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1.
Sci Rep ; 8(1): 9625, 2018 06 25.
Article in English | MEDLINE | ID: mdl-29941972

ABSTRACT

Besides improved mineral nutrition, plants colonised by arbuscular mycorrhizal (AM) fungi often display increased biomass and higher tolerance to biotic and abiotic stresses. Notwithstanding the global importance of wheat as an agricultural crop, its response to AM symbiosis has been poorly investigated. We focused on the role of an AM fungus on mineral nutrition of wheat, and on its potential protective effect against Xanthomonas translucens. To address these issues, phenotypical, molecular and metabolomic approaches were combined. Morphological observations highlighted that AM wheat plants displayed an increased biomass and grain yield, as well as a reduction in lesion area following pathogen infection. To elucidate the molecular mechanisms underlying the mycorrhizal phenotype, we investigated changes of transcripts and proteins in roots and leaves during the double (wheat-AM fungus) and tripartite (wheat-AM fungus-pathogen) interaction. Transcriptomic and proteomic profiling identified the main pathways involved in enhancing plant biomass, mineral nutrition and in promoting the bio-protective effect against the leaf pathogen. Mineral and amino acid contents in roots, leaves and seeds, and protein oxidation profiles in leaves, supported the omics data, providing new insight into the mechanisms exerted by AM symbiosis to confer stronger productivity and enhanced resistance to X. translucens in wheat.


Subject(s)
Gene Expression Profiling , Metabolomics , Mycorrhizae/physiology , Proteomics , Symbiosis , Triticum/growth & development , Triticum/microbiology , Disease Resistance/genetics , Environment, Controlled , Phenotype , Plant Diseases/immunology , Plant Diseases/microbiology , Plant Leaves/microbiology , Plant Roots/microbiology , RNA, Messenger/genetics , RNA, Messenger/metabolism , Triticum/genetics , Triticum/metabolism
2.
PLoS One ; 10(11): e0142639, 2015.
Article in English | MEDLINE | ID: mdl-26559418

ABSTRACT

Application of a plant growth promoting rhizobacterium (PGPR), Pseudomonas fluorescens N21.4, to roots of blackberries (Rubus sp.) is part of an optimised cultivation practice to improve yields and quality of fruit throughout the year in this important fruit crop. Blackberries are especially rich in flavonoids and therefore offer potential benefits for human health in prevention or amelioration of chronic diseases. However, the phenylpropanoid pathway and its regulation during ripening have not been studied in detail, in this species. PGPR may trigger flavonoid biosynthesis as part of an induced systemic response (ISR) given the important role of this pathway in plant defence, to cause increased levels of flavonoids in the fruit. We have identified structural genes encoding enzymes of the phenylpropanoid and flavonoid biosynthetic pathways catalysing the conversion of phenylalanine to the final products including flavonols, anthocyanins and catechins from blackberry, and regulatory genes likely involved in controlling the activity of pathway branches. We have also measured the major flavonols, anthocyanins and catechins at three stages during ripening. Our results demonstrate the coordinated expression of flavonoid biosynthetic genes with the accumulation of anthocyanins, catechins, and flavonols in developing fruits of blackberry. Elicitation of blackberry plants by treatment of roots with P.fluorescens N21.4, caused increased expression of some flavonoid biosynthetic genes and an accompanying increase in the concentration of selected flavonoids in fruits. Our data demonstrate the physiological mechanisms involved in the improvement of fruit quality by PGPR under field conditions, and highlight some of the genetic targets of elicitation by beneficial bacteria.


Subject(s)
Flavonoids/chemistry , Anthocyanins/chemistry , Anthocyanins/metabolism , Catechin/chemistry , Catechin/metabolism , Chromatography, High Pressure Liquid , Flavonoids/metabolism , Flavonols/chemistry , Flavonols/metabolism , Fruit/chemistry , Fruit/metabolism , Mass Spectrometry , Plant Proteins/genetics , Plant Proteins/metabolism , Plant Roots/growth & development , Plant Roots/metabolism , Plant Roots/microbiology , Pseudomonas fluorescens/isolation & purification , Real-Time Polymerase Chain Reaction , Rubus/chemistry , Rubus/growth & development , Rubus/metabolism , Symbiosis/physiology
3.
Plant Foods Hum Nutr ; 70(2): 170-5, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25724576

ABSTRACT

Blackberry (Rubus sp.) fruit has a high content of anthocyanins, but its health benefits have not been sufficiently explored in healthy individuals. Thus, the aim of the study was to determine the effects of blackberry extract on lipid and glucose variables in female and male rats. Sprague Dawley rats were given a standard pellet (SD) or cafeteria (CD) diet supplemented (SD+R and CD+R) or not with Rubus extract for 80 days. Female rats given SD+R had lower body and liver weights than SD females; both sexes given SD+R showed lower plasma glucose and insulin, higher plasma NEFA, glycerol and 3-hydroxybutyrate, and higher liver concentration of triacylglycerols than SD rats. The homeostasis model of insulin resistance (HOMA) was lower in SD+R rats than in SD rats, but higher in CD rats. No effects of Rubus extract were observed in CD rats. In conclusion, Rubus extract, in rats given SD, decreased glycemia and increased insulin sensitivity. It also increased lipid breakdown in adipose tissue. The effects were greater in females than in males. No effect was seen in rats given CD, probably as a result of their high insulin resistance.


Subject(s)
Dietary Supplements , Insulin Resistance , Plant Extracts/administration & dosage , Rubus/chemistry , Animals , Blood Glucose/metabolism , Cholesterol/blood , Diet/veterinary , Female , Insulin/blood , Male , Rats , Rats, Sprague-Dawley , Triglycerides/blood
4.
BMC Genomics ; 16: 5, 2015 Jan 22.
Article in English | MEDLINE | ID: mdl-25608670

ABSTRACT

BACKGROUND: There is an increasing interest in berries, especially blackberries in the diet, because of recent reports of their health benefits due to their high content of flavonoids. A broad range of genomic tools are available for other Rosaceae species but these tools are still lacking in the Rubus genus, thus limiting gene discovery and the breeding of improved varieties. RESULTS: De novo RNA-seq of ripe blackberries grown under field conditions was performed using Illumina Hiseq 2000. Almost 9 billion nucleotide bases were sequenced in total. Following assembly, 42,062 consensus sequences were detected. For functional annotation, 33,040 (NR), 32,762 (NT), 21,932 (Swiss-Prot), 20,134 (KEGG), 13,676 (COG), 24,168 (GO) consensus sequences were annotated using different databases; in total 34,552 annotated sequences were identified. For protein prediction analysis, the number of coding DNA sequences (CDS) that mapped to the protein database was 32,540. Non redundant (NR), annotation showed that 25,418 genes (73.5%) has the highest similarity with Fragaria vesca subspecies vesca. Reanalysis was undertaken by aligning the reads with this reference genome for a deeper analysis of the transcriptome. We demonstrated that de novo assembly, using Trinity and later annotation with Blast using different databases, were complementary to alignment to the reference sequence using SOAPaligner/SOAP2. The Fragaria reference genome belongs to a species in the same family as blackberry (Rosaceae) but to a different genus. Since blackberries are tetraploids, the possibility of artefactual gene chimeras resulting from mis-assembly was tested with one of the genes sequenced by RNAseq, Chalcone Synthase (CHS). cDNAs encoding this protein were cloned and sequenced. Primers designed to the assembled sequences accurately distinguished different contigs, at least for chalcone synthase genes. CONCLUSIONS: We prepared and analysed transcriptome data from ripe blackberries, for which prior genomic information was limited. This new sequence information will improve the knowledge of this important and healthy fruit, providing an invaluable new tool for biological research.


Subject(s)
Rubus/genetics , Sequence Analysis, RNA , Transcriptome , Databases, Genetic , Gene Expression Profiling , High-Throughput Nucleotide Sequencing , Molecular Sequence Annotation
5.
Plant Physiol Biochem ; 82: 9-16, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24869797

ABSTRACT

Glycine max (L.) Merr. plays a crucial role in both the field of food and the pharmaceutical industry due to their input as plant protein and to the benefits of isoflavones (IF) for health. In addition, IF play a key role in nodulation and plant defense and therefore, an increase in IF would be desirable for better field performance. IF are secondary metabolites and therefore, inducible, so finding effective agents to increase IF contents is interesting. Among these agents, plant growth promoting rhizobacteria (PGPR) have been used to trigger systemic induction of plant's secondary metabolism through their microbe associated molecular patterns (MAMPs) that fit in the plant's receptors to start a systemic response. The aim of this study was to evaluate the ability of 4 PGPR that had a contrasted effect on IF metabolism, to protect plants against biotic stress and to establish the relation between IF profile and the systemic response triggered by the bacteria. Apparently, the response involves a lower sensitivity to ethylene and despite the decrease in effective photosynthesis, growth is only compromised in the case of M84, the most effective in protection. All strains protected soybean against Xanthomonas axonopodis pv. glycines (M84 > N5.18 > Aur9>N21.4) and only M84 and N5.18 involved IF. N5.18 stimulated accumulation of IF before pathogen challenge. M84 caused a significant increase on IF only after pathogen challenge and N21.4 caused a significant increase on IF content irrespective of pathogen challenge. Aur9 did not affect IF. These results point out that all 4 strains have MAMPs that trigger defensive metabolism in soybean. Protection induced by N21.4 and Aur9 involves other metabolites different to IF and the role of IF in defence depends on the previous metabolic status of the plant and on the bacterial MAMP.


Subject(s)
Glycine max/metabolism , Glycine max/microbiology , Isoflavones/metabolism , Rhizobium/metabolism , Rhizobium/physiology , Xanthomonas axonopodis/pathogenicity , Gene Expression Regulation, Plant/physiology , Plant Diseases/immunology , Plant Diseases/microbiology
6.
J Hazard Mater ; 260: 220-30, 2013 Sep 15.
Article in English | MEDLINE | ID: mdl-23770488

ABSTRACT

In this work we assess the capacity of maize (Zea mays) plants to phytoremediate spent metal working fluids (MWFs) and its effects on photosynthesis and ultrastructure of mesophyll and root cells. A corn-esparto fibre system patented by us has been used to phytoremediate MWFs in hydroponic culture. Furthermore, a plant growth promoting rhizobacteria (PGPR) has been used to improve the process. The results show that this system is capable of significantly reducing the chemical oxygen demand, under local legislation limits. However, plant systems are really damaged, mainly its photosynthetic system, as shown by the photosynthetical parameters. Nevertheless, strain inoculated improves these parameters, especially Hill reaction. The ultrastructure of photosynthetic apparatus was also affected. Chloroplast number decreased and becomes degraded in the mesophyll of MWFs treated plants. In some cases even plasmolysis of chloroplast membrane was detected. Early senescence symptoms were detected in root ultrastructural study. Severe cellular damage was observed in the parenchymal root cells of plants grown with MWFs, while vascular bundles cell remained unchanged. It seems that the inoculation minimises the damage originated by the MWFs pollutants, appearing as less degenerative organelles and higher chloroplast number than in non-inoculated ones.


Subject(s)
Photosynthesis/drug effects , Plant Leaves/drug effects , Plant Roots/drug effects , Water Pollutants, Chemical/chemistry , Zea mays/drug effects , Bacteria/growth & development , Biodegradation, Environmental , Chlorophyll/chemistry , Chloroplasts/drug effects , Hydrogen-Ion Concentration , Industrial Waste , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Plant Roots/microbiology , Zea mays/microbiology
7.
Electrophoresis ; 34(15): 2251-8, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23712878

ABSTRACT

Berries are a rich source of antioxidants compounds, among which is the catechin group. Determination of the monomers (catechin and epicatechin) in fruits is a first step in the way to establish a relationship between polyphenols and their effects on human health. The purpose of this work is to develop a method to determine free catechins in blackberry by MEKC and to characterize levels of catechins in fresh fruits of Rubus fruticosus var. Lochness throughout the annual production period. A methanolic extract was prepared from fresh fruit. Then, it was evaporated and the residue was extracted with diethyl ether. MEKC conditions: phosphoric acid, 30 mmol/L; SDS, 40 mmol/L and triethylamine, 0.1% v/v at pH 2.3; -15 kV of voltage; 10-s hydrodynamic injection; 25°C temperature; and detection at 200 nm. Instrumental and interday precision were lower than 4.7 and 10% RSD, respectively. Only (-)-epicatechin was quantified in blackberries and ranged from 120 to 620 mg/kg fresh weight, which were the lowest values in December and the highest in June. A solid-liquid extraction and an MEKC method were successfully applied to determine (-)-epicatechins in blackberry for the first time. A strong dependence of (-)-epicatechin on the annual average temperature was observed.


Subject(s)
Catechin/analysis , Chromatography, Micellar Electrokinetic Capillary/methods , Fruit/chemistry , Catechin/isolation & purification , Limit of Detection , Plant Extracts/chemistry , Reproducibility of Results , Solid Phase Extraction , Stereoisomerism
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