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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.

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

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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