This thesis investigates the impact of avian malaria (Haemosporidia) parasites on the outcome of interspecific competition between two closely related bird species, pied (Ficedula hypoleuca) and collared (F. albicollis) flycatchers. I further investigated how variation in timing of breeding, life history strategies and immune competence genes (MHC genes) modulate the fitness effects of malaria parasites in one of the two species i.e. collared flycatchers. Collared flycatchers colonized the Baltic island Öland in the late 1950-ties and has since then been expanding their breeding range while competitively excluding pied flycatchers from the favourable habitats (deciduous forests). I investigated the underlying mechanisms behind this exclusion by combining detailed long-term breeding data with modern molecular genetic techniques identifying both the presence/absence and lineage specificity of haemosporidian blood parasites. I found that the rapid decline of pied flycatchers can be explained by the combined effects of competition over nestling sites, hybridization and haemosporidian infections. Haemosporidian infections have a negative impact on survival of pied flycatcher females but no detectable effect on collared flycatchers’ longevity or reproductive success. This may be due to the fact that collared flycatchers carry (and are potentially exposed to) a higher diversity of parasites than pied flycatchers, which in turn may select for a higher diversity of MHC genes and hence a better overall protection from the negative impact of parasites. Indeed, functional MHC diversity correlates negatively with malaria prevalence among collared flycatchers from Gotland. Moreover, I found that both, malaria infection intensity and immunoglobulin level influences how infected collared flycatchers respond to increased nestling food-demands. The latter results mean that there is variation in allocation strategies (i.e. in resource allocation between reproductive effort and immune competence) within the collared flycatcher population. Hence, this population has the ability to respond to novel selection pressures in terms of optimal allocation of resources into immune functions. In summary, my results show that local parasites may facilitate the expansion of a new colonizer. This is important in the context of global climate change that will probably increase the colonization rate of southern species and lead to novel host-parasite interactions.