Gunawardene Chaminda D, Wong Lok-Yin Roy
Center for Virus-Host Innate Immunity, Rutgers New Jersey Medical School, Newark, New Jersey, USA.
Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers New Jersey Medical School, Newark, New Jersey, USA.
J Virol. 2025 Feb 25;99(2):e0135324. doi: 10.1128/jvi.01353-24. Epub 2025 Jan 6.
Betacoronaviruses express a small internal (I) protein that is encoded by the same subgenomic RNA (sgRNA) as the nucleocapsid (N) protein. Translation of the +1 reading frame of the N sgRNA through leaky ribosomal scanning leads to expression of the I protein. The I protein is an accessory protein reported to evade host innate immune responses during coronavirus infection. Previous studies have shown that the I proteins of severe acute respiratory syndrome coronavirus (SARS-CoV), SARS-CoV-2, and Middle East respiratory syndrome coronavirus suppress type I interferon production by distinct mechanisms. In this review, we summarize the current knowledge on the I proteins of betacoronaviruses from different subgenera, with emphasis on its function and role in pathogenesis.
β冠状病毒表达一种小的内部(I)蛋白,该蛋白由与核衣壳(N)蛋白相同的亚基因组RNA(sgRNA)编码。通过核糖体渗漏扫描对N sgRNA的+1读码框进行翻译,从而导致I蛋白的表达。I蛋白是一种辅助蛋白,据报道在冠状病毒感染期间可逃避宿主的先天免疫反应。先前的研究表明,严重急性呼吸综合征冠状病毒(SARS-CoV)、SARS-CoV-2和中东呼吸综合征冠状病毒的I蛋白通过不同机制抑制I型干扰素的产生。在这篇综述中,我们总结了目前关于不同亚属β冠状病毒I蛋白的知识,重点是其在发病机制中的功能和作用。