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The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection
Parasitic fungi are the only pathogens that can infect insect hosts directly through their proteinaceous exoskeleton. Penetration of the cuticle requires the release of fungal enzymes, including proteinases, which act as virulence factors. Insects can sense fungal infections and activate innate immu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955202/ https://www.ncbi.nlm.nih.gov/pubmed/29166834 http://dx.doi.org/10.1080/21505594.2017.1405190 |
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author | Mukherjee, Krishnendu Vilcinskas, Andreas |
author_facet | Mukherjee, Krishnendu Vilcinskas, Andreas |
author_sort | Mukherjee, Krishnendu |
collection | PubMed |
description | Parasitic fungi are the only pathogens that can infect insect hosts directly through their proteinaceous exoskeleton. Penetration of the cuticle requires the release of fungal enzymes, including proteinases, which act as virulence factors. Insects can sense fungal infections and activate innate immune responses, including the synthesis of antifungal peptides and proteinase inhibitors that neutralize the incoming proteinases. This well-studied host response is epigenetically regulated by histone acetylation/deacetylation. Here we show that entomopathogenic fungi can in turn sense the presence of insect-derived antifungal peptides and proteinase inhibitors, and respond by inducing the synthesis of chymotrypsin-like proteinases and metalloproteinases that degrade the host-derived defense molecules. The rapidity of this response is dependent on the virulence of the fungal strain. We confirmed the specificity of the pathogen response to host-derived defense molecules by LC/MS and RT-PCR analysis, and correlated this process with the epigenetic regulation of histone acetylation/deacetylation. This cascade of responses reveals that the coevolution of pathogens and hosts can involve a complex series of attacks and counterattacks based on communication between the invading fungal pathogen and its insect host. The resolution of this process determines whether or not pathogenesis is successful. |
format | Online Article Text |
id | pubmed-5955202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-59552022018-05-21 The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection Mukherjee, Krishnendu Vilcinskas, Andreas Virulence Research Paper Parasitic fungi are the only pathogens that can infect insect hosts directly through their proteinaceous exoskeleton. Penetration of the cuticle requires the release of fungal enzymes, including proteinases, which act as virulence factors. Insects can sense fungal infections and activate innate immune responses, including the synthesis of antifungal peptides and proteinase inhibitors that neutralize the incoming proteinases. This well-studied host response is epigenetically regulated by histone acetylation/deacetylation. Here we show that entomopathogenic fungi can in turn sense the presence of insect-derived antifungal peptides and proteinase inhibitors, and respond by inducing the synthesis of chymotrypsin-like proteinases and metalloproteinases that degrade the host-derived defense molecules. The rapidity of this response is dependent on the virulence of the fungal strain. We confirmed the specificity of the pathogen response to host-derived defense molecules by LC/MS and RT-PCR analysis, and correlated this process with the epigenetic regulation of histone acetylation/deacetylation. This cascade of responses reveals that the coevolution of pathogens and hosts can involve a complex series of attacks and counterattacks based on communication between the invading fungal pathogen and its insect host. The resolution of this process determines whether or not pathogenesis is successful. Taylor & Francis 2018-03-01 /pmc/articles/PMC5955202/ /pubmed/29166834 http://dx.doi.org/10.1080/21505594.2017.1405190 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Research Paper Mukherjee, Krishnendu Vilcinskas, Andreas The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection |
title | The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection |
title_full | The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection |
title_fullStr | The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection |
title_full_unstemmed | The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection |
title_short | The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection |
title_sort | entomopathogenic fungus metarhizium robertsii communicates with the insect host galleria mellonella during infection |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955202/ https://www.ncbi.nlm.nih.gov/pubmed/29166834 http://dx.doi.org/10.1080/21505594.2017.1405190 |
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