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Bioluminescence Imaging to Detect Late Stage Infection of African Trypanosomiasis
Published on: May 18, 2016
Effect of dibutyltin(IV) on the ultrastructure of African Trypanosoma spp
M N Shuaibu1, H Kanbara, T Yanagi
1Protozoology Department, Institute of Tropical Medicine, Nagasaki University, 1-12-4 Sakamoto, 852-8523 Nagasaki-shi, Japan. nshuaibu@yahoo.com
Abstract:
Diorganotins (R2SnX2) are compounds with a wide variety of biological properties. In an attempt to follow the morphological events and to characterize the toxic effects of diorganotins on in vitro cultured African Trypanosoma spp., the ultrastructural alterations induced on the parasites by dibutyltins (Bu2SnX2) were followed. The data obtained indicate that these compounds induced irreparable damage to the in vitro cultured bloodstream forms of the parasites. Transmission and scanning electron microscopy allowed observations on the perturbation of the kinetoplast, extensive cytoplasmic swellings, disconfiguration around the flagellar pocket and membrane disintegration. Fluorescence microscopy with 4,6-diamidine-2-phenylindole stain was also used to visualize the survival or degeneration of kDNA. Understanding the collateral cellular toxic effect of these compounds on the parasites may shed light on the possible mechanism by which they kill trypanosomes. Agarose gel electrophoresis resolution of isolated kDNAs revealed no fragmentation by these compounds following in vitro incubation at 37 degrees C. However, fragmentation was observed from the gel electrophoresis of kDNA isolated from in vitro cultured Bu2SnX2-exposed parasites. Transmission electron microscopy of the kDNAs revealed the same pattern as observed with gel electrophoresis. These results provide evidence for the possible involvement of the Bu2Sn moiety in the in vivo-induced fragmentation of trypanosomal kDNA and consequent trypanolysis. This observation also underlies the relevance of organometallics in the therapy of African trypanosomiasis.
Insights
Dibutyltins cause severe damage to African trypanosomes, including kinetoplast and DNA fragmentation. This organometallic compound shows potential for treating African trypanosomiasis.
Area of Science:
- Parasitology
- Toxicology
- Medicinal Chemistry
Background:
- Diorganotins (R2SnX2) exhibit diverse biological activities.
- African trypanosomiasis remains a significant health concern, necessitating novel therapeutic strategies.
- Understanding the mechanisms of anti-parasitic compounds is crucial for drug development.
Purpose of the Study:
- To investigate the ultrastructural effects of dibutyltins (Bu2SnX2) on in vitro cultured African Trypanosoma spp.
- To characterize the toxic mechanisms and potential of diorganotins in trypanosome cell death.
Main Methods:
- Transmission and scanning electron microscopy to observe morphological changes in parasites.
- Fluorescence microscopy using 4,6-diamidine-2-phenylindole stain to assess kinetoplast DNA (kDNA) integrity.
- Agarose gel electrophoresis to analyze kDNA fragmentation patterns.
Main Results:
- Dibutyltins induced significant ultrastructural damage, including kinetoplast perturbation, cytoplasmic swelling, and membrane disintegration.
- kDNA fragmentation was observed in parasites exposed to dibutyltins, correlating with cell death.
- No direct fragmentation of isolated kDNA by dibutyltins in vitro was detected, suggesting an indirect mechanism.
Conclusions:
- Dibutyltins induce severe, irreparable damage to African trypanosomes, involving kDNA fragmentation.
- The findings suggest a potential therapeutic role for organometallic compounds, specifically dibutyltins, in treating African trypanosomiasis.
- Further research into organometallic compounds could lead to novel anti-trypanosomal drugs.
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