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津巴布韦第二波疫情中诊断基因靶点的 SARS-CoV-2 突变:回顾性基因组分析。

SARS-CoV-2 mutations on diagnostic gene targets in the second wave in Zimbabwe: A retrospective genomic analysis.

机构信息

Microbiology Unit, Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe; National Microbiology Reference Laboratory, Ministry of Health and Child Care, Harare, Zimbabwe.

Quadram Institute Bioscience, Norwich, UK.

出版信息

S Afr Med J. 2023 Mar 2;113(3):141-147. doi: 10.7196/SAMJ.2023.v113i3.16762.

Abstract

BACKGROUND

SARS-CoV-2 continues to be a major issue in resource-limited settings, particularly owing to the limited supply of vaccinescaused by inequitable distribution.

OBJECTIVE

To monitor diagnostic gene targets to identify potential test failures caused by mutations, which is important for public health.

METHODS

Here we analysed the genome sequence of SARS-CoV-2 from the second wave in Zimbabwe. A total of 377 samples weresequenced at Quadram Institute Bioscience. After quality control, 192 sequences passed and were analysed.

RESULTS

The Beta variant was dominant during this period, contributing 77.6% (149) of the genomes sequenced and having a total of 2994mutations in diagnostic polymerase chain reaction target genes. Many single nucleotide polymorphism mutations resulted in amino acidsubstitution that had the potential to impact viral fitness by increasing the rate of transmission or evading the immune response to previousinfection or vaccination.

CONCLUSION

There were nine lineages circulating in Zimbabwe during the second wave. The B.1.351 was dominant, accounting for >75%.There were over 3 000 mutations on the diagnostic genes and lineage B.1.351, contributing almost two-thirds of the mutations. The S-genehad the most mutations and the E-gene was the least mutated.

摘要

背景

SARS-CoV-2 在资源有限的环境中仍然是一个主要问题,特别是由于疫苗分配不均导致供应有限。

目的

监测诊断基因靶标,以识别可能由突变引起的测试失败,这对公共卫生很重要。

方法

在这里,我们分析了津巴布韦第二波疫情中的 SARS-CoV-2 基因组序列。总共在 Quadram Institute Bioscience 对 377 个样本进行了测序。经过质量控制,有 192 个序列通过并进行了分析。

结果

在此期间,Beta 变体占主导地位,占测序基因组的 77.6%(149 个),在诊断聚合酶链反应靶基因中共有 2994 个突变。许多单核苷酸多态性突变导致氨基酸替换,这有可能通过增加传播速度或逃避对先前感染或疫苗接种的免疫反应来影响病毒适应性。

结论

在第二波疫情期间,津巴布韦有 9 个谱系在循环。B.1.351 占主导地位,占比超过 75%。在诊断基因和谱系 B.1.351 上有超过 3000 个突变,占突变的近三分之二。S 基因的突变最多,E 基因的突变最少。

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