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Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans

Drosophila C virus (DCV) is a natural pathogen of Drosophila and a useful model for studying antiviral defences. The Drosophila host is also commonly infected with the widespread endosymbiotic bacteria Wolbachia pipientis. When DCV coinfects Wolbachia-infected D. melanogaster, virus particles accumu...

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Autores principales: Osborne, Sheree E., Leong, Yi San, O'Neill, Scott L., Johnson, Karyn N.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768908/
https://www.ncbi.nlm.nih.gov/pubmed/19911047
http://dx.doi.org/10.1371/journal.ppat.1000656
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author Osborne, Sheree E.
Leong, Yi San
O'Neill, Scott L.
Johnson, Karyn N.
author_facet Osborne, Sheree E.
Leong, Yi San
O'Neill, Scott L.
Johnson, Karyn N.
author_sort Osborne, Sheree E.
collection PubMed
description Drosophila C virus (DCV) is a natural pathogen of Drosophila and a useful model for studying antiviral defences. The Drosophila host is also commonly infected with the widespread endosymbiotic bacteria Wolbachia pipientis. When DCV coinfects Wolbachia-infected D. melanogaster, virus particles accumulate more slowly and virus induced mortality is substantially delayed. Considering that Wolbachia is estimated to infect up to two-thirds of all insect species, the observed protective effects of Wolbachia may extend to a range of both beneficial and pest insects, including insects that vector important viral diseases of humans, animals and plants. Currently, Wolbachia-mediated antiviral protection has only been described from a limited number of very closely related strains that infect D. melanogaster. We used D. simulans and its naturally occurring Wolbachia infections to test the generality of the Wolbachia-mediated antiviral protection. We generated paired D. simulans lines either uninfected or infected with five different Wolbachia strains. Each paired fly line was challenged with DCV and Flock House virus. Significant antiviral protection was seen for some but not all of the Wolbachia strain-fly line combinations tested. In some cases, protection from virus-induced mortality was associated with a delay in virus accumulation, but some Wolbachia-infected flies were tolerant to high titres of DCV. The Wolbachia strains that did protect occurred at comparatively high density within the flies and were most closely related to the D. melanogaster Wolbachia strain wMel. These results indicate that Wolbachia-mediated antiviral protection is not ubiquitous, a finding that is important for understanding the distribution of Wolbachia and virus in natural insect populations.
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spelling pubmed-27689082009-11-13 Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans Osborne, Sheree E. Leong, Yi San O'Neill, Scott L. Johnson, Karyn N. PLoS Pathog Research Article Drosophila C virus (DCV) is a natural pathogen of Drosophila and a useful model for studying antiviral defences. The Drosophila host is also commonly infected with the widespread endosymbiotic bacteria Wolbachia pipientis. When DCV coinfects Wolbachia-infected D. melanogaster, virus particles accumulate more slowly and virus induced mortality is substantially delayed. Considering that Wolbachia is estimated to infect up to two-thirds of all insect species, the observed protective effects of Wolbachia may extend to a range of both beneficial and pest insects, including insects that vector important viral diseases of humans, animals and plants. Currently, Wolbachia-mediated antiviral protection has only been described from a limited number of very closely related strains that infect D. melanogaster. We used D. simulans and its naturally occurring Wolbachia infections to test the generality of the Wolbachia-mediated antiviral protection. We generated paired D. simulans lines either uninfected or infected with five different Wolbachia strains. Each paired fly line was challenged with DCV and Flock House virus. Significant antiviral protection was seen for some but not all of the Wolbachia strain-fly line combinations tested. In some cases, protection from virus-induced mortality was associated with a delay in virus accumulation, but some Wolbachia-infected flies were tolerant to high titres of DCV. The Wolbachia strains that did protect occurred at comparatively high density within the flies and were most closely related to the D. melanogaster Wolbachia strain wMel. These results indicate that Wolbachia-mediated antiviral protection is not ubiquitous, a finding that is important for understanding the distribution of Wolbachia and virus in natural insect populations. Public Library of Science 2009-11-13 /pmc/articles/PMC2768908/ /pubmed/19911047 http://dx.doi.org/10.1371/journal.ppat.1000656 Text en Osborne 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
Osborne, Sheree E.
Leong, Yi San
O'Neill, Scott L.
Johnson, Karyn N.
Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans
title Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans
title_full Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans
title_fullStr Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans
title_full_unstemmed Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans
title_short Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans
title_sort variation in antiviral protection mediated by different wolbachia strains in drosophila simulans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768908/
https://www.ncbi.nlm.nih.gov/pubmed/19911047
http://dx.doi.org/10.1371/journal.ppat.1000656
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