Modelling the Dynamics of an Experimental Host-Pathogen Microcosm within a Hierarchical Bayesian Framework

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Abstract

The advantages of Bayesian statistical approaches, such as flexibility and the ability to acknowledge uncertainty in all parameters, have made them the prevailing method for analysing the spread of infectious diseases in human or animal populations. We introduce a Bayesian approach to experimental host-pathogen systems that shares these attractive features. Since uncertainty in all parameters is acknowledged, existing information can be accounted for through prior distributions, rather than through fixing some parameter values. The non-linear dynamics, multi-factorial design, multiple measurements of responses over time and sampling error that are typical features of experimental host-pathogen systems can also be naturally incorporated. We analyse the dynamics of the free-living protozoan Paramecium caudatum and its specialist bacterial parasite Holospora undulata. Our analysis provides strong evidence for a saturable infection function, and we were able to reproduce the two waves of infection apparent in the data by separating the initial inoculum from the parasites released after the first cycle of infection. In addition, the parameter estimates from the hierarchical model can be combined to infer variations in the parasite's basic reproductive ratio across experimental groups, enabling us to make predictions about the effect of resources and host genotype on the ability of the parasite to spread. Even though the high level of variability between replicates limited the resolution of the results, this Bayesian framework has strong potential to be used more widely in experimental ecology. © 2013 Lunn et al.

Figures

  • Figure 1. Compartmental models. (a) without distinction between the inoculum and newly-produced parasites, (b) with distinction. doi:10.1371/journal.pone.0069775.g001
  • Table 1. Symbols and summaries of prior information for variables used in this study.
  • Figure 2. Experimental data. (a) Time series of the number of paramecia in each of the 12 populations of each clone, classified by inoculum and food level treatments; note the logarithmic scale. (b) Time series of the mean proportions of paramecia in each of the three stages of infection (green: S, amber: C, brown: I) across all populations. doi:10.1371/journal.pone.0069775.g002
  • Table 2. Posterior mean deviance D of the six models considered.
  • Figure 3. Model fits for clone K8, replicate A. Each panel shows a different variable (from top to bottom: S, C, I and G) in low food (left) and high food (right). The dots show experimental data and the lines show the predicted dynamics obtained from each of the five fitted models. doi:10.1371/journal.pone.0069775.g003
  • Table 3. Food-level-specific posterior medians and 95% intervals (Lower, Upper) for overall parameters of the two-wave, Gsaturating model.
  • Figure 4. Posterior median and 95%-credible intervals of parameters for the two-wave, G-saturating model. The parameters r1 , b and E are shown for each population. Darker grey areas show the prior ranges (see Table 1). A vague prior is assigned to b. doi:10.1371/journal.pone.0069775.g004
  • Figure 5. Posterior 95%-credible intervals for clone K8, replicate A, in high food. The dots show experimental data and the lines show the predicted dynamics for the two-wave, G-saturating model. In the central panel on the right-hand side, the red line shows the predicted dynamics of C1 and the blue line the predicted dynamics of C2. doi:10.1371/journal.pone.0069775.g005

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APA

Lunn, D., Goudie, R. J. B., Wei, C., Kaltz, O., & Restif, O. (2013). Modelling the Dynamics of an Experimental Host-Pathogen Microcosm within a Hierarchical Bayesian Framework. PLoS ONE, 8(8). https://doi.org/10.1371/journal.pone.0069775

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