Original article Biomath 1 (2012), 1209255, 1–7 B f Volume ░, Number ░, 20░░ BIOMATH ISSN 1314-684X Editor–in–Chief: Roumen Anguelov B f BIOMATH h t t p : / / w w w . b i o m a t h f o r u m . o r g / b i o m a t h / i n d e x . p h p / b i o m a t h / Biomath Forum Multiregional SIR Model with Infection during Transportation Diána H. Knipl∗ and Gergely Röst† ∗Analysis and Stochastics Research Group – Hungarian Academy of Sciences, Bolyai Institute, University of Szeged, Szeged, Hungary Email: knipl@math.u-szeged.hu † Bolyai Institute, University of Szeged, Szeged, Hungary Email: rost@math.u-szeged.hu Received: 12 July 2012, accepted: 25 September 2012, published: 18 October 2012 Abstract—We present a general epidemic model to describe the spread of an infectious disease in several regions connected by transportation. We take into account that infected individuals not only carry the disease to a new place while traveling from one region to another, but transmit the disease during travel as well. We obtain that a model structured by travel time is equivalent to a large system of differential equations with multiple delays. By showing the local Lipschitz property of the dynamically defined delayed feedback function, we obtain existence and uniqueness of solutions of the system. Keywords-epidemic spread; transportation model; dy- namically defined delay; Lipschitz continuity I. INTRODUCTION We consider an arbitrary n number of regions which are connected by transportation, and present an SIR based model which describes the spread of infection in the regions and also during travel between them. We show that our model is equivalent to a system of functional differential equations x′(t) = F(xt), (1) where t ∈ R, t ≥ 0 and x : R � R3n. We use the nota- tion xt ∈ C, xt(θ) = x(t + θ) for θ ∈ [−σ, 0], where for σ > 0, we define our phase space C = C([−σ, 0], R3n) as the Banach space of continuous functions from [−σ, 0] to R3n, equipped with the usual supremum norm || · ||. In the sequel we use the notation |v| for the Euclidean TABLE I VARIABLES AND KEY MODEL PARAMETERS (j, k ∈ {1, . . . n}) Sj , Ij , susceptible, infected, recovered, all Rj , Nj individuals in region j sk,j , ik,j , susceptible, infected, recovered, all rk,j , nk,j individuals during travel from region k to j Λj incidence in region j λk,j incidence during travel from region k to j αj recovery rate of infected individuals in region j αk,j recovery rate during travel from region k to j µj,k travel rate from region j to region k τk,j duration of travel from region k to j norm of any vector v ∈ Rm for m ∈ Z+. In order to obtain the general existence and uniqueness result for the system, we prove that F : C � R3n satisfies the local Lipschitz condition on each bounded subset of C, that is, for every M > 0 there exists a constant K = K(M) such that the inequality |F(φ) − F(ψ)| ≤ K||φ − ψ|| holds for every φ,ψ ∈ C with ||φ||, ||ψ|| ≤ M. The paper is organised as follows. In Section 2 we introduce our model, then we obtain the compact form of the system in Section 3. Section 4 concerns with the proof of the local Lipschitz condition for various types of incidence (new cases per unit of time). Citation: D. Knipl, G. Röst, Multiregional SIR Model with Infection during Transportation, Biomath 1 (2012), 1209255, http://dx.doi.org/10.11145/j.biomath.2012.09.255 Page 1 of 7 http://www.biomathforum.org/biomath/index.php/biomath http://dx.doi.org/10.11145/j.biomath.2012.09.255 D. Knipl et al., Multiregional SIR Model with Infection during Transportation II. MODEL DESCRIPTION We formulate a dynamical model describing the spread of an infectious disease in n regions and also during travel from one region to another. Divide the entire populations of the n regions into the disjoint classes Sj, Ij, Rj, j ∈ {1, . . .n}, where Sj(t) Ij(t), Rj(t), j ∈ {1, . . .n} denote the number of susceptible, infected and recovered individuals at time t in region j. For the total population in region j at time t, we use the notation Nj(t) = Sj(t) + Ij(t) + Rj(t). The incidence in region j is denoted by Λj ( Sj(t),Ij(t),Rj(t) ) , model parameter αj represents the recovery rate of infected individuals in region j. We denote the travel rate from region j to region k by µj,k and we set µj,j = 0 for j,k ∈ {1, . . .n}. Let sk,j, ik,j, rk,j denote susceptible, infected and recovered travelers, where lower index-pair {k,j}, j,k ∈ {1, . . .n} indicates that individuals are traveling from region k to region j. Let τk,j > 0 denote the time required to complete the travel from region k to region j, which is assumed to be fixed. To describe the disease dynamics during travel, for each t∗ we define sk,j(u; t∗), ik,j(u; t∗), rk,j(u; t∗), j,k ∈ {1, . . .n} as the densities of individuals with respect to u who started travel at time t∗ and belong to classes sk,j, ik,j, rk,j, where u ∈ [0,τk,j] denotes the time elapsed since the beginning of the travel. Then sk,j(τk,j; t − τk,j), ik,j(τk,j; t − τk,j), rk,j(τk,j; t − τk,j) express the inflow of individuals arriving from region k to compartments Sj, Ij, Rj at time t, respectively. Let nk,j(u; t∗) = sk,j(u; t∗) + ik,j(u; t∗) + rk,j(u; t∗) denote the total density of individuals during travel from region k to j, where j,k ∈ {1, . . .n}. The total density is constant during travel, i.e. nk,j(u; t∗) = nk,j(0, t∗) for all u ∈ [0,τk,j]. During the course of travel from region k to j, λk,j ( sk,j(u; t∗), ik,j(u; t∗),rk,j(u; t∗) ) represents the incidence, and let αk,j denote the recovery rate. All variables and model parameters are listed in Table I. Based on the assumptions formulated above, we obtain the following system of differential equations for the disease transmission in region j, j ∈ {1, . . .n}:  Ṡj(t) = −Λj(·) − ( n∑ k=1 µj,k ) Sj(t) + n∑ k=1 sk,j(τk,j; t − τk,j), İj(t) = Λj(·) − ( n∑ k=1 µj,k ) Ij(t) − αjIj(t) + n∑ k=1 ik,j(τk,j; t − τk,j), Ṙj(t) = αjIj(t) − ( n∑ k=1 µj,k ) Rj(t) + n∑ k=1 rk,j(τk,j; t − τk,j). (Lj) For each j,k ∈ {1, . . .n} and for each t∗, the following system (Tk,j) describes the evolution of the densities during the travel from region k to region j which started at time t∗:   d du sk,j(u; t∗) = −λk,j(·), d du ik,j(u; t∗) = λk,j(·) − αk,jik,j(u; t∗), d du rk,j(u; t∗) = αk,jik,j(u; t∗). (Tk,j) For sake of simplicity, in systems (Lj) and (Tk,j) we use the notations Λj(·) and λk,j(·) for the incidences, where these functions are meant to be evaluated at the appropriate points. For u = 0, the densities are determined by the rates individuals start their travels from region k to region j at time t∗. Hence, the initial values for system (Tk,j) at u = 0 are given by  sk,j(0; t∗) = µk,jSk(t∗), ik,j(0; t∗) = µk,jIk(t∗), rk,j(0; t∗) = µk,jRk(t∗). (IV Tk,j) Notice that µj,j = 0 for j ∈ {1, . . .n} implies that for each t∗, it holds that sj,j(u; t∗) = ij,j(u; t∗) = rj,j(u; t∗) ≡ 0, as there is no travel from region j to itself. Since travel from region k to region j takes τk,j units of time to complete, we need to assure that there exists a unique solution of system (Tk,j) on [0,τk,j] (see Proposition IV.1). Now we turn our attention to the terms sk,j(τk,j; t−τk,j), ik,j(τk,j; t−τk,j), rk,j(τk,j; t−τk,j), j,k ∈ {1, . . .n} in Biomath 1 (2012), 1209255, http://dx.doi.org/10.11145/j.biomath.2012.09.255 Page 2 of 7 http://dx.doi.org/10.11145/j.biomath.2012.09.255 D. Knipl et al., Multiregional SIR Model with Infection during Transportation system (Lj), which give the inflow of individuals arriving to classes Sj, Ij, Rj at time t, upon completing a travel from region k. At time t, these terms are determined by the solution of system (Tk,j) at u = τk,j with initial values (IV Tk,j) for t∗ = t − τk,j, since individuals who left region k with rate µk,j at time t − τk,j will enter region j at time t. Next we specify initial values for system (Lj) at t = 0. Since for k ∈ {1, . . .n}, travel from region k to region j takes τk,j units of time to complete, arrivals to region j at time t are determined by the state of the classes of region k at t−τk,j, via the solution of system (Tk,j) and initial values (IV Tk,j). Thus, we set up initial values as follows:   Sj(θ) = ϕS,j(θ), Ij(θ) = ϕI,j(θ), Rj(θ) = ϕR,j(θ), (IV Lj) where θ ∈ [−τ, 0] for τ := maxj,k∈{1,...n} τk,j, moreover ϕS,j, ϕI,j and ϕR,j are continuous functions for j ∈ {1, . . .n}. III. THE COMPACT FORM OF THE SYSTEM For each j,k ∈ {1, . . .n} and t∗ ≥ 0, we define y(u) = yt∗k,j(u) = (sk,j(u; t∗), ik,j(u; t∗), rk,j(u; t∗)) T and g = gk,j = (gS,gI,gR)T , where y : [0,τk,j] � R3, g : R3 � R3 and gS(y) = −λk,j(y1,y2,y3), gI(y) = λk,j(y1,y2,y3) − αk,jy2, gR(y) = αk,jy2. Then for each j,k and t∗, system{ y′(u) = g(y(u)), y(0) = y0 (2) is a compact form of system (Tk,j) with initial values (IV Tk,j) for y0 = (µk,jSk(t∗), µk,jIk(t∗), µk,jRk(t∗))T . Let y(u, 0; y0) denote the solution of system (2) at time u with initial value y0. The feasible phase space is the nonnegative cone C+ = C([−τ, 0], R3n+ ) of the Banach space of continuous func- tions from [−τ, 0] to R3n with the sup norm. For every j,k ∈ {1, . . .n}, let hk,j : R3n � R3 be defined by hk,j = (hS,k,j, hI,k,j, hR,k,j)T , where hS,k,j(v) = µk,jv3k−2, hI,k,j(v) = µk,jv3k−1, hR,k,j(v) = µk,jv3k. For φ ∈ C+, we use the notation ŷφ(−τk,j )(u) = y(u, 0; hk,j(φ(−τk,j))). Furthermore we define Wk : C+ � R3n as Wk(φ) = ( ŷφ(−τk,1)(τk,1), . . . ŷφ(−τk,n)(τk,n) )T . Let x(t) = (S1(t), I1(t), R1(t), . . .Sn(t),In(t),Rn(t))T for t ≥ 0, and f = (fS,1,fI,1,fR,1, . . .fS,n,fI,n,fR,n)T , where for j ∈ {1, . . .n}, fS,j(x) = −Λj(x3j−2,x3j−1,x3j) − ( n∑ k=1 µj,k ) x3j−2, fI,j(x) = Λj(x3j−2,x3j−1,x3j) − αjx3j−1 − ( n∑ k=1 µj,k ) x3j−1, fR,j(x) = αjx3j−1 − ( n∑ k=1 µj,k ) x3j. Clearly the union of systems (Lj) with initial conditions (IV Lj), j ∈ {1, . . .n} can be written in a closed form as   x′(t) = f(x(t)) + n∑ k=1 Wk(xt) =: F(xt), x0 = ϕ, (3) where F : C+ � R3n and for ϕ ∈ C+, ϕ := (ϕS,1,ϕI,1,ϕR,1, . . . ,ϕS,n,ϕI,n,ϕR,n)T . IV. THE LOCAL LIPSCHITZ PROPERTY This section is devoted to the proof of the general existence and uniqueness result of system (3). First, we obtain the following simple result. Proposition IV.1. Assume that λk,j possesses the lo- cal Lipschitz property on each bounded subset of R3. Moreover, assume that λk,j(q1,q2,q3) ≥ 0 and λk,j(0,q2,q3) = 0 hold for q1,q2,q3 ≥ 0. Then there exists a unique solution of system (2) which continuously depends on the initial data, and for u ∈ [0,τ] and y0 ≥ 0 the following inequality holds componentwise: 0 ≤ y(u, 0; y0) ≤ √ 3 |y0|. Proof: The local Lipschitz condition guarantees the existence of a unique solution which continuously depends on the initial data (see Picard-Lindelöf theorem in Chapter II, Theorem 1.1 and Chapter V, Theorem 2.1 in [1]). We have also seen that nk,j(u; t∗) is constant for all u in the maximal interval of existence, moreover from the nonnegativity condition of λk,j it follows that Biomath 1 (2012), 1209255, http://dx.doi.org/10.11145/j.biomath.2012.09.255 Page 3 of 7 http://dx.doi.org/10.11145/j.biomath.2012.09.255 D. Knipl et al., Multiregional SIR Model with Infection during Transportation nonnegative initial data give rise to nonnegative solution. Hence we obtain 0 ≤ nk,j(0; t∗) = nk,j(u; t∗), 0 ≤ sk,j(0; t∗) + ik,j(0; t∗) + rk,j(0; t∗) = sk,j(u; t∗) + ik,j(u; t∗) + rk,j(u; t∗) = µk,j(Sk(t∗) + Ik(t∗) + Rk(t∗)), 0 ≤ sk,j(u; t∗), ik,j(u; t∗),rk,j(u; t∗) ≤ µk,j(Sk(t∗) + Ik(t∗) + Rk(t∗)), (4) where we used (IV Tk,j). Using the definition of y, (4) implies that the inequality 0 ≤ ( y(u, 0; y0) ) 1 , ( y(u, 0; y0) ) 2 , ( y(u, 0; y0) ) 3 ≤ (y0)1 + (y0)2 + (y0)3 ≤ √ 3 √ ((y0)1) 2 + ((y0)2) 2 + ((y0)3) 2 holds for u ∈ [0,∞), where y0 = ( (y0)1, (y0)2, (y0)3 )T is the initial value and we used the arithmetic-quadratic mean inequality. We conclude that the solution exists on [0,τ] and is bounded. Now we prove that if we assume that Λj and λk,j possess the local Lipschitz property, then F is also locally Lipschitz continuous. Lemma IV.2. Let us suppose that for all j,k ∈ {1, . . .n}, Λj and λk,j possess the local Lipschitz prop- erty, λk,j(q1,q2,q3) ≥ 0 and λk,j(0,q2,q3) = 0 hold for q1,q2,q3 ≥ 0. Then F satisfies the local Lipschitz condition on each bounded subset of C+. Proof: We claim that for every M > 0 there exists a constant K = K(M) such that the inequality |F(φ) −F(ψ)| ≤ K||φ−ψ|| holds for every φ,ψ ∈ C+ with ||φ||, ||ψ|| ≤ M. Fix indices j,k ∈ {1, . . .n}. For ||ψ|| ≤ M it holds componentwise that 0 ≤ ψ(−τk,j) ≤ M, so due to the continuity of hk,j, there exists a constant L h k,j(M) such that 0 ≤ hk,j(ψ(−τk,j)) ≤ Lhk,j is satisfied component- wise. For y0 = hk,j(ψ(−τk,j)) Proposition IV.1 implies that there exists a Jk,j = Jk,j(Lhk,j) = Jk,j(M) such that the inequality |ŷψ(−τk,j )(u)| ≤ Jk,j holds for u ∈ [0,τ] (for instance we can choose Jk,j = √ 3Lhk,j). The local Lipschitz property of hk,j follows from its definition. We assumed that λk,j is Lipschitz contin- uous, this implies the Lipschitz continuity of g. Let Khk,j = K h k,j(M) be the Lipschitz constant of hk,j on the set {v ∈ R3n : |v| ≤ M}, we denote the Lipschitz constant of g = gk,j on the set {v ∈ R3 : |v| ≤ Jk,j} by K g k,j = K g k,j(J) = K g k,j(M). For any ||φ||, ||ψ|| ≤ M, it holds that |φ(−τk,j)|, |ψ(−τk,j)| ≤ M. Since solu- tions of (2) can be expressed as y(u, 0; y0) = y0 +∫u 0 g(y(r, 0; y0)) dr, we have∣∣ŷφ(−τk,j )(u) − ŷψ(−τk,j )(u)∣∣ = ∣∣∣∣hk,j(φ(−τk,j)) + ∫ u 0 g(ŷφ(−τk,j )(r)) dr − ( hk,j(ψ(−τk,j)) + ∫ u 0 g(ŷψ(−τk,j )(r)) dr )∣∣∣∣ ≤ |hk,j(φ(−τk,j)) − hk,j(ψ(−τk,j))| + ∫ u 0 ∣∣g(ŷφ(−τk,j )(r)) − g(ŷψ(−τk,j )(r))∣∣ dr ≤ Khk,j||φ − ψ|| + ∫ u 0 K g k,j ∣∣ŷφ(−τk,j )(r) − ŷψ(−τk,j )(r)∣∣ dr (5) for u ∈ [0,τ]. Define Γ(u) = ∣∣ŷφ(−τk,j )(u) − ŷψ(−τk,j )(u)∣∣ for u ∈ [0,τ]. Then (5) gives Γ(u) ≤ Khk,j||φ − ψ|| + K g k,j ∫ u 0 Γ(r) dr, and from Gronwall’s inequality we have Γ(u) ≤ Khk,j||φ − ψ||e K g k,ju. (6) Applying the definition of Wk, we arrive to the inequal- ity |(Wk(φ))j − (Wk(ψ))j| = ∣∣ŷφ(−τk,j )(τk,j) − ŷψ(−τk,j )(τk,j)∣∣ ≤ Khk,je K g k,jτk,j||φ − ψ||, where we used (6) at u = τk,j. It is straightforward that Wk has the Lipschitz con- dition for any k ∈ {1, . . .n}, KWk = KWk (M) =√∑n j=1 ( Khk,je K g k,jτk,j )2 is a suitable choice for the Lipschitz constant. Finally, the assumption that Λj is Lipschitz continuous for any j ∈ {1, . . .n} implies the Lipschitz continuity of f, so let Kf = Kf (M) be the Lipschitz constant of f on the set {v ∈ R3n : |v| ≤ M}. Then for any ||φ||, ||ψ|| ≤ M, |φ(0)|, |ψ(0)|, |φ(−τ)|, |ψ(−τ)| ≤ M hold and thus |F(φ) − F(ψ)| ≤ |f(φ(0)) − f(ψ(0))| + n∑ k=1 |Wk(φ) − Wk(ψ)| ≤ Kf||φ − ψ|| + n∑ k=1 KWk||φ − ψ||. Biomath 1 (2012), 1209255, http://dx.doi.org/10.11145/j.biomath.2012.09.255 Page 4 of 7 http://dx.doi.org/10.11145/j.biomath.2012.09.255 D. Knipl et al., Multiregional SIR Model with Infection during Transportation |Λ1(p) − Λ1(q)| = β1 ∣∣∣∣ q1q2q1 + q2 + q3 − p1p2p1 + p2 + p3 ∣∣∣∣ = β1 ∣∣∣∣ q1q2q1 + q2 + q3 − q1p2q1 + q2 + q3 + q1p2q1 + q2 + q3 − q1p2 q1 + p2 + q3 + q1p2 q1 + p2 + q3 − q1p2 q1 + p2 + p3 + q1p2 q1 + p2 + p3 − q1p2 p1 + p2 + p3 + q1p2 p1 + p2 + p3 − p1p2 p1 + p2 + p3 ∣∣∣∣ ≤ β1 (∣∣∣∣ q1q2q1 + q2 + q3 − q1p2q1 + q2 + q3 ∣∣∣∣ + ∣∣∣∣ q1p2q1 + q2 + q3 − q1p2q1 + p2 + q3 ∣∣∣∣ + ∣∣∣∣ q1p2q1 + p2 + q3 − q1p2q1 + p2 + p3 ∣∣∣∣ + ∣∣∣∣ q1p2q1 + p2 + p3 − q1p2p1 + p2 + p3 ∣∣∣∣ + ∣∣∣∣ q1p2p1 + p2 + p3 − p1p2p1 + p2 + p3 ∣∣∣∣ ) = β1 ( |q2 − p2| ∣∣∣∣ q1q1 + q2 + q3 ∣∣∣∣ + |p2 − q2| ∣∣∣∣ q1p2(q1 + q2 + q3)(q1 + p2 + q3) ∣∣∣∣ +|p3 − q3| ∣∣∣∣ q1p2(q1 + p2 + q3)(q1 + p2 + p3) ∣∣∣∣ +|p1 − q1| ∣∣∣∣ q1p2(q1 + p2 + p3)(p1 + p2 + p3) ∣∣∣∣ + |q1 − p1| ∣∣∣∣ p2p1 + p2 + p3 ∣∣∣∣ ) ≤ β1 (2|q2 − p2| + |p3 − q3| + 2|p1 − q1|) ≤ 5β1|q − p| (7) Hence Kf + ∑n k=1 √∑n j=1 ( Khk,je K g k,jτk,j )2 is a suit- able choice for K, the Lipschitz constant of F for the set {ψ ∈ C+ : ||ψ|| ≤ M}. The assumptions of Lemma IV.2 on the incidences Λj(Sj(t),Ij(t),Rj(t)) and λk,j(sk,j(u; t∗), ik,j(u; t∗),rk,j(u; t∗)) can be fulfilled by several choices on the type of disease transmission. For instance, let βj > 0 be the transmission rate in region j and let βTk,j > 0 denote the transmission rates during travel. For j,k ∈ {1, . . .n} and for q = (q1,q2,q3) ∈ R3, define Λj(q) = −βj q1 q1 + q2 + q3 q2, λk,j(q) = −βTk,j q1 q1 + q2 + q3 q2. This implies that Λj and λk,j have the form Λj(Sj,Ij,Rj) = −βj Sj Nj Ij, λk,j(sk,j, ik,j,rk,j) = −βTk,j sk,j nk,j ik,j, (8) which is called standard incidence. Now we prove the following existence-uniqueness theorem. Theorem IV.3. With the incidences Λj and λk,j defined in (8), there exists a unique solution of system (3). Proof: Recall Theorem 3.7 from [2]: Suppose that F satisfies the local Lipschitz property on each bounded subset of C+ = C+([−τ, 0], R3n+ ), moreover let M > 0. There exists A > 0, depending only on M such that if φ ∈ C+ satisfies ||φ|| ≤ M, then there exists a unique solution x(t) = x̂(t, 0; φ) of (3), defined on [−τ,A]. In addition, if K is the Lipschitz constant for F corresponding to M, then max −τ≤η≤A |x(η, 0; φ) − x(η, 0; ψ)| ≤ ||φ − ψ||eKA holds for ||φ||, ||ψ|| ≤ M. We showed in Lemma IV.2 that the local Lipschitz continuity of F follows from the local Lipschitz property of the incidences and the nonnegativity condition of λk,j. The latter condition clearly holds, hence it is sufficient to prove that the incidences defined in (8) possess the local Lipschitz property. As one may observe, the definition of the Λj-s and λk,j- Biomath 1 (2012), 1209255, http://dx.doi.org/10.11145/j.biomath.2012.09.255 Page 5 of 7 http://dx.doi.org/10.11145/j.biomath.2012.09.255 D. Knipl et al., Multiregional SIR Model with Infection during Transportation s (j,k ∈ {1, . . .n}) only differ in a constant multiplier, hence it is sufficent to prove the local Lipschitz property only for one of them, i.e. for Λ1. Moreover, we prove this property only on the nonnegative cone R3+, which is invariant under systems (3) and (2). For p, q ∈ R3+, by (7) we obtain the Lipschitz constant K = 5β1, where we used that for any a,b,c > 0, it holds that a a+b+c < 1. Remark 1. It follows from the proof of Theorem IV.3 that the incidences Λj and λk,j defined in (8) also satisfy the global Lipschitz property, meaning that the Lipschitz constant K arises independently of M. In this case, the solution of system (3) exists on [0,∞). Another natural choice for the incidences can be the following: for q = (q1,q2,q3) ∈ R3 and for j,k ∈ {1, . . .n}, let Λj(q) = −βjq1q2, λk,j(q) = −βTk,jq1q2, which leads to the mass action-type disease transmission, therefore Λj and λk,j have the form Λj(Sj,Ij,Rj) = −βjSjIj, λk,j(sk,j, ik,j,rk,j) = −βTk,jsk,jik,j. (9) Theorem IV.4. With incidences Λj and λk,j defined in (9), there exists a unique solution of system (3). Proof: Similarly as by Theorem IV.3, it is enough to show that Λj and λk,j satisfy the local Lipschitz property, we detail the proof only for Λ1 and consider the nonnegative subspace R3+. For any M > 0, for any p, q ∈ R3+ such that |p|, |q| ≤ M, we obtain |Λ1(p) − Λ1(q)| = | − β1p1p2 + β1q1q2| ≤ β1|p1p2 − q1q2| ≤ β1|p1p2 − p1q2 + p1q2 − q1q2| ≤ β1(|p1p2 − p1q2| + |p1q2 − q1q2|) ≤ β1(p1|p2 − q2| + q2|p1 − q1|) ≤ 2Mβ1|q − p|, so we can choose K(M) = 2Mβ1. Remark 2. Although the global Lipschitz property does not hold for Λj and λk,j defined in (9), it is possible to show that the solution of (3) is bounded and hence exists on [0,∞). V. CONCLUSION The topic of epidemic spread of infectious diseases via transportation networks has recently been examined in several studies (see [3], [4], [5], [6], [7]), although these works mostly consider only two connected regions. We introduced a dynamic model which describes the spread of an infectious disease in and between n regions which are connected by transportation. We used the commonly applied SIR model as a basic epidemic building block in the regions and also during the travel. The model formulation led to a system structured by travel time, which turned out to be equivalent to a system of differen- tial equations with multiple dynamically defined delays. We showed that under local Lipschitz conditions on the infection terms within the regions and during travel, the usual existence and uniqueness results hold. Recent epidemics like the 2002-2003 SARS outbreak and the 2009 pandemic influenza A(H1N1) highlighted the importance of the global air travel network in the study of epidemic spread. During long distance travel such as intercontinental flights, a single infected indi- vidual may infect several other passengers during the flight, and since the progress of these diseases is fast, even a short delay (a fraction of a day) arising due to transportation may play a significant role in the disease dynamics. In this paper we illustrated by proving an existence and uniqueness result that such epidemiologi- cal situations can be studied in the framework of delay differential equations. ACKNOWLEDGMENT DHK was partially supported by the Hungarian Re- search Fund grant OTKA K75517 and the TÁMOP- 4.2.2/B-10/1-2010-0012 program of the Hungarian Na- tional Development Agency. RG was supported by Eu- ropean Research Council StG Nr. 259559, Hungarian Research Fund grant OTKA K75517 and the Bolyai Re- search Scholarship of Hungarian Academy of Sciences. REFERENCES [1] P. Hartman, “Ordinary differential equations”, Classics in Ap- plied Mathematics, vol. 38, SIAM, 2002. [2] H. L. Smith, An Introduction to Delay Differential Equations with Applications to the Life Sciences, Springer, 2010. [3] D. H. Knipl, “Fundamental properties of differential equation with dynamically defined delayed feedback”, preprint, 2012. [4] D. H. Knipl, G. Röst, J. Wu,“Epidemic spread of infectious diseases on long distance travel networks”, preprint, 2012. [5] J. Liu, J. Wu, Y. Zhou, “Modeling disease spread via transport- related infection by a delay differential equation”, Rocky Moun- tain J. Math., vol. 38 No 5, pp. 1225–1541, 2008. Biomath 1 (2012), 1209255, http://dx.doi.org/10.11145/j.biomath.2012.09.255 Page 6 of 7 http://dx.doi.org/10.11145/j.biomath.2012.09.255 D. Knipl et al., Multiregional SIR Model with Infection during Transportation [6] Y. Nakata, “On the global stability of a delayed epidemic model with transport-related infection”, Nonlinear Analysis Series B: Real World Applications, vol. 12 No 6, pp. 3028–3034 2011. http://dx.doi.org/10.1016/j.nonrwa.2011.05.004 [7] Y. Nakata, G. Röst, “Global analysis for spread of an infectious disease via global transportation”, submitted, 2012. Biomath 1 (2012), 1209255, http://dx.doi.org/10.11145/j.biomath.2012.09.255 Page 7 of 7 http://dx.doi.org/10.1016/j.nonrwa.2011.05.004 http://dx.doi.org/10.11145/j.biomath.2012.09.255 Introduction Model Description The Compact Form of the System The Local Lipschitz Property Conclusion References