Suppr超能文献

一项用于揭示南亚地区严重急性呼吸综合征冠状病毒2(SARS-CoV-2)基因组和蛋白质组突变图谱的新一代测序(NGS)分析。

A next generation sequencing (NGS) analysis to reveal genomic and proteomic mutation landscapes of SARS-CoV-2 in South Asia.

作者信息

Mahmood Tousif Bin, Saha Ayan, Hossan Mohammad Imran, Mizan Shagufta, Arman S M Abu Sufian, Chowdhury Afrin Sultana

机构信息

Department of Biotechnology and Genetic Engineering, Noakhali Science and Technology University, Noakhali 3814, Bangladesh.

Department of Genetic Engineering and Biotechnology, East West University, Dhaka 1212, Bangladesh.

出版信息

Curr Res Microb Sci. 2021 Aug 24;2:100065. doi: 10.1016/j.crmicr.2021.100065. eCollection 2021 Dec.

Abstract

Counts for SARS-CoV-2 associated infections and fatalities are on the rise globally even in regions which contained the spread momentarily. The pattern of infections has been found to be controlled by the distinctive selection pressures exerted by fluctuating environmental nature and hosts. A total of 410 whole-genome sequences submitted by the South Asian countries were retrieved from the GISAID database and analyzed to assess the impact and pattern of mutations in this region. Most common and frequent mutations in the South Asian countries are 241C > , 3037C > , 14408C > , and 23403A >  and about 85% SNPs are localized in ORF1ab, spike protein, and nucleocapsid. Among the identified mutations, the proportion of missense type (54.17%) was highest, followed by the synonymous (41.66%) and the non-coding types (4.17%). While analyzing transmission source in terms of geolocation, the largest clustered group from the South Asian countries was based on the G-clade (D614G) (81.7%; 335/410 samples), tracing the inception and transmission of SARS-CoV-2 infections in the South Asian countries from European regions. Phylogenetic analysis also revealed that the South Asian strains are highly related to the South American and European strains. We found that G-clade mutations are more prevalent (96.19%) in the samples of Bangladesh which were also prevalent in the European isolates. Surprisingly, one missense mutation (1163A > ) in ORF1ab gene became dominant only in Bangladesh (78.8%), which led to debates regarding effects on the pathogenicity and transmissibility of the virus. Overall, the findings of this study highlight the frequently mutated SARS-CoV-2 variants among the COVID-19 patients in the South Asian countries which might ease containment of the disease in this region through investigating the virulence reducing factors as the identified mutations are strongly correlated with low infection and mortality rate.

摘要

即使在曾暂时控制住病毒传播的地区,全球范围内与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)相关的感染和死亡病例数仍在上升。已发现感染模式受环境变化性质和宿主所施加的独特选择压力控制。从全球共享流感数据倡议组织(GISAID)数据库中检索了南亚国家提交的410个全基因组序列,并进行分析以评估该地区突变的影响和模式。南亚国家最常见和频繁出现的突变是241C>、3037C>、14408C>和23403A>,约85%的单核苷酸多态性(SNP)位于开放阅读框1ab(ORF1ab)、刺突蛋白和核衣壳中。在已识别的突变中,错义类型的比例最高(54.17%),其次是同义类型(41.66%)和非编码类型(4.17%)。在按地理位置分析传播源时,南亚国家最大的聚类组基于G分支(D614G)(81.7%;410个样本中的335个),追踪了南亚国家SARS-CoV-2感染从欧洲地区的起源和传播。系统发育分析还显示,南亚毒株与南美和欧洲毒株高度相关。我们发现G分支突变在孟加拉国的样本中更为普遍(96.19%),在欧洲分离株中也很普遍。令人惊讶的是,ORF1ab基因中的一个错义突变(1163A>)仅在孟加拉国占主导地位(78.8%),这引发了关于其对病毒致病性和传播性影响的争论。总体而言,本研究结果突出了南亚国家2019冠状病毒病(COVID-19)患者中频繁突变的SARS-CoV-2变体,由于已识别的突变与低感染率和死亡率密切相关,通过研究毒力降低因素,这可能有助于该地区控制疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbb9/8610355/feb6af82094b/gr4.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验