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Stochastic dynamics of Francisella tularensis infection and replication

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  • Jonathan Carruthers
  • Grant Lythe
  • Martín López-García
  • Joseph Gillard
  • Thomas R Laws
  • Roman Lukaszewski
  • Carmen Molina-París

Abstract

We study the pathogenesis of Francisella tularensis infection with an experimental mouse model, agent-based computation and mathematical analysis. Following inhalational exposure to Francisella tularensis SCHU S4, a small initial number of bacteria enter lung host cells and proliferate inside them, eventually destroying the host cell and releasing numerous copies that infect other cells. Our analysis of disease progression is based on a stochastic model of a population of infectious agents inside one host cell, extending the birth-and-death process by the occurrence of catastrophes: cell rupture events that affect all bacteria in a cell simultaneously. Closed expressions are obtained for the survival function of an infected cell, the number of bacteria released as a function of time after infection, and the total bacterial load. We compare our mathematical analysis with the results of agent-based computation and, making use of approximate Bayesian statistical inference, with experimental measurements carried out after murine aerosol infection with the virulent SCHU S4 strain of the bacterium Francisella tularensis, that infects alveolar macrophages. The posterior distribution of the rate of replication of intracellular bacteria is consistent with the estimate that the time between rounds of bacterial division is less than 6 hours in vivo.Author summary: Infecting a host cell is required for the replication of many types of bacteria and viruses. In some cases, infected cells release new infectious agents continuously over their lifetime. In others, such as the Francisella tularensis bacterium studied here, they are released in a single burst that coincides with the cell’s death. We show how a stochastic model, the birth-and-death process with catastrophe, can be used to characterise infection in a single cell, thereby allowing us to account for burst events and quantify the kinetics of pathogenesis in the lung, the initial site of infection, as well as in other organs that the infection spreads to. We learn about the parameters of the mathematical model of Francisella tularensis infection making use of the experimental measurements of bacterial loads, together with approximate Bayesian statistical inference methods. The most important parameter describing the pathogenesis is the rate of replication of intracellular bacteria.

Suggested Citation

  • Jonathan Carruthers & Grant Lythe & Martín López-García & Joseph Gillard & Thomas R Laws & Roman Lukaszewski & Carmen Molina-París, 2020. "Stochastic dynamics of Francisella tularensis infection and replication," PLOS Computational Biology, Public Library of Science, vol. 16(6), pages 1-26, June.
  • Handle: RePEc:plo:pcbi00:1007752
    DOI: 10.1371/journal.pcbi.1007752
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