characterization of Phaeoacremonium aleophilum isolated from grapevines in Castilla y León (Spain). Phytopathologia Mediterranea, 49, 111. es_ES
dc.description.references Mead, R., Curnow, R. N., & Hasted, A. M. (2003). Statistical methods in agriculture and experimental biology (3rd ed.). Washington: CRS. es_ES
dc.description.references Mostert, L., Crous, P. W., Groenewald, J. Z., Gams, W., & Summerbell, R. C. (2003). Togninia (Calosphaeriales) is confirmed as teleomorph of Phaeoacremonium by means of morphology, sexual compatibility and DNA phylogeny. Mycologia, 95, 646–649. es_ES
dc.description.references Mostert, L., Groenewald, J. Z., Summerbell, R. C., Sutton, D. A., Padhye, A. A., & Crous, P. W. (2005). Species of Phaeoacremonium associated with human infections and environmental reservoirs in infected woody plants. Journal of Clinical Microbiology, 43, 1752–1767. es_ES
dc.description.references Mostert, L., Groenewald, J. Z., Summerbell, R. C., Gams, W., & Crous, P. W. (2006). Taxonomy and pathology of Togninia (Diaporthales) and its Phaeoacremonium anamorphs. Studies in Mycology, 54, 1–115. es_ES
dc.description.references Mugnai, L., Graniti, A., & Surico, G. (1999). Esca (black measles) and brown wood-streaking: two old and elusive diseases of grapevines. Plant Disease, 83, 404–416. es_ES
dc.description.references Nei, M. (1973). Analysis of gene diversity in subdivided populations. Proceedings of the National Academy of Sciences of the United States of America, 70, 3321–3323. es_ES
dc.description.references O’Donnell, K., & Cigelnik, E. (1997). Two divergent intragenomic rDNA ITS2 types within a monophyletic lineage of the fungus Fusarium are nonorthologous. Molecular and Phylogenetic Evolution, 7, 103–116. es_ES
dc.description.references Pascoe, I. G., Edwards, J., Cunnington, J. H., & Cottral, E. (2004). Detection of the Togninia teleomorph of Phaeoacremonium aleophilum in Australia. Phytopathologia Mediterranea, 43, 51–58. es_ES
dc.description.references Péros, J. P., & Berger, G. (1994). A rapid method to assess the aggressiveness of Euypa lata isolates and the susceptibility of grapevine cultivars to Eutypa dieback. Agronomie, 14, 515–523. es_ES
dc.description.references Péros, J. P., Jamaux-Despréaux, I., & Berger, G. (2000). Population genetics of fungi associated with esca disease in French vineyards. Phytopathologia Mediterranea, 39, 150–155. es_ES
dc.description.references Pritchard, J. K., Stephens, M., & Donnelly, P. (2000). Inference of population structure using multilocus genotype data. Genetics, 155, 945–959. es_ES
dc.description.references Réblová, M., & Mostert, L. (2007). Romellia is congeneric with Togninia, and description of Conidiotheca gen. nov. for one species of this genus with polysporous asci. Mycological Research, 111, 299–307. es_ES
dc.description.references Réblová, M., Mostert, L., Gams, W., & Crous, P. W. (2004). New genera in Calosphaeriales: Togniniella and its anamorph Phaeocrella, and Calosphaeriophora as Anamorph of Calosphaeria. Studies in Mycology, 50, 533–550. es_ES
dc.description.references Rice, W. R. (1989). Analyzing table of statistical tests. Evolution, 43, 223–225. es_ES
dc.description.references Rooney-Latham, S., Eskalen, A., & Gubler, W. D. (2005a). Teleomorph formation of Phaeoacremonium aleophilum, cause of esca and grapevine decline in California. Plant Disease, 89, 177–184. es_ES
dc.description.references Rooney-Latham, S., Eskalen, A., & Gubler, W. D. (2005b). Occurrence of Togninia minima perithecia in esca-affected vineyards in California. Plant Disease, 89, 867–871. es_ES
dc.description.references Rumbos, I. C. (1986). Phialophora parasitica, causal agent of cherry dieback. Journal of Phytopathology, 117, 283–287. es_ES
dc.description.references Scheck, H. J., Vasquez, S. J., & Gubler, W. D. (1998). First report of three Phaeoacremonium spp. causing young grapevine decline in California. Plant Disease, 82, 590. es_ES
dc.description.references Stoddart, J. A., & Taylor, J. F. (1988). Genotype diversity: estimation and prediction in samples. Genetics, 118, 705–711. es_ES
dc.description.references Tegli, S., Santilli, E., Bertelli, E., & Surico, G. (2000). Genetic variation within Phaeoacremonium aleophilum and P. chlamydosporum in Italy. Phytopathologia Mediterranea, 39, 125–133. es_ES
dc.description.references Tibayrenc, M., Kjellberg, F., Arnaud, J., Oury, B., Brenière, S. F., Dardé, M. L., et al. (1991). Are eukaryotic microorganisms clonal or sexual? A population genetics vantage. Proceedings of the National Academy of Sciences, 88, 5129–5133. es_ES
dc.description.references Williams, J. G. K., Kubelik, A. R., Livak, K. J., Rafalski, J. A., & Tingey, S. V. (1990). DNA polymorphism amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Research, 18, 6531–6535. es_ES
dc.description.references Yeh, F. C., Yang, R. C., & Boyle, T. (1999). POPGENE version 1.32, The Microsoft Window based freeware for Population Genetic Analysis, Edmanton, Alberta: University of Alberta, available in the internet at http://www.ualberta.ca/~fyeh/fyeh . es_ES
dc.description.references Zanzotto, A., Gardiman, M., & Lovat, L. (2008). Effect of Phaeomoniella chlamydospora and Phaeoacremonium sp. on in vitro grapevine plants. Scientia Horticulturae, 116, 404–408. es_ES
dc.description.references Zhan, J., Kema, G. H. J., Waalwijk, C., & McDonald, B. A. (2002). Distribution of mating type alleles in the wheat pathogen Mycosphaerella graminicola over spatial scales from lesions to continents. Fungal Genetics and Biology, 36, 128–136. es_ES


Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem