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Cell2Cell SIGNED

What makes a successfull pathogen? Understanding the impact of cell-to-cell heterogeneity in chromatin structure on infection and adaptation

Total Cost €

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EC-Contrib. €

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Partnership

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 Cell2Cell project word cloud

Explore the words cloud of the Cell2Cell project. It provides you a very rough idea of what is the project "Cell2Cell" about.

yeast    hypothesized    plays    signal    genome    unveiling    challenged    multicellular    give    bioinformatics    stage    prepared    outcome    cell    noise    of    modern    infections    genomics    models    infection    adapt    heterogeneity    scientists    decrease    organisms    burden    overcome    employ    proposes    infectious    structural    serve    establishment    size    renders    variability    lack    population    skilled    cellular    cancer    revolutionize    decades    demands    enormous    previously    small    degree    experts    chromatin    host    genetic    pathogens    mechanisms    revealed    industry    organization    people    unicellular    insights    changing    plasticity    technologies    train    molecular    tools    millions    little    environments    pathogen    kill    developmental    successful    single    biology    understand    enabled    lasting    started    endeavor    sequence    phenotypic    immune    individual    establishing    microbial    worldwide    cell2cell    limitations    species    evade    diseases    barriers    caused    academia    epigenetic    dna    elucidation   

Project "Cell2Cell" data sheet

The following table provides information about the project.

Coordinator
LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN 

Organization address
address: GESCHWISTER SCHOLL PLATZ 1
city: MUENCHEN
postcode: 80539
website: www.uni-muenchen.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 3˙889˙769 €
 EC max contribution 3˙889˙769 € (100%)
 Programme 1. H2020-EU.1.3.1. (Fostering new skills by means of excellent initial training of researchers)
 Code Call H2020-MSCA-ITN-2019
 Funding Scheme MSCA-ITN-ETN
 Starting year 2019
 Duration (year-month-day) from 2019-11-01   to  2023-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN DE (MUENCHEN) coordinator 1˙011˙153.00
2    HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH DE (NEUHERBERG) participant 505˙576.00
3    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD UK (OXFORD) participant 303˙172.00
4    KAROLINSKA INSTITUTET SE (STOCKHOLM) participant 281˙982.00
5    SCHWEIZERISCHES TROPEN- UND PUBLIC HEALTH-INSTITUT CH (Basel) participant 281˙276.00
6    INSTITUT CURIE FR (PARIS) participant 274˙802.00
7    STICHTING KATHOLIEKE UNIVERSITEIT NL (NIJMEGEN) participant 265˙619.00
8    WEIZMANN INSTITUTE OF SCIENCE IL (REHOVOT) participant 263˙500.00
9    INSTITUTO DE MEDICINA MOLECULAR JOAO LOBO ANTUNES PT (LISBOA) participant 237˙720.00
10    EPIGENETIKS GENETIK BIYOINFORMATIK YAZILIM AS TR (ISTANBUL) participant 235˙248.00
11    CELLSORTER MUSZAKI KUTATO ES FEJLESZTO KFT HU (BUDAPEST) participant 229˙715.00

Map

 Project objective

Infectious diseases kill millions of people worldwide every year. Decades of research have revealed important insights into the molecular mechanisms pathogens employ to establish lasting infections, yet little is known about what renders individual pathogens within a microbial population more successful at establishing an infection than others. Recent advances in single-cell technologies have started to revolutionize modern biology, unveiling an enormous degree of cell-to-cell heterogeneity. Often, phenotypic variability is not caused by genetic changes in the DNA sequence, but by epigenetic changes in the structural organization of DNA called chromatin. In multicellular organisms, this epigenetic plasticity plays a key role in developmental processes and cancer. In unicellular pathogens, cell-to-cell heterogeneity is hypothesized to promote the establishment of infections by allowing the pathogen to adapt to changing environments or evade the host immune response. To decrease the burden of infectious diseases, it is therefore, necessary to better understand how infections are enabled by cellular heterogeneity at the chromatin level of the pathogen. Several limitations have previously challenged this endeavor, including small genome size (i.e. low signal-to-noise) and the lack of knowledge of how chromatin is organized in pathogens. Cell2Cell proposes to overcome these barriers by bringing together (1) experts in pathogen biology; (2) the use of unicellular yeast species to serve as chromatin models; (3) single-cell technologies; (4) bioinformatics tools. Using state of the art technologies, we will train early stage researchers to identify the molecular mechanisms that control cell-to-cell heterogeneity in pathogens. The proposed research will contribute to the elucidation of how heterogeneity affects the outcome of diseases and give rise to highly skilled scientists that are well prepared to face the demands of modern genomics research in academia and industry.

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The information about "CELL2CELL" are provided by the European Opendata Portal: CORDIS opendata.

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