31 research outputs found

    In Memoriam Dr. Luigi Carraro

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    Guazuma ulmifolia (Sterculiaceae), a new natural host of 16SrXV phytoplasma in Costa Rica

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    Guacimo trees (Guazuma ulmifolia, Sterculiaceae) showing witches' broom symptoms (GWB), small leaves, short internodes, stunting and no flower and fruit production were observed on side roads and fences in different areas of Costa Rica. The occurrence of phytoplasma infection in GWB trees was evaluated by transmission electron microscopy (TEM), and by molecular analyses based on 16SrDNA: nested-PCR/RFLP, sequencing and phylogenetics. Phytoplasmas were observed only in the sieve cells of symptomatic trees by TEM. The infection was confirmed by nested-PCR; amplicons of about 1.2 kb were obtained from all DNA samples from symptomatic trees. The RFLP analysis generated patterns identical among GWB samples and showed a relationship of this phytoplasma to hibiscus witches' broom group (16SrXV). The 16S rDNA sequence (1460 nt), obtained from the P1A/16S-SR semi-nested-PCR products of two phytoplasma strains, shared 98.8% similarity with 'Candidatus Phytoplasma brasiliense' (GenBank accession: AF147708). The virtual RFLP pattern indicated a similarity coefficient of 0.95 with 16Sr group XV-A (AF147708), suggesting that the GWB phytoplasma may represent a new subgroup within this group. This is the first report of a phytoplasma infecting the neotropical tree species G. ulmifolia and the natural occurrence of a phytoplasma strain closely related to 'Ca. Phytoplasma brasiliense' in Costa Rica. En varias zonas de Costa Rica se observaron árboles de guácimo (Guazuma ulmifolia, Sterculiaceae) con síntomas de escoba de bruja (GWB), hoja pequeña, acortamiento de entrenudos, dando al árbol un aspecto general de enanismo. La infección por fitoplasmas en los árboles de guácimo se evaluó mediante microscopia electrónica de transmisión (TEM), análisis moleculares del 16S rDNA mediante PCR anidado, RFLP´s, secuenciación y filogenia. En la TEM, los fitoplasmas se observaron sólo en las células del floema de los árboles sintomáticos. La infección se confirmó por PCR anidada, los productos amplificados de aproximadamente 1,2 kb se obtuvieron para todas las muestras sintomáticas evaluadas. El análisis de RFLP generó patrones idénticos entre las muestras con GWB y mostró relación de este fitoplasma con el de la "escoba de bruja del hibisco" (16SrXV). La secuencia de ADNr 16S (1460 nt) de los productos obtenidos por PCR semi-anidado (P1A/16S-SR) de dos muestras de GWB mostraron 98,8% de similitud con "Candidatus Phytoplasma brasiliense" (GenBank, registro AF147708). El patrón RFLP virtual reveló 95% de similitud con el grupo 16Sr XV-A (AF147708), lo que sugiere que el fitoplasma GWB puede representar un nuevo subgrupo dentro del 16Sr XV. Este es el primer informe de un fitoplasma infectando a la especie neotropical G. ulmifolia y de la ocurrencia natural de un fitoplasma estrechamente relacionado con "Ca. Phytoplasma brasiliense" en Costa Rica Universidad de Costa Rica/[801-A7-602]/UCR/Costa Rica Universidad de Costa Rica/[801-A1-801]/UCR/Costa Rica UCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias Básicas::Centro de Investigación en Biología Celular y Molecular (CIBCM) UCR::Vicerrectoría de Docencia::Ciencias Agroalimentarias::Facultad de Ciencias Agroalimentarias::Escuela de Agronomí

    Phloem cytochemical modification and gene expression following the recovery of apple plants from apple proliferation

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    Recovery of apple trees from apple proliferation was studied by combining ultrastructural, cytochemical, and gene expression analyses to possibly reveal changes linked to recovery-associated resistance. When compared with either healthy or visibly diseased plants, recovered apple trees showed abnormal callose and phloem-protein accumulation in their leaf phloem. Although cytochemical localization detected Ca2+ ions in the phloem of all the three plant groups, Ca2+ concentration was remarkably higher in the phloem cytosol of recovered trees. The expression patterns of five genes encoding callose synthase and of four genes encoding phloem proteins were analyzed by quantitative real-time reverse transcription- polymerase chain reaction. In comparison to both healthy and diseased plants, four of the above nine genes were remarkably upregulated in recovered trees. As in infected apple trees, phytoplasma disappear from the crown during winter, but persist in the roots, and it is suggested that callose synthesis/deposition and phloem-protein plugging of the sieve tubes would form physical barriers preventing the recolonization of the crown during the following spring. Since callose deposition and phloem-protein aggregation are both Ca2+-dependent processes, the present results suggest that an inward flux of Ca2+ across the phloem plasma membrane could act as a signal for activating defense reactions leading to recovery in phytoplasma-infected apple trees.L'articolo é disponibile sul sito dell'editore: http://www.apsjournals.apsnet.or

    Population dynamics of Cacopsylla pruni and 'Candidatus Phytoplasma prunorum' infection in North-Eastern Italy

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    Abstract A two year surveys was conducted in Friuli Venezia Giulia region (north-eastern Italy) with the aims to improve knowledge about biological characteristics of Cacopsylla pruni Scopoli, and to ascertain its role in the spread of different 'Candidatus Phytoplasma prunorum' strains. Insects were captured starting from March till the end of April in apricot orchards with high European stone fruit yellows incidence. For phytoplasma detection a nested PCR protocol based on aceF gene was adopted. Results confirmed that the percentage of phytoplasma positive insects increased from March to April, because they fed on infected trees. During the reimmigration season the percentage of females was higher than that of males, especially after coupling time. Besides a very high percentage of infected C. pruni, no significant differences related to the sex were observed. 'Ca. P. prunorum' strains of aceF-A, aceF-C and aceF-E subgroups, were mainly found in the captured C. pruni population
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