Short-term starvation of immune deficient Drosophila improves survival to gram-negative bacterial infections.

BACKGROUND: Primary immunodeficiencies are inborn errors of immunity that lead to life threatening conditions. These predispositions describe human immunity in natura and highlight the important function of components of the Toll-IL-1- receptor-nuclear factor kappa B (TIR-NF-kappaB) pathway. Since...

Full description

Bibliographic Details
Main Authors: Brown, A, Baumbach, J, Cook, P, Ligoxygakis, P
Format: Journal article
Language:English
Published: Public Library of Science 2009
_version_ 1797096597564162048
author Brown, A
Baumbach, J
Cook, P
Ligoxygakis, P
author_facet Brown, A
Baumbach, J
Cook, P
Ligoxygakis, P
author_sort Brown, A
collection OXFORD
description BACKGROUND: Primary immunodeficiencies are inborn errors of immunity that lead to life threatening conditions. These predispositions describe human immunity in natura and highlight the important function of components of the Toll-IL-1- receptor-nuclear factor kappa B (TIR-NF-kappaB) pathway. Since the TIR-NF-kappaB circuit is a conserved component of the host defence in higher animals, genetically tractable models may contribute ideas for clinical interventions. METHODOLOGY/PRINCIPAL FINDINGS: We used immunodeficient fruit flies (Drosophila melanogaster) to address questions pertaining to survival following bacterial infection. We describe here that flies lacking the NF-kappaB protein Relish, indispensable for countering Gram-negative bacteria, had a greatly improved survival to such infections when subject to dietary short-term starvation (STS) prior to immune challenge. STS induced the release of Nitric Oxide (NO), a potent molecule against pathogens in flies, mice and humans. Administering the NO Synthase-inhibitory arginine analog N-Nitro-L-Arginine-Methyl-Ester (L-NAME) but not its inactive enantiomer D-NAME increased once again sensitivity to infection to levels expected for relish mutants. Surprisingly, NO signalling required the NF-kappaB protein Dif, usually needed for responses against Gram-positive bacteria. CONCLUSIONS/SIGNIFICANCE: Our results show that NO release through STS may reflect an evolutionary conserved process. Moreover, STS could be explored to address immune phenotypes related to infection and may offer ways to boost natural immunity.
first_indexed 2024-03-07T04:44:07Z
format Journal article
id oxford-uuid:d2a6af61-369b-4cca-bc97-4ab9c71759a0
institution University of Oxford
language English
last_indexed 2024-03-07T04:44:07Z
publishDate 2009
publisher Public Library of Science
record_format dspace
spelling oxford-uuid:d2a6af61-369b-4cca-bc97-4ab9c71759a02022-03-27T08:05:35ZShort-term starvation of immune deficient Drosophila improves survival to gram-negative bacterial infections.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d2a6af61-369b-4cca-bc97-4ab9c71759a0EnglishSymplectic Elements at OxfordPublic Library of Science2009Brown, ABaumbach, JCook, PLigoxygakis, P BACKGROUND: Primary immunodeficiencies are inborn errors of immunity that lead to life threatening conditions. These predispositions describe human immunity in natura and highlight the important function of components of the Toll-IL-1- receptor-nuclear factor kappa B (TIR-NF-kappaB) pathway. Since the TIR-NF-kappaB circuit is a conserved component of the host defence in higher animals, genetically tractable models may contribute ideas for clinical interventions. METHODOLOGY/PRINCIPAL FINDINGS: We used immunodeficient fruit flies (Drosophila melanogaster) to address questions pertaining to survival following bacterial infection. We describe here that flies lacking the NF-kappaB protein Relish, indispensable for countering Gram-negative bacteria, had a greatly improved survival to such infections when subject to dietary short-term starvation (STS) prior to immune challenge. STS induced the release of Nitric Oxide (NO), a potent molecule against pathogens in flies, mice and humans. Administering the NO Synthase-inhibitory arginine analog N-Nitro-L-Arginine-Methyl-Ester (L-NAME) but not its inactive enantiomer D-NAME increased once again sensitivity to infection to levels expected for relish mutants. Surprisingly, NO signalling required the NF-kappaB protein Dif, usually needed for responses against Gram-positive bacteria. CONCLUSIONS/SIGNIFICANCE: Our results show that NO release through STS may reflect an evolutionary conserved process. Moreover, STS could be explored to address immune phenotypes related to infection and may offer ways to boost natural immunity.
spellingShingle Brown, A
Baumbach, J
Cook, P
Ligoxygakis, P
Short-term starvation of immune deficient Drosophila improves survival to gram-negative bacterial infections.
title Short-term starvation of immune deficient Drosophila improves survival to gram-negative bacterial infections.
title_full Short-term starvation of immune deficient Drosophila improves survival to gram-negative bacterial infections.
title_fullStr Short-term starvation of immune deficient Drosophila improves survival to gram-negative bacterial infections.
title_full_unstemmed Short-term starvation of immune deficient Drosophila improves survival to gram-negative bacterial infections.
title_short Short-term starvation of immune deficient Drosophila improves survival to gram-negative bacterial infections.
title_sort short term starvation of immune deficient drosophila improves survival to gram negative bacterial infections
work_keys_str_mv AT browna shorttermstarvationofimmunedeficientdrosophilaimprovessurvivaltogramnegativebacterialinfections
AT baumbachj shorttermstarvationofimmunedeficientdrosophilaimprovessurvivaltogramnegativebacterialinfections
AT cookp shorttermstarvationofimmunedeficientdrosophilaimprovessurvivaltogramnegativebacterialinfections
AT ligoxygakisp shorttermstarvationofimmunedeficientdrosophilaimprovessurvivaltogramnegativebacterialinfections