Evolutionary drivers of parasite-induced changes in insect life-history traits from theory to underlying mechanisms

Many hosts are able to tolerate infection by altering life-history traits that are traded-off one against another. Here the reproductive fitness of insect hosts and vectors is reviewed in the context of theories concerning evolutionary mechanisms driving such alterations. These include the concepts that changes in host reproductive fitness are by-products of infection, parasite manipulations, host adaptations, mafia-like strategies or host compensatory responses. Two models are examined in depth, a tapeworm/beetle association, Hymenolepis diminuta/Tenebrio molitor and malaria infections in anopheline mosquitoes. Parasite-induced impairment of vitellogenesis ultimately leads to a decrease in female reproductive success in both cases, though by different means. Evidence is put forwards for both a manipulator molecule of parasite origin and for host-initiated regulation. These models are backed by other examples in which mechanisms underlying fecundity reduction or fecundity compensation are explored. It is concluded that evolutionary theories must be supported by empirical evidence gained from studying molecular, biochemical and physiological mechanisms underlying changes in host life-history traits, ideally using organisms that have evolved together and that are in their natural environment.