CONACyT Facultad de Medicina y Cirugía, Universidad Autónoma "Benito Juárez" de Oaxaca, Oaxaca, Mexico.
Centro de Investigación Facultad de Medicina UNAM-UABJO, Facultad de Medicina y Cirugía, Universidad Autónoma "Benito Juárez" de Oaxaca, Oaxaca, Mexico.
J Med Virol. 2021 Apr;93(4):2099-2114. doi: 10.1002/jmv.26591. Epub 2020 Nov 1.
The genomic sequences of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) worldwide are publicly available and are derived from studies due to the increase in the number of cases. The importance of study of mutations is related to the possible virulence and diagnosis of SARS-CoV-2. To identify circulating mutations present in SARS-CoV-2 genomic sequences in Mexico, Belize, and Guatemala to find out if the same strain spread to the south, and analyze the specificity of the primers used for diagnosis in these samples. Twenty three complete SARS-CoV-2 genomic sequences, available in the GISAID database from May 8 to September 11, 2020 were analyzed and aligned versus the genomic sequence reported in Wuhan, China (NC_045512.2), using Clustal Omega. Open reading frames were translated using the ExPASy Translate Tool and UCSF Chimera (v.1.12) for amino acid substitutions analysis. Finally, the sequences were aligned versus primers used in the diagnosis of COVID-19. One hundred and eighty seven distinct variants were identified, of which 102 are missense, 66 synonymous and 19 noncoding. P4715L and P5828L substitutions in replicase polyprotein were found, as well as D614G in spike protein and L84S in ORF8 in Mexico, Belize, and Guatemala. The primers design by CDC of United States showed a positive E value. The genomic sequences of SARS-CoV-2 in Mexico, Belize, and Guatemala present similar mutations related to a virulent strain of greater infectivity, which could mean a greater capacity for inclusion in the host genome and be related to an increased spread of the virus in these countries, furthermore, its diagnosis would be affected.
全球严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的基因组序列均可公开获取,这些序列是基于病例数量增加而从研究中获得的。研究突变的重要性与 SARS-CoV-2 的可能毒力和诊断有关。为了确定在墨西哥、伯利兹和危地马拉的 SARS-CoV-2 基因组序列中存在的循环突变,以了解是否有相同的病毒株传播到南部,并分析这些样本中用于诊断的引物的特异性。对 2020 年 5 月 8 日至 9 月 11 日 GISAID 数据库中可用的 23 个完整的 SARS-CoV-2 基因组序列进行了分析,并与中国武汉报告的基因组序列(NC_045512.2)进行了比对,使用 Clustal Omega。使用 ExPASy Translate Tool 和 UCSF Chimera(v.1.12)对开放阅读框进行翻译,以分析氨基酸替换。最后,将序列与用于诊断 COVID-19 的引物进行比对。共鉴定出 187 个不同的变体,其中 102 个为错义,66 个为同义,19 个为非编码。在复制酶多蛋白中发现了 P4715L 和 P5828L 替换,以及在墨西哥、伯利兹和危地马拉的 Spike 蛋白中的 D614G 和 ORF8 中的 L84S。美国 CDC 设计的引物显示出阳性的 E 值。墨西哥、伯利兹和危地马拉的 SARS-CoV-2 基因组序列存在相似的突变,与更具感染力的毒力株有关,这可能意味着更大的宿主基因组纳入能力,并与这些国家病毒的传播增加有关,此外,其诊断也将受到影响。