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1.
Microb Biotechnol ; 12(6): 1346-1358, 2019 11.
Article in English | MEDLINE | ID: mdl-31452345

ABSTRACT

Seaweeds have been used as a source of natural fertilizer and biostimulant in agriculture for centuries. However, their effects on soil and crop root microbiota remain unclear. Here, we used a commercially available Ascophyllum nodosum extract (ANE) to test its effect on bacterial and fungal communities of rhizospheric soils and roots of pepper and tomato plants in greenhouse trials. Two independent trials were conducted in a split-block design. We used amplicon sequencing targeting fungal ITS and bacterial 16S rRNA gene to determine microbial community structure changes. We find that productivity parameters of root, shoot and fruit biomass were positively and significantly influenced by the ANE amendment. In addition, a-diversity differed significantly between amended and control plants, but only in some of the experimental conditions. Species composition among sites (b-diversity) differed according to the amendment treatment in all four communities (fungal-root, fungal-soil, bacterial-root and bacterial-soil). Finally, we identified a number of candidate taxa most strongly correlated with crop yield increases. Further studies on isolation and characterization of these microbial taxa linked to the application of liquid seaweed extract may help to enhance crop yield in sustainable agro-ecosystems.


Subject(s)
Ascophyllum/chemistry , Capsicum/growth & development , Capsicum/microbiology , Complex Mixtures/metabolism , Microbiota/drug effects , Solanum lycopersicum/growth & development , Solanum lycopersicum/microbiology , Bacteria/classification , Bacteria/drug effects , Bacteria/genetics , Cluster Analysis , Complex Mixtures/isolation & purification , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Fungi/classification , Fungi/drug effects , Fungi/genetics , Phylogeny , RNA, Ribosomal, 16S/genetics , Seaweed/chemistry , Sequence Analysis, DNA
2.
Mar Drugs ; 16(7)2018 Jun 28.
Article in English | MEDLINE | ID: mdl-29958402

ABSTRACT

Insects and pathogenic infections (bacteria, viruses and fungi) cause huge losses in agriculturally important crops yearly. Due to the rise in pesticide and antibiotic resistance, our crops and livestock are increasingly at risk. There is a rising demand for environmentally friendly solutions to prevent crop decreases. Components of Ascophyllum nodosum seaweed extracts were recently found to boost plant immunity. The stimulatory activities of the A.nodosum marine alga-derived extract (Stella Maris®) were investigated in a broad range of immune assays. Elevated hydrogen peroxide production measured in a chemiluminescence assay suggested that the extract elicited a strong burst of reactive oxygen species. Arabidopsis seedlings treated with Stella Maris® activated the expression of WRKY30, CYP71A12 and PR-1 genes, the induction of which represent early, mid and late plant immune response, respectively. Finally, this study found that Stella Maris® inhibited the growth of multiple bacterial pathogens, including an opportunistic human pathogen that has demonstrated pathogenicity in plants. In summary, the pre-treatment with the seaweed extract protected Arabidopsis against subsequent infection by these pathogens.


Subject(s)
Arabidopsis/drug effects , Immunity, Innate/drug effects , Plant Diseases/immunology , Plant Extracts/pharmacology , Seaweed/chemistry , Arabidopsis/immunology , Ascophyllum/chemistry , Protective Agents/pharmacology , Reactive Oxygen Species/metabolism
3.
J Microbiol Methods ; 68(1): 60-8, 2007 Jan.
Article in English | MEDLINE | ID: mdl-16887226

ABSTRACT

Strains of Trichoderma spp. are known for their antagonistic properties against plant pathogens, some are already on the market, others are under development. In order to launch a strain on the market its perfect identification at the species and strain levels is needed. The aim of this study is to (i) design a SCAR marker for specific identification of strain T1 of Trichoderma atroviride and (ii) monitor population dynamics of this strain in soil by real time PCR. A primer pair targeting a 141-bp fragment enabled specific detection of this strain without cross detection of autochthonous populations of Trichoderma in several field soils. In two soils, population dynamics assessed by real time PCR and the soil plate technique gave similar results. The molecular tools developed in this study satisfy the requirement for specific identification of the biocontrol strain and for detection and quantification of T. atroviride T1 population in complex environments.


Subject(s)
DNA Fingerprinting/methods , Polymerase Chain Reaction/methods , Soil Microbiology , Trichoderma/growth & development , Trichoderma/genetics , DNA, Fungal/chemistry , DNA, Fungal/genetics , Random Amplified Polymorphic DNA Technique , Sequence Analysis, DNA
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