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COMMANDEER

COMMANDEER: Disrupting microbial resistance using rationally designed signalling molecules

Total Cost €

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EC-Contrib. €

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Partnership

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 COMMANDEER project word cloud

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

until    route    inhabitant    treatment    disease    molecules    once    receptors    body    expectancies    again    combining    life    defence    fits    abnormally    susceptible    whereby    resistance    serious    signal    shield    respiratory    prevalent    synthesise    mucus    80    thick    infecting    lungs    sticky    airways    multidisciplinary    aeruginosa    off    disable    usually    young    strains    microbiologists    subtle    diffusible    emergency    chronic    pseudomonas    inherited    mimic    35    flare    patients    commandeering    approximately    causes    biological    commandeer    behaves    age    worldwide    uk    messenger    excrete    switches    cystic    populations    chemical    circumventing    antibiotics    ireland    infected    bacterial    cenocepacia    switch    mechanism    succumb    acts    chemists    activates    50    significantly    strategy    people    co    infection    cf    fit    fibrosis    dsf    special    resistant    60    biofilm    settle    protects    collaborative    talents    signalling    burkholderia    quality    shown    bacteria    lock   

Project "COMMANDEER" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY COLLEGE CORK - NATIONAL UNIVERSITY OF IRELAND, CORK 

Organization address
address: WESTERN ROAD
city: Cork
postcode: T12 YN60
website: www.ucc.ie

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 Ireland [IE]
 Project website https://sites.google.com/view/commandeer
 Total cost 187˙866 €
 EC max contribution 187˙866 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-07-01   to  2017-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE CORK - NATIONAL UNIVERSITY OF IRELAND, CORK IE (Cork) coordinator 187˙866.00

Map

 Project objective

Cystic Fibrosis (CF) is an inherited disease which affects 100,000 people worldwide and is prevalent in European populations. CF causes the body to produce an abnormally sticky mucus in the lungs making patients susceptible to serious bacterial infection. By age 8, 50% of CF patients are infected with Pseudomonas aeruginosa increasing to 80% by 20 years of age. Eventually, the infecting strains of bacteria become resistant to antibiotics and remain a chronic inhabitant of the lungs of CF patients until they succumb to respiratory failure, usually by the young age of 30-35. Approximately 60% of CF patients are co-infected with Burkholderia cenocepacia that settle into the thick mucus of the airways. These bacteria have evolved a special type of defence mechanism to antibiotics whereby they excrete a chemical messenger on treatment. This chemical messenger -Diffusible Signal Factor or DSF - activates bacterial biofilm formation. Previous work has shown that DSF effectively behaves as an ‘emergency flare’ to other bacteria, which produce a biofilm in response. This biofilm acts as a shield which protects the bacteria from the effects of antibiotics.

As a key fits in a lock, DSF fits into bacterial receptors and “switches on” biofilm formation. In this COMMANDEER project, we will synthesise molecules which mimic DSF and fit into the same biological receptors. However, due to subtle changes in their design, our molecules will “switch off” biofilm formation. Using this novel strategy of effectively commandeering the bacteria’s signalling system, we will disable biofilm formation, making the bacteria susceptible to antibiotics once again. We will adopt a multidisciplinary and collaborative approach combining the talents of chemists in Ireland and microbiologists in the UK. This project, therefore, represents a new and exciting route of circumventing bacterial resistance, offering significantly improved quality of life for CF patients and increased life expectancies.

 Publications

year authors and title journal last update
List of publications.
2017 Kate O`Reilly, Manoj Gupta, Hirenkumar Gandhi, Pavan Kumar, Tim O`Sullivan
Asymmetric Peroxidation of α,β-Unsaturated Aldehydes Under Diarylprolinol Ether Catalysis
published pages: 1-4, ISSN: 1385-2728, DOI: 10.2174/1385272821666170412113323
Current Organic Chemistry 21/999 2019-07-23
2016 Kate O’Reilly, Manoj K. Gupta, Hiren K. Gandhi, Vydyuta P. Kumar, Kevin S. Eccles, Simon E. Lawrence, Timothy P. O’Sullivan
Cinchona-catalysed, Enantioselective Synthesis of β-Peroxycarboxylic Acids, β-Peroxyesters and β-Peroxyalcohols
published pages: 2633-2638, ISSN: 1385-2728, DOI: 10.2174/1385272820666160513164417
Current Organic Chemistry 20/24 2019-07-23

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