9 research outputs found
Senescence can play an essential role in modelling and estimation of vector based epidemiological indicators: demographical approach
In the paper basic epidemiological indicators, produced by an aging population of vectors, are calculated. In the study we follow two lines: calculations for demographically structured population and individual life-history approach. We discuss the advantages and limitations of these approaches and compare the results of our calculations with epidemiological indicators obtained for non-aging population of vectors.Gibraltar, age effect, disease control, gerontology
An Age-Structured Extension to the Vectorial Capacity Model
Vectorial capacity and the basic reproductive number (R(0)) have been instrumental in structuring thinking about vector-borne pathogen transmission and how best to prevent the diseases they cause. One of the more important simplifying assumptions of these models is age-independent vector mortality. A growing body of evidence indicates that insect vectors exhibit age-dependent mortality, which can have strong and varied affects on pathogen transmission dynamics and strategies for disease prevention.Based on survival analysis we derived new equations for vectorial capacity and R(0) that are valid for any pattern of age-dependent (or age-independent) vector mortality and explore the behavior of the models across various mortality patterns. The framework we present (1) lays the groundwork for an extension and refinement of the vectorial capacity paradigm by introducing an age-structured extension to the model, (2) encourages further research on the actuarial dynamics of vectors in particular and the relationship of vector mortality to pathogen transmission in general, and (3) provides a detailed quantitative basis for understanding the relative impact of reductions in vector longevity compared to other vector-borne disease prevention strategies.Accounting for age-dependent vector mortality in estimates of vectorial capacity and R(0) was most important when (1) vector densities are relatively low and the pattern of mortality can determine whether pathogen transmission will persist; i.e., determines whether R(0) is above or below 1, (2) vector population growth rate is relatively low and there are complex interactions between birth and death that differ fundamentally from birth-death relationships with age-independent mortality, and (3) the vector exhibits complex patterns of age-dependent mortality and R(0) ∼ 1. A limiting factor in the construction and evaluation of new age-dependent mortality models is the paucity of data characterizing vector mortality patterns, particularly for free ranging vectors in the field
Illustration of mortality models examined with different parameter values.
<p>Parameter values not listed; Gompertz: α = 0.01, declining: µ = 0.7, <i>g</i> = 0.1, logistic: <i>α = </i>0.007, <i>s</i> = 0.2, U-Shaped: <i>µ</i> = 0.001, <i>e<sub>0</sub></i> = 24, unimodal: <i>g</i> = 0.05, <i>e<sub>0</sub></i> = 30.</p
Hypothetical survivorship curves for different values of <i>H,</i> entropy.
<p>Hypothetical survivorship curves for different values of <i>H,</i> entropy.</p
Formulas for vectorial capacity in stable and stationary vector populations.
<p>Formulas for vectorial capacity in stable and stationary vector populations.</p
Transmission dynamics when an infectious host is introduced at time = 0.
<p>(A) age-dependent mortality, <i>m = </i>1.5, (B) age-independent mortality <i>m</i> = 1.5, (C) age-dependent mortality, <i>m = </i>0.007, (D) age-independent mortality <i>m</i> = 0.007. Solid line denotes humans and dashed line mosquitoes.</p
Vectorial capacity in a stable population for three mortality models (see Table 3 for functions).
<p>Parameters used in calculations are: exponential (dotted line, <i>g</i> = 0.0313), Gompertz (dashed line, α = 0.00662, <i>β</i> = 0.06234), and logistic (solid line, <i>α</i> = 0.00662, <i>β</i> = 0.06234, <i>s</i> = 1.073); taken from Styer et al. 2007a.</p