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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.

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

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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