Received 20 June 2016; accepted 21 August 2016; published 24 August 2016
Dengue disease is regarded as a serious infectious disease. The four serotypes of viruses DEN 1 to DEN 4 are responsible for the disease. It is one of the re-emerging diseases in tropical and subtropical countries. A person infected by one of the four serotypes of dengue viruses will never be infected again by the same serotype, but the person loses immunity to other serotype of viruses and becomes more susceptible in developing dengue hemorrhagic fever  . The prevalence of the disease has been increasing dramatically and the disease has become a major public health problem in recent years. According to World Health Organization, dengue has shown 30 fold increase globally over five decades. About 50 - 100 million new infections are estimated to occur annually in more than 100 endemic countries. Almost fifty percent of the world’s population lives in the countries where dengue is endemic  .
There have been many mathematical studies to understand the dynamics of infectious diseases. Mathematical models can help in providing guides and suggestions for the control of the disease to the concerned authorities. Kermack and McKendrick introduced an SIR model to study the transmission of infectious diseases  which became very popular in the mathematical study of epidemic diseases. Esteva and Vargas proposed an SIR-SI model to study the transmission dynamics of dengue disease considering constant  and variable  host populations. Since then, different mathematical models have been proposed to study dengue disease transmission. Authors in   studied the impact of awareness in the transmission of dengue disease. Pinho et al.  used mathematical model for dengue disease transmission with the aim of analyzing and comparing two dengue epidemics that occurred in Brazil. Pongsumpun  studied the incubation period of dengue viruses using SEIR model. Edy and Supriatna proposed a two dimensional epidemic model to study the transmission of dengue disease restricting the dynamics for two dimensions for the constant host and vector populations  .
Emerging and re-emerging diseases like dengue disease spread very quickly due to the travel of infective human population from one region to the other. They spread the disease in new regions. Different spatial models have been developed to study infectious diseases. Arino and Driessche   studied the disease spread in meta-populations and they developed multicity model to study the infectious diseases in different cities. Wang and Mulone  ; and Wang and Zhao  proposed epidemic models with population dispersal to describe the dynamics of disease spread between n patches and two patches. Hsieh et al. proposed a multi-patch epidemic model to study the impact travel between patches for the spatial spread of influenza  .
Lee and Castillo-Chavez  formulated the two patch dengue transmission model to explore the role of residence times in dengue transmission dynamics and optimal control strategies assuming that only the human budgets their residence time across the patches. In the present work, we have discussed the multi-patch SIR-SI model to study the transmission dynamics of dengue disease among n-patches. We have investigated the impact of travel rates of humans in the transmission dynamics and control of dengue disease. We have assumed different travel rates and different disease prevalences in different patches.
2. Model Formulation
For the formulation of the model, we divide human population in three classes, susceptible, infective and recovered. Let, , respectively denote the number of susceptible humans, infective humans and recovered humans in patch i. Also, we divide mosquito population in two compartments only, susceptible and infective mosquitoes. Let, respectively denote the number of susceptible mosquitoes and infective mosquitoes in patch.
Figure 1. Flow chart of the model.
Table 1. Parameters used in the model.
(Total host population in patch i in time t)
(Total vector population in patch i in time t)
The total host and vector population sizes in all n-patches in time t is
Theorem 1. The system of Equations (2.1) has a unique disease free equilibrium point.
Proof: A disease free equilibrium (DFE) for the system of Equations (2.1) is a steady state solution of the system where and for.
In disease free situation,
In matrix form,
Here, has all off-diagonal entries negative and every column has positive sum. So, is a non-singular M-matrix. Since all the off diagonal elements are non-zero, is irreducible  . Hence, has a positive inverse and the system of Equations (2.2) has a unique solution. So, is the solution of the system, i.e., for. Hence, in disease free situation, , , for all. Also, ,.
Now, we show that the disease free equilibrium is unique. From the system of Equations (2.1), in disease free situation:
For the host populations only:
For vector populations only:
Here, the matrix C has positive column sums and each non-diagonal element is negative. So, the matrix C is an irreducible and non-singular M-matrix. Again, since C is an irreducible non-singular M-matrix, C must have positive inverse, i.e.,  . Hence, there is a unique solution.
Also, the matrix D is a diagonal matrix with positive diagonal elements. So, there exists with positive diagonal elements. Hence, is unique solution of. The results show that there always exists a unique disease free equilibrium point.
3. Basic Reproduction Number
Basic reproduction number is defined as the expected number of secondary cases produced by a typical infective individual introduced into a completely susceptible population.
We use next generation matrix method   to find the basic reproduction number. For, we order the infected variables by. Then,
Here, the matrix has column sums, and all off diagonal elements are negative. So, the matrix is an irreducible non-negative M-matrix. Hence, exists and is positive, i.e.,.
Also, is a diagonal matrix with positive entries. So, nonnegative exists. The basic reproduction number for the system (2.1) is the spectral radius of.
Theorem 2. If R0 < 1, then the disease free equilibrium is locally asymptotically stable and unstable if R0 > 1.
Proof: Let and be the matrices of partial derivatives evaluated at the disease free equilibrium. The Jacobian matrix for the linearization of the system about the disease free equilibrium is obtained as the block structure
Matrix J is triangular. So, the eigenvalues of J are those of the partition matrices and. Also,
Matrices C and D (matrices defined in Theorem 1) are non-singular M matrices. So, spectral abscissa,  and eigenvalues of the matrix have negative real parts.
Hence, the matrix J will have eigenvalues all with negative real parts if the matrix has all eigenvalues with negative real parts. Also, F is non-negative matrix and V is non-singular M-matrix. So, eigenvalues of will have negative real parts if and only if  . i.e., disease free equilibrium is locally asymptotically stable if and only if the basic reproduction number.
If, then. It shows that at least one eigenvalue lies in right half plane. So, the disease free equilibrium is unstable if.
Theorem 3. If R0 < 1, then the disease free equilibrium is globally asymptotically stable and unstable if R0 > 1.
Proof: Since, and, we have from the system of Equations (2.1),
Consider the linear system
The system of Equations (3.2) can be written as
where, Here, F is a non-negative matrix and V is a non-negative M- matrix. So,
i.e., Eigenvalues of lie on left half plane if. Hence, each positive solution of (3.3) satisfies
i.e., for all
Since all the variables in the system of Equations (2.1) are non-negative, the use of Comparison theorem   leads to
for all (3.5)
From the system of Equations (2.1), we have
i.e., (In matrix form)
Here, (matrix defined in Theorem 1) is non-singular M-matrix. So, all eigenvalues of lie in the left half plane. Hence,
In matrix form
Here, matrices C and D are non-singular M-matrices, all their eigenvalues lie in left half plane. Therefore, if and be the homogeneous solutions of Equation (3.8) and Equation (3.9), then
Matrix C is an irreducible, non-singular M-matrix. So, the matrix C has positive inverse. is a particular solution and is the general solution of Equation (3.8). Also, Matrix D is diagonal matrix with positive diagonal elements. So, D has an inverse with positive diagonal elements. Hence, is a particular solution and is the general solution of Equation (3.9). And,
Thus, as, we obtain the equilibrium point. Hence, the disease free equilibrium is globally asymptotically stable if. If  , Theorem 2 admits that the disease free equilibrium point is unstable.
4. For n = 2 (Considering Two Patches Only)
Basic Reproduction Number
(Basic reproduction number, Patch 1)
(Basic reproduction number, Patch 2)
5. Numerical Results and Discussions
We considered the case of two patches and computed basic reproduction number for the numerical results. The parameter values chosen for the simulation are:,  , , ,  , , ,  , ,  ,  ,  . With and. Thus, patch 1 is a high disease dominant patch and patch 2 is a low disease dominant patch.
Figure 2 shows the dynamics of susceptible hosts of patch 1 and patch 2. Patch 1 is a high disease dominant patch, so the susceptible host population in the patch decreases most rapidly over the time. Patch 2 is a low disease dominant patch. So, the number of susceptible hosts in patch 2 increases initially due to the travel of susceptible hosts from patch 1. Afterwards, due to the interaction of susceptible hosts with infectious mosquitoes and due to the natural death of some humans, the susceptible host population starts decreasing.
When the susceptible hosts come in contact with infectious mosquitoes, hosts get infected. So, the population size of infected hosts increases (Figure 3). Eventually, the infected host population decreases to zero due to their recovery from the disease and due to the natural death of some humans.
Changes in basic reproduction number with the changes in travel rates are illustrated in Figure 4. It is observed that basic reproduction number decreases with the increasing values of. Also, the number increases when the values of travel rate are increased. The figure shows that, the burden of disease reduces when the travel rates of hosts from high disease dominant patch to low disease dominant patch are high. The burden of disease increases when the travel rates of hosts from low disease dominant patch to the high disease
Figure 2. Dynamics of susceptible host population.
Figure 3. Dynamics of infected host population.
dominant patch are high. Thus, we should increase the travel rates of hosts from high disease dominant patch to the low disease dominant patch to bring the disease under control.
Basic reproduction number of two patches is determined by the basic reproduction numbers, of patch 1 and of patch 2. Figure 5 shows that increases together with and. If basic reproduction numbers of the both patches are high, then the basic reproduction number gets higher. Thus, if any one of the two patches is more disease dominant and there is mobility between the two patches, then this can cause the whole system to be more endemic.
6. Discussion of Travel Restrictions
In this section, the dynamics of the host population is observed with the restriction of the travel of symptomatic hosts from one patch to the other patch.
Restricting the travel of symptomatic hosts from low disease dominant patch to high disease dominant patch
Figure 4. Basic reproduction number against and.
Figure 5. Basic reproduction number against and.
Similarly, when and all other parameters are same i.e., on restricting the travel of symptomatic travelers from high disease dominant patch to low disease dominant patch, we find that basic reproduction number of patch 1 increases (Figure 8) and basic reproduction number of patch 2 decreases (Figure 9). Thus, the disease in low disease dominant patch can be controlled by restricting the travel of symptomatic hosts from high disease dominant patch to low disease dominant patch.
Dynamics of infected host populations are observed in Figure 10 and Figure 11 with travel restrictions. When infected hosts of patch 1 are restricted to travel (Figure 10) more hosts in patch 1 (very few hosts in patch 2) are observed infected of the disease when compared with the case that infected hosts of patch 2 are restricted (Figure 11) to travel. The graphical results (Figure 10, Figure 11) suggest that the disease spread in patch 2 can be brought under control by restricting the travel of infected hosts from patch 1 to patch 2.
Figure 6. Basic reproduction number of patch 1 against with.
Figure 7. Basic reproduction number of patch 2 against with.
Figure 8. Basic reproduction number of patch 1 against with.
Figure 9. Basic reproduction number of patch 2 against with.
In the present work, we have studied the effect of travel of humans on the transmission dynamics of dengue disease. We discussed the disease transmission dynamics between n-patches by subdividing vector population in susceptible and infectious class and host population in susceptible, infectious and recovered class.
We defined the multi-patch basic reproduction number by taking each patch together. Basic reproduction number of patch 1 and of patch 2 are calculated. The results show that the disease dies out if and invades the population if. Theorem 2 and Theorem 3 show that the disease free equilibrium is locally and globally asymptotically stable if and unstable if.
Travel of human from one place to another place affects the whole dynamics of the dengue disease transmission. We have shown that traveling of infected human changes the less disease dominant patch to high disease
Figure 10. Dynamics of infected host population with.
Figure 11. Dynamics of infected host population with.
dominant patch. Also, restricting the travel of infected hosts helps in controlling the disease. Basic reproduction number is seen higher when there is higher travel rate from low disease dominant patch to the high disease dominant patch. The basic reproduction number is seen lowered when there is higher travel rate from high dominant disease patch to the low disease dominant patch. Thus, we can control the disease in low disease dominant patch by restricting the travel of infected hosts from high disease dominant patch.
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