The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei.
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
Texto Completo: | http://dx.doi.org/10.3389/fmicb.2015.01181 http://www.alice.cnptia.embrapa.br/alice/handle/doc/1032746 |
Resumo: | Species of Trichoderma exert direct biocontrol activity against soil-borne plant pathogens due to their ability to compete for nutrients and to inhibit or kill their targets through the production of antibiotics and/or hydrolytic enzymes. In addition to these abilities, Trichoderma spp. have beneficial effects for plants, including the stimulation of defenses and the promotion of growth. Here we study the role in biocontrol of the T. parareesei Tparo7 gene, encoding a chorismate mutase (CM), a shikimate pathway branch point leading to the production of aromatic amino acids, which are not only essential components of protein synthesis but also the precursors of a wide range of secondary metabolites. We isolated T. parareesei transformants with the Tparo7 gene silenced. Compared with the wild-type, decreased levels of Tparo7 expression in the silenced transformants were accompanied by reduced CM activity, lower growth rates on different culture media, and reduced mycoparasitic behavior against the phytopathogenic fungi Rhizoctonia solani, Fusarium oxysporum and Botrytis cinerea in dual cultures. By contrast, higher amounts of the aromatic metabolites tyrosol, 2-phenylethanol and salicylic acid were detected in supernatants from the silenced transformants, which were able to inhibit the growth of F. oxysporum and B. cinerea. In in vitro plant assays, Tparo7-silenced transformants also showed a reduced capacity to colonize tomato roots. The effect of Tparo7-silencing on tomato plant responses was examined in greenhouse assays. The growth of plants colonized by the silenced transformants was reduced and the plants exhibited an increased susceptibility to B. cinerea in comparison with the responses observed for control plants. In addition, the plants turned yellowish and were defective in jasmonic acid- and ethylene-regulated signaling pathways which was seen by expression analysis of lipoxygenase 1 (LOX1), ethylene-insensitive protein 2 (EIN2) and pathogenesis-related protein 1 (PR-1) genes. |
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The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei.Tparo7 gene2-phenylethanolTyrosolTrichodermaControle biológicoShikimate pathwayGene silencingAntifungal agentsPhenylethyl alcoholSalicylic acidSpecies of Trichoderma exert direct biocontrol activity against soil-borne plant pathogens due to their ability to compete for nutrients and to inhibit or kill their targets through the production of antibiotics and/or hydrolytic enzymes. In addition to these abilities, Trichoderma spp. have beneficial effects for plants, including the stimulation of defenses and the promotion of growth. Here we study the role in biocontrol of the T. parareesei Tparo7 gene, encoding a chorismate mutase (CM), a shikimate pathway branch point leading to the production of aromatic amino acids, which are not only essential components of protein synthesis but also the precursors of a wide range of secondary metabolites. We isolated T. parareesei transformants with the Tparo7 gene silenced. Compared with the wild-type, decreased levels of Tparo7 expression in the silenced transformants were accompanied by reduced CM activity, lower growth rates on different culture media, and reduced mycoparasitic behavior against the phytopathogenic fungi Rhizoctonia solani, Fusarium oxysporum and Botrytis cinerea in dual cultures. By contrast, higher amounts of the aromatic metabolites tyrosol, 2-phenylethanol and salicylic acid were detected in supernatants from the silenced transformants, which were able to inhibit the growth of F. oxysporum and B. cinerea. In in vitro plant assays, Tparo7-silenced transformants also showed a reduced capacity to colonize tomato roots. The effect of Tparo7-silencing on tomato plant responses was examined in greenhouse assays. The growth of plants colonized by the silenced transformants was reduced and the plants exhibited an increased susceptibility to B. cinerea in comparison with the responses observed for control plants. In addition, the plants turned yellowish and were defective in jasmonic acid- and ethylene-regulated signaling pathways which was seen by expression analysis of lipoxygenase 1 (LOX1), ethylene-insensitive protein 2 (EIN2) and pathogenesis-related protein 1 (PR-1) genes.ESCLAUDYS PEREZ, Universidad de Salamanca; MARIA BELEN RUBIO, Universidad de Salamanca; ROSA ELENA CARDOSA, Universidad de León; SANTIAGO GUTIERREZ, Universidad de León; WAGNER BETTIOL, CNPMA; ENRIQUE MONTE, Universidad de Salamanca; ROSA HERMOSA, Universidad de Salamanca.PÉREZ, E.RUBIO, M. B.CARDOZA, R. E.GUTIÉRREZ, S.BETTIOL, W.MONTE, E.HERMOSA, R.2016-01-04T11:11:11Z2016-01-04T11:11:11Z2016-01-0420152016-01-25T11:11:11Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article14 p.Frontiers in Microbiology, Lausanne, v. 6, 2015. Article 1181.http://dx.doi.org/10.3389/fmicb.2015.01181http://www.alice.cnptia.embrapa.br/alice/handle/doc/1032746enginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2017-08-16T03:28:10Zoai:www.alice.cnptia.embrapa.br:doc/1032746Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542017-08-16T03:28:10falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542017-08-16T03:28:10Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false |
dc.title.none.fl_str_mv |
The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei. |
title |
The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei. |
spellingShingle |
The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei. PÉREZ, E. Tparo7 gene 2-phenylethanol Tyrosol Trichoderma Controle biológico Shikimate pathway Gene silencing Antifungal agents Phenylethyl alcohol Salicylic acid |
title_short |
The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei. |
title_full |
The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei. |
title_fullStr |
The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei. |
title_full_unstemmed |
The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei. |
title_sort |
The importance of chorismate mutase in the biocontrol potential of Trichoderma parareesei. |
author |
PÉREZ, E. |
author_facet |
PÉREZ, E. RUBIO, M. B. CARDOZA, R. E. GUTIÉRREZ, S. BETTIOL, W. MONTE, E. HERMOSA, R. |
author_role |
author |
author2 |
RUBIO, M. B. CARDOZA, R. E. GUTIÉRREZ, S. BETTIOL, W. MONTE, E. HERMOSA, R. |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
ESCLAUDYS PEREZ, Universidad de Salamanca; MARIA BELEN RUBIO, Universidad de Salamanca; ROSA ELENA CARDOSA, Universidad de León; SANTIAGO GUTIERREZ, Universidad de León; WAGNER BETTIOL, CNPMA; ENRIQUE MONTE, Universidad de Salamanca; ROSA HERMOSA, Universidad de Salamanca. |
dc.contributor.author.fl_str_mv |
PÉREZ, E. RUBIO, M. B. CARDOZA, R. E. GUTIÉRREZ, S. BETTIOL, W. MONTE, E. HERMOSA, R. |
dc.subject.por.fl_str_mv |
Tparo7 gene 2-phenylethanol Tyrosol Trichoderma Controle biológico Shikimate pathway Gene silencing Antifungal agents Phenylethyl alcohol Salicylic acid |
topic |
Tparo7 gene 2-phenylethanol Tyrosol Trichoderma Controle biológico Shikimate pathway Gene silencing Antifungal agents Phenylethyl alcohol Salicylic acid |
description |
Species of Trichoderma exert direct biocontrol activity against soil-borne plant pathogens due to their ability to compete for nutrients and to inhibit or kill their targets through the production of antibiotics and/or hydrolytic enzymes. In addition to these abilities, Trichoderma spp. have beneficial effects for plants, including the stimulation of defenses and the promotion of growth. Here we study the role in biocontrol of the T. parareesei Tparo7 gene, encoding a chorismate mutase (CM), a shikimate pathway branch point leading to the production of aromatic amino acids, which are not only essential components of protein synthesis but also the precursors of a wide range of secondary metabolites. We isolated T. parareesei transformants with the Tparo7 gene silenced. Compared with the wild-type, decreased levels of Tparo7 expression in the silenced transformants were accompanied by reduced CM activity, lower growth rates on different culture media, and reduced mycoparasitic behavior against the phytopathogenic fungi Rhizoctonia solani, Fusarium oxysporum and Botrytis cinerea in dual cultures. By contrast, higher amounts of the aromatic metabolites tyrosol, 2-phenylethanol and salicylic acid were detected in supernatants from the silenced transformants, which were able to inhibit the growth of F. oxysporum and B. cinerea. In in vitro plant assays, Tparo7-silenced transformants also showed a reduced capacity to colonize tomato roots. The effect of Tparo7-silencing on tomato plant responses was examined in greenhouse assays. The growth of plants colonized by the silenced transformants was reduced and the plants exhibited an increased susceptibility to B. cinerea in comparison with the responses observed for control plants. In addition, the plants turned yellowish and were defective in jasmonic acid- and ethylene-regulated signaling pathways which was seen by expression analysis of lipoxygenase 1 (LOX1), ethylene-insensitive protein 2 (EIN2) and pathogenesis-related protein 1 (PR-1) genes. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015 2016-01-04T11:11:11Z 2016-01-04T11:11:11Z 2016-01-04 2016-01-25T11:11:11Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
Frontiers in Microbiology, Lausanne, v. 6, 2015. Article 1181. http://dx.doi.org/10.3389/fmicb.2015.01181 http://www.alice.cnptia.embrapa.br/alice/handle/doc/1032746 |
identifier_str_mv |
Frontiers in Microbiology, Lausanne, v. 6, 2015. Article 1181. |
url |
http://dx.doi.org/10.3389/fmicb.2015.01181 http://www.alice.cnptia.embrapa.br/alice/handle/doc/1032746 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
14 p. |
dc.source.none.fl_str_mv |
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Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
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EMBRAPA |
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EMBRAPA |
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Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
collection |
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
repository.name.fl_str_mv |
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
repository.mail.fl_str_mv |
cg-riaa@embrapa.br |
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1794503415532879872 |