Contrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster.

Although host-parasitoid interactions are becoming well characterized at the organismal and cellular levels, much remains to be understood of the molecular bases for the host immune response and the parasitoids' ability to defeat this immune response. Leptopilina boulardi and L. heterotoma, two...

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Autores principales: Todd A Schlenke, Jorge Morales, Shubha Govind, Andrew G Clark
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Publicado: Public Library of Science (PLoS) 2007
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spelling oai:doaj.org-article:679149fa42084df0bcfc9b2ef92a35912021-11-25T05:46:21ZContrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster.1553-73661553-737410.1371/journal.ppat.0030158https://doaj.org/article/679149fa42084df0bcfc9b2ef92a35912007-10-01T00:00:00Zhttps://doi.org/10.1371/journal.ppat.0030158https://doaj.org/toc/1553-7366https://doaj.org/toc/1553-7374Although host-parasitoid interactions are becoming well characterized at the organismal and cellular levels, much remains to be understood of the molecular bases for the host immune response and the parasitoids' ability to defeat this immune response. Leptopilina boulardi and L. heterotoma, two closely related, highly infectious natural parasitoids of Drosophila melanogaster, appear to use very different infection strategies at the cellular level. Here, we further characterize cellular level differences in the infection characteristics of these two wasp species using newly derived, virulent inbred strains, and then use whole genome microarrays to compare the transcriptional response of Drosophila to each. While flies attacked by the melanogaster group specialist L. boulardi (strain Lb17) up-regulate numerous genes encoding proteolytic enzymes, components of the Toll and JAK/STAT pathways, and the melanization cascade as part of a combined cellular and humoral innate immune response, flies attacked by the generalist L. heterotoma (strain Lh14) do not appear to initiate an immune transcriptional response at the time points post-infection we assayed, perhaps due to the rapid venom-mediated lysis of host hemocytes (blood cells). Thus, the specialist parasitoid appears to invoke a full-blown immune response in the host, but suppresses and/or evades downstream components of this response. Given that activation of the host immune response likely depletes the energetic resources of the host, the specialist's infection strategy seems relatively disadvantageous. However, we uncover the mechanism for one potentially important fitness tradeoff of the generalist's highly immune suppressive infection strategy.Todd A SchlenkeJorge MoralesShubha GovindAndrew G ClarkPublic Library of Science (PLoS)articleImmunologic diseases. AllergyRC581-607Biology (General)QH301-705.5ENPLoS Pathogens, Vol 3, Iss 10, Pp 1486-1501 (2007)
institution DOAJ
collection DOAJ
language EN
topic Immunologic diseases. Allergy
RC581-607
Biology (General)
QH301-705.5
spellingShingle Immunologic diseases. Allergy
RC581-607
Biology (General)
QH301-705.5
Todd A Schlenke
Jorge Morales
Shubha Govind
Andrew G Clark
Contrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster.
description Although host-parasitoid interactions are becoming well characterized at the organismal and cellular levels, much remains to be understood of the molecular bases for the host immune response and the parasitoids' ability to defeat this immune response. Leptopilina boulardi and L. heterotoma, two closely related, highly infectious natural parasitoids of Drosophila melanogaster, appear to use very different infection strategies at the cellular level. Here, we further characterize cellular level differences in the infection characteristics of these two wasp species using newly derived, virulent inbred strains, and then use whole genome microarrays to compare the transcriptional response of Drosophila to each. While flies attacked by the melanogaster group specialist L. boulardi (strain Lb17) up-regulate numerous genes encoding proteolytic enzymes, components of the Toll and JAK/STAT pathways, and the melanization cascade as part of a combined cellular and humoral innate immune response, flies attacked by the generalist L. heterotoma (strain Lh14) do not appear to initiate an immune transcriptional response at the time points post-infection we assayed, perhaps due to the rapid venom-mediated lysis of host hemocytes (blood cells). Thus, the specialist parasitoid appears to invoke a full-blown immune response in the host, but suppresses and/or evades downstream components of this response. Given that activation of the host immune response likely depletes the energetic resources of the host, the specialist's infection strategy seems relatively disadvantageous. However, we uncover the mechanism for one potentially important fitness tradeoff of the generalist's highly immune suppressive infection strategy.
format article
author Todd A Schlenke
Jorge Morales
Shubha Govind
Andrew G Clark
author_facet Todd A Schlenke
Jorge Morales
Shubha Govind
Andrew G Clark
author_sort Todd A Schlenke
title Contrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster.
title_short Contrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster.
title_full Contrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster.
title_fullStr Contrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster.
title_full_unstemmed Contrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster.
title_sort contrasting infection strategies in generalist and specialist wasp parasitoids of drosophila melanogaster.
publisher Public Library of Science (PLoS)
publishDate 2007
url https://doaj.org/article/679149fa42084df0bcfc9b2ef92a3591
work_keys_str_mv AT toddaschlenke contrastinginfectionstrategiesingeneralistandspecialistwaspparasitoidsofdrosophilamelanogaster
AT jorgemorales contrastinginfectionstrategiesingeneralistandspecialistwaspparasitoidsofdrosophilamelanogaster
AT shubhagovind contrastinginfectionstrategiesingeneralistandspecialistwaspparasitoidsofdrosophilamelanogaster
AT andrewgclark contrastinginfectionstrategiesingeneralistandspecialistwaspparasitoidsofdrosophilamelanogaster
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