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PREMNEC SIGNED

PReterm Enteroids to determine the Mechanism of Necrotising EnteroColitis

Total Cost €

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EC-Contrib. €

0

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.

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

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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