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Effects of heterogeneous self-protection awareness on resource-epidemic coevolution dynamics

Xiaolong Chen Kai Gong Ruijie Wang [email protected] Shimin Cai Wei Wang [email protected] School of Economic Information Engineering, Southwestern University of Finance and Economics, Chengdu 611130, China A Ba Teachers University, A Ba 623002, China School of Computer Science and Engineering, University of Electronic Science and Technology of China, Chengdu 610054, China Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 610054, China Big Data Research Center, University of Electronic Science and Technology of China, Chengdu 610054,China Cybersecurity Research Institute, Sichuan University, Chengdu 610065, China
Abstract

Recent studies have demonstrated that the allocation of individual resources has a significant influence on the dynamics of epidemic spreading. In the real scenario, individuals have a different level of awareness for self-protection when facing the outbreak of an epidemic. To investigate the effects of the heterogeneous self-awareness distribution on the epidemic dynamics, we propose a resource-epidemic coevolution model in this paper. We first study the effects of the heterogeneous distributions of node degree and self-awareness on the epidemic dynamics on artificial networks. Through extensive simulations, we find that the heterogeneity of self-awareness distribution suppresses the outbreak of an epidemic, and the heterogeneity of degree distribution enhances the epidemic spreading. Next, we study how the correlation between node degree and self-awareness affects the epidemic dynamics. The results reveal that when the correlation is positive, the heterogeneity of self-awareness restrains the epidemic spreading. While, when there is a significant negative correlation, strong heterogeneous or strong homogeneous distribution of the self-awareness is not conducive for disease suppression. We find an optimal heterogeneity of self-awareness, at which the disease can be suppressed to the most extent. Further research shows that the epidemic threshold increases monotonously when the correlation changes from most negative to most positive, and a critical value of the correlation coefficient is found. When the coefficient is below the critical value, an optimal heterogeneity of self-awareness exists; otherwise, the epidemic threshold decreases monotonously with the decline of the self-awareness heterogeneity. At last, we verify the results on four typical real-world networks and find that the results on the real-world networks are consistent with those on the artificial network.

keywords:
Coevolution dynamics , Epidemic spreading, Resource allocation, Self-protection awareness, Complex networks

1 Introduction

Resources, such as funds, medical and protective equipment, play a vital role in constraining or mitigating the outbreak of an epidemic. However, the pandemics always announced themselves with a sudden explosion of cases, inducing a severe shortage of public resources [1, 2]. Examples including the SARS coronavirus in 2003 [3] and Ebola virus in 2014 [4] etc.. At the end of 2019, a new type of coronavirus called COVID-19 broke out in Wuhan, China, and it quickly spreads around the world. By the end of April 2020, more than three million cases worldwide have been officially reported [5]. The increasing demands for protection and treatment have led to a severe shortage of public resources [6].

Facing the shortage of public resources, the topic of optimal resource allocation in suppressing disease spreading has aroused extensive attention from varies communities [7, 8, 9, 10, 11, 12]. For example, Andrey et al. [8] solved the problem of optimal deployment of limited resources by studying the interplay between network topology and spreading dynamics. Based on a scalable dynamic message-passing approach [9], they got the optimal distribution of available resources and demonstrated the universality of the method on a variety of real-world examples. Preciado et al. [7] researched the problem of how to optimally allocate the vaccination resources on complex networks. Through a convex framework, they found the cost-optimal distribution of the resources. Nicholas et al. [13] developed a framework to find an optimal strategy of resource allocation to eliminate one of the epidemics when two competitive epidemics spreading on a bilayer network. Besides, Nowzari et al.  [14] studied the problem of containing an initial epidemic outbreak under budget constraints based on the analysis of a generalized epidemic model over arbitrary directed graphs with heterogeneous nodes. Chen et al. [15] studied the problem of optimally allocate the limited resources to minimize the prevalence. They solved the problem under the premise of the positive correlation between node degree and resource own by each node.

The previous works only considered the optimization of public resources and addressed the problem from a mathematical perspective. However, during the outbreak of epidemics, public resources such as medical staff, protective equipment are in a severe shortage. Usually, public resources are allocated preferentially to meet the needs of severe and critical patients [16]. The treatment and protection of mild or susceptible individuals mainly depend on the accumulation of individual resources and the support of resources among individuals. The topic that the influence of individual resource on the epidemic spreading has attracted wide attention in physic community [17, 18, 19]. For instance, Böttcher [17] considered that the healthy individuals could contribute resources during an outbreak of an epidemic. By studying the coevolution of the resource and disease, they found an “explosive” increase of infected nodes induced by resource constraints. Chen et al. [18] studied the interplay between resource allocation and disease spreading on top of multiplex networks, and found a hybrid phase transition. In this multiplex network framework, they further investigated the impact of preferential resource allocation on the dynamics of epidemic spreading [19].

In real scenario, the diffusion of information/awareness can change human behaviors, such as wearing masks or staying at home to reduce the frequency of face-to-face contact [20, 21]. The interplay between information/awarenss diffusion and epidemic spreading is another topic that has inspired a wide range of research by scholars [22, 23, 24, 25]. For example, Granell et al. [26] studied the dynamical interplay between the epidemic spreading and information diffusion on top of multiplex networks. Funk et al. [27] studied the coevolution of information and disease on well-mixed populations and lattices, and found that in a well-mixed population, the information about the disease can suppress the disease. Kabir et al. [28] proposed a two-layer susceptible-infected-recovered/unaware-aware (SIR-UA) epidemic model to investigate the impact of awareness on epidemic spreading on top of different heterogeneous networks. Moreover, Kabir et al. [29] further studied the effects of awareness on the epidemic spreading based on a metapopulation model combined with a SIS-UA (susceptible-infected-susceptible-unaware-aware) epidemic model.

Information or awareness can also change the individuals’ willingness of resource donation  [30]. In reality, the susceptible individuals would weigh whether to help others or protect themselves when they are aware of the disease. Since individuals are in various circumstances and have different personalities, there is a heterogeneous distribution of awareness for self-protection. For example, a cautious person is more likely to reserve resources for self-protection than a generous person during an outbreak, or a person who has received help from others will have a stronger willingness to donate resources than others. There remains a question that how the heterogeneous distribution of awareness for self-protection influence the epidemic dynamics. To answer this question, a resource-epidemic coevolution model is proposed, which is based on the following assumption: Namely, each susceptible individual has both a probability of resource donation and a certain level of self-awareness. A larger self-awareness of an individual indicates a stronger sense of self-protection and a lower willingness of resource donation. Besides, we also consider that the susceptible individuals can perceive the disease from immediate neighbors. With the increase of infected neighbors, the susceptible individuals will reduce the probability of resource donation, since the donation behavior will lead to fewer resources for self-protection and a higher probability of been infected. Then the interplay between resource allocation and epidemic spreading is studied in our paper.

We first study the effects of degree and self-awareness heterogeneity on epidemic dynamics on the artificial networks. Through extensive Monte Carlo simulations, we find that the heterogeneity of degree distribution enhances the epidemic spreading, which is consistent with the classical results on scale-free networks [31, 32]. Besides, we find that the self-awareness heterogeneity suppresses the outbreak of an epidemic. Next, we study the influence of the correlation between node degree and self-awareness on the epidemic dynamics on artificial networks. We find that when there is a positive correlation between node degree and self-awareness, the heterogeneity of self-awareness restrains the outbreak of the epidemic. While, when there is a strong negative correlation, the epidemic threshold first increases and then decreases with the decline of the self-awareness heterogeneity. Furthermore, we find an optimal self-awareness distribution, at which the disease can be suppressed to the most extent. By exploring the relationship between the epidemic threshold and correlation coefficient, we reveal that the more positive correlation between node degree and self-awareness, the better the disease can be suppressed. Besides, a critical value of the correlation coefficient is found. When the coefficient is below the critical value, an optimal heterogeneity of self-awareness exists. In contrast, the epidemic threshold decreases monotonously with the decline of the self-awareness heterogeneity. At last, we verify the results on four typical real-world networks, and find that the results on the real-world networks are consistent with those on the artificial network.

2 Model descriptions

In this section, a resource-epidemic coevolution model that is named as the resource-based epidemiological susceptible-infected-susceptible model (r-SIS) is proposed.

2.1 Epidemic spreading model

For the epidemic spreading model, each node has two possible states: the infected (I) and the susceptible (S) state [33]. At any time step tt, each I-state node ii can transmit the disease to its susceptible neighbors, at the same time it recoveries to S-state with the rate μi(t)\mu_{i}(t), which depends on the resource quantity ωi(t)\omega_{i}(t) received from its healthy neighbors. We consider that the resource, such as funds and medical, can promote the recovery of the I-state individuals [34, 35]. Thus, the recovery rate μi(t)\mu_{i}(t) is assumed to be proportional to resource quantity ωi(t)\omega_{i}(t) in this paper and is defined as:

μi(t)=1(1μ0)εωi(t),\mu_{i}(t)=1-(1-\mu_{0})^{\varepsilon{\omega_{i}(t)}}, (1)

where μ0\mu_{0} is the spontaneous recovery rate that is independent of resource. Since the value of μ0\mu_{0} does not qualitatively affect the results [36], without loss of generality, it is set at a small value μ0=0.1\mu_{0}=0.1 in this paper. Besides, resource wastes widely exist in the real scene of the medical system during the treatment process [37]. To mimic the phenomenon of resource wasting, a parameter ε\varepsilon is introduced to represent the resource utilization rate, which has been proved to not qualitatively affect the dynamical properties [18, 36]. Thus, without loss of generality, it is set to be ε=0.6\varepsilon=0.6 in this paper. In the spreading process of the epidemic, every S-state node has a probability of being infected by its I-state neighbors. We consider that the healthy (S-state) nodes are the source of resources, they can both generate new resources and donate them to the I-state neighbors. If an S-state node chooses to donate its resources, it will have fewer resources for self-protection, which leads to a greater risk of been infected. Otherwise, if it refuses to donate resources for self-protection, the infection rate will reduce by a factor cc. As there is a heterogeneous distribution of self-awareness in populations, the infection rate varies from node to node. To reflect the relationship between the donation behavior and infection probability, we denote the basic infection rate as β\beta, and define the actual infection of node ii as:

βi(t)={β,if donating resource;cβ,otherwise. \beta_{i}(t)=\left\{\begin{array}[]{ll}\beta,&\hbox{if donating resource;}\\ c\beta,&\hbox{otherwise. }\end{array}\right. (2)

According to the individual-based mean-field theory [38, 39], the dynamical process of the r-SIS model can be expressed as:

dρi(t)dt=μi(t)ρi(t)+βi(t)[1ρi(t)]j=1Naijρj(t),\frac{d\rho_{i}(t)}{dt}=-\mu_{i}(t)\rho_{i}(t)+\beta_{i}(t)[1-\rho_{i}(t)]\sum_{j=1}^{N}a_{ij}\rho_{j}(t), (3)

where aija_{ij} is the element of adjacency matrix AA. If there is an edge between nodes ii and jj, aij=1a_{ij}=1, otherwise, aij=0a_{ij}=0. Besides, to calculate the spreading size of the epidemic, a parameter ρi(t)\rho_{i}(t) is introduced to represent the probability that node ii is in I-state. Thus we can calculate the fraction of infected nodes in a network of size NN at time tt by averaging overall NN nodes:

ρ(t)=1Ni=1Nρi(t).\rho(t)=\frac{1}{N}\sum_{i=1}^{N}\rho_{i}(t). (4)

At last, the prevalence of the epidemic in the stationary state is defined as ρρ()\rho\equiv\rho(\infty).

2.2 Resource allocation model

As the statements above, the healthy individuals can generate and donate resources to support the recovery of their I-state neighbors during the outbreak of an epidemic. For the sake of simplicity, we assume that each susceptible node will generate one unit resource at each time step. Besides, the S-state nodes can perceive the severity of an outbreak from the state of infection in the neighborhood. The parameter mim_{i} is defined to represent the amount of the I-state neighbors of node ii. Generally, the larger the value of mim_{i}, the lower probability of resource donation of node ii [40, 41]. Besides, the parameter αi\alpha_{i} is defined to represent the awareness of self-protection for each node ii. A larger value of αi\alpha_{i} indicates more sensitive of node ii to the disease, and a lower intention to donate resource. We consider that αi\alpha_{i} obeys the heterogeneous distribution g(α)αγαg(\alpha)\sim{\alpha}^{-\gamma_{\alpha}}, where γα\gamma_{\alpha} is the self-awareness exponent. Thus, the resource donation probability of a healthy node ii is related to its intrinsic self-awareness and a total of mim_{i} infected neighbors, which is defined as:

qi(t)=q0(1αi)mi(t),q_{i}(t)=q_{0}(1-\alpha_{i})^{m_{i}(t)}, (5)

where q0q_{0} is a basic donation probability. We consider that the resource of an S-state node will be distributed equally among neighbors.

Based on the above resource allocation scheme, the amount of resource that node ii donates to node jj at a time can be expressed as:

ωij(t)=qi(t)1mi(t).\omega_{i\rightarrow j}(t)=q_{i}(t)\frac{1}{m_{i}(t)}. (6)

With the resource allocation scheme defined in Eq. (6), we can further define the resource quantity ωi(t)\omega_{i}(t), which is expressed as:

ωi(t)=j𝒩i[1ρj(t)]ωji(t)=j𝒩i[1ρj(t)]qj(t)mj(t).\begin{split}\omega_{i}(t)&=\sum_{j\in\mathcal{N}_{i}}[1-\rho_{j}(t)]\omega_{j\rightarrow i}(t)\\ &=\sum_{j\in\mathcal{N}_{i}}[1-\rho_{j}(t)]\frac{q_{j}(t)}{m_{j}(t)}.\end{split} (7)

where 𝒩i\mathcal{N}_{i} represents the neighbor set of node ii, and the expression [1ρj(t)][1-\rho_{j}(t)] represents the probability that a neighbor jj is in S-state. Combining Eq.( 6), we can get the expression of infection rate of any node ii at time tt as:

βi(t)=qi(t)β+[1qi(t)]cβ\beta_{i}(t)=q_{i}(t)\beta+[1-q_{i}(t)]c\beta (8)

3 Simulation results

Although various theoretical methods such as the heterogeneous mean-field (HMF), quench mean-field (QMF) and dynamical message passing (DMP) approaches have been proposed to analyze both the single dynamical process [42] and the multiple coupled dynamical processes [25, 43], the nonlinearity of the model described in section 2 and the strong dynamic correlations make it infeasible to obtain precise theoretical solutions for epidemic size and threshold by utilizing the existing theoretical methods. Therefore, extensive Monte Carlo simulations are carried out to study the coevolution of resource allocation and epidemic spreading in this section. First, we study the impact of heterogeneous distributions of self-awareness and node degree on the epidemic dynamics, and then investigate the effects of correlation between node degree and self-awareness on the spreading dynamics on artificial networks through Monte Carlo simulations. At last, we will verify the results by conducting simulations on several typical real-world networks.

A specific simulation is carried out as follows [44]: during each time time interval [t,t+Δt][t,t+\Delta{t}], each S-state node ii changes to I-state in rate βi\beta_{i}, which can be defined as [45]

βi(t)=limΔt0P(St+Δti=Iinfectedbyj|Sti=S,Stj=I)Δt,\beta_{i}(t)={\rm lim}_{\Delta{t}\rightarrow{0}}\frac{P(S_{t+\Delta{t}}^{i}=I{\rm~{}infected~{}by~{}}{j}|S_{t}^{i}=S,S_{t}^{j}=I)}{\Delta{t}}, (9)

where StiS_{t}^{i} is denoted as the state of node ii at time tt, and (St+Δti=Iinfectedbyj)(S_{t+\Delta{t}}^{i}=I{\rm~{}infected~{}by~{}}{j}) represents that node ii is infected by an I-state neighbor jj [46]. At the same time, the I-state node will recover to S-state with rate of μi(t)\mu_{i}(t), which defines as

μi(t)=limΔt0P(St+Δti=S|Sti=I)Δt.\mu_{i}(t)={\rm lim}_{\Delta{t}\rightarrow{0}}\frac{P(S_{t+\Delta{t}}^{i}=S|S_{t}^{i}=I)}{\Delta{t}}. (10)

The infection rate βj(t)\beta_{j}(t) and recovery rate μi(t)\mu_{i}(t) are dependent on the resource donation probability qj(t)q_{j}(t) and resource quantity ωi(t)\omega_{i}(t) respectively. The process of resource allocation takes place with the propagation of disease. In synchronous updating, the Δt\Delta{t} is finite, and the infection and recovery probability of node ii is βi~=βiΔt\tilde{\beta_{i}}=\beta_{i}\Delta{t}, and μ~i=μiΔt\tilde{\mu}_{i}=\mu_{i}{\Delta{t}}. According to Eqs.(9) and (10), the transition probabilities can be expressed as:

βiΔt=P(St+Δti=Iinfectedbyj|Sti=S,Stj=I),\beta_{i}{\Delta{t}}=P(S_{t+\Delta{t}}^{i}=I{\rm~{}infected~{}by~{}}j|S_{t}^{i}=S,S_{t}^{j}=I), (11)
μiΔt=P(St+Δti=S|Sti=I).\mu_{i}\Delta{t}=P(S_{t+\Delta{t}}^{i}=S|S_{t}^{i}=I). (12)

At the end of each time step, the state of all nodes in the network update synchronously. To ensure that the dynamical processes enter a stationary, in which the prevalence fluctuates within a small range, each simulation will run a sufficiently long time. Besides, in order to avoid the influence of other factors on the results, without loss of generality, we set the coefficient cc at a constant value c=0.05c=0.05, such that if any healthy individual jj chooses to reserve its resource, the probability that it is infected in one contact with an infected neighbor reduces to βj=0.05β\beta_{j}=0.05\beta.

3.1 Effects of heterogeneous self-awareness and degree distributions

In order to investigate the effects of heterogeneous distributions of self-awareness and node degree on the epidemic dynamics, we first generate networks with degree distribution P(k)kγDP(k)\sim{k^{-\gamma_{D}}} using the uncorrelated configuration model (UCM) [47, 48], where γD\gamma_{D} is the degree exponent. The maximum and minimum degree of the network are set to be kmaxNk_{\rm max}\sim\sqrt{N} and kmin=3k_{\rm min}=3 respectively, which assures no degree correlation of the network when NN is sufficient large [49, 50], and the mean degree is set to be k=8\langle{k}\rangle=8. Then we generate a self-awareness sequence {αi}i=1N\{\alpha_{i}\}_{i=1}^{N} according to the distribution g(α)αγαg(\alpha)\sim{\alpha}^{-\gamma_{\alpha}}. The maximum and minimum values are set to be αmaxN1/2\alpha_{\rm max}\sim{N}^{1/2}, αmin=5\alpha_{\rm min}=5 respectively. To ensure α[0,1]\alpha\in[0,1], we rescale each value as α/αmax\alpha/\alpha_{\rm max}. At last, each node is assigned an value of self-awareness randomly.

In addition, we employ the susceptibility measure  [51] χ\chi to numerically determine the epidemic threshold:

χ=Nρ2ρ2ρ,\chi=N\frac{\langle\rho^{2}\rangle-\langle\rho\rangle^{2}}{\langle\rho\rangle}, (13)

where \langle\cdots\rangle is the ensemble averaging. To obtain a reliable value of χ\chi, we perform at least 2×1032\times 10^{3} independent realizations on a specific network with fixed self-awareness distribution for each basic infection rate β\beta. At the threshold βc\beta_{c}, the value of χ\chi exhibits a maximum value. And then, by performing the simulations on 100 different networks, we can obtain the average value of βc\beta_{c}.

Refer to caption
Figure 1: The influence of degree and awareness distributions on the spreading dynamics without correlations. (a) The prevalence ρ\rho in the stationary state versus the basic infection rate β\beta for γD=2.1\gamma_{D}=2.1, γα=2.1\gamma_{\alpha}=2.1 (red up-triangles), γD=2.1\gamma_{D}=2.1, γα=4.0\gamma_{\alpha}=4.0 (blue circles), γD=4.0\gamma_{D}=4.0, γα=2.1\gamma_{\alpha}=2.1 (orange squares), and γD=4.0\gamma_{D}=4.0, γα=4.0\gamma_{\alpha}=4.0 (yellow rhombus) respectively. (b) The relative epidemic threshold βc/βc0\beta_{c}/\beta^{0}_{c} as a function of awareness exponent γα\gamma_{\alpha} for degree exponent γD=2.1\gamma_{D}=2.1 (blue circles), γD=2.5\gamma_{D}=2.5 (orange squares), and γD=4.0\gamma_{D}=4.0 (yellow right-triangles), where βc00.041\beta^{0}_{c}\approx 0.041 is the threshold at γD=4.0,γα=2.1\gamma_{D}=4.0,\gamma_{\alpha}=2.1. Data are obtained by averaging over 500 independent simulations.

Fig. 1 (a) displays the prevalence ρ\rho in the stationary state as a function of basic infection rate β\beta at different degree and awareness exponents. We can observe that the dynamic process converges to two possible stationary states: the completely healthy state when β<βc\beta<\beta_{c}, and nearly all infected state β>βc\beta>\beta_{c}, which indicates a first-order transition at βc\beta_{c}. As shown in Fig. 1 (a), the epidemic threshold βc\beta_{c} decreases with the heterogeneity of degree distribution, which is consistent with the epidemic outbreak on networks without self-awareness [52]. The phenomenon is induced by the hub nodes that exist on strong heterogeneous networks. When a given heterogeneity of degree distribution, the value of βc\beta_{c} increases with the heterogeneity of self-awareness distribution, which is in contrast to the effects of degree heterogeneity. For instance, when γD=2.1\gamma_{D}=2.1, the βc\beta_{c} for γα=2.1\gamma_{\alpha}=2.1 is larger than that for γα=4.0\gamma_{\alpha}=4.0. Fig 1 (b) exhibits the value of relative threshold βc/βc0\beta_{c}/\beta_{c}^{0} as a function of γα\gamma_{\alpha} for three degree exponents γD=2.1\gamma_{D}=2.1, γD=2.5\gamma_{D}=2.5 and γD=4.0\gamma_{D}=4.0 respectively. We can observe that the epidemic threshold βc\beta_{c} decreases gradually with the increases of γα\gamma_{\alpha}, which reveals that the self-awareness heterogeneity restrains the epidemic spreading.

Refer to caption
Figure 2: Plots of the critical parameters versus time tt. (a) Top pane: time evolution of the average resource donation probability q\langle{q}\rangle for γD=2.1\gamma_{D}=2.1, γα=2.1\gamma_{\alpha}=2.1 (blue up-triangles), γD=2.1\gamma_{D}=2.1, γα=4.0\gamma_{\alpha}=4.0 (orange circles), γD=4.0\gamma_{D}=4.0, γα=2.1\gamma_{\alpha}=2.1 (yellow squares), and γD=4.0\gamma_{D}=4.0, γα=4.0\gamma_{\alpha}=4.0 (green snowflakes) respectively; Bottom pane: the corresponding time evolution of the average number of infected neighbors m\langle{m}\rangle. (b) The average recovery rate μ\langle{\mu}\rangle versus tt. (c) The time evolution of average effective infection rate λ\langle{\lambda}\rangle. (d) The time evolution of the fraction of infected nodes ρ(t)\rho(t). Data are obtained by averaging over 500 independent Monte Carlo simulations.

Next, we explain qualitatively the results above by exploring the time evolutions of the critical parameters when the basic infection rate is set to be β=0.04\beta=0.04. Fig 2 (a) plots the time evolution of the average donation probability q\langle{q}\rangle (top pane) and average number of infected neighbors m\langle{m}\rangle for varies values of γD\gamma_{D} and γα\gamma_{\alpha} (bottom panel). It shows that when γD=2.1\gamma_{D}=2.1, the donation probability q\langle{q}\rangle first decreases and then increases with time tt for γα=2.1\gamma_{\alpha}=2.1 (see blue upper-circles). While, for γα=4.0\gamma_{\alpha}=4.0 (see red circles), the value of q\langle{q}\rangle first decreases, and then increases slightly in the middle time, at last, it declines with time tt. This phenomenon can be qualitatively explained as follows: When there is a strong heterogeneity of the self-awareness distribution, for instance, γα=2.1\gamma_{\alpha}=2.1, the network has a larger number of nodes with very low self-awareness, and more nodes with high self-awareness. Since the more nodes with large self-awareness means a lower willingness to donation resources, and a lower donation probability in the early stage, thus the value of q\langle{q}\rangle drops more abruptly than that for γα=4.0\gamma_{\alpha}=4.0, which induces a larger number of infected neighbors m\langle{m}\rangle, as less resource is donated from healthy nodes to their neighbors. This phenomenon can be verified by studying the bottom pane of Fig. 2 (a). With less resource, the I-state nodes will recovery with a relatively lower recovery rate [see blue upper-triangles and red circles in Fig. 2(b)]. With the spread of the disease, more nodes with a very small value of α\alpha participate in the behavior of donating resources. The smaller value of α\alpha means a larger willingness to donate resource, which leads to a greater growth of q\langle{q}\rangle for γα=2.1\gamma_{\alpha}=2.1 that γα=4.0\gamma_{\alpha}=4.0 [see the blue upper-triangles and red circles in the top pane of Fig 2 (a)]. Consequently, with the increase of donation probability of the entire network, the value of m\langle{m}\rangle decreases gradually, which leading to a slower decrease of μ\langle{\mu}\rangle for γα=2.1\gamma_{\alpha}=2.1 that γα=4.0\gamma_{\alpha}=4.0 [see the blue upper-triangles and red circles in Fig 2 (b)]. The relative larger recovery rate leads to a lower effective infection rate, which is defined as λ=β/μ\langle{\lambda}\rangle=\langle\beta\rangle/\langle{\mu}\rangle, as shown in Fig. 2 (c). Thus the prevalence ρ(t)\rho(t) increases slower for γα=2.1\gamma_{\alpha}=2.1 than γα=4.0\gamma_{\alpha}=4.0, as shown in Fig 2 (d). From the statement above, we can explain the reason why the heterogeneity of self-awareness distribution can suppress the outbreak of an epidemic.

When the degree heterogeneity of the network decreases, for instance, γD=4.0\gamma_{D}=4.0, the donation probability for both q\langle{q}\rangle for γα=2.1\gamma_{\alpha}=2.1 that γα=4.0\gamma_{\alpha}=4.0 increases with time tt [see the yellow squares and green snowflakes in the top pane of Fig 2 (a)], which leads to an increase of the recovery rate of the whole network, as shown in Fig. 2 (b). Consequently, the effective infection rate of the network λ\langle{\lambda}\rangle decreases gradually to a very small value with time tt. Thus we see that the prevalence decreases gradually to zero [see Fig 2 (d)]. From the statement above, we can also explain the phenomenon that the threshold βc\beta_{c} decreases with an increase of λD\lambda_{D}.

3.2 Effects of degree-awareness correlations

In this section, we focus on how the correlation between the node degree and self-awareness affects the spreading dynamics. A network with a given correlation coefficient is built as follows:

  • 1.

    A network with degree distribution P(k)kγDP(k)\sim{k}^{-\gamma_{D}} is built by the steps in Section 3.1;

  • 2.

    A self-awareness sequence is generated from the distribution P(α)αγαP(\alpha)\sim\alpha^{-\gamma_{\alpha}};

  • 3.

    Sorting the nodes of the network by the degree in ascending order, and then sorting the self-awareness sequence in ascending or descending order, respectively.

  • 4.

    Rearranging the order of each self-awareness value with a given probability π\pi, and then assigning each self-awareness value to the corresponding node.

According to the steps above, we can get a network with a given awareness-degree correlation. The correlation coefficient is:

σ=1π.\sigma=1-\pi. (14)

If the self-awareness sequence is sorted in ascending order, we can get a positive awareness-degree correlation with coefficient σ\sigma; otherwise, we can get a negative awareness-degree correlation with coefficient σ\sigma.

First of all, we study the case when there is a positive degree-awareness correlation, i.e., σ=0.8\sigma=0.8. Figs. 3 (a), (b) and (c) exhibit the prevalence ρ\rho in the stationary as a function of β\beta when degree exponent is γD=2.1\gamma_{D}=2.1, γD=2.5\gamma_{D}=2.5 and γD=4.0\gamma_{D}=4.0, respectively. It shows that for a network with a fixed structure, the epidemic threshold βc\beta_{c} increases with self-awareness heterogeneity. To verify the results obtained in Figs. 3 (a) to (c), we explore the relationship between βc\beta_{c} and the awareness exponent γα\gamma_{\alpha} in Fig. 3 (d). Obviously, for each fixed γD\gamma_{D}, the value of βc\beta_{c} decreases gradually with the γα\gamma_{\alpha}, which suggests that when node degree and self-awareness correlated positively, the heterogeneity of self-awareness inhibits the epidemic spreading.

Refer to caption
Figure 3: Impacts of self-awareness heterogeneity on spreading dynamics with positive correlation between node degree and self-awareness. (a) The prevalence ρ\rho in the stationary state as a function of basic infection rate β\beta for γα=2.1\gamma_{\alpha}=2.1 (red upper-triangles), γα=2.5\gamma_{\alpha}=2.5 (blue circles), γα=2.9\gamma_{\alpha}=2.9 (orange squares), and γα=3.5\gamma_{\alpha}=3.5 (yellow rhombuses) respectively when degree exponent is fixed at γD=2.1\gamma_{D}=2.1. (b) The value of ρ\rho versus β\beta for the corresponding γα\gamma_{\alpha} when γD=2.5\gamma_{D}=2.5. (c) The value of ρ\rho as a function of β\beta for the corresponding γα\gamma_{\alpha} when γD=4.0\gamma_{D}=4.0. (d) The epidemic threshold βc\beta_{c} as a function of γα\gamma_{\alpha} for γD=2.1\gamma_{D}=2.1 (orange upper-triangles), γD=2.5\gamma_{D}=2.5 (green squares), and γD=4.0\gamma_{D}=4.0 (yellow circles) respectively. The correlation coefficient is σ=0.8\sigma=0.8. Data are obtained by averaging over 500 independent Monte Carlo simulations.
Refer to caption
Figure 4: The influence of self-awareness heterogeneity on spreading dynamics with negative correlation between node degree and self-awareness. (a) The prevalence ρ\rho in the stationary state as a function of basic infection rate β\beta for γα=2.1\gamma_{\alpha}=2.1 (blue upper-triangles), γα=2.5\gamma_{\alpha}=2.5 (orange circles), γα=2.9\gamma_{\alpha}=2.9 (yellow squares), and γα=3.5\gamma_{\alpha}=3.5 (purple rhombuses) respectively when degree exponent is fixed at γD=2.1\gamma_{D}=2.1. (b) The value of ρ\rho versus β\beta for the corresponding γα\gamma_{\alpha} when γD=2.5\gamma_{D}=2.5. (c) The value of ρ\rho as a function of β\beta for the corresponding γα\gamma_{\alpha} when γD=4.0\gamma_{D}=4.0. (d) The epidemic threshold βc\beta_{c} as a function of γα\gamma_{\alpha} for γD=2.1\gamma_{D}=2.1 (green upper-triangles), γD=2.5\gamma_{D}=2.5 (orange cirlces), and γD=4.0\gamma_{D}=4.0 (yellow squares) respectively. The correlation coefficient is σ=0.8\sigma=-0.8. Data are obtained by averaging over 500 independent Monte Carlo simulations.

Next, we explore the case when there is a negative degree-awareness correlation. Figs. 4 (a) to (c) display the value of ρ\rho versus β\beta for γD=2.1\gamma_{D}=2.1, γD=2.5\gamma_{D}=2.5 and γD=4.0\gamma_{D}=4.0 when σ=0.8\sigma=-0.8 respectively. It shows that for a fixed network, for instance γD=2.1\gamma_{D}=2.1, the epidemic threshold βc\beta_{c} first increases when γα\gamma_{\alpha} increase from γα=2.1\gamma_{\alpha}=2.1 to γα=2.5\gamma_{\alpha}=2.5, and then it decreases when γα\gamma_{\alpha} increases from γα=2.5\gamma_{\alpha}=2.5 to γα=4.0\gamma_{\alpha}=4.0. We next study systematically the effects of negative correlation between node degree and self-awareness on the spreading dynamics by exploring the relationship between threshold βc\beta_{c} and awareness exponent γα\gamma_{\alpha} in Fig. 4 (d) for γD=2.1\gamma_{D}=2.1 (green upper-triangles), γD=2.5\gamma_{D}=2.5 (red circles), and γD=4.0\gamma_{D}=4.0 (yellow squares) respectively. It shows that the threshold βc\beta_{c} first increases and then decreases with γα\gamma_{\alpha}, and an optimal value γαopt\gamma_{\alpha}^{\rm opt} (γαopt\gamma_{\alpha}^{\rm opt} is around 2.62.6) exists, at which the value of βc\beta_{c} reaches maximum. This result can be qualitatively explained as follow: When the self-awareness heterogeneity is very strong, e.g., γα=2.1\gamma_{\alpha}=2.1, there is a large number of nodes with very small values of self-awareness α\alpha (strong willingness of resource donation), and many nodes with very large values α\alpha (weak willingness of resource donation). When the coefficient σ=0.8\sigma=-0.8, there is a strong negative correlation between node degree and self-awareness. Under this circumstance, the large degree nodes will have a strong willingness to donate resource, while the small degree nodes (covering most nodes of the network) have a weak willingness to donate resource, which leads to a high infection rate of these hub nodes. Besides, the epidemic spreading dynamics exhibits hierarchical features [32]. That is to say, the hubs with large degrees are more likely to be infected firstly, and then the disease propagates from hubs to the intermediate nodes, and finally to nodes with small degrees. Therefore, the large numbers of small degrees will be infected rapidly by the hub nodes in this situation, and the epidemic will outbreak easily.

When the heterogeneity of self-awareness distribution is weak, i.e., γα=4.0\gamma_{\alpha}=4.0, there is a small fraction of nodes with very large or small value of α\alpha, many nodes have an intermediate α\alpha around the mean value α\langle{\alpha}\rangle. The awareness level of the small degree nodes reduces compared to the case of γα=2.1\gamma_{\alpha}=2.1, which leads to a raise of both the donation probability q\langle{q}\rangle and effective infection rate λ\langle{\lambda}\rangle of these nodes. As the strong negative correlation between node degree and self-awareness, the hub nodes still have a very small value of α\alpha (large value of donation probability q\langle{q}\rangle). During the outbreak of an epidemic, these hubs nodes are more likely to be infected in the early stage, and then transmit the disease to those small degree nodes rapidly as they have a highly effective infection rate λ\langle{\lambda}\rangle. Thus the epidemic will break out more easily than the case of γα=2.1\gamma_{\alpha}=2.1 in this situation.

According to the above statement, we have qualitatively explained the optimal phenomenon by explaining why diseases are more likely to break out when there is a strong heterogeneity (γα=2.1\gamma_{\alpha}=2.1) and weak heterogeneity (γα=4.0\gamma_{\alpha}=4.0).

Refer to caption
Figure 5: The epidemic threshold βc\beta_{c} as a function of correlation coefficient σ\sigma for γα=2.1\gamma_{\alpha}=2.1 (blue circles), γα=2.5\gamma_{\alpha}=2.5 (red squares), and γα=3.1\gamma_{\alpha}=3.1 (yellow upper-triangles). The degree exponent is fixed at γD=2.5\gamma_{D}=2.5. Phase II and phase IIII are separated by critical value σc0.4\sigma_{c}\approx-0.4. Data are obtained by averaging over 500 independent Monte Carlo simulations.

Next, we study the effects of correlation between node degree and self-awareness by exploring the relationship between epidemic threshold βc\beta_{c} systematically and correlation coefficient. Fig. 5 displays the βc\beta_{c} as a function of σ\sigma for γα=2.1\gamma_{\alpha}=2.1, γα=2.5\gamma_{\alpha}=2.5, γα=3.1\gamma_{\alpha}=3.1 respectively. We find that for each fixed heterogeneity of self-awareness, the epidemic threshold βc\beta_{c} increases monotonously with correlation coefficient σ\sigma. For instance, for γα=2.1\gamma_{\alpha}=2.1, the threshold increases from βc0.027\beta_{c}\approx 0.027 to βc0.044\beta_{c}\approx 0.044, which suggests that the more positive of the correlation between node degree and self-awareness, the better the disease can be suppressed. This phenomenon can be qualitatively explained as follows: When there is a larger positive correlation, the hub nodes will have a larger value of α\alpha, which indicates a smaller probability of resource donation q\langle{q}\rangle, and consequently a lower effective infection rate λ\langle{\lambda}\rangle of the hubs. This phenomenon reduces the infection probability of the hub nodes in the early stage. Meanwhile, the small degree nodes have a larger probability of resource donation, which increases the recovery rate of the I-state neighbors, including the hub nodes. Thus the outbreak of the epidemic is effectively delayed. In addition, it also shows that the parameter pane (σβc)(\sigma-\beta_{c}) is separated into two phases: phase I and phase II, by a critical value of σ0.4\sigma\approx 0.4. In phase II, the threshold βc\beta_{c} first increases and then decreases with the increase of γα\gamma_{\alpha}, namely the optimal value γαopt\gamma_{\alpha}^{\rm opt} exists in this region, as shown the curves in Fig. 4 (d) for σ=0.8\sigma=-0.8. In phase IIII, the threshold βc\beta_{c} decreases monotonously with γα\gamma_{\alpha}, as shown the curves in Fig. 1 (b) for σ=0\sigma=0, and the curves Fig. 3 (d) for σ=0.8\sigma=0.8 respectively.

3.3 Verification on real-world networks

In this section, we verify the results obtained on artificial networks by conducting the simulations on the real-world networks. The following four typical real-world networks are chosen in our paper: (i). The OpenFlights network [53]. This network describes the flights between airports in the world. The nodes represent a portion of the world’s airports, and edges represent flights from one airport to another. There are N=2939N=2939 nodes and Ve=30501V_{e}=30501 edges in the network with maximum degree kmax=473k_{\rm max}=473 [54]. (ii). The Euroroad network [55] is a international road network. Most road in the network is located in Europe. The nodes of the network represent cities, and the edge between two nodes denotes that an E-road connects them. There are N=1174N=1174 nodes and Ve=1417V_{e}=1417 edges with kmax=10k_{\rm max}=10. (iii). The face-to-face contact network [56]. Nodes in this network represent the individuals who attended the exhibition INFECTIOUS: STAY AWAY in 2009 at the Science Gallery in Dublin, edges describe the face-to-face contacts that were active for at least 20 seconds among individuals during the exhibition [57]. There are a total numbers of N=410N=410 nodes and Ve=17298V_{e}=17298 edges (contacts) in the network. The maximum degree is kmax=294k_{\rm max}=294. (iv) The Facebook network [58]. This dataset consists of ’circles’ (or ’friends lists’) from Facebook. Facebook data was collected from survey participants using this Facebook app. The dataset includes node features (profiles), circles, and ego networks. There are N=4039N=4039 nodes and Ve=88234V_{e}=88234 edges in the network.

Refer to caption
Figure 6: The effects of awareness distribution on the epidemic spreading on real world networks. (a) The prevalence ρ\rho as a function of basic infection rate β\beta on the OpenFlights network for awareness exponent γα=2.1\gamma_{\alpha}=2.1 (blue upper-triangle), γα=2.5\gamma_{\alpha}=2.5 (red circles), and γα=4.0\gamma_{\alpha}=4.0 (yellow squares) respectively. (b) The prevalence ρ\rho versus β\beta for the corresponding values of awareness exponent on the Euroroad network. (c) The value of ρ\rho as a function of β\beta for the four typical values of γα\gamma_{\alpha} on the face-to-face contact network. (d) The results on Facebook network. The correlation coefficient between self-awareness and node degree is σ=0\sigma=0.

Figs. 6 (a) to (d) display the prevalence ρ\rho in stationary state as a function of β\beta when there is no degree-awareness correlation on OpenFlights network, Euroroad network, face-to-face contact network and the Facebook network respectively for different heterogeneities of self-awareness. We find that on the OpenFlights network, the threshold βc\beta_{c} decreases with the increase of γα\gamma_{\alpha}, which is consistent with the result on artificial networks [see Fig. 1 (a)], and the prevalence ρ\rho increases with γα\gamma_{\alpha} for a fixed basic infection rate β\beta. However, there is a difference when disease propagates on the other three real-world networks, i.e., the awareness heterogeneity does not alter the threshold of βc\beta_{c}. Besides, it shows that the prevalence increases with the decreases of awareness heterogeneity, which is consistent with the result on OpenFlights network. The results above reveal that the awareness heterogeneity can suppress the outbreak of epidemic on real-world networks when there is no correlation between node degree and self-awareness.

Refer to caption
Figure 7: The influence of correlation between self-awareness and node degree on the epidemic spreading on real world networks. (a) The prevalence ρ\rho as a function of basic infection rate β\beta on the OpenFlights network for σ=0.8\sigma=-0.8 (blue upper-triangle), σ=0.4\sigma=-0.4 (red circles), σ=0.4\sigma=0.4 (yellow squares), and σ=0.8\sigma=0.8 (green rhombuses) respectively. (b) The prevalence ρ\rho versus β\beta for the corresponding values of σ\sigma on the Euroroad network. (c) The value of ρ\rho as a function of β\beta for the four typical values of σ\sigma on the face-to-face contact network. (d) The results on Facebook network. The awareness exponent is set to be γα=2.5\gamma_{\alpha}=2.5 .

At last, we study the effects of degree-awareness correlation on the epidemic spreading on the four real-world networks. The awareness exponent is fixed at γα=2.5\gamma_{\alpha}=2.5. It shows that when disease propagates on the OpenFlights and face-to-face contact networks, the threshold βc\beta_{c} does not be altered, but the prevalence ρ\rho decreases with correlation coefficient σ\sigma. This result indicates that a more positive correlation between node degree and self-awareness can better suppress the disease spreading, which is consistent with the result of artificial networks. When disease propagates on the Euroroad network, the correlation does not alter both threshold βc\beta_{c} and prevalence ρ\rho. At last, when disease propagates on the Facebook network, the threshold βc\beta_{c} increases with σ\sigma, which is consistent with the result on artificial networks [see Fig. 5],

Based on the above research, we can see that the results on the real-world networks are consistent with those on the artificial network. However, the complex structural features of the real networks, such as clustering, community structure, and small-world characteristics, have an important impact on the results, and needs to be further studied in our future research.

4 Discussion

In summary, we have studied systematically the impact of heterogeneous awareness of self-protection on the dynamics of epidemic spreading. A coevolution dynamical model of resources and epidemic on complex networks has been proposed. The two processes of resource allocation and disease spreading are coevolving in such a way that the generation and allocation of resource depend on the S-state nodes, and the recovery rate of I-state nodes rely on the resources from their S-state neighbors. Both the effective infection rate and the recovery rate of the nodes will be alerted due to the resource factor. First of all, we have studied the effects of the heterogeneity of both degree and self-awareness distributions on the epidemic dynamics on artificial networks. Through extensive Monte Carlo simulations, we have found that the degree heterogeneity enhances the epidemic spreading, which is consistent with the classical results on scale-free networks. Besides, the threshold βc\beta_{c} increases with the growth of self-awareness heterogeneity for a fixed network structure, which indicates that the self-awareness heterogeneity suppresses the outbreak of an epidemic.

Then we have studied the impact of correlation between node degree and self-awareness on the epidemic dynamics on artificial networks. We have found that when there is a positive correlation between node degree and self-awareness, the threshold βc\beta_{c} increases monotonously with the heterogeneity of self-awareness. When there is a strong negative correlation, e.g., σ=0.8\sigma=-0.8, the epidemic threshold βc\beta_{c} first increases and then decreases with γα\gamma_{\alpha}. An optimal value γαopt\gamma_{\alpha}^{\rm opt} have been found, at which the disease can be suppressed to the most extent. Besides, we have studied systematically the effects of degree-awareness correlation on the epidemic dynamics by exploring the relationship between βc\beta_{c} and correlation coefficient σ\sigma. We have found that the epidemic threshold βc\beta_{c} increases monotonously with σ\sigma in [1.0,1.0][-1.0,1.0], which reveals that the stronger the positive correlation, the more likely the disease can be suppressed. Besides, we have also found a critical value σc0.4\sigma_{c}\approx 0.4, when σ<σc\sigma<\sigma_{c}, an optimal value γαopt\gamma_{\alpha}^{\rm opt} exists, the threshold βc\beta_{c} increases with γα\gamma_{\alpha} before γαopt\gamma_{\alpha}^{\rm opt} and decreases after γαopt\gamma_{\alpha}^{\rm opt}. When σ>σc\sigma>\sigma_{c}, βc\beta_{c} decreases monotonously with the increase of γα\gamma_{\alpha}.

At last, to verify our results, we have conducted Monte Carlo simulations on four typical real-world networks. It reveals that the results on the real-world networks are consistent with those on the artificial network. However, the sophisticated structural features of the real networks, such as clustering, community structure, and small-world characteristics, have an essential impact on the results. For instance, the self-awareness heterogeneity does not alter the threshold βc\beta_{c} on the Euroroad network, face-to-face contact network, and Facebook network. Besides, the correlation does not change both the threshold βc\beta_{c} and prevalence ρ\rho, when disease propagates on the Euroroad network.

Our findings make a substantial contribution to the understanding of how the heterogeneous distribution of individual awareness for self-protection influences the dynamics of epidemic spreading. The results in this paper are of practical significance for controlling the outbreak of infectious diseases, especially in the context of the outbreak of COVID-19. It will also guide us to make the most reasonable choice between resource contribution and self-protection when perceiving the threat of disease, and also have a direct application in the development of strategies to suppress the outbreaks of epidemics.

The present work mainly focus on the spreading dynamics of infectious diseases that can be described by the susceptible-infected-susceptible model, such as seasonal influenza. However, the findings obtained in this paper could still shed light on the control of the diseases with similar characteristics, such as the SIRS and SIR-like epidemics that have been widely studied in recent years [59, 60, 61, 62]. There are still some limitations of our work. For example, as the SIS model can not describe the spread of an irreversible epidemic, there would be difference in the dynamical characteristics such as the transition type and phase diagram between the SIS model and the irreversible epidemic models. Thus, a coupled dynamic model of resource allocation and epidemic spreading based on the SIR,SIRV and SEIR models will be studied in our future works. In addition, the theoretical analysis will also be researched.

Acknowledgements

This work was supported by the Fundamental Research Funds for the Central Universities (No. JBK190972), the Financial Intelligence and Financial Engineering Key Laboratory of Sichuan Province, School of Economic Information Engineering, and the National Natural Science Foundation of China (No. 61673086,61903266), the China Postdoctoral Science Special Foundation (No. 2019T120829), and Sichuan Science and Technology Program (No.20YYJC4001).

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