Institut Pasteur
Pasteur

AMR Spread

Welcome to the AMR Spread user interface!

Using a mechanistic deterministic multi-country model of the transmission of antibiotic-resistant bacteria, simulate the spread of an emergent carbapenem-resistant E. coli worldwide.

Select the emergent resistant E. coli characteristics, national antibiotic consumption levels, international travel flows and index country where emergence starts. Then, simulate for 20 years the emergence corresponding to the selected scenario.

After simulation, visualize two outputs:

  • a map of antibiotic resistance proportion for healthy carriage
  • a timeline to visualize at what year surveillance system detects 5 antibiotic resistant infections by country

  • Run simulation

    Choose the characteristics of the emergent resistant bacteria for simulations.

    Choose national antibiotics consumption: decrease, keep or increase consumption for the 20 years of simulation compared to true national antibiotic sales from IQVIA data.

    Choose proportion of travelers from a country traveling to any country worldwide: decrease, keep or increase travel flows for the 20 years of simulation compared to estimated travel matrix from KCMD data.

    Choose one index country where emergence of carbapenem-resistant E. coli will start and let it spread to the whole world.
    Optional: Choose a second index country with the possibility to compare with simulations of first index country.




    AMR Model



    MODEL USED FOR SIMULATIONS

    We build a mechanistic deterministic between-host model of the transmission of antibiotic-resistant Escherichia coli. The model is calibrated using empirical data of endemic ESBL-producing E. coli. Then, the model is used to simulate the spread of an emergent resistant bacteria worldwide, such as carbapenem-resistant E. coli.


    The model is initialized by defining the characteristics of an emerging resistant bacterium, which is introduced at the start of the simulation in a given index country. National antibiotic consumption levels in every country and travel fluxes between every country can be varied. The model simulates, over 20 years, the spread of the emerging resistant bacteria between individuals within a country, and between different countries connected by travel flows. A "simulation" thus corresponds to the spread of an emerging resistant bacterium from an index country to other countries over time.


    Schematic of the between-host model used for simulations




    EQUATIONS FOR THE MODEL



    INPUT PARAMETERS


    NORMAL BUG
    SCENARIO
    SUPER BUG
    SCENARIO
    FITNESS COST BUG
    SCENARIO
    MULTI-DRUG RESISTANT BUG
    SCENARIO
    βi Estimated per country βi x 1.1 βi x 0.9
    σS i Estimated per country
    ai Estimated per country
    σR i σR i = ai x σS i
    α 8 days
    α' 60 days
    γ 1/120 days-1
    φant 9.83
    k 0.80
    τy,i Carbapenems treatment rate per year y and country i

    Data source: IQVIA

    Carbapenems and β-lactams treatment rate per year y and country i

    Data source: IQVIA

    Δy,i,j travel matrix (% of inhabitants of country i traveling to country j per year y)

    Data source: KCMD



    INITIAL CONDITIONS


    CS = Ni x (1 - τ1,i)
    CSr = n
    CsR = 0
    CSA = Ni x (τ1,i)
    CsRA = 0

    Ni is population size of country i (data: World Bank)
    n is initial number of resistant bacteria carriers at the beginning of the simulation (n = 1000)







    Data



    DATA USED FOR SIMULATIONS

    Model calibrated using antibiotic resistance data from the Pfizer ATLAS database. https://atlas-surveillance.com/#/login

    Synthetic data representing trends of antibiotic consumption by country and by year.

    Data obtained from the Knowledge Center for Migration and Demography (KCMD) data hub, from the Global Transnational Mobility dataset. Data represent the estimated number of travelers country by country, for year periods between 2011-2016.
    https://migration-demography-tools.jrc.ec.europa.eu/data-hub/

    Contact



    TEAM

    Eve Rahbé

    Eve.Rahbe@pasteur.fr

    Doctorante en biostatistiques santé publique, Paris-Saclay

    Equipe Epidémiologie et Modélisation de l’échappement aux anti-infectieux, Institut Pasteur, INSERM

    Philippe Glaser

    Philippe.Glaser@pasteur.fr

    Directeur de recherche

    Equipe Ecologie et Evolution de la résistance aux antimicrobiens,
    Institut Pasteur

    Lulla Opatowski

    Lulla.Opatowski@pasteur.fr

    Professeure, Chercheure-enseignante, UVSQ

    Equipe Epidémiologie et Modélisation de l’échappement aux anti-infectieux, Institut Pasteur, INSERM



    HOME PAGE TEAM/PROJECT

    https://research.pasteur.fr/fr/team/epidemiology-and-modelling-of-bacterial-escape-to-antimicrobials/



    Credits



    CONTRIBUTORS

    Eve Rahbé

    eve.rahbe@pasteur.fr

    Author of simulation code

    PhD Student in biostatistics public health, Paris-Saclay

    Epidemiology and modelling of antibacteiral evasion(EMAE) team, Institut Pasteur, INSERM

    Elodie Chapeaublanc

    elodie.chapeaublanc@pasteur.fr

    Implementation and Deployment

    Research Engineer - Web Developer

    Head of Web INTERface Group
    Hub Bioinformatique et Biostatistique,
    Institut Pasteur, Paris

    Rachel Torchet

    rachel.torchet@pasteur.fr

    Develop User Interface

    Research Engineer - UX/UI Designer

    Hub Bioinformatique et Biostatistique,
    Institut Pasteur, Paris



    TECHNICAL IMPLEMENTATION DETAILS

    The website was developed in R Shiny and deployed on Kubernetes cluster of Institut Pasteur.

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