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■Bio-mathematics, Statistics and Nano-Technologies: Mosquito Control Strategies
fully in analyzing a whole class of compartmental models dealing with the transition from
the disease-free to the endemic state or the reverse situation leading to the disease elimina-
tion. The number R0 is used frequently as a rule-of-thumb for determining the presence of
an epidemic. The following threshold is established: whenever R0 > 1 the disease persists
and there is an epidemic, and whenever R0 < 1 there is no epidemic and the disease fades
away.
The transition between the elimination and endemic disease can also be studied by
bifurcation theory: in which case the threshold is fixed by a so called transcritical bifur-
cation. That is R0 = 1 at the TC-point and therefore the associated threshold values are
equal. The stable disease-free becomes unstable when a parameter is varied and there origi-
nates a stable (for a non-catastrophic or supercritical TC) or an unstable (for a catastrophic
or subcritical TC) endemic equilibrium. In the second case, the second rule that R0 < 1
implying no epidemic is violated. Therein the transcritical bifurcation produces an unsta-
ble endemic equilibrium, and the term used in the epidemiology literature is a backward
bifurcation [29, 53] instead of subcritical often used in the nonlinear dynamical system
theory literature. Consequently, in the parameter region where R0 < 1 a bistable regime of
another stable endemic equilibrium (or limit cycle) may coexist with the stable disease-free
equilibrium and an epidemic can occur despite R0 being under the threshold value [27].
Coming back to a multi-strain model, the characteristic long-term dynamics, in addi-
tion to an equilibrium could exhibit several features such as limit cycles or chaotic be-
havior, because of the large number of equations and highly non-linear couplings among
them. Besides the trivial disease-free equilibrium, endemic equilibria with a single strain
(also known as boundary or exclusion equilibria) and endemic equilibria where multiple
strains are present, are possible.
As an example, the presence of multiple strains in the model [25, 41] gives rise to multi-
ple equilibria. Depending on the parameter values, their local asymptotic stability changes.
In [25] the boundary equilibria are always locally asymptotically stable. While the general
structure of these models is broadly similar, the presence of intermediate recovered host
classes R1,R2 in the model [41] allows both boundary equilibria to be locally asymptoti-
cally unstable. This shows that the nonlinear interactions between the model compartments
are an important factor in driving the asymptotic behavior of the model.
Furthermore, in realistic dengue models with infection/recovery rates above the R0
threshold the endemic equilibrium becomes unstable leading to more complex long-term
dynamical behavior such as limit cycles and chaos. These types of dynamics can be studied
using bifurcation analysis. Limit cycles describe periodic behaviour and typically arise
from a Hopf bifurcation. For chaotic dynamics another tool for the study of non-linear
dynamical systems, namely the calculation of Lyapunov exponents can be used [52]. Many
of the multi-strain models show mathematical symmetry and this property governs specific
types of bifurcations [2, 1, 34, 41].
6.2.2
Time scale separation
Mathematical models for vector-borne diseases are natural candidates for time
scale separation analysis based on singular perturbation theory. Typically the vector