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Identification of natural antimicrobial agents to treat dengue infection: In vitro analysis of latarcin peptide activity against dengue virus

机译:鉴定治疗登革热感染的天然抗菌药物:拉塔霉素肽对登革热病毒活性的体外分析

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Background Although there have been considerable advances in the study of dengue virus, no vaccines or anti-dengue drugs are currently available for humans. Therefore, new approaches are necessary for the development of potent anti-dengue drugs. Natural antimicrobial peptides (AMPs) with potent antiviral activities are potential hits-to-leads for antiviral drug discovery. We performed this study to identify and characterise the inhibitory potential of the latarcin peptide (Ltc 1, SMWSGMWRRKLKKLRNALKKKLKGE) against dengue virus replication in infected cells. Results The Ltc 1 peptide showed a significantly inhibitory effect against the dengue protease NS2B-NS3pro at 37°C, a physiological human temperature, (IC50, 12.68?±?3.2?μM), and greater inhibitory effect was observed at 40°C, a temperature similar to a high fever (IC50, 6.58?±?4.1?μM). A greater reduction in viral load (p.f.u./ml) was observed at simultaneous (0.7?±?0.3 vs. 7.2?±?0.5 control) and post-treatment (1.8?±?0.7 vs. 6.8?±?0.6 control) compared to the pre-treatment (4.5?±?0.6 vs. 6.9?±?0.5 control). Treatment with the Ltc 1 peptide reduced the viral RNA in a dose-dependent manner with EC50 values of 8.3?±?1.2, 7.6?±?2.7 and 6.8?±?2.5?μM at 24, 48 and 72?h, respectively. Conclusions The Ltc 1 peptide exhibited significant inhibitory effects against dengue NS2B-NS3pro and virus replication in the infected cells. Therefore, further investigation is necessary to develop the Ltc 1 peptide as a new anti-dengue therapeutic.
机译:背景技术尽管在登革热病毒的研究方面已经取得了很大的进展,但是目前尚无用于人类的疫苗或抗登革热药物。因此,开发有效的抗登革热药物需要新的方法。具有有效抗病毒活性的天然抗微生物肽(AMPs)是潜在的抗病毒药物发现途径。我们进行了这项研究,以鉴定和表征latarcin肽(Ltc 1,SMWSGMWRRKLKKLRNALKKKKKKGE)对登革热病毒在感染细胞中复制的抑制潜力。结果Ltc 1肽在37°C,生理温度(IC 50 ,12.68?±?3.2?μM)和更大的抑制作用下对登革热蛋白酶NS2B-NS3pro具有明显的抑制作用。在40°C,类似于高烧的温度(IC 50 ,6.58?±?4.1?μM)下观察到效果。与同时(0.7±±0.3对比7.2±±0.5对照)和治疗后(1.8±±0.7对比6.8±±0.6对照)观察到的病毒载量(pfu / ml)有更大的降低。达到治疗前的水平(对照组为4.5±±0.6,而对照组为6.9±±0.5)。 Ltc 1肽的处理以剂量依赖的方式减少病毒RNA,在24, 48和72?h。结论Ltc 1肽对登革热NS2B-NS3pro和感染细胞中的病毒复制具有明显的抑制作用。因此,有必要进一步研究以开发Ltc 1肽作为一种新的抗登革热治疗剂。

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