Document Detail


Genetic ablation of Drosophila phagocytes reveals their contribution to both development and resistance to bacterial infection.
MedLine Citation:
PMID:  20375589     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Drosophila phagocytes participate in development and immune responses through their abilities to perform phagocytosis and/or secrete extra-cellular matrix components, antimicrobial peptides, clotting factors and signalling molecules. However, our knowledge of their functional impact on development and host resistance to infection is limited. To address this, we have used a genetic cell ablation strategy to generate Drosophila individuals lacking functional phagocytes. Our results highlight the essential contribution of phagocytes to embryonic development including central nervous system morphogenesis. Phagocytes also ensure optimal viability during post-embryonic development through immune functions. The use of phagocyte-depleted flies reveals the contribution of phagocytes in the resistance of Drosophila adults upon systemic infections with specific bacteria. Phagocytes were not involved in the expression of antimicrobial peptides by the fat body indicating a clear separation between cellular and humoral immune responses at this stage. Finally, we confirm that phagocytosis is a critical effector mechanism of the cellular arm by demonstrating that phagocytosis contributes to resistance to infection with Staphylococcus aureus in adults. Our results highlight the power of this cell ablation strategy to reveal the contribution of phagocytes to specific biological processes. We now provide a blueprint of phagocyte importance during both development and innate immune responses in Drosophila.
Authors:
Arnaud Defaye; Iwan Evans; Michèle Crozatier; Will Wood; Bruno Lemaitre; François Leulier
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-04-01
Journal Detail:
Title:  Journal of innate immunity     Volume:  1     ISSN:  1662-8128     ISO Abbreviation:  J Innate Immun     Publication Date:  2009  
Date Detail:
Created Date:  2010-04-08     Completed Date:  2010-08-05     Revised Date:  2011-11-04    
Medline Journal Info:
Nlm Unique ID:  101469471     Medline TA:  J Innate Immun     Country:  Switzerland    
Other Details:
Languages:  eng     Pagination:  322-34     Citation Subset:  IM    
Copyright Information:
Copyright 2009 S. Karger AG, Basel.
Affiliation:
Centre de Génétique Moléculaire, CNRS FRE 3144, Gif sur Yvette, France.
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MeSH Terms
Descriptor/Qualifier:
Animals
Central Nervous System / embryology
Drosophila melanogaster / embryology,  immunology*,  microbiology*
Female
Phagocytes / immunology*
Phagocytosis / genetics,  immunology*
Phagosomes / genetics,  immunology
Staphylococcus aureus / immunology
Grant Support
ID/Acronym/Agency:
//Wellcome Trust

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