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. 2010 May;91(5):1263-8.
doi: 10.1890/09-1243.1.

Benefits of host genetic diversity for resistance to infection depend on parasite diversity

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Benefits of host genetic diversity for resistance to infection depend on parasite diversity

Holly H Ganz et al. Ecology. 2010 May.

Abstract

Host populations with high genetic diversity are predicted to have lower levels of infection prevalence. This theory assumes that host genetic diversity results in variation in susceptibility and that parasites exhibit variation in infectivity. Empirical studies on the effects of host heterogeneity typically neglect the role of parasite diversity. We conducted three laboratory experiments designed to test if genetic variation in Daphnia magna populations and genetic variation in its parasites together influence the course of parasite spread after introduction. We found that a natural D. magna population exhibited variation in susceptibility to infection by three parasite species and had strong host clone-parasite species interactions. There was no effect of host heterogeneity in experimental host populations (polycultures and monocultures) separately exposed to single strains of three parasite species. When we manipulated the genetic diversity of a single parasite species and exposed them to host monocultures and polycultures, we found that parasite prevalence increased with the number of parasite strains. Host monocultures exposed to several parasite strains had higher mean parasite prevalence and higher variance than polycultures. These results indicate that effect of host genetic diversity on the spread of infection depends on the level of genetic diversity in the parasite population.

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Figures

Fig. 1
Fig. 1
Mean parasite prevalence (±SE) in monoclonal host populations 30 days after they were exposed to three gut parasite species (Glugoides intestinalis, Ordospora colligata, and Microsporidium sp.). Fifteen different host clones are indicated by color.
Fig. 2
Fig. 2
Mean prevalence (and SE) in monoclonal (white bars) and polyclonal (black bars) populations of D. magna 30 days after exposure to three different parasite species (G. intestinalis, O. colligata, and Microsporidium sp.).
Fig. 3
Fig. 3
Mean parasite prevalence (± variance) in monoclonal (black circles) and polyclonal (red triangles) populations of D. magna 24 days after exposure to as many as four different strains of a single parasite species (O. colligata).

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