We incorporate a representation of Plasmodium falciparum recombination with
in a discrete-event model of malaria transmission. We simulate the introduc
tion of a new parasite genotype into a human population in which another ge
notype has reached equilibrium prevalence and compare the emergence and per
sistence of the novel recombinant forms under differing cross-reactivity re
lationships between the genotypes. Cross-reactivity between the parental (i
nitial and introduced) genotypes reduces the frequency of appearance of rec
ombinants within three years of introduction from 100% to 14%, and delays t
heir appearance by more than a year, on average. Cross-reactivity between p
arental and recombinant genotypes reduces the frequency of appearance to 36
% and increases the probability of recombinant extinction following appeara
nce from 0% to 83%. When a recombinant is cross-reactive with its parental
types, its probability of extinction is influenced by cross-reactivity betw
een the parental types in the opposite manner; that is, its probability of
extinction after appearance decreases. Frequencies of P. falciparum outcros
sing are mediated by frequencies of mixed-genotype infections in the host p
opulation, which are in turn mediated by the structure of cross-reactivity
between parasite genotypes. The three leading hypotheses about how meiosis
relates to oocyst production lead to quantitative, but no qualitative, diff
erences in these results.