Essential oil of oregano (Origanum vulgare L.) reduces infection and proliferation of Toxoplasma gondii in BeWo cells with induction of autophagy and death of tachyzoites through a mechanism similar to necrosis
Toxoplasmosis poses a global health threat, ranging from asymptomatic cases to severe, potentially fatal manifestations, especially in immunocompromised individuals and congenital transmission. Prior research suggests that oregano essential oil (OEO) exhibits diverse biological effects, including an...
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Veröffentlicht in: | Parasitology research (1987) 2024-05, Vol.123 (5), p.217, Article 217 |
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Sprache: | eng |
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Zusammenfassung: | Toxoplasmosis poses a global health threat, ranging from asymptomatic cases to severe, potentially fatal manifestations, especially in immunocompromised individuals and congenital transmission. Prior research suggests that oregano essential oil (OEO) exhibits diverse biological effects, including antiparasitic activity against
Toxoplasma gondii.
Given concerns about current treatments, exploring new compounds is important. This study was to assess the toxicity of OEO on BeWo cells and
T. gondii
tachyzoites, as well as to evaluate its effectiveness in in vitro infection models and determine its direct action on free tachyzoites. OEO toxicity on BeWo cells and
T. gondii
tachyzoites was assessed by MTT and trypan blue methods, determining cytotoxic concentration (CC
50
), inhibitory concentration (IC
50
), and selectivity index (SI). Infection and proliferation indices were analyzed. Direct assessments of the parasite included reactive oxygen species (ROS) levels, mitochondrial membrane potential, necrosis, and apoptosis, as well as electron microscopy. Oregano oil exhibited low cytotoxicity on BeWo cells (CC
50
: 114.8 µg/mL ± 0.01) and reduced parasite viability (IC
50
12.5 ± 0.06 µg/mL), demonstrating 9.18 times greater selectivity for parasites than BeWo cells. OEO treatment significantly decreased intracellular proliferation in infected cells by 84% after 24 h with 50 μg/mL. Mechanistic investigations revealed increased ROS levels, mitochondrial depolarization, and lipid droplet formation, linked to autophagy induction and plasma membrane permeabilization. These alterations, observed through electron microscopy, suggested a necrotic process confirmed by propidium iodide labeling. OEO treatment demonstrated anti-
T. gondii
action through cellular and metabolic change while maintaining low toxicity to trophoblastic cells.
Graphical abstract |
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ISSN: | 0932-0113 1432-1955 1432-1955 |
DOI: | 10.1007/s00436-024-08231-z |