Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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
_version_ 1784607330819637248
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
work_keys_str_mv AT francoflaviap fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT tuleramandac fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT gallandiegoz fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT goncalvesfelipeg fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT favarisarodip fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT penaflormariafernandagv fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT lealwalters fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT mouradaniels fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT bentojosemauricios fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination
AT silvafilhomarcioc fungalphytopathogenmodulatesplantandinsectresponsestopromoteitsdissemination