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Dernière mise à jour : Mai 2018

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Institut Sophia Agrobiotech

UMR INRA - Univ. Nice Sophia Antipolis - Cnrs

http://www.paca.inra.fr/institut-sophia-agrobiotech_eng/

Persistence of Bacillus thuringiensis spores : Impacts on innate immune response of non-target organisms

Vendredi 28 Mai à 11h00 - Sophia Antipolis - INRAE PACA - Visioconférence

Séminaire scientifique
For the scientific animation of this week at ISA, we will have the pleasure to listen to Salma Hachfi, PhD student of the BES team, who will present her work.

The presentation will be in english on Zoom:

https://univ-cotedazur.zoom.us/j/89486088416?pwd=d2Jkc0FEa1QxcllFTzR3MEhtdW9JQT09

 

ID de réunion : 894 8608 8416

Code secret : 343929

 

Pour vous connecter depuis un téléphone fixe:

1. Composer le +33 1 8699 5831

2. Entrer l'ID 894 8608 8416 puis #

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Abstract :

The Gram-positive sporulating bacterium Bacillus thuringiensis (Bt) is a worldwide used biopesticide to fight lepidopteran pests. Upon ingestion of Bt spores, target insects die in 3 days. The increasing environmental dispersion of Bt products raises the question about their potential risks on non-target animals. Indeed, Bt belongs to the phylogenetic group of B.cereus, the third cause of food poisoning in Europe and the second in France. Using Drosophila melanogaster, we have previously demonstrated that Bt vegetative cells are rapidly cleared from the intestine of non-target organisms. This rapid elimination is due to the activation of the local innate immune response in the anterior midgut (Benguettat et al., 2018). However, few studies suggest that Bt spores can persist in human and rodent guts (Oliviera-Filho et al., 2009, Wilcks et al., 2008). To understand why and how Bt/Bc spores persist in the gut of non-target organisms and the the innate immune response to the persistence of spores, we have used two powerful models: Drosophila melanogaster and mice. First, I showed that Bt/Bc spores can persist up to 10 days after acute contamination in the Drosophila gut and at least 48 hours in mouse intestine with severe diarrhea. These findings prompted me to further investigate the possible spore germination in the intestines. For this, I generated an innovative tool consisting in red fluorescent spores which once germinated fluoresce in green to mark vegetative bacteria. Using this tool, I showed that spores did not trigger any immune response in the anterior midgut while accumulating mainly in the posterior midgut where they could germinate. My data suggest that, in the posterior midgut, the innate immune response is inefficient to promptly eliminate germinated bacteria.  Finally, using in vitro culture of  mouse macrophages, I showed that Bt/Bc vegetative cells could activate the NLRP3 inflammasome pathway causing a high level of cells death. On the other side, spores were phagocytosed but did not activate the inflammasome pathway. Altogether, these data will help to understand why and how ingestion of Bt/Bc spores can trigger food poisoning. Moreover, my data suggest that Bt biopesticides could be responsible for unintended effects in non-target organisms.