Leucocytozoon pterotenuis sp. nov. (Haemosporida, Leucocytozoidae): description of the morphologically unique species from the Grallariidae birds, with remarks on the distribution of Leucocytozoon parasites in the Neotropics

We describe morphologically unique Leucocytozoon pterotenuis sp. nov. (Haemosporida, Leucocytozoidae), the first reported leucocytozoid species developing in fusiform host cell found in a Neotropical passeriform bird. The type host of this parasite is the Chestnut-crowned Antpitta (Grallaria ruficap...

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Veröffentlicht in:Parasitology research (1987) 2015-03, Vol.114 (3), p.1031-1044
Hauptverfasser: Lotta, Ingrid A, Gonzalez, Angie D, Pacheco, M. Andreína, Escalante, Ananias A, Valkiūnas, Gediminas, Moncada, Ligia I, Matta, Nubia E
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container_title Parasitology research (1987)
container_volume 114
creator Lotta, Ingrid A
Gonzalez, Angie D
Pacheco, M. Andreína
Escalante, Ananias A
Valkiūnas, Gediminas
Moncada, Ligia I
Matta, Nubia E
description We describe morphologically unique Leucocytozoon pterotenuis sp. nov. (Haemosporida, Leucocytozoidae), the first reported leucocytozoid species developing in fusiform host cell found in a Neotropical passeriform bird. The type host of this parasite is the Chestnut-crowned Antpitta (Grallaria ruficapilla, Grallariidae), an elusive native passerine bird whose natural history remains, to a large degree, unexplored. This bird was captured in Palacio forest in the damping zone of Chingaza National Natural Park, Cundinamarca, Colombia, at 2900 m above sea level (asl). Gametocytes of the new species develop both in roundish and fusiform host cells. This parasite is readily morphologically distinguishable from the described Leucocytozoon species because its host cells possess the narrow (needle-like) spindle-shaped processes, which length markedly exceeds their width. Additionally, the host cell nucleus markedly extends into the processes. Phylogenetic relationships were constructed based on a fragment of the mitochondrial cytochrome b gene and the complete mitochondrial genome. Phylogenetic analysis placed the lineage of L. pterotenuis in different positions depending on the length of the sequence analyzed that is likely due to poor sampling of Leucocytozoon species, especially from rare or non-passerine hosts, as well as a paucity of complete mitochondrial sequences of these parasites. Available data indicate that Leucocytozoon parasites are distributed mainly in mountain regions of the Neotropics where unique morphological forms have been recently discovered. To a better knowledge of the diversity of Leucocytozoon spp. and their host–vector–parasite interactions in Neotropical countries, additional deep and intensive samplings are needed, particularly in orders different to Passeriformes.
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The type host of this parasite is the Chestnut-crowned Antpitta (Grallaria ruficapilla, Grallariidae), an elusive native passerine bird whose natural history remains, to a large degree, unexplored. This bird was captured in Palacio forest in the damping zone of Chingaza National Natural Park, Cundinamarca, Colombia, at 2900 m above sea level (asl). Gametocytes of the new species develop both in roundish and fusiform host cells. This parasite is readily morphologically distinguishable from the described Leucocytozoon species because its host cells possess the narrow (needle-like) spindle-shaped processes, which length markedly exceeds their width. Additionally, the host cell nucleus markedly extends into the processes. Phylogenetic relationships were constructed based on a fragment of the mitochondrial cytochrome b gene and the complete mitochondrial genome. Phylogenetic analysis placed the lineage of L. pterotenuis in different positions depending on the length of the sequence analyzed that is likely due to poor sampling of Leucocytozoon species, especially from rare or non-passerine hosts, as well as a paucity of complete mitochondrial sequences of these parasites. Available data indicate that Leucocytozoon parasites are distributed mainly in mountain regions of the Neotropics where unique morphological forms have been recently discovered. 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Andreína</creatorcontrib><creatorcontrib>Escalante, Ananias A</creatorcontrib><creatorcontrib>Valkiūnas, Gediminas</creatorcontrib><creatorcontrib>Moncada, Ligia I</creatorcontrib><creatorcontrib>Matta, Nubia E</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Parasitology research (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lotta, Ingrid A</au><au>Gonzalez, Angie D</au><au>Pacheco, M. 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The type host of this parasite is the Chestnut-crowned Antpitta (Grallaria ruficapilla, Grallariidae), an elusive native passerine bird whose natural history remains, to a large degree, unexplored. This bird was captured in Palacio forest in the damping zone of Chingaza National Natural Park, Cundinamarca, Colombia, at 2900 m above sea level (asl). Gametocytes of the new species develop both in roundish and fusiform host cells. This parasite is readily morphologically distinguishable from the described Leucocytozoon species because its host cells possess the narrow (needle-like) spindle-shaped processes, which length markedly exceeds their width. Additionally, the host cell nucleus markedly extends into the processes. Phylogenetic relationships were constructed based on a fragment of the mitochondrial cytochrome b gene and the complete mitochondrial genome. Phylogenetic analysis placed the lineage of L. pterotenuis in different positions depending on the length of the sequence analyzed that is likely due to poor sampling of Leucocytozoon species, especially from rare or non-passerine hosts, as well as a paucity of complete mitochondrial sequences of these parasites. Available data indicate that Leucocytozoon parasites are distributed mainly in mountain regions of the Neotropics where unique morphological forms have been recently discovered. To a better knowledge of the diversity of Leucocytozoon spp. and their host–vector–parasite interactions in Neotropical countries, additional deep and intensive samplings are needed, particularly in orders different to Passeriformes.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>25544705</pmid><doi>10.1007/s00436-014-4269-y</doi><tpages>14</tpages></addata></record>
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ispartof Parasitology research (1987), 2015-03, Vol.114 (3), p.1031-1044
issn 0932-0113
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language eng
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source MEDLINE; SpringerLink Journals
subjects Animals
Biomedical and Life Sciences
Biomedicine
Bird Diseases - epidemiology
Bird Diseases - parasitology
birds
cell nucleus
Colombia
Colombia - epidemiology
cytochrome b
Cytochromes b - genetics
forests
gametocytes
genes
Genome, Mitochondrial - genetics
Haemosporida - classification
Haemosporida - cytology
Haemosporida - genetics
Health aspects
Host-parasite relationships
hosts
Identification and classification
Immunology
Leucocytozoon
Medical Microbiology
Microbiology
mitochondria
mitochondrial DNA
mitochondrial genome
Morphology (Biology)
natural history
Neotropics
new species
Original Paper
parasites
parasitology
Passeriformes
Passeriformes - parasitology
Perching birds
Phylogeny
Protozoan Infections, Animal - epidemiology
Protozoan Infections, Animal - parasitology
Protozoans
species
Species Specificity
tropics
title Leucocytozoon pterotenuis sp. nov. (Haemosporida, Leucocytozoidae): description of the morphologically unique species from the Grallariidae birds, with remarks on the distribution of Leucocytozoon parasites in the Neotropics
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