Cargando…

Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome

Plants produce suites of defenses that can collectively deter and reduce herbivory. Many defenses target the insect digestive system, with some altering the protective peritrophic matrix (PM) and causing increased permeability. The PM is responsible for multiple digestive functions, including reduci...

Descripción completa

Detalles Bibliográficos
Autores principales: Mason, Charles J., Ray, Swayamjit, Shikano, Ikkei, Peiffer, Michelle, Jones, Asher G., Luthe, Dawn S., Hoover, Kelli, Felton, Gary W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689943/
https://www.ncbi.nlm.nih.gov/pubmed/31332013
http://dx.doi.org/10.1073/pnas.1908748116
_version_ 1783443118351187968
author Mason, Charles J.
Ray, Swayamjit
Shikano, Ikkei
Peiffer, Michelle
Jones, Asher G.
Luthe, Dawn S.
Hoover, Kelli
Felton, Gary W.
author_facet Mason, Charles J.
Ray, Swayamjit
Shikano, Ikkei
Peiffer, Michelle
Jones, Asher G.
Luthe, Dawn S.
Hoover, Kelli
Felton, Gary W.
author_sort Mason, Charles J.
collection PubMed
description Plants produce suites of defenses that can collectively deter and reduce herbivory. Many defenses target the insect digestive system, with some altering the protective peritrophic matrix (PM) and causing increased permeability. The PM is responsible for multiple digestive functions, including reducing infections from potential pathogenic microbes. In our study, we developed axenic and gnotobiotic methods for fall armyworm (Spodoptera frugiperda) and tested how particular members present in the gut community influence interactions with plant defenses that can alter PM permeability. We observed interactions between gut bacteria with plant resistance. Axenic insects grew more but displayed lower immune-based responses compared with those possessing Enterococcus, Klebsiella, and Enterobacter isolates from field-collected larvae. While gut bacteria reduced performance of larvae fed on plants, none of the isolates produced mortality when injected directly into the hemocoel. Our results strongly suggest that plant physical and chemical defenses not only act directly upon the insect, but also have some interplay with the herbivore’s microbiome. Combined direct and indirect, microbe-mediated assaults by maize defenses on the fall armyworm on the insect digestive and immune system reduced growth and elevated mortality in these insects. These results imply that plant–insect interactions should be considered in the context of potential mediation by the insect gut microbiome.
format Online
Article
Text
id pubmed-6689943
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-66899432019-08-14 Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome Mason, Charles J. Ray, Swayamjit Shikano, Ikkei Peiffer, Michelle Jones, Asher G. Luthe, Dawn S. Hoover, Kelli Felton, Gary W. Proc Natl Acad Sci U S A Biological Sciences Plants produce suites of defenses that can collectively deter and reduce herbivory. Many defenses target the insect digestive system, with some altering the protective peritrophic matrix (PM) and causing increased permeability. The PM is responsible for multiple digestive functions, including reducing infections from potential pathogenic microbes. In our study, we developed axenic and gnotobiotic methods for fall armyworm (Spodoptera frugiperda) and tested how particular members present in the gut community influence interactions with plant defenses that can alter PM permeability. We observed interactions between gut bacteria with plant resistance. Axenic insects grew more but displayed lower immune-based responses compared with those possessing Enterococcus, Klebsiella, and Enterobacter isolates from field-collected larvae. While gut bacteria reduced performance of larvae fed on plants, none of the isolates produced mortality when injected directly into the hemocoel. Our results strongly suggest that plant physical and chemical defenses not only act directly upon the insect, but also have some interplay with the herbivore’s microbiome. Combined direct and indirect, microbe-mediated assaults by maize defenses on the fall armyworm on the insect digestive and immune system reduced growth and elevated mortality in these insects. These results imply that plant–insect interactions should be considered in the context of potential mediation by the insect gut microbiome. National Academy of Sciences 2019-08-06 2019-07-22 /pmc/articles/PMC6689943/ /pubmed/31332013 http://dx.doi.org/10.1073/pnas.1908748116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Mason, Charles J.
Ray, Swayamjit
Shikano, Ikkei
Peiffer, Michelle
Jones, Asher G.
Luthe, Dawn S.
Hoover, Kelli
Felton, Gary W.
Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome
title Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome
title_full Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome
title_fullStr Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome
title_full_unstemmed Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome
title_short Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome
title_sort plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689943/
https://www.ncbi.nlm.nih.gov/pubmed/31332013
http://dx.doi.org/10.1073/pnas.1908748116
work_keys_str_mv AT masoncharlesj plantdefensesinteractwithinsectentericbacteriabyinitiatingaleakygutsyndrome
AT rayswayamjit plantdefensesinteractwithinsectentericbacteriabyinitiatingaleakygutsyndrome
AT shikanoikkei plantdefensesinteractwithinsectentericbacteriabyinitiatingaleakygutsyndrome
AT peiffermichelle plantdefensesinteractwithinsectentericbacteriabyinitiatingaleakygutsyndrome
AT jonesasherg plantdefensesinteractwithinsectentericbacteriabyinitiatingaleakygutsyndrome
AT luthedawns plantdefensesinteractwithinsectentericbacteriabyinitiatingaleakygutsyndrome
AT hooverkelli plantdefensesinteractwithinsectentericbacteriabyinitiatingaleakygutsyndrome
AT feltongaryw plantdefensesinteractwithinsectentericbacteriabyinitiatingaleakygutsyndrome