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FERRANDON, D.

Publications and source records attributed to FERRANDON, D..

2 recordsLinked to original sources

Distinct Bomanins at the Drosophila 55C locus function in resistance and resilience to infections

Host defense against many Gram-positive bacteria and fungal pathogens is mainly provided by the Toll-dependent systemic immune response in Drosophila. While antimicrobial peptides active against these categories of pathogens contribute only modestly to protection, Bomanin peptides are major effectors of the Toll pathway. Remarkably, flies deleted for the 55C locus that contains 10 Bomanin genes are as sensitive as Toll pathway mutant flies to these infections. Yet, the exact functions of single Bomanins in resistance or resilience to infections remain poorly characterized. Here, we have extensively studied the role of these Bomanin genes. BomT1 functions in resistance to Enterococcus faecalis while playing a role in resilience against Metarhizium robertsii infection, like BomS2. BomT1 and BomT2 prevent the dissemination of Candida albicans throughout the host, even though they are not sufficient to confer protection to immunodeficient flies against this pathogen in survival experiments. Furthermore, BomT1 and BomBc1 mutants are sensitive to an Aspergillus fumigatus ribotoxin. We conclude that 55C Bomanins have defined albeit sometimes overlapping roles in the different facets of host defense against infections.

immunology↗

The BaramicinA gene is required at several steps of the host defense against Enterococcus faecalis and Metarhizium robertsii in a septic wound infection model in Drosophila melanogaster

The Drosophila systemic immune response against many Gram-positive bacteria and fungi is mediated by the Toll pathway. How Toll-regulated effectors actually fulfill this role remains poorly understood as the known antimicrobial peptide (AMP) genes it controls are essentially active only against filamentous fungi and not against Gram-positive bacteria or yeasts. BaramicinA gene expression is transcriptionally regulated by the Toll pathway. BaraA encodes a polyprotein precursor that releases processed proteins into the hemolymph upon immune challenge. Here, we demonstrate that BaraA is required specifically in the host defense against Enterococcus faecalis and against the entomopathogenic fungus Metarhizium robertsii. It does so by protecting the fly from the action of distinct toxins secreted by Gram-positive and fungal pathogens but not by directly attacking them. Thus, in complement to the current paradigm, innate immunity can cope with toxins, effectively, through the secretion of peptides that are not AMPs, independently of xenobiotics detoxification pathways.

immunology↗