While avian chronic haemoparasite infections induce reproductive costs, infection has not previously been shown to affect survival. Here, we experimentally reduced, through medication, the intensity of infection by Haemoproteus parasites in wild-breeding female blue tits Cyanistes caeruleus. However, this treatment did not reduce the intensity of infection in males or the intensity of infection by Leucocytozoon. Medicated females, but not males, showed increased local survival until the next breeding season compared with control birds. To our knowledge, this is the first empirical evidence showing long-term direct survival costs of chronic Haemoproteus infections in wild birds.
Parasitism is a major selection force affecting wild animals. The phylum Apicomplexa forms a large and cosmopolitan assemblage of protozoan parasites. Within this phylum are the haemospororins, including malaria parasites, which infect blood-feeding dipterans acting as vectors, and several classes of vertebrates. These parasites are common infections in many bird species and there are evidences for short-term costs of chronic infections by the haemospororins parasites Plasmodium, Haemoproteus and Leucocytozoon on wild bird's reproductive performance (e.g. Merino et al. 2000; Marzal et al. 2005; Knowles et al. 2010). However, effects of these parasites on survival have remained elusive in wild avian populations (e.g. Stjernman et al. 2004). Thus, it has been unclear whether infections can have long-term fitness consequences, which is an important assumption of many studies of host–parasite interactions.
Intraspecific (Richner et al. 1995; Nordling et al. 1998; Marzal et al. 2008) and comparative studies (Møller & Nielsen 2007) suggest a role of blood parasites in reducing avian survival under natural conditions. However, these studies have not controlled for differences in capture probability, making previous conclusions open to alternative interpretations. In addition, no study has experimentally investigated host survival in relation to infections by Haemoproteus parasites in wild populations, probably owing to the difficulty of manipulating parasite loads. The use of the antimalarial drug primaquine has overcome this challenge allowing experimental reductions of Haemoproteus loads in birds and investigation of subsequent effects on post-breeding body condition (e.g. Merino et al. 2000) or reproduction (e.g. Merino et al. 2000; Marzal et al. 2005).
We tested whether experimental reduction in the intensity of infection by Haemoproteus parasites increases local survival in its avian host. Owing to the effect of host sex on parasite load and the efficacy of antiparasitic treatments (e.g. Klein 2004; Martínez-de la Puente et al. 2007), we also explored a potential differential effect of medication on parasite load and subsequent survival between sexes. Because treatment causes detectable reductions in Haemoproteus load in females, but not in males (Martínez-de la Puente et al. 2007), we predicted an increase in female, but not in male survival following medication.
2. Material and methods
This study was conducted on blue tits (Cyanistes caeruleus) breeding in nest boxes in Spain (40°53′ N, 4°01′ W, 1200 m above sea level). During 2004, birds were captured and blood sampled when their nestlings were 3 days old (initial sample). Birds attending nests with similar clutch size (±1 egg) and hatching date (±1 day) were randomly assigned to one of the two treatments (medicated or control). Previous studies revealed that the prevalence of infection by Haemoproteus spp. and Leucocytozoon spp. in our population is very high, thus allowing blind assignment of treatments. This assumption was later confirmed (see §3). Medicated birds were injected subcutaneously with 0.1 mg primaquine (Sigma, St Louis, MO, USA) diluted in 0.1 ml saline solution, whereas control birds were injected with saline solution only (Merino et al. 2000). Ten days later birds were recaptured and a second blood sample obtained (final sample). All birds breeding in nest boxes in the study area were captured each season until 2007, allowing analysis of local survival in relation to treatment.
A drop of blood from each sample was immediately smeared, air-dried, fixed in absolute ethanol and stained with Giemsa for 45 min. Smears were used to quantify intensity of infection by Haemoproteus spp. and Leucocytozoon spp. (see electronic supplementary material). An additional drop of blood was collected in a plastic tube and frozen for molecular detection of parasite infection. Blood samples from birds diagnosed as uninfected by inspection of smears at the initial capture were also analysed with polymerase chain reaction (see electronic supplementary material). Blood samples from one female and five males were insufficient for conducting DNA analyses.
We used repeated-measures ANOVA to test for an effect of treatment on change in intensity of infection by Haemoproteus and Leucocytozoon parasites between initial and final samples in the two sexes separately. Intensities of infection were log-transformed to allow use of parametric statistics. Survival analyses were carried out using two different methods. First, for simplicity, we tested for an effect of treatment and sex (as factors) on local survival using a generalized linear model (GLZ) model. The main problem with this approach is that it does not consider either capture probability or permanent emigration. Therefore, we also estimated survival using capture–mark–recapture models for open populations (see electronic supplementary material).
A total of 95 females (47 medicated, 48 controls) and 92 males (47 medicated, 45 controls) were included in the experiment. At first capture, 85 per cent of females and 88 per cent of males were infected with Haemoproteus spp. (see also table S1 in the electronic supplementary material), whereas 92 per cent of females and 87 per cent of males were infected by Leucocytozoon spp. All except one male and one female were infected by at least one parasite.
Repeated-measures ANOVA revealed that medicated females experienced a significantly greater reduction in intensity of infection by Haemoproteus parasites from initial to final samples than control females (figure 1a; F1,77 = 4.25, p = 0.04). In males, change in intensity was not significantly affected by treatment (figure 1b; F1,73 = 0.34, p = 0.56). There were no significant treatment effects on change in intensity of infection by Leucocytozoon parasites in either sex (all p > 0.35).
Of all birds included in the study in 2004, 28 females (19 medicated and nine controls) and 26 males (11 medicated and 15 controls) were recaptured at least once between 2005 and 2007. Sex and treatment were not significantly associated with local survival, but there was a significant interaction effect on survival (GLZ: treatment: Wald = 0.77, p = 0.38; sex: Wald = 0.001, p = 0.97; treatment × sex interaction: Wald = 5.56, p = 0.02), supporting an effect of medication on survival in females only. Accordingly, the best model for survival included an interaction between sex and treatment in the first year post-treatment (model 1, table S2 in the electronic supplementary material). The other three competing models included within two Akaike Information Criterion with second order correction units of the best model (table S2 in the electronic supplementary material) support the interaction between sex and treatment on survival between 2004 and 2005, although differing in effect of treatment on survival to subsequent years. Furthermore, the only partial coefficient of the log-linear function for survival for the best-fit model with a 95% confidence interval that did not overlap with zero included the interaction between sex and treatment (Beta (s.e.) = 1.71 (0.60), 95% confidence interval = 0.53–2.89). This indicates that survival probability of treated females was higher than for controls, and there was no significant effect of primaquine treatment on male survival. We estimated survival probabilities for males and females assigned to different treatments by model averaging, and the higher survival probability was obtained for medicated females (table 1). For additional information, see the electronic supplementary material.
There was a sex-specific effect of medication on Haemoproteus parasite intensity. Host sex is an important determinant of intensity of infection by parasites (Møller et al. 1998), with males usually having stronger infections (Klein 2004). Although reports on the pharmacokinetics of treatments against parasites in wild animals of different sexes are scarce, the literature reports sex effects on drug kinetics (e.g. Klein 2004; Dimitrova et al. 2009), including studies with antimalarial drugs (Gordi et al. 2002). Different factors tightly related to sex, such as hormone concentrations and genetic characteristics, may affect the absorption and metabolism of drugs (Lashev et al. 1995; Pinsonneault & Sadée 2004). These factors may be implicated in the observed different efficacy of primaquine treatment between sexes.
Experimental reductions of helminth loads increase adult survival in red grouse Lagopus lagopus (Hudson & Dobson 1991) and common eiders Somateria mollissima (Hanssen et al. 2003). By direct experimental manipulation of intensity of infection of a common avian parasite through medication, we have, to our knowledge, shown for the first time that chronic Haemoproteus parasite infections have detrimental effects on survival. In accord with expectations, female but not male blue tits increased survival following medication, consistent with the fact that females were the only sex in which medication effectively reduced the intensity of infection. Reductions of parasite loads may imply beneficial effects for hosts in terms of reduction of adverse effects of parasitism, including the amount of resources drained by the parasite and the amount of resources devoted by hosts to immune defence (de Lope et al. 1998; Martínez et al. 2004). In addition, both infection status and immunological response of hosts may increase metabolic rate (Martínez et al. 2004) and, as a consequence, reduce survival by increasing susceptibility to infection by other pathogens or capture by predators (Hudson et al. 1992; Møller & Nielsen 2007). Our findings add to previous studies showing short-term costs of Haemoproteus parasite infections on avian post-breeding body condition (Merino et al. 2000) and reproductive success (Merino et al. 2000; Marzal et al. 2005).
The study complies with current laws in Spain.
The study was supported by projects CGL2006-14129-C02-01 and CGL2007-61251. See electronic supplementary material for additional information.
- Received January 18, 2010.
- Accepted February 4, 2010.
- © 2010 The Royal Society