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      A comparative evaluation of modelling strategies for the effect of treatment and host interactions on the spread of drug resistance

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          Abstract

          The evolutionary responses of infectious pathogens often have ruinous consequences for the control of disease spread in the population. Drug resistance is a well-documented instance that is generally driven by the selective pressure of drugs on both the replication of the pathogen within hosts and its transmission between hosts. Management of drug resistance therefore requires the development of treatment strategies that can impede the emergence and spread of resistance in the population. This study evaluates various treatment strategies for influenza infection as a case study by comparing the long-term epidemiological outcomes predicted by deterministic and stochastic versions of a homogeneously mixing (mean-field) model and those predicted by a heterogeneous model that incorporates spatial pair-wise correlation. We discuss the importance of three major parameters in our evaluation: the basic reproduction number, the population level of treatment, and the degree of clustering as a key parameter determining the structure of heterogeneous interactions. The results show that, as a common feature in all models, high treatment levels during the early stages of disease outset can result in large resistant outbreaks, with the possibility of a second wave of infection appearing in the pair-approximation model. Our simulations demonstrate that, if the basic reproduction number exceeds a threshold value, the population-wide spread of the resistant pathogen emerges more rapidly in the pair-approximation model with significantly lower treatment levels than in the homogeneous models. We tested an antiviral strategy that delays the onset of aggressive treatment for a certain amount of time after the onset of the outbreak. The findings indicate that the overall disease incidence is reduced as the degree of clustering increases, and a longer delay should be considered for implementing the large-scale treatment.

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          Network theory and SARS: predicting outbreak diversity

          Many infectious diseases spread through populations via the networks formed by physical contacts among individuals. The patterns of these contacts tend to be highly heterogeneous. Traditional “compartmental” modeling in epidemiology, however, assumes that population groups are fully mixed, that is, every individual has an equal chance of spreading the disease to every other. Applications of compartmental models to Severe Acute Respiratory Syndrome (SARS) resulted in estimates of the fundamental quantity called the basic reproductive number R 0 —the number of new cases of SARS resulting from a single initial case—above one, implying that, without public health intervention, most outbreaks should spark large-scale epidemics. Here we compare these predictions to the early epidemiology of SARS. We apply the methods of contact network epidemiology to illustrate that for a single value of R 0 , any two outbreaks, even in the same setting, may have very different epidemiological outcomes. We offer quantitative insight into the heterogeneity of SARS outbreaks worldwide, and illustrate the utility of this approach for assessing public health strategies.
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            Oseltamivir resistance during treatment of influenza A (H5N1) infection.

            Influenza A (H5N1) virus with an amino acid substitution in neuraminidase conferring high-level resistance to oseltamivir was isolated from two of eight Vietnamese patients during oseltamivir treatment. Both patients died of influenza A (H5N1) virus infection, despite early initiation of treatment in one patient. Surviving patients had rapid declines in the viral load to undetectable levels during treatment. These observations suggest that resistance can emerge during the currently recommended regimen of oseltamivir therapy and may be associated with clinical deterioration and that the strategy for the treatment of influenza A (H5N1) virus infection should include additional antiviral agents. Copyright 2005 Massachusetts Medical Society.
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              The Importance of Being Discrete (and Spatial)

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                Author and article information

                Contributors
                Journal
                J Theor Biol
                J. Theor. Biol
                Journal of Theoretical Biology
                Published by Elsevier Ltd.
                0022-5193
                1095-8541
                1 April 2009
                21 July 2009
                1 April 2009
                : 259
                : 2
                : 253-263
                Affiliations
                [a ]Institute for Biodiagnostics, National Research Council Canada, Winnipeg, Manitoba, Canada R3B 1Y6
                [b ]Department of Physics, University of Winnipeg, Winnipeg, Manitoba, Canada R3B 2E9
                [c ]Department of Statistics, University of Manitoba, Winnipeg, Manitoba, Canada R3T 2N2
                [d ]Department of Mathematics and Statistics, University of Winnipeg, Winnipeg, Manitoba, Canada R3B 2E9
                Author notes
                [* ]Corresponding author at: Institute for Biodiagnostics, National Research Council Canada, Winnipeg, Manitoba, Canada R3B 1Y6. Tel.: +1 204 984 6573; fax: +1 204 984 5472. seyed.moghadas@ 123456nrc-cnrc.gc.ca
                Article
                S0022-5193(09)00136-2
                10.1016/j.jtbi.2009.03.029
                7127136
                19344730
                96862c16-1ee2-4e32-beef-7b63668aa17f
                Crown copyright © 2009 Published by Elsevier Ltd. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 8 October 2008
                : 11 March 2009
                : 23 March 2009
                Categories
                Article

                Comparative biology
                drug resistance,treatment strategies,epidemic models,pair-approximation,monte carlo simulations

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