Ysrafil, Ysrafil and Mus, Rosdiana and Gama, Noviyanty Indjar and Rahmaisyah, Dwi and Nur'amalia, Riskah (2021) Emerging mutation in SARS-CoV-2 spike: Widening distribution over time in different geographic areas. Biomedical Journal, 44 (5). 570 – 581. ISSN 23194170
Full text not available from this repository. (Request a copy)Abstract
Background: Recently, differences in mortality rates of COVID-19 in different geographic areas have become an important subject of research because these different mortality rates appear to be associated with mutations that appeared in SARS-CoV-2. The part of the viral body called the spike protein plays a critical role in the viral attachment and entry of the virus into the host cell. Accordingly, we hypothesized that mutations in this area will affect viral infectivity. Methods: A total of 193 sequences of spike SARS-CoV-2 were randomly retrieved from five different geographic areas and collection dates (from December 2019 until July 2020). Multiple sequence alignment for mutation and phylogenetic analyses was conducted using Bioedit, UniProt, and MEGA X. Results: We found 169 total mutations with 37 different mutations across the included samples. The D614G is the first and most frequently established mutation in different regions including Europe, Asia, America, Africa and Australia with the number of mutations of 49, 33, 17, 16 and 4, respectively. Furthermore, we also found mutations in several important domains in this virus including NTD and CTR/RBD of S1 subunit and at S2 subunit area, namely the peptide fusion (FP), and both heptad repetition (HR1 and 2) domains that suggested this could influence virus binding and virus-host cell membrane fusion. Conclusion: In summary, we concluded that mutation had generated diversity of spike SARS-CoV-2 sequences worldwide and is still growing. This analysis may provide important evidence that should be considered in vaccine development in different geographic areas. © 2021 Chang Gung University
Item Type: | Article |
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Additional Information: | Cited by: 5; All Open Access, Gold Open Access, Green Open Access |
Uncontrolled Keywords: | COVID-19; Humans; Mutation; Phylogeny; SARS-CoV-2; Spike Glycoprotein, Coronavirus; coronavirus spike glycoprotein; Severe acute respiratory syndrome coronavirus 2 spike protein; unclassified drug; coronavirus spike glycoprotein; Africa; Article; Asia; Australia; cell membrane; Europe; nonhuman; phylogeny; post hoc analysis; sequence alignment; Severe acute respiratory syndrome coronavirus 2; virus mutation; Western Hemisphere; genetics; human; mutation |
Subjects: | R Medicine > RB Biomedical Sciences |
Divisions: | Faculty of Medicine, Public Health and Nursing > Biomedical Sciences |
Depositing User: | Sri JUNANDI |
Date Deposited: | 27 Sep 2024 02:52 |
Last Modified: | 27 Sep 2024 02:52 |
URI: | https://ir.lib.ugm.ac.id/id/eprint/4570 |