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Fundamental biological adaptations underlying persister formation and multi-stress tolerance in Mycobacterium abscessus and their impact on host-pathogen interactions

Project description

Targeting bacterial persisters to combat antimicrobial resistance

Bacteria live in communities and employ various strategies to ensure viability. A bacterial subpopulation called persisters can withstand temporary stresses such as antibiotics, nutrient depletion, or acidic environments. Clinical evidence indicates that persisters can regrow once antibiotic treatment stops, driving chronic and relapsing infections while accelerating the evolution of resistance. With the support of the Marie Skłodowska-Curie Actions programme, the MabADAPT project aims to uncover the biological mechanisms behind persister formation and their role in host-pathogen interactions. Researchers will study Mycobacterium abscessus as a clinically relevant model, following a multidisciplinary approach. Project findings could lead to novel strategies against antimicrobial resistance.

Objective

The rapid spread of bacterial antimicrobial resistance (AMR) poses a major global health threat, leading to treatment failures. Beyond resistance, bacteria employ also other strategies to counteract antibiotics. Persisters represent a bacterial subpopulation that can survive transient exposure to different stresses, such as nutrient depletion, low pH or the presence of antibiotics. Increasing evidence suggests clinical importance of persister formation, since their ability to regrow after termination of antibiotic treatment is a cause for prolonged and relapsing course of many bacterial infections. Formation of persisters also accelerates the emergence of antibiotic resistance, worsening the problem of bacterial AMR. Recent research indicates that mechanisms involved in persister formation may also enhance the overall adaptability of bacteria to antibiotics and stresses imposed by host immune system. Targeting these dual mechanisms could represent a unique two-pronged strategy to improve treatment efficiency, preventing resistance development and decreasing bacterial survival within the host. However, our understanding of these mechanisms is very limited. Combining microbiology, molecular biology and infection models, together with cutting-edge techniques such as metabolomics and transcriptomics, I propose to identify key biological adaptations underlying the formation of bacterial persisters and to explore their impact on host-pathogen interactions and infection outcomes. As an emerging pathogen known for its high antibiotic resistance and ability to endure harsh conditions during infection, I selected Mycobacterium abscessus (Mabs) as a clinically relevant model for this study. Discovery of such adaptations can lead to the development of innovative treatments tackling not only Mabs infections, but also the broader challenge of AMR.

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Topic(s)

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HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

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Call for proposal

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(opens in new window) HORIZON-MSCA-2024-PF-01

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Coordinator

CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 226 420,56
Address
RUE MICHEL ANGE 3
75794 PARIS
France

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Ile-de-France Ile-de-France Paris
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Research Organisations
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