12 research outputs found
Desfolha e nutrição do S no rabanete: crescimento, polifenóis e atividade antiradical
ABSTRACT Experiments were carried out to study patterns of artificial defoliation in radish in combination with sulphur (S) fertilization, to evaluate the contribution of younger and older leaves on plant growth and phenolics accumulation in storage roots. Biomass accumulation and partitioning were related to leaf age, magnitude and timing of the clipping treatments. Older leaves increased biomass production and translocation into the storage organ; besides, they induced higher accumulation of phenolic compounds compared to the younger leaves. The highest S fertilization rate (120 kg ha-1) significantly enhanced the polyphenols accumulation, as well as the antiradical activity. The modulation of S inputs in combination with slightly induced stress from defoliation could effectively enhance the concentration of some important phytochemicals, providing higher nutritionally improved vegetables, without affecting yield
Corrigendum: Transcriptome Analysis of the Melon-Fusarium oxysporum f. sp. melonis Race 1.2 Pathosystem in Susceptible and Resistant Plants
Distinct colonization patterns and cDNA-AFLP transcriptome profiles in compatible and incompatible interactions between melon and different races of Fusarium oxysporum f. sp. melonis
Background: Fusarium oxysporum f. sp. melonis Snyd. & Hans. (FOM) causes Fusarium wilt, the most important infectious disease of melon (Cucumis melo L.). The four known races of this pathogen can be distinguished only by infection on appropriate cultivars. No molecular tools are available that can discriminate among the races, and the molecular basis of compatibility and disease progression are poorly understood. Resistance to races 1 and 2 is controlled by a single dominant gene, whereas only partial polygenic resistance to race 1,2 has been described. We carried out a large-scale cDNA-AFLP analysis to identify host genes potentially related to resistance and susceptibility as well as fungal genes associated with the infection process. At the same time, a systematic reisolation procedure on infected stems allowed us to monitor fungal colonization in compatible and incompatible host-pathogen combinations. Results: Melon plants (cv. Charentais Fom-2), which are susceptible to race 1,2 and resistant to race 1, were artificially infected with a race 1 strain of FOM or one of two race 1,2 w strains. Host colonization of stems was assessed at 1, 2, 4, 8, 14, 16, 18 and 21 days post inoculation (dpi), and the fungus was reisolated from infected plants. Markedly different colonization patterns were observed in compatible and incompatible host-pathogen combinations. Five time points from the symptomless early stage (2 dpi) to obvious wilting symptoms (21 dpi) were considered for cDNA-AFLP analysis. After successful sequencing of 627 transcript-derived fragments (TDFs) differentially expressed in infected plants, homology searching retrieved 305 melon transcripts, 195 FOM transcripts expressed in planta and 127 orphan TDFs. RNA samples from FOM colonies of the three strains grown in vitro were also included in the analysis to facilitate the detection of in planta-specific transcripts and to identify TDFs differentially expressed among races/strains. Conclusion: Our data suggest that resistance against FOM in melon involves only limited transcriptional changes, and that wilting symptoms could derive, at least partially, from an active plant response. We discuss the pathogen-derived transcripts expressed in planta during the infection process and potentially related to virulence functions, as well as transcripts that are differentially expressed between the two FOM races grown in vitro. These transcripts provide candidate sequences that can be further tested for their ability to distinguish between races. Sequence data from this article have been deposited in GenBank, Accession Numbers: HO867279-HO867981
Reference gene selection for gene expression analysis in melon infected by Fusarium oxysporum f.sp. melonis.
Eleven candidate reference genes were evaluated in stem tissues of two melon (Cucumis melo L) genotypes infected with Fusarium oxysporum f.sp. melonis (FOM) race 1, to investigate the most stable internal control gene to use in gene expression study in melon under biotic stress. The candidate reference genes, utilized in the qRT-PCR, were selected among the most common reference genes reported in melon literature as well as on melon sequences found in available databases. The expression stability of the reference genes selected, was tested by using the geNorm and NormFinder statistical algorithms. Irrespective of the plant response to FOM infection, there was substantial agreement in gene ranks of both software. The ribosomal protein L2 gene had the high transcript stability while the elongation factor, cyclophilin7 and 18S rRNA were the least stable. The best three reference genes, ribosomal protein L2, actin* and cyclophilin were used to normalize the expression data of the glutathione S-transferase in the resistant and susceptible plants. Differences in the expression data emerged for both genotypes and were more evident in the resistant one. The ribosomal protein L2 showed similar normalized expression values in both genotypes and thus it could be indicated as unique internal control for gene expression analysis in melon under FOM infection. This work represents the first in-depth study on reference genes validation in melon under biotic stress condition. The identification of such genes would improve the accuracy and reliability of gene expression studies and speed up candidate disease resistant gene analysis in melon
Adaptive Responses to Nitrogen and Light Supplies of a Local Varieties of Sweet Pepper from the Abruzzo Region, Southern Italy
Local varieties represent a heritage for plant biodiversity and, thanks to their resilience, are characterized by a better adaptation and rusticity to environmental variables. This work reports the morphological and physiological responses of a local ecotype of sweet pepper grown in Southern Italy, i.e., Altino, to N and light supplied at optimal and sub-optimal levels. In 2017, two open-field experiments were set up, comparing increasing N rates (0, 100 and 200 kg N ha−1, 0_N, 100_N and 200_N, respectively) and different percentages of shading and/or manipulations of the transmitted solar radiation, obtained through photoselective nets (red net, RN; black net, BN; unshaded Control). The unfertilized plants reduced growth (by 32% on average, at 83 days after transplanting, DAT), especially in terms of number of leaves, leaf area and effectiveness (chlorophyll content) of photosynthetic apparatus; no differences were recorded among fertilization treatments. On the other hand, the shading avoidance mechanisms resulted in higher biomass partitioned to leaves at the expense of sink organs, the building of more expanse (higher total leaf area) and thinner (higher specific leaf area and lower leaf-cuticular waxes) photosynthetic apparatus, and in a greater concentration of leaf pigments. The effects on yield and fruit quality of Altino ecotype deserve to be further explored
Modulation of Light and Nitrogen for Quality-Traits Improvement: A Case Study of Altino Sweet Pepper
Local varieties are known to cope more efficiently with stressful and/or low-input conditions than cultivated ones by activating secondary metabolisms and, hence, are supposed to have higher nutraceutical potential. In this work, we investigate the effects of N and light, supplied at optimal and sub-optimal levels, on the fruit yield and quality of a local ecotype of sweet pepper, Altino, grown in the Abruzzo Region (Southern Italy). In 2017, two open-field experiments were carried out, comparing increasing N rates (0, 100 and 200 kg N ha−1, 0_N, 100_N and 200_N, respectively) and different percentages of shading and/or manipulations of the transmitted solar radiation, obtained through photoselective nets (red net, RN; black net, BN; unshaded Control). Both N and light were preconditions to obtain stable yields in terms of both fruit number and fruit weights. However, BN significantly reduced the number of sunscalded fruits (0.39 vs. 3.38 and 2.59 fruit plant−1 for BN, Control and RN, respectively), leading to lower waste. N deficiency favoured higher total polyphenol (TPC) and flavonoid (TFC) contents in ripened fruits; on the other hand, shading significantly reduced TPC (−12.4%) in immature and TFC (−18.2%) in red fruits. The variations in nutraceuticals were also evaluated in terms of the variations of the single phenolic acids in fruits during ripening; the most interesting results were associated with light treatments. Further research should be directed to the in-depth study of nutrition regimes, in combination with other photoselective nets applications (i.e., pearl nets), that could be suitable for the Altino genotype to enhance the yield and nutraceutical potentials of its fruits
A Newly Developed Real-Time PCR Assay for Detection and Quantification of Fusarium oxysporum and Its Use in Compatible and Incompatible Interactions with Grafted Melon Genotypes
A reliable and species-specific real-time quantitative polymerase chain reaction (qPCR) assay was developed for detection of the complex soilborne anamorphic fungus Fusarium oxysporum. The new primer pair, designed on the translation elongation factor 1-\u3b1 gene with an amplicon of 142 bp, was highly specific to F. oxysporum without cross reactions with other Fusarium spp. The protocol was applied to grafted melon plants for the detection and quantification of F. oxysporum f. sp. melonis, a devastating pathogen of this cucurbit. Grafting technologies are widely used in melon to confer resistance against new virulent races of F. oxysporum f. sp. melonis, while maintaining the properties of valuable commercial varieties. However, the effects on the vascular pathogen colonization have not been fully investigated. Analyses were performed on \u2018Charentais-T\u2019 (susceptible) and \u2018Nad-1\u2019 (resistant) melon cultivars, both used either as rootstock and scion, and inoculated with F. oxysporum f. sp. melonis race 1 and race 1,2. Pathogen development was compared using qPCR and isolations from stem tissues. Early asymptomatic melon infections were detected with a quantification limit of 1 pg of fungal DNA. The qPCR protocol clearly showed that fungal development was highly affected by host\u2013pathogen interaction (compatible or incompatible) and time (days postinoculation). The principal significant effect (P 64 0.01) on fungal development was due to the melon genotype used as rootstock, and this effect had a significant interaction with time and F. oxysporum f. sp. melonis race. In particular, the amount of race 1,2 DNA was significantly higher compared with that estimated for race 1 in the incompatible interaction at 18 days postinoculation. The two fungal races were always present in both the rootstock and scion of grafted plants in either the compatible or incompatible interaction
Transcriptome Analysis of the Melon-Fusarium oxysporum f. sp. melonis Race 1.2 Pathosystem in Susceptible and Resistant Plants
The Effect of Water Stress on the Glucosinolate Content and Profile: A Comparative Study on Roots and Leaves of <i>Brassica oleracea</i> L. Crops
Drought is one of the major challenges of global crop production, and its severity is increasing because of climate change. This abiotic stress is an important target for Brassica species, which are generally grown in arid and semi-arid climates. This study was conducted to investigate the effects of water deficit on a set of accessions belonging to the Brassica core collection of the EU H2020 BRESOV project, represented by Brassica oleracea L. crops and Brassica oleracea complex species (n = 9). In particular, the variation in the amount and profile of the glucosinolates (GLSs) compounds was analyzed on the root and the leaf tissues. The plant morphometric traits and GLSs amount and profile were detected for the plants grown in cold greenhouse in Catania (Sicily) during the autumn–winter season for ten weeks. The results showed a wide qualitative and quantitative variation among the Brassica accessions. The GLSs profile varied qualitatively and quantitively among both genotypes and portions of the plants (hypogenous-root and epigeous-leaf). Plants grown under drought stress, for the last two weeks of the growing cycle under consideration, showed a higher amount of GLS in their leaves (190.1 ± 8.9 µmol. g−1 d.w.) compared to their roots (17.3 ± 1.9 µmol. g−1 d.w.). Under water stress conditions, the highest increase in the glucosinolate amount was detected in broccoli (the accession BR1) with 85.4% and in cauliflower (the accession CV1) with 72.8% in the roots and leaves, respectively. Positive correlations were found between the major leaf and root GLSs identified. The selection of chemotypes allows for an important time reduction during the breeding programs after crossing accessions with the specific profiles of glucosinolates