Cargando…
Pathogenic bacteria enhance dispersal through alteration of Drosophila social communication
Pathogens and parasites can manipulate their hosts to optimize their own fitness. For instance, bacterial pathogens have been shown to affect their host plants’ volatile and non-volatile metabolites, which results in increased attraction of insect vectors to the plant, and, hence, to increased patho...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559524/ https://www.ncbi.nlm.nih.gov/pubmed/28814724 http://dx.doi.org/10.1038/s41467-017-00334-9 |
_version_ | 1783257534537138176 |
---|---|
author | Keesey, Ian W. Koerte, Sarah Khallaf, Mohammed A. Retzke, Tom Guillou, Aurélien Grosse-Wilde, Ewald Buchon, Nicolas Knaden, Markus Hansson, Bill S. |
author_facet | Keesey, Ian W. Koerte, Sarah Khallaf, Mohammed A. Retzke, Tom Guillou, Aurélien Grosse-Wilde, Ewald Buchon, Nicolas Knaden, Markus Hansson, Bill S. |
author_sort | Keesey, Ian W. |
collection | PubMed |
description | Pathogens and parasites can manipulate their hosts to optimize their own fitness. For instance, bacterial pathogens have been shown to affect their host plants’ volatile and non-volatile metabolites, which results in increased attraction of insect vectors to the plant, and, hence, to increased pathogen dispersal. Behavioral manipulation by parasites has also been shown for mice, snails and zebrafish as well as for insects. Here we show that infection by pathogenic bacteria alters the social communication system of Drosophila melanogaster. More specifically, infected flies and their frass emit dramatically increased amounts of fly odors, including the aggregation pheromones methyl laurate, methyl myristate, and methyl palmitate, attracting healthy flies, which in turn become infected and further enhance pathogen dispersal. Thus, olfactory cues for attraction and aggregation are vulnerable to pathogenic manipulation, and we show that the alteration of social pheromones can be beneficial to the microbe while detrimental to the insect host. |
format | Online Article Text |
id | pubmed-5559524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55595242017-08-23 Pathogenic bacteria enhance dispersal through alteration of Drosophila social communication Keesey, Ian W. Koerte, Sarah Khallaf, Mohammed A. Retzke, Tom Guillou, Aurélien Grosse-Wilde, Ewald Buchon, Nicolas Knaden, Markus Hansson, Bill S. Nat Commun Article Pathogens and parasites can manipulate their hosts to optimize their own fitness. For instance, bacterial pathogens have been shown to affect their host plants’ volatile and non-volatile metabolites, which results in increased attraction of insect vectors to the plant, and, hence, to increased pathogen dispersal. Behavioral manipulation by parasites has also been shown for mice, snails and zebrafish as well as for insects. Here we show that infection by pathogenic bacteria alters the social communication system of Drosophila melanogaster. More specifically, infected flies and their frass emit dramatically increased amounts of fly odors, including the aggregation pheromones methyl laurate, methyl myristate, and methyl palmitate, attracting healthy flies, which in turn become infected and further enhance pathogen dispersal. Thus, olfactory cues for attraction and aggregation are vulnerable to pathogenic manipulation, and we show that the alteration of social pheromones can be beneficial to the microbe while detrimental to the insect host. Nature Publishing Group UK 2017-08-16 /pmc/articles/PMC5559524/ /pubmed/28814724 http://dx.doi.org/10.1038/s41467-017-00334-9 Text en © The Author(s) 2017 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 Keesey, Ian W. Koerte, Sarah Khallaf, Mohammed A. Retzke, Tom Guillou, Aurélien Grosse-Wilde, Ewald Buchon, Nicolas Knaden, Markus Hansson, Bill S. Pathogenic bacteria enhance dispersal through alteration of Drosophila social communication |
title | Pathogenic bacteria enhance dispersal through alteration of Drosophila social communication |
title_full | Pathogenic bacteria enhance dispersal through alteration of Drosophila social communication |
title_fullStr | Pathogenic bacteria enhance dispersal through alteration of Drosophila social communication |
title_full_unstemmed | Pathogenic bacteria enhance dispersal through alteration of Drosophila social communication |
title_short | Pathogenic bacteria enhance dispersal through alteration of Drosophila social communication |
title_sort | pathogenic bacteria enhance dispersal through alteration of drosophila social communication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559524/ https://www.ncbi.nlm.nih.gov/pubmed/28814724 http://dx.doi.org/10.1038/s41467-017-00334-9 |
work_keys_str_mv | AT keeseyianw pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication AT koertesarah pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication AT khallafmohammeda pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication AT retzketom pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication AT guillouaurelien pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication AT grossewildeewald pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication AT buchonnicolas pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication AT knadenmarkus pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication AT hanssonbills pathogenicbacteriaenhancedispersalthroughalterationofdrosophilasocialcommunication |