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Research article Special Issues

On the date of the epidemic peak


  • Epidemiologists have used the timing of the peak of an epidemic to guide public health interventions. By determining the expected peak time, they can allocate resources effectively and implement measures such as quarantine, vaccination, and treatment at the right time to mitigate the spread of the disease. The peak time also provides valuable information for those modeling the spread of the epidemic and making predictions about its future trajectory. In this study, we analyze the time needed for an epidemic to reach its peak by presenting a straightforward analytical expression. Utilizing two epidemiological models, the first is a generalized SEIR model with two classes of latent individuals, while the second incorporates a continuous age structure for latent infections. We confirm the conjecture that the peak occurs at approximately T(lnN)/λ, where N is the population size and λ is the largest eigenvalue of the linearized system in the first model or the unique positive root of the characteristic equation in the second model. Our analytical results are compared to numerical solutions and shown to be in good agreement.

    Citation: Ali Moussaoui, Mohammed Meziane. On the date of the epidemic peak[J]. Mathematical Biosciences and Engineering, 2024, 21(2): 2835-2855. doi: 10.3934/mbe.2024126

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  • Epidemiologists have used the timing of the peak of an epidemic to guide public health interventions. By determining the expected peak time, they can allocate resources effectively and implement measures such as quarantine, vaccination, and treatment at the right time to mitigate the spread of the disease. The peak time also provides valuable information for those modeling the spread of the epidemic and making predictions about its future trajectory. In this study, we analyze the time needed for an epidemic to reach its peak by presenting a straightforward analytical expression. Utilizing two epidemiological models, the first is a generalized SEIR model with two classes of latent individuals, while the second incorporates a continuous age structure for latent infections. We confirm the conjecture that the peak occurs at approximately T(lnN)/λ, where N is the population size and λ is the largest eigenvalue of the linearized system in the first model or the unique positive root of the characteristic equation in the second model. Our analytical results are compared to numerical solutions and shown to be in good agreement.



    Epidemic modeling has become a current issue with the 2020 pandemic caused by a coronavirus. Technical concepts, such as the parameter R0, have emerged in the discourse of policymakers. This type of modeling is necessary to understand the transmission dynamics of infectious diseases, forecast the future trajectory of outbreaks, and assess strategies for epidemic control [1,2,3,4]. Its significance has been emphasized by a series of viral infection epidemics, including HIV since the 1980s [5,6], the SARS epidemic in 2002–2003 [7,8,9], H5N1 influenza in 2005 [10,11], H1N1 in 2009 [12,13], Ebola in 2014 [14,15], and the recent COVID-19 pandemic [16,17,18,19].

    The most important features to assess the severity of an epidemic are its final size and timescale. The final size of the epidemic, typically measured by the number of people ultimately affected by the disease, serves as a crucial indicator for the assessment of the extent of the disease's impact on the population. Grasping this dimension allows authorities to effectively plan for necessary resources, such as hospital beds, medical equipment, and healthcare personnel. This, in turn, helps to prevent healthcare systems from becoming overwhelmed and ensures an appropriate response to the increasing demand during the epidemic's peak. Nevertheless, effective resource management during an epidemic can be optimized with precise knowledge of the peak time [20]. Researchers use various data sources and mathematical models to determine peak date of the epidemic and gain insights into the dynamics of the disease spread. In [21], the authors present an analytical method for determining the peak time of an epidemic outbreak by utilizing the SIR (susceptible-infected-recovered) model. The formula takes into account variables such as the fraction of susceptible individuals, the infectious ratio, and the initial count of infected and susceptible individuals. Empirical testing has confirmed the accuracy and utility of the formula in terms of predicting the peak time of different epidemic diseases, including COVID-19. More recently, in [22], the author proposes a simple yet accurate formula, relying on Pade approximations, to estimate the peak date of an epidemic in an SIR-type epidemic model. The author compares the results of their estimation with those of other existing formulas, highlighting that the current estimation is the most accurate with a negligible error margin across the entire parameter regime of the SIR model. In [23], the SEIR model is being studied to understand the spread of infectious diseases like COVID-19, and to provide analytical expressions for the peak and and their timing, as well as the long-term behavior of the affected populations. In [20, Chapter 1], the author examines the asymptotic behavior of the time T required for an epidemic, as modeled by SIR differential system, to reach its peak when the population size N is large. The formula derived by the author for T is T1ab{logNI0+log[(1ba)logab]+logab01+eu+uu(1eubau)du}, where I0 is the initial number of infected individuals, a is the effective contact rate and b is the recovery rate, with the assumption that a>b. In [20, Chapter 2], the authors evaluated the SEIR epidemic model with the aim of finding the date of the peak. They determined a lower bound for the date of the epidemic peak and conjectured that it occurs at time T(lnN)/λ, where λ is the largest eigenvalue of the linearized system.

    Based on these works, we aim to determine the lower bound for the date of the epidemic peak and the final number of individuals who contract the disease in two epidemiological models. Our first model is a non-structured SEIR epidemic model that includes two latent classes (SE1E2IR), while the second model incorporates a continuous age structure for latent infections. The results confirm the conjecture that the peak occurs at approximately T(lnN)/λ where N is the population size and λ is the largest eigenvalue of the linearized system in the first model or the unique positive root of the characteristic equation in the second model. The findings from this study will contribute to the understanding of the dynamics of disease spread and inform public health interventions and planning for future outbreaks.

    Consider a population of size N subjected to a contagious disease outbreaks. The population is divided into four classes: susceptible S(t), exposed E(t), infectious I(t) or recovered from infection R(t). The following model describes the evolution of this epidemic in time [24,25]:

    S(t)=aS(t)I(t)N (2.1)
    E1(t)=aS(t)I(t)Nb1E1(t) (2.2)
    E2(t)=b1E1(t)b2E2(t) (2.3)
    I(t)=b2E2(t)cI(t) (2.4)
    R(t)=cI(t) (2.5)

    In this model, there are two latent (exposed) periods. Individuals remain in the exposed class for a certain latent period, passing through two stages E1(t) and E2(t) before becoming infective [24]. Recovered individuals are assumed to be immune and retain their immunity without a time limit. The parameter a (a>0) represents the average number of contacts per unit time that a susceptible individual has with an infectious individual. b1 (b1>0) is the rate of progression from the first exposed class to the second exposed class. b2 (b2>0) is the rate at which the exposed individuals in the second exposed class become infectious and c (c>0) is the rate of recovery. The figure below displays the transfer diagram for the SE1E2IR system. Consider the initial conditions

    S(0)=N(nE1+nE2+nI)>0, E1(0)=nE10, E2(0)=nE20, I(0)=nI0, R(0)=0, (2.6)

    with nE1+nE2+nI>0.

    Figure 1.  Flow diagram representing the structure of the model described by Eqs (2.1)–(2.5).

    One may argue that an infective individual in a totally susceptible population causes a new infections per unit time, and the mean time spent in the infective compartment is 1/c. Thus, at the beginning of the epidemic, an infected individual will infect on average R0=a/c secondary cases before entering the compartment R, despite undergoing the latent phase. The parameter R0 is called the basic reproduction number. It is one of the most important parameters in epidemiology, and it is defined as the average number of secondary cases generated by a single case in a completely susceptible population [26]. The basic reproduction number is an important measure in the spread of infectious diseases, as it helps to predict the potential magnitude and speed of an outbreak. The value of R0 can vary depending on several factors, including the contagiousness of the disease, the susceptibility of the population, and the effectiveness of public health interventions. If R0>1, then the disease may emerge in the population. However, if R0<1, the disease disappears [27]. We assume throughout this paper that a>c, which means that R0>1.

    Let us commence by recalling the following proposition, proven via the same method as in the classical SEIR model.

    Proposition 1. The system defined by Eqs (2.1)-(2.5) has a unique solution which is defined for all t>0. Furthermore, S(t)>0,E1(t)>0,E2(t)>0,I(t)>0,R(t)>0 and S(t)+E1(t)+E2(t)+I(t)+R(t)=N for all t>0.

    Proof

    The Cauchy-Lipschitz theorem [28, p. 74] ensures the existence and uniqueness of a solution to the system described by Eqs (2.1)–(2.5) over a maximal interval [0;Tmax]. Additionally, for all t]0,Tmax[, we have

    S(t)=S(0)exp(aNt0I(u)du)>0

    since S(0)>0. Let

    X(t)=(E1(t)E2(t)I(t)),    F(t)=(b10aS(t)/Nb1b200b2c) (2.7)

    We then have

    dXdt=F(t)X(t) (2.8)

    We observe that X(0)0 and X(0)0 because nE1+nE2+nI>0, where the inequality between vectors signifies an inequality for all respective components. Additionally, because the off-diagonal entries of the matrix F(t) are non-negative for all t[0;Tmax) and F(0) is irreducible, the system (2.8) is consequently cooperative and irreducible; then, it is strongly monotone [20,29,30]. Therefore, for all t]0;Tmax[, E1(t)>0, E2(t)>0, and I(t)>0. Since

    R(t)=ct0I(u)du

    we also deduce that R(t)>0 for all t]0;Tmax[. Note that

    ddt(S+E1+E2+I+R)=0

    we derive

    S(t)+E1(t)+E2(t)+I(t)+R(t)=S(0)+E1(0)+E2(0)+I(0)+R(0)=N

    and

    0<S(t)<N,  0<E1(t)<N,  0<E2(t)<N,0<I(t)<N,0<R(t)<N

    for all 0<t<Tmax. Since the solutions remain bounded on the maximal interval ]0;Tmax[, it follows that Tmax=+ [31, Corollary A.5]. Therefore, the system described by (2.1)–(2.5) has a unique solution defined for all t>0.

    The final size of an epidemic, represents the ultimate number of infected individuals in a population during the course of an outbreak. It is a mathematical measure used to evaluate the spread and impact of a disease.

    The function S(t) is a non-negative, smooth, and decreasing function which converges to a limit S0 as t+. The function R(t) is a non-negative, smooth, and increasing function which converges to a limit RN as t+. The sum of Eqs (2.4) and (2.5) is given by

    (I+R)(t)=b2E2(t)0 (2.9)

    Thus, I+R is a non-negative, smooth, and increasing function, and it converges to a limit as t+. As R(t) converges, I(t) also converges to a limit I0. The sum of Eqs (2.3)–(2.5) is given by

    (E2+I+R)(t)=b1E1(t)0 (2.10)

    Therefore, E2+I+R is a non-negative and smooth increasing function that is bounded by N; hence it converges to a limit as t+. As both R(t) and I(t) converge, E2(t) also converges to a limit E2,0. By utilizing Eqs (2.2)–(2.5), it can be proven that E1+E2+I+R is a non-negative, smooth, increasing, and bounded function that also converges to a limit as t+. Consequently, as E2(t), R(t), and I(t) converge, E1(t) converges to a limit E1,0.

    Let us prove that I=E2,=E1,=0. Integration of Eq (2.5) gives

    R(t)=ct0I(u)du (2.11)

    Because R(t) is bounded by N, I(t) cannot converge to a strictly positive limit; then I=0.

    Similarly, using the sum of the equations for I and R, gives

    I(t)+R(t)I(0)=b2t0E2(u)du (2.12)

    from which we conclude that E2,=0.

    By performing a similar calculation using the sum of the equations for E2, I, and R, we obtain

    E2(t)+I(t)+R(t)E2(0)I(0)=b1t0E1(u)du (2.13)

    it follows that E1,=0.

    By utilizing the equations for S and R, Eq (2.5) can be written as

    R(t)=cNaS(t)S(t) (2.14)

    Then

    R(t)=cNalnS(t)S(0) (2.15)

    we obtain the following at the limit

    R=cNalnSS(0) (2.16)

    this shows that S>0, and it leads to the equation

    S=NR=N+cNalnSS(0) (2.17)

    Denote by x=SN, x0=S(0)N and define the function

    f(x)=1x+calnxx0 (2.18)

    Clearly f(x)=0 and 0<x1. In addition

    f(x)=cax1>0if0<x<caf(x)<0  ifca<x<1 (2.19)

    On the other hand

    f(1)=caln1x0>0f(x)ifx0+f(ca)=1ca+calncax0>1ca+calnca>0 (2.20)

    The last inequality stems from the assumption that c/a<1 and the property of g(u)=1u+ulnu being a monotonically decreasing function in the interval ]0,1[ with g(1)=0 and g(u)>0 for u]0,1[.

    As a result, the function f increases from to f(ca)>0 on the interval ]0,ca[ and decreases from f(ca)>0 to f(1)>0 on the interval ]ca,1[. Therefore, the equation f(x)=0 has a unique solution in the interval ]0,1[, and this solution lies within the interval ]0,ca[. We conclude that

    0<SN<ca (2.21)

    To start, clarify the definition of the epidemic peak; we have

    (E1+E2+I)(t)=(aS(t)Nc)I(t) (2.22)

    Suppose that

    S(0)N=1(nE1+nE2+nI)N>ca (2.23)

    Under the assumption that a>c, this inequality holds as long as N is sufficiently large. Because I(t)>0 for all t>0, the function S(t) is monotonically decreasing from S(0)>cN/a to S<cN/a on the interval [0,+[ also, there exists a unique time T>0 such that S(T)=cN/a. According to Eq (2.22), the function E1+E2+I is monotonically increasing on the interval [0,T] and monotonically decreasing on the interval [T,+[. We refer to T as the time of the epidemic peak. It is worth noting that in general, this time does not correspond to the maximum of I or the maximum of Ei (i=1,2). Using Eq (2.15), we get

    E1(T)+E2(T)+I(T)=NS(T)R(T)=NcNa+cNalncaS(0)N (2.24)

    Consider the following linear system

    e1(t)=b1e1(t)+ai(t)e2(t)=b1e1(t)b2e2(t)i(t)=b2e2(t)ci(t) (2.25)

    Define

    A=(b10ab1b200b2c) (2.26)

    Note that the determinant of matrix A is given by det(A)=b1b2(ac)>0. Whether A has three real eigenvalues or one real eigenvalue and two complex conjugates, it always has at least one eigenvalue that is strictly positive. Define

    σ(A)={λC | det(AλI)=0}  the spectrum of A

    and

    λ+=max{Re(λ) | λσ(A)}  the stability modulus of matrix A

    From Eq (2.2), we have

    E1(t)b1E1(t)+aI(t) (2.27)

    Due to the non-negative off-diagonal coefficients of matrix A, we can apply a comparison theorem for cooperative systems [20, Corollary 2.3.1]; we obtain

    (E1(t)E2(t)I(t))etA(nE1nE2nI) (2.28)

    for all t0, where the inequality between vectors is component by component. Thus

    E1(T)+E2(T)+I(T)(1 1 1) eTA(nE1nE2nI)(nE1+nE2+nI)eTA (2.29)

    Because A is a Metzler matrix (the off-diagonal coefficients are non-negative [32]) and

    A2=(b21ab2a(b1+c)b1(b1+b2)b22ab1b1b2b2(b2+c)c2)0

    A is irreducible [33]; thus, λ+ is an eigenvalue of multiplicity equal to 1 [29, Corollary 4.3.2]. Therefore there exists an invertible matrix X [34] such that

    A=XJX1 (2.30)

    We distinguish two cases:

    ● Case 1: A is diagonalizable. Thus

    J=(λ+000λ1000λ2) (2.31)

    and

    eJT=(eλ+T000eλ1T000eλ2T) (2.32)

    Consequently, there exists a constant k1>0, independent of T and N, such that

    ||eAT||k1eλ+T (2.33)

    ● Case 2: A is not diagonalizable. Thus

    J=(λ+000λ1100λ1) (2.34)

    and

    eJT=(eλ+T000eλ1TTeλ1T00eλ1T) (2.35)

    Let us define the function g(T)=Te(λ1λ+)T; this function increases on the interval [0,1/(λ+λ1)] and decreases on the interval [1/(λ+λ1),+]. Moreover g(0)=0 and limT+g(T)=0. Hence

    g(T)g(1λ+λ1)=1λ+λ1e1 (2.36)

    We get

    Teλ1T1λ+λ1e1+λ+T (2.37)

    Consequently, there exists a constant k2>0, independent of T and N, such that

    ||eAT||k2eλ+T (2.38)

    It then follows from Eq (2.29) that

    E1(T)+E2(T)+I(T)(nE1+nE2+nI)||eAT||keλ+T (2.39)

    where k>0 is a constant which depends only on a, b1, b2, c, nE1, nE2 and nI, but not on N.

    Because S(0)/N<1, it follows that ln(S(0)/N)>0. Hence, we obtain from Eq (2.24) the following inequality

    N(1ca+calnca)E1(T)+E2(T)+I(T) (2.40)

    In conclusion, based on Eqs (2.39) and (2.40), the following inequalities are derived

    N(1ca+calnca)E1(T)+E2(T)+I(T)keλ+T (2.41)

    Finally, there exists another constant KR that only depends on the parameters a, b1, b2, c, nE1, nE2 and nI, but not on N, such that

    TlnNλ++K (2.42)

    This lower bound supports the following conjecture

    TlnNλ+,   N (2.43)

    In the previous section, a model was presented by using ordinary differential equations to describe the progression of an infection. This section extends that model by stratifying the latency phase based on the time since infection. The new model tracks the time since infection, represented by the variable x, and considers individuals who have been in the exposed class for a duration of x. These individuals move to the infected class at a rate of b(x), which is a non-negative function of x. The model is described by the following system, with notation from the previous section

    {S(t)=aS(t)I(t)NEt+Ex=b(x)E(t,x)E(t,0)=aS(t)I(t)NI(t)=0b(x)E(t,x)dxcI(t)R(t)=cI(t) (3.1)

    The following assumptions are made regarding the parameters of the system:

    (H1) a,c>0.

    (H2) bL(R+), with the essential upper bound ˉb.

    (H3) We suppose that there exist B>0 and X>0 such that for all x>X, b(x)>B.

    The phase space for the system is defined as Y=R+×L1+×R+×R+, where L1+ represents the space of non-negative and integrable functions on (0,), with a norm defined by

    ||(y1,y2,y3,y4)||Y=|y1|+0|y2(x)|dx+|y3|+|y4|

    Biologically, this norm gives the total population size N. In our case, N=S+0E(t,x)dx+I+R which is constant. The initial condition for Eq (3.1) is

    (S(0),E(0,.),I(0),R(0))Y

    where

    S(0)=NnEnI>0,  0E(0,x)dx=nE0,  I(0)=nI0,  R(0)=0 (3.2)

    with nE+nI>0.

    Let π(x) denote the probability of survival in the exposed class until age x, where for x0, π(x) is defined as

    π(x)=ex0b(s)ds (3.3)

    It can be proved, as done in Subsection 2.1, that

    S=limtS(t)>0 and R=limtR(t)<N (3.4)

    The sum of the equations for I and R gives

    (I+R)(t)=0b(x)E(t,x)dx0 (3.5)

    Hence I+R is an increasing function that is bounded by N; also, it follows that it has a limit. Because R(t) converges, I(t) also converges to a limit of I0.

    Therefore, because R(t)=ct0I(s)ds is bounded by N, I(t) cannot converge to a positive limit and instead reaches I=0. Furthermore,

    (0E(t,x)dx+I(t)+R(t))=aS(t)I(t)N0 (3.6)

    Therefore, because 0E(.,x)dx+I+R is a increasing and bounded function, it converges to a limit. Because I and R also converge, it can be concluded that 0E(t,x)dx converges to a limit as well.

    Next, we will prove that limt0E(t,x)dx=0.

    Integrating the second equation of Eq (3.1) with the boundary equation and initial condition, yields

    E(t,x)={E(tx,0)π(x)t>xE(0,xt)π(x)π(xt)tx (3.7)

    It follows that

    0E(t,x)dx=t0E(t,x)dx+tE(t,x)dx=t0E(tx,0)π(x)dx+tE(0,xt)π(x)π(xt)dx=G1(t)+G2(t) (3.8)

    where G1(t)=t0E(tx,0)π(x)dx and G2(t)=tE(0,xt)π(x)π(xt)dx

    It follows that

    limt0E(t,x)dx=limtG1(t)+limtG2(t) (3.9)

    We have the following inequalities

    0G1(t)0E(tx,0)π(x)dx (3.10)

    then

    0limtG1(t)limt0E(tx,0)π(x)dx (3.11)

    Bacause limtI(t)=0, it follows that

    1) limtE(tx,0)π(x)=limtaS(tx)NI(tx)π(x)=0

    2) E(tx,0)π(x)=aS(tx)NI(tx)π(x)aNπ(x); then, |E(tx,0)π(x)|aNπ(x)

    Therefore, by the dominated convergence theorem [35], we obtain

    limt0E(tx,0)π(x)dx=0limtE(tx,0)π(x)dx=0 (3.12)

    On the other hand, we have

    G2(t)=tE(0,xt)π(x)π(xt)dx=0E(0,x)π(x+t)π(x)dx (3.13)

    Using (H3), we obtain

    G2(t)=0E(0,x)ex+txb(s)dsdx0E(0,x)dxeBt (3.14)

    It can be deduced that

    limtG2(t)=0 (3.15)

    To summarize, we have established that

    limt0E(t,x)dx=0 (3.16)

    Bacause N=S+0E(t,x)dx+I+R, we obtain, at the limit, that S+R=N.

    By utilizing arguments similar to those in Subsection 2.1, it can be demonstrated that

    0<SN<ca (3.17)

    First, clarify the definition of the epidemic peak; we have

    (0E(t,x)dx+I(t))=(aS(t)Nc)I(t) (3.18)

    Assume that S(0)N=1(nE+nI)N>ca<1, which is true for sufficiently large N; we have that I(t)>0 for all t>0. The function S(t) decreases monotonically from S(0)>Nca to S<Nca on the interval [0,+[. Therefore, there exists a unique time T>0 such that S(T)=cNa. As in Subsection 3.2, the time of the epidemic peak is referred to as T.

    We have

    0E(T,x)dx+I(T)=NS(T)R(T)=NcNa+cNalncaS(0)N (3.19)

    Let (S(t),E(t,x),I(t),R(t)) be a solution of Eq (3.1) with the initial condition given by Eq (3.2). The fact that S/N1 implies that (E(t,x),I(t)) satisfies the following conditions:

    {Et=Exb(x)E(t,x)E(t,0)aI(t),I(t)=0b(x)E(t,x)dxcI(t) (3.20)

    Let (ˉE(t,x),ˉI(t)) be the solution of the following auxiliary system

    {ˉEt=ˉExb(x)ˉE(t,x)ˉE(t,0)=aˉI(t)ˉI(t)=0b(x)ˉE(t,x)dxcˉI(t) (3.21)

    with (ˉE(0,x),ˉI(0))=(E(0,x),I(0)).

    Let F(t,x)=ˉE(t,x)E(t,x), J(t)=ˉI(t)I(t); then, (F(t,x),J(t)) satisfies

    {Ft=Fxb(x)F(t,x)F(t,0)=aJ(t)+W(t)J(t)=0b(x)F(t,x)dxcJ(t)F(0,x)=J(0)=0 (3.22)

    where W(t)=aI(t)(1S(t)N)0.

    Next, we need to show that (F,J)(0,0).

    The integration of the first equation of Eq (3.22) with the specified boundary and initial conditions yields

    F(t,x)=F(tx,0)π(x) (3.23)

    The integration of the equation for J in Eq (3.22), combined with Eq (3.23), yields

    J(t)=t0ec(ts)t0b(x)F(sx,0)π(x)dxds (3.24)

    Define B(t)=F(t,0); then,

    B(t)=t0t0Ψ(x)B(sx)dxec(ts)ds+W(t) (3.25)

    where Ψ(x)=ab(x)π(x).

    Let us consider the following sequence

    {Bn+1(t)=t0t0ec(ts)Ψ(x)Bn(sx)dxds+W(t)nNB0(t)=W(t)0 (3.26)

    Because B0, Ψ and W are non-negative and continuous functions, by the induction method, we can prove that it is the same for Bn, for all n0.

    Next, we prove the convergence of {Bn(t)}n to B(t) for all t[0,˜T] by using the contraction mapping principle. For this purpose, we introduce a variable

    ˉBn(t)=eˉλtBn(t) for some ˉλ>0 (3.27)

    Multiplying both sides of Eq (3.26) by eˉλt yields

    ˉBn+1(t)=t0t0Ψ(x)ˉBn(sx)eˉλ(sx)dxec(ts)ˉλtds+ˉW(t) (3.28)

    where ˉW(t)=eˉλtW(t).

    It can be deduced that if convergence of ˉBn(t) to ˉB(t) for any t[0,˜T] is established, then Bn(t) will converge to B(t).

    For any nN, we have

    ||ˉBn+1(t)ˉBn(t)||t0t0Ψ(x)|ˉBn(sx)ˉBn1(sx)|eˉλ(sx)dxec(ts)ˉλtdst0t0Ψ(x)eˉλ(sx)dxec(ts)ˉλtds||ˉBn(sx)ˉBn1(sx)|| (3.29)

    or t0t0Ψ(x)eˉλ(sx)dxec(ts)ˉλtdsaˉbˉλ2:=Mˉλ for ˉλ>0, where ˉb is defined in (H2).

    Substituting this estimate into Eq (3.29) yields

    ||ˉBn+1(t)ˉBn(t)||Mˉλ||ˉBn(t)ˉBn1(t)||Mnˉλ||ˉB1(t)ˉB0(t)|| (3.30)

    As a result, for any m,nN (m>n) and ˉλ that is sufficiently large,

    ||ˉBm(t)ˉBn(t)||||ˉBm(t)ˉBm1(t)||+....+||ˉBn+1(t)ˉBn(t)||(Mm1ˉλ+....+Mnˉλ)||ˉB1(t)ˉB0(t)||Mmnˉλ1Mˉλ||ˉB1(t)ˉB0(t)|| (3.31)

    We choose ˉλ large enough such that Mˉλ<1.

    Therefore, as m and n approach infinity, ||ˉBm(t)ˉBn(t)|| tends to zero, which means that {ˉBn(t)}n is a Cauchy sequence. It follows that ˉBn(t) converges to ˉB(t); thus, Bn(t) also converges to B(t) as n approaches infinity.

    Let

    ˉN(t)=0F(t,x)dx+J(t) (3.32)

    for t[0,˜T); we have

    ˉN(t)=(ac)J(t)+W(t)(ac)ˉN(t)+aN (3.33)

    for t[0,˜T). By using the standard comparison lemma [36], we can conclude that

    ˉN(t)aNac(e(ac)t1) (3.34)

    which implies that limt˜TsupˉN(t)<. Thus, the maximal interval of existence for the solution of Eq (3.22) is R+.

    To summarize, we have shown that the solution of Eq (3.22) is non-negative, which implies that

    E(t,x)ˉE(t,x),  I(t)ˉI(t)      t0, x0 (3.35)

    When looking for solutions of Eq (3.21) of the form ˉE(t,x)=u(x)eλt and ˉI(t)=veλt where λ is constant, by substituting in Eq (3.21), we obtain the following:

    {λu=uxb(x)u(x)u(0)=avλv=0b(x)u(x)dxcv (3.36)

    Solving the first equation of Eq (3.36) yields

    u(x)=aveλxx0b(s)ds (3.37)

    By inserting Eq (3.37) into the last equation of Eq (3.36), we obtain the following characteristic equation,

    a0b(x)eλxx0b(s)dsdx=λ+c (3.38)

    The characteristic equation can be rewritten in the following form:

    R(λ)=1 (3.39)

    where

    R(λ)=a0b(x)eλxx0b(s)dsdxλ+c (3.40)

    We define the basic reproduction number by

    R0=R(0)=ac(1e0b(x)dx) (3.41)

    For λ<c, R(λ) is negative and the characteristic equation Eq (3.39) does not have a solution.

    For λ>c, R(λ) is a decreasing function of λ which approaches as λc and zero as λ. As a result, the characteristic equation given by Eq (3.39) has a unique real solution λ. In addition, if R0>1, this real solution satisfies that λ>0.

    Therefore, the solution of Eq (3.21) is given by:

    ˉE(t,x)=aveλ(tx)x0b(s)ds,ˉI(t)=veλt (3.42)

    We denote u(x)=aveλxx0b(s)ds. Using Eq (3.35), we get

    0E(t,x)dx+I(t)0u(x)dxeλt+veλt(0u(x)dx+v)eλtkeλT (3.43)

    where k is a positive constant that is independent of both N and T.

    Because S(0)/N<1, we have that ln(S(0)/N)>0. We can deduce the following inequality from Eq (3.19):

    N(1ca+caln(ca))0E(T,x)dx+I(T) (3.44)

    Therefore, from Eqs (3.43) and (3.44), we arrive at the following inequalities:

    N(1ca+caln(ca))0E(T,x)dx+I(T)keλT (3.45)

    Hence, there exists another constant KR that is independent of both N and T such that

    TlnNλ+K (3.46)

    This lower bound suggests the following conjecture

    TlnNλ,   N (3.47)

    We have chosen the parameters a=9/10, b1=3/4, and b2=2/5, with the initial conditions nE1=nE2=0 and nI(0)=1. We have also chosen three values of the recovery rate c such that R0=a/c{2,2.5,4.5}. We have considered various values of the population N ranging from 103 to 106. We have solved the system of equations for SE1E2IR and determined the peak time T, which is the time at which the number of cases reaches its maximum, represented by the sum of E1, E2, and I. Figure 2 depicts the variation of T as a function of lnN (represented by solid lines), as well as (lnN)/λ+ (represented by small circles). The curves appear to align, which is consistent with the conjecture. Additionally, Figure 2 suggests that the next term in the asymptotic expansion of T is a constant, which is negative when R0 is close to 1 and becomes positive as R0 increases.

    Figure 2.  Epidemic peak time in the SE1E2IR model as a function of lnN with solid lines, and (lnN)/λ+ with small circles.

    For the model given by Eq (3.1), we have applied the following:

    b(x)={0ifx10.75ifx>1

    The value of a is set to 9/10, nE is zero, and nI(0)=1. We have also considered three different recovery rates c to obtain R0 values of {2.5,3,4.5}. The population N is varied between 103 and 108. We have solved Eq (3.1) and determined the peak time T, which is the time at which the maximum of 0E(t,x)dx+I(t) is reached. Figure 3 displays the relationship between T and lnN with continuous lines, and (lnN)/λ with small circles. The data appear to indicate that the two sets of values coincide, in accordance with the conjecture.

    Figure 3.  Epidemic peak time in the age-structured SEIR model as a function of lnN with solid lines and (lnN)/λ with small circles.

    The calculation of the peak epidemic is important because it gives information about the timing and severity of an outbreak. Assuming that the contact coefficient already incorporates certain health restrictions, having an idea of the peak date may allow one to at least predict the order of magnitude of the duration of these restrictions (weeks or months).

    In this work, we have established a lower bound for the peak date of two epidemic models. The first model is an SE1E2IR epidemic model with two latent categories. These categories encompass two chains of different lengths and are placed between the susceptible and infectious compartments. The second model includes a continuous age structure for latently infected individuals. We have demonstrated that the formula for the lower bound of the peak date is given by T(lnN)/λ, where N is the population size and λ represents the largest eigenvalue of the linearized system for the first model, and the unique positive root of the characteristic equation given by Eq (3.39) for the second model.

    Although we were unable to prove that the epidemic peak is reached at T(lnN)/λ, our numerical findings support this conjecture. Looking ahead, a future avenue for this research involves endeavors to formally demonstrate this equality and extend the technique employed in this work to determine the date of the epidemic peak for other models that are more general, complex, and realistic.

    The authors declare that they have not used artificial intelligence tools in the creation of this article.

    This research was supported by DGRSDT, Algeria and the PHC (Partenariat Hubert Curien) FRANCE-MAGHREB project grant number 22MAG22–47518WK. We express our gratitude to Nicolas Bacaër from IRD-Bondy for the valuable discussions that have greatly assisted us in finalizing this article. The authors would like to thank the referees for valuable comments and suggestions that have helped to improve the quality of this work.

    The authors declare that there is no conflict of interest.



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