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PREMNEC SIGNED

PReterm Enteroids to determine the Mechanism of Necrotising EnteroColitis

Total Cost €

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EC-Contrib. €

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Partnership

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 PREMNEC project word cloud

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

co    invasive    colonisation    protection    mechanisms    disease    crosstalk    longstanding    pathobiology    packages    enteroid    regarded    enterocolitis    otherwise    resected    divided    nec    treatment    prematurity    pathogenesis    microbial    crypt    few    causes    characterisation    metagenomics    poorly    risk    premnec    newcastle    human    relates    preterm    utilise    vivo    pioneered    added    yielded    transcriptomics    bacterial    phie    isolate    wps    cells    inflammatory    microbiome    extremely    surgically    expertise    pathology    fellowship    imaging    isolated    beneficial    discarded    abnormal    single    tissue    explore    university    wp    cellular    accurate    week    bacteria    robustly    utilising    first    model    functioning    deaths    interaction    species    proteomics    intestinal    inability    mediated    lack    bowel    utilised    translating    gut    culture    mechanistic    enteroids    overcome    host    infants    undergo    progress    technologies    reproducible    potentially    necrotising    hurdle    stool    life    phies    24    completion    samples    ex    concurrently    fresh    permit    vixo    systematically    wp1   

Project "PREMNEC" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF NEWCASTLE UPON TYNE 

Organization address
address: KINGS GATE
city: NEWCASTLE UPON TYNE
postcode: NE1 7RU
website: http://www.ncl.ac.uk/

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 United Kingdom [UK]
 Total cost 183˙454 €
 EC max contribution 183˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-07-01   to  2020-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF NEWCASTLE UPON TYNE UK (NEWCASTLE UPON TYNE) coordinator 183˙454.00

Map

 Project objective

Necrotising enterocolitis (NEC) is an inflammatory mediated bowel disease that causes more deaths after the first week of life in extremely preterm infants than any other single pathology, with prematurity and abnormal bacterial colonisation regarded as the most significant risk factors. However, 40 years of research have yielded few advances in treatment and the mechanisms of disease remain poorly understood. A major reason for this lack of progress relates to challenges in translating findings from non-invasive samples (e.g., stool) and the inability to robustly model bacterial-host crosstalk. To overcome this longstanding hurdle, the proposed PREMNEC (PReterm Enteroids to determine the Mechanisms of Necrotising EnteroColitis) fellowship will utilise a novel ex vivo preterm human intestinal enteroid (PHIE) co-culture model to systematically explore the gut microbiome and host functioning in preterm infants. The fellowship is divided in three distinct work packages (WPs). In WP1, surgically resected intestinal tissue (otherwise discarded) from NEC and non-NEC infants will undergo characterisation utilising metagenomics, transcriptomics, proteomics, and cellular imaging directly on the fresh tissue. Concurrently, WP 2 will isolate crypt cells from the tissue to establish PHIEs that permit accurate and reproducible ex vixo co-culture of bacterial-host interaction. In WP 3, bacterial species isolated from preterm infants will be systematically added to the ex vixo co-culture model and comparable technologies utilised in WP 1 will be applied to determine the pathobiology of disease. Newcastle University will provide expertise in state-of-the-art transcriptomics and cellular imaging technologies. Upon completion of this 24-month fellowship, I will have pioneered significant advancement in the mechanistic understanding of microbial-host interaction in the pathogenesis of NEC and identified potentially beneficial bacteria that may provide protection from NEC.

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