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Abstract
We prove a threshold theorem for the Reed-Frost chain-binomial model
which is analogous to the threshold theorem of Williams (1971) for the general
stochastic epidemic. We show that when the population size is large a 'true
epidemic' occurs with a non-zero probability if and only if an initial infective
individual infects on average more than one susceptible individual.
EPIDEMICS; THRESHOLD THEOREMS; SIZE OF EPIDEMIC; RANDOM GRAPH; TREES
1. Introduction
The Reed-Frost chain-binomial epidemic (see e.g. Bailey (1975), Chapter 14),
assumes a constant latent period, an infectious period that is reduced to a single
point in time and at this point a given infective individual infects a given
susceptible individual with probability p, all infections being independent. These
assumptions give rise to epidemics consisting of a series of infections, each set of
infections occurring at a time, equal to the latent period, after the previous set.
Suppose that initially there are a infectives and n susceptibles. As we are only
going to be concerned with the total size of an epidemic it is sufficient to view the
process as a random graph on n + a labelled points, in which the arc joining two
points, i, and i2 say, is present with probability p, independent of the presence or
absence of any other arc. The graph is interpreted as follows. The a initial
infectives are the infectives of the Oth generation. For n = 1,2, - - - the infectives
of the n th generation consist of those susceptible individuals that are joined by
at least one arc to infectives of the (n - 1)th generation. The epidemic ceases
when a generation of infectives have no arcs joining them to the remaining
susceptibles. Note that there may be connected components at the graph that
play no role in the spread of infection. Clearly an individual i, is infected by an
epidemic if and only if there is a connected chain of arcs joining an initial
infective to
i,.
Received 3 March 1982; revision received 15 April 1982.
* Present address: Department of Applied Statistics, The University of Reading, Reading, RG6
2AN, U.K.
153
(1) p) 1n i = - - -, n
0,,
Pa•n,(i)=1P.0(i)(l
-
since the probability that (n i) susceptibles avoid infection from (a + i)
infectives is (1 -p)a'"+)(n" as (a + i)(n - i) arcs have to be absent. This is
essentially the same argument used by Ludwig (1975), except that he did not use
the concept of a graph.
Now let Pa, = P,,n(n) be the probability that an epidemic infects all n
susceptibles, i.e. the probability of a complete epidemic. P,,n is a polynomial in p
whose lowest term is of order p". Fix upon any n - 1 of these susceptibles and
consider the sub-epidemic amongst them alone, ignoring any part the other
susceptible might play. Conditioning on the size of this sub-epidemic we have
that
n-I
3. Threshold behaviour
To elaborate the threshold behaviour we write p = 0/n and let n tend to xc
with 0 fixed; thus 0 is the mean number of infections made by an initial infective.
(Note that two or more initial infectives may infect the same susceptible.) Write
(i) as Pn, (i, 0), and consider Equation (1) and the fact that every term in Pa.,
P•.n
Pa (0) = Pa(i, 0)
i=O
=
e-aOi=0 a,(a)(Oe-')'/i!
= e-Oha (Oe-) say.
We shall show that 300 > 0 such that Pa(0)= 1 if 0 5<00 and Pa(0)< 1 if
0 > 00, i.e. a 'true epidemic' occurs with non-zero probability if and only if
0 > 00. Now to obtain such a result Pa (0) = 1 over (0, 0o) and hence ha(0e-) =
eae over this interval, which uniquely defines the function ha(). In fact it is
readily seen that
(4) ha(x) = (f-'(x)/x)a X> 0
where f-' is the inverse function of f(x) = xe-x defined only for 0 5 x 5 1.
To prove that (4) does hold we first equate the coefficients of p" in (2) to
obtain
0 1.1 1.2 1.4 1.6 1.8 2.0 2.5 3.0 4.0 6.0 8.0 10.0
f-'(Oe-0)/6 0.82 0.69 0.49 0.36 0.27 ).20 0.11 0.050 0.020 0.0025 0.00033 0.000045
When there are a > 1 initial infectives the graphs of epidemics contributing to
the coefficient of p' will be disjoint unions of trees rooted at the initial infectives,
i.e. forests. The number of such forests can be obtained from a result of Clarke
(1958), which says that if N1,, is the number of trees on n labelled points in which
1 lines meet at a specified vertex then
n- n - 1.
(7) NI, = (n- 1)"'' I=1 2,...
To apply (7) to our problem we consider the number of trees on i + a + 1
labelled points with a lines joined to our additional point. There are Na.i+a+i
such trees but we have specified the a initial infectives, which could have been
chosen in (i'a) ways, and thus
5. Comment
The threshold theorem proved here is contained in Theorem 1 of von Bahr
and Martin-Lof (1980). However, although their theorem also contains an
asymptotic distribution for the size of a 'true epidemic', their proof is consider-
ably more complicated than ours and provides little insight into the mechanism
underlying the threshold behaviour.
Acknowledgements
I should like to thank John Haigh for commenting on drafts of this paper and
the referee for his useful suggestions.
References
VON BAHR, B. AND MARTIN-LOF, A. (1980) Threshold limit theorems for some epidemic
processes. Adv. Appl. Prob. 12, 319-349.
BAILEY, N. T. J. (1975) The Mathematical Theoryof Infectious Diseases and its Applications, 2nd
edn. Griffin, London.
CLARKE,L. E. (1958) Cayley's formula for counting trees. J. London Math. Soc. 33, 471-474.
LUDWIG,D. (1975) Final size distributions for epidemics. Math. Biosci. 23, 33-46.
RIORDAN, J. (1958) An Introduction to Combinatorial Analysis. Princeton University Press,
Princeton, NJ.
WILLIAMS, T. (1971) An algebraic proof of the threshold theorem for the general stochastic
epidemic (abstract). Adv. Appl. Prob. 3, 223.