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PHARMS SIGNED

Bacteriophage inhibition of antibiotic-resistant pathogenic microbes and founding for novel therapeutic strategies

Total Cost €

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EC-Contrib. €

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Partnership

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 PHARMS project word cloud

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

strategies    validation    framework    phages    mechanisms    people    haemophilus    resistant    antibiotics    mediated    700    elucidating    pathogens    killed    vitro    phage    inhibitors    positioned    time    wp3    plan    universal    amr    bacteria    treating    functions    wp1    modes    nucleotide    diseases    therapies    therapeutic    mimic    deploy    employ    sequence    alien    pharms    interdisciplinary    encoded    pylori    discoveries    life    baumannii    resistance    influenzae    grand    synthetic    translation    engineer    vivo    action    bactericidal    obstacles    ways    isolate    infectious    threatening    fight    inhibition    molecular    peptides    array    vectors    delivered    biology    unknown    elucidate    building    independent    transport    complement    antimicrobial    group    battery    throughput    revolutionary    bacterial    utilizes    multiple    helicobacter    emergence    driving    acinetobacter    lines    culture    multifaceted    natural    enzymes    worldwide    tools    discovered    isolates    genes    transcription    discover    therapy    rational    screen    wp2    limited    viruses    ranging    bacteriophages    levels    scientific    confirmation    host    clinical   

Project "PHARMS" data sheet

The following table provides information about the project.

Coordinator
HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH 

Organization address
address: INGOLSTADTER LANDSTRASSE 1
city: NEUHERBERG
postcode: 85764
website: www.helmholtz-muenchen.de

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 Germany [DE]
 Total cost 1˙499˙650 €
 EC max contribution 1˙499˙650 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2023-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH DE (NEUHERBERG) coordinator 1˙499˙650.00

Map

 Project objective

Emergence of antimicrobial resistance (AMR) is a grand scientific challenge of our time that has killed more than 700,000 people worldwide. Phage therapy, a promising complement to antibiotics, utilizes viruses of bacteria (bacteriophages) or phage-derived inhibitors as natural ways to fight AMR. The main obstacles in the clinical application of phage-based AMR therapy are the limited number of phage isolates and the unknown molecular mechanisms of phage-delivered bactericidal action. Building on the recent advances of my group in high-throughput, culture-independent but host-targeted methodologies, PHARMS aims to deploy a revolutionary approach: to screen for all possible phages of a resistant bacterial isolate, characterize multiple lines of their bactericidal functions, and use this information for the design of a whole battery of phage-based therapies that employ multifaceted modes of action.

Using an interdisciplinary research plan, PHARMS will discover phage-specific bactericidal action modes at all possible levels ranging from nucleotide sequence and transcription to translation, in order to elucidate the molecular mechanisms driving phage-mediated inhibition of AMR Acinetobacter baumannii, Helicobacter pylori, & Haemophilus influenzae (WP1). These discoveries, together with novel synthetic biology tools, will enable us to engineer an array of phage vectors that mimic phage-deployed bactericidal modes discovered under WP1, including transport of alien genes to deliver bactericidal effects (WP2). PHARMS will provide molecular confirmation and in vitro & in vivo validation of the functions of phage-encoded bactericidal peptides and enzymes (WP3). By elucidating universal and specific mechanisms of phage-delivered inhibition of AMR pathogens, PHARMS is positioned to provide the rational framework for the design of novel therapeutic strategies aimed at treating common and life-threatening infectious diseases.

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