Cargando…
The route of infection determines Wolbachia antibacterial protection in Drosophila
Bacterial symbionts are widespread among metazoans and provide a range of beneficial functions. Wolbachia-mediated protection against viral infection has been extensively demonstrated in Drosophila. In mosquitoes that are artificially transinfected with Drosophila melanogaster Wolbachia (wMel), prot...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474083/ https://www.ncbi.nlm.nih.gov/pubmed/28592678 http://dx.doi.org/10.1098/rspb.2017.0809 |
_version_ | 1783244404157317120 |
---|---|
author | Gupta, Vanika Vasanthakrishnan, Radhakrishnan B. Siva-Jothy, Jonathon Monteith, Katy M. Brown, Sam P. Vale, Pedro F. |
author_facet | Gupta, Vanika Vasanthakrishnan, Radhakrishnan B. Siva-Jothy, Jonathon Monteith, Katy M. Brown, Sam P. Vale, Pedro F. |
author_sort | Gupta, Vanika |
collection | PubMed |
description | Bacterial symbionts are widespread among metazoans and provide a range of beneficial functions. Wolbachia-mediated protection against viral infection has been extensively demonstrated in Drosophila. In mosquitoes that are artificially transinfected with Drosophila melanogaster Wolbachia (wMel), protection from both viral and bacterial infections has been demonstrated. However, no evidence for Wolbachia-mediated antibacterial protection has been demonstrated in Drosophila to date. Here, we show that the route of infection is key for Wolbachia-mediated antibacterial protection. Drosophila melanogaster carrying Wolbachia showed reduced mortality during enteric—but not systemic—infection with the opportunist pathogen Pseudomonas aeruginosa. Wolbachia-mediated protection was more pronounced in male flies and is associated with increased early expression of the antimicrobial peptide Attacin A, and also increased expression of a reactive oxygen species detoxification gene (Gst D8). These results highlight that the route of infection is important for symbiont-mediated protection from infection, that Wolbachia can protect hosts by eliciting a combination of resistance and disease tolerance mechanisms, and that these effects are sexually dimorphic. We discuss the importance of using ecologically relevant routes of infection to gain a better understanding of symbiont-mediated protection. |
format | Online Article Text |
id | pubmed-5474083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-54740832017-06-19 The route of infection determines Wolbachia antibacterial protection in Drosophila Gupta, Vanika Vasanthakrishnan, Radhakrishnan B. Siva-Jothy, Jonathon Monteith, Katy M. Brown, Sam P. Vale, Pedro F. Proc Biol Sci Development and Physiology Bacterial symbionts are widespread among metazoans and provide a range of beneficial functions. Wolbachia-mediated protection against viral infection has been extensively demonstrated in Drosophila. In mosquitoes that are artificially transinfected with Drosophila melanogaster Wolbachia (wMel), protection from both viral and bacterial infections has been demonstrated. However, no evidence for Wolbachia-mediated antibacterial protection has been demonstrated in Drosophila to date. Here, we show that the route of infection is key for Wolbachia-mediated antibacterial protection. Drosophila melanogaster carrying Wolbachia showed reduced mortality during enteric—but not systemic—infection with the opportunist pathogen Pseudomonas aeruginosa. Wolbachia-mediated protection was more pronounced in male flies and is associated with increased early expression of the antimicrobial peptide Attacin A, and also increased expression of a reactive oxygen species detoxification gene (Gst D8). These results highlight that the route of infection is important for symbiont-mediated protection from infection, that Wolbachia can protect hosts by eliciting a combination of resistance and disease tolerance mechanisms, and that these effects are sexually dimorphic. We discuss the importance of using ecologically relevant routes of infection to gain a better understanding of symbiont-mediated protection. The Royal Society 2017-06-14 2017-06-07 /pmc/articles/PMC5474083/ /pubmed/28592678 http://dx.doi.org/10.1098/rspb.2017.0809 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Development and Physiology Gupta, Vanika Vasanthakrishnan, Radhakrishnan B. Siva-Jothy, Jonathon Monteith, Katy M. Brown, Sam P. Vale, Pedro F. The route of infection determines Wolbachia antibacterial protection in Drosophila |
title | The route of infection determines Wolbachia antibacterial protection in Drosophila |
title_full | The route of infection determines Wolbachia antibacterial protection in Drosophila |
title_fullStr | The route of infection determines Wolbachia antibacterial protection in Drosophila |
title_full_unstemmed | The route of infection determines Wolbachia antibacterial protection in Drosophila |
title_short | The route of infection determines Wolbachia antibacterial protection in Drosophila |
title_sort | route of infection determines wolbachia antibacterial protection in drosophila |
topic | Development and Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474083/ https://www.ncbi.nlm.nih.gov/pubmed/28592678 http://dx.doi.org/10.1098/rspb.2017.0809 |
work_keys_str_mv | AT guptavanika therouteofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT vasanthakrishnanradhakrishnanb therouteofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT sivajothyjonathon therouteofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT monteithkatym therouteofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT brownsamp therouteofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT valepedrof therouteofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT guptavanika routeofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT vasanthakrishnanradhakrishnanb routeofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT sivajothyjonathon routeofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT monteithkatym routeofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT brownsamp routeofinfectiondetermineswolbachiaantibacterialprotectionindrosophila AT valepedrof routeofinfectiondetermineswolbachiaantibacterialprotectionindrosophila |