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Metacyclic Trypanosoma vivax possess a surface coat
Parasitology
|February 1, 1986
Summary
Coated metacyclic Trypanosoma vivax were found in tsetse fly hypopharynges. Electron microscopy confirmed these parasites acquire a surface coat before infecting mammals, crucial for antigenic variation.
Area of Science:
- Parasitology
- Molecular Biology
- Entomology
Background:
- Trypanosoma vivax is a protozoan parasite transmitted by tsetse flies.
- Metacyclic trypanosomes are the infective stage transmitted to mammalian hosts.
- The presence and timing of the surface coat acquisition in T. vivax metacyclics were previously debated.
Purpose of the Study:
- To investigate the presence and ultrastructure of metacyclic Trypanosoma vivax within the tsetse fly vector.
- To determine when T. vivax metacyclics acquire their surface coat in relation to transmission.
- To understand the functional implications of the T. vivax surface coat in the context of antigenic variation.
Main Methods:
- Tsetse flies infected with Trypanosoma vivax were dissected.
- Proboscides of infected flies were extensively searched for metacyclic trypanosomes.
- A specialized process was used to examine single, extruded, metacyclic trypanosomes.
- Electron microscopy was employed to visualize the surface coat of metacyclic T. vivax.
Main Results:
- Coated metacyclic Trypanosoma vivax were identified in the hypopharynges of infected tsetse flies.
- Metacyclic T. vivax were extruded in low numbers upon probing by the tsetse fly.
- Electron microscopic evidence demonstrated that metacyclic T. vivax acquire a surface coat prior to host contact, contradicting earlier findings.
- The surface coat plays a role in the antigenic variation of T. vivax.
Conclusions:
- Metacyclic Trypanosoma vivax are coated within the tsetse fly vector before transmission.
- The acquisition of a surface coat by metacyclic T. vivax is an early event, preceding mammalian host infection.
- The surface coat of T. vivax is functionally analogous to that of other tsetse-transmitted trypanosomes, likely mediating antigenic variation.