Cargando…
Interspecific Nematode Signals Regulate Dispersal Behavior
BACKGROUND: Dispersal is an important nematode behavior. Upon crowding or food depletion, the free living bacteriovorus nematode Caenorhabditis elegans produces stress resistant dispersal larvae, called dauer, which are analogous to second stage juveniles (J2) of plant parasitic Meloidogyne spp. and...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368880/ https://www.ncbi.nlm.nih.gov/pubmed/22701701 http://dx.doi.org/10.1371/journal.pone.0038735 |
_version_ | 1782235003540733952 |
---|---|
author | Kaplan, Fatma Alborn, Hans T. von Reuss, Stephan H. Ajredini, Ramadan Ali, Jared G. Akyazi, Faruk Stelinski, Lukasz L. Edison, Arthur S. Schroeder, Frank C. Teal, Peter E. |
author_facet | Kaplan, Fatma Alborn, Hans T. von Reuss, Stephan H. Ajredini, Ramadan Ali, Jared G. Akyazi, Faruk Stelinski, Lukasz L. Edison, Arthur S. Schroeder, Frank C. Teal, Peter E. |
author_sort | Kaplan, Fatma |
collection | PubMed |
description | BACKGROUND: Dispersal is an important nematode behavior. Upon crowding or food depletion, the free living bacteriovorus nematode Caenorhabditis elegans produces stress resistant dispersal larvae, called dauer, which are analogous to second stage juveniles (J2) of plant parasitic Meloidogyne spp. and infective juveniles (IJ)s of entomopathogenic nematodes (EPN), e.g., Steinernema feltiae. Regulation of dispersal behavior has not been thoroughly investigated for C. elegans or any other nematode species. Based on the fact that ascarosides regulate entry in dauer stage as well as multiple behaviors in C. elegans adults including mating, avoidance and aggregation, we hypothesized that ascarosides might also be involved in regulation of dispersal behavior in C. elegans and for other nematodes such as IJ of phylogenetically related EPNs. METHODOLOGY/PRINCIPAL FINDINGS: Liquid chromatography-mass spectrometry analysis of C. elegans dauer conditioned media, which shows strong dispersing activity, revealed four known ascarosides (ascr#2, ascr#3, ascr#8, icas#9). A synthetic blend of these ascarosides at physiologically relevant concentrations dispersed C. elegans dauer in the presence of food and also caused dispersion of IJs of S. feltiae and J2s of plant parasitic Meloidogyne spp. Assay guided fractionation revealed structural analogs as major active components of the S. feltiae (ascr#9) and C. elegans (ascr#2) dispersal blends. Further analysis revealed ascr#9 in all Steinernema spp. and Heterorhabditis spp. infected insect host cadavers. CONCLUSIONS/SIGNIFICANCE: Ascaroside blends represent evolutionarily conserved, fundamentally important communication systems for nematodes from diverse habitats, and thus may provide sustainable means for control of parasitic nematodes. |
format | Online Article Text |
id | pubmed-3368880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33688802012-06-13 Interspecific Nematode Signals Regulate Dispersal Behavior Kaplan, Fatma Alborn, Hans T. von Reuss, Stephan H. Ajredini, Ramadan Ali, Jared G. Akyazi, Faruk Stelinski, Lukasz L. Edison, Arthur S. Schroeder, Frank C. Teal, Peter E. PLoS One Research Article BACKGROUND: Dispersal is an important nematode behavior. Upon crowding or food depletion, the free living bacteriovorus nematode Caenorhabditis elegans produces stress resistant dispersal larvae, called dauer, which are analogous to second stage juveniles (J2) of plant parasitic Meloidogyne spp. and infective juveniles (IJ)s of entomopathogenic nematodes (EPN), e.g., Steinernema feltiae. Regulation of dispersal behavior has not been thoroughly investigated for C. elegans or any other nematode species. Based on the fact that ascarosides regulate entry in dauer stage as well as multiple behaviors in C. elegans adults including mating, avoidance and aggregation, we hypothesized that ascarosides might also be involved in regulation of dispersal behavior in C. elegans and for other nematodes such as IJ of phylogenetically related EPNs. METHODOLOGY/PRINCIPAL FINDINGS: Liquid chromatography-mass spectrometry analysis of C. elegans dauer conditioned media, which shows strong dispersing activity, revealed four known ascarosides (ascr#2, ascr#3, ascr#8, icas#9). A synthetic blend of these ascarosides at physiologically relevant concentrations dispersed C. elegans dauer in the presence of food and also caused dispersion of IJs of S. feltiae and J2s of plant parasitic Meloidogyne spp. Assay guided fractionation revealed structural analogs as major active components of the S. feltiae (ascr#9) and C. elegans (ascr#2) dispersal blends. Further analysis revealed ascr#9 in all Steinernema spp. and Heterorhabditis spp. infected insect host cadavers. CONCLUSIONS/SIGNIFICANCE: Ascaroside blends represent evolutionarily conserved, fundamentally important communication systems for nematodes from diverse habitats, and thus may provide sustainable means for control of parasitic nematodes. Public Library of Science 2012-06-06 /pmc/articles/PMC3368880/ /pubmed/22701701 http://dx.doi.org/10.1371/journal.pone.0038735 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Kaplan, Fatma Alborn, Hans T. von Reuss, Stephan H. Ajredini, Ramadan Ali, Jared G. Akyazi, Faruk Stelinski, Lukasz L. Edison, Arthur S. Schroeder, Frank C. Teal, Peter E. Interspecific Nematode Signals Regulate Dispersal Behavior |
title | Interspecific Nematode Signals Regulate Dispersal Behavior |
title_full | Interspecific Nematode Signals Regulate Dispersal Behavior |
title_fullStr | Interspecific Nematode Signals Regulate Dispersal Behavior |
title_full_unstemmed | Interspecific Nematode Signals Regulate Dispersal Behavior |
title_short | Interspecific Nematode Signals Regulate Dispersal Behavior |
title_sort | interspecific nematode signals regulate dispersal behavior |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368880/ https://www.ncbi.nlm.nih.gov/pubmed/22701701 http://dx.doi.org/10.1371/journal.pone.0038735 |
work_keys_str_mv | AT kaplanfatma interspecificnematodesignalsregulatedispersalbehavior AT albornhanst interspecificnematodesignalsregulatedispersalbehavior AT vonreussstephanh interspecificnematodesignalsregulatedispersalbehavior AT ajrediniramadan interspecificnematodesignalsregulatedispersalbehavior AT alijaredg interspecificnematodesignalsregulatedispersalbehavior AT akyazifaruk interspecificnematodesignalsregulatedispersalbehavior AT stelinskilukaszl interspecificnematodesignalsregulatedispersalbehavior AT edisonarthurs interspecificnematodesignalsregulatedispersalbehavior AT schroederfrankc interspecificnematodesignalsregulatedispersalbehavior AT tealpetere interspecificnematodesignalsregulatedispersalbehavior |