从尼日利亚奥贡州奥塔一名患者的呼吸道样本中分离出的 SARS-CoV-2 全基因组回顾性测序结果

IF 1 Q4 GENETICS & HEREDITY
Olajumoke Olufunmilayo Joseph , Samuel Olatunde Dahunsi , Anthony Okoh
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引用次数: 0

摘要

造成 COVID-19 大流行的严重急性呼吸系统综合症冠状病毒-2(SARS-CoV-2)现在已被认为是一种地方性病毒,会在全球不同的社区持续爆发。尽管包括尼日利亚在内的全球范围内对 SARS-CoV-2 进行了多项监测研究,但仍有必要了解大流行后立即流行的该病毒株的独特性,以充实全球信息数据库,从而帮助疫苗生产和未来应对另一场 SARS 相关 CoV 大流行。我们在南非 Inqaba 生物技术公司对之前报告的阳性样本中的 SARS-CoV-2 进行了回顾性全基因组测序(WGS)分析。RNA 提取使用 Quick - RNA 病毒试剂盒(Zymo),文库制备使用 NEBNext ARTIC SARS-CoV-2 FS 文库制备试剂盒(Illumina),按照制造商的说明进行。WGS 在 Illumina 的 NextSeq500 平台上进行。包含未组装原始序列读数的 fastq 文件已提交给 NCBI SARS-CoV-2 资源,并获得了 BioProject 加入号 PRJNA1076330。研究序列中的尖峰(s)基因有7个突变(G142D, A163V, V213G, D614G, H655Y, N679K, P681H),与武汉参考序列WIV04中的尖峰(s)基因有99.4%的相同性。非结构蛋白(NSP)--7、8、9、10 和 16 与 GISAID 上的蝙蝠/云南/RaTG13(一种在蝙蝠中发现的 SARS 相关 CoV)序列具有 100 % 的同一性。虽然研究序列是从一个无症状的个体身上获得的,但观察到的 S 突变与毒力、抗原转变、传播性增强和宿主改变有关。因此,在成功利用这种无症状变异体后,它有可能转变为未来 SARS-CoV-2 疫苗的潜在候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A retrospective whole genome sequencing of SARS-CoV-2 isolate from respiratory sample of an individual from Ota – Ogun State, Nigeria

Severe acute respiratory syndrome coronavirus – 2 (SARS-CoV-2) which was responsible for the COVID-19 pandemic has now been considered an endemic virus, that will continually produce sporadic outbreaks in different communities around the globe. Although, there are several surveillance studies on SARS-CoV-2 globally, including Nigeria, there is still an important need to understand the uniqueness of the strains of the virus that was circulating immediately after the pandemic, to add to the global database of information that will aid vaccine production and future preparedness against another SARS - related CoV pandemic.

Towards the end of the pandemic, between February – August 2022, SARS-CoV-2 was detected in a surveillance project in Ota – Ogun State Nigeria. We carried out a retrospective whole genome sequencing (WGS) analysis of SARS-CoV-2 in the previously reported positive sample, at Inqaba biotech in South Africa. RNA extraction was carried out using the Quick – RNA viral kit (Zymo) and library preparation was done by NEBNext ARTIC SARS-CoV-2 FS Library Prep kit (Illumina) according to the manufacturer's instruction. The WGS was carried out on the NextSeq500 platform by Illumina. The fastq file containing the unassembled raw sequence reads were submitted to NCBI SARS-CoV-2 resources, and a BioProject accession number PRJNA1076330 was issued. The DRAGEN Targeted Microbial, GISAID-CoVsurver mutation, BLAST and MAFFT applications were used for analysis.

The spike (s) gene of the study sequence possessed seven mutations (G142D, A163V, V213G, D614G, H655Y, N679K, P681H) and shared 99.4 % identity with those of the Wuhan reference sequence WIV04. The non-structural proteins (NSP) – 7,8,9,10 and 16 shared 100 % identity with bat/Yunnan/RaTG13 (a SARS- related CoV found in bats) sequence on GISAID. Although, the study sequence was obtained from an asymptomatic individual, the S mutations observed are known to be related to virulence, antigenic shift, enhanced transmissibility and host change. Thus, upon successful exploitation of this asymptomatic variant, it may possibly be transformed to a potential candidate for SARS-CoV-2 vaccine in future.

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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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