Revealing the genotypic variants and proteomic mutations in Turkish SARS-CoV-2 driving evolution and virulence

Ragothaman Prathiviraj , K. Prinsha , Saqib Hassan , S. Hari Krishna Kumar , George Seghal Kiran , Joseph Selvin
{"title":"Revealing the genotypic variants and proteomic mutations in Turkish SARS-CoV-2 driving evolution and virulence","authors":"Ragothaman Prathiviraj ,&nbsp;K. Prinsha ,&nbsp;Saqib Hassan ,&nbsp;S. Hari Krishna Kumar ,&nbsp;George Seghal Kiran ,&nbsp;Joseph Selvin","doi":"10.1016/j.meomic.2023.100024","DOIUrl":null,"url":null,"abstract":"<div><p>Turkey is a transcontinental nation with much of its territory in western Asia and southeast Europe, and it is the 6th most affected country by SARS-CoV-2 globally, so far, many mutations have occurred within this short period of time. The present study mainly focused on identifying genotypic variants and proteomic mutations, along with the folding rate and virulence action of Turkey SARS-CoV-2 isolates. The phylogenomic study reveals that the first origination of SARS-CoV-2 isolates (2020) in Turkey has more chance of an occurrence of mutation rate during evolution/new origination. 53 genotypic- and 45 proteomic variants among 83 isolates were found. The genotypic and proteomic variants from 2022 isolates have six times higher mutation rates than 2020 isolates. The highest number of mutations occurred in the 2022 isolate (ERAGEM-OM-1104/2022), with 60 mutations in the G53 variant, followed by 44 mutations in the G49 variant (ERAGEM-DEL-1103/2021) and 42 mutations in the G50 variant (Ank_DLT/2021). Also, we identified 38 novel mutations among 45 proteomic variants. The predicted virulence mechanism of some ORFs such as Nsp1, Nsp3, Nsp4, Nsp5, Nsp8, 2′O-ribose, Spike, Orf3a, Envelope, Orf7b, Orf8, and Nucleocapsid shows high virulence and transmission rate. Hence, our findings would help the researchers to develop new anti-virals against new variants from Turkey’s SARS-CoV-2 isolates.</p></div>","PeriodicalId":100914,"journal":{"name":"Medicine in Omics","volume":"9 ","pages":"Article 100024"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicine in Omics","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590124923000056","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Turkey is a transcontinental nation with much of its territory in western Asia and southeast Europe, and it is the 6th most affected country by SARS-CoV-2 globally, so far, many mutations have occurred within this short period of time. The present study mainly focused on identifying genotypic variants and proteomic mutations, along with the folding rate and virulence action of Turkey SARS-CoV-2 isolates. The phylogenomic study reveals that the first origination of SARS-CoV-2 isolates (2020) in Turkey has more chance of an occurrence of mutation rate during evolution/new origination. 53 genotypic- and 45 proteomic variants among 83 isolates were found. The genotypic and proteomic variants from 2022 isolates have six times higher mutation rates than 2020 isolates. The highest number of mutations occurred in the 2022 isolate (ERAGEM-OM-1104/2022), with 60 mutations in the G53 variant, followed by 44 mutations in the G49 variant (ERAGEM-DEL-1103/2021) and 42 mutations in the G50 variant (Ank_DLT/2021). Also, we identified 38 novel mutations among 45 proteomic variants. The predicted virulence mechanism of some ORFs such as Nsp1, Nsp3, Nsp4, Nsp5, Nsp8, 2′O-ribose, Spike, Orf3a, Envelope, Orf7b, Orf8, and Nucleocapsid shows high virulence and transmission rate. Hence, our findings would help the researchers to develop new anti-virals against new variants from Turkey’s SARS-CoV-2 isolates.

揭示土耳其严重急性呼吸系统综合征冠状病毒2型的基因型变异和蛋白质组突变驱动进化和毒力
土耳其是一个横贯大陆的国家,其大部分领土位于西亚和东南欧,是全球受严重急性呼吸系统综合征冠状病毒2型影响第六大的国家,到目前为止,在这段短时间内发生了许多突变。本研究主要集中于鉴定土耳其严重急性呼吸系统综合征冠状病毒2型分离株的基因型变异和蛋白质组突变,以及折叠率和毒力作用。系统发育学研究表明,土耳其首次起源的严重急性呼吸系统综合征冠状病毒2型分离株(2020)在进化/新起源过程中发生突变率的可能性更大。在83个分离株中发现53个基因型和45个蛋白质组变异。2022分离株的基因型和蛋白质组变异的突变率是2020分离株的六倍。突变数量最多的是2022分离株(ERAGEM-OM-104/2022),G53变体中有60个突变,其次是G49变体中的44个突变(ERAGEM-DEL-1103/2021)和G50变体中的42个突变(Ank_DLT/2021)。此外,我们在45个蛋白质组变体中鉴定出38个新突变。一些ORF如Nsp1、Nsp3、Nsp4、Nsp5、Nsp8、2′O-核糖、Spike、Orf3a、Envelope、Orf7b、Orf4和核衣壳的毒力机制预测显示出高毒力和高传播率。因此,我们的发现将有助于研究人员开发针对土耳其严重急性呼吸系统综合征冠状病毒2型分离株新变种的新抗病毒药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信