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The Journal of eukaryotic microbiology2004; 50 Suppl; 689-690; doi: 10.1111/j.1550-7408.2003.tb00689.x

Mode of action of ponazuril against Toxoplasma gondii tachyzoites in cell culture.

Abstract: Toxoplasma gondii is an important apicomplexan parasite of humans and other warm-blooded animals. Ponazuril is a triazine anticoccidial recently approved for use in horses in the United States. We investigated the mode of action of ponazuril against developing RH strain T. gondii tachyzoites in African green monkey kidney cells. Host cells were infected with 2.0 x 10(5) tachyzoites and treated with 5 microg/ml ponazuril. Cultures were fixed and examined by transmission electron microscopy 3 days after treatment. Ponazuril interfered with normal parasite division. This led to the presence of multinucleate schizonts stages. Up to six tachyzoites were observed partially budded from the surface of these schizonts. Large vacuoles developed in these schizonts and they eventually degenerated.
Publication Date: 2004-01-23 PubMed ID: 14736221DOI: 10.1111/j.1550-7408.2003.tb00689.xGoogle Scholar: Lookup
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  • Journal Article

Summary

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This research study explores how the drug ponazuril affects the growth and survival of Toxoplasma gondii, a parasite, in infected African green monkey kidney cells.

Introduction to Toxoplasma gondii and Ponazuril

  • Toxoplasma gondii is a type of parasite that can infect humans and various warm-blooded animals.
  • Ponazuril is an anti-parasitic drug that is mainly used to treat infections caused by parasites. Recently, the drug has been approved for use in horses in the United States.
  • The aim of this study was to understand how ponazuril works to combat the T. gondii infection within cell cultures, specifically within African green monkey kidney cells.

Methodology

  • In order to observe the action of the drug, the researchers infected African green monkey kidney cells with a strain of T. gondii called the RH strain.
  • The cells were then treated with ponazuril in a concentration of 5 micrograms per milliliter.
  • After treatment, the cells were fixed and observed under a transmission electron microscope after three days.

Observations and Conclusions

  • When examined under the electron microscope, the researchers noticed abnormalities in the division process of the parasites. Ponazuril seemed to hinder the normal division of the parasites.
  • This interference caused the formation of multinucleate schizont stages, a stage in the life cycle of the parasite in which it holds more than one nucleus.
  • In certain schizont stages, the formation of as many as six tachyzoites, or rapidly dividing forms of the parasite, was observed partially budding from the surface.
  • Large vacuoles, which are enclosed compartments within a cell that contain various substances, were seen within these schizonts. Over time, these schizonts with large vacuoles appeared to degenerate.
  • The study concluded that ponazuril induces changes in the life cycle and division process of T. gondii, leading to abnormal forms and eventual degeneration of the parasites.

Cite This Article

APA
Mitchell SM, Zajac AM, Davis WL, Lindsay DS. (2004). Mode of action of ponazuril against Toxoplasma gondii tachyzoites in cell culture. J Eukaryot Microbiol, 50 Suppl, 689-690. https://doi.org/10.1111/j.1550-7408.2003.tb00689.x

Publication

ISSN: 1066-5234
NlmUniqueID: 9306405
Country: United States
Language: English
Volume: 50 Suppl
Pages: 689-690

Researcher Affiliations

Mitchell, Sheila M
  • Center for Molecular Medicine and Infectious Diseases, Department of Biomedical Sciences and Pathobiology, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Tech, 1410 Prices Fork Road, Blacksburg, Virginia 24061-0342, USA.
Zajac, Anne M
    Davis, Wendell L
      Lindsay, David S

        MeSH Terms

        • Animals
        • Antiprotozoal Agents / toxicity
        • Cell Line
        • Chlorocebus aethiops
        • Kidney
        • Toxoplasma / drug effects
        • Toxoplasma / growth & development
        • Toxoplasma / ultrastructure
        • Triazines / toxicity

        Citations

        This article has been cited 1 times.
        1. Uddin T, McFadden GI, Goodman CD. Validation of Putative Apicoplast-Targeting Drugs Using a Chemical Supplementation Assay in Cultured Human Malaria Parasites. Antimicrob Agents Chemother 2018 Jan;62(1).
          doi: 10.1128/AAC.01161-17pubmed: 29109165google scholar: lookup