Alendronate repositioning as potential anti-parasitic agent targeting Trichinella spiralis inorganic pyrophosphatase, in vitro supported molecular docking and molecular dynamics simulation study

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Marmar A. Hanafy, Doaa A. Nassar, Fatima M. Zahran, Magdy M. D. Mohammed
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Abstract

Trichinellosis represents great public health and economic problems worldwide. Moreover, the development of parasitic resistance against conventional anthelminthic treatment led to the urgent search for new therapeutic strategies, including drug repurposing. Bisphosphonates have been used to inhibit the growth of many parasites and have also emerged as promising candidates for the treatment of cryptosporidiosis and amoebic liver abscess. Alendronate is a second-generation bisphosphonate that is widely used for the treatment and prevention of osteoporosis. Till date, there is not enough data on the effect of this drug on Trichinella spiralis and it is unknown whether the regular use of this drug in osteoporotic patients may alter the course of the infection. ALN showed a significant lethal effect on both adult worms and juveniles, with severe tegumental damage in the form of fissures in the cuticle, widening of the hypodermal gland, and flattening of the cuticular annulation, ending with the appearance of multiple vesicles and large cauliflower masses. Molecular docking outcomes unveiled the potential inhibition of ALN against T. spiralis surface proteins (i.e., Ts-SP, Ts-PPase, Ts-MAPRC2, Ts-TS, Ts-MIF, etc.), with promising results confirmed its ability to defeat T. spiralis via targeting its surface proteins. Moreover, molecular dynamics simulation, through the analysis of RMSD, RMSF, RG, SASA and cluster analysis, proved the prolonged effective inhibition of ALN on T. spiralis inorganic pyrophosphatase, as an essential surface protein required for molting and developmental process of intestinal larval stages. Thus, ALN might be a valuable drug candidate for the treatment of trichinellosis and warrant further investigation in animal models of disease.

阿仑膦酸重新定位作为旋毛虫无机焦磷酸酶潜在抗寄生虫剂的体外支持分子对接及分子动力学模拟研究
旋毛虫病在世界范围内构成了严重的公共卫生和经济问题。此外,寄生虫对传统驱虫治疗的耐药性的发展导致迫切需要寻找新的治疗策略,包括药物再利用。双膦酸盐已被用于抑制许多寄生虫的生长,也已成为治疗隐孢子虫病和阿米巴肝脓肿的有希望的候选人。阿仑膦酸盐是第二代双膦酸盐,广泛用于治疗和预防骨质疏松症。迄今为止,关于该药对旋毛虫的影响尚无足够的数据,骨质疏松症患者经常使用该药是否会改变感染的过程尚不清楚。ALN对成虫和幼虫都有显著的致死作用,其被皮严重受损,表现为角质层裂缝、皮下腺变宽、角质层环变平,最终出现多个囊泡和大菜花团块。分子对接结果揭示了ALN对螺旋体表面蛋白(即Ts-SP、Ts-PPase、Ts-MAPRC2、Ts-TS、Ts-MIF等)的潜在抑制作用,并证实了其通过靶向螺旋体表面蛋白来击败螺旋体的能力。分子动力学模拟,通过RMSD、RMSF、RG、SASA分析和聚类分析,证明ALN对螺旋藻无机焦磷酸酶有较长时间的有效抑制作用,而无机焦磷酸酶是肠道幼虫期蜕皮和发育过程中必需的表面蛋白。因此,ALN可能是治疗旋毛虫病的一种有价值的候选药物,值得在动物模型中进一步研究。
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来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
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