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BIOFAGE SIGNED

Interaction Dynamics of Bacterial Biofilms with Bacteriophages

Total Cost €

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EC-Contrib. €

0

Partnership

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 BIOFAGE project word cloud

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

inside    nothing    communities    resolution    termed    population    mechanistic    life    exposure    function    mathematical    methodology    altogether    time    varying    spatial    cells    single    genetically    combine    expression    experimental    promises    imaging    species    either    biofilms    microscopic    ecology    manipulate    dwelling    interactions    lastly    enrich    modeling    gap    light    determinants    track    bacteria    dominant    spread    antibiotic    insights    susceptible    mechanisms    evolutionary    motivate    cell    manipulating    environmental    members    image    generational    phenotypes    engineer    subtraction    strategies    occupy    individual    structure    gene    designed    tracking    almost    proximate    dynamics    parasites    hosts    bacterial    fundamental    technique    composition    mode    phages    earth    combination    biological    phage    biofilm    community    microbial    attack    combined    uncover    first    physical    force    resistance    scales    viral    nature    surfaces    surprisingly    moist    resistant    urgent    sessile    fill   

Project "BIOFAGE" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: Munich
postcode: 80539
website: www.mpg.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˙494˙963 €
 EC max contribution 1˙494˙963 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-STG
 Funding Scheme ERC-STG
 Starting year 2017
 Duration (year-month-day) from 2017-01-01   to  2021-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (Munich) coordinator 1˙494˙963.00

Map

 Project objective

Biofilms are antibiotic-resistant, sessile bacterial communities that occupy most moist surfaces on Earth and represent a major mode of bacterial life. Another common feature of bacterial life is exposure to viral parasites (termed phages), which are a dominant force in bacterial population control throughout nature. Surprisingly, almost nothing is known about the interactions between biofilm-dwelling bacteria and phages. This proposal is designed to fill this gap using a combination of novel methodology, experimental systems, and mathematical modeling. We have recently developed a new microscopic imaging technique that allows us to image and track all individual cells and their gene expression inside biofilms. First, we will use this technique for tracking the population dynamics of bacteria and phages within biofilms at single cell resolution. By genetically manipulating bacterial hosts and their phages, and by varying environmental conditions, we will investigate the fundamental biological and physical determinants of phage spread within biofilm communities. Second, we will study how biofilms respond to phage attack on both intra-generational and evolutionary time scales, focusing in particular on proximate response mechanisms and the population dynamics of phage-resistant and phage-susceptible cells as a function of biofilm spatial structure. Lastly, we will combine our novel insights to engineer phages that manipulate the composition of biofilm communities, either by subtraction of particular bacterial species or by addition of novel phenotypes to existing biofilm community members. Altogether, the proposed research promises to uncover the major mechanistic and evolutionary elements of biofilm-phage interactions. This combined work will greatly enrich our knowledge of microbial ecology and motivate novel strategies for bacterial biofilm control, an increasingly urgent priority in light of widespread antibiotic resistance.

 Publications

year authors and title journal last update
List of publications.
2018 Anna Dragoš, Heiko Kiesewalter, Marivic Martin, Chih-Yu Hsu, Raimo Hartmann, Tobias Wechsler, Carsten Eriksen, Susanne Brix, Knut Drescher, Nicola Stanley-Wall, Rolf Kümmerli, Ákos T. Kovács
Division of Labor during Biofilm Matrix Production
published pages: 1903-1913.e5, ISSN: 0960-9822, DOI: 10.1016/j.cub.2018.04.046
Current Biology 28/12 2019-06-13
2018 Lucia Vidakovic, Praveen K. Singh, Raimo Hartmann, Carey D. Nadell, Knut Drescher
Dynamic biofilm architecture confers individual and collective mechanisms of viral protection
published pages: 26-31, ISSN: 2058-5276, DOI: 10.1038/s41564-017-0050-1
Nature Microbiology 3/1 2019-06-13
2018 Ricardo Martínez-García, Carey D. Nadell, Raimo Hartmann, Knut Drescher, Juan A. Bonachela
Cell adhesion and fluid flow jointly initiate genotype spatial distribution in biofilms
published pages: e1006094, ISSN: 1553-7358, DOI: 10.1371/journal.pcbi.1006094
PLOS Computational Biology 14/4 2019-06-13
2017 Praveen K. Singh, Sabina Bartalomej, Raimo Hartmann, Hannah Jeckel, Lucia Vidakovic, Carey D. Nadell, Knut Drescher
Vibrio cholerae Combines Individual and Collective Sensing to Trigger Biofilm Dispersal
published pages: 3359-3366.e7, ISSN: 0960-9822, DOI: 10.1016/j.cub.2017.09.041
Current Biology 27/21 2019-06-13
2017 Matthew Simmons, Knut Drescher, Carey D Nadell, Vanni Bucci
Phage mobility is a core determinant of phage–bacteria coexistence in biofilms
published pages: 531-543, ISSN: 1751-7362, DOI: 10.1038/ismej.2017.190
The ISME Journal 12/2 2019-06-13

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