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Symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity

Obligate symbioses occur when organisms require symbiotic relationships to survive. Some parasitic wasps of caterpillars possess obligate mutualistic viruses called “polydnaviruses.” Along with eggs, wasps inject polydnavirus inside their caterpillar hosts where the hatching larvae develop inside th...

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Autores principales: Tan, Ching-Wen, Peiffer, Michelle, Hoover, Kelli, Rosa, Cristina, Acevedo, Flor E., Felton, Gary W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960290/
https://www.ncbi.nlm.nih.gov/pubmed/29712862
http://dx.doi.org/10.1073/pnas.1717934115
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author Tan, Ching-Wen
Peiffer, Michelle
Hoover, Kelli
Rosa, Cristina
Acevedo, Flor E.
Felton, Gary W.
author_facet Tan, Ching-Wen
Peiffer, Michelle
Hoover, Kelli
Rosa, Cristina
Acevedo, Flor E.
Felton, Gary W.
author_sort Tan, Ching-Wen
collection PubMed
description Obligate symbioses occur when organisms require symbiotic relationships to survive. Some parasitic wasps of caterpillars possess obligate mutualistic viruses called “polydnaviruses.” Along with eggs, wasps inject polydnavirus inside their caterpillar hosts where the hatching larvae develop inside the caterpillar. Polydnaviruses suppress the immune systems of their caterpillar hosts, which enables egg hatch and wasp larval development. It is unknown whether polydnaviruses also manipulate the salivary proteins of the caterpillar, which may affect the elicitation of plant defenses during feeding by the caterpillar. Here, we show that a polydnavirus of the parasitoid Microplitis croceipes, and not the parasitoid larva itself, drives the regulation of salivary enzymes of the caterpillar Helicoverpa zea that are known to elicit tomato plant-defense responses to herbivores. The polydnavirus suppresses glucose oxidase, which is a primary plant-defense elicitor in the saliva of the H. zea caterpillar. By suppressing plant defenses, the polydnavirus allows the caterpillar to grow at a faster rate, thus improving the host suitability for the parasitoid. Remarkably, polydnaviruses manipulate the phenotypes of the wasp, caterpillar, and host plant, demonstrating that polydnaviruses play far more prominent roles in shaping plant–herbivore interactions than ever considered.
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spelling pubmed-59602902018-05-21 Symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity Tan, Ching-Wen Peiffer, Michelle Hoover, Kelli Rosa, Cristina Acevedo, Flor E. Felton, Gary W. Proc Natl Acad Sci U S A Biological Sciences Obligate symbioses occur when organisms require symbiotic relationships to survive. Some parasitic wasps of caterpillars possess obligate mutualistic viruses called “polydnaviruses.” Along with eggs, wasps inject polydnavirus inside their caterpillar hosts where the hatching larvae develop inside the caterpillar. Polydnaviruses suppress the immune systems of their caterpillar hosts, which enables egg hatch and wasp larval development. It is unknown whether polydnaviruses also manipulate the salivary proteins of the caterpillar, which may affect the elicitation of plant defenses during feeding by the caterpillar. Here, we show that a polydnavirus of the parasitoid Microplitis croceipes, and not the parasitoid larva itself, drives the regulation of salivary enzymes of the caterpillar Helicoverpa zea that are known to elicit tomato plant-defense responses to herbivores. The polydnavirus suppresses glucose oxidase, which is a primary plant-defense elicitor in the saliva of the H. zea caterpillar. By suppressing plant defenses, the polydnavirus allows the caterpillar to grow at a faster rate, thus improving the host suitability for the parasitoid. Remarkably, polydnaviruses manipulate the phenotypes of the wasp, caterpillar, and host plant, demonstrating that polydnaviruses play far more prominent roles in shaping plant–herbivore interactions than ever considered. National Academy of Sciences 2018-05-15 2018-04-30 /pmc/articles/PMC5960290/ /pubmed/29712862 http://dx.doi.org/10.1073/pnas.1717934115 Text en Copyright © 2018 the Author(s). Published by PNAS. 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
Tan, Ching-Wen
Peiffer, Michelle
Hoover, Kelli
Rosa, Cristina
Acevedo, Flor E.
Felton, Gary W.
Symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity
title Symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity
title_full Symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity
title_fullStr Symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity
title_full_unstemmed Symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity
title_short Symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity
title_sort symbiotic polydnavirus of a parasite manipulates caterpillar and plant immunity
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960290/
https://www.ncbi.nlm.nih.gov/pubmed/29712862
http://dx.doi.org/10.1073/pnas.1717934115
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