摩洛哥 SARS-CoV-2 大流行头 3 年的遗传多样性和基因组流行病学:综合序列分析,包括摩洛哥的独特血统 B.1.528。

Access microbiology Pub Date : 2024-10-07 eCollection Date: 2024-01-01 DOI:10.1099/acmi.0.000853.v4
Soulandi Djorwé, Abderrahim Malki, Néhémie Nzoyikorera, Joseph Nyandwi, Samuel Privat Zebsoubo, Kawthar Bellamine, Amale Bousfiha
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引用次数: 0

摘要

在 COVID-19 大流行出现后的 3 年中,非洲大陆与世界其他地区一样,受到 COVID-19 的严重影响。在摩洛哥,COVID-19 大流行的特点是多种 SARS-CoV-2 变体的出现和传播,导致感染和死亡人数大幅增加。然而,在摩洛哥,对几个病毒系的遗传多样性、进化和流行病学的全面了解仍然有限。本研究试图通过回顾性分析加深对 SARS-CoV-2 基因组流行病学的了解。本研究的主要目的是利用基因组流行病学方法分析 SARS-CoV-2 的遗传多样性,确定不同的病毒系,并评估它们在摩洛哥大流行期间的演变情况。此外,研究还强调了不同病毒系中功能蛋白的几个关键突变,并分析了这些毒株之间的遗传关系,以更好地了解它们的进化途径。研究人员从 GISAID EpiCoV 数据库中提取了 2020 年至 2023 年期间在摩洛哥分离到的 2274 个 SARS-CoV-2 基因组序列,并对其进行了分析。根据 GISAID、Nextstrain 和 Pangolin 的命名法对品系和支系进行了分类。该研究按照 STROBE(加强流行病学观察性研究的报告)指南进行和报告。通过对 2274 个基因组序列的详尽分析,确定了 157 个 PANGO 系,包括 B.1、B.1.1、B.1.528 和 B.1.177 等著名系,以及 B.1.1.7、B.1.621、B.1.525、B.1.351、B.1.617.1、B.1.617.2 等变体,以及其显著的亚系 AY.33、AY.72、AY.112、AY.121,这些变体在 2021 年 12 月被 Omicron 取代之前,随着时间的推移不断演化。在分析的 2274 个序列中,Omicron 及其亚变种的流行率为 59.5%。最主要的支系是 21K、21L 和 22B,它们在系统发育上分别与 BA.1、BA.2 和 BA.5 相关。2022 年 6 月,摩洛哥迅速观察到感染病例的再次爆发,22B 支系的亚变种如 BA.5.2.20、BA.5、BA.5.1、BA.5.2.1 和 BF.5 等出现并同时共存,取代了亚变种 BA.1(支系显示 21K)和 BA.2(支系显示 21L),成为边缘变种。然而,XBB(支系 22F)及其后代,如 XBB.1.5(23A)、XBB.1.16(23B)、CH.1.1(23C)、XBB.1.9(23D)、XBB.2.3(23E)、EG.5.1(23F)和 XBB.1.5.70(23G) 等,却在零星地进化。此外,还发现了一些显著的突变,如 H69del/V70del、G142D、K417N、T478K、E484K、E484A、L452R、F486P、N501Y、Q613H、D614G 和 P681H/R。已知这些 SARS-CoV-2 变异中的一些参与了增加传播性、毒力和抗体逃逸。这项研究确定了摩洛哥分离株基因多样性中涉及的几个不同的品系和突变,并分析了它们的进化趋势。这些发现为更好地了解不同变异及其在传播性、致病性和抗原性(免疫逃避/再感染)变异中的作用提供了坚实的基础。此外,在摩洛哥发现的不同品系数量显著,这凸显了对 COVID-19 进行持续监测的重要性。此外,扩大疫苗接种覆盖面也有助于保护患者免受更严重临床疾病的侵袭。
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Genetic diversity and genomic epidemiology of SARS-CoV-2 during the first 3 years of the pandemic in Morocco: comprehensive sequence analysis, including the unique lineage B.1.528 in Morocco.

During the 3 years following the emergence of the COVID-19 pandemic, the African continent, like other regions of the world, was substantially impacted by COVID-19. In Morocco, the COVID-19 pandemic has been marked by the emergence and spread of several SARS-CoV-2 variants, leading to a substantial increase in the incidence of infections and deaths. Nevertheless, the comprehensive understanding of the genetic diversity, evolution, and epidemiology of several viral lineages remained limited in Morocco. This study sought to deepen the understanding of the genomic epidemiology of SARS-CoV-2 through a retrospective analysis. The main objective of this study was to analyse the genetic diversity of SARS-CoV-2 and identify distinct lineages, as well as assess their evolution during the pandemic in Morocco, using genomic epidemiology approaches. Furthermore, several key mutations in the functional proteins across different viral lineages were highlighted along with an analysis of the genetic relationships amongst these strains to better understand their evolutionary pathways. A total of 2274 genomic sequences of SARS-CoV-2 isolated in Morocco during the period of 2020 to 2023, were extracted from the GISAID EpiCoV database and subjected to analysis. Lineages and clades were classified according to the nomenclature of GISAID, Nextstrain, and Pangolin. The study was conducted and reported in accordance with STROBE (Strengthening the Reporting of Observational Studies in Epidemiology) guidelines. An exhaustive analysis of 2274 genomic sequences led to the identification of 157 PANGO lineages, including notable lineages such as B.1, B.1.1, B.1.528, and B.1.177, as well as variants such as B.1.1.7, B.1.621, B.1.525, B.1.351, B.1.617.1, B.1.617.2, and its notable sublineages AY.33, AY.72, AY.112, AY.121 that evolved over time before being supplanted by Omicron in December 2021. Among the 2274 sequences analysed, Omicron and its subvariants had a prevalence of 59.5%. The most predominant clades were 21K, 21L, and 22B, which are respectively related phylogenetically to BA.1, BA.2, and BA.5. In June 2022, Morocco rapidly observed a recrudescence of cases of infection, with the emergence and concurrent coexistence of subvariants from clade 22B such as BA.5.2.20, BA.5, BA.5.1, BA.5.2.1, and BF.5, supplanting the subvariants BA.1 (clade display 21K) and BA.2 (clade display 21L), which became marginal. However, XBB (clade 22F) and its progeny such XBB.1.5(23A), XBB.1.16(23B), CH.1.1(23C), XBB.1.9(23D), XBB.2.3(23E), EG.5.1(23F), and XBB.1.5.70(23G) have evolved sporadically. Furthermore, several notable mutations, such as H69del/V70del, G142D, K417N, T478K, E484K, E484A, L452R, F486P, N501Y, Q613H, D614G, and P681H/R, have been identified. Some of these SARS-CoV-2 mutations are known to be involved in increasing transmissibility, virulence, and antibody escape. This study has identified several distinct lineages and mutations involved in the genetic diversity of Moroccan isolates, as well as the analysis of their evolutionary trends. These findings provide a robust basis for better understanding the distinct mutations and their roles in the variation of transmissibility, pathogenicity, and antigenicity (immune evasion/reinfection). Furthermore, the noteworthy number of distinct lineages identified in Morocco highlights the importance of maintaining continuous surveillance of COVID-19. Moreover, expanding vaccination coverage would also help protect patients against more severe clinical disease.

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