Enhancement of adventitious root differentiation and growth of in vitro grapevine shoots inoculated with plant growth promoting rhizobacteria

The effect of Burkholderia spp. strain IF25 on adventitious rooting was evaluated in micropropagated grapevine explants. Data on rooting time, stem length, number of stem nodes, basal callus development, number of roots and root length per rooted microcutting were detected at 6, 8, 10, 13, 19, 26 and 30 days after bacterial inoculation. Results suggest that bacterization of in vitro grapevine explants by strain IF25 affected root differentiation, as the earliest rooting occurred in inoculated shoots, whether or not exogenous IBA had been applied, and increased the average number of roots per explant

Leaf morphological characteristics and stilbene production differently affect downy mildew resistance of Vitis vinifera varieties grown in Italy

The degree of resistance to downy mildew of grape varieties belonging to the oenological tradition of Central Italy was evaluated by the analysis of plant responses to pathogen infections carried out in natural and controlled environments. Leaf morphological traits, such as hair and stornata! density, were determined for each variety, and the percentage of infected stornata and pathogen colonization of host mesophyll at 24, 48, and 72 hours post inoculation were assessed by epifluorescence microscopy. Furthermore, stilbene production at the site of Plasmopara viticola infection was analyzed at 72 hours post inoculation. Results indicate differences in resistance to downy mildew among selected varieties. Different significant values were detected among grapevines in the percentage of infected stornata and average number of successfully penetrated zoospores per stornata and per leaf surface unit. Differences also emerged in the rate of pathogen growth and stilbene production, signifying that defence mechanisms involved or induced during pathogen infection could be differentially effective among grapevine cultivars in limiting disease progression.Peer reviewe

Intra-varietal variability of Romanesco variety (Vitis vinifera L.)

Most historical sources that describe the presence of Romanesco variety in vine-growing areas of Lazio Region (Italy) highlighted the variability of morphological traits within the variety. This partly justifies the presence of different synonyms, true or presumed, reported by many authors for this grape variety. With the aim of analysing this variability, eight accessions related to the variety, collected in Lazio Region and grown in the DAFNE grape germplasm collection, have been characterized over five productive seasons. The ampelographic description was carried out using 50 OIV morphological descriptors and ampelometric analyses were carried out on mature leaves by SuperAmpelo software. The DNA of the different accessions, extracted from young leaves, was analyzed using 14 microsatellite loci. Furthermore, at harvest, the grapes of each accession were sampled to assess main compositive characteristics. Results showed differences among accessions on some ampelographic descriptors of the mature leaf, of the bunch, and on phenological stages. Microsatellite profiles allowed for classification of the accessions into three distinct groups. Qualitative analysis of the berry skin showed differences among accessions in the content of the main classes of phenolic compounds

Berry Flesh and Skin Ripening Features in Vitis vinifera as Assessed by Transcriptional Profiling

Background Ripening of fleshy fruit is a complex developmental process involving the differentiation of tissues with separate functions. During grapevine berry ripening important processes contributing to table and wine grape quality take place, some of them flesh- or skin-specific. In this study, transcriptional profiles throughout flesh and skin ripening were followed during two different seasons in a table grape cultivar ‘Muscat Hamburg’ to determine tissue-specific as well as common developmental programs. Methodology/Principal Findings Using an updated GrapeGen Affymetrix GeneChip® annotation based on grapevine 12×v1 gene predictions, 2188 differentially accumulated transcripts between flesh and skin and 2839 transcripts differentially accumulated throughout ripening in the same manner in both tissues were identified. Transcriptional profiles were dominated by changes at the beginning of veraison which affect both pericarp tissues, although frequently delayed or with lower intensity in the skin than in the flesh. Functional enrichment analysis identified the decay on biosynthetic processes, photosynthesis and transport as a major part of the program delayed in the skin. In addition, a higher number of functional categories, including several related to macromolecule transport and phenylpropanoid and lipid biosynthesis, were over-represented in transcripts accumulated to higher levels in the skin. Functional enrichment also indicated auxin, gibberellins and bHLH transcription factors to take part in the regulation of pre-veraison processes in the pericarp, whereas WRKY and C2H2 family transcription factors seems to more specifically participate in the regulation of skin and flesh ripening, respectively. Conclusions/Significance A transcriptomic analysis indicates that a large part of the ripening program is shared by both pericarp tissues despite some components are delayed in the skin. In addition, important tissue differences are present from early stages prior to the ripening onset including tissue-specific regulators. Altogether, these findings provide key elements to understand berry ripening and its differential regulation in flesh and skin.This study was financially supported by GrapeGen Project funded by Genoma España within a collaborative agreement with Genome Canada. The authors also thank The Ministerio de Ciencia e Innovacion for project BIO2008-03892 and a bilateral collaborative grant with Argentina (AR2009-0021). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Peer reviewe