Back to Search Start Over

A comparative genomics-based study of positive strand RNA viruses emphasizing on SARS-CoV-2 utilizing dinucleotide signature, codon usage and codon context analyses.

Authors :
Saha J
Bhattacharjee S
Pal Sarkar M
Saha BK
Basak HK
Adhikary S
Roy V
Mandal P
Chatterjee A
Pal A
Source :
Gene reports [Gene Rep] 2021 Jun; Vol. 23, pp. 101055. Date of Electronic Publication: 2021 Feb 17.
Publication Year :
2021

Abstract

The novel corona virus disease or COVID-19 caused by a positive strand RNA virus (PRV) called SARS-CoV-2 is plaguing the entire planet as we conduct this study. In this study a multifaceted analysis was carried out employing dinucleotide signature, codon usage and codon context to compare and unravel the genomic as well as genic characteristics of the SARS-CoV-2 isolates and how they compare to other PRVs which represents some of the most pathogenic human viruses. The main emphasis of this study was to comprehend the codon biology of the SARS-CoV-2 in the backdrop of the other PRVs like Poliovirus, Japanese encephalitis virus, Hepatitis C virus, Norovirus , Rubella virus, Semliki Forest virus, Zika virus, Dengue virus, Human rhinoviruses and the Betacoronaviruses since codon usage pattern along with the nucleotide composition prevalent within the viral genome helps to understand the biology and evolution of viruses. Our results suggest discrete genomic dinucleotide signature within the PRVs. Some of the genes from the different SARS-CoV-2 isolates were also found to demonstrate heterogeneity in terms of their dinucleotide signature. The SARS-CoV-2 isolates also demonstrated a codon context trend characteristically dissimilar to the other PRVs. The findings of this study are expected to contribute to the developing global knowledge base in countering COVID-19.<br />Competing Interests: All the authors declare that they have no conflict of interest.<br /> (© 2021 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2452-0144
Volume :
23
Database :
MEDLINE
Journal :
Gene reports
Publication Type :
Academic Journal
Accession number :
33615042
Full Text :
https://doi.org/10.1016/j.genrep.2021.101055