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KryptonInt SIGNED

Erasing the superintegron to understand the role of chromosomal integrons in bacterial evolution

Total Cost €

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EC-Contrib. €

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Partnership

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 KryptonInt project word cloud

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

deleting    adaptability    genesis    causative    medicine    situation    antibiotic    mobility    cholerae    platforms    environment    scis    integrons    power    eons    toxin    sci    modern    bacteria    resistance    humans    pathogens    agent    inaccessible    deadliest    circulation    seqdelta    fundamental    functions    mi    exapted    sedentary    food    proof    good    mobile    preliminary    despite    paradigm    size    disease    chromosomes    extremely    located    understand    functional    bacterial    paradoxical    i3c    17    named    adaptive    threat    module    biosynthetic    stabilized    cassettes    giving    chromosomal    model    evolvability    context    chromosome    acquisition    gene    transposons    integron    cholera    explore    native    hundreds    nature    tool    evolution    association    antitoxin    interferes    historically    little    multidrug    found    background    genetic    stockpiling    history    si    acquired    experimental    performed    conjugative    kryptonint    precludes    animals    class    vibrio    126    plasmids    unravel    unexpected    kb    excellent    caused    superintegron    encoded    environmental    genes    elucidate    poorly   

Project "KryptonInt" data sheet

The following table provides information about the project.

Coordinator
UNIVERSIDAD COMPLUTENSE DE MADRID 

Organization address
address: AVENIDA DE SENECA 2
city: MADRID
postcode: 28040
website: http://www.ucm.es

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 Spain [ES]
 Total cost 1˙499˙516 €
 EC max contribution 1˙499˙516 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2023-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSIDAD COMPLUTENSE DE MADRID ES (MADRID) coordinator 1˙499˙516.00

Map

 Project objective

Integrons are genetic platforms that enhance bacterial evolvability through the acquisition and stockpiling of new genes encoded in mobile elements named cassettes. They are found in the chromosomes of environmental bacteria but some have acquired mobility through their association to transposons and conjugative plasmids. These mobile integrons (MI) caused the unexpected rise of multidrug resistance that is now a major threat to modern medicine, and are good proof of the adaptive power of integrons. Class 1 integrons are the most relevant MI and the major experimental model. Yet little is known about the hundreds of sedentary chromosomal integrons (SCI) that have driven bacterial evolution for eons. The paradigm of SCI is the superintegron (SI), an extremely large integron located in the chromosome of Vibrio cholerae, the causative agent of Cholera disease. Despite its role in the adaptability of one of the deadliest pathogens in history, the SI is poorly characterized because it is only functional in its native genetic background, yet its presence interferes with, and precludes all studies performed in V. cholerae. I propose to solve this paradoxical situation by deleting the SI, an ambitious project not only for its size (126 Kb) but because it is highly stabilized by 17 toxin-antitoxin systems. To do so, I have developed SeqDelTA, a novel method that is already giving excellent preliminary results. I will then use V. cholerae∆SI to study fundamental aspects of SCIs, yet out of reach. I will elucidate the functions encoded in SI cassettes to understand the role and adaptive value of integrons in nature; I will also unravel the genesis of cassettes: how a gene is exapted from its genetic context to become a mobile module; and I will explore the circulation of antibiotic resistance cassettes among humans, animals, food, and the environment with a novel biosynthetic tool (the I3C). KryptonInt will open and explore the historically inaccessible field of study of SCIs.

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

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