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      Trichoderma volatiles effecting Arabidopsis: from inhibition to protection against phytopathogenic fungi

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          Abstract

          Trichoderma species are present in many ecosystems and some strains have the ability to reduce the severity of plant diseases by activating various defense pathways via specific biologically active signaling molecules. Hence we investigated the effects of low molecular weight volatile compounds of Trichoderma asperellum IsmT5 on Arabidopsis thaliana. During co-cultivation of T. asperellum IsmT5 without physical contact to A. thaliana we observed smaller but vital and robust plants. The exposed plants exhibit increased trichome numbers, accumulation of defense-related compounds such as H 2O 2, anthocyanin, camalexin, and increased expression of defense-related genes. We conclude that A. thaliana perceives the Trichoderma volatiles as stress compounds and subsequently initiates multilayered adaptations including activation of signaling cascades to withstand this environmental influence. The prominent headspace volatile of T. asperellum IsmT5 was identified to be 6-pentyl-α-pyrone (6PP), which was solely applied to A. thaliana to verify the growth and defense reactions. Most noticeable is that A. thaliana preexposed to 6PP showed significantly reduced symptoms when challenged with Botrytis cinerea and Alternaria brassicicola, indicating that defense-activated plants subsequently became more resistant to pathogen attack. Together, these results support that products that are based on Trichoderma volatiles have the potential being a useful biocontrol agent in agriculture.

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          Pre- and postinvasion defenses both contribute to nonhost resistance in Arabidopsis.

          Nonhost resistance describes the immunity of an entire plant species against nonadapted pathogen species. We report that Arabidopsis PEN2 restricts pathogen entry of two ascomycete powdery mildew fungi that in nature colonize grass and pea species. The PEN2 glycosyl hydrolase localizes to peroxisomes and acts as a component of an inducible preinvasion resistance mechanism. Postinvasion fungal growth is blocked by a separate resistance layer requiring the EDS1-PAD4-SAG101 signaling complex, which is known to function in basal and resistance (R) gene-triggered immunity. Concurrent impairment of pre- and postinvasion resistance renders Arabidopsis a host for both nonadapted fungi.
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            Growth stimulation and fruit yield improvement of greenhouse tomato plants by inoculation with Pseudomonas putida or Trichoderma atroviride: Possible role of indole acetic acid (IAA)

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              A novel role for Trichoderma secondary metabolites in the interactions with plants

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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                29 September 2015
                2015
                : 6
                : 995
                Affiliations
                [1] 1Institute for Biological Sciences, University of Rostock Rostock, Germany
                [2] 2Biocenter, Botanical Institute and Cluster of Excellence on Plant Sciences, University of Cologne Cologne, Germany
                [3] 3Department of Plant and Environmental Sciences, Copenhagen Plant Science Centre, University of Copenhagen Taastrup, Denmark
                [4] 4Institute of Plant Sciences, University of Graz Graz, Austria
                Author notes

                Edited by: Paolina Garbeva, Netherlands Institute of Ecology (NIOO-KNAW), Netherlands

                Reviewed by: Ruth Schmidt, Netherlands Institute of Ecology (NIOO-KNAW), Netherlands; Olaf Tyc, The Royal Netherlands Academy of Arts and Sciences, Netherlands; Tomislav Cernava, Graz University of Technology, Austria

                *Correspondence: Birgit Piechulla, Institute for Biological Sciences, University of Rostock, Albert-Einstein-Str. 3, 18059 Rostock, Germany birgit.piechulla@ 123456uni-rostock.de

                This article was submitted to Plant Biotic Interactions, a section of the journal Frontiers in Microbiology

                †Present Address: Metwally Kottb, Botany Department, Faculty of Science, Suez Canal University, Ismailia, Egypt

                Article
                10.3389/fmicb.2015.00995
                4586454
                26483761
                be59b346-e001-4335-8516-5f5b05f65a94
                Copyright © 2015 Kottb, Gigolashvili, Großkinsky and Piechulla.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 18 June 2015
                : 07 September 2015
                Page count
                Figures: 8, Tables: 1, Equations: 1, References: 107, Pages: 14, Words: 11103
                Funding
                Funded by: University of Rostock
                Categories
                Plant Science
                Original Research

                Microbiology & Virology
                trichoderma asperellum ismt5,botrytis cinerea,alternaria brassicicola,arabidopsis thaliana,mvocs,6-pentyl-α-pyrone,glucosinolates,camalexin

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