Department of Immunology, Parasitology and General Pathology - Laboratory of Experimental Immunoparasitology, State University of Londrina, Londrina, Paraná, Brazil.
Department of Immunology, Parasitology and General Pathology - Laboratory of Immunoparasitology of Neglected Diseases and Cancer, State University of Londrina, Londrina, Paraná, Brazil.
Parasitol Res. 2024 May 22;123(5):217. doi: 10.1007/s00436-024-08231-z.
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), inhibitory concentration (IC), 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: 114.8 µg/mL ± 0.01) and reduced parasite viability (IC 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.
弓形虫病构成全球性健康威胁,可表现为无症状感染乃至严重、甚至可能致命的感染,尤其在免疫功能低下个体和先天性感染中更为常见。既往研究表明,牛至精油(oregano essential oil,OEO)具有多种生物学效应,包括针对刚地弓形虫的抗寄生虫活性。鉴于对现有治疗方法的担忧,探索新的化合物非常重要。本研究旨在评估 OEO 对 BeWo 细胞和刚地弓形虫速殖子的毒性,评估其在体外感染模型中的效果,并确定其对游离速殖子的直接作用。采用 MTT 和台盼蓝法评估 OEO 对 BeWo 细胞和刚地弓形虫速殖子的毒性,确定细胞毒性浓度(cytotoxic concentration,CC)、抑制浓度(inhibitory concentration,IC)和选择性指数(selectivity index,SI)。分析感染和增殖指数。直接评估寄生虫包括活性氧(reactive oxygen species,ROS)水平、线粒体膜电位、坏死和凋亡,以及电子显微镜。牛至油对 BeWo 细胞的细胞毒性较低(CC:114.8 ± 0.01 μg/mL),且降低寄生虫活力(IC 12.5 ± 0.06 μg/mL),对寄生虫的选择性比 BeWo 细胞高 9.18 倍。OEO 处理可使感染细胞内增殖在 24 小时时降低 84%,有效浓度为 50 μg/mL。机制研究显示 ROS 水平增加、线粒体去极化和脂滴形成,与自噬诱导和质膜通透性增加有关。通过电子显微镜观察到这些变化,提示发生坏死过程,碘化丙啶标记进一步证实。OEO 通过细胞和代谢变化发挥抗弓形虫作用,同时对滋养层细胞保持低毒性。