Rothan Hussin A, Bahrani Hirbod, Rahman Noorsaadah Abd, Yusof Rohana
Department of Molecular Medicine, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
BMC Microbiol. 2014 May 31;14:140. doi: 10.1186/1471-2180-14-140.
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.
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.
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.
尽管登革病毒的研究已取得相当大的进展,但目前尚无用于人类的疫苗或抗登革病毒药物。因此,开发有效的抗登革病毒药物需要新的方法。具有强大抗病毒活性的天然抗菌肽是抗病毒药物发现的潜在先导化合物。我们进行本研究以鉴定和表征latarcin肽(Ltc 1,SMWSGMWRRKLKKLRNALKKKLKGE)对感染细胞中登革病毒复制的抑制潜力。
Ltc 1肽在人体生理温度37°C时对登革病毒蛋白酶NS2B - NS3pro表现出显著的抑制作用(IC50,12.68 ± 3.2 μM),在与高烧相似的温度40°C时观察到更大的抑制作用(IC50,6.58 ± 4.1 μM)。与预处理(4.5 ± 0.6 vs. 6.9 ± 0.5对照)相比,同时处理(0.7 ± 0.3 vs. 7.2 ± 0.5对照)和处理后(1.8 ± 0.7 vs. 6.8 ± 0.6对照)观察到病毒载量(p.f.u./ml)有更大程度的降低。用Ltc 1肽处理以剂量依赖性方式降低病毒RNA,在24、48和72小时时的EC50值分别为8.3 ± 1.2、7.6 ± 2.7和6.8 ± 2.5 μM。
Ltc 1肽对感染细胞中的登革病毒NS2B - NS3pro和病毒复制表现出显著的抑制作用。因此,有必要进一步研究将Ltc 1肽开发为一种新的抗登革热治疗药物。