Abstract
Behavior change significantly influences the transmission of diseases during outbreaks. To incorporate spontaneous preventive measures, we propose a model that integrates behavior change with disease transmission. The model represents behavior change through an imitation process, wherein players exclusively adopt the behavior associated with higher payoff. We find that relying solely on spontaneous behavior change is insufficient for eradicating the disease. The dynamics of behavior change are contingent on the basic reproduction number \(R_a\) corresponding to the scenario where all players adopt non-pharmaceutical interventions (NPIs). When \(R_a<1\), partial adherence to NPIs remains consistently feasible. We can ensure that the disease stays at a low level or maintains minor fluctuations around a lower value by increasing sensitivity to perceived infection. In cases where oscillations occur, a further reduction in the maximum prevalence of infection over a cycle can be achieved by increasing the rate of behavior change. When \(R_a>1\), almost all players consistently adopt NPIs if they are highly sensitive to perceived infection. Further consideration of saturated recovery leads to saddle-node homoclinic and Bogdanov–Takens bifurcations, emphasizing the adverse impact of limited medical resources on controlling the scale of infection. Finally, we parameterize our model with COVID-19 data and Tokyo subway ridership, enabling us to illustrate the disease spread co-evolving with behavior change dynamics. We further demonstrate that an increase in sensitivity to perceived infection can accelerate the peak time and reduce the peak size of infection prevalence in the initial wave.
Similar content being viewed by others
References
Arefin MR, Masaki T, Tanimoto J (2020) Vaccinating behaviour guided by imitation and aspiration. Proc R Soc A 476(2239):20200327
Bauch CT (2005) Imitation dynamics predict vaccinating behaviour. Proc R Soc B Biol Sci 272(1573):1669–1675
Betti MI, Abouleish AH, Spofford V, Peddigrew C, Diener A, Heffernan JM (2023) Covid-19 vaccination and healthcare demand. Bull Math Biol 85(5):32
Buonomo B, Della Marca R (2020) Effects of information-induced behavioural changes during the COVID-19 lockdowns: the case of Italy. R Soc Open Sci 7(10):201635
Butler G, Freedman HI, Waltman P (1986) Uniformly persistent systems. Proc Am Math Soc 93:425–430
Castillo-Chavez C, Song B (2004) Dynamical models of tuberculosis and their applications. Math Biosci Eng 1(2):361
Chang SL, Piraveenan M, Pattison P, Prokopenko M (2020) Game theoretic modelling of infectious disease dynamics and intervention methods: a review. J Biol Dyn 14(1):57–89
Change in positive cases by reported day. https://stopcovid19.metro.tokyo.lg.jp/en/cards/number-of-confirmed-cases/. Accessed 28 Mar 2023
Cooney DB, Morris DH, Levin SA, Rubenstein DI, Romanczuk P (2022) Social dilemmas of sociality due to beneficial and costly contagion. PLoS Comput Biol 18(11):1010670
Cross G (1978) Three types of matrix stability. Linear Algebra Appl 20(3):253–263
Cui J, Mu X, Wan H (2008) Saturation recovery leads to multiple endemic equilibria and backward bifurcation. J Theor Biol 254(2):275–283
Current Situation of Infection, March 23, 2023. https://www.niid.go.jp/niid/en/2019-ncov-e/11990-covid19-ab119th-en.html. Accessed 28 Mar 2023
Current Situation of Infection, September 14, 2022. https://www.niid.go.jp/niid/en/2019-ncov-e/11525-covid19-ab99th-en.html. Accessed 28 March 2023
Dhooge A, Govaerts W, Kuznetsov YA, Mestrom W, Riet A, Sautois B (2006) MATCONT and CL MATCONT: continuation toolboxes in Matlab. Universiteit Gent, Belgium and Utrecht University, The Netherlands
Diekmann O, Heesterbeek JAP, Metz JA (1990) On the definition and the computation of the basic reproduction ratio R0 in models for infectious diseases in heterogeneous populations. J Math Biol 28(4):365–382
Ge J, Wang W (2022) Vaccination games in prevention of infectious diseases with application to Covid-19. Chaos Solitons Fractals 161:112294
Greenberger M (2018) Better prepare than react: reordering public health priorities 100 years after the Spanish flu epidemic. Am J Public Health 108(11):1465–1468
Guckenheimer J, Kuznetsov YA (2007) Bogdanov–Takens bifurcation. Scholarpedia 2(1):1854. https://doi.org/10.4249/scholarpedia.1854
Heffernan JM, Smith RJ, Wahl LM (2005) Perspectives on the basic reproductive ratio. J R Soc Interface 2(4):281–293
Hofbauer J, Sigmund K et al (1998) Evolutionary games and population dynamics. Cambridge University Press
Hota AR, Maitra U, Elokda E, Bolognani S (2023) Learning to mitigate epidemic risks: a dynamic population game approach. Dyn Games Appl, 1–24
Korobeinikov A (2007) Global properties of infectious disease models with nonlinear incidence. Bull Math Biol 69(6):1871–1886
Kuznetsov YA, Kuznetsov IA, Kuznetsov Y (1998) Elements of applied bifurcation theory. Springer
Kuznetsov YA (2006) Saddle-node bifurcation. Scholarpedia 1(10):1859. https://doi.org/10.4249/scholarpedia.1859. (revision #151865)
Lau JT, Yang X, Tsui H, Pang E (2004) SARS related preventive and risk behaviours practised by Hong Kong-mainland China cross border travellers during the outbreak of the SARS epidemic in Hong Kong. J Epidemiol Commun Health 58(12):988–996
Laxmi, Ngonghala CN, Bhattacharyya S (2022) An evolutionary game model of individual choices and bed net use: elucidating key aspect in malaria elimination strategies. R Soc Open Sci 9(11):220685
Liu S, Zhao Y, Zhu Q (2022) Herd behaviors in epidemics: a dynamics-coupled evolutionary games approach. Dyn Games Appl 12(1):183–213
Lupica A, Volpert V, Palumbo A, Manfredi P, d’Onofrio A et al (2020) Spatio-temporal games of voluntary vaccination in the absence of the infection: the interplay of local versus non-local information about vaccine adverse events. Math Biosci Eng 17(2):1090–1131
Marsden JE, McCracken M (2012) The Hopf bifurcation and its applications. Springer
Martcheva M, Tuncer N, Ngonghala CN (2021) Effects of social-distancing on infectious disease dynamics: an evolutionary game theory and economic perspective. J Biol Dyn 15(1):342–366
Nations U (2023) The World’s Cities in 2018. https://www.un.org/en/events/citiesday/assets/pdf/the_worlds_cities_in_2018_data_booklet.pdf. Accessed 28 March 2023
Phillips B, Anand M, Bauch CT (2020) Spatial early warning signals of social and epidemiological tipping points in a coupled behaviour-disease network. Sci Rep 10(1):7611
Poletti P, Caprile B, Ajelli M, Pugliese A, Merler S (2009) Spontaneous behavioural changes in response to epidemics. J Theor Biol 260(1):31–40
Poletti P, Ajelli M, Merler S (2012) Risk perception and effectiveness of uncoordinated behavioral responses in an emerging epidemic. Math Biosci 238(2):80–89
Redheffer R (1985) Volterra multipliers I. SIAM J Algebraic Discret. Methods 6(4):592–611
Redheffer R (1986) Erratum: volterra multipliers II. SIAM J Algebraic Discret Methods 7(2):336–336
Riley S, Fraser C, Donnelly CA, Ghani AC, Abu-Raddad LJ, Hedley AJ, Leung GM, Ho L-M, Lam T-H, Thach TQ et al (2003) Transmission dynamics of the etiological agent of SARS in Hong Kong: impact of public health interventions. Science 300(5627):1961–1966
Rinaldi F (1990) Global stability results for epidemic models with latent period. Math Med Biol J IMA 7(2):69–75
Saad-Roy CM, Traulsen A (2023) Dynamics in a behavioral-epidemiological model for individual adherence to a nonpharmaceutical intervention. Proc Natl Acad Sci 120(44):2311584120
Satapathi A, Dhar NK, Hota AR, Srivastava V (2023) Coupled evolutionary behavioral and disease dynamics under reinfection risk. IEEE Trans Control Netw Syst
Seale H, Heywood AE, McLaws M-L, Ward KF, Lowbridge CP, Van D, MacIntyre CR (2010) Why do I need it? I am not at risk! Public perceptions towards the pandemic (H1N1) 2009 vaccine. BMC Infect Dis 10(1):1–9
Squires H, Kelly MP, Gilbert N, Sniehotta F, Purshouse RC (2023) The long-term effectiveness and cost-effectiveness of public health interventions; How can we model behavior? a review. Health Econ 32(12):2836–2854
SteelFisher GK, Blendon RJ, Bekheit MM, Lubell K (2010) The public’s response to the 2009 H1N1 influenza pandemic. N. Engl. J. Med. 362(22):65
Sun C, Hsieh Y-H (2010) Global analysis of an SEIR model with varying population size and vaccination. Appl Math Model 34(10):2685–2697
Tang B, Zhou W, Wang X, Wu H, Xiao Y (2022) Controlling multiple COVID-19 epidemic waves: an insight from a multi-scale model linking the behaviour change dynamics to the disease transmission dynamics. Bull Math Biol 84(10):1–31
Toei subway passengers. https://stopcovid19.metro.tokyo.lg.jp/en/cards/predicted-number-of-toei-subway-passengers. Accessed 28 March 2023
Van den Driessche P, Watmough J (2002) Reproduction numbers and sub-threshold endemic equilibria for compartmental models of disease transmission. Math Biosci 180(1–2):29–48
Vegvari C, Abbott S, Ball F, Brooks-Pollock E, Challen R, Collyer BS, Dangerfield C, Gog JR, Gostic KM, Heffernan JM et al (2022) Commentary on the use of the reproduction number R during the COVID-19 pandemic. Stat Methods Med Res 31(9):1675–1685
Walker JA (1974) Literature review: qualitative theory of second-order dynamic systems. Shock Vib Digest 6(10):74–74
Wang W (2006) Backward bifurcation of an epidemic model with treatment. Math Biosci 201(1–2):58–71
Wang X, Wang W (2012) An HIV infection model based on a vectored immunoprophylaxis experiment. J Theor Biol 313:127–135
Wang X, Li Q, Sun X, He S, Xia F, Song P, Shao Y, Wu J, Cheke RA, Tang S et al (2021) Effects of medical resource capacities and intensities of public mitigation measures on outcomes of COVID-19 outbreaks. BMC Public Health 21(1):1–11
Wang X, Zhou L, McAvoy A, Li A (2023) Imitation dynamics on networks with incomplete information. Nat Commun 14(1):7453
Weibull JW (1997) Evolutionary game theory. MIT press
Xin Y, Gerberry D, Just W (2019) Open-minded imitation can achieve near-optimal vaccination coverage. J Math Biol 79(4):1491–1514
Yin H, Wang S, Zhu Y, Zhang R, Ye X, Wei J, Hou PC (2020) The development of critical care medicine in china: from SARS to COVID-19 pandemic. Crit Care Res Pract
Zhang T, Nishiura H (2023) Estimating infection fatality risk and ascertainment bias of COVID-19 in Osaka, Japan from February 2020 to January 2022. Sci Rep 13(1):5540
Zhao X-Q (2003) Dynamical systems in population biology. Springer
Zhou X, Cui J (2011) Analysis of stability and bifurcation for an SEIR epidemic model with saturated recovery rate. Commun Nonlinear Sci Numer Simul 16(11):4438–4450
Funding
The authors were supported by the National Key R &D Program of China2022YFA1003704 (YX), the National Natural Science Foundation of China (NSFC12220101001(YX), 12031010(YX), 12071366(TL)), the Natural Science and Engineering Research Council of Canada (NSERC (JH)) and the York Research Chair Program (JH).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare no Conflict of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Appendices
Dynamical Behaviors of System (3)
1.1 Comparing Trajectories from the Full Model (3) and its approximation (5)
To illustrate the rationale for analyzing the approximate system, we compared the solutions of the full System (3) and the approximate System (5) across a wide range of parameters. Through this comparison, we demonstrated that Model (5) can be considered a numerically validated approximation of Model (3). Figures 13 and 14 represent two specific examples under two different conditions outlined in Sect. 3.3. It is stated that the approximation arising from Assumption (4) in the main text is not restrictive and does not affect the dynamics behavior. As a consequence, for the sake of simplicity, only the approximated model is analyzed in both the main text.
1.2 The Proof Theorem 3
In what follows, we first introduce some necessary concepts and notations that facilitate our global stability analysis.
Assumption A. 1
The matrix \(A>0 \ (<0)\) if A is symmetric positive (negative) definite.
Lemma A.1
(Cross 1978). Let A is an \(n\times n\) real matrix. Then, all the eigenvalues of A have negative real parts if and only if there is a matrxia \(H>0\), such that
where \(A^T\) is the transpose of A.
Lemma A.2
(Cross 1978). The \(n\times n\) matrix A is Volterra–Lyapunov stable if there is a positive diagonal \(n\times n\) matrix M, such that
where \(M^T\) is the transpose of M.
Lemma A.3
(Cross 1978; Rinaldi 1990). Let \(D=\left[ \begin{array}{ll} d_{11} &{}\quad d_{12} \\ d_{21} &{}\quad d_{22} \\ \end{array} \right] \) be a \(2\times 2\) matrix. Then D is Volterra–Lyapunov stable if and only if
Lemma A.4
(Redheffer 1985, 1986). Consider the nonsingular matrix \(A=[a_{ij}]_{n\times n} (n\ge 2)\) and a positive diagonal \(n\times n\) matrix \(M=diag(m_1,...,m_n)\). Let \(E=A^{-1}\) and \(\widetilde{A}\) denote the \((n-1)\times (n-1)\) matrix obtained from A by deleting its last row and last column. Then, if
there is a \(m_n>0\) such that \(MA+A^TM^T>0\).
Theorem A.1
The matrix M is Volterra–Lyapunov stable when
Proof
As for Matrix (17), we have
and
with
And if \(k<1-X_{1}\), \(m_{33}>0\) is true. Let \(\widetilde{M}\) and \(\widetilde{M^{-1}}\) denote the \((n-1)\times (n-1)\) matrix obtained from M and \(M^{-1}\) by deleting its last row and last column respectively. According to Lemma A.3, we get that the matrix \(\widetilde{M}\) and \(\widetilde{M^{-1}}\) are all Volterra–Lyapunov stable (Cross 1978) if \(k<1-X_{1}\) since
and the diagonal elements of \(\widetilde{M}\) or \(\widetilde{M^{-1}}\) are all negative in this case. Let \(\mathbb {M}=-M\), combining Lemma A.4, we get that if there is a constant diag matrix \(W=diag(1,m,w_3)\) such that
and
for any \((y_1,y_2,y_3)\in \Omega _y\), the matrix M is Volterra–Lyapunov stable if \(k<1-X_{1}\). Equation (A2) is equivalent to
Since Eq. (A4) has to be true for any \(0<1-X_{1}-y_1<1\),
has to be satisfied. Then, we have
Substituting Eq. (A5) into Eq. (A4) gives
which is true if \( R_a <4\frac{\mu +\gamma +\delta }{\delta }.\) Substituting Eq. (A5) into Eq. (A3) gives
Algebraic calculations show that if \( R_a <4\frac{\mu +\gamma +\delta }{\delta }\),
holds true. And if \(\delta >\frac{1}{2}\),
is true. Based on the above analysis, we can testify that the matrix M is Volterra–Lyapunov stable if
That completes the proof. \(\square \)
1.3 The Local Stability of \(\text {EE}^{*}\)
The Jacobian matrix of System (6) evaluated at \(E_{*}^{*}=(E_{*},I_{*},x_{*})\) is
where
The corresponding characteristic equation is
where
According to the Hurwitz stability criterion, we know that the real parts of the eigenvalues of \(J_{E_{*}^{*}}\) are negative if \(b_1b_2-b_3>0\), indicating the local stability of the endemic equilibrium \(E_{*}^{*}\).
Especially, when \(k<I_M\), if \(\phi \rightarrow +\infty \), \(I_{*}\rightarrow k^{-}\) is true, then we have \(a_{32}\rightarrow +\infty \), and \(a_{11}\), \(a_{12}\), \(a_{13}\) and \(a_{33}\) are values that fall within a finite range. Then \(b_1b_2-b_3\rightarrow -\infty \) is true in this case, which indicates the unstable of the endemic equilibrium \(E_{*}^{*}\). When \(k>I_M\), if \(\phi \rightarrow +\infty \), \(I_{*}\rightarrow I_M^{-}\) is true, then we have \(x_{*}\rightarrow 1^{-}\), which means that \(a_{33}\rightarrow -\infty \), and \(a_{11}\), \(a_{12}\), \(a_{13}\) and \(a_{32}\) are values that fall within a finite range. Then \(b_1b_2-b_3\rightarrow +\infty \) is true in this case, which indicates the local stability of the endemic equilibrium \(E_{*}^{*}\).
And beyond that, \(b_1b_2-b_3>0\) is equivalent to \(Q_1(I_{*})>Q_2(I_{*})\), where
Algebraic calculations show that \(Q_1'(I)>0\) and \(Q_2'(I)>0\) in the interval \([\mathbb {I}_{m},\mathbb {I}_{M}]\) (see Eq. 11 for the specific form for this interval). If
and
\(Q_1(I_{m})>Q_2(I_{M})\) is true, where
and
Combining the monotonicity of \(Q_i(I)\) with \(i=1,2\) and \(I_{m}>0\) if \( R_a >1\), we can conclude that if
\(Q_1(I)>Q_2(I)\) holds true when \(\mathbb {I}_{m}<I<\mathbb {I}_{M}\), that is to say, \(b_1b_2-b_3>0\) holds true in this case.
1.4 Uniform Persistence
Let X be a locally compact metric space with metric d and \(\Gamma \) be a closed nonempty subset of X. \(\Gamma _0\in \Gamma \) is an open set. Define \(\partial \Gamma _0:=\Gamma \setminus \Gamma _0\). \(\partial \Gamma _0\) need not be the boundary of \(\Gamma _0\) as the notation suggests (Zhao 2003). \(\Phi _t\) is a dynamical system defined on \(\Gamma \). A set B in X is said to be invariant if \(\Phi (B,t)=B\). Define \(M_{\partial }:=\{ x\in \partial \Gamma _0:\Phi _t x\in \partial \Gamma _0,\forall t\ge 0 \}\). We have the following lemma.
Lemma A.5
(Zhao 2003; Sun and Hsieh 2010). Assume
-
(\(A_1\)) \(\Phi _t\) has a global attractor;
-
(\(A_2\)) There exists an \(M=\{M_1,...,M_k\}\) of pair-wise disjoint, compact, and isolated invariant set on \(\partial \Gamma _0\) such that
-
(a)
\(\cup _{x\in M_{\partial }}w(x)\subset \cup _{j=1}^{k}M_j\);
-
(b)
No subsets of M form a cycle on \(\partial \Gamma _0\);
-
(c)
Each \(M_j\) is also isolated in \(\Gamma \);
-
(d)
\(W^s(M_j)\cap \Gamma _0 = \emptyset \) for each \(1\le j \le k\), where \(W^s(M_j)\) is the stable manifold of \(M_j\).
-
(a)
Then \(\Phi _t\) is uniformly persistent with respect to \(\Gamma _0\).
As for System (6), let
Obviously, \(M_{\partial }=\{(0,0,x)\mid x\ge 0\}\). Since \(\Omega \) is a positively invariant set of System (6), there always admits a global attractor, making (\(A_1\)) true. We can prove that \(M=\{E_0^{0},E_0^{1}\}\), \(w(x)={E_0^{1}}\) for all \(x\in M_{\partial }{\setminus } E_0^{0}\). On \(M_{\partial }\), System (6) reduces to \(\dot{x}(t)= \phi x(1-x)k\) with \(0\le x(0)\le 1\), in which \(x(t)\rightarrow 1\) as \(t\rightarrow \infty \) if \(0<x(0)\le 1\). That means that hypothesis (a) and (b) hold. \(E_0^{0}\) is always unstable and \(E_0^{1}\) is unstable if \( R_0>1\) according to Theorem 2. And beyond that, \(W^s(M)\subset \partial \Gamma _0\). Hypothesis (c) and (d) are then satisfied. To sum up, we can reach the Theorem 5.
1.5 Hopf Bifurcations of System (6)
Figure 15 displays time series under various large \(\phi \) values when periodic solutions are present. It indicates that as \(\phi \) increases, not only does the maximum prevalence of infection decrease during a cycle, but both the period and cumulative cases over one cycle also decrease.
Dynamical Behaviors of System (21)
1.1 Existence of Equilibria
Theorem B.1
The following statements on \(\text {EE}^0\) of System (21) are true.
-
(a)
When \(\frac{\mu }{\mu +\gamma }<R_a<1\), if \(R_a<R_m\) or \(R_a>R_M\), Model (21) has two \(\text {EE}^0\)s, represented by \(E_{{*}_1}^0=(E_a,I_a,0)\) and \(E_{{*}_2}^0=(E_b,I_b,0)\) with \(I_a<I_b\). Further, \(E_{{*}_1}^0\) is unstable saddle, \(E_{{*}_2}^0\) is locally asymptotically stable node or focus if \(\hat{H}(I_{b})<0\), but unstable node or focus if \(\hat{H}(I_{b})>0\).
-
(b)
Model (21) has a unique \(\text {EE}^0\) if one of the following conditions holds,
-
(b-1)
\(\frac{\mu }{\mu +\gamma }< R_a = R_m\) and \(h>h_0\);
-
(b-2)
\(\frac{\mu }{\mu +\gamma }< R_a = R_M\) and \(h>h_0\);
-
(b-3)
\( R_a >max\{1,R_M\}\) or \(1<R_a<R_m\). In this case, this unique \(\text {EE}^0\) is represented by (\(E_b,I_b,0\)), which is locally asymptotically stable node or focus if \(\hat{H}(I_{b})<0\), but unstable node or focus if \(\hat{H}(I_{b})>0\).
-
(b-1)
Here
Proof
As for System (21), the possible EE (E, I, x) with all players adopting an “altered” behavior satisfies
where
The discriminant of Eq. (B1) is
and \(\Delta >0\) holds true if \(R_a<R_{m}\) or \(R_a>R_{M}\), where
According to the relationship between the roots and the coefficients of quadratic equations, the following can be obtained: If \( R_m<R_a < R_M\), Eq. (B1) has no real roots. If \(R_a=R_m\) or \(R_a=R_M\), Eq. (B1) has a unique real and non-zero root, represented by \(I_{c}=\delta \frac{-H_0}{2h(\mu +\delta )}\), which is positive if \(H_0<0\). If \(R_a<R_m\) or \(R_a>R_M\), Eq. (B1) possesses two distinct real and non-zero roots, represented by
And beyond that, \(I_a<0<I_b\) holds true if \(R_a>1\); \(0<I_a<I_b\) is true if \(R_a<1\) and \(H_0<0\); \(I_a<I_b<0\) is true if \(R_a<1\) and \(H_0>0\). \(H_0<0\) holds true if
Furthermore,
holds true if \(I_{j}>0\), where \(E_{j}=\frac{\mu }{\delta }I_{j}+\frac{\gamma }{\delta }\frac{I_{j}}{1+hI_{j}}\) and \(j\in \{a,b,c,d\}\). Then the existence of \(\text {EE}^0\) can be obtained.
By checking the Jacobian matrix of System (21) at the possible EE (E, I, 0) with \(E=\frac{\mu }{\delta }I+\frac{\gamma }{\delta }\frac{I}{1+hI}\), we get the corresponding characteristic equation
where
When System (21) has two \(\text {EE}^0\),
with \(I_{a}<I_{b}\). Combing with Eq. (B1), we have
which means that \(\lambda ^2+\hat{a_1}(I_{a}) \lambda +\hat{a_2}(I_{a})=0\) has a positive real root and a negative real root, and the real parts of the roots of \(\lambda ^2+\hat{a_1}(I_{b}) \lambda +\hat{a_2}(I_{b})=0\) are all negative. That is to say, \(E_{{*}_1}^0\) is a unstable saddle and \(E_{{*}_2}^0\) is locally asymptotically stable node or focus if \(\hat{H}(I_{b})< 0\) but unstable node or focus if \(\hat{H}(I_{b})> 0\). Evidenced by the same token, if System (21) has the unique \(\text {EE}^0\) (\(E_b,I_b,0\)), which is locally asymptotically stable node or focus if \(\hat{H}(I_{b})<0\) but unstable node or focus if \(\hat{H}(I_{b})>0\); That completes the proof. \(\square \)
It was evident that as for Model (21), the EE with all players adopting “normal” behaviors does not exist. But the EE where a fixed proportion of the players adopt “normal” behavior (denoted as \(\text {EE}^{*}\)) may exist, i.e., the equilibrium
with \(0<x_{*}<1\) and \(I_{*}>0\) is feasible.
Theorem B.2
Model (21) may have 0-2 \(\text {EE}^{*}\) if one of the following conditions holds,
-
(a)
\( R_0> 1\);
-
(b)
\( \frac{\mu }{\mu +\gamma }< R_0<1\) and \(h>h_1\doteq \frac{\mu +\delta +\gamma }{\delta }\frac{(\mu +\gamma )R_0}{(\mu +\gamma )R_0-\mu }\).
Proof
As for System (21), the possible \(\text {EE}^{*}\) (E, I, x) where a fixed proportion of the players adopt an “normal” behavior satisfies
Due to requirement \(0<x<1\), we know from Eq. (B4)b that
which is equivalent to
where \(H_1=\frac{\mu +\delta +\gamma }{\delta }-h+\frac{\mu }{\mu +\gamma }\frac{1}{R_0}h\), \(H_0=\frac{\mu +\delta +\gamma }{\delta }-h+\frac{\mu }{\mu +\gamma }\frac{1}{R_a}h\) and \(H_1<H_0\). Let
with
we have that \(\Delta _1>0\) if and only if \( R_0<R_{m}\) or \(R_0>R_{M}\), where
According to the relationship between the roots and the coefficients of quadratic equations, the following can be obtained: if \(R_m< R_0< R_M\), Inequality (B6)a cannot be true for all \(I>0\), which means that System (21) doesn’t have any \(\text {EE}^{*}\) in this case; if \(R_0<R_{m}\) or \(R_0>R_{M}\), Inequality (B6)a is true for \(I_1^1<I<I_2^1\), where
And beyond that, \(I_1^1<0<I_2^1\) holds true if \(R_0>1\); \(0<I_1^1<I_2^1\) is true if \(R_0<1\) and \(H_1<0\). And \(H_1<0\) holds true if
That is to say, except for the condition \(R_0<R_{m}\) or \(R_0>R_{M}\), \(EE^{*}\) is feasible if \(R_0>1\), or \(\frac{\mu }{\mu +\gamma }<R_0<1\) and \(h>h_1\).
Similarly, let
\(\Delta _2>0\) is true if \(R_a<R_{m}\) or \(R_a>R_{M}\). Note that \(H_0\) is the same as Eq. (B2). We can also testify that if \(R_{m}<R_a<R_{M}\), Inequality (B6)b holds true for all \(I>0\); if \(R_a<R_{m}\) or \(R_a>R_{M}\), Inequality (B6)b is true if \(I<I_1^2\) or \(I>I_2^2\), where
And beyond that, \(I_1^2<0<I_2^2\) holds true if \(R_a>1\); \(0<I_1^2<I_2^2\) is true if \(R_a<1\) and \(H_0<0\); and \(I_1^2<I_2^2<0\) is true if \(R_a<1\) and \(H_0>0\). And \(H_0<0\) holds true if
Inequality (B5)a means that
then Inequality (B4)c holds true provided \(I<k\). We can also testify that Eq. (B4)c is equivalent to \(F_1(I)=F_2(I)\), where
Algebraic calculation shows that \(F'_1(I)>0\), \(F'_2(I)>0\) and the non-zero solution to \(F_1(I)=F_2(I)\) is equivalent to
Since functions \(G_1(I)\) and \(G_2(I)\) are both monotonically increasing concave functions on the interval [0, 1], there are at most two non-zero solutions to equation \(F_1(I)=F_2(I)\), which means that System (21) has at most two \(\text {EE}^{*}\). Besides, we have
Considering the zero point theorem and combining the monotonicity of \(G_i(I)\), we can get the existence of \(\text {EE}^{*}\) of System (21), which is shown in Table 2. That completes the proof. \(\square \)
1.2 A Saddle-Node Homoclinic Bifurcation
A saddle-node homoclinic bifurcation, i.e., the birth of a limit cycle when the saddle-node disappears (Kuznetsov 2006), is illustrated in Fig. 11. It shows that, System (21) always has two unstable DFEs. When \(0<h<4.0253\), System (21) has a locally asymptotically stable \(\text {EE}^{*}\). As h increases beyond 4.0253, \(\text {EE}^{*}\) becomes unstable through a Hopf bifurcation (say, H). Numerical simulation shows that the solutions of System (21) undergo oscillation when \(4.0253<h<7.2935\). Further as h increases beyond 7.2935, the limit cycle disappears through a saddle-node homoclinic bifurcation and two \(\text {EE}^0\)s exist (say, SNH). Numerical simulation shows that the \(\text {EE}^0\) with smaller I is always unstable and the \(\text {EE}^0\) with larger I is locally asymptotically stable when \(7.2935<h<10\). Besides, \(\text {EE}^{*}\) disappears after colliding with the \(\text {EE}^0\) with smaller I when h lies near 8.0105 (say, BP).
To further analyze how periodic orbits change, we plot the variation in period of cycles versus h in Fig. 11e, which shows that the periods eventually go to infinity at \(h=7.2935\). Besides, we also draw phase diagrams with different parameters h, show in Fig. 16. When \(h=7.2935\), System (21) exists a unstable saddle-node point, the location of this point is shown in the red dot marked with \(E_{LP}\) in Fig. 16. Figure 16 shows that as h gets closer and closer to 7.2935, the minimum distance between all points on the stable periodic solution and \(E_{LP}\) gets smaller and smaller and eventually approaches zero. These all indicate that a saddle-node homoclinic bifurcations does occur when \(h=7.2935\).
1.3 A Hopf Bifurcation
Here, we analyze the case where \(R_a>1\). In this scenario, a Hopf bifurcation can still occur, as shown in Fig. 17. It is noteworthy that when h is large, even though all players take “altered” behaviors, the prevalence of infection increases with the magnitude of h. This emphasizes the critical role of medical resources in controlling the scale of infection.
A Model Under the SEIRS Scheme
If we use an SEIRS scheme to describe disease and immunity states and consider the principles, the corresponding full equation is
where, m is the rate which recovered individuals return to the susceptible statue due to loss of immunity and d is the mortality rate caused by the disease. As for recovered individual, they face no risk of infection, so they don’t need to take any precautions. When they return to a susceptible status, they will take “altered” behaviors to mitigate the risk of reinfection. If condition (4) is still true, the approximated model would be System (22) of the main text. The corresponding positively invariant set is
The basic reproduction number without behavior change, represented by System (22) with \(x\equiv 1\), is given by:
The basic reproduction number where all individuals adopt “altered” behaviors, represented by System (22) with \(x\equiv 0\), is given by:
It is evident that System (22) always has two DFEs: one where all players adopt “altered” behaviors \(E_0^{0}=(1,0,0,0,0)\) (denoted as \(\text {DFE}^0\)), and another where all players adopt “normal” behaviors \(E_0^{1}=(1,0,0,0,1)\) (denoted as \(\text {DFE}^1\)). Here, \(\text {DFE}^0\) is always unstable. \(\text {DFE}^1\) is locally asymptotically stable if \(R_{0d}<1\) and unstable if \(R_{0d}>1\). When \(R_{ad}>1\), System (22) has an EE with all players adopting “altered” behaviors, denoted as \(EE^0\), given by:
where
It’s worth noting that
meaning that for the EE where all players adopt “altered” behaviors, the corresponding infection prevalence in the SEIRS-based model is smaller than that in the SEIS-based model. The stability of this equilibrium can be examined.
Theorem C.1
Assume \(R_{ad}>1\). \(EE^{0}\) of System (22) is locally asymptotically stable if \(k<\texttt {k}\) and unstable if \(k>\texttt {k}\), where
Proof
The Jacobian matrix of System (22) evaluated at \(EE^{0}\) gives characteristic equation
where
Since \(\widetilde{a_3}\widetilde{a_2}-\widetilde{a_1}>0\) and \(\widetilde{a_3}\widetilde{a_2}\widetilde{a_1}-\widetilde{a_0}(\widetilde{a_3})^2-(\widetilde{a_1})^2>0\), the real parts of the roots of \(\lambda ^4+\widetilde{a_3}\lambda ^3+\widetilde{a_2}\lambda ^2+\widetilde{a_1}\lambda +\widetilde{a_0}=0\) are negative, implying that the local stability of \(EE^0\) is determined only by the eigenvalue \(\lambda _5=\widetilde{a_{55}}\). Algebraic calculation shows \(\widetilde{a_{55}}<0\) is equivalent to \(k<\texttt {k}\). That completes the proof. \(\square \)
An EE where a fixed proportion of the players adopt “normal” behavior, denoted as \(EE^{*}\), is also feasible.
Theorem C.2
System (22) has a unique \(EE^{*}\) if \(R_{ad}<1<R_{0d}\), or \(R_{ad}>1\) and \(k>\texttt {k}\). When this equilibrium exists, it locally asymptotically stable if Conditions (C8) hold true.
Proof
The potential \(EE^{*}\), represented by \(E_{*}^{*}=(S_{*},E_{*},I_{*},x_{*})\) with \(0<x_{*}<1\), satisfies
and \(I_{*}\) is the root of \(F_1(I)=F_2(I)\), where
Combing the inequality \(0<x_{*}<1\) with Eq. (C6)d, we have \(I_m<I_{*}<I_M\), where
\(I_M>0\) provided \(R_{0d}>1\), implying that System (22) may have \(EE^{*}\) only if \(R_{0d}>1\). Further considering the equation \(F_1(I)=F_2(I)\), we have \(0<F_2(I_{*})<1\) and
Then, we only need to consider the root of \(F_1(I)=F_2(I)\) in the interval \((\mathbb {I}_{m},\mathbb {I}_{M})\).
It’s evident that on the interval \((\mathbb {I}_{m},\mathbb {I}_{M})\), the function \(F_1(I)\) is increasing, while \(F_2(I)\) is decreasing. When \(R_{ad}<1<R_{0d}\), \(\mathbb {I}_{m}=0\) and \(F_1(0)<1=F_2(0)\) hold true. If \(I_M<k\), we have \(F_1(I_M)=1>F_2(I_M)\). If \(I_M>k\), we have
Thus System (22) has a unique \(EE^{*}\) when \(R_{ad}<1<R_{0d}\). Now, we focus on the case where \(R_{0d}>1\). In this case, we have \(\mathbb {I}_{m}=I_m\) and \(F_1(\mathbb {I}_{M})>F_2(\mathbb {I}_{M}^{-})\) still holds true. Thus, when \(R_{0d}>1\), System (22) has a unique \(EE^{*}\) if \(F_1(I_m)<F_2(I_m)\). The condition \(F_1(I_m)<F_2(I_m)\) is further equivalent to \(k>\texttt {k}\). See Eq. (C5) for the specific expression for \(\texttt {k}\).
The characteristic equation at this EE is
where
The real parts of the roots of this equation are all negative if the following conditions hold:
That completes the proof. \(\square \)
Numerical simulations additionally demonstrate that when this interior EE exists, if \(R_{ad}<1<R_{0d}\), this EE is either globally asymptotically stable or unstable but with a stable periodic solution around it. Oscillations are also observed when k is small and \(\phi \) is large, as illustrated in Fig. 18. Moreover, if \(R_{ad}>1\), periodic solutions around this EE are also possible, occurring when k is at an intermediate value or when \(\phi \) is large, as depicted in Fig. 19. Generally, the dynamic behaviors of System (22) and System (6) are similar.
Then, we utilize similar data to parameterize this SEIRS-based model (22), we can observe comparable results regarding the impact of behavioral changes on the timing and magnitude of the peak of the first wave, as shown in Fig. 20.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Li, T., Xiao, Y. & Heffernan, J. Linking Spontaneous Behavioral Changes to Disease Transmission Dynamics: Behavior Change Includes Periodic Oscillation. Bull Math Biol 86, 73 (2024). https://doi.org/10.1007/s11538-024-01298-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s11538-024-01298-w