Assessment of the Activity of Decoquinate and Its Quinoline-O-Carbamate Derivatives against Toxoplasma gondii In Vitro and in Pregnant Mice Infected with T. gondii Oocysts
Autor: | Ramseier, Jessica, Imhof, Dennis, Anghel, Nicoleta, Hänggeli, Kai, Beteck, Richard M., Balmer, Vreni, Ortega Mora, Luis-Miguel, Sánchez Sánchez, Roberto, Ferre, Ignacio, Haynes, Richard K., Hemphill, Andrew |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Sanidad animal
proliferation Antiprotozoal Agents Toxoplasma gondii oocysts Organic chemistry 610 Medicine & health Article resistance Mice decoquinate QD241-441 quinolone Pregnancy Animals bradyzoites Molecular Structure 630 Agriculture tachyzoites 500 Science Infectious Disease Transmission Vertical Disease Models Animal Toxoplasmosis Animal Quinolines 570 Life sciences biology 590 Animals (Zoology) Female vertical transmission Carbamates Toxoplasma |
Zdroj: | Ramseier, Jessica; Imhof, Dennis; Anghel, Nicoleta; Hänggeli, Kai; Beteck, Richard M.; Balmer, Vreni; Ortega-Mora, Luis-Miguel; Sanchez-Sanchez, Roberto; Ferre, Ignacio; Haynes, Richard K.; Hemphill, Andrew (2021). Assessment of the Activity of Decoquinate and Its Quinoline-O-Carbamate Derivatives against Toxoplasma gondii In Vitro and in Pregnant Mice Infected with T. gondii Oocysts. Molecules, 26(21), p. 6393. Molecular Diversity Preservation International MDPI 10.3390/molecules26216393 Molecules, Vol 26, Iss 6393, p 6393 (2021) Molecules Volume 26 Issue 21 |
DOI: | 10.3390/molecules26216393 |
Popis: | The quinolone decoquinate (DCQ) is widely used in veterinary practice for the treatment of bacterial and parasitic infections, most notably, coccidiosis in poultry and in ruminants. We have investigated the effects of treatment of Toxoplasma gondii in infected human foreskin fibroblasts (HFF) with DCQ. This induced distinct alterations in the parasite mitochondrion within 24 h, which persisted even after long-term (500 nM, 52 days) treatment, although there was no parasiticidal effect. Based on the low half-maximal effective concentration (IC50) of 1.1 nM and the high selectivity index of > 5000, the efficacy of oral treatment of pregnant mice experimentally infected with T. gondii oocysts with DCQ at 10 mg/kg/day for 5 days was assessed. However, the treatment had detrimental effects, induced higher neonatal mortality than T. gondii infection alone, and did not prevent vertical transmission. Thus, three quinoline-O-carbamate derivatives of DCQ, anticipated to have better physicochemical properties than DCQ, were assessed in vitro. One such compound, RMB060, displayed an exceedingly low IC50 of 0.07 nM, when applied concomitantly with the infection of host cells and had no impact on HFF viability at 10 µM. As was the case for DCQ, RMB060 treatment resulted in the alteration of the mitochondrial matrix and loss of cristae, but the changes became apparent at just 6 h after the commencement of treatment. After 48 h, RMB060 induced the expression of the bradyzoite antigen BAG1, but TEM did not reveal any other features reminiscent of bradyzoites. The exposure of infected cultures to 300 nM RMB060 for 52 days did not result in the complete killing of all tachyzoites, although mitochondria remained ultrastructurally damaged and there was a slower proliferation rate. The treatment of mice infected with T. gondii oocysts with RMB060 did reduce parasite burden in non-pregnant mice and dams, but vertical transmission to pups could not be prevented. |
Databáze: | OpenAIRE |
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