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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.

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

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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