Centro de Investigación en Enfermedades Tropicales (CIET) & Facultad de Microbiología, Universidad de Costa Rica, Costa Rica.
Instituto Costarricense de Investigación y Enseñanza en Nutrición y Salud (INCIENSA), Tres Ríos, Cartago, Costa Rica.
Infect Genet Evol. 2021 Aug;92:104872. doi: 10.1016/j.meegid.2021.104872. Epub 2021 Apr 24.
Genome sequencing is a key strategy in the surveillance of SARS-CoV-2, the virus responsible for the COVID-19 pandemic. Latin America is the hardest-hit region of the world, accumulating almost 20% of COVID-19 cases worldwide. In Costa Rica, from the first detected case on March 6th to December 31st almost 170,000 cases have been reported. We analyzed the genomic variability during the SARS-CoV-2 pandemic in Costa Rica using 185 sequences, 52 from the first months of the pandemic, and 133 from the current wave. Three GISAID clades (G, GH, and GR) and three PANGOLIN lineages (B.1, B.1.1, and B.1.291) were predominant, suggesting multiple re-introductions from other regions. The whole-genome variant calling analysis identified a total of 283 distinct nucleotide variants, following a power-law distribution with 190 single nucleotide mutations in a single sequence, and only 16 mutations were found in >5% sequences. These mutations were distributed through the whole genome. The prevalence of worldwide-found variant D614G in the Spike (98.9% in Costa Rica), ORF8 L84S (1.1%) is similar to what is found elsewhere. Interestingly, the frequency of mutation T1117I in the Spike has increased during the current pandemic wave beginning in May 2020 in Costa Rica, reaching 29.2% detection in the full genome analyses in November 2020. This variant has been observed in less than 1% of the GISAID reported sequences worldwide in 2020. Structural modeling of the Spike protein with the T1117I mutation suggests a potential effect on the viral oligomerization needed for cell infection, but no differences with other genomes on transmissibility, severity nor vaccine effectiveness are predicted. In conclusion, genome analyses of the SARS-CoV-2 sequences over the course of the COVID-19 pandemic in Costa Rica suggest the introduction of lineages from other countries and the detection of mutations in line with other studies, but pointing out the local increase in the detection of Spike-T1117I variant. The genomic features of this virus need to be monitored and studied in further analyses as part of the surveillance program during the pandemic.
基因组测序是监测导致 COVID-19 大流行的 SARS-CoV-2 病毒的关键策略。拉丁美洲是受疫情影响最严重的地区,累计病例数占全球近 20%。在哥斯达黎加,自 3 月 6 日首例确诊病例至 12 月 31 日,已报告近 17 万例病例。我们使用 185 条序列分析了哥斯达黎加 SARS-CoV-2 大流行期间的基因组变异性,其中 52 条来自大流行的最初几个月,133 条来自当前疫情。三个 GISAID 进化枝(G、GH 和 GR)和三个 PANGOLIN 谱系(B.1、B.1.1 和 B.1.291)占主导地位,表明有来自其他地区的多次重新输入。全基因组变异呼叫分析总共鉴定出 283 个不同的核苷酸变异,遵循幂律分布,在单个序列中有 190 个单核苷酸突变,只有 16 个突变出现在>5%的序列中。这些突变分布在整个基因组中。Spike 中发现的全球变异 D614G 在哥斯达黎加的流行率为 98.9%(在哥斯达黎加),ORF8 L84S(1.1%)与其他地方的发现相似。有趣的是,2020 年 5 月哥斯达黎加开始的当前疫情波期间,Spike 中的 T1117I 突变的频率增加,在 2020 年 11 月的全基因组分析中达到 29.2%的检测率。在 2020 年全球 GISAID 报告的序列中,这种变体的观察不到 1%。带有 T1117I 突变的 Spike 蛋白的结构建模表明,这可能会影响病毒感染所需的寡聚化,但没有预测到与其他基因组在传染性、严重程度或疫苗效力方面的差异。总之,对哥斯达黎加 COVID-19 大流行期间 SARS-CoV-2 序列的基因组分析表明,来自其他国家的谱系被引入,并检测到与其他研究一致的突变,但指出 Spike-T1117I 变异的检测有所增加。在大流行期间,作为监测计划的一部分,需要对这种病毒的基因组特征进行监测和进一步研究。