Department of Epidemiology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Accra, Ghana.
Department of Epidemiology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Accra, Ghana.
Infect Genet Evol. 2024 Apr;119:105568. doi: 10.1016/j.meegid.2024.105568. Epub 2024 Feb 15.
Genetic variations in the human angiotensin converting enzyme gene (ACE) influence ACE enzyme expression levels in humans and subsequently influence both communicable and non-communicable disease outcomes. More recently, polymorphisms in this gene have been linked to susceptibility and outcomes of infectious diseases such as the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and malaria infections. This study is the first to investigate the genetic diversity of ACE and ACE2 polymorphisms in the Ghanaian population. Archived filter blood blot samples from malaria patients aged ≤9 years were used. Molecular analysis for the detection of ACE rs4646994 (I/D), ACE2 rs2106809 (C/T) and rs2285666 (G/A) alleles as well as ACE2 exons 1-4 polymorphisms was conducted on 300 samples. The D allele (54%,162/300) was the most dominant polymorphism observed in the ACE rs4646994 gene whilst the G (68%, 204/300) and T alleles (59.3%,178/300) were the most frequent ACE2 rs2285666 and rs2106809 polymorphisms observed. For the 300 samples sequenced for ACE2 exons 1-4, analyses were done on 268, 282 and 137 quality sequences for exons 1, 2 and 3-4 respectively. For exon 1, the mutation D38N (2.2%; 6/268) was the most prevalent. The S19P and E37K mutations previously reported to influence COVID-19 infections were observed at low frequencies (0.4%, 1/268 each). No mutations were observed in exon 2. The N121K/T variants were the most seen in exons 3-4 at frequencies of 5.1% (K121, 7/137) and 2.9% (T121, 4/137) respectively. Most of the variants observed in the exons were novel compared to those reported in other populations in the world. This is the first study to investigate the genetic diversity of ACE and ACE2 genes in Ghanaians. The observation of novel mutations in the ACE2 gene is suggesting selection pressure. The importance of the mutations for communicable and non-communicable diseases (malaria and COVID-19) are further discussed.
人类血管紧张素转换酶基因(ACE)的遗传变异影响 ACE 酶在人类中的表达水平,进而影响传染病和非传染性疾病的结局。最近,该基因的多态性与严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)和疟疾感染等传染病的易感性和结局有关。本研究首次调查了加纳人群中 ACE 和 ACE2 多态性的遗传多样性。使用了年龄≤9 岁的疟疾患者的存档过滤血斑样本。对 300 个样本进行了 ACE rs4646994(I/D)、ACE2 rs2106809(C/T)和 rs2285666(G/A)等位基因以及 ACE2 外显子 1-4 多态性的分子分析。ACE rs4646994 基因中观察到最常见的多态性是 D 等位基因(54%,162/300),而 ACE2 rs2285666 和 rs2106809 多态性中最常见的是 G(68%,204/300)和 T 等位基因(59.3%,178/300)。对 300 个进行 ACE2 外显子 1-4 测序的样本进行了分析,外显子 1、2 和 3-4 的质量序列分别为 268、282 和 137。对于外显子 1,最常见的突变是 D38N(2.2%,6/268)。以前报道过影响 COVID-19 感染的 S19P 和 E37K 突变频率较低(0.4%,各 1/268)。在外显子 2 中未观察到突变。在 3-4 个外显子中,最常见的 N121K/T 变体频率分别为 5.1%(K121,7/137)和 2.9%(T121,4/137)。与世界其他人群报告的多态性相比,大多数在这些外显子中观察到的变体是新的。这是首次在加纳人中研究 ACE 和 ACE2 基因的遗传多样性。ACE2 基因中的新突变表明存在选择压力。进一步讨论了这些突变对传染病和非传染病(疟疾和 COVID-19)的重要性。