4.4 Article

SIS and SIR Epidemic Models Under Virtual Dispersal

Journal

BULLETIN OF MATHEMATICAL BIOLOGY
Volume 77, Issue 11, Pages 2004-2034

Publisher

SPRINGER
DOI: 10.1007/s11538-015-0113-5

Keywords

Epidemiology; SIS-SIR models; Dispersal; Residence times; Global stability; Adaptive behavior; Final size relationship

Funding

  1. National Institute of General Medical Sciences (NIGMS) at National Institutes of Health [1R01GM100471-01]
  2. NSF-DMS [1313312]
  3. Direct For Biological Sciences
  4. Division Of Environmental Biology [1414374] Funding Source: National Science Foundation
  5. Direct For Mathematical & Physical Scien
  6. Division Of Mathematical Sciences [1313312] Funding Source: National Science Foundation

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We develop a multi-group epidemic framework via virtual dispersal where the risk of infection is a function of the residence time and local environmental risk. This novel approach eliminates the need to define and measure contact rates that are used in the traditional multi-group epidemic models with heterogeneous mixing. We apply this approach to a general n-patch SIS model whose basic reproduction number is computed as a function of a patch residence-time matrix . Our analysis implies that the resulting n-patch SIS model has robust dynamics when patches are strongly connected: There is a unique globally stable endemic equilibrium when , while the disease-free equilibrium is globally stable when . Our further analysis indicates that the dispersal behavior described by the residence-time matrix has profound effects on the disease dynamics at the single patch level with consequences that proper dispersal behavior along with the local environmental risk can either promote or eliminate the endemic in particular patches. Our work highlights the impact of residence-time matrix if the patches are not strongly connected. Our framework can be generalized in other endemic and disease outbreak models. As an illustration, we apply our framework to a two-patch SIR single-outbreak epidemic model where the process of disease invasion is connected to the final epidemic size relationship. We also explore the impact of disease-prevalence-driven decision using a phenomenological modeling approach in order to contrast the role of constant versus state-dependent on disease dynamics.

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