Tissue Architecture and Regeneration Research Group, School of Life Sciences, University of Westminster, London W1W 6UW, UK.
Institute of Biotechnology, Gebze Technical University, Gebze, 41400 Kocaeli, Turkey.
Viruses. 2021 Jan 16;13(1):117. doi: 10.3390/v13010117.
Our recent study identified seven key microRNAs (miR-8066, 5197, 3611, 3934-3p, 1307-3p, 3691-3p, 1468-5p) similar between SARS-CoV-2 and the human genome, pointing at miR-related mechanisms in viral entry and the regulatory effects on host immunity. To identify the putative roles of these miRs in zoonosis, we assessed their conservation, compared with humans, in some key wild and domestic animal carriers of zoonotic viruses, including bat, pangolin, pig, cow, rat, and chicken. Out of the seven miRs under study, miR-3611 was the most strongly conserved across all species; miR-5197 was the most conserved in pangolin, pig, cow, bat, and rat; miR-1307 was most strongly conserved in pangolin, pig, cow, bat, and human; miR-3691-3p in pangolin, cow, and human; miR-3934-3p in pig and cow, followed by pangolin and bat; miR-1468 was most conserved in pangolin, pig, and bat; while miR-8066 was most conserved in pangolin and pig. In humans, miR-3611 and miR-1307 were most conserved, while miR-8066, miR-5197, miR-3334-3p and miR-1468 were least conserved, compared with pangolin, pig, cow, and bat. Furthermore, we identified that changes in the miR-5197 nucleotides between pangolin and human can generate three new miRs, with differing tissue distribution in the brain, lung, intestines, lymph nodes, and muscle, and with different downstream regulatory effects on KEGG pathways. This may be of considerable importance as miR-5197 is localized in the spike protein transcript area of the SARS-CoV-2 genome. Our findings may indicate roles for these miRs in viral-host co-evolution in zoonotic hosts, particularly highlighting pangolin, bat, cow, and pig as putative zoonotic carriers, while highlighting the miRs' roles in KEGG pathways linked to viral pathogenicity and host responses in humans. This in silico study paves the way for investigations into the roles of miRs in zoonotic disease.
我们最近的研究确定了七种在 SARS-CoV-2 和人类基因组之间相似的关键 microRNAs(miR-8066、5197、3611、3934-3p、1307-3p、3691-3p、1468-5p),这些 microRNAs 指向病毒进入和宿主免疫调节的 microRNA 相关机制。为了确定这些 miRs 在人畜共患病中的潜在作用,我们评估了它们在一些关键的野生动物和家畜携带的人畜共患病病毒中的保守性,包括蝙蝠、穿山甲、猪、牛、鼠和鸡。在研究的七种 miRs 中,miR-3611 在所有物种中最保守;miR-5197 在穿山甲、猪、牛、蝙蝠和大鼠中最保守;miR-1307 在穿山甲、猪、牛、蝙蝠和人类中最保守;miR-3691-3p 在穿山甲、牛和人类中最保守;miR-3934-3p 在猪和牛中最保守,其次是穿山甲和蝙蝠;miR-1468 在穿山甲、猪和蝙蝠中最保守;而 miR-8066 在穿山甲和猪中最保守。在人类中,miR-3611 和 miR-1307 最保守,而 miR-8066、miR-5197、miR-3334-3p 和 miR-1468 与穿山甲、猪、牛和蝙蝠相比最不保守。此外,我们发现穿山甲和人类之间的 miR-5197 核苷酸变化可以产生三种新的 miRs,它们在大脑、肺、肠道、淋巴结和肌肉中的组织分布不同,对 KEGG 途径的下游调节作用也不同。这可能非常重要,因为 miR-5197 定位于 SARS-CoV-2 基因组的刺突蛋白转录区域。我们的发现可能表明这些 miRs 在人畜共患病宿主中的病毒-宿主共同进化中发挥作用,特别是突出穿山甲、蝙蝠、牛和猪作为可能的人畜共患病携带者,同时突出 miRs 在与病毒致病性和人类宿主反应相关的 KEGG 途径中的作用。这项计算机研究为研究 miRs 在人畜共患病中的作用铺平了道路。