Computational insight into the protective mechanism of Allium iranicum Wendelbo. Alliaceae in a mouse model of Staphylococcosis: focus on dietary phytocannabinoid trans-caryophyllene.

In Silico Pharmacology Pub Date : 2021-02-07 eCollection Date: 2021-01-01 DOI:10.1007/s40203-021-00078-x
Layth Jasim Mohammed, Khosrow Chehri, Isaac Karimi, Nasser Karimi
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Abstract

This study was aimed to investigate the prophylactic effects of hydro-alcoholic extract derived from bulbs of Allium iranicum Wendelbo. (Alliaceae; AI) on mouse model of Staphylococcosis, and to decipher which phytochemicals of AI may involve in its anti-staphylococcal property. Male mice were allocated into four groups, i.e. normal control (NC) and three other groups received AI at 0.192, 0.384 and 0.768 mg/ml in drinking water for 9 days. Thereafter, mice were intravenously injected 106 colony forming unites (CFUs/ml) of Staphylococcus aureus suspension at 10th day and tissue homogenates were colony counted for S. aureus 9 days post-inoculation. Molecular docking among cardinal proteins involved in Staphylococcosis and phytochemicals of AI has been performed using PyRx software and the best ligand submitted to compute molecular and biological attributes. Induction of murine Staphylococcosis and inclusion of AI did not adversely alter bodyweights of mice while colony counts in selected tissues of mice infected with S. aureus were different among groups (PANOVA = 0.016). Generally, the colony counts tended to decrease in AI 0.192 (P = 0.099) and AI 0.768 (P = 0.818) groups as compared to NC, however AI 0.384 (P = 0.005) group showed lesser colony counts than NC. In addition, colony counts decreased in AI 0.384 as compared to AI 0.768 (P = 0.009). The colony counts in kidneys of AI 0.0384 group were lesser than those of NC (P = 0.051) and AI 0.768 (P = 0.048). Among target proteins, trans-caryophyllene (TCP) showed reliable binding affinities (kcal/mol) to three hydrolase enzymes [beta toxin (sphingomyelin phosphodiesterase - 8.1), sortase B (protease - 8.1), and FtsZ (GTPase - 8.7) of S. aureus]. The ADMET properties of TCP showed that it followed the Lipinski's rule of five with one violation with respect to its miLogP 5.17. In addition, Molinspiration bioactivity score indicated ion channel modulatory and enzyme inhibitory effect for TCP. Computational findings of admetSAR software revealed that TCP leads to carcinogenicity, Tetrahymena pyriformis, fish, rat, and honey bee toxicities, weak inhibition of human ether-a-go-go-related gene, and cytochromes inhibitory promiscuity. The TCP showed promising in human intestinal absorption, blood-brain barrier permeability, Caco-2 penetration, and solubility. The results of Toxtree software showed that TCP is not an endogenous molecule of the body and contains no functional groups associated with enhanced toxicity and considered as class I toxic compound close to terpenes. In conclusion, we found the hydro-alcoholic extract derived from of bulbs AI has a significant protective effect against Staphylococcosis in mouse model. In silico findings demonstrated that TCP has acceptable ADMET score to be considered as a bioactive compound for designing phytobiotics.

Supplementary information: The online version contains supplementary material available at 10.1007/s40203-021-00078-x.

通过计算深入了解薤白在葡萄球菌病小鼠模型中的保护机制:重点关注膳食中的植物大麻素-反式叶绿素。万年青在葡萄球菌病小鼠模型中的作用:关注膳食中的植物大麻素-反式茶叶烯。
本研究旨在探讨从鸢尾科植物薤白(Allium iranicum Wendelbo.(AI)的水醇提取物对葡萄球菌病小鼠模型的预防作用,并研究AI中哪些植物化学物质可能参与了其抗葡萄球菌特性。雄性小鼠被分为四组,即正常对照组(NC)和其他三组,每组在饮用水中添加 0.192、0.384 和 0.768 毫克/毫升的 AI,连续 9 天。然后,在第 10 天给小鼠静脉注射 106 个菌落形成单位(CFUs/ml)的金黄色葡萄球菌悬浮液,并在接种后 9 天对组织匀浆进行金黄色葡萄球菌菌落计数。使用 PyRx 软件在葡萄球菌病相关的主要蛋白和 AI 植物化学物之间进行分子对接,并提交最佳配体以计算分子和生物属性。诱导小鼠葡萄球菌病和加入 AI 不会对小鼠体重产生不利影响,而感染金黄色葡萄球菌的小鼠选定组织中的菌落计数在各组之间存在差异(PANOVA = 0.016)。一般来说,与 NC 组相比,AI 0.192 组(P = 0.099)和 AI 0.768 组(P = 0.818)的菌落数呈下降趋势,但 AI 0.384 组(P = 0.005)的菌落数低于 NC 组。此外,与 AI 0.768(P = 0.009)相比,AI 0.384 组的菌落数有所减少。AI 0.0384 组肾脏中的菌落数少于 NC 组(P = 0.051)和 AI 0.768 组(P = 0.048)。在靶蛋白中,反式茶碱(TCP)与金黄色葡萄球菌的三种水解酶[β毒素(鞘磷脂磷酸二酯酶 - 8.1)、分类酶 B(蛋白酶 - 8.1)和 FtsZ(GTP 酶 - 8.7)]具有可靠的结合亲和力(kcal/mol)。TCP 的 ADMET 特性表明,它遵循利宾斯基的五项规则,只有一项违反了 miLogP 5.17。此外,Molinspiration 生物活性评分表明 TCP 具有离子通道调节和酶抑制作用。admetSAR 软件的计算结果表明,TCP 具有致癌性,对四膜虫、鱼类、大鼠和蜜蜂有毒性,对人类醚-a-go-go 相关基因有弱抑制作用,并具有细胞色素抑制性。TCP 在人体肠道吸收性、血脑屏障渗透性、Caco-2 穿透性和溶解性方面表现良好。Toxtree 软件的结果表明,TCP 不是人体的内源性分子,不含与增强毒性相关的官能团,被认为是接近萜类的一类毒性化合物。总之,我们发现鳞茎 AI 的水醇提取物对小鼠模型中的葡萄球菌病有显著的保护作用。硅学研究结果表明,TCP具有可接受的ADMET评分,可作为设计植物生物制剂的生物活性化合物:在线版本包含补充材料,可查阅 10.1007/s40203-021-00078-x。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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