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Wardlaw, A. M.

Publications and source records attributed to Wardlaw, A. M..

2 recordsLinked to original sources

Virulence evolution of a parasite infecting male and female hosts

Parasites experience different tradeoffs between transmission and virulence in male and female hosts if the sexes vary in life history or disease-related traits. We determine the evolutionarily stable levels of exploitation by pathogens under two scenarios: an unconstrained pathogen that expresses different exploitation rates within each host type as well as a pathogen constrained to express the same exploitation rate in each sex. We show that an unconstrained horizontally-transmitted parasite evolves to express the same sex-specific exploitation rate within each sex as it would in a host population composed entirely of hosts with that sexs resistance and intrinsic death rate. In contrast, the ESS exploitation rate of a constrained pathogen is affected by sex-differences in susceptibility and non-random contact patterns between host types that differ in resistance. As the amount of within-sex transmission increases, the ESS shifts closer to the optimum trait value in the more susceptible sex. Allowing for some degree of vertical transmission, the exploitation rate expressed in females (but not males) changes with contact pattern even in unconstrained pathogens. Differences in contact pattern and susceptibility play an important role in determining the ESS exploitation rate by shifting the reproductive value of each host type.

evolutionary biology

Sexual conflict and STDs: coevolution of sexually antagonistic host traits with a sexually transmitted disease

In many taxa, there is a conflict between the sexes over mating rate. The outcome of sexually antagonistic coevolution depends on the costs of mating and natural selection against sexually antagonistic traits. A sexually transmitted infection (STI) changes the relative strength of these costs. We study the three-way evolutionary interaction between male persistence, female resistance, and STI virulence for two types of STIs: a viability-reducing STI and a reproduction-reducing STI. A viability-reducing STI escalates conflict between the sexes. This leads to increased STI virulence (i.e., full coevolution) if the costs of sexually antagonistic traits occur through viability but not if the costs occur through reproduction. In contrast, a reproduction-reducing STI de-escalates the sexual conflict but STI virulence does not coevolve in response. We also investigated the establishment probability of STIs under different combinations of evolvability. Successful invasion by a viability-reducing STI becomes less likely if hosts (but not parasite) are evolvable, especially if only the female trait can evolve. A reproduction-reducing STI can almost always invade because it does not kill its host. We discuss how the evolution of host and parasite traits in a system with sexual conflict differ from a system with female mate choice.

evolutionary biology