UR-Génomes et Milieux, Université de Nouakchott, Nouakchott BP 880, Mauritania.
Institut National de Recherche en Santé Publique, Nouakchott BP 695, Mauritania.
Genes (Basel). 2024 Mar 14;15(3):361. doi: 10.3390/genes15030361.
The rapid genetic evolution of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) during the coronavirus disease 2019 (COVID-19) pandemic has greatly challenged public health authorities worldwide, including in Mauritania. Despite the presence of the virus in Mauritania, only one study described its genomic variation during the course of the epidemic. The purpose of the present study was to document the genomic pattern of SARS-CoV-2 variants from clinical isolates during the COVID-19 outbreak in Mauritania, from September to November 2021. The whole genomes from 54 SARS-CoV-2 strains detected in nasopharyngeal swabs with a cycle threshold value ≤ 30 were successfully sequenced using next-generation sequencing (NGS) and the Illumina protocol. The mean genome coverage (±standard deviation) was 96.8% (±3.7). The most commonly identified clade was 21J (57.4%), followed by 21D (16.7%), 20A (11.1%), and 20B (9.2%). At the level of lineages, the majority of the samples were Delta variants with the sub-lineage AY.34 (or B.1.617.2.34). Among the 54 SARS-CoV-2 isolates that were successfully sequenced, 33 (61.1%) came from vaccinated individuals, and 21 (38.9%) were from unvaccinated individuals. Several SARS-CoV-2 variants were present in Mauritania between September and November 2021. As Mauritania, like many West African countries, is resource-limited regarding viral genome sequencing facilities, establishment of mutualized sub-regional sequencing platforms will be necessary to ensure continuous monitoring of mutations in viral genomes and track potential reduction in COVID-19 vaccine efficacy, increased transmissibility, and disease severity.
新型冠状病毒 2(SARS-CoV-2)在 2019 年冠状病毒病(COVID-19)大流行期间的快速遗传进化给全球公共卫生当局带来了巨大挑战,毛里塔尼亚也不例外。尽管该病毒存在于毛里塔尼亚,但只有一项研究描述了其在疫情期间的基因组变异情况。本研究的目的是记录 2021 年 9 月至 11 月毛里塔尼亚 COVID-19 爆发期间从临床分离株中检测到的 SARS-CoV-2 变异的基因组模式。使用下一代测序(NGS)和 Illumina 方案成功地对 54 株来自鼻咽拭子的 SARS-CoV-2 株的全基因组进行了测序,这些株的循环阈值值≤30。平均基因组覆盖率(±标准偏差)为 96.8%(±3.7)。最常见的亚谱系是 21J(57.4%),其次是 21D(16.7%)、20A(11.1%)和 20B(9.2%)。在谱系水平上,大多数样本是带有亚谱系 AY.34(或 B.1.617.2.34)的 Delta 变体。在成功测序的 54 株 SARS-CoV-2 分离株中,33 株(61.1%)来自接种疫苗的个体,21 株(38.9%)来自未接种疫苗的个体。2021 年 9 月至 11 月期间,毛里塔尼亚存在几种 SARS-CoV-2 变体。由于毛里塔尼亚与许多西非国家一样,在病毒基因组测序设施方面资源有限,因此有必要建立相互化的次区域测序平台,以确保对病毒基因组的突变进行持续监测,并跟踪 COVID-19 疫苗效力降低、传染性增加和疾病严重程度增加的潜在情况。