Mortazavi S A R, Kaveh-Ahangar K, Mortazavi S M J, Firoozi D, Haghani M
MD, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
MSc, Vice-Chancellery for Research, Shiraz University of Medical Sciences, Shiraz, Iran.
J Biomed Phys Eng. 2021 Feb 1;11(1):109-114. doi: 10.31661/jbpe.v0i0.2010-1218. eCollection 2021 Feb.
Neanderthal genes possibly gave modern human protection against viruses. However, a recent study revealed that that a long sequence of DNA that is inherited from our Neanderthal ancestors can be linked to severe COVID-19 infection and hospitalization. Substantial evidence now indicates that our genetic background may be involved in the transmissibility of SARS-CoV-2 and the rapid progress of COVID-19 in some infected individuals. Although both morbidity and mortality of COVID-19 strongly depends on key factors such as age and co-existing health conditions, potential classes of human genomic variants possibly affect the likelihood of SARS-CoV-2 infection and its progress. Despite Iran and Mongolia seem to share the same SARS-CoV-2 mutation cluster, the COVID-19 mortality rates in these two countries are drastically different. While the population in Iran is 25.8 times higher than that of Mongolia, the number of confirmed cases is 1170 times higher. Moreover, the death rate shows a drastic difference. Since Neanderthals interbred with modern humans in Middle East between 47,000 and 65,000 years ago before going extinct 40,000 years ago, some Iranians have much more Neanderthal DNA than other people. Although neither genetic background nor environmental factors alone can determine our risk of developing severe COVID-19, our genes clearly affect both the development and progression of infectious diseases including COVID-19. Given these considerations, we believe that these great differences, at least to some extent, can be due to the proportion of Neanderthal genes among the people of these two countries.
尼安德特人的基因可能赋予了现代人类抵御病毒的能力。然而,最近一项研究表明,从我们的尼安德特人祖先那里遗传下来的一长段DNA序列可能与严重的新冠病毒感染及住院情况有关。现在有大量证据表明,我们的基因背景可能与新冠病毒的传播能力以及新冠病毒在一些感染者体内的快速发展有关。尽管新冠病毒的发病率和死亡率在很大程度上取决于年龄和并存的健康状况等关键因素,但人类基因组变异的潜在类别可能会影响感染新冠病毒的可能性及其发展进程。尽管伊朗和蒙古似乎共享相同的新冠病毒突变簇,但这两个国家的新冠病毒死亡率却截然不同。伊朗的人口比蒙古多25.8倍,而确诊病例数却高出1170倍。此外,死亡率也存在巨大差异。由于尼安德特人在4万年前灭绝之前,于4.7万至6.5万年前在中东地区与现代人类进行了杂交,一些伊朗人拥有比其他人更多的尼安德特人DNA。尽管基因背景和环境因素都不能单独决定我们患重症新冠的风险,但我们的基因显然会影响包括新冠病毒在内的传染病的发生和发展。考虑到这些因素,我们认为,至少在某种程度上,这些巨大差异可能是由于这两个国家人群中尼安德特人基因的比例不同所致。