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Träfflista för sökning "L773:0031 949X OR L773:1943 7684 "

Sökning: L773:0031 949X OR L773:1943 7684

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1.
  • Abreha, Kibrom Berhe, et al. (författare)
  • Late Blight Resistance Screening of Major Wild Swedish Solanum Species: S. dulcamara, S. nigrum, and S. physalifolium
  • 2018
  • Ingår i: Phytopathology. - 0031-949X .- 1943-7684. ; 108, s. 847-857
  • Tidskriftsartikel (refereegranskat)abstract
    • To understand the contribution of wild Solanum species to the epidemiology of potato late blight in Sweden, we characterized the resistance of the three putative alternative hosts: S. physalifolium, S. nigrum, and S. dulcamara to Phytophthora infestans, the causal agent of late blight. The pathogen sporulated in all 10 investigated S. physalifolium genotypes, suggesting susceptibility (S phenotype). Field-grown S. physalifolium was naturally infected but could regrow, though highly infected genotypes were smaller at the end of the season. In 75 S. nigrum genotypes, there were no symptoms (R phenotype) or a lesion restricted to the point of inoculation (RN phenotype), indicating resistance. In 164 S. dulcamara genotypes, most resistance variability was found within sibling groups. In addition to the three resistance phenotypes (R, RN, and S), in S. dulcamara a fourth new resistance phenotype (SL) was identified with lesions larger than the point of inoculation but without visible sporulation of the pathogen. Quantitative PCR confirmed P. infestans growth difference in RN, SL, and S phenotypes. Thus, in Sweden S. physalifolium is susceptible and could be a player in epidemiology. A limited role of S. dulcamara leaves in the epidemiology of late blight was suggested, since no major symptoms have been found in the field.
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  • Berlin, Anna, et al. (författare)
  • Genetic variation in Puccinia graminis collected from oats, rye, and barberry
  • 2012
  • Ingår i: Phytopathology. - 0031-949X .- 1943-7684. ; 102, s. 1006-1012
  • Tidskriftsartikel (refereegranskat)abstract
    • Puccinia graminis, the causal agent of stem rust, was collected from its alternate host barberry (Berberis spp.) and two different uredinial hosts, oats (Avena sativa) and rye (Secale cereale). The samples were analyzed using 11 polymorphic simple sequence repeat (SSR) markers. There were large differences between fungal populations on oats (P. graminis f. sp. avenae) and rye (P. graminis f. sp. secalis), and the genetic variation within the different formae speciales was also high. It was possible to distinguish between the two formae speciales on barberry. Additional genotypic groups not present in the field samples from oats and rye were also identified on barberry. Our results confirm the importance of barberry in maintaining the populations of P. graminis in Sweden and the importance of the sexual stage for the survival of the pathogen.
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  • Berlin, Anna (författare)
  • Isolate Specificity and Polygenic Inheritance of Resistance in Barley to the Heterologous Rust Pathogen Puccinia graminis f. sp avenae
  • 2016
  • Ingår i: Phytopathology. - 0031-949X .- 1943-7684. ; 106, s. 1029-1037
  • Tidskriftsartikel (refereegranskat)abstract
    • Barley is a near-nonhost to numerous heterologous (nonadapted) rust pathogens because a small proportion of genotypes are somewhat susceptible. We assessed 66 barley accessions and three mapping populations (Vada x SusPtrit, Cebada Capa x SusPtrit, and SusPtrit x Golden Promise) for response to three Swedish oat stem rust (Puccinia graminis f. sp. avenae) fungal isolates and determined that barley is a near-nonhost to P. graminis f. sp. avenae and that resistance was polygenically inherited. The parental genotypes Vada and Golden Promise were immune to all three isolates, whereas Cebada Capa was immune to two isolates and moderately resistant to the third. Phenotypic data from the Vada x SusPtrit mapping population and the barley accessions tested also demonstrated isolate-specific resistance. In particular, the SusPtrit parent and several other accessions allowed sporulation by isolate Ingeberga but were resistant to isolate Evertsholm. Nine chromosomal regions carried quantitative trait loci (QTL) (Rpgaql to Rpgaq9) of varying effect, most of which colocated to previously identified QTL for resistance to other heterologous rust pathogens. Rpgaql on chromosome 1H (Vada and Golden Promise) was effective toward all isolates tested. Microscopic examination indicated that resistance was prehaustorial in Vada whereas, in SusPtrit, both pre- and posthaustorial mechanisms play a role.
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  • Blandón-Díaz, Jorge Ulises, et al. (författare)
  • Phenotypic Variation Within a Clonal Lineage of Phytophthora infestans Infecting both Tomato and Potato in Nicaragua
  • 2012
  • Ingår i: Phytopathology. - 0031-949X .- 1943-7684. ; 102, s. 323-330
  • Tidskriftsartikel (refereegranskat)abstract
    • Late blight caused by Phytophthora infestans (Mont.) de Bary is a constraint to both potato and tomato crops in Nicaragua. The hypothesis that the Nicaraguan population of P. infestans is genotypically and phenotypically diverse and potentially subdivided based on host association was tested. A collection of isolates was analyzed using genotypic markers (microsatellites and mitochondrial DNA haplotype) and phenotypic markers (mating type, virulence, and fungicide sensitivity). The genotypic analysis revealed no polymorphism in 121 of 132 isolates of P. infestans tested. Only the Ia haplotype and the A2 mating type were detected. Most of the tested isolates were resistant to metalaxyl. The virulence testing showed variation among isolates of P. infestans. No evidence was found of population differentiation among potato and tomato isolates of P. infestans based on the genotypic and phenotypic analysis. We conclude that the Nicaraguan population of P. infestans consists of a single clonal lineage (NI-1) which belongs to the A2 mating type and the Ia mitochondrial DNA haplotype. Moreover, based on the markers used, this population of P. infestans does not resemble the population in countries from which potato seed is imported to Nicaragua or the population in neighboring countries. The data presented here indicate that the NI-1 clonal lineage is the primary pathogen on both potato and tomato, and its success on both host species is unique in a South American context.
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  • Chawade, Aakash (författare)
  • Mapping for Adult-Plant Resistance Against Septoria Tritici Blotch in a Common Wheat Line Murga
  • 2021
  • Ingår i: Phytopathology. - 0031-949X .- 1943-7684. ; 111, s. 1001-1007
  • Tidskriftsartikel (refereegranskat)abstract
    • Septoria tritici blotch (STB) is a major foliar disease globally that is notorious for quickly developing fungicide resistance, making host resistance an indispensable component in mitigating STB. The International Maize and Wheat Improvement Center (CIMMYT) wheat line Murga is well known for its high, durable, and broad-spectrum resistance against STB infection. This study aimed to investigate the resistance mechanism of Murga to facilitate its utilization in breeding. A recombinant inbred line population was derived from a cross between Murga and STB-susceptible line Huirivis#1, comprising 297 progenies. The population was evaluated for adult-plant STB resistance in Toluca, Mexico (from 2017 to 2019), and in La Estanzuela, Uruguay (from 2016 to 2018). Genotyping was performed with the DArTseq platform. Quantitative trait locus (QTL) mapping indicated a major and stable QTL on chromosome 3DL, explaining a phenotypic variation for STB of 41.2 to 62.5% in Mexico and 27.5 to 40.3% in Uruguay. This QTL was regarded as Stb16 based on the comparison of its physical position, the possible origin from synthetic wheat, and its broad-spectrum resistance. Additional QTLs with minor effects were identified on chromosomes 2B, 2D, 3A, 3B, and 5B. The QTL on 5BS was significant in four of the six environments and must be new. Murga was the resistant donor for all QTLs except for those on 2B and 3A. Being an elite breeding line, Stb16 carrier Murga could be used as a promising STB resistance donor. Rational employment of Stb16 could contribute to STB management yet avoid the rapid emergence of Stb16-virulent isolates.
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