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      Effect of fungicide on Fusarium verticillioides mycelial morphology and fumonisin B 1 production

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          Abstract

          The effect of fludioxonil + metalaxyl-M on the mycelial morphology, sporulation and fumonisin B 1 production by Fusarium verticillioides 103 F was evaluated. Scanning electron microscopy analysis showed that the fungicide caused inhibition of hyphal growth and defects on hyphae morphology such as cell wall disruption, withered hyphae, and excessive septation. In addition, extracellular material around the hyphae was rarely observed in the presence of fludioxonil + metalaxyl-M. While promoting the reduction of mycelial growth, the fungicide increased sporulation of F. verticillioides compared to the control, and the highest production occurred on the 14 th day in the treatments and on the 10 th day in the control cultures. Fumonisin B 1 production in the culture media containing the fungicide (treatment) was detected from the 7 th day incubation, whereas in cultures without fungicide (control) it was detected on the 10 th day. The highest fumonisin B 1 production occurred on the 14 th day, both for the control and for the treatment. Fludioxonil + metalaxyl - M can interfere in F. verticillioides mycelial morphology and sporulation and increase fumonisin B 1 levels. These data indicate the importance of understanding the effects of fungicide to minimize the occurrence of toxigenic fungi and fumonisins.

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          Most cited references52

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          Approved Methods of the American Association of Cereal Chemist

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            Production of fumonisin analogs by Fusarium species.

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              How to build a biofilm: a fungal perspective.

              Biofilms are differentiated masses of microbes that form on surfaces and are surrounded by an extracellular matrix. Fungal biofilms, especially those of the pathogen Candida albicans, are a cause of infections associated with medical devices. Such infections are particularly serious because biofilm cells are relatively resistant to many common antifungal agents. Several in vitro models have been used to elucidate the developmental stages and processes required for C. albicans biofilm formation, and recent studies have begun to define biofilm genetic control. It is clear that cell-substrate and cell-cell interactions, hyphal differentiation and extracellular matrix production are key steps in biofilm development. Drug resistance is acquired early in biofilm formation, and appears to be governed by different mechanisms in early and late biofilms. Quorum sensing might be an important factor in dispersal of biofilm cells. The past two years have seen the emergence of several genomic strategies to uncover global events in biofilm formation and directed studies to understand more specific events, such as hyphal formation, in the biofilm setting.
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                Author and article information

                Journal
                Braz J Microbiol
                Braz. J. Microbiol
                Brazilian Journal of Microbiology
                Sociedade Brasileira de Microbiologia
                1517-8382
                1678-4405
                31 March 2015
                March 2015
                : 46
                : 1
                : 293-299
                Affiliations
                [1 ]Departamento de Bioquímica e Biotecnologia, Universidade Estadual de Londrina, Londrina, PR, Brazil.
                [2 ]Departamento de Biologia Geral, Universidade Estadual de Londrina, Londrina, PR, Brazil.
                [3 ]Departamento de Ciências Patológicas, Universidade Estadual de Londrina, Londrina, PR, Brazil.
                [4 ]Departamento de Ciência e Tecnologia de Alimentos, Universidade Estadual de Londrina, Londrina, PR, Brazil.
                [5 ]Departamento de Estatística, Universidade Estadual de Londrina, Londrina, PR, Brazil.
                Author notes
                Send correspondence to E.Y.S. Ono. Departamento de Bioquímica e Biotecnologia, Universidade Estadual de Londrina, 86057-970 Londrina, Paraná, Brazil. E-mail: eysono@ 123456uel.br .

                Associate Editor: Ulysses Garcia Casado Lins

                Article
                10.1590/S1517-838246120120383
                4512075
                26221120
                aeb0f2bb-2226-4753-a7e3-07592873ddae

                All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License CC BY-NC.

                History
                : 05 December 2012
                : 06 June 2014
                Page count
                Figures: 2, Tables: 4, Equations: 0, References: 39, Pages: 0
                Categories
                Microbial Physiology

                toxigenic fungi,mycotoxin,scanning electron microscopy,electron micrographs,extracellular material

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