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Bioinformatics prediction of siRNAs as potential antiviral agents against dengue viruses
Dengue virus (DENV 1-4) represents the major emerging arthropod-borne viral infection in the world. Currently, there is neither an available vaccine nor a specific treatment. Hence, there is a need of antiviral drugs for these viral infections; we describe the prediction of short interfering RNA (si...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398769/ https://www.ncbi.nlm.nih.gov/pubmed/22829722 http://dx.doi.org/10.6026/97320630008519 |
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author | Villegas-Rosales, Paula M Méndez-Tenorio, Alfonso Ortega-Soto, Elizabeth Barrón, Blanca L |
author_facet | Villegas-Rosales, Paula M Méndez-Tenorio, Alfonso Ortega-Soto, Elizabeth Barrón, Blanca L |
author_sort | Villegas-Rosales, Paula M |
collection | PubMed |
description | Dengue virus (DENV 1-4) represents the major emerging arthropod-borne viral infection in the world. Currently, there is neither an available vaccine nor a specific treatment. Hence, there is a need of antiviral drugs for these viral infections; we describe the prediction of short interfering RNA (siRNA) as potential therapeutic agents against the four DENV serotypes. Our strategy was to carry out a series of multiple alignments using ClustalX program to find conserved sequences among the four DENV serotype genomes to obtain a consensus sequence for siRNAs design. A highly conserved sequence among the four DENV serotypes, located in the encoding sequence for NS4B and NS5 proteins was found. A total of 2,893 complete DENV genomes were downloaded from the NCBI, and after a depuration procedure to identify identical sequences, 220 complete DENV genomes were left. They were edited to select the NS4B and NS5 sequences, which were aligned to obtain a consensus sequence. Three different servers were used for siRNA design, and the resulting siRNAs were aligned to identify the most prevalent sequences. Three siRNAs were chosen, one targeted the genome region that codifies for NS4B protein and the other two; the region for NS5 protein. Predicted secondary structure for DENV genomes was used to demonstrate that the siRNAs were able to target the viral genome forming double stranded structures, necessary to activate the RNA silencing machinery. |
format | Online Article Text |
id | pubmed-3398769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-33987692012-07-24 Bioinformatics prediction of siRNAs as potential antiviral agents against dengue viruses Villegas-Rosales, Paula M Méndez-Tenorio, Alfonso Ortega-Soto, Elizabeth Barrón, Blanca L Bioinformation Hypothesis Dengue virus (DENV 1-4) represents the major emerging arthropod-borne viral infection in the world. Currently, there is neither an available vaccine nor a specific treatment. Hence, there is a need of antiviral drugs for these viral infections; we describe the prediction of short interfering RNA (siRNA) as potential therapeutic agents against the four DENV serotypes. Our strategy was to carry out a series of multiple alignments using ClustalX program to find conserved sequences among the four DENV serotype genomes to obtain a consensus sequence for siRNAs design. A highly conserved sequence among the four DENV serotypes, located in the encoding sequence for NS4B and NS5 proteins was found. A total of 2,893 complete DENV genomes were downloaded from the NCBI, and after a depuration procedure to identify identical sequences, 220 complete DENV genomes were left. They were edited to select the NS4B and NS5 sequences, which were aligned to obtain a consensus sequence. Three different servers were used for siRNA design, and the resulting siRNAs were aligned to identify the most prevalent sequences. Three siRNAs were chosen, one targeted the genome region that codifies for NS4B protein and the other two; the region for NS5 protein. Predicted secondary structure for DENV genomes was used to demonstrate that the siRNAs were able to target the viral genome forming double stranded structures, necessary to activate the RNA silencing machinery. Biomedical Informatics 2012-06-16 /pmc/articles/PMC3398769/ /pubmed/22829722 http://dx.doi.org/10.6026/97320630008519 Text en © 2012 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited. |
spellingShingle | Hypothesis Villegas-Rosales, Paula M Méndez-Tenorio, Alfonso Ortega-Soto, Elizabeth Barrón, Blanca L Bioinformatics prediction of siRNAs as potential antiviral agents against dengue viruses |
title | Bioinformatics prediction of siRNAs as potential antiviral agents against dengue viruses |
title_full | Bioinformatics prediction of siRNAs as potential antiviral agents against dengue viruses |
title_fullStr | Bioinformatics prediction of siRNAs as potential antiviral agents against dengue viruses |
title_full_unstemmed | Bioinformatics prediction of siRNAs as potential antiviral agents against dengue viruses |
title_short | Bioinformatics prediction of siRNAs as potential antiviral agents against dengue viruses |
title_sort | bioinformatics prediction of sirnas as potential antiviral agents against dengue viruses |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398769/ https://www.ncbi.nlm.nih.gov/pubmed/22829722 http://dx.doi.org/10.6026/97320630008519 |
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