Cardillo Natalia M, Villarino Nicolas F, Lacy Paul A, Riscoe Michael K, Doggett Joseph Stone, Ueti Massaro W, Chung Chungwon J, Suarez Carlos E
Animal Disease Research Unit, United States Department of Agriculture-Animal Research Unit (USDA-ARS), 3003 ADBF, WSU, Pullman, WA 99163, USA.
Estación Experimental INTA Paraná, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires 2290, Argentina.
Pharmaceutics. 2024 Oct 31;16(11):1402. doi: 10.3390/pharmaceutics16111402.
Bovine babesiosis is a vector-borne disease transmitted by ticks that causes important losses in livestock worldwide. Recent research performed on the drugs currently used to control bovine babesiosis reported several issues including drug resistance, toxicity impact, and residues in edible tissue, suggesting the need for developing novel effective therapies. The endochin-like quinolones ELQ-316 and buparvaquone (BPQ) act as cytochrome 1 inhibitors and have been proven to be safe and efficacious against related apicomplexans, such as spp. and , without showing toxicity in mammals. The objectives of this study are investigating whether ELQ-316, BPQ, and their combination treatment could be effective against in an in vitro culture model and comparing with imidocarb (ID), the routinely used drug. In vitro cultured parasites starting at 2% percentage of parasitemia (PPE) were treated with BPQ, ELQ-316, ID, and the combinations of BPQ + ELQ-316 and ID + ELQ-316 at drug concentrations that ranged from 25 to 1200 nM, during four consecutive days. The IC50% and IC99% were reported. Parasitemia levels were evaluated daily using microscopic examination. Data were compared using the non-parametrical Mann-Whitney and Kruskall-Wallis test. All drugs tested, whether used alone or in combination, significantly decreased the survival ( < 0.05) of in in vitro cultures. The combination of BPQ + ELQ-316 had the lowest calculated inhibitory concentration 50% (IC50%) values, 31.21 nM (IC95%: 15.06-68.48); followed by BPQ, 77.06 nM (IC95%: 70.16-86.01); ID + ELQ316, 197 nM (IC95%:129.0-311.2); ID, 635.1 nM (IC95%: 280.9-2119); and ELQ316, 654.9 nM (IC95%: 362.3-1411). The results reinforce the higher efficacy of BPQ at affecting survival and the potential synergistic effects of its combination with ELQ-316, providing a promising treatment option against .
牛巴贝斯虫病是一种由蜱传播的媒介传播疾病,在全球范围内给牲畜造成重大损失。最近对目前用于控制牛巴贝斯虫病的药物进行的研究报告了几个问题,包括耐药性、毒性影响和可食用组织中的残留,这表明需要开发新的有效疗法。类内二喹啉ELQ - 316和丁萘脒(BPQ)作为细胞色素1抑制剂,已被证明对相关顶复门原虫(如某些种类)安全有效,且对哺乳动物无毒性。本研究的目的是调查ELQ - 316、BPQ及其联合治疗在体外培养模型中对[具体病原体名称缺失]是否有效,并与常规使用的药物咪唑苯脲(ID)进行比较。以2%的寄生虫血症百分比(PPE)开始的体外培养寄生虫,在连续四天内用BPQ、ELQ - 316、ID以及BPQ + ELQ - 316和ID + ELQ - 316的组合进行处理,药物浓度范围为25至1200 nM。报告了半数抑制浓度(IC50%)和99%抑制浓度(IC99%)。每天使用显微镜检查评估寄生虫血症水平。使用非参数曼 - 惠特尼检验和克鲁斯卡尔 - 沃利斯检验比较数据。所有测试药物,无论是单独使用还是联合使用,均显著降低了体外培养物中[具体病原体名称缺失]的存活率(P < 0.05)。BPQ + ELQ - 316组合的计算半数抑制浓度(IC50%)值最低,为31.21 nM(IC95%:15.06 - 68.48);其次是BPQ,为77.06 nM(IC95%:70.16 - 86.01);ID + ELQ316,为197 nM(IC95%:129.0 - 311.2);ID,为635.1 nM(IC95%:280.9 - 2119);ELQ316,为654.9 nM(IC95%:362.3 - 1411)。结果强化了BPQ在影响[具体病原体名称缺失]存活率方面的更高疗效及其与ELQ - 316联合的潜在协同作用,为对抗[具体病原体名称缺失]提供了一种有前景的治疗选择。