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mARs SIGNED

mARs: Mobile DNA driven antibiotic resistance spreading: molecular strategies, control and evolution for broad distribution

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 mARs project word cloud

Explore the words cloud of the mARs project. It provides you a very rough idea of what is the project "mARs" about.

spread    superbugs    biochemistry    insights    genomic    resort    resistance    drive    microbial    environments    sparse    elucidate    mobile    functional    communities    confer    mechanisms    drugs    bioinformatics    rare    unclear    promiscuous    resistant    bioinformatic    functionally    limited    significance    prevalence    annotated    movies    protein    transfer    clinical    underlying    cells    quests    carriers    meta    hotspots    transposons    mechanistic    situ    disciplines    antibiotic    reveal    bridging    interaction    genetics    vitro    molecular    bacteria    virulent    strategies    spreading    determinants    biology    gut    evolution    genes    interplay    movement    draw    multidrug    intervention    occurs    implications    dissect    machineries    biochemical    bacterial    data    drug    structural    model    chart    regulation    integrons    pathogens    microbiology    dna    view    era    reducing    humans    last    ar    natural    gene    health    gained    diversity    combining    structure    preventive    broad    care    promotes   

Project "mARs" data sheet

The following table provides information about the project.

Coordinator
EUROPEAN MOLECULAR BIOLOGY LABORATORY 

Organization address
address: Meyerhofstrasse 1
city: HEIDELBERG
postcode: 69117
website: http://www.embl.de

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 1˙999˙118 €
 EC max contribution 1˙999˙118 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-COG
 Funding Scheme ERC-COG
 Starting year 2021
 Duration (year-month-day) from 2021-01-01   to  2025-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    EUROPEAN MOLECULAR BIOLOGY LABORATORY DE (HEIDELBERG) coordinator 1˙999˙118.00

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 Project objective

Antibiotic resistance (AR) is spreading rapidly, leading to the development of highly virulent pathogens and multidrug-resistant ‘superbugs’, a major health concern of our era. Mobile DNA elements, transposons and integrons, effectively drive the spread of AR genes in microbial interaction hotspots, such as bacterial communities in humans and natural environments. Yet, our knowledge of their mechanisms remains very sparse. It is unclear how DNA movement occurs on the molecular level and how it is controlled in cells and communities; biochemical and structural data are rare and our view on their diversity and evolution is limited. Here I propose an integrated approach combining bioinformatics, genetics, microbiology, biochemistry, and structural biology to elucidate the mechanisms and diversity of mobile DNA driven resistance spreading. I want to (a) investigate the molecular mechanisms and regulation of AR gene movement in vitro, in model bacteria and in gut bacterial communities; (b) dissect the structure of the underlying molecular machineries to reveal how protein-DNA interplay promotes gene transfer; and (c) characterize the diversity, evolution and functional success of distinct molecular pathways. Mechanistic work will focus on selected mobile elements that confer resistance to last resort drugs and promiscuous gene carriers with high prevalence in health care. Bioinformatic quests will draw on recent (meta)genomic data to chart the clinical significance of molecular insights in situ. By bridging disciplines, I want to provide functionally annotated molecular movies of gene movement and explain how specific molecular strategies evolved to enable broad dissemination of resistance determinants. The insights gained in this research will provide in-depth knowledge on major AR transfer pathways and will have key implications for the development of novel intervention strategies and preventive measures aimed at reducing dissemination of drug resistance in bacteria.

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The information about "MARS" are provided by the European Opendata Portal: CORDIS opendata.

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