Next-generation matrix explained

In epidemiology, the next-generation matrix is used to derive the basic reproduction number, for a compartmental model of the spread of infectious diseases. In population dynamics it is used to compute the basic reproduction number for structured population models. It is also used in multi-type branching models for analogous computations.[1]

The method to compute the basic reproduction ratio using the next-generation matrix is given by Diekmann et al. (1990)[2] and van den Driessche and Watmough (2002).[3] To calculate the basic reproduction number by using a next-generation matrix, the whole population is divided into

n

compartments in which there are

m<n

infected compartments. Let

xi,i=1,2,3,\ldots,m

be the numbers of infected individuals in the

ith

infected compartment at time t. Now, the epidemic model is
dxi
dt

=Fi(x)-Vi(x)

, where

Vi(x)=

+
[V
i(x)]

In the above equations,

Fi(x)

represents the rate of appearance of new infections in compartment

i

.
+
V
i
represents the rate of transfer of individuals into compartment

i

by all other means, and
-
V
i

(x)

represents the rate of transfer of individuals out of compartment

i

.The above model can also be written as
dx
dt

=F(x)-V(x)

where

F(x)=\begin{pmatrix} F1(x),&F2(x),&\ldots,&Fm(x) \end{pmatrix}T

and

V(x)=\begin{pmatrix} V1(x),&V2(x),&\ldots,&Vm(x) \end{pmatrix}T.

Let

x0

be the disease-free equilibrium. The values of the parts of the Jacobian matrix

F(x)

and

V(x)

are:

DF(x0)=\begin{pmatrix} F&0\\ 0&0 \end{pmatrix}

and

DV(x0)=\begin{pmatrix} V&0\\ J3&J4 \end{pmatrix}

respectively.

Here,

F

and

V

are m × m matrices, defined as

F=

\partialFi
\partialxj

(x0)

and
V=\partialVi
\partialxj

(x0)

.

Now, the matrix

FV-1

is known as the next-generation matrix. The basic reproduction number of the model is then given by the eigenvalue of

FV-1

with the largest absolute value (the spectral radius of

FV-1

. Next generation matrices can be computationally evaluated from observational data, which is often the most productive approach where there are large numbers of compartments.

See also

Sources

Notes and References

  1. Book: Mode, Charles J., 1927-. Multitype branching processes; theory and applications. 1971. American Elsevier Pub. Co. 0-444-00086-0. New York. 120182.
  2. 10.1007/BF00178324. On the definition and the computation of the basic reproduction ratio R0 in models for infectious diseases in heterogeneous populations. Journal of Mathematical Biology. 28. 4. 365–382. 1990. Diekmann . O.. Heesterbeek . J. A. P.. Metz . J. A. J. . 22275430. 2117040. 1874/8051. free.
  3. 10.1016/S0025-5564(02)00108-6. 12387915. Reproduction numbers and sub-threshold endemic equilibria for compartmental models of disease transmission. Mathematical Biosciences. 180. 1–2. 29–48. 2002. van den Driessche . P. . Pauline van den Driessche . Watmough . J.. 17313221.