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Intensity of Mutualism Breakdown Is Determined by Temperature Not Amplification of Wolbachia Genes
Wolbachia are maternally transmitted intracellular bacterial symbionts that infect approximately 40% of all insect species. Though several strains of Wolbachia naturally infect Drosophila melanogaster and provide resistance against viral pathogens, or provision metabolites during periods of nutritio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035075/ https://www.ncbi.nlm.nih.gov/pubmed/27661080 http://dx.doi.org/10.1371/journal.ppat.1005888 |
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author | Rohrscheib, Chelsie E. Frentiu, Francesca D. Horn, Emilie Ritchie, Fiona K. van Swinderen, Bruno Weible, Michael W. O’Neill, Scott L. Brownlie, Jeremy C. |
author_facet | Rohrscheib, Chelsie E. Frentiu, Francesca D. Horn, Emilie Ritchie, Fiona K. van Swinderen, Bruno Weible, Michael W. O’Neill, Scott L. Brownlie, Jeremy C. |
author_sort | Rohrscheib, Chelsie E. |
collection | PubMed |
description | Wolbachia are maternally transmitted intracellular bacterial symbionts that infect approximately 40% of all insect species. Though several strains of Wolbachia naturally infect Drosophila melanogaster and provide resistance against viral pathogens, or provision metabolites during periods of nutritional stress, one virulent strain, wMelPop, reduces fly lifespan by half, possibly as a consequence of over-replication. While the mechanisms that allow wMelPop to over-replicate are still of debate, a unique tandem repeat locus in the wMelPop genome that contains eight genes, referred to as the “Octomom” locus has been identified and is thought to play an important regulatory role. Estimates of Octomom locus copy number correlated increasing copy number to both Wolbachia bacterial density and increased pathology. Here we demonstrate that infected fly pathology is not dependent on an increased Octomom copy number, but does strongly correlate with increasing temperature. When measured across developmental time, we also show Octomom copy number to be highly variable across developmental time within a single generation. Using a second pathogenic strain of Wolbachia, we further demonstrate reduced insect lifespan can occur independently of a high Octomom locus copy number. Taken together, this data demonstrates that the mechanism/s of wMelPop virulence is more complex than has been previously described. |
format | Online Article Text |
id | pubmed-5035075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50350752016-10-10 Intensity of Mutualism Breakdown Is Determined by Temperature Not Amplification of Wolbachia Genes Rohrscheib, Chelsie E. Frentiu, Francesca D. Horn, Emilie Ritchie, Fiona K. van Swinderen, Bruno Weible, Michael W. O’Neill, Scott L. Brownlie, Jeremy C. PLoS Pathog Research Article Wolbachia are maternally transmitted intracellular bacterial symbionts that infect approximately 40% of all insect species. Though several strains of Wolbachia naturally infect Drosophila melanogaster and provide resistance against viral pathogens, or provision metabolites during periods of nutritional stress, one virulent strain, wMelPop, reduces fly lifespan by half, possibly as a consequence of over-replication. While the mechanisms that allow wMelPop to over-replicate are still of debate, a unique tandem repeat locus in the wMelPop genome that contains eight genes, referred to as the “Octomom” locus has been identified and is thought to play an important regulatory role. Estimates of Octomom locus copy number correlated increasing copy number to both Wolbachia bacterial density and increased pathology. Here we demonstrate that infected fly pathology is not dependent on an increased Octomom copy number, but does strongly correlate with increasing temperature. When measured across developmental time, we also show Octomom copy number to be highly variable across developmental time within a single generation. Using a second pathogenic strain of Wolbachia, we further demonstrate reduced insect lifespan can occur independently of a high Octomom locus copy number. Taken together, this data demonstrates that the mechanism/s of wMelPop virulence is more complex than has been previously described. Public Library of Science 2016-09-23 /pmc/articles/PMC5035075/ /pubmed/27661080 http://dx.doi.org/10.1371/journal.ppat.1005888 Text en © 2016 Rohrscheib et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rohrscheib, Chelsie E. Frentiu, Francesca D. Horn, Emilie Ritchie, Fiona K. van Swinderen, Bruno Weible, Michael W. O’Neill, Scott L. Brownlie, Jeremy C. Intensity of Mutualism Breakdown Is Determined by Temperature Not Amplification of Wolbachia Genes |
title | Intensity of Mutualism Breakdown Is Determined by Temperature Not Amplification of Wolbachia Genes |
title_full | Intensity of Mutualism Breakdown Is Determined by Temperature Not Amplification of Wolbachia Genes |
title_fullStr | Intensity of Mutualism Breakdown Is Determined by Temperature Not Amplification of Wolbachia Genes |
title_full_unstemmed | Intensity of Mutualism Breakdown Is Determined by Temperature Not Amplification of Wolbachia Genes |
title_short | Intensity of Mutualism Breakdown Is Determined by Temperature Not Amplification of Wolbachia Genes |
title_sort | intensity of mutualism breakdown is determined by temperature not amplification of wolbachia genes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035075/ https://www.ncbi.nlm.nih.gov/pubmed/27661080 http://dx.doi.org/10.1371/journal.ppat.1005888 |
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