Development of two species of the Trypanosoma theileri complex in tabanids.


Journal

Parasites & vectors
ISSN: 1756-3305
Titre abrégé: Parasit Vectors
Pays: England
ID NLM: 101462774

Informations de publication

Date de publication:
21 Mar 2022
Historique:
received: 07 12 2021
accepted: 18 02 2022
entrez: 22 3 2022
pubmed: 23 3 2022
medline: 24 3 2022
Statut: epublish

Résumé

Trypanosoma theileri species complex includes parasites of Bovidae (cattle, sheep, goat, etc.) and Cervidae (deer) transmitted mainly by Tabanidae (horse flies and deerflies) and keds (Hippoboscidae). While morphological discrimination of species is challenging, two big clades, TthI and TthII, each containing parasites isolated from bovids and cervids, have been identified phylogenetically. To date, the development in the vector has been studied in detail only for the ked-transmitted sheep parasite T. melophagium (TthII), while the fate of trypanosomes in tabanids was described only briefly by light microscopy. We collected infected tabanids of various species and identified trypanosomes by molecular phylogenetic analysis. The morphology and development of trypanosomes was studied using the combination of statistical analyses as well as light and electron microscopy. Two trypanosome species belonging to both TthI and TthII clades of the T. theileri complex were identified. The phylogenetic position of these two trypanosomes suggests that they parasitize deer. Both species were indiscernible by morphology in the vector and showed the same development in its intestine. In contrast to the previously described development of T. melophagium, both trypanosomes of tabanids only transiently infected midgut and settled mainly in the ileum, while pylorus and rectum were neglected. Meanwhile, the flagellates developing in the tabanid ileum (pyriform epimastigotes and metacyclic trypomastigotes) showed similarities to the corresponding stages in T. melophagium by morphology, mode of attachment to the host cuticle and formation of the fibrillar matrix surrounding the mass of developing parasites. In addition, for the first time to our knowledge we documented extraintestinal stages in these trypanosomes, located in the space between the epithelium and circular muscles. The development of different species of flagellates of the T. theileri complex in their insect vectors shows many similarities, which can be explained not only by their common origin, but also the same transmission mode, i.e. contamination of the oral mucosa with the gut content released after squashing the insect either by tongue or teeth. The observed differences (concerning primarily the distribution of developmental stages in the intestine) are associated rather with the identity of vectors than the phylogenetic position of parasites.

Sections du résumé

BACKGROUND BACKGROUND
Trypanosoma theileri species complex includes parasites of Bovidae (cattle, sheep, goat, etc.) and Cervidae (deer) transmitted mainly by Tabanidae (horse flies and deerflies) and keds (Hippoboscidae). While morphological discrimination of species is challenging, two big clades, TthI and TthII, each containing parasites isolated from bovids and cervids, have been identified phylogenetically. To date, the development in the vector has been studied in detail only for the ked-transmitted sheep parasite T. melophagium (TthII), while the fate of trypanosomes in tabanids was described only briefly by light microscopy.
METHODS METHODS
We collected infected tabanids of various species and identified trypanosomes by molecular phylogenetic analysis. The morphology and development of trypanosomes was studied using the combination of statistical analyses as well as light and electron microscopy.
RESULTS RESULTS
Two trypanosome species belonging to both TthI and TthII clades of the T. theileri complex were identified. The phylogenetic position of these two trypanosomes suggests that they parasitize deer. Both species were indiscernible by morphology in the vector and showed the same development in its intestine. In contrast to the previously described development of T. melophagium, both trypanosomes of tabanids only transiently infected midgut and settled mainly in the ileum, while pylorus and rectum were neglected. Meanwhile, the flagellates developing in the tabanid ileum (pyriform epimastigotes and metacyclic trypomastigotes) showed similarities to the corresponding stages in T. melophagium by morphology, mode of attachment to the host cuticle and formation of the fibrillar matrix surrounding the mass of developing parasites. In addition, for the first time to our knowledge we documented extraintestinal stages in these trypanosomes, located in the space between the epithelium and circular muscles.
CONCLUSIONS CONCLUSIONS
The development of different species of flagellates of the T. theileri complex in their insect vectors shows many similarities, which can be explained not only by their common origin, but also the same transmission mode, i.e. contamination of the oral mucosa with the gut content released after squashing the insect either by tongue or teeth. The observed differences (concerning primarily the distribution of developmental stages in the intestine) are associated rather with the identity of vectors than the phylogenetic position of parasites.

Identifiants

pubmed: 35313955
doi: 10.1186/s13071-022-05212-y
pii: 10.1186/s13071-022-05212-y
pmc: PMC8935851
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

95

Subventions

Organisme : Russian Science Foundation
ID : 21-14-00191
Organisme : European Regional Development Fund
ID : CZ.02.1.01/16_019/0000759

Informations de copyright

© 2022. The Author(s).

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Auteurs

Alexei Yu Kostygov (AY)

Zoological Institute of the Russian Academy of Sciences, St. Petersburg, 190121, Russia. kostygov@gmail.com.
Life Science Research Centre, Faculty of Science, University of Ostrava, 71000, Ostrava, Czech Republic. kostygov@gmail.com.

Alexander O Frolov (AO)

Zoological Institute of the Russian Academy of Sciences, St. Petersburg, 190121, Russia.

Marina N Malysheva (MN)

Zoological Institute of the Russian Academy of Sciences, St. Petersburg, 190121, Russia.

Anna I Ganyukova (AI)

Zoological Institute of the Russian Academy of Sciences, St. Petersburg, 190121, Russia.

Daria Drachko (D)

Zoological Institute of the Russian Academy of Sciences, St. Petersburg, 190121, Russia.

Vyacheslav Yurchenko (V)

Life Science Research Centre, Faculty of Science, University of Ostrava, 71000, Ostrava, Czech Republic.
Martsinovsky Institute of Medical Parasitology, Sechenov University, Moscow, 119435, Russia.

Vera V Agasoi (VV)

Zoological Institute of the Russian Academy of Sciences, St. Petersburg, 190121, Russia.
Natural-Geographical Faculty, Pskov State University, Pskov, 180000, Russia.

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