Activated entomopathogenic nematode infective juveniles release lethal venom proteins.

Entomopathogenic nematodes (EPNs) are unique parasites due to their symbiosis with entomopathogenic bacteria and their ability to kill insect hosts quickly after infection. It is widely believed that EPNs rely on their bacterial partners for killing hosts. Here we disproved this theory by demonstrat...

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Main Authors: Dihong Lu, Marissa Macchietto, Dennis Chang, Mirayana M Barros, James Baldwin, Ali Mortazavi, Adler R Dillman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-04-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC5398726?pdf=render
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spelling doaj-baf6338ffc514d51b0fcc07c2a7379f32020-11-24T21:25:54ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742017-04-01134e100630210.1371/journal.ppat.1006302Activated entomopathogenic nematode infective juveniles release lethal venom proteins.Dihong LuMarissa MacchiettoDennis ChangMirayana M BarrosJames BaldwinAli MortazaviAdler R DillmanEntomopathogenic nematodes (EPNs) are unique parasites due to their symbiosis with entomopathogenic bacteria and their ability to kill insect hosts quickly after infection. It is widely believed that EPNs rely on their bacterial partners for killing hosts. Here we disproved this theory by demonstrating that the in vitro activated infective juveniles (IJs) of Steinernema carpocapsae (a well-studied EPN species) release venom proteins that are lethal to several insects including Drosophila melanogaster. We confirmed that the in vitro activation is a good approximation of the in vivo process by comparing the transcriptomes of individual in vitro and in vivo activated IJs. We further analyzed the transcriptomes of non-activated and activated IJs and revealed a dramatic shift in gene expression during IJ activation. We also analyzed the venom proteome using mass spectrometry. Among the 472 venom proteins, proteases and protease inhibitors are especially abundant, and toxin-related proteins such as Shk domain-containing proteins and fatty acid- and retinol-binding proteins are also detected, which are potential candidates for suppressing the host immune system. Many of the venom proteins have conserved orthologs in vertebrate-parasitic nematodes and are differentially expressed during IJ activation, suggesting conserved functions in nematode parasitism. In summary, our findings strongly support a new model that S. carpocapsae and likely other Steinernema EPNs have a more active role in contributing to the pathogenicity of the nematode-bacterium complex than simply relying on their symbiotic bacteria. Furthermore, we propose that EPNs are a good model system for investigating vertebrate- and human-parasitic nematodes, especially regarding the function of excretory/secretory products.http://europepmc.org/articles/PMC5398726?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Dihong Lu
Marissa Macchietto
Dennis Chang
Mirayana M Barros
James Baldwin
Ali Mortazavi
Adler R Dillman
spellingShingle Dihong Lu
Marissa Macchietto
Dennis Chang
Mirayana M Barros
James Baldwin
Ali Mortazavi
Adler R Dillman
Activated entomopathogenic nematode infective juveniles release lethal venom proteins.
PLoS Pathogens
author_facet Dihong Lu
Marissa Macchietto
Dennis Chang
Mirayana M Barros
James Baldwin
Ali Mortazavi
Adler R Dillman
author_sort Dihong Lu
title Activated entomopathogenic nematode infective juveniles release lethal venom proteins.
title_short Activated entomopathogenic nematode infective juveniles release lethal venom proteins.
title_full Activated entomopathogenic nematode infective juveniles release lethal venom proteins.
title_fullStr Activated entomopathogenic nematode infective juveniles release lethal venom proteins.
title_full_unstemmed Activated entomopathogenic nematode infective juveniles release lethal venom proteins.
title_sort activated entomopathogenic nematode infective juveniles release lethal venom proteins.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2017-04-01
description Entomopathogenic nematodes (EPNs) are unique parasites due to their symbiosis with entomopathogenic bacteria and their ability to kill insect hosts quickly after infection. It is widely believed that EPNs rely on their bacterial partners for killing hosts. Here we disproved this theory by demonstrating that the in vitro activated infective juveniles (IJs) of Steinernema carpocapsae (a well-studied EPN species) release venom proteins that are lethal to several insects including Drosophila melanogaster. We confirmed that the in vitro activation is a good approximation of the in vivo process by comparing the transcriptomes of individual in vitro and in vivo activated IJs. We further analyzed the transcriptomes of non-activated and activated IJs and revealed a dramatic shift in gene expression during IJ activation. We also analyzed the venom proteome using mass spectrometry. Among the 472 venom proteins, proteases and protease inhibitors are especially abundant, and toxin-related proteins such as Shk domain-containing proteins and fatty acid- and retinol-binding proteins are also detected, which are potential candidates for suppressing the host immune system. Many of the venom proteins have conserved orthologs in vertebrate-parasitic nematodes and are differentially expressed during IJ activation, suggesting conserved functions in nematode parasitism. In summary, our findings strongly support a new model that S. carpocapsae and likely other Steinernema EPNs have a more active role in contributing to the pathogenicity of the nematode-bacterium complex than simply relying on their symbiotic bacteria. Furthermore, we propose that EPNs are a good model system for investigating vertebrate- and human-parasitic nematodes, especially regarding the function of excretory/secretory products.
url http://europepmc.org/articles/PMC5398726?pdf=render
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