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Serine Protease Inhibitors Block Invasion of Host Cells by Toxoplasma gondii
Author(s) -
Valérie Conseil,
M Soete,
JeanFrançois Dubremetz
Publication year - 1999
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.43.6.1358
Subject(s) - toxoplasma gondii , serine protease , biology , parasite hosting , protease , microbiology and biotechnology , serine , motility , protease inhibitor (pharmacology) , protozoa , enzyme , biochemistry , virology , immunology , virus , antibody , world wide web , computer science , antiretroviral therapy , viral load
We investigated the effect of protease inhibitors on the asexual development of the protozoan parasite Toxoplasma gondii. Among the inhibitors tested only two irreversible serine protease inhibitors, 3,4-dichloroisocoumarin and 4-(2-aminoethyl)-benzenesulfonyl fluoride, clearly prevented invasion of the host cells by specifically affecting parasite targets in a dose-dependent manner, with 50% inhibitory concentrations between 1 and 5 and 50 and 100 microM, respectively. Neither compound significantly affected parasite morphology, basic metabolism, or gliding motility within the range of the experimental conditions in which inhibition of invasion was demonstrated. No partial invasion was observed, meaning that inhibition occurred at an early stage of the interaction. These results suggest that at least one serine protease of the parasite is involved in the invasive process of T. gondii.

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