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Sequence analysis of the Spike, RNA-dependent RNA polymerase, and protease genes reveals a distinct evolutionary pattern of SARS-CoV-2 variants circulating in Yogyakarta and Central Java provinces, Indonesia.

Authors :
Hakim, Mohamad Saifudin
Gunadi
Rahayu, Ayu
Wibawa, Hendra
Eryvinka, Laudria Stella
Supriyati, Endah
Vujira, Khanza Adzkia
Iskandar, Kristy
Afiahayati
Daniwijaya, Edwin Widyanto
Oktoviani, Farida Nur
Annisa, Luthvia
Utami, Fadila Dyah Trie
Amadeus, Verrell Christopher
Nurhidayah, Setiani Silvy
Leksono, Tiara Putri
Halim, Fiqih Vidiantoro
Arguni, Eggi
Nuryastuti, Titik
Wibawa, Tri
Source :
Virus Genes; Apr2024, Vol. 60 Issue 2, p105-116, 12p
Publication Year :
2024

Abstract

During the Covid-19 pandemic, the resurgence of SARS-CoV-2 was due to the development of novel variants of concern (VOC). Thus, genomic surveillance is essential to monitor continuing evolution of SARS-CoV-2 and to track the emergence of novel variants. In this study, we performed phylogenetic, mutation, and selection pressure analyses of the Spike, nsp12, nsp3, and nsp5 genes of SARS-CoV-2 isolates circulating in Yogyakarta and Central Java provinces, Indonesia from May 2021 to February 2022. Various bioinformatics tools were employed to investigate the evolutionary dynamics of distinct SARS-CoV-2 isolates. During the study period, 213 and 139 isolates of Omicron and Delta variants were identified, respectively. Particularly in the Spike gene, mutations were significantly more abundant in Omicron than in Delta variants. Consistently, in all of four genes studied, the substitution rates of Omicron were higher than that of Delta variants, especially in the Spike and nsp12 genes. In addition, selective pressure analysis revealed several sites that were positively selected in particular genes, implying that these sites were functionally essential for virus evolution. In conclusion, our study demonstrated a distinct evolutionary pattern of SARS-CoV-2 variants circulating in Yogyakarta and Central Java provinces, Indonesia. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09208569
Volume :
60
Issue :
2
Database :
Complementary Index
Journal :
Virus Genes
Publication Type :
Academic Journal
Accession number :
176338708
Full Text :
https://doi.org/10.1007/s11262-023-02048-1