Blood parasite infection causes marginal temporary costs in juvenile birds of prey

This is a Preprint and has not been peer reviewed. This is version 6 of this Preprint.

Add a Comment

You must log in to post a comment.


Comments

There are no comments or no comments have been made public for this article.

Downloads

Download Preprint

Supplementary Files
Authors

Tony Rinaud , Oliver Krüger, Meinolf Ottensmann, Nayden Chakarov

Abstract

Physiological costs from parasites arise by host colonization and defence activation and can vary according to the interactions of host and parasite traits and states. Parasite-induced costs crucially differ between stages of infection but this is difficult to assess in wild vertebrates. To evaluate the effects of blood parasite infection in juvenile birds, we compared physiological measures of common buzzard nestlings (Buteo buteo) between stages of infection with Leucocytozoon toddi, a Plasmodium-like pathogen. We related proxies of infection damage to experimentally manipulated infection intensity. We expected infection costs to be higher at the onset of infection and during peak parasitemia, compared with hosts with decreasing parasitemia and uninfected ones. We found body condition to be initially negatively related to infection intensity, but this relationship disappeared by the late stages of infection. Furthermore, there was no difference in growth rate and other physiological measures among infection stages. This indicates negligible costs of parasitism and transient virulence of Leucocytozoon in the nestling stage of host. To diminish infection-driven mortality, juveniles may evolve to be particularly parasite-tolerant which further enhances parasite transmission in the population. Our results demonstrate the necessity of including infection courses, rather than point estimates in models of fitness costs of infection.

DOI

https://doi.org/10.32942/osf.io/4tcqu

Subjects

Ecology and Evolutionary Biology, Immunology and Infectious Disease, Life Sciences, Other Ecology and Evolutionary Biology, Parasitology

Keywords

Avian malaria, Bird of prey, Host-parasite interaction, Immune system, infection burden, nestlings, physiology, tolerance

Dates

Published: 2022-02-24 23:16

Last Updated: 2025-01-08 16:24

Older Versions
License

CC-By Attribution-ShareAlike 4.0 International