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COVID-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review
The Covid-19 pandemic is highly contagious and has spread rapidly across the globe. To date there have been no specific treatment options available for this life-threatening disease. During this medical emergency, target-based drug repositioning/repurposing with a continuous monitoring and recording...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868660/ https://www.ncbi.nlm.nih.gov/pubmed/33555378 http://dx.doi.org/10.1007/s00203-021-02183-z |
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author | Raj, C. T. Dhanya Kandaswamy, Dinesh Kumar Danduga, Ravi Chandra Sekhara Reddy Rajasabapathy, Raju James, Rathinam Arthur |
author_facet | Raj, C. T. Dhanya Kandaswamy, Dinesh Kumar Danduga, Ravi Chandra Sekhara Reddy Rajasabapathy, Raju James, Rathinam Arthur |
author_sort | Raj, C. T. Dhanya |
collection | PubMed |
description | The Covid-19 pandemic is highly contagious and has spread rapidly across the globe. To date there have been no specific treatment options available for this life-threatening disease. During this medical emergency, target-based drug repositioning/repurposing with a continuous monitoring and recording of results is an effective method for the treatment and drug discovery. This review summarizes the recent findings on COVID-19, its genomic organization, molecular evolution through phylogenetic analysis and has recapitulated the drug targets by analyzing the viral molecular machinery as drug targets and repurposing of most frequently used drugs worldwide and their therapeutic applications in COVID-19. Data from solidarity trials have shown that the treatment with Chloroquine, hydroxychloroquine and lopinavir-ritonavir had no effect in reducing the mortality rate and also had adverse side effects. Remdesivir, Favipiravir and Ribavirin might be a safer therapeutic option for COVID-19. Recent clinical trial has revealed that dexamethasone and convalescent plasma treatment can reduce mortality in patients with severe forms of COVID-19. |
format | Online Article Text |
id | pubmed-7868660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-78686602021-02-09 COVID-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review Raj, C. T. Dhanya Kandaswamy, Dinesh Kumar Danduga, Ravi Chandra Sekhara Reddy Rajasabapathy, Raju James, Rathinam Arthur Arch Microbiol Original Paper The Covid-19 pandemic is highly contagious and has spread rapidly across the globe. To date there have been no specific treatment options available for this life-threatening disease. During this medical emergency, target-based drug repositioning/repurposing with a continuous monitoring and recording of results is an effective method for the treatment and drug discovery. This review summarizes the recent findings on COVID-19, its genomic organization, molecular evolution through phylogenetic analysis and has recapitulated the drug targets by analyzing the viral molecular machinery as drug targets and repurposing of most frequently used drugs worldwide and their therapeutic applications in COVID-19. Data from solidarity trials have shown that the treatment with Chloroquine, hydroxychloroquine and lopinavir-ritonavir had no effect in reducing the mortality rate and also had adverse side effects. Remdesivir, Favipiravir and Ribavirin might be a safer therapeutic option for COVID-19. Recent clinical trial has revealed that dexamethasone and convalescent plasma treatment can reduce mortality in patients with severe forms of COVID-19. Springer Berlin Heidelberg 2021-02-08 2021 /pmc/articles/PMC7868660/ /pubmed/33555378 http://dx.doi.org/10.1007/s00203-021-02183-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Raj, C. T. Dhanya Kandaswamy, Dinesh Kumar Danduga, Ravi Chandra Sekhara Reddy Rajasabapathy, Raju James, Rathinam Arthur COVID-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review |
title | COVID-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review |
title_full | COVID-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review |
title_fullStr | COVID-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review |
title_full_unstemmed | COVID-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review |
title_short | COVID-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review |
title_sort | covid-19: molecular pathophysiology, genetic evolution and prospective therapeutics—a review |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868660/ https://www.ncbi.nlm.nih.gov/pubmed/33555378 http://dx.doi.org/10.1007/s00203-021-02183-z |
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