Multi-Strain Host-Vector Dengue Modeling: Dynamics and Control
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O(ε2)
QSSA
full model
S(t)
I(t)
260
240
220
1.5
1
0.5
0
equilibrium
O(ε)
QSSA
full model
S(t)
I(t)
270
240
210
180
150
3
2.5
2
1.5
1
0.5
0
Figure 6.1: Trajectory in (S,I)-plane of (6.4) and trajectories with two approximations of
V : the O(ε0) or QSSA approximation and for terms up to O(ε) (left) and up to O(ε2)
(right).
only when ε > 0.175482. When ε = 0.175482 the spurious equilibrium equals S = N and
I = 0. Consequently the first order approximation approach can fail for ε > 0.175482 when
the initial data of the trajectory is far from the expected endemic equilibrium close in the
full model.
The second-order approximation does not have this shortcoming. However, for the
initial condition used the calculated transient dynamics is also poor for the second-order
approximation with ε = 1. The technique is applicable only when the starting point is suffi-
ciently close to the equilibrium as in the case of the QSSA trajectory in Figure 6.1 (QSSA
green curve). In (6.4) a value for ε was quantified by its interpretation as the ratio of the
rates of changes of the state variables of the host and vector population near equilibrium.
It was argued that ε = 1/365 is suitable value for the SIR-UV model. Simulations (not
shown) for the first- and second-order approximations indicate that when starting close to
the M0-plane defined in the Appendix 6.A, there are no spurious equilibria but higher-
order approximations do not improve much the QSSA solutions when ε = 1/365.
6.3
TWO-STRAIN DENGUE MODELS
In this section we describe the two-strain dengue models, namely the Host-only and
the host-vector model. The analysis of these models relies heavily on numerical techniques
where the time dependency on parameter values is obtained by simulations and bifurcation
analysis. Besides equilibria and limit cycles, both models show also chaotic dynamics.
6.3.1
Host-only models
In host-only models [2, 1, 12, 26, 34], the vector dynamics is considered implicitly in
the parameters by assuming that the size of the infected vector population is proportional
to that of the infected host population. In that respect this modeling approach closely re-