Cargando…

Effects of co-occurring Wolbachia and Spiroplasma endosymbionts on the Drosophila immune response against insect pathogenic and non-pathogenic bacteria

BACKGROUND: Symbiotic interactions between microbes and animals are common in nature. Symbiotic organisms are particularly common in insects and, in some cases, they may protect their hosts from pathogenic infections. Wolbachia and Spiroplasma endosymbionts naturally inhabit various insects includin...

Descripción completa

Detalles Bibliográficos
Autores principales: Shokal, Upasana, Yadav, Shruti, Atri, Jaishri, Accetta, Julia, Kenney, Eric, Banks, Katherine, Katakam, Akash, Jaenike, John, Eleftherianos, Ioannis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746768/
https://www.ncbi.nlm.nih.gov/pubmed/26862076
http://dx.doi.org/10.1186/s12866-016-0634-6
_version_ 1782414859843928064
author Shokal, Upasana
Yadav, Shruti
Atri, Jaishri
Accetta, Julia
Kenney, Eric
Banks, Katherine
Katakam, Akash
Jaenike, John
Eleftherianos, Ioannis
author_facet Shokal, Upasana
Yadav, Shruti
Atri, Jaishri
Accetta, Julia
Kenney, Eric
Banks, Katherine
Katakam, Akash
Jaenike, John
Eleftherianos, Ioannis
author_sort Shokal, Upasana
collection PubMed
description BACKGROUND: Symbiotic interactions between microbes and animals are common in nature. Symbiotic organisms are particularly common in insects and, in some cases, they may protect their hosts from pathogenic infections. Wolbachia and Spiroplasma endosymbionts naturally inhabit various insects including Drosophila melanogaster fruit flies. Therefore, this symbiotic association is considered an excellent model to investigate whether endosymbiotic bacteria participate in host immune processes against certain pathogens. Here we have investigated whether the presence of Wolbachia alone or together with Spiroplasma endosymbionts in D. melanogaster adult flies affects the immune response against the virulent insect pathogen Photorhabdus luminescens and against non-pathogenic Escherichia coli bacteria. RESULTS: We found that D. melanogaster flies carrying no endosymbionts, those carrying both Wolbachia and Spiroplasma, and those containing Wolbachia only had similar survival rates after infection with P. luminescens or Escherichia coli bacteria. However, flies carrying both endosymbionts or Wolbachia only contained higher numbers of E. coli cells at early time-points post infection than flies without endosymbiotic bacteria. Interestingly, flies containing Wolbachia only had lower titers of this endosymbiont upon infection with the pathogen P. luminescens than uninfected flies of the same strain. We further found that the presence of Wolbachia and Spiroplasma in D. melanogaster up-regulated certain immune-related genes upon infection with P. luminescens or E. coli bacteria, but it failed to alter the phagocytic ability of the flies toward E. coli inactive bioparticles. CONCLUSION: Our results suggest that the presence of Wolbachia and Spiroplasma in D. melanogaster can modulate immune signaling against infection by certain insect pathogenic and non-pathogenic bacteria. Results from such studies are important for understanding the molecular basis of the interactions between endosymbiotic bacteria of insects and exogenous microbes.
format Online
Article
Text
id pubmed-4746768
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-47467682016-02-10 Effects of co-occurring Wolbachia and Spiroplasma endosymbionts on the Drosophila immune response against insect pathogenic and non-pathogenic bacteria Shokal, Upasana Yadav, Shruti Atri, Jaishri Accetta, Julia Kenney, Eric Banks, Katherine Katakam, Akash Jaenike, John Eleftherianos, Ioannis BMC Microbiol Research Article BACKGROUND: Symbiotic interactions between microbes and animals are common in nature. Symbiotic organisms are particularly common in insects and, in some cases, they may protect their hosts from pathogenic infections. Wolbachia and Spiroplasma endosymbionts naturally inhabit various insects including Drosophila melanogaster fruit flies. Therefore, this symbiotic association is considered an excellent model to investigate whether endosymbiotic bacteria participate in host immune processes against certain pathogens. Here we have investigated whether the presence of Wolbachia alone or together with Spiroplasma endosymbionts in D. melanogaster adult flies affects the immune response against the virulent insect pathogen Photorhabdus luminescens and against non-pathogenic Escherichia coli bacteria. RESULTS: We found that D. melanogaster flies carrying no endosymbionts, those carrying both Wolbachia and Spiroplasma, and those containing Wolbachia only had similar survival rates after infection with P. luminescens or Escherichia coli bacteria. However, flies carrying both endosymbionts or Wolbachia only contained higher numbers of E. coli cells at early time-points post infection than flies without endosymbiotic bacteria. Interestingly, flies containing Wolbachia only had lower titers of this endosymbiont upon infection with the pathogen P. luminescens than uninfected flies of the same strain. We further found that the presence of Wolbachia and Spiroplasma in D. melanogaster up-regulated certain immune-related genes upon infection with P. luminescens or E. coli bacteria, but it failed to alter the phagocytic ability of the flies toward E. coli inactive bioparticles. CONCLUSION: Our results suggest that the presence of Wolbachia and Spiroplasma in D. melanogaster can modulate immune signaling against infection by certain insect pathogenic and non-pathogenic bacteria. Results from such studies are important for understanding the molecular basis of the interactions between endosymbiotic bacteria of insects and exogenous microbes. BioMed Central 2016-02-09 /pmc/articles/PMC4746768/ /pubmed/26862076 http://dx.doi.org/10.1186/s12866-016-0634-6 Text en © Shokal et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Shokal, Upasana
Yadav, Shruti
Atri, Jaishri
Accetta, Julia
Kenney, Eric
Banks, Katherine
Katakam, Akash
Jaenike, John
Eleftherianos, Ioannis
Effects of co-occurring Wolbachia and Spiroplasma endosymbionts on the Drosophila immune response against insect pathogenic and non-pathogenic bacteria
title Effects of co-occurring Wolbachia and Spiroplasma endosymbionts on the Drosophila immune response against insect pathogenic and non-pathogenic bacteria
title_full Effects of co-occurring Wolbachia and Spiroplasma endosymbionts on the Drosophila immune response against insect pathogenic and non-pathogenic bacteria
title_fullStr Effects of co-occurring Wolbachia and Spiroplasma endosymbionts on the Drosophila immune response against insect pathogenic and non-pathogenic bacteria
title_full_unstemmed Effects of co-occurring Wolbachia and Spiroplasma endosymbionts on the Drosophila immune response against insect pathogenic and non-pathogenic bacteria
title_short Effects of co-occurring Wolbachia and Spiroplasma endosymbionts on the Drosophila immune response against insect pathogenic and non-pathogenic bacteria
title_sort effects of co-occurring wolbachia and spiroplasma endosymbionts on the drosophila immune response against insect pathogenic and non-pathogenic bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746768/
https://www.ncbi.nlm.nih.gov/pubmed/26862076
http://dx.doi.org/10.1186/s12866-016-0634-6
work_keys_str_mv AT shokalupasana effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria
AT yadavshruti effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria
AT atrijaishri effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria
AT accettajulia effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria
AT kenneyeric effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria
AT bankskatherine effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria
AT katakamakash effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria
AT jaenikejohn effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria
AT eleftherianosioannis effectsofcooccurringwolbachiaandspiroplasmaendosymbiontsonthedrosophilaimmuneresponseagainstinsectpathogenicandnonpathogenicbacteria