Hostname: page-component-848d4c4894-pftt2 Total loading time: 0 Render date: 2024-06-03T00:25:30.031Z Has data issue: false hasContentIssue false

Special issue: avian malaria

Published online by Cambridge University Press:  11 January 2024

Lisa C. Ranford-Cartwright*
Affiliation:
School of Biodiversity, One Health and Veterinary Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow UK
*
Corresponding author: Lisa C. Ranford-Cartwright; Email: Lisa.ranford-cartwright@glasgow.ac.uk

Abstract

Avian malaria parasites or haemosporidia are found in bird species worldwide. This special issue focuses on 3 most commonly studied genera: Haemoproteus, Plasmodium and Leucocytozoon. Seven research articles and reviews are provided to illustrate the breadth of knowledge of the diversity of avian malaria parasites in different regional habitats and across bird species, and the use of avian haemosporidian systems to examine host–parasite eco-evolutionary questions.

Type
Editorial
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press

Introduction

Haemosporidia are a large group of intracellular parasitic protozoa which infect amphibians, reptiles, birds and mammals, and which use haematophagous dipteran insects as vectors. This special issue focuses on Avian haemosporidia, often called Avian malaria parasites, which played important roles in early research on human malaria (Cox, Reference Cox2010), but also are of major importance in their own right as parasites of bird species across the world (Valkiunas, Reference Valkiunas2005). Avian haemosporidia are important economically for their effects on productivity and mortality in domestic birds, and in captive birds in zoos and aviaries. In wild birds, they have been shown to impact negatively on the body condition, survival, migration and reproduction of their hosts (Lapointe et al., Reference Lapointe, Atkinson and Samuel2012). Avian haemosporidian parasites have also been useful as model systems to explore evolutionary and ecological parasite–host relationships (Dunn and Outlaw, Reference Dunn and Outlaw2019).

The different haemosporidian genera have different lifecycles in the avian host. Depending on the genus, asexual (mitotic) replication takes place in the reticuloendothelial cells of the tissues, and/or the red blood cells, where the parasites multiply as haploid clones. The sexual stages (gametocytes) of all genera are found in the circulating red blood cells, where they are taken up by the insect vectors during blood feeding, and the sexual phase is completed in the vector.

Avian haemosporidia are found on all continents except Antarctica, infecting a very large range of host species. There are more than 200 morphologically-distinct species of Plasmodium, Haemoproteus and Leucocytozoon that develop in a variety of bird and vector species. Plasmodium is often considered to be a generalist, transmitted between different avian orders, whereas Leucocytozoon and Haemoproteus species tend to exhibit a higher degree of specialism towards their vertebrate hosts (Valkiunas, Reference Valkiunas2005). The diversity of haemosporidia is closely linked to the richness of avian species, so the parasite community present in a specific location is influenced by the composition of avian host species, as well as by the distribution of vectors.

Haemoproteus are, globally, the most prevalent of the haemosporidia. Over 150 species have been defined, categorized into 2 subgenera: Haemoproteus comprises species that are transmitted by Hippoboscidae (louse flies), and Parahaemoproteus are species transmitted by Ceratopogonidae (biting midges). Over 40 species within the genus Plasmodium affect birds; the parasites are transmitted by mosquitoes, mainly Culicidae (e.g. Culex). Plasmodium relictum is one of the most widespread avian malaria parasites in the world, and has been linked to the extinction of some bird species (Atkinson and Samuel, Reference Atkinson and Samuel2010). Leucocytozoon parasites are unique amongst the avian haemosporidia as they only infect birds. The genus is the least studied of the avian haemosporidia. There are over 45 morphologically distinct species (Valkiunas and Iezhova, Reference Valkiunas and Iezhova2023). Leucocytozoa are transmitted by black flies (Simuliidae), except for 1 species, Leucocytozoon caulleryi, which is transmitted by biting midges (Ceratopogonidae).

The prevalence of avian haemosporidia was shown to be influenced by factors including temperature, altitude, latitude and season (reviewed in Sehgal, Reference Sehgal2015). Generally, Haemoproteus is more prevalent at higher elevations and in more arid environments. Leucocytozoon is also found more commonly at higher elevations, whereas Plasmodium species are more frequently found at lower elevations. Prevalence has also been shown in some studies to be affected by the bird host age, sex, migratory status, foraging behaviour (whether at ground level or in the canopy), body mass and plumage colour (reviewed in Fecchio et al., Reference Fecchio, Clark, Bell, Skeen, Lutz, De La Torre, Vaughan, Tkach, Schunck, Ferreira, Braga, Lugarini, Wamiti, Dispoto, Galen, Kirchgatter, Sagario, Cueto, González-Acuña, Inumaru, Sato, Schumm, Quillfeldt, Pellegrino, Dharmarajan, Gupta, Robin, Ciloglu, Yildirim, Huang, Chapa-Vargas, Álvarez-Mendizábal, Santiago-Alarcon, Drovetski, Hellgren, Voelker, Ricklefs, Hackett, Collins, Weckstein and Wells2021). Part of the explanation for these observations lies in the vector distribution and behaviour: blackflies which transmit Leucocytozoon species are more prevalent at higher altitudes, whereas mosquitoes which transmit Plasmodium are found in higher abundance at lower elevations. For Haemoproteus species, the Hippoboscidae vectors (louse flies) live most of their adult life on their host (obligate ectoparasitism), and therefore may be less influenced by different habitats in which their hosts move, whereas Parahaemoproteus vectors, biting midges (Ceratopogonidae), are opportunistic feeders on birds (free living ectoparasites).

The avian haemosporidia have very high genetic diversity. Studies on species diversity, host range and geographical distribution of avian haemosporidia were greatly aided by the development of a sequence database of cytochrome b gene lineages, known as MalAvi (Bensch et al., Reference Bensch, Hellgren and Perez-Tris2009). The database currently catalogues parasites from over 2000 bird species with around 5000 unique lineages in total, over 2000 of which are Haemoproteus species, and the remaining lineages are split evenly between Leucocytozoon and Plasmodium species.

Scope of the special issue

The present special issue has 6 articles and 1 review. It begins with 3 papers describing the diversity of avian haemosporidia in 2 distinct habitats in Northern and Southern America respectively, and within larid seabirds in South Africa. The 4th paper describes a detailed phylogenetic analysis of a new species of Leucocytozoon, identified in a terrestrial bird in Brazil. The next 2 papers address evolutionary questions in avian malaria parasites, one examining host–parasite co-phylogeny in Haemoproteus infections in passerine birds in the United Kingdom, and the other haemosporidian infections in suboscine passerine birds, the Asities, native to Madagascar. Finally, the issue closes with a review of vector immune responses to infection with haemosporidian parasites. A brief summary of the individual contributions is given below.

Viridiana Martinez and colleagues report on the diversity of avian haemosporidia in the Davis Mountain sky islands of West Texas (Martinez et al., Reference Martinez, Keith, Grace and Voelker2023). Sky islands are distinct, isolated mountain habitats, characterized by great species richness, surrounded by radically different lowland habitats such as deserts. The Davis Mountain region has rich species diversity with over 277 bird species, and also forms a temperate breeding ground for migrating birds. Both resident and migratory bird species were sampled, and more than 40% were found to be infected with haemosporidian parasites. Haemoproteus was the most common genus, but Plasmodium and Leucocytozoon were also present, and a small number of birds were infected with multiple species or lineages. The overall prevalence of infection, and the lineages present, were comparable to that seen in similar habitats in New Mexico, although 55% of the lineages found were previously unreported. Specialist lineages were more common amongst Haemoproteus than Plasmodium infections, which were mostly generalist. Comparing migratory and resident species, the authors concluded that host phylogeny played a more significant role in parasite prevalence than migratory status. Adult birds had higher prevalence than hatch-year birds, which the authors suggest could be due to a down-regulation of immune responses during reproduction, an increased exposure to vectors during nesting or foraging activities, or a higher mortality in infected juveniles.

Daniela de Angeli Dutra and co-authors studied how host phylogeny and seasonality influenced haemosporidian infection in the Caatinga, a seasonally dry tropical forest in Brazil, with over 200 bird species (de Angeli Dutra et al., Reference de Angeli Dutra, Khan, Ferreira, Beirão, Pichorim, Moreira and Braga2023). Over 900 samples were taken over 4 seasons, and they found a higher diversity and prevalence of haemosporidian infections than has been reported from other regions of Brazil: an average prevalence of 51% with 32 different lineages. Haemoproteus was the most common genus, followed by Plasmodium (Leucocytozoon was not studied as it is believed to be at low prevalence in Brazil). Five lineages of Haemoproteus were found, mainly in columbiformes, with 2 lineages found in passerines. Seventeen lineages of Plasmodium were found, mainly in passerines. Parasite prevalence was found to be influenced by seasonality, with higher prevalence in the rainy season for Plasmodium, but in the dry season for Haemoproteus. This was perhaps surprising since the vectors are most abundant during the rainy season, but columbiformes were more common in the dry season. Overall, the study revealed a very high level of phylogenetic association between haemosporidian infection in birds: closely-related avian hosts harboured similar prevalence patterns within the community. In contrast with previous studies in Brazil which found Plasmodium to be the most common haemosporidian genus, the high prevalence of Haemoproteus observed could be explained by the high abundance of columbiformes in the Caatinga.

Ralph Vanstreels and co-authors present a survey of infections in Laridae aquatic birds – a suborder with more than 170 species including gulls, skuas and puffins (Vanstreels et al., Reference Vanstreels, Chagas, Valkiūnas, dos Anjos, Parsons, Roberts, Snyman, Hurtado, Kirchgatter, Ludynia and Pistorius2023). Previous studies in this avian suborder revealed a low diversity of haemosporidian parasites, which could be explained by a limited sampling effort, or to their occupation of habitats with less abundant vectors. They reported 4 species of Haemoproteus in 2 gull species in South Africa. Almost 20% of wild kelp gulls (Larus dominicanus) were found to be infected with Haemoproteus jenniae, the first record of this species in Africa, and only the 4th previous recording globally, forming a new cytb lineage different to the existing H. jenniae lineages. This species was also found, for the first time, in 1 sample of a Hartlaub's gull (Larus hartlaubii), and thus appears to be distributed across Laridae seabirds. In addition, the authors provide a redescription of Haemoproteus skuae taken from a brown skua – previously described only once from the same host species, in the same location in Cape Town, in 2010.

Utilizing morphological and molecular data, Lis Vieira and co-authors report on the analysis of the first mitochondrial genome of a new species of Leucocytozoon found in a non-migratory Brazilian bird, the Red-legged Seriema (Cariama cristata), the first report of a competent host for leucocytozoa in Brazil (Vieira et al., Reference Vieira, Pereira, Vilela, Landau, Pacheco, Escalante, Ferreira and Braga2023). The new species is named Leucocytozoon cariamae, and is distinguished from the Leucocytozoon fringillarum group by its microgamete morphology. The most closely-related species based on the mitochondrial genomes are leucocytozoa found in birds of different orders (tawny owls, American kestrel), but with different and distinct morphology. Leucocytozoon transmission has previously been deemed negligible outside the highland areas of Brazil, despite the presence of the vector blackflies, but the authors suggest that submicroscopic infections may be present in the Neotropics at low- and mid-elevations. The bird was also coinfected with Haemoproteus pulcher, and the authors present additional analyses of the mitochondrial genomes of H. pulcher and Haemoproteus catharti that suggest these species are more closely related to the reptile parasites Haemocystidium, with which they form a monophyletic group.

Cospeciation, co-phylogeny and the origins of haemosporidia

As parasites and their hosts co-evolved, some parasites specialized to 1 host species, with high efficiency, whereas others adapted to several hosts, with a trade-off of lower efficiency. Specialization can trigger evolutionary arms races and can result in speciation in both parasite and host (co-speciation). Processes such as host-switching, where parasites successfully infect and adapt to a new host, duplication, where a parasite diverges and speciates within its original host, sorting, where a parasite becomes extinct within a host species, and inertia, where hosts speciate but parasites fail to diverge, all affect host–parasite relationships.

Charlie Woodrow and co-authors have used Haemoproteus infections in passeriform bird hosts to investigate host–parasite co-phylogeny (Woodrow et al., Reference Woodrow, Rosca, Fletcher, Hone, Ruta, Hamer and Dunn2023). Sampling 32 passerine species in the south of England, they found almost 60% to be infected with Haemoproteus, and identified 30 lineages, 9 of which were novel (i.e. not in the MalAvi database). 23 lineages were found only in 1 bird species. The highest parasite richness was found in the blackcap Sylvia atricapilla, which also had the highest parasite specificity – 7 lineages were found, 6 of which were exclusive to the blackcap. The presence of a generalist parasite lineage masked an underlying co-phylogeny – removing this from the analysis allowed the identification of host-switching and duplication as contributory factors favouring coevolution of parasite and host.

Hannah Barbon and co-authors present a study of haemosporidian infections in a family of birds – the Asities (Philepittidae) – that are native to Madagascar (Barbon et al., Reference Barbon, Berthoud, Woog and Musa2023). The Asities represent a single radiation, with 4 extant species in 2 genera, that feed on fruit (Philepitta spp.) and nectar (Neodrepanis spp.). They compared parasite infection in Neodrepanis spp. to that found in Malagasy sunbirds (Cinnyris spp.), with which they share habitat and nectar foraging behaviour, to test if ecological factors were stronger influences on parasite prevalence than phylogenetic relationships between the avian hosts. They found a high prevalence of haemosporidian infection in all bird taxa studied. Cinnyris species were found to have predominantly specialist haemosporidian lineages, whereas Philepittidae were found to have mainly generalist lineages, with no Haemoproteus and few mixed infections, suggesting that these birds may be resistant to the parasite species circulating in Madagascar. Haemosporidian parasite composition was more similar for more closely related avian hosts than those that shared habitat and foraging behaviour, and the authors conclude that haemosporidian infections are driven primarily by host phylogenetic rather than ecological factors.

Vectors

Finally, Irene Hernandez-Caballero and colleagues present a systematic review of vector responses to infection with haemosporidian parasites, focussing on gene expression in Culex quinquefasciatus mosquitoes during infection with P. relictum, and comparing the results with Anopheles infection with human malaria Plasmodium falciparum (Hernandez-Caballero et al., Reference Hernandez-Caballero, Hellgren and Garcia-Longoria2023). They discuss the relative importance of the 3 main immune response pathways: Toll, Imd and JAK/STAT, as well as changes in metabolic pathways observed during infection in the different parasite–vector combinations. The authors also highlight the relative paucity of studies on avian malaria – vector interactions.

Summary

The papers presented in this special issue serve to highlight the extreme diversity within the avian malaria parasites, and the growing use of these parasites to explore evolutionary questions. Avian hosts globally exhibit a high prevalence of infection with haemosporidian parasites. Both generalist and specialist lineages of haemosporidians are common, and all papers report novel lineages, adding to the thousands already in the MalAvi database. Host phylogeny is repeatedly identified in the papers presented here as significant in explaining lineage prevalence. The description of a new species, Haemoproteus cariamae, and the redescription of H. skuae continue the long history of Parasitology in the taxonomy of parasite species.

Financial support

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

Competing interest

None.

References

Atkinson, CT and Samuel, MD (2010) Avian malaria Plasmodium relictum in native Hawaiian forest birds: epizootiology and demographic impacts on `apapane Himatione sanguinea. Journal of Avian Biology 41, 357366.CrossRefGoogle Scholar
Barbon, H, Berthoud, JL, Woog, F and Musa, S (2023) Haemosporidian parasite infections of Malagasy Philepittidae and Nectariniidae are driven by phylogeny rather than ecology. Parasitology 150, 13161329.Google Scholar
Bensch, S, Hellgren, O and Perez-Tris, J (2009) MalAvi: a public database of malaria parasites and related haemosporidians in avian hosts based on mitochondrial cytochrome b lineages. Molecular Ecology Resources 9, 13531358.CrossRefGoogle ScholarPubMed
Cox, FEG (2010) History of the discovery of the malaria parasites and their vectors. Parasites & Vectors 3, 5.CrossRefGoogle ScholarPubMed
de Angeli Dutra, D, Khan, AU, Ferreira, FC, Beirão, MV, Pichorim, M, Moreira, PA and Braga, ÉM (2023) Host phylogeny and seasonality shapes avian haemosporidian prevalence in a Brazilian biodiverse and dry forest: the Caatinga. Parasitology 150, 12771285.Google Scholar
Dunn, JC and Outlaw, DC (2019) Flying into the future: avian haemosporidians and the advancement of understanding host–parasite systems. Parasitology 146, 14871489.CrossRefGoogle ScholarPubMed
Fecchio, A, Clark, NJ, Bell, JA, Skeen, HR, Lutz, HL, De La Torre, GM, Vaughan, JA, Tkach, VV, Schunck, F, Ferreira, FC, Braga, ÉM, Lugarini, C, Wamiti, W, Dispoto, JH, Galen, SC, Kirchgatter, K, Sagario, MC, Cueto, VR, González-Acuña, D, Inumaru, M, Sato, Y, Schumm, YR, Quillfeldt, P, Pellegrino, I, Dharmarajan, G, Gupta, P, Robin, VV, Ciloglu, A, Yildirim, A, Huang, X, Chapa-Vargas, L, Álvarez-Mendizábal, P, Santiago-Alarcon, D, Drovetski, SV, Hellgren, O, Voelker, G, Ricklefs, RE, Hackett, SJ, Collins, MD, Weckstein, JD and Wells, K (2021) Global drivers of avian haemosporidian infections vary across zoogeographical regions. Global Ecology and Biogeography 30, 23932406.CrossRefGoogle Scholar
Hernandez-Caballero, I, Hellgren, O and Garcia-Longoria, L (2023) Genomic advances in the study of the mosquito vector during avian malaria infection. Parasitology 150, 13301339.Google Scholar
Lapointe, DA, Atkinson, CT and Samuel, MD (2012) Ecology and conservation biology of avian malaria. Annals of the New York Academy of Sciences 1249, 211226.CrossRefGoogle ScholarPubMed
Martinez, V, Keith, KD, Grace, JK and Voelker, G (2023) Avian haemosporidians of breeding birds in the Davis Mountains sky-islands of west Texas. Parasitology 150, 12661276.Google Scholar
Sehgal, RNM (2015) Manifold habitat effects on the prevalence and diversity of avian blood parasites. International Journal for Parasitology: Parasites and Wildlife 4, 421430.Google ScholarPubMed
Valkiunas, G (2005) Avian Malaria Parasites and Other Haemosporidia. Boca Raton, Florida: CRC Press.Google Scholar
Valkiunas, G and Iezhova, TA (2023) Insights into the biology of leucocytozoon species (Haemosporida, Leucocytozoidae): why is there slow research progress on agents of leucocytozoonosis? Microorganisms 11, 1251. https://doi.org/10.3390/microorganisms11051251CrossRefGoogle ScholarPubMed
Vanstreels, RET, Chagas, CRF, Valkiūnas, G, dos Anjos, CC, Parsons, NJ, Roberts, DG, Snyman, A, Hurtado, R, Kirchgatter, K, Ludynia, K and Pistorius, PA (2023) Haemoproteus jenniae (Haemoproteidae, Haemosporida) infects gulls (Larus spp.) in South Africa, with redescription of Haemoproteus skuae. Parasitology 150, 12861295.Google Scholar
Vieira, LMC, Pereira, PHO, Vilela, DAR, Landau, I, Pacheco, MA, Escalante, AA, Ferreira, FC and Braga, ÉM (2023) Leucocytozoon cariamae n. sp. and Haemoproteus pulcher coinfection in Cariama cristata (Aves: Cariamiformes): first mitochondrial genome analysis and morphological description of a leucocytozoid in Brazil. Parasitology 150, 12961306.Google Scholar
Woodrow, C, Rosca, AT, Fletcher, RM, Hone, AL, Ruta, M, Hamer, KC and Dunn, JC (2023) Haemoproteus parasites and passerines: the effect of local generalists on inferences of host–parasite co-phylogeny in the British Isles. Parasitology 150, 13071315.Google Scholar