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Identification of Drosophila Mutants Affecting Defense to an Entomopathogenic Fungus

Fungi cause the majority of insect disease. However, to date attempts to model host–fungal interactions with Drosophila have focused on opportunistic human pathogens. Here, we performed a screen of 2,613 mutant Drosophila lines to identify host genes affecting susceptibility to the natural insect pa...

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Autores principales: Lu, Hsiao-Ling, Wang, Jonathan B., Brown, Markus A., Euerle, Christopher, St. Leger, Raymond J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511952/
https://www.ncbi.nlm.nih.gov/pubmed/26202798
http://dx.doi.org/10.1038/srep12350
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author Lu, Hsiao-Ling
Wang, Jonathan B.
Brown, Markus A.
Euerle, Christopher
St. Leger, Raymond J.
author_facet Lu, Hsiao-Ling
Wang, Jonathan B.
Brown, Markus A.
Euerle, Christopher
St. Leger, Raymond J.
author_sort Lu, Hsiao-Ling
collection PubMed
description Fungi cause the majority of insect disease. However, to date attempts to model host–fungal interactions with Drosophila have focused on opportunistic human pathogens. Here, we performed a screen of 2,613 mutant Drosophila lines to identify host genes affecting susceptibility to the natural insect pathogen Metarhizium anisopliae (Ma549). Overall, 241 (9.22%) mutant lines had altered resistance to Ma549. Life spans ranged from 3.0 to 6.2 days, with females being more susceptible than males in all lines. Speed of kill correlated with within-host growth and onset of sporulation, but total spore production is decoupled from host genotypes. Results showed that mutations affected the ability of Drosophila to restrain rather than tolerate infections and suggested trade-offs between antifungal and antibacterial genes affecting cuticle and gut structural barriers. Approximately, 13% of mutations where in genes previously associated with host pathogen interactions. These encoded fast-acting immune responses including coagulation, phagocytosis, encapsulation and melanization but not the slow-response induction of anti-fungal peptides. The non-immune genes impact a wide variety of biological functions, including behavioral traits. Many have human orthologs already implicated in human disorders; while others were mutations in protein and non-protein coding genes for which disease resistance was the first biological annotation.
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spelling pubmed-45119522015-07-28 Identification of Drosophila Mutants Affecting Defense to an Entomopathogenic Fungus Lu, Hsiao-Ling Wang, Jonathan B. Brown, Markus A. Euerle, Christopher St. Leger, Raymond J. Sci Rep Article Fungi cause the majority of insect disease. However, to date attempts to model host–fungal interactions with Drosophila have focused on opportunistic human pathogens. Here, we performed a screen of 2,613 mutant Drosophila lines to identify host genes affecting susceptibility to the natural insect pathogen Metarhizium anisopliae (Ma549). Overall, 241 (9.22%) mutant lines had altered resistance to Ma549. Life spans ranged from 3.0 to 6.2 days, with females being more susceptible than males in all lines. Speed of kill correlated with within-host growth and onset of sporulation, but total spore production is decoupled from host genotypes. Results showed that mutations affected the ability of Drosophila to restrain rather than tolerate infections and suggested trade-offs between antifungal and antibacterial genes affecting cuticle and gut structural barriers. Approximately, 13% of mutations where in genes previously associated with host pathogen interactions. These encoded fast-acting immune responses including coagulation, phagocytosis, encapsulation and melanization but not the slow-response induction of anti-fungal peptides. The non-immune genes impact a wide variety of biological functions, including behavioral traits. Many have human orthologs already implicated in human disorders; while others were mutations in protein and non-protein coding genes for which disease resistance was the first biological annotation. Nature Publishing Group 2015-07-23 /pmc/articles/PMC4511952/ /pubmed/26202798 http://dx.doi.org/10.1038/srep12350 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lu, Hsiao-Ling
Wang, Jonathan B.
Brown, Markus A.
Euerle, Christopher
St. Leger, Raymond J.
Identification of Drosophila Mutants Affecting Defense to an Entomopathogenic Fungus
title Identification of Drosophila Mutants Affecting Defense to an Entomopathogenic Fungus
title_full Identification of Drosophila Mutants Affecting Defense to an Entomopathogenic Fungus
title_fullStr Identification of Drosophila Mutants Affecting Defense to an Entomopathogenic Fungus
title_full_unstemmed Identification of Drosophila Mutants Affecting Defense to an Entomopathogenic Fungus
title_short Identification of Drosophila Mutants Affecting Defense to an Entomopathogenic Fungus
title_sort identification of drosophila mutants affecting defense to an entomopathogenic fungus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511952/
https://www.ncbi.nlm.nih.gov/pubmed/26202798
http://dx.doi.org/10.1038/srep12350
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