Search arXivSearch

arXiv · 2112.14208

Spread of variants of epidemic disease based on the microscopic numerical simulations on networks

Abstract

Viruses constantly undergo mutations with genomic changes. The propagation of variants of viruses is an interesting problem. We perform numerical simulations of the microscopic epidemic model based on network theory for the spread of variants. Assume that a small number of individuals infected with the variant are added to widespread infection with the original virus. When a highly infectious variant that is more transmissible than the original lineage is added, the variant spreads quickly to the wide space. On the other hand, if the infectivity is about the same as that of the original virus, the infection will not spread. The rate of spread is not linear as a function of the infection strength but increases non-linearly. This cannot be explained by the compartmental model of epidemiology but can be understood in terms of the dynamic absorbing state known from the contact process.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yutaka Okabe, Akira Shudo. 2021-12-28. Spread of variants of epidemic disease based on the microscopic numerical simulations on networks. https://doi.org/10.1038/s41598-021-04520-0

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Beta-coalescents when sample size is large

Sweepstakes reproduction refers to a highly skewed individual recruitment success without involving natural selection and may apply to individuals in broadcast spawning populations characterised by Type III survivorship. We consider an extension of the model of sweepstakes reproduction for a haploid panmictic population of constant size $N$; the extension also works as an alternative to the Wright-Fisher model. Our model incorporates an upper bound on the random number of potential offspring (juveniles) produced by a given individual. Depending on how the bound behaves relative to the total population size, we obtain the Kingman coalescent, an incomplete Beta-coalescent, or the (complete) Beta-coalescent. We argue that applying such an upper bound is biologically reasonable. Moreover, we estimate the error of the coalescent approximation. The error estimates reveal that convergence can be slow, and small sample size can be sufficient to invalidate convergence, for example if the stated bound is of the form $N/\log N$. We use simulations to investigate the effect of increasing sample size on the site-frequency spectrum. When the limit is a Beta-coalescent, the site frequency spectrum will be as predicted by the limiting tree even though the full coalescent tree may deviate from the limiting one. When in the domain of attraction of the Kingman coalescent the effect of increasing sample size depends on the effective population size as has been noted in the case of the Wright-Fisher model. Conditioning on the population ancestry (the random ancestral relations of the entire population at all times) may have little effect on the site-frequency spectrum for the models considered here (as evidenced by simulation results).

q-bio.PE

The role of nestedness and saturating feedback in bipartite ecological systems

Large ecosystems balance competition and cooperation, yet standard generalized Lotka--Volterra models make mutualism destabilizing by amplifying disorder and driving unbounded growth. We show that Monod-like saturation resolves this paradox: dynamical mean-field theory and random-matrix analysis reveal a broader stable phase and enhanced survival. Network architecture provides a second control mechanism, but nestedness offers no intrinsic stability advantage. Instead, it is a byproduct of degree distributions with high connectivity necessary for stability.

q-bio.PE

TreeFlow: probabilistic modelling and automatic differentiation for phylogenetics

Probabilistic modelling frameworks are powerful tools for statistical modelling and inference. They are not immediately generalizable to phylogenetic problems due to the particular computational properties of the phylogenetic tree object. TreeFlow is a software library for probabilistic modelling and automatic differentiation with phylogenetic trees. It embeds phylogenetic trees in the TensorFlow Probability framework, and implements inference algorithms for phylogenetic models given a fixed tree topology. We demonstrate how TreeFlow can be used to quickly implement and assess new models. We also show that it provides reasonable performance for gradient-based inference algorithms compared to specialized computational libraries for phylogenetics.

q-bio.PE