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      Measurability of the epidemic reproduction number in data-driven contact networks

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          The analysis of real epidemiological data has raised issues of the adequacy of the classic homogeneous modeling framework and quantities, such as the basic reproduction number in real-world situations. Based on high-quality sociodemographic data, here we generate a multiplex network describing the contact pattern of the Italian and Dutch populations. By using a microsimulation approach, we show that, for epidemics spreading on realistic contact networks, it is not possible to define a steady exponential growth phase and a basic reproduction number. We show the operational use of the instantaneous reproduction rate as a good descriptor of the transmission dynamics.

          Abstract

          The basic reproduction number is one of the conceptual cornerstones of mathematical epidemiology. Its classical definition as the number of secondary cases generated by a typical infected individual in a fully susceptible population finds a clear analytical expression in homogeneous and stratified mixing models. Along with the generation time (the interval between primary and secondary cases), the reproduction number allows for the characterization of the dynamics of an epidemic. A clear-cut theoretical picture, however, is hardly found in real data. Here, we infer from highly detailed sociodemographic data two multiplex contact networks representative of a subset of the Italian and Dutch populations. We then simulate an infection transmission process on these networks accounting for the natural history of influenza and calibrated on empirical epidemiological data. We explicitly measure the reproduction number and generation time, recording all individual-level transmission events. We find that the classical concept of the basic reproduction number is untenable in realistic populations, and it does not provide any conceptual understanding of the epidemic evolution. This departure from the classical theoretical picture is not due to behavioral changes and other exogenous epidemiological determinants. Rather, it can be simply explained by the (clustered) contact structure of the population. Finally, we provide evidence that methodologies aimed at estimating the instantaneous reproduction number can operationally be used to characterize the correct epidemic dynamics from incidence data.

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          Most cited references46

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          Mitigation strategies for pandemic influenza in the United States.

          Recent human deaths due to infection by highly pathogenic (H5N1) avian influenza A virus have raised the specter of a devastating pandemic like that of 1917-1918, should this avian virus evolve to become readily transmissible among humans. We introduce and use a large-scale stochastic simulation model to investigate the spread of a pandemic strain of influenza virus through the U.S. population of 281 million individuals for R(0) (the basic reproductive number) from 1.6 to 2.4. We model the impact that a variety of levels and combinations of influenza antiviral agents, vaccines, and modified social mobility (including school closure and travel restrictions) have on the timing and magnitude of this spread. Our simulations demonstrate that, in a highly mobile population, restricting travel after an outbreak is detected is likely to delay slightly the time course of the outbreak without impacting the eventual number ill. For R(0) < 1.9, our model suggests that the rapid production and distribution of vaccines, even if poorly matched to circulating strains, could significantly slow disease spread and limit the number ill to <10% of the population, particularly if children are preferentially vaccinated. Alternatively, the aggressive deployment of several million courses of influenza antiviral agents in a targeted prophylaxis strategy may contain a nascent outbreak with low R(0), provided adequate contact tracing and distribution capacities exist. For higher R(0), we predict that multiple strategies in combination (involving both social and medical interventions) will be required to achieve similar limits on illness rates.
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            Multilayer Networks

            In most natural and engineered systems, a set of entities interact with each other in complicated patterns that can encompass multiple types of relationships, change in time, and include other types of complications. Such systems include multiple subsystems and layers of connectivity, and it is important to take such "multilayer" features into account to try to improve our understanding of complex systems. Consequently, it is necessary to generalize "traditional" network theory by developing (and validating) a framework and associated tools to study multilayer systems in a comprehensive fashion. The origins of such efforts date back several decades and arose in multiple disciplines, and now the study of multilayer networks has become one of the most important directions in network science. In this paper, we discuss the history of multilayer networks (and related concepts) and review the exploding body of work on such networks. To unify the disparate terminology in the large body of recent work, we discuss a general framework for multilayer networks, construct a dictionary of terminology to relate the numerous existing concepts to each other, and provide a thorough discussion that compares, contrasts, and translates between related notions such as multilayer networks, multiplex networks, interdependent networks, networks of networks, and many others. We also survey and discuss existing data sets that can be represented as multilayer networks. We review attempts to generalize single-layer-network diagnostics to multilayer networks. We also discuss the rapidly expanding research on multilayer-network models and notions like community structure, connected components, tensor decompositions, and various types of dynamical processes on multilayer networks. We conclude with a summary and an outlook.
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              Modeling targeted layered containment of an influenza pandemic in the United States.

              Planning a response to an outbreak of a pandemic strain of influenza is a high public health priority. Three research groups using different individual-based, stochastic simulation models have examined the consequences of intervention strategies chosen in consultation with U.S. public health workers. The first goal is to simulate the effectiveness of a set of potentially feasible intervention strategies. Combinations called targeted layered containment (TLC) of influenza antiviral treatment and prophylaxis and nonpharmaceutical interventions of quarantine, isolation, school closure, community social distancing, and workplace social distancing are considered. The second goal is to examine the robustness of the results to model assumptions. The comparisons focus on a pandemic outbreak in a population similar to that of Chicago, with approximately 8.6 million people. The simulations suggest that at the expected transmissibility of a pandemic strain, timely implementation of a combination of targeted household antiviral prophylaxis, and social distancing measures could substantially lower the illness attack rate before a highly efficacious vaccine could become available. Timely initiation of measures and school closure play important roles. Because of the current lack of data on which to base such models, further field research is recommended to learn more about the sources of transmission and the effectiveness of social distancing measures in reducing influenza transmission.
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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                11 December 2018
                21 November 2018
                21 November 2018
                : 115
                : 50
                : 12680-12685
                Affiliations
                [1] aWeb Sciences Center, University of Electronic Science and Technology of China , Chengdu 611731, Sichuan, People’s Republic of China;
                [2] bBig Data Research Center, University of Electronic Science and Technology of China , Chengdu 611731, Sichuan, People’s Republic of China;
                [3] cLaboratory for the Modeling of Biological and Socio-Technical Systems, Northeastern University , Boston, MA 02115;
                [4] dBruno Kessler Foundation , 38123 Trento, Italy;
                [5] eInstitute for Biocomputation and Physics of Complex Systems, University of Zaragoza , 50018 Zaragoza, Spain;
                [6] fDepartment of Theoretical Physics, University of Zaragoza , 50009 Zaragoza, Spain;
                [7] gISI Foundation , 10126 Turin, Italy
                Author notes
                1To whom correspondence should be addressed. Email: a.vespignani@ 123456northeastern.edu .

                Edited by Simon A. Levin, Princeton University, Princeton, NJ, and approved October 16, 2018 (received for review June 27, 2018)

                Author contributions: Q.-H.L., M.A., A.A., S.M., Y.M., and A.V. designed research, performed research, analyzed data, and wrote the paper.

                Author information
                http://orcid.org/0000-0002-0895-1893
                http://orcid.org/0000-0003-3419-4205
                Article
                201811115
                10.1073/pnas.1811115115
                6294899
                30463945
                e6606ec2-8aa2-490d-b8cf-6447d79affdd
                Copyright © 2018 the Author(s). Published by PNAS.

                This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).

                History
                Page count
                Pages: 6
                Funding
                Funded by: MINECO | Consejo Superior de Investigaciones Científicas (CSIC) 501100003339
                Award ID: FIS2017-87519-P
                Award Recipient : Yamir Moreno
                Funded by: Chinese Scholarship Council
                Award ID: 201606070059
                Award Recipient : Quan-Hui Liu Award Recipient : Marco Ajelli Award Recipient : Alessandro Vespignani
                Funded by: NIH MIDAS
                Award ID: U54GM111274
                Award Recipient : Quan-Hui Liu Award Recipient : Marco Ajelli Award Recipient : Alessandro Vespignani
                Categories
                Physical Sciences
                Biophysics and Computational Biology
                Biological Sciences
                Population Biology

                computational modeling,infectious diseases,multiplex networks,reproduction number,generation time

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