Web of Science: 3 cites, Scopus: 2 cites, Google Scholar: cites,
Interspecific potato breeding lines display differential colonization patterns and induced defense responses after Ralstonia solanacearum infection
Ferreira, Virginia (Universidad de la República (Uruguai). Departamento de Biociencias)
Pianzzola, María J. (Universidad de la República (Uruguai). Departamento de Biociencias)
Vilaró, Francisco L. (Instituto Nacional de Investigación Agropecuaria (Uruguai))
Galván, Guillermo A. (Universidad de la República (Uruguai). Departamento de Producción Vegetal)
Tondo, María L. (Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Área de Biología Molecular)
Rodriguez, María V. (Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Área Biología Vegetal)
Orellano, Elena G. (Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Área de Biología Molecular)
Valls, Marc (Centre de Recerca en Agrigenòmica)
Siri, María I. (Universidad de la República (Uruguai). Departamento de Biociencias)

Data: 2017
Resum: Potato (Solanum tuberosum L. ) is one of the main hosts of Ralstonia solanacearum, the causative agent of bacterial wilt. This plant pathogen bacteria produce asymptomatic latent infections that promote its global spread, hindering disease control. A potato breeding program is conducted in Uruguay based on the introgression of resistance from the wild native species S. commersonii Dun. Currently, several backcrosses were generated exploiting the high genetic variability of this wild species resulting in advanced interspecific breeding lines with different levels of bacterial wilt resistance. The overall aim of this work was to characterize the interaction of the improved potato germplasm with R. solanacearum. Potato clones with different responses to R. solanacearum were selected, and colonization, dissemination and multiplication patterns after infection were evaluated. A R. solanacearum strain belonging to the phylotype IIB-sequevar 1, with high aggressiveness on potato was genetically modified to constitutively generate fluorescence and luminescence from either the green fluorescence protein gene or lux operon. These reporter strains were used to allow a direct and precise visualization of fluorescent and luminescent cells in plant tissues by confocal microscopy and luminometry. Based on wilting scoring and detection of latent infections, the selected clones were classified as susceptible or tolerant, while no immune-like resistance response was identified. Typical wilting symptoms in susceptible plants were correlated with high concentrations of bacteria in roots and along the stems. Tolerant clones showed a colonization pattern restricted to roots and a limited number of xylem vessels only in the stem base. Results indicate that resistance in potato is achieved through restriction of bacterial invasion and multiplication inside plant tissues, particularly in stems. Tolerant plants were also characterized by induction of anatomical and biochemical changes after R. solanacearum infection, including hyperplasic activity of conductor tissue, tylose production, callose and lignin deposition, and accumulation of reactive oxygen species. This study highlights the potential of the identified tolerant interspecific potato clones as valuable genetic resources for potato-breeding programs and leads to a better understanding of resistance against R. solanacearum in potato.
Drets: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Llengua: Anglès.
Document: article ; recerca ; publishedVersion
Matèria: Bacterial wilt ; Ralstonia solanacearum ; Potato ; Solanum commersonii ; Plant breeding ; Disease resistance ; Latent infections
Publicat a: Frontiers in plant science, Vol. 8 (Aug. 2017) , art. 1424, ISSN 1664-462X

DOI: 10.3389/fpls.2017.01424
PMID: 28894453


14 p, 6.9 MB

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Documents de recerca > Documents dels grups de recerca de la UAB > Centres i grups de recerca (producció científica) > Ciències > CRAG (Centre de Recerca en Agrigenòmica)
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 Registre creat el 2017-08-28, darrera modificació el 2018-10-21



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