Department of Pharmacology, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
Center for Emerging Viruses, University of Minnesota, Minneapolis, Minnesota, United States of America.
PLoS Pathog. 2024 May 6;20(5):e1012204. doi: 10.1371/journal.ppat.1012204. eCollection 2024 May.
Since the COVID-19 outbreak, raccoon dogs have been suggested as a potential intermediary in transmitting SARS-CoV-2 to humans. To understand their role in the COVID-19 pandemic and the species barrier for SARS-CoV-2 transmission to humans, we analyzed how their ACE2 protein interacts with SARS-CoV-2 spike protein. Biochemical data showed that raccoon dog ACE2 is an effective receptor for SARS-CoV-2 spike protein, though not as effective as human ACE2. Structural comparisons highlighted differences in the virus-binding residues of raccoon dog ACE2 compared to human ACE2 (L24Q, Y34H, E38D, T82M, R353K), explaining their varied effectiveness as receptors for SARS-CoV-2. These variations contribute to the species barrier that exists between raccoon dogs and humans regarding SARS-CoV-2 transmission. Identifying these barriers can help assess the susceptibility of other mammals to SARS-CoV-2. Our research underscores the potential of raccoon dogs as SARS-CoV-2 carriers and identifies molecular barriers that affect the virus's ability to jump between species.
自 COVID-19 爆发以来,貉被认为是 SARS-CoV-2 向人类传播的潜在中间宿主。为了了解它们在 COVID-19 大流行中的作用以及 SARS-CoV-2 向人类传播的物种屏障,我们分析了它们的 ACE2 蛋白如何与 SARS-CoV-2 刺突蛋白相互作用。生化数据表明,貉 ACE2 是 SARS-CoV-2 刺突蛋白的有效受体,尽管不如人类 ACE2 有效。结构比较突出了貉 ACE2 与人类 ACE2 (L24Q、Y34H、E38D、T82M、R353K)在病毒结合残基上的差异,解释了它们作为 SARS-CoV-2 受体的有效性不同。这些差异导致了 SARS-CoV-2 在貉和人类之间传播的物种屏障。确定这些障碍可以帮助评估其他哺乳动物对 SARS-CoV-2 的易感性。我们的研究强调了貉作为 SARS-CoV-2 携带者的潜力,并确定了影响病毒在物种间跳跃能力的分子障碍。