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R E S E A R C H

Open Access

Analysis of an SIS epidemic model with

treatment

Jinghai Wang

*

and Qiaohong Jiang

*Correspondence: fzwjh@163.com

College of Mathematics and Computer Science, Fuzhou University, Fuzhou, Fujian 350002, P.R. China

Abstract

An SIS epidemic model with saturated incidence rate and treatment is considered. According to different recovery rates, we use differential stability theory and

qualitative theory to analyze the various kinds of endemic equilibria and disease-free equilibrium. Finally, we get complete configurations of different endemic equilibria and disease-free equilibrium.

Keywords: epidemic model; incidence rates; treatment; globally asymptotically stable

1 Introduction and model

Infectious diseases have tremendous influence on human life and will bring huge panic and disaster to mankind once out of control. Every year millions of human beings suffer from or die of various infectious diseases. In order to predict the spreading of infectious diseases, many epidemic models have been proposed and analyzed in recent years (see [–]). Some new conditions should be considered into SIS model to extend the results. Liet al. (see []) studied an SIS model with bilinear incidence rateβSIand treatment. The model takes into account the medical conditions. The recovery of the infected rate is divided into natural and unnatural recovery rates. Because of the medical conditions, when the number of infected persons reaches a certain amountI, the unnatural recovery

rate will be a fixed valueδI. The study of this model should be divided into two cases to

discuss withIIandI>I. In this paper, we study an SIS model with saturated incidence

rate+βSIαS and treatment, and we extend some recent results.

By a saturated incidence rate +βSIαS, we consider an SIS epidemic model which consists of the susceptible individualsS(t), the infectious individualsI(t) and the total population N(t) at timet:

dS

dt =AdS

βSI

+αS+γI+T(I), dI

dt =

βSI

+αS– (d+ε+γ)IT(I),

N(t) =S(t) +I(t),

(.)

whereT(I) =δI, if≤II,

k, ifII (k=δI) is the rate at which infected individuals are treated;

Ais the recruitment rate of individuals (including newborns and immigrants) into the susceptible population; +βSIαS is the nonlinear incidence rate;dis the natural death rate;

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γ is the rate at which infected individuals are recovered;εis the disease-related death rate,A,d,γ,δ,ε,αare all positive numbers.

Thus, if ≤II, model (.) implies

dS

dt =AdS

βSI

+αS+γI+δI, dI

dt=

βSI

+αS– (d+ε+γ)IδI.

(.)

IfI>I, model (.) implies

dS

dt =AdS

βSI

+αS+γI+k, dI

dt=

βSI

+αS– (d+ε+γ)Ik.

(.)

2 Existence of equilibria

Now, we study equilibria of model (.). Steady states of model (.) satisfy the following equations:

AdS+βSIαS+γI+T(I) = , βSI

+αS– (d+ε+γ)IT(I) = .

(.)

We easily see that model (.) has a disease-free equilibriumP(Ad, ).

If  <II, it follows from equation (.) that

AdS+βSIαS+γI+δI= , βSI

+αS– (d+ε+γ)IδI= ,

(.)

and ifI>I, we get

AdS+βSIαS+γI+k= , βSI

+αS– (d+ε+γ)Ik= .

(.)

From two equations of (.), we have

S=A– (d+ε)I

d . (.)

By substituting (.) into the second equation of (.), we obtain the following equations:

βAβ(d+ε)I

d+α(d+ε)I – (d+ε+γ +δ) = ,

(d+ε)–β+α(d+ε+γ+δ)I= (d+)(d+ε+γ +δ) –βA.

(.)

LetR=(d+Aα)(d+βAε+γ+δ). We study equation (.) as follows.

Ifα(d+ε+γ +δ) >β,R<  holds if and only if

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with

S= d

A– (d+ε)(d+)(d+ε+γ+δ)( –R) (d+ε)[–β+α(d+ε+γ +δ)]

= – d+ε+γ+δ

β+α(d+ε+γ +δ)< .

So this case need not be considered.

Ifα(d+ε+γ +δ) <β,R>  holds if and only if

I=(d+)(d+ε+γ +δ)(R– ) (d+ε)[βα(d+ε+γ+δ)] > 

with

S= d+ε+γ+δ

βα(d+ε+γ+δ)> .

Then we get a positive equilibriumP∗(S∗,I∗) of (.), where

I∗=(d+)(d+ε+γ+δ)(R– ) (d+ε)[βα(d+ε+γ+δ)] ,

S∗= d+ε+γ +δ

βα(d+ε+γ+δ).

Furthermore, if  <I∗≤I,P∗(S∗,I∗) is an endemic equilibrium of model (.) when

 <R≤ +

(d+ε)[βα(d+ε+γ+δ)] (d+)(d+ε+γ +δ) I.

Define

n=  +

(d+ε)[βα(d+ε+γ +δ)] (d+)(d+ε+γ+δ) I.

Therefore model (.) has a disease-free equilibriumP(Ad, ) and has an endemic

equilib-riumP∗(S∗,I∗) except the disease-free equilibriumP(Ad, ) when  <R≤n.

By substituting (.) into the second equation of (.), we obtain the following equation:

(d+ε)βα(d+ε+γ)I+(+d)(d+ε+γ) –βA(d+ε)I+k(+d) = . (.)

Letb= (+d)(d+ε+γ) –βA(d+ε). We study equation (.) as follows. Ifβ=α(d+ε+γ), (.) has a positive root ifb< , then

I= k(+d) (d+ε) –d(d+ε+γ),

S= –k(d+ε) +A(d+ε+γ) (d+ε) –d(d+ε+γ)< .

So this case need not be considered.

Ifβ<α(d+ε+γ), it follows from (.) that

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Then

=

βA+(d+ε) – (+d)(d+ε+γ)+ k(d+ε)α(d+ε+γ) –β(+d) > .

Denoting two roots of (.) byIandI, we have

I+I= –

βA+(d+ε) – (+d)(d+ε+γ) (d+ε)[α(d+ε+γ) –β] ,

I·I=

k(+d)

(d+ε)[α(d+ε+γ) –β]< .

So (.) has only one positive root, denote it byI,

I=

b+√

(d+ε)[α(d+ε+γ) –β],

S=

d

A– (d+ε)I

.

ThenS>  holds only if

R<

(d)(d+ε+γ) +(d+ε) –√

(+d)(d+ε+γ+δ) .

Define

n=

(d)(d+ε+γ) +(d+ε) –√

(+d)(d+ε+γ +δ) .

The pointP(S,I) satisfies (.), thenI>I,i.e.,

b+√

(d+ε)[α(d+ε+γ) –β]>I,

we have

> –b+ (d+ε)α(d+ε+γ) –βI. (.)

Then –b+ (d+ε)[α(d+ε+γ) –β]I< .

And

R<  –

δ(+d) +(d+ε) (+d)(d+ε+γ +δ)–

(d+ε)[α(d+ε+γ) –β]I

(d+ε+γ+δ)(+d) .

Define

n=  –

δ(+d) +(d+ε) (+d)(d+ε+γ +δ)–

(d+ε)[α(d+ε+γ) –β]I

(d+ε+γ +δ)(+d) .

Then (.) holds only if

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Then

n<R≤ –

δ(+d) +(d+ε) (+d)(d+ε+γ+δ)+

k (d+ε+γ +δ)I

+(d+ε)[βα(d+ε+γ)]I (+d)(d+ε+γ+δ) ,

define

n=  –

δ(+d) +(d+ε) (+d)(d+ε+γ +δ)+

k (d+ε+γ+δ)I

+(d+ε)[βα(d+ε+γ)]I (+d)(d+ε+γ+δ) .

So, ifR≤nandR≤n,P(S,I) is an endemic equilibrium, where

I=

b+√

(d+ε)[α(d+ε+γ) –β], S=  d

A– (d+ε)I

.

Ifβ>α(d+ε+γ), it is easy to see that (.) has no positive root ifb≥. Ifb< ,

=b– k(d+ε)(+d)

βα(d+ε+γ),

b= –R(d+ε+γ +δ)(+d) + (+d)(d+ε+δ+γ) –(d+ε) –δ(+d).

Then≥ impliesb≥k(d+ε)(+d)[βα(d+ε+γ)], we get

R≤ –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)–

k(+d)(d+ε)[βα(d+ε+γ)] (+d)(d+ε+δ+γ)

or

R≥ –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)+

k(+d)(d+ε)[βα(d+ε+γ)] (+d)(d+ε+δ+γ) .

Define

n=  –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)–

k(+d)(d+ε)[βα(d+ε+γ)] (+d)(d+ε+δ+γ) ,

n=  –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)+

k(+d)(d+ε)[βα(d+ε+γ)] (+d)(d+ε+δ+γ) .

At the same time,b<  holds if and only ifR>  –(Aδ(Aαα+d)(d++d)+kεα+(d+δ+γε)).

Define

n=  –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ).

Therefore, ifR≥n, we haveb<  and≥, then (.) has two positive rootsI,I,

where

I=

b–√

(d+ε)[βα(d+ε+γ)], I=

b+√

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ThenSi=d[A– (d+ε)Ii] >  (i= , ) holds only if

R<  –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)+

A[βα(d+ε+γ)] +√

(+d)(d+ε+δ+γ) ,

R<  –

δ(+d) +(d+ε) +√

(+d)(d+ε+δ+γ) +

A[βα(d+ε+γ)] (+d)(d+ε+δ+γ).

Define

n=  –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)+

A[βα(d+ε+γ)] +√

(+d)(d+ε+δ+γ) ,

n=  –

δ(+d) +(d+ε) +√

(+d)(d+ε+δ+γ) +

A[βα(d+ε+γ)] (+d)(d+ε+δ+γ).

It is easy to see thatn<n, which implies that (.) has two positive equilibrium points

P(S,I),P(S,I) ifR<n, (.) has only one positive equilibrium pointP(S,I) if

n<R<n, (.) has no positive equilibrium point ifR≥n.

Now, we consider the conditions forIi>I(i= , ).

I>I ⇒ –b

> (d+ε)

βα(d+ε+γ)I

b+ (d+ε)βα(d+ε+γ)I< .

Then

R>  –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)+

(d+ε)[βα(d+ε+γ)]I

(+d)(d+ε+δ+γ) .

Define

n=  –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)+

(d+ε)[βα(d+ε+γ)]I

(+d)(d+ε+δ+γ) .

Furthermore,

b> (d+ε)

βα(d+ε+γ)I ⇒

b+ (d+ε)βα(d+ε+γ)I 

>,

i.e.,

R<  –

δ(+d) +(d+ε) (+d)(d+ε+δ+γ)+

k (d+ε+δ+γ)I

+(d+ε)[βα(d+ε+γ)]I (+d)(d+ε+δ+γ) .

Therefore, ifn<R<n,I>Iholds.

Similarly, ifI>I,

b+ (d+ε)βα(d+ε+γ)I≤

or

b+ (d+ε)[βα(d+ε+γ)]I> , >{(d+ε)[βα(d+ε+γ)]I+b},

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From the above discussion, we get the following conclusions.

Theorem . If R< ,model(.)has only one disease-free equilibrium P(Ad, );if R> ,

model(.)has a unique endemic equilibrium P∗(S∗,I∗)except the disease-free equilibrium P(Ad, );if <R<n,P∗(S∗,I∗)is a unique endemic equilibrium of model(.).

Theorem . Ifβ<α(d+ε+γ),then P(S,I)is a unique endemic equilibrium of model

(.)if R≤n;P(S,I)is a unique endemic equilibrium of model(.) if R≤nand

R≤n.

Ifβ>α(d+ε+γ),model(.)has two positive equilibrium points P(S,I),P(S,I)if

R<n;model(.)has only one positive equilibrium point P(S,I)if n<R<n;model

(.)has no positive point if R≥n;P(S,I)is an endemic equilibrium of model(.)if

n<R<n;P(S,I)is an endemic equilibrium of model(.)if R<nor n<R<n.

Ifβ=α(d+ε+γ),model(.)has no endemic equilibrium.

3 Stability of equilibria

Theorem . The disease-free equilibrium P(Ad, )is stable if R< and is a saddle point

if R> ;the endemic equilibrium P∗(S∗,I∗)is a stable node if it exists;the endemic

equi-librium P(S,I)is a stable node if it exists;if the endemic equilibrium points P(S,I),

P(S,I)exist,then P(S,I)is a stable node of model(.)if –b–

(d+α)[βα(d+α+γ)]D+D> 

and P(S,I)is a stable node of model(.)if –b+

(d+α)[βα(d+α+γ)]D+D> .

Proof The Jacobi matrix of model (.) is

J=

d(+βαIS) –

βS +αS+δ+γ

βI (+αS)

βS

+αS– (d+ε+δ+γ)

,

then

J(P) =

dd+βAαA+γ +δ

d+βAαA– (d+ε+γ+δ)

,

detJ(P) =d(d+ε+δ+γ)( –R),

trJ(P) = –d– (d+ε+δ+γ)( –R).

Thus,P(Ad, ) is a stable node ifR< , and is a saddle point ifR> .

ForP∗(S∗,I∗),

J(P∗) =

d(+βαIS

∗) –

βS

+αS∗+δ+γ βI

(+αS∗)

βS

+αS∗– (d+ε+δ+γ)

=

d(+βαIS

∗) –(d+ε)

βI

(+αS∗) 

,

trJ(P∗) = –dβI∗ ( +αS∗)< ,

detJ(P∗) = (d+ε) βI∗ ( +αS∗) > .

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The Jacobi matrix of model (.) is

BecauseIsatisfies equation (.), we get

(9)

If –b–

Proof Consider the Dulac functionD=

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Then there is no limit cycle of model (.) if βα(d+ε+γ). This completes the

proof.

4 Numerical simulation and conclusion

With differentA,d,γ,δ,ε,α, it is easy to test and verify the above results, so numerical simulation is omitted. In this paper, we study an SIS model with saturated incidence rate

βSI

+αS and treatment. We get some relatively complex conclusions by stability theory and

qualitative theory of differential equations. These conclusions will help policy makers to make decisions.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

The authors are entirely responsible for this research. The authors read and approved the final manuscript.

Acknowledgements

The research was supported by the Fujian Nature Science Foundation under Grant No. 2014J01008.

Received: 11 August 2014 Accepted: 5 September 2014 Published: 24 September 2014 References

1. Jin, Y, Wang, W, Xiao, S: An SIRS model with a nonlinear incidence rate. Chaos Solitons Fractals34, 1482-1497 (2007) 2. Cai, L-M, Li, X-Z: Analysis of a SEIV epidemic model with a nonlinear incidence rate. Appl. Math. Model.33, 2919-2926

(2009)

3. Xu, R, Ma, Z: Stability of a delayed SIRS epidemic model with a nonlinear incidence rate. Chaos Solitons Fractals41, 2319-2325 (2009)

4. Wang, X, Tao, Y, Song, X: Pulse vaccination on SEIR epidemic model with nonlinear incidence rate. Appl. Math. Comput.210, 398-404 (2009)

5. Jiang, Q, Wang, J: Qualitative analysis of a harvested predator-prey system with Holling type III functional response. Adv. Differ. Equ.2013, 249 (2013)

6. Wang, J, Pan, L: Qualitative analysis of a harvested predator-prey system with Holling-type III functional response incorporating a prey refuge. Adv. Differ. Equ.2012, 96 (2012)

7. Wang, J: Analysis of an SEIS epidemic model with a changing delitescence. Abstr. Appl. Anal.2012, Article ID 318150 (2012). doi:10.1155/2012/318150

8. Zhang, T, Teng, Z: Global behavior and permanence of SIRS epidemic model withttime delay. Nonlinear Anal., Real World Appl.9, 1409-1424 (2008)

9. Mukhopadhyay, B, Bhattacharyya, R: Analysis of a spatially extended non-linear SEIS epidemic model with distinct incidence for exposed and infectives. Nonlinear Anal., Real World Appl.9(2), 585-598 (2008)

10. Zhang, J, Ma, Z: Global dynamics of an SEIRS epidemic model with saturating contact rate. Math. Biosci.185, 15-32 (2003)

11. Hethcote, H, Ma, Z, Liao, S: Effects of quarantine in six endemic models for infectious diseases. Math. Biosci.180, 141-160 (2002)

12. Martcheva, M, Castillo-Chavez, C: Diseases with chronic stage in a population with varying size. Math. Biosci.182, 1-25 (2003)

13. Li, X-Z, Li, W-S, Ghosh, M: Stability and bifurcation for an SIS epidemic model with treatment. Chaos Solitons Fractals

42, 2822-2832 (2009)

doi:10.1186/1687-1847-2014-246

References

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