Abstract

BackgroundHaemosporidian parasites of the genus Haemoproteus (Haemoproteidae) are widespread and cause haemoproteosis in birds and therefore, their diversity, ecology and evolutionary biology have become subjects of intensive research. However, the vectors and transmission patterns of haemoproteids as well as the epidemiology of haemoproteosis remain insufficiently investigated. Several species of Culicoides (Ceratopogonidae) support complete sporogony of haemoproteids belonging to the subgenus Parahaemoproteus. However, experimental research with these fragile insects is difficult to design in the field, particularly because their abundance markedly depends on seasonality. This is an obstacle for continuous sampling of sufficient numbers of naturally infected or experimentally exposed midges from wildlife. We developed simple methodology for accessing sporogonic development of haemoproteids in laboratory-reared Culicoides nubeculosus. This study aimed to describe the mosaic of methods constituting this methodology, which was applied for investigation of the sporogonic development of Haemoproteus (Parahaemoproteus) pastoris, a widespread parasite of the common starling Sturnus vulgaris.MethodsThe methodology consists of the following main stages: (i) laboratory rearing of C. nubeculosus from the egg stage to adult insects; (ii) selection of naturally infected birds, the donors of mature gametocytes to expose biting midges; (iii) experimental exposure of insects and their laboratory maintenance; and (iv) dissection of exposed insects. Biting midges were exposed to H. pastoris (cytochrome b lineage hLAMPUR01) detected in one naturally infected common starling. Engorged insects were dissected at intervals in order to follow sporogony. Microscopic examination and PCR-based methods were used to identify the sporogonic stages and to confirm the presence of the parasite lineage in infected insects, respectively.ResultsCulicoides nubeculosus females were successfully reared and exposed to H. pastoris, which completed sporogonic development 7–9 days post-infection when sporozoites were observed in the salivary glands.ConclusionsThe new methodology is easy to use and non-harmful for birds, providing opportunities to access the sporogonic stages of Parahaemoproteus parasites, which might be used in a broad range of parasitology and genetic studies. Culicoides nubeculosus is an excellent experimental vector of subgenus Parahaemoproteus and is recommended for various experimental studies aiming investigation of sporogony of these pathogens.

Highlights

  • Haemosporidian parasites of the genus Haemoproteus (Haemoproteidae) are widespread and cause haemoproteosis in birds and their diversity, ecology and evolutionary biology have become subjects of intensive research

  • The primers HaemF and HaemR2 were applied for the second polymerase chain reaction (PCR), which amplifies deoxyribonucleic acid (DNA) of Haemoproteus and Plasmodium parasites

  • Culicoides nubeculosus is an excellent experimental vector of avian haemoproteids belonging to the subgenus Parahaemoproteus due to easy maintaining in laboratory

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Summary

Introduction

Haemosporidian parasites of the genus Haemoproteus (Haemoproteidae) are widespread and cause haemoproteosis in birds and their diversity, ecology and evolutionary biology have become subjects of intensive research. Haemoproteus parasites were discovered in 1890 [12], and it took over 60 years to determine that Culicoides biting midges are involved in the transmission of haemoproteids belonging to the subgenus Parahaemoproteus [13] Experimental research with these tiny and fragile insects is challenging due to difficulties in sampling and maintaining sufficient numbers of females that support complete sporogonic development in laboratory conditions [1, 14]. There is still not much progress in experimental research with avian haemoproteids due to the insufficiently developed methodology for accessing the invasive stages of these parasites, sporozoites, as well as other sporogonic stages (ookinetes and oocysts) We developed such methodology using laboratory-reared biting midges Culicoides nubeculosus. It consists of several steps, each involving an array of simple methods, which can be applied in any laboratory

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