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新生霉素作为热休克蛋白 90 抑制剂对体外培养的马媾疫锥虫和马巴贝斯虫的抗焦虫活性。

Anti-piroplasmic activity of novobiocin as heat shock protein 90 inhibitor against in vitro cultured Theileria equi and Babesia caballi parasites.

机构信息

ICAR - National Research Centre on Equines, Sirsa Road, Hisar, 125001, India; Division of Veterinary Medicine, Indian Veterinary Research Institute, Izatnagar, 243122, Uttar Pradesh, India; Department of Medicine, College of Veterinary Science & Animal Husbandry, Sardarkrushinagar Dantiwada Agricultural University, Dantiwada, 385506, Gujarat, India.

ICAR - National Research Centre on Equines, Sirsa Road, Hisar, 125001, India; Subject matter specialist (Animal Health), North 24 Praganas Krishi Vigyan Kendra, WBUAFS, Ashokenagar, 743223, West Bengal, India.

出版信息

Ticks Tick Borne Dis. 2021 Jul;12(4):101696. doi: 10.1016/j.ttbdis.2021.101696. Epub 2021 Feb 27.

Abstract

Theileria equi and Babesia caballi are the causative agents of equine piroplasmosis (EP). Currently, imidocarb dipropionate (ID) is the only available drug for treating the clinical form of EP. Serious side effects and incomplete clearance of infection is a major drawback of ID. Heat-shock proteins (Hsp) play a vital role in the life cycle of these haemoprotozoans by preventing alteration in protein conformation. These Hsp are activated during transmission of EP sporozoites from the tick vector (poikilotherm) to the natural host (homeotherm) and facilitate parasite survival. In the present study, we targeted the heat shock protein 90 (Hsp-90) pathway of T. equi and B. caballi by using its inhibitor drug - novobiocin. Dose-dependent efficacy of novobiocin on the growth of T. equi and B. caballi was observed in in vitro culture. Additionally, we examined dose-dependent cell cytotoxicity on host peripheral mononuclear cells (PBMCs) and haemolytic activity on equine red blood cells (RBC). In vivo organ toxicity of novobiocin was also assessed in a mouse model. The IC (50 % inhibitory concentration) value of novobiocin against T. equi and B. caballi was 165 μM and 84.85 μM, respectively. Novobiocin significantly arrested the in vitro growth of T. equi and B. caballi parasites at 100 μM and 200 μM drug concentration, respectively. In vitro treated parasites had distorted nuclear material and showed no further viability. Based on the equine PBMCs and RBC, the drug was found to be safe even at 1000 μM concentration and the CC (50 % cytotoxicity concentration) values were 11.63 mM and 261.97 mM. Very high specific selective index (SSI) values (70.47 and 1587) were observed for equine PBMCs and RBC, respectively. Organ-specific biochemical markers and histopathological examination indicated no adverse effect of the drug at a dose rate of 50 mg kg body weight in the mouse model. The results demonstrate the growth inhibitory effect of novobiocin against T. equi and B. caballi parasites and its safety for host cell lines with very high SSI. Hence, it can be inferred that the Theileria/Babesia Hsp-90 family are potential drug targets worthy of further investigation.

摘要

马媾疫锥虫和马巴贝斯虫是马媾疫(EP)的病原体。目前,二硝托胺丙二醇(ID)是治疗 EP 临床症状的唯一可用药物。ID 存在严重的副作用和不完全清除感染的问题。热休克蛋白(Hsp)在这些血液原生动物的生命周期中起着至关重要的作用,可防止蛋白质构象改变。这些 Hsp 在 EP 孢子从蜱(变温动物)传播到天然宿主(恒温动物)时被激活,并促进寄生虫的存活。在本研究中,我们通过使用其抑制剂药物 - 新生霉素,针对 T. equi 和 B. caballi 的热休克蛋白 90(Hsp-90)途径。在体外培养中观察到新生霉素对 T. equi 和 B. caballi 生长的剂量依赖性功效。此外,我们还检查了对宿主外周血单核细胞(PBMCs)的剂量依赖性细胞细胞毒性和对马红细胞(RBC)的溶血活性。还在小鼠模型中评估了新生霉素的体内器官毒性。新生霉素对 T. equi 和 B. caballi 的 IC(50%抑制浓度)值分别为 165 μM 和 84.85 μM。新生霉素在 100 μM 和 200 μM 药物浓度下可显著抑制 T. equi 和 B. caballi 寄生虫的体外生长。体外处理的寄生虫核物质扭曲,且无进一步活力。基于马 PBMCs 和 RBC,即使在 1000 μM 浓度下,该药物也被发现是安全的,CC(50%细胞毒性浓度)值分别为 11.63 mM 和 261.97 mM。对马 PBMCs 和 RBC 的特异性选择性指数(SSI)值分别高达 70.47 和 1587。在小鼠模型中,以 50mgkg 体重的剂量率给药时,特定的器官特异性生化标志物和组织病理学检查表明该药物无不良反应。结果表明,新生霉素对 T. equi 和 B. caballi 寄生虫具有生长抑制作用,并且对宿主细胞系具有非常高的 SSI,安全性良好。因此,可以推断 Theileria/Babesia Hsp-90 家族是值得进一步研究的潜在药物靶标。

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