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

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...

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Autores principales: Alhoot, Mohammed Abdelfatah, Rathinam, Alwin Kumar, Wang, Seok Mui, Manikam, Rishya, Sekaran, Shamala Devi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638295/
https://www.ncbi.nlm.nih.gov/pubmed/23630436
http://dx.doi.org/10.7150/ijms.5037
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author Alhoot, Mohammed Abdelfatah
Rathinam, Alwin Kumar
Wang, Seok Mui
Manikam, Rishya
Sekaran, Shamala Devi
author_facet Alhoot, Mohammed Abdelfatah
Rathinam, Alwin Kumar
Wang, Seok Mui
Manikam, Rishya
Sekaran, Shamala Devi
author_sort Alhoot, Mohammed Abdelfatah
collection PubMed
description 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.
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spelling pubmed-36382952013-04-29 Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides Alhoot, Mohammed Abdelfatah Rathinam, Alwin Kumar Wang, Seok Mui Manikam, Rishya Sekaran, Shamala Devi Int J Med Sci Research Paper 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. Ivyspring International Publisher 2013-04-16 /pmc/articles/PMC3638295/ /pubmed/23630436 http://dx.doi.org/10.7150/ijms.5037 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Alhoot, Mohammed Abdelfatah
Rathinam, Alwin Kumar
Wang, Seok Mui
Manikam, Rishya
Sekaran, Shamala Devi
Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides
title Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides
title_full Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides
title_fullStr Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides
title_full_unstemmed Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides
title_short Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides
title_sort inhibition of dengue virus entry into target cells using synthetic antiviral peptides
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638295/
https://www.ncbi.nlm.nih.gov/pubmed/23630436
http://dx.doi.org/10.7150/ijms.5037
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