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      PGPR control Phytophthora capsici in tomato through induced systemic resistance, early hypersensitive response and direct antagonism in a cultivar-specific manner

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          Abstract

          Plant pathogens cause significant crop losses worldwide and present significant challenges to reliable food systems. The hemibiotroph Phytophthora capsici is ranked within the top 10 most problematic oomycete plant pathogens. P. capsici induces significant damage to plants by causing root rot, stem blight, and fruit rot, leading to decreased crop yields, economic losses, and increased plant susceptibility to secondary infections. The current study tested the hypothesis that plant growth promoting rhizobacteria (PGPR), namely Bacillus velezensis UQ9000N and Pseudomonas azotoformans UQ4510An, have inhibitory effects against various fungi and oomycetes. This study also hypothesised that the plant genotype affects the capability of UQ4510An to control P. capsici infection. Our results revealed that B. velezensis UQ9000N and P. azotoformans UQ4510An inhibited the growth of several plant pathogens by 50% or higher. These bacteria also induced abnormal mycelial morphology of P. capsici and Fusarium oxysporum f. sp. lycopersici. Moreover, P. azotoformans UQ4510An exhibited anti-oomycete activity in vitro and in planta, by reducing symptoms of P. capsici infection in various tomato plant cultivars in a genotype-dependent manner. Some tomato cultivars which presented less improvements of phenotypic parameters from the UQ4510An inoculation in the absence of the pathogen had a more pronounced reduction in symptoms upon P. capsici infection. Furthermore, our results indicated that the main biocontrol mechanism of P. azotoformans UQ4510An against P. capsici is a combination of direct antagonism and induction of induced systemic resistance (ISR) involving a hypersensitive response (HR) in the plant host at early stages of infection.

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          Most cited references106

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          A new mathematical model for relative quantification in real-time RT-PCR.

          M. Pfaffl (2001)
          Use of the real-time polymerase chain reaction (PCR) to amplify cDNA products reverse transcribed from mRNA is on the way to becoming a routine tool in molecular biology to study low abundance gene expression. Real-time PCR is easy to perform, provides the necessary accuracy and produces reliable as well as rapid quantification results. But accurate quantification of nucleic acids requires a reproducible methodology and an adequate mathematical model for data analysis. This study enters into the particular topics of the relative quantification in real-time RT-PCR of a target gene transcript in comparison to a reference gene transcript. Therefore, a new mathematical model is presented. The relative expression ratio is calculated only from the real-time PCR efficiencies and the crossing point deviation of an unknown sample versus a control. This model needs no calibration curve. Control levels were included in the model to standardise each reaction run with respect to RNA integrity, sample loading and inter-PCR variations. High accuracy and reproducibility (<2.5% variation) were reached in LightCycler PCR using the established mathematical model.
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            Universal chemical assay for the detection and determination of siderophores

            A universal method to detect and determine siderophores was developed by using their high affinity for iron(III). The ternary complex chrome azurol S/iron(III)/hexadecyltrimethylammonium bromide, with an extinction coefficient of approximately 100,000 M-1 cm-1 at 630 nm, serves as an indicator. When a strong chelator removes the iron from the dye, its color turns from blue to orange. Because of the high sensitivity, determination of siderophores in solution and their characterization by paper electrophoresis chromatography can be performed directly on supernatants of culture fluids. The method is also applicable to agar plates. Orange halos around the colonies on blue agar are indicative of siderophore excretion. It was demonstrated with Escherichia coli strains that biosynthetic, transport, and regulatory mutations in the enterobactin system are clearly distinguishable. The method was successfully used to screen mutants in the iron uptake system of two Rhizobium meliloti strains, DM5 and 1021.
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              JAZ repressor proteins are targets of the SCF(COI1) complex during jasmonate signalling.

              Jasmonate and related signalling compounds have a crucial role in both host immunity and development in plants, but the molecular details of the signalling mechanism are poorly understood. Here we identify members of the jasmonate ZIM-domain (JAZ) protein family as key regulators of jasmonate signalling. JAZ1 protein acts to repress transcription of jasmonate-responsive genes. Jasmonate treatment causes JAZ1 degradation and this degradation is dependent on activities of the SCF(COI1) ubiquitin ligase and the 26S proteasome. Furthermore, the jasmonoyl-isoleucine (JA-Ile) conjugate, but not other jasmonate-derivatives such as jasmonate, 12-oxo-phytodienoic acid, or methyl-jasmonate, promotes physical interaction between COI1 and JAZ1 proteins in the absence of other plant proteins. Our results suggest a model in which jasmonate ligands promote the binding of the SCF(COI1) ubiquitin ligase to and subsequent degradation of the JAZ1 repressor protein, and implicate the SCF(COI1)-JAZ1 protein complex as a site of perception of the plant hormone JA-Ile.
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                Author and article information

                Contributors
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                Journal
                European Journal of Plant Pathology
                Eur J Plant Pathol
                Springer Science and Business Media LLC
                0929-1873
                1573-8469
                December 2023
                August 04 2023
                December 2023
                : 167
                : 4
                : 811-832
                Article
                10.1007/s10658-023-02734-8
                8b5bb585-5036-4e8f-9ebe-8b3e309879e1
                © 2023

                https://creativecommons.org/licenses/by/4.0

                https://creativecommons.org/licenses/by/4.0

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