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Fungal phytopathogen modulates plant and insect responses to promote its dissemination
Vector-borne plant pathogens often change host traits to manipulate vector behavior in a way that favors their spread. By contrast, infection by opportunistic fungi does not depend on vectors, although damage caused by an herbivore may facilitate infection. Manipulation of hosts and vectors, such as...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8630062/ https://www.ncbi.nlm.nih.gov/pubmed/34127802 http://dx.doi.org/10.1038/s41396-021-01010-z |
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author | Franco, Flávia P. Túler, Amanda C. Gallan, Diego Z. Gonçalves, Felipe G. Favaris, Arodí P. Peñaflor, Maria Fernanda G. V. Leal, Walter S. Moura, Daniel S. Bento, José Maurício S. Silva-Filho, Marcio C. |
author_facet | Franco, Flávia P. Túler, Amanda C. Gallan, Diego Z. Gonçalves, Felipe G. Favaris, Arodí P. Peñaflor, Maria Fernanda G. V. Leal, Walter S. Moura, Daniel S. Bento, José Maurício S. Silva-Filho, Marcio C. |
author_sort | Franco, Flávia P. |
collection | PubMed |
description | Vector-borne plant pathogens often change host traits to manipulate vector behavior in a way that favors their spread. By contrast, infection by opportunistic fungi does not depend on vectors, although damage caused by an herbivore may facilitate infection. Manipulation of hosts and vectors, such as insect herbivores, has not been demonstrated in interactions with fungal pathogens. Herein, we establish a new paradigm for the plant-insect-fungus association in sugarcane. It has long been assumed that Fusarium verticillioides is an opportunistic fungus, where it takes advantage of the openings left by Diatraea saccharalis caterpillar attack to infect the plant. In this work, we show that volatile emissions from F. verticillioides attract D. saccharalis caterpillars. Once they become adults, the fungus is transmitted vertically to their offspring, which continues the cycle by inoculating the fungus into healthy plants. Females not carrying the fungus prefer to lay their eggs on fungus-infected plants than mock plants, while females carrying the fungus prefer to lay their eggs on mock plants than fungus-infected plants. Even though the fungus impacts D. saccharalis sex behavior, larval weight and reproduction rate, most individuals complete their development. Our data demonstrate that the fungus manipulates both the host plant and insect herbivore across life cycle to promote its infection and dissemination. |
format | Online Article Text |
id | pubmed-8630062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86300622021-12-01 Fungal phytopathogen modulates plant and insect responses to promote its dissemination Franco, Flávia P. Túler, Amanda C. Gallan, Diego Z. Gonçalves, Felipe G. Favaris, Arodí P. Peñaflor, Maria Fernanda G. V. Leal, Walter S. Moura, Daniel S. Bento, José Maurício S. Silva-Filho, Marcio C. ISME J Article Vector-borne plant pathogens often change host traits to manipulate vector behavior in a way that favors their spread. By contrast, infection by opportunistic fungi does not depend on vectors, although damage caused by an herbivore may facilitate infection. Manipulation of hosts and vectors, such as insect herbivores, has not been demonstrated in interactions with fungal pathogens. Herein, we establish a new paradigm for the plant-insect-fungus association in sugarcane. It has long been assumed that Fusarium verticillioides is an opportunistic fungus, where it takes advantage of the openings left by Diatraea saccharalis caterpillar attack to infect the plant. In this work, we show that volatile emissions from F. verticillioides attract D. saccharalis caterpillars. Once they become adults, the fungus is transmitted vertically to their offspring, which continues the cycle by inoculating the fungus into healthy plants. Females not carrying the fungus prefer to lay their eggs on fungus-infected plants than mock plants, while females carrying the fungus prefer to lay their eggs on mock plants than fungus-infected plants. Even though the fungus impacts D. saccharalis sex behavior, larval weight and reproduction rate, most individuals complete their development. Our data demonstrate that the fungus manipulates both the host plant and insect herbivore across life cycle to promote its infection and dissemination. Nature Publishing Group UK 2021-06-14 2021-12 /pmc/articles/PMC8630062/ /pubmed/34127802 http://dx.doi.org/10.1038/s41396-021-01010-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Franco, Flávia P. Túler, Amanda C. Gallan, Diego Z. Gonçalves, Felipe G. Favaris, Arodí P. Peñaflor, Maria Fernanda G. V. Leal, Walter S. Moura, Daniel S. Bento, José Maurício S. Silva-Filho, Marcio C. Fungal phytopathogen modulates plant and insect responses to promote its dissemination |
title | Fungal phytopathogen modulates plant and insect responses to promote its dissemination |
title_full | Fungal phytopathogen modulates plant and insect responses to promote its dissemination |
title_fullStr | Fungal phytopathogen modulates plant and insect responses to promote its dissemination |
title_full_unstemmed | Fungal phytopathogen modulates plant and insect responses to promote its dissemination |
title_short | Fungal phytopathogen modulates plant and insect responses to promote its dissemination |
title_sort | fungal phytopathogen modulates plant and insect responses to promote its dissemination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8630062/ https://www.ncbi.nlm.nih.gov/pubmed/34127802 http://dx.doi.org/10.1038/s41396-021-01010-z |
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