Affiliations 

  • 1 Department of Animal Ecology and Systematics, Justus-Liebig Universität Gießen, Heinrich-Buff-Ring 26, D-35392, Gießen, Germany. juan.f.masello@bio.uni-giessen.de
  • 2 Departamento de Biomedicina y Biotecnologıía, Area Parasitologıía, Facultad de Farmacia, Universidad de Alcalá (UAH), NII Km 33.600, 28805 Alcalá de Henares, Madrid, Spain
  • 3 Department of Animal Ecology and Systematics, Justus-Liebig Universität Gießen, Heinrich-Buff-Ring 26, D-35392, Gießen, Germany
  • 4 Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, INF 364, 69120, Heidelberg, Germany
  • 5 Centro de Ecología, Instituto Venezolano de Investigaciones Científicas, Altos de Pipe, Venezuela
  • 6 Museum and Institute of Zoology, Polish Academy of Sciences, Wilcza 64, 00-679, Warsaw, Poland
  • 7 Institute of Natural and Mathematical Sciences, Massey University, Auckland, New Zealand
  • 8 Instituto Multidisciplinario sobre Ecosistemas y Desarrollo Sustentable, Universidad Nacional del Centro de la Provincia de Buenos Aires, Tandil, Argentina
  • 9 Fundación para la Investigación y la Conservación de los Loros en Bolivia (CLB), Avenida Francisco Mora, Santa Cruz de la Sierra, Bolivia
  • 10 Department of Animal Biology, School of Integrative Biology, University of Illinois, Urbana-Champaign, IL, 61801, USA
  • 11 ZoologyDepartment (CRUB-UNCo), INIBIOMA (Universidad Nacional del Comahue-CONICET), 8400, Bariloche, Argentina
  • 12 Province des Iles Loyauté, Direction du Développement Economique, BP 50 98820, Wé, Lifou, New Caledonia
  • 13 Auckland Zoological Park, Motions Road, Western Springs, Auckland, 1022, New Zealand
  • 14 Centro de Bioquímica y Biofísica, Instituto Venezolano de Investigaciones Científicas, Altos de Pipe, Venezuela
  • 15 Projeto Papagaio-verdadeiro, Fundação Neotropica do Brasil, Campo Grande, Brazil
  • 16 Base Multifuncional do CEMAVE em Florianópolis/SC, Estação Ecológica Carijós - ICMBio, Florianópolis, Brazil
  • 17 Projeto de Conservação do papagaio-de-cara-roxa, SPVS - Sociedade de Pesquisa em Vida Selvagem e Educação Ambiental, Curitiba, Brazil
  • 18 Institute of Ecology and Biodiversity, Departamento de Ciencias Ecológicas, Facultad de Ciencias Universidad de Chile, Santiago, Chile
  • 19 Katala Foundation, Inc., Puerto Princesa City, Palawan, Philippines
  • 20 Departamento de Ecología Evolutiva, Museo Nacional de Ciencias Naturales, Consejo Superior de Investigaciones Científicas, 28006, Madrid, Spain
Parasit Vectors, 2018 Jun 19;11(1):357.
PMID: 29921331 DOI: 10.1186/s13071-018-2940-3

Abstract

BACKGROUND: Parasites can exert selection pressure on their hosts through effects on survival, on reproductive success, on sexually selected ornament, with important ecological and evolutionary consequences, such as changes in population viability. Consequently, hemoparasites have become the focus of recent avian studies. Infection varies significantly among taxa. Various factors might explain the differences in infection among taxa, including habitat, climate, host density, the presence of vectors, life history and immune defence. Feeding behaviour can also be relevant both through increased exposure to vectors and consumption of secondary metabolites with preventative or therapeutic effects that can reduce parasite load. However, the latter has been little investigated. Psittaciformes (parrots and cockatoos) are a good model to investigate these topics, as they are known to use biological control against ectoparasites and to feed on toxic food. We investigated the presence of avian malaria parasites (Plasmodium), intracellular haemosporidians (Haemoproteus, Leucocytozoon), unicellular flagellate protozoans (Trypanosoma) and microfilariae in 19 Psittaciformes species from a range of habitats in the Indo-Malayan, Australasian and Neotropical regions. We gathered additional data on hemoparasites in wild Psittaciformes from the literature. We considered factors that may control the presence of hemoparasites in the Psittaciformes, compiling information on diet, habitat, and climate. Furthermore, we investigated the role of diet in providing antiparasitic secondary metabolites that could be used as self-medication to reduce parasite load.

RESULTS: We found hemoparasites in only two of 19 species sampled. Among them, all species that consume at least one food item known for its secondary metabolites with antimalarial, trypanocidal or general antiparasitic properties, were free from hemoparasites. In contrast, the infected parrots do not consume food items with antimalarial or even general antiparasitic properties. We found that the two infected species in this study consumed omnivorous diets. When we combined our data with data from studies previously investigating blood parasites in wild parrots, the positive relationship between omnivorous diets and hemoparasite infestation was confirmed. Individuals from open habitats were less infected than those from forests.

CONCLUSIONS: The consumption of food items known for their secondary metabolites with antimalarial, trypanocidal or general antiparasitic properties, as well as the higher proportion of infected species among omnivorous parrots, could explain the low prevalence of hemoparasites reported in many vertebrates.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.