The Susceptible-Infected-Susceptible (SIS) model, along with its various adaptations (e.g., accounting for mortality rates, population density changes, birth rates, and vaccination-based immunization), serves as a framework for describing scenarios in which susceptible individuals become infected and then self-immunize after a certain period, reverting back to a susceptible state. For more information on different SIS model variations, refer to relevant resources.
This model considers a uniform and homogeneous population where individuals are randomly distributed and classified as either Susceptible
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$S+I=1$ : The total population$N$ remains constant, allowing for the assumption that mortality and birth rates fluctuate in a manner that maintains this constancy. In this context, the epidemic can be observed over a brief period. Here,$S=n_s/N$ and$I=n_i/N$ , where$n_s$ and$n_i$ represent the number of susceptible and infected individuals, respectively, and$N=n_i+n_s$ . This approach focuses solely on population densities. -
$S\overset{\lambda}{\Longrightarrow}I$ : Susceptible individuals transition to the infected state with a probability of$\lambda$ per unit of time following contact with another infected individual. The rate$\lambda$ reflects a population's predisposition to an epidemic.- For this process to unfold, a susceptible individual (probability
$S$ ), an infected individual (probability$I$ ), and successful contagion (probability per unit of time$\lambda$ ) must be present. Therefore, the probability of a susceptible individual becoming infected after contact is given by$P_{S\to I}=\lambda SI$ .
- For this process to unfold, a susceptible individual (probability
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$I\overset{\alpha}{\Longrightarrow}S$ : Infected individuals spontaneously revert to the susceptible state with a probability of$\alpha$ at each point in time. The factor$\alpha$ can be interpreted as an intrinsic recovery mechanism within the population.- This process requires the presence of an infected individual (probability
$I$ ) and their successful recovery (probability per unit of time$\alpha$ ). The probability of an infected individual spontaneously transitioning back to a susceptible state is thus$P_{S\to I}=\alpha I$ .
- This process requires the presence of an infected individual (probability
To illustrate this model, consider the following diagram:
The dynamics of the SIS model can be expressed using a set of coupled ordinary differential equations (ODEs), which represent the rates of change of susceptible and infected populations over time:
These coupled ODEs capture the continuous interplay between the susceptible and infected populations within the SIS model, providing a mathematical representation of the epidemic's progression.
Temporal evolution of infected and susceptible agent densities for the parameters
This diagram provides a comprehensive view of the active and absorbing phases. As the fixed parameter
In this diagram, we can more clearly see each of the phases and where exactly the critical point (
Here we consider the stationary density of infected individuals
Introducing a separate group for vaccinated individuals alters the dynamics we previously observed in the SIS model. Consequently, an individual can now be categorized as susceptible (S), infected (I), or vaccinated (V). It assumes that any disease affecting the population follows the same dynamics:
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$S+I+V=1$ : The total population$N$ is constant. I considered$S=n_s/N$ ,$I=n_i/N$ , and$V=n_v/N$ where$n_s$ ,$n_i$ , and$n_v$ are the numbers of susceptible, infected, and vaccinated individuals, respectively, and$N=n_i+n_s+n_v$ ; since we will be dealing exclusively with population densities. -
$S\overset{\gamma}{\Longrightarrow}V$ : A susceptible individual has a probability of$\gamma$ per unit of time to get vaccinated.- The process occurs when we find a susceptible individual (with probability S) and with probability
$\gamma$ , this individual gets vaccinated. The probability of a susceptible individual becoming vaccinated will be$P_{S\to V}=\gamma S$ .
- The process occurs when we find a susceptible individual (with probability S) and with probability
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$S\overset{(1-\gamma)\lambda}{\Longrightarrow}I$ : A susceptible individual will be transferred to the infected state with a probability of$(1-\gamma)\lambda$ per unit of time after coming into contact with a second infected individual. Here, the predisposition rate for a given population to face an epidemic will be$(1-\gamma)\lambda$ .- The process occurs similarly to the SIS model \eqref{StoI}. The probability of a susceptible individual becoming infected after contact will be
$P_{S\to I}=(1-\gamma)\lambda SI$ .
- The process occurs similarly to the SIS model \eqref{StoI}. The probability of a susceptible individual becoming infected after contact will be
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$I\overset{\alpha}{\Longrightarrow}S$ : Here, again, it will occur as already discussed for the SIS model \eqref{ItoS}.- The probability of an infected individual spontaneously transforming into a susceptible individual is
$P_{I\to S}=\alpha I$ .
- The probability of an infected individual spontaneously transforming into a susceptible individual is
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$V\overset{\phi}{\Longrightarrow}S$ A vaccinated individual can become susceptible again with a probability of$\phi$ . We can interpret$\phi$ as a rate of loss of immunity for the individual who was vaccinated.- For this process to occur, it is necessary to find a vaccinated individual (with probability V), and for that individual to lose the immunity provided by the vaccine (with probability
$\phi$ ). The probability of a vaccinated individual becoming susceptible is$P_{V\to S}= \phi V$ .
- For this process to occur, it is necessary to find a vaccinated individual (with probability V), and for that individual to lose the immunity provided by the vaccine (with probability
To illustrate this model, consider the following diagram:
In the SISV (Susceptible-Infected-Susceptible-Vaccinated) framework, the population dynamics are depicted by the following set of coupled ordinary differential equations (ODEs):
The rate of change of the susceptible population over time,
In the SISV (Susceptible-Infectious-Susceptible-Vaccinated) model, a crucial factor is the reproductive rate of the infection. This rate is particularly significant during the early stages of an outbreak. We can obtain an expression for the reproductive rate by examining how the infected population changes over time.
Consider the following equation representing the rate of change of the infected population at time
In this equation, the term
- If
$(1-\gamma)\lambda S_0/\alpha > 1$ , the rate of change of the infected population ($d{I}/d{t}$ ) is positive, indicating that the infection is proliferating within the community. - If
$(1-\gamma)\lambda S_0/\alpha < 1$ , the rate of change of the infected population ($d{I}/d{t}$ ) is negative, suggesting that the infection is declining.
This leads us to the definition of the reproductive rate of the infection, denoted by
The reproductive rate
Moreover, considering
This threshold represents the critical level of vaccination coverage (
Consider the following diagram for
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$R_e > 1$ : This scenario corresponds to an endemic outbreak period, which could either persist indefinitely within the population or eventually extinguish over time. This scenario unfolds when a primary infected individual generates more than one secondary infection on average, thereby increasing the number of infected individuals in the population. As a result, the rate of change of the infected population over time,$\frac{dI}{dt}$ , is positive at the initial stages. -
$R_e = 1$ : This value represents the threshold that delineates the two potential scenarios. Here, the rate of change in the density of infected individuals remains constant, indicating a stable state of the infection within the population. -
$R_e < 1$ : In this case, the population will not experience an epidemic outbreak at any time. Here, fewer than one secondary infection is produced on average by a primary infected individual, leading to a decline in the number of infected individuals over time. Consequently, the rate of change of the infected population over time,$\frac{dI}{dt}$ , is negative at the initial stages.
By examining the ordinary differential equations (ODEs) in a steady state, we can analytically determine the critical point. It is given by:
We can also identify the threshold parameter
We see three possible scenarios represented as regions I, II, and III from the driagram
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In region I, the population experiences a persistent (endemic) phase of the disease due to a low vaccination rate, as indicated by the parameter
$\gamma$ . -
As we increase
$\gamma$ , more people get vaccinated. By the time we reach region II, the disease can be wiped out from the population after some time. -
Once we enter region III, we find that regardless of the value of
$\lambda$ (which determines how infectious the disease is), the endemic phase disappears. This happens because$\lambda$ is always less than the critical point$\lambda_c$ in this region, considering that$\lambda_c$ is greater than 1.
In Diagram
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Case
$(\lambda_c > 1)$ : This shows that for certain values of$\gamma$ , regardless of the vaccine's validity dictated by the parameter$\phi$ , the population can get rid of the epidemic. -
Case
$(\lambda_c = 1)$ : Walking along this line, we will not observe the possibility of an endemic phase, being the limit that separates the case$\lambda_c > 1$ from the case$\lambda_c < 1$ . -
Case
$(\lambda_c < 1)$ : Here we can find the population in an endemic phase or in a disease-free phase, which will depend on the value of$\lambda$ . If$\lambda < \lambda_c$ , the epidemic can be eliminated from the population. Otherwise, if$\lambda < \lambda_c$ , the epidemic will persist in the population until some other measure is taken.
We can now plot the Stationary density of infected individuals versus
As we increase the value of
Let's plot the Density of susceptible, infected, and vaccinated individuals over time for these parameters. Here, we've used the parameters
Density of susceptible, infected, and vaccinated individuals over time. The parameters used here were
Dinâmica de epidemias sem e com vacinação: Aproximação de campo médio e simulações de Monte Carlo