Abstract
In this paper, we study a diffusive SIS epidemic model with a logistic source, saturation rate, and spontaneous infection mechanism. Based on the uniform bounds of parabolic system, the global attractivity of the endemic equilibrium is established in a homogeneous environment. Moreover, we prove the existence of the endemic equilibrium via the topological degree theory. We mainly analyze the effects of dispersal, saturation, and spontaneous infection on the limiting behaviors of the endemic equilibrium. These results show that spontaneous infection and the logistic source can enhance the persistence of infectious disease, causing the disease to become more threatening.
Keywords:
SIS epidemic model with logistic source; saturation; spatially heterogeneous; global stability; asymptotic profile MSC:
35K57; 35J57; 35B40; 92D25
1. Introduction
It has been commonly recognized in the study of epidemiology that reaction-diffusion equations are efficient and indispensable tools for understanding the spatial spread of infectious diseases in a heterogeneous environment and for predicting and controlling the transmission of diseases in these environments [1,2,3,4,5].
In the past few decades, more works have been devoted to investigating the following diffusive SIS epidemic model:
where and denote the density of the susceptible and infected populations at ; the positive coefficients and , respectively, represent the motility of susceptible and infected individuals; the positive function is the disease transmission rate; is the recovery rate; and indicates the infection mechanism. In order to make the infection mechanism easier to understand, we have grouped things into three general forms: (standard incidence rate); (bilinear infection mechanism); and (saturated incidence). In the context of epidemiology, the impact of the spatial heterogeneity of the environment and the dispersal of individuals has been studied by many authors. For example, Allen et al. [6] and Peng et al. [7,8,9] considered the SIS model with a standard incidence mechanism. The main results of their work investigated the existence, uniqueness, and global asymptotic stability of the unique endemic equilibrium in two special cases, as well as the asymptotic profile with respect to the small/large diffusion coefficient of the susceptible or infected individuals. From their results, we can assert that limiting the migration of susceptible individuals is a better control strategy than limiting the migration of infected individuals. Let us mention that for the SIS epidemic model with a bilinear infection mechanism (i.e., ), the dynamics and asymptotic behaviors of endemic equilibrium have been considered in [10,11,12]. In terms of a model with a saturation mechanism, one can find an example of such a SIS epidemic model in [13]. We also refer the readers to the SIS epidemic model in advective heterogeneous environments. The authors discussed some classes of the diffusion-advection SIS epidemic equation in [14,15,16,17,18,19,20,21,22,23]. These works focused on the effects of dispersal and advection on the dynamics of infectious disease and the asymptotic profile of endemic equilibrium.
Recently, further studies on the mathematical analysis of such an SIS diffusive equation with a varying total population have been conducted.
where represents the birth/death effect of the susceptible population, which takes a form similar to the linear source (), logistic source (), and so on. The dynamics and asymptotic behavior of the system have been investigated by [24,25,26,27,28,29,30,31], and their results indicate that the birth/death effect can enhance disease persistence. In [32,33], Hill et al. adapted the classic epidemic model to describe the effect of a “spontaneous” infection mechanism by adding a term whereby uninfected populations can become infected independent of direct contacts. The “spontaneous factors” can occur when the pathogen transmission to susceptible hosts occurs via environmental reservoirs (e.g., air, water, soil) or fomites, independent of direct host-to-host contact. We note that in the class of epidemic model with a spontaneous infection mechanism, the rate of spontaneous infection is proportional to the number of susceptible populations, which in turn contributes to the migration of infected populations. Thus, the spontaneous infection can be adopted independently of direct contact between the infected and susceptible individual, which indicates that there is no longer a threshold for the extinction and persistence of the infectious disease. In recent works [34,35,36,37,38], the authors considered the diffusive SIS epidemic model with a spontaneous infection mechanism and studied the effects of spatial heterogeneity and the spontaneous infection mechanism on the dynamics and spatial behavior of the diseases.
Most existing diffusion-based SIS studies focus solely on single transmission mechanisms (e.g., contact transmission) without simultaneously incorporating the logistic source and spontaneous infection mechanisms, resulting in a lack of in-depth understanding of the coupled mechanisms between resource constraints and environmental transmission.
Motivated by these models, in this work we will explore a diffusive SIS epidemic model with spontaneous infection. The model is described by the following parabolic equations:
where , and have the same interpretation as in (1), and the constant stands for the saturation coefficient; the nonlinear term represents that the susceptible individual satisfies logistic growth; denotes the spontaneous infection rate; the habitat is a bounded domain in with smooth boundary ; and the boundary conditions mean that the habitat is closed and no individuals flux crosses the boundary . We assume that , and are positive and Hölder continuous functions on , and the nonnegative initial data and are continuous functions on which satisfy .
Corresponding to (3), the steady state problem fulfills
where and denote the density of susceptible and infected populations, respectively. Moreover, from the strong maximum principle, we know that and are positive on . A positive steady state solution of (4) is called an endemic equilibrium of (3).
This work focuses on characterizing the asymptotic behavior of the endemic equilibrium under diverse dispersal regimes with a small/large dispersal rate of susceptible/infected contacts and a large saturated coefficient. From the biological point of view, our purpose is to explore the influence of population dispersal, infection mechanism, and environmental heterogeneity on the spatial profiles of infectious diseases. These results may have some useful implications for disease prevention and control.
This work is organized as follows. In Section 2, based on the uniform bounds of the parabolic solution of (3), we obtain the global attractivity of the endemic equilibrium in a homogeneous environment. In Section 3, using the topological degree theory, we prove the existence of the endemic equilibrium. Section 4 is devoted to analyzing the asymptotic profiles of the endemic equilibrium as the dispersal rates or approach zero or infinity, and the saturated coefficient goes to infinity.
2. Uniform Boundedness and Global Stability
In this section, we will study the uniform boundedness of parabolic solutions to (3), and then investigate the global stability of endemic equilibrium in the case that , and are positive constants. From now on, for convenience, we write
An iterative method is a numerical algorithm used to approximate solutions to differential equations by progressively refining an initial guess through repeated application of a specific procedure. Iterative methods are often preferred for large-scale or computationally intensive problems due to their memory efficiency and adaptability. We first apply the iteration method in [39] to establish the ultimate uniform bounds of solutions to (3). We omit the details, as the proof is similar to that of Theorem 2.3 in [26] (see also Theorem 2.3 in [37]).
Proposition 1.
There exists a positive constant K independent of initial value such that
for some large .
Next, we discuss the global stability of the endemic equilibrium of (3) in a special case: the homogeneous environment. In this case, the coefficients , and are assumed to be positive constants. It is not hard to see that (3) has a unique endemic equilibrium, denoted by
Using Lyapunov’s theory, is a Lyapunov functional for system (3), on account of the uniform boundedness (5) in Proposition 1, from the standard parabolic regularity.
Theorem 1.
For any , , the endemic equilibrium is globally attractive.
Proof.
For any solution of (3), we consider the following functional
with
Then, for all , it follows from the elementary computations that
Note that for any , along all trajectories except at and if and only if . From the Sobolev embedding theorem and some compactness arguments in [40] (see also similar arguments in Theorem 3.1 of [41]), we can deduce
Clearly, is globally attractive. □
3. The Existence of Endemic Equilibrium
In this section, we study the existence of the endemic equilibrium of (3) when , , , , and are positive Hölder continuous functions on . By using the topological degree approach, we establish the existence of positive solutions to (4) and resort to the auxiliary problem:
where , and are given positive constants satisfying , , and and the parameter . It is clear that the system (6) with becomes (4).
Theorem 2.
Proof. 1. A priori bounds for u and v.
and
Thus, it is evident that (6) has no positive solution . For any , we consider the operator
here denotes the inverse operator in . The standard elliptic regularity theory implies that is a compact operator. Note that for any and , it turns out that is well-defined and independent of . It follows from Theorem 1 that
is the unique fixed point of in , and thus
For the system (4) (i.e., the system (6) with ) from Theorem 1, it is clear that is stable. Hence, it follows from the standard Leray–Schauder degree index formula ([43], Theorem 2.8.1) that
Therefore, it follows from the homotopy invariance property that
As a consequence, by the properties of the degree, we know that possesses at least one fixed point in , which implies the existence of the positive solution of (4). □
Assume that is a positive solution of (6). For convenience, we denote . In view of the maximum principle ([42], Proposition 2.2), letting , we have
and
It follows from (9) that
then
Combining (8) and (10), we have
Via straightforward calculation, one can obtain
and
Similarly, set . We deduce from the maximum principle that
which implies that
In the same fashion, we have
As a result,
It should be noted that
From the above inequality and (12), we know that
Substituting the above inequality into (11), we have
Consequently, by the above arguments, let and . Thus, we know that
here, and are independent of , and .
2. Existence.
For the above and , we denote
4. Asymptotic Profiles of Endemic Equilibrium
In this section, we are concerned with the asymptotic profiles of endemic equilibrium to (3) in the following cases: (i) small dispersal ( or ); (ii) large dispersal ( or ); and (iii) large saturation ().
4.1. Small Dispersal
In this subsection, we study the limiting profile of the positive solutions of (4) as the dispersal rate of the susceptible/infected individual is small. First we investigate the case of a small mobility rate in susceptible individuals.
Theorem 3.
Proof.
It follows from Theorem 2 that the steady state system (4) possesses at least one endemic equilibrium .
We first consider the convergence of I. From the arguments in the proof of Theorem 2, we know that
where the positive constants and are independent of and . In light of the standard elliptic regularity theory, we can take a subsequence satisfying as and the corresponding positive solution with , such that
where and on due to (15).
Next, we investigate the convergence of u and analyze the the following equation:
In view of (16), for any small , there exists such that for all ,
Consequently, for all , we have
where
It is easy to see that and on . Note that for any , M and is a pair of upper-lower solutions of the following auxiliary equation:
where M is a positive constant satisfying on . Then, for any , (19) admits at least one positive solution, denoted by , which satisfies on . From the the maximum principle, we have
As an application of a singular perturbation technique ([44], Lemma 2.1; see also [45], Lemma 2.4), we know that any positive solution of (19) satisfies
It follows from on that we obtain
At the same time, for all , we have
where
with on . By a similar argument, one can obtain
We further obtain
It follows from (20) and (21) that
As a result, it is clear that solves (14). This completes the proof. □
We next study the limiting behavior of the endemic equilibrium to (4) in the case of small dispersal of an infected individual.
Theorem 4.
Proof.
It should be noted that the estimate (15) holds for any . From the standard elliptic regularity theory and Sobolev embedding theorem, we know that there exists a subsequence with convergence to 0 as , and the corresponding positive solution of (4) with such that
where on due to (15).
It is clear that fulfills:
In view of (24), for any small , there exists such that for all ,
Thus, for any , it follows that
where
We know that and on . Note that for any , M and is a pair of upper-lower solutions of
where the positive constant M satisfies on . Therefore, for all , (27) admits at least one positive solution , which satisfies on . By similar arguments, we deduce
and
At the same time, for any , we deduce from (26)
where
with on . In a similar fashion as above, we can conclude that
Notice that
From (28) and (29), we know that
According to the expression of , it is easy to see that solves (23). The proof is thus complete. □
4.2. Large Dispersal
This subsection is devoted to discussing the limiting behavior of positive solutions in relation to a large dispersal rate of susceptible individuals in Theorem 5 and a large dispersal rate of infected individuals in Theorem 6.
Theorem 5.
Proof.
Since the estimate (15) is valid for all sufficiently large , from the standard elliptic regularity theory and Sobolev embedding theorem, we can take a subsequence satisfying as and a corresponding positive solution with , such that in as , where on due to (15). It is easy to see that solves
Consequently, the maximum principle ensures that is a positive constant. It follows from some direct calculation that . By a similar analysis, from the equation of v in (4), and by passing to a further subsequence if necessary, we know that
It follows from the similar technique explained in the Appendix in [46] that is the unique positive solution of (30). The proof is complete. □
The limiting behavior of the endemic equilibrium for the case of can be deduced in the same fashion. Thus, we omit the details.
4.3. Large Saturation
In this subsection, we investigate the limiting behavior of the endemic equilibrium of (3) with being fixed and .
Theorem 7.
Proof.
Is is evident that the estimate (15) still holds true for any . By the standard elliptic regularity and Sobolev embedding theorem, we can derive that there exists a subsequence satisfying as , such that the corresponding positive solution of (4) fulfills
where on due to (15). We can deduce that solves (32). This proves Theorem 7. □
A comparative discussion of results with previous SIS models is given. First, the incidence rate mechanisms differ significantly between the two models, with the model studied in this paper exhibiting greater complexity. Second, the proposed model incorporates both natural host population growth and resource constraints, whereas the first model represents a simplified infectious disease framework that neglects host population dynamics. Third, the introduction of a spontaneous infection mechanism in the second model accounts for environmental transmission pathways absent in the first model, potentially leading to divergent transmission patterns and distinct equilibrium states.
There are many diseases governed by these mechanisms, such as COVID-19, dengue fever, and multidrug-resistant tuberculosis. The results in this paper can aid in determining ICU beds/vaccine production capacity aligned with Logistic model-predicted peaks and adjust social distancing policies to slow transmission rates, such as through the establishment of public campaigns to reduce contact frequency (e.g., staggered commuting).
5. Conclusions
By integrating multiple mechanisms such as diffusion, nonlinear infection rates, and spontaneous infection, this study extends the mathematical framework of the classical SIS model, addressing the limitations of single-mechanism studies. Through analyzing the stability, periodicity, and threshold conditions of model solutions, it reveals the emergent mechanisms underlying complex epidemiological behaviors. Future work will employ stochastic differential equations (SDEs) to model the stochastic dynamics of pathogen decay and reactivation in environmental reservoirs linked to spontaneous infection.
Author Contributions
H.Z.: Writing—original draft; J.Z. and X.H.: Methodology, Writing—review and editing. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by Heilongjiang Provincial Universities, grant number 145409333.
Data Availability Statement
No new data were created or analyzed in this study.
Conflicts of Interest
The authors declare no conflicts of interest.
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