Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides

被引:54
作者
Alhoot, Mohammed Abdelfatah [1 ,2 ]
Rathinam, Alwin Kumar [3 ,4 ]
Wang, Seok Mui [5 ]
Manikam, Rishya [6 ]
Sekaran, Shamala Devi [1 ]
机构
[1] Univ Malaya, Fac Med, Dept Med Microbiol, Kuala Lumpur 50603, Malaysia
[2] Management & Sci Univ, Int Med Sch, Dept Med Microbiol, Shah Alam 40100, Selangor, Malaysia
[3] Univ Malaya, Virtual Real Centre, Kuala Lumpur 50603, Malaysia
[4] Univ Malaya, Ctr Biomed Technol Intergrat Pte Ltd, Kuala Lumpur 50603, Malaysia
[5] Univ Teknol Mara, Fac Med, Inst Med Mol Biotechnol, Shah Alam, Selangor, Malaysia
[6] Univ Malaya, Med Ctr, Dept Trauma & Emergency Med, Kuala Lumpur, Malaysia
关键词
Dengue virus; Antiviral peptides; Inhibitory Peptides; Viral entry; Envelope protein; Domain III; HERPES-SIMPLEX-VIRUS; HEPATITIS-B-VIRUS; PROTEIN-STRUCTURE PREDICTION; ENVELOPE PROTEIN; RNA INTERFERENCE; HEPARAN-SULFATE; MEMBRANE-FUSION; IN-VITRO; REPLICATION; BINDING;
D O I
10.7150/ijms.5037
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite the importance of DENV as a human pathogen, there is no specific treatment or protective vaccine. Successful entry into the host cells is necessary for establishing the infection. Recently, the virus entry step has become an attractive therapeutic strategy because it represents a barrier to suppress the onset of the infection. Four putative antiviral peptides were designed to target domain III of DENV-2 E protein using BioMoDroid algorithm. Two peptides showed significant inhibition of DENV when simultaneously incubated as shown by plaque formation assay, RT-qPCR, and Western blot analysis. Both DET4 and DET2 showed significant inhibition of virus entry (84.6% and 40.6% respectively) using micromolar concentrations. Furthermore, the TEM images showed that the inhibitory peptides caused structural abnormalities and alteration of the arrangement of the viral E protein, which interferes with virus binding and entry. Inhibition of DENV entry during the initial stages of infection can potentially reduce the viremia in infected humans resulting in prevention of the progression of dengue fever to the severe life-threatening infection, reduce the infected vector numbers, and thus break the transmission cycle. Moreover these peptides though designed against the conserved region in DENV-2 would have the potential to be active against all the serotypes of dengue and might be considered as Hits to begin designing and developing of more potent analogous peptides that could constitute as promising therapeutic agents for attenuating dengue infection.
引用
收藏
页码:719 / 729
页数:11
相关论文
共 42 条
[1]   RNA Interference Mediated Inhibition of Dengue Virus Multiplication and Entry in HepG2 Cells [J].
Alhoot, Mohammed Abdelfatah ;
Wang, Seok Mui ;
Sekaran, Shamala Devi .
PLOS ONE, 2012, 7 (03)
[2]   Inhibition of Dengue Virus Entry and Multiplication into Monocytes Using RNA Interference [J].
Alhoot, Mohammed Abdelfatah ;
Wang, Seok Mui ;
Sekaran, Shamala Devi .
PLOS NEGLECTED TROPICAL DISEASES, 2011, 5 (11)
[3]   Antiviral peptides targeting the west nile virus envelope protein [J].
Bai, Fengwei ;
Town, Terrence ;
Pradhan, Deepti ;
Cox, Jonathan ;
Ashish ;
Ledizet, Michel ;
Anderson, John F. ;
Flavell, Richard A. ;
Krueger, Joanna K. ;
Koski, Raymond A. ;
Fikrig, Erol .
JOURNAL OF VIROLOGY, 2007, 81 (04) :2047-2055
[4]   In vitro and in vivo antimicrobial activity of two α-helical cathelicidin peptides and of their synthetic analogs [J].
Benincasa, M ;
Skerlavaj, B ;
Gennaro, R ;
Pellegrini, A ;
Zanetti, M .
PEPTIDES, 2003, 24 (11) :1723-1731
[5]   Amino acid size, charge, hydropathy indices and matrices for protein structure analysis [J].
Biro, J. C. .
THEORETICAL BIOLOGY AND MEDICAL MODELLING, 2006, 3
[6]   Structure of a flavivirus envelope glycoprotein in its low-pH-induced membrane fusion conformation [J].
Bressanelli, S ;
Stiasny, K ;
Allison, SL ;
Stura, EA ;
Duquerroy, S ;
Lescar, J ;
Heinz, FX ;
Rey, FA .
EMBO JOURNAL, 2004, 23 (04) :728-738
[7]   Demonstration of binding of dengue virus envelope protein to target cells [J].
Chen, YP ;
Maguire, T ;
Marks, RM .
JOURNAL OF VIROLOGY, 1996, 70 (12) :8765-8772
[8]   Dengue virus infectivity depends on envelope protein binding to target cell heparan sulfate [J].
Chen, YP ;
Maguire, T ;
Hileman, RE ;
Fromm, JR ;
Esko, JD ;
Linhardt, RJ ;
Marks, RM .
NATURE MEDICINE, 1997, 3 (08) :866-871
[9]   Recent advances in deciphering viral and host determinants of dengue virus replication and pathogenesis [J].
Clyde, Karen ;
Kyle, Jennifer L. ;
Harris, Eva .
JOURNAL OF VIROLOGY, 2006, 80 (23) :11418-11431
[10]   Structural Optimization and De Novo Design of Dengue Virus Entry Inhibitory Peptides [J].
Costin, Joshua M. ;
Jenwitheesuk, Ekachai ;
Lok, Shee-Mei ;
Hunsperger, Elizabeth ;
Conrads, Kelly A. ;
Fontaine, Krystal A. ;
Rees, Craig R. ;
Rossmann, Michael G. ;
Isern, Sharon ;
Samudrala, Ram ;
Michael, Scott F. .
PLOS NEGLECTED TROPICAL DISEASES, 2010, 4 (06)