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Sex-dependent Differences in Avian Malaria Prevalence and Consequences of Infections on Nestling Growth and Adult Condition in the Tawny Pipit, Anthus Campestris

Overview
Journal Malar J
Publisher Biomed Central
Specialty Tropical Medicine
Date 2016 Mar 23
PMID 27001667
Citations 14
Authors
Affiliations
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Abstract

Background: Parasites play pivotal roles in host population dynamics and can have strong ecological impacts on hosts. Knowledge of the effects of parasites on hosts is often limited by the general observation of a fraction of individuals (mostly adults) within a population. The aim of this study was to assess the prevalence of malaria parasites in adult (≥ 1 year old) and nestling (7-11 day old) Tawny pipits Anthus campestris, to evaluate the influence of the host sex on parasite prevalence in both groups of age, and explore the association between infections and body condition (adults) and growth (nestlings).

Methods: Two hundred Tawny pipits (105 adults and 95 nestlings) from one Spanish population were screened for avian malaria parasites (Haemoproteus and Plasmodium) using the polymerase chain reaction (PCR)-based methods. Body condition (body mass against a linear measure of size) was measured in adults and growth rate (daily mass gain) was calculated for nestlings.

Results: The overall prevalence of infection was 46%. Sixteen different mitochondrial cytochrome b haplotypes of Plasmodium spp. and one Haemoproteus spp. haplotype were found. Malaria parasites were equally prevalent in nestlings and adults (45 and 46%, respectively). Males were more likely to be infected by parasites than females, and this sex-bias parasitism was evident in both adults and nestlings. Furthermore, a lower daily mass gain during nestling growth in males than in females following infections were found, whereas the effect of infections on body condition of adults was detrimental for females but not for males.

Conclusions: Age-specific differences in physiological trade-offs and ecological factors, such as nest predation would explain, at least in part, the observed host sex and age-related patterns in Tawny pipits.

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References
1.
Atkinson C, Dusek R, Woods K, Iko W . Pathogenicity of avian malaria in experimentally-infected Hawaii Amakihi. J Wildl Dis. 2000; 36(2):197-204. DOI: 10.7589/0090-3558-36.2.197. View

2.
Merino S, Moreno J, Sanz J, Arriero E . Are avian blood parasites pathogenic in the wild? A medication experiment in blue tits (Parus caeruleus). Proc Biol Sci. 2001; 267(1461):2507-10. PMC: 1690848. DOI: 10.1098/rspb.2000.1312. View

3.
Atkinson C, Dusek R, Lease J . Serological responses and immunity to superinfection with avian malaria in experimentally-infected Hawaii amakihi. J Wildl Dis. 2001; 37(1):20-7. DOI: 10.7589/0090-3558-37.1.20. View

4.
Jarvi S, Schultz J, Atkinson C . PCR diagnostics underestimate the prevalence of avian malaria (Plasmodium relictum) in experimentally-infected passerines. J Parasitol. 2002; 88(1):153-8. DOI: 10.1645/0022-3395(2002)088[0153:PDUTPO]2.0.CO;2. View

5.
Remes V, Martin T . Environmental influences on the evolution of growth and developmental rates in passerines. Evolution. 2003; 56(12):2505-18. DOI: 10.1111/j.0014-3820.2002.tb00175.x. View