Cargando…
Conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence
Ascaroside pheromones stimulate dispersal, a key nematode behavior to find a new food source. Ascarosides produced by entomopathogenic nematodes (EPNs) drive infective juvenile (IJ) emergence from consumed cadavers and dispersal in soil. Without ascarosides from host cadavers, Steinernema feltiae (E...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109026/ https://www.ncbi.nlm.nih.gov/pubmed/32235877 http://dx.doi.org/10.1038/s41598-020-62817-y |
_version_ | 1783512873019899904 |
---|---|
author | Kaplan, Fatma Perret-Gentil, Abigail Giurintano, Julie Stevens, Glen Erdogan, Hilal Schiller, Karl C. Mirti, Amaleah Sampson, Edith Torres, Cedric Sun, Jiayi Lewis, Edwin E. Shapiro-Ilan, David |
author_facet | Kaplan, Fatma Perret-Gentil, Abigail Giurintano, Julie Stevens, Glen Erdogan, Hilal Schiller, Karl C. Mirti, Amaleah Sampson, Edith Torres, Cedric Sun, Jiayi Lewis, Edwin E. Shapiro-Ilan, David |
author_sort | Kaplan, Fatma |
collection | PubMed |
description | Ascaroside pheromones stimulate dispersal, a key nematode behavior to find a new food source. Ascarosides produced by entomopathogenic nematodes (EPNs) drive infective juvenile (IJ) emergence from consumed cadavers and dispersal in soil. Without ascarosides from host cadavers, Steinernema feltiae (EPN) reduce dispersal substantially. To determine whether other Steinernema spp. exhibit the same behavior, we compared S. feltiae and S. carpocapsae IJs without host cadaver pheromones. Unlike S. feltiae, S. carpocapsae IJs continued to disperse. However, S. carpocapsae IJs exhibited a temperature-dependent quiescent period. The IJ quiescent period increased at ≤20 °C but did not appear at ≥25 °C. Consistent with this, S. carpocapsae IJ quiescence increased from 30 min to 24 h at ≤20 °C over 60 days. The quiescent period was overcome by dispersal pheromone extracts of their own, other Steinernema spp. and Heterorhabditis spp. Furthermore, S. carpocapsae IJ ambush foraging associated behaviors (tail standing, waving, and jumping) were unaffected by the absence or presence of host cadaver pheromones. For S. feltiae, IJ dispersal declined at all temperatures tested. Understanding the interaction between foraging strategies and pheromone signals will help uncover molecular mechanisms of host seeking, pathogenicity and practical applications to improve the EPN’s efficacy as biocontrol agents. |
format | Online Article Text |
id | pubmed-7109026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71090262020-04-06 Conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence Kaplan, Fatma Perret-Gentil, Abigail Giurintano, Julie Stevens, Glen Erdogan, Hilal Schiller, Karl C. Mirti, Amaleah Sampson, Edith Torres, Cedric Sun, Jiayi Lewis, Edwin E. Shapiro-Ilan, David Sci Rep Article Ascaroside pheromones stimulate dispersal, a key nematode behavior to find a new food source. Ascarosides produced by entomopathogenic nematodes (EPNs) drive infective juvenile (IJ) emergence from consumed cadavers and dispersal in soil. Without ascarosides from host cadavers, Steinernema feltiae (EPN) reduce dispersal substantially. To determine whether other Steinernema spp. exhibit the same behavior, we compared S. feltiae and S. carpocapsae IJs without host cadaver pheromones. Unlike S. feltiae, S. carpocapsae IJs continued to disperse. However, S. carpocapsae IJs exhibited a temperature-dependent quiescent period. The IJ quiescent period increased at ≤20 °C but did not appear at ≥25 °C. Consistent with this, S. carpocapsae IJ quiescence increased from 30 min to 24 h at ≤20 °C over 60 days. The quiescent period was overcome by dispersal pheromone extracts of their own, other Steinernema spp. and Heterorhabditis spp. Furthermore, S. carpocapsae IJ ambush foraging associated behaviors (tail standing, waving, and jumping) were unaffected by the absence or presence of host cadaver pheromones. For S. feltiae, IJ dispersal declined at all temperatures tested. Understanding the interaction between foraging strategies and pheromone signals will help uncover molecular mechanisms of host seeking, pathogenicity and practical applications to improve the EPN’s efficacy as biocontrol agents. Nature Publishing Group UK 2020-03-31 /pmc/articles/PMC7109026/ /pubmed/32235877 http://dx.doi.org/10.1038/s41598-020-62817-y Text en © The Author(s) 2020 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/. |
spellingShingle | Article Kaplan, Fatma Perret-Gentil, Abigail Giurintano, Julie Stevens, Glen Erdogan, Hilal Schiller, Karl C. Mirti, Amaleah Sampson, Edith Torres, Cedric Sun, Jiayi Lewis, Edwin E. Shapiro-Ilan, David Conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence |
title | Conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence |
title_full | Conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence |
title_fullStr | Conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence |
title_full_unstemmed | Conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence |
title_short | Conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence |
title_sort | conspecific and heterospecific pheromones stimulate dispersal of entomopathogenic nematodes during quiescence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109026/ https://www.ncbi.nlm.nih.gov/pubmed/32235877 http://dx.doi.org/10.1038/s41598-020-62817-y |
work_keys_str_mv | AT kaplanfatma conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT perretgentilabigail conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT giurintanojulie conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT stevensglen conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT erdoganhilal conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT schillerkarlc conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT mirtiamaleah conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT sampsonedith conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT torrescedric conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT sunjiayi conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT lewisedwine conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence AT shapiroilandavid conspecificandheterospecificpheromonesstimulatedispersalofentomopathogenicnematodesduringquiescence |