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Impact of behavioral change on the epidemic characteristics of an epidemic model without vital dynamics

  • Received: 14 January 2018 Accepted: 11 June 2018 Published: 01 December 2018
  • MSC : Primary: 92D30, 34C37; Secondary: 37G35

  • The epidemic characteristics of an epidemic model with behavioral change in [V. Capasso, G. Serio, A generalizaition of the Kermack-McKendrick deterministic epidemic model, Math. Bios., 42 (1978), 43-61] are investigated, including the epidemic size, peak and turning point. The conditions on the appearance of the peak state and turning point are represented clearly, and the expressions determining the corresponding time for the peak state and turning point are described explicitly. Moreover, the impact of behavioral change on the characteristics is discussed.

    Citation: Jianquan Li, Xiaoqin Wang, Xiaolin Lin. Impact of behavioral change on the epidemic characteristics of an epidemic model without vital dynamics[J]. Mathematical Biosciences and Engineering, 2018, 15(6): 1425-1434. doi: 10.3934/mbe.2018065

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  • The epidemic characteristics of an epidemic model with behavioral change in [V. Capasso, G. Serio, A generalizaition of the Kermack-McKendrick deterministic epidemic model, Math. Bios., 42 (1978), 43-61] are investigated, including the epidemic size, peak and turning point. The conditions on the appearance of the peak state and turning point are represented clearly, and the expressions determining the corresponding time for the peak state and turning point are described explicitly. Moreover, the impact of behavioral change on the characteristics is discussed.


    1. Introduction

    Dynamical models for epidemic spread have made a great contribution to understanding transmission mechanism of the infection and controlling the spread. In 1927, Kermack and McKendrick [5] established the following simple SIR epidemic model to investigate the outbreak of the Great Plague lasting from 1665 to 1666 in London

    {S=βSI,I=βSIαI,R=αR, (1)

    where the population is divided into three classes, susceptible (S), infective (I) and removed (R); S(t),I(t) and R(t) denote their numbers respectively at time t; β is the infection rate coefficient, and α is the removal rate coefficient. A threshold theorem of epidemic spread was found by Kermack and McKendrick [5] for system (1). Since then a lot of epidemic models are established based on model (1)[9,2] and references therein.

    In 1978, after a study of the cholera epidemic spread in Bari in 1973, Capasso and Serio [3] proposed a saturation incidence rate βSI/(1+εI) to measure the inhibition effect due to behavioral change (e.g. reduction of contact rate, strengthening of protection measures, etc.) of the susceptible individuals when the number of infective individuals increases, where ε is referred to as inhibition parameter reflecting the intensity of behavioral change of susceptible individuals during the disease spread. The replacement of the bilinear incidence in model (1) with the saturation incidence yields the following model with behavioral change

    {S=βSI1+εI,I=βSI1+εIαI,R=αR, (2)

    For model (1), the epidemic final size (i.e. the number of individuals who are infected over the course of the epidemic) can be determined easily by dividing the first two equations of the model and then integrating it[1,6,8,10], and the epidemic peak (i.e. the largest number of real-time infected individuals in the population (not cumulative cases)) can also be found directly from the first integral and the second equation of model (1) [6].

    In [3], Capasso and Serio compared the two models (1) and (2) in a qualitative way, and extended the threshold theorem for model (1) by replacing the threshold line of model (1) with the threshold curve of model (2). But with respect to the epidemic final size and peak state of model (2), there is not an investigation in detail. Especially, the role of the inhibition parameter ε for the epidemic characteristics has not been discussed.

    During an epidemic outbreak, for the local public health department to control the spread of the disease, while concerning about the peak state of disease spread and the epidemic final size, the turning point and the associated state of population are also the important characteristics that need to be paid attention too. The turning point denotes the time at which the rate of cumulative cases changes from increasing to decreasing or vice versa [4]. Recently, we theoretically investigated the epidemic characteristics including the epidemic final size, the peak and the turning point of some simple epidemic models without vita dynamics including model (1), and analyzed the dependence of the related quantities on the initial conditions [6,7,11]. However, in the preceding models considered by us, no behavioral intervention was involved. In this paper, our aim is to investigate the impact of behavioral change on the epidemic characteristics for model (2). Based on some fundamental and elegant mathematical deductions, the dependence of the epidemic characteristics on the initial condition and the inhibition parameter is established.


    2. Formulation of model and preliminary

    Since the variable R does not appear in the first two equations of (2), and the system (called as SI model) consisting of the first two equations of (2) can determine its dynamics and epidemic characteristics, we consider the reduced model

    {S=βSI1+εI,I=βSI1+εIαI (3)

    with the initial condition S(0)=S0>0 and I(0)=I0>0, where α may represent the sum of the recovery and disease-induced death rates.

    Obviously, the initial condition implies that S(t)>0 and I(t)>0 for t>0. Moreover, S(t) is decreasing since S(t)<0 for t>0. Thus S(t)S0 for t0.

    From model (3) we have

    dIdS=α(1+εI)βSβS. (4)

    Correspondingly, I|S=S0=I0. Then equation (4) with condition I|S=S0=I0 has the following solution

    I=I0SS0+αβ(SS01)SlnSS0   for   β=αε, (5)

    and

    I=I0(SS0)αεβ1ε[1(SS0)αεβ]βSβαε[1(SS0)αεβ1]   for   βαε. (6)

    For simplicity, we denote x=S/S0 and σ=αε/β. Here x=x(t)(0,1] for t>0 since S(t)S0 for t0.

    Further, for σ=1 and σ1, (5) and (6) can be rewritten as

    I=1ε[(εI0+1)x1εS0xlnx]=:1εf1(x), (7)

    and

    I=1ε[(εI0+1+εS01σ)xσ1εS0x1σ]=:1εf2(x), (8)

    respectively. In particular, when σ=1+εS0/(1+εI0), function f2(x) becomes f0(x)=(1+εI0)x1.

    Additionally, we state the following lemmas and inequalities, which will be used in our later inferences.

    Lemma 2.1. For function g(x)C2[a,b] with g(x)0 (0), there is a unique zero point in (a,b) if g(a)g(b)<0; it is always positive (negative) in [a,b] if g(x)0 (0) and both g(a) and g(b) are positive (negative).

    Lemma 2.2. For function g(x)C1[a,b], if there is at most one local extreme point, then there is a unique zero of function g(x) in (a,b) if and only if g(a)g(b)<0.

    Lemma 2.3. The inequality

    Φ(u)=u1lnu0

    for u>0, and the equality holds if and only if u=1.

    Lemma 2.4. For any positive number σ with σ1, the inequality

    Ψ(u)=uσ+σuσ11σ11σ0

    for u>0, and the equality holds if and only if u=1.

    It is easy to prove the above lemmas and inequalities by applying the fundamental knowledge of differential calculus, so we omit them.


    3. Analysis of epidemic characteristics

    In this section, we analyze the epidemic characteristics of SI model (3) including the final state, the peak state and the turning point by means of Lemmas and the relation between variable S and I obtained in Section 2.


    3.1. Epidemic final state

    Epidemic final size is the number of the cumulative cases. According to the character of SI model (3), there is no reinfection for the model. Then the size can be obtained by subtracting the number of the individuals, who have not been infected when the spread of the disease terminates, from the initial number of susceptible individuals. The termination of infection is indicated by the fact that there is no infected individuals.

    In what follows, we will determine the final size by analyzing the zeros of fi(x) (i=0,1,2) on (0,1]. It is easy to know that

    limx0+f1(x)=f2(0)=1,

    and

    f1(1)=f2(1)=εI0.

    Moreover, the direct calculation gives

    f1(x)=εS0x,f2(x)= σ(σ1)(εI0+1+εS01σ)xσ2.

    So the signs of f1(x) and f2(x) are unchanged for σ1+εS0/(1+εI0). Then, according to Lemma 2.1, when σ1+εS0/(1+εI0), both f1(x) and f2(x) have a unique zero in the interval (0,1), denoted by x. Further, we know that fi(x)<0 for 0<x<x and fi(x)>0 for x<x<1 (i=1,2).

    For σ=1+εS0/(1+εI0), it is obvious that f0(x) has a unique positive zero, 1/(1+εI0), denoted by x0.

    The above inference implies that x or x0 represents the fraction of the susceptible individuals, who have not been infected when the spread of the disease terminates, and that the feasible region of the variable x is (x,1] for σ1+εS0/(1+εI0), and (x0,1] for σ=1+εS0/(1+εI0). Therefore, when the infection terminates, the number of susceptible individuals is S0x for σ1+εS0/(1+εI0), and S0/(1+εI0) for σ=1+εS0/(1+εI0). Correspondingly, the epidemic final size is S0(1x) for σ1+εS0/(1+εI0), and εS0I0/(1+εI0) for σ=1+εS0/(1+εI0).

    Remark 1. Although we have introduced how to determine the epidemic state, the related expressions are not formulated explicitly since the equations determining them could be a transcendental one. Then it is necessary to turn to mathematical softwares for finding them.

    Additionally, with respect to x, we have the following statement which will be used later.

    Proposition 1. When σ=1, x<1/(εS0). When σ1 and σ1+εS0/(1+εI0), x<s/(εS0).

    Proof. First, substituting x=1/(εS0) into function f1(x) yields

    f1(1εS0)=I0S0+Φ(1εS0).

    From Lemma 2.3 it follows that f1(1/(εS0))>0. By the property of function f1(x) we know that x<1/(εS0).

    Next the substitution of x=σ/(εS0) into function f2(x) yields

    f2(σεS0)=εI0(σεS0)σ+Ψ(σεS0).

    By Lemma 2.4 we know that f2(σ/(εS0))>0. Further, the property of function f2(x) implies that x<σ/(εS0).

    This completes the proof of Proposition 1.


    3.2. Peak state

    The peak state corresponds to time at which the number of infected individuals attains the maximum. It can be found by determining the state at which I(t)=0. That is, the peak state satisfies the equation

    βS1+εI=α. (9)

    Note that σ=αε/β. Then (9) can become

    εI+1εσS=0. (10)

    In Section 2, we have expressed I by a function of x. Then, for the cases σ=1+εS0/(1+εI0), σ=1 and σ1,1+εS0/(1+εI0), substituting S=S0x and I=fi(x) (i=0,1,2) into the left hand side of (10) gives gi(x)=0, where

    g0(x)=εS0xσ(1σ),g1(x)=x(1+εI0εS0εS0lnx)=:xˉg1(x),g2(x)=x[(εI0+1+εS01σ)xσ1εS0σ(1σ)]=:xˉg2(x).

    Thus, the zero of functions gi(x) (i=0,1,2) corresponds to the peak state of the associated cases.

    Obviously, g0(x)>0 for x(x0,1). Then there is no peak state as σ=1+εS0/(1+εI0).

    For σ=1, from f1(x)=0, i.e. 1+εI0εS0lnx=1/x, it follows that ˉg1(x)=(1εS0x)/x. From Proposition 1 we have ˉg1(x)>0. Then, according to the monotonicity of ˉg1(x), there is a unique zero of ˉg1(x) (i.e. g1(x)), x1p, in the interval (x,1) if and only if g1(1)=1+εI0εS0<0, i.e. εS0/(1+εI0)>1, where

    x1p=e(1+εI0εS0)/(εS0).

    For function ˉg2(x) with σ1,1+εS0/(1+εI0), applying f2(x)=0 gives ˉg2(x)=1/xεS0/s. From Proposition 1 we know that ˉg2(x)>0. It is evident that ˉg2(x) is monotone, then ˉg2(x) (i.e. g2(x)) has a unique zero x2p in the interval (x,1) if and only if ˉg2(1)=1+εI0εS0/σ<0, i.e., σ<εS0/(1+εI0), where

    x2p={εS0σ[(1σ)(εI0+1)+εS0]}1/(σ1).

    Further, substituting x=xip (i=1,2) into S=S0x and I=fi(x)/ε (i=1,2), we obtain the peak state (S1p,I1p) for σ=1, and (S2p,I2p) for σ1,1+εS0/(1+εI0), respectively, where

    S1p=S0e1+εI0εS0εS0,I1p=S0e1+εI0εS0εS01ε;S2p=S0{εS0σ[(1σ)(εI0+1)+εS0]}1σ1,I2p=S0σ{εS0σ[(1σ)(εI0+1)+εS0]}1σ11ε.

    Moreover, the time of the peak state can also be found by substituting S=S0x and I=fi(x)/ε (i=1,2) into the first equation of (3) and then integrating it. In detail, we first substitute S=S0x and I= fi(x)/ε (i=1,2) into the first equation of (3) yields

    dxdt=βxfi(x)ε[1+fi(x)]

    with x<x<1, that is,

    dt=ε[1+fi(x)]βxfi(x)dx. (11)

    Note that x(0)=1 since S(0)=S0. Denote the time of the peak state by tp. Then tp can be determined by integrating the right hand side of (11) from 1 to xip, that is,

    tp=xip1ε[1+fi(x)]βxfi(x)dx=εβ[1xipdxxfi(x)lnxip].

    3.3. Turning point

    Let C(t) represent the number of the cumulative cases at time t. Then the turning point of the infection spread corresponds to the inflection point of function C(t), and C(t)=βSI/(1+εI) for model (3).

    The expressions (5) and (6) show that the variable I can be expressed by the variable S. Then

    C(t)=ddS(βSI1+εI)dSdt=β(1+εI)2[I(1+εI)+SdIdS]dSdt.

    Since dSdt<0, the inflection point of function C(t) is determined by equation

    I(1+εI)+SdIdS=0. (12)

    Substituting S=S0x and I=fi(x)/ε (i=0,1,2) into the left hand side of (12) gives

    h0(x)=(εI0+1)2x2ε,h1(x)=1ε[f1(x)(1+f1(x))+xf1(x)]=x2ε{[(εI0+1)εS0lnx]2εS0x}=:x2εh+1(x)h1(x),h2(x)=1ε[f2(x)(1+f2(x))+xf2(x)]=:x2εˉh2(x),

    respectively, where

    h+1(x)=(εI0+1)εS0lnx+εS0x,h1(x)=(εI0+1)εS0lnxεS0x,ˉh2(x)=[(εI0+1)xσ1εS0(1xσ1)1σ]2[(1σ)(εI0+1)+εS0]xσ2.

    Thus, the zeros of functions hi(x) (i=0,1,2) in (x,1) correspond to the inflection points of C(t) (i.e. the turning point of the infection) under the cases σ=1+εS0/(1+εI0), σ=1 and σ1,1+εS0/(1+εI0), respectively.

    (1) Note that h0(x)>0. Then there is no inflection point of function C(t) for σ=1+εS0/(1+εI0).

    (2) When σ=1, from f1(x)>0 for x<x<1 it follows that (εI0+1)εS0lnx>1/x>0 for x<x<1. Then h+1(x)>0 for xx<1.

    From f1(x)=0 it follows that h1(x)=(1εS0x)/x. Further we know that h1(x)>0 by Proposition 1. Note that

    h1(x)=εS0(12xεS0)1x

    implies that function ˉh1(x) has at most one local extreme point. Then from Lemma 2.2 it follows that there is one zero of h1(x) in (x,1) if and only if h1(1)=(εI0+1)εS0<0, i.e. εI0+1<εS0.

    Therefore, when σ=1, there is a unique inflection point of C(t) for x(x,1) if and only if εI0+1<εS0.

    (3) It is easy to see that function ˉh2(x)>0 (i.e. h2(x)>0) for x<x<1 when σ>1+εS0/(1+εI0).

    When σ<1+εS0/(1+εI0) and σ1, function ˉh2(x) can be expressed as ˉh2(x)=h+2(x)h2(x), where

    h+2(x)=[(εI0+1)xσ1εS0(1xσ1)1σ]+[(1σ)(εI0+1)+εS0]xσ2,h2(x)=[(εI0+1)xσ1εS0(1xσ1)1σ][(1σ)(εI0+1)+εS0]xσ2.

    From f2(x)>0 for x<x<1 we know that

    (εI0+1)xσ1εS0(1xσ1)1σ>1x>0

    for x<x<1. Then h+2(x)>0 for xx<1.

    For function h2(x),

    h2(x)=(1σ)(εI0+1)+εS0xσ22×{(1σ)(εI0+1)+εS0xσ2+σ22}.

    Then function h2(x) has at most one local extreme point in (x,1).

    On the other hand, applying f2(x)=0 gives h2(x)=(σεS0x)/ε>0 by Proposition 1. Further we have h2(x)>0 since h+2(x)>0 for xx<1.

    Therefore, from Lemma 2.2 function h2(x) has one zero in (x,1) if and only if

    h2(1)=(εI0+1)(εI0+σ)εS0(εI0+1)+(1σ)(εI0+1)+εS0<0,

    i.e., σ<εS0/(1+εI0)εI0. Note that εS0/(1+εI0)εI0<1+εS0/(1+εI0). Hence, when σ1, 1+εS0/(1+εI0), function h2(x)(i.e. h2(x)) has one zero in (x,1) if and only if σ<εS0/(1+εI0)εI0. That is, when σ1, 1+εS0/(1+εI0), there is a unique inflection point of C(t) for x(x,1) if and only if (εI0+1)(εI0+σ)<εS0.

    Summarizing the above inference, the conditions on the existence of the turning point can be unified as the expression (εI0+σ)(εI0+1)<εS0.

    Since functions hi(x) (i=1,2) are transcendental functions, the value of x corresponding to the inflection point of C(t) could not expressed explicitly. If it exists, denoted by xt, then, similar to the determination of time corresponding to the peak state, the time of the turning point of epidemic spread can be found by the following expression

    tt=εβ[1xtdxxfi(x)lnxt],

    and the corresponding state is (St,It), where St=S0xt and It=fi(xt)/ε (i=1,2.)


    4. Conclusion and discussion

    In Section 3, we have discussed the epidemic characteristics of model (3) with behavioral change, obtained the condition on the existence of the peak state, σ(1+εI0)<εS0, and the condition on the appearance of the turning point of epidemic spread, (εI0+σ)(1+εI0)<εS0, and provided the methods or expressions determining the associated quantities.

    In order to make the dependence of the related conditions on the parameters and the initial conditions more clear, we replace the parameter σ with αε/b in the associated expressions. Correspondingly, the condition on the existence of the peak state is that ε<(βS0/a1)/I0, and the condition on the appearance of the turning point is that ε<[βS0/(α+βI0)1]/I0. Conversely, when ε(βS0/a1)/I0, the peak can not appear; when ε[βS0/(α+βI0)1]/I0, there is no turning point. Note that βS0/(α+βI0)<βS0/a. Then, when ε<[βS0/(α+βI0)1]/I0, both the peak and the turning point can appear; when [βS0/(α+βI0)1]/I0ε<(βS0/a1)/I0, there is a peak but no turning point; if ε(βS0/a1)/I0, both the two characteristics could not exist. These statements show the impact of the behavioral change on the existence of the two characteristics. From another point of view, when the turning point can appear, there must be the peak state. But there may not be the turning point if the peak state exists. The inequalities above also provide the threshold condition on the appearance of the peak and/or the turning point. The results obtained here would be useful to make the effective control strategy for disease spread.

    In order to visually show the impact of behavioral change on the peak state and turning point of disease spread, we plot a set of graphes (Figures 1, 2 and 3) of the curves of I=I(t) and C=C(t), denoting the real-time numbers of infected individuals and cumulative cases, respectively. Here, the chosen values of parameters and the initial conditions do not represent any real data. Corresponding to all the three graphes, parameters α=2 and β=0.2, initial values S(0)=200 and I(0)=2, then

    Figure 1. The case that both the peak and the turning point can appear.
    Figure 2. The case that there is the peak and no turning point.
    Figure 3. The case that both the peak and the turning point can not appear.
    1I0(βS0α+βI01)=7.8333,1I0(βS0α1)=9.5000.

    According to the obtained results, there are both the peak and the turning point if ε<7.8333, there is the peak and no turning point if 7.8333ε<9.8, and there is neither peak and no turning point for ε9.5. These theoretic results are verified by Figures 1, 2 and 3. In Figure 1 for ε=0.08, the peak I=75.53400 achieves at t=0.57065, and the turning point is (0.16853,37.07000). In Figure 2 for ε=8, the peak is I=2.29549 at t=1.36570 and there is no turning point. For Figure 3 for ε=9.8, I=I(t) is decreasing, and C=C(t) is convex upwards. That is, both the peak and the turning point do not appear.


    Acknowledgments

    The authors would like to thank the anonymous referees and the editor for their helpful suggestions and comments which led to the improvement of our original manuscript.


    [1] [ F. Brauer, The Kermack-McKendrick epidemic model revisited, Math. Bios., 198 (2005), 119-131.
    [2] [ F. Brauer and C. Castillo-Chávez, Mathematical Models in Population Biology and Epidemiology, 2nd edn. Springer, New York, 2001.
    [3] [ V. Capasso and G. Serio, A generalizaition of the Kermack-McKendrick deterministic epidemic model, Math. Bios., 42 (1978), 43-61.
    [4] [ Y. H. Hsieh and C. W. S. Chen, Turning points, reproduction number, and impact of climatological events for multi-wave dengue outbreaks, Trop. Med. Int. Heal., 14 (2009), 628-638.
    [5] [ W. O. Kermack and A. G. McKendrick, A contribution to the mathematical theory of epidemics, Proc. R. Soc. Lond. A, 115 (1927), 700-721.
    [6] [ J. Li, Y. Li and Y. Yang, Epidemic characteristics of two classic models and the dependence on the initial conditions, Math. Bios. Eng., 13 (2016), 999-1010.
    [7] [ J. Li and Y. Lou, Characteristics of an epidemic outbreak with a large initial infection size, J. Biol. Dyn., 10 (2016), 366-378.
    [8] [ J. Ma and D. J. D. Earn, Generality of the final size formula for an epidemic of a newly invading infectious disease, Bull. Math. Biol., 68 (2006), 679-702.
    [9] [ Z. Ma and J. Li, Dynamical Modeling and Analysis of Epidemics, Singapore, 2009.
    [10] [ J. C. Miller, A note on the derivation of epidemic final sizes, Bull. Math. Biol., 74 (2012), 2125-2141.
    [11] [ F. Zhang, J. Li and J. Li, Epidemic characteristics of two classic SIS models with disease-induced death, J. Theoret. Biol., 424 (2017), 73-83.
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