Tomo Sojit, Saikiran Gangam, Banerjee Mithu, Paul Sushmita
Department of Biochemistry, All India Institute of Medical Sciences, Jodhpur, India.
Indian Institute of Technology, Jodhpur, India.
EXCLI J. 2021 Apr 16;20:781-791. doi: 10.17179/excli2021-3530. eCollection 2021.
The disruption of antioxidant defense has been demonstrated in severe acute respiratory syndrome due to SARS-CoV infection. Selenium plays a major role in decreasing the ROS produced in response to various viral infections. Selenoprotein enzymes are essential in combating oxidative stress caused due to excessive generation of ROS. Selenium also has a role in inhibiting the activation of NF-κB, thus alleviating inflammation. In viral infections, selenoproteins have also been found to inhibit type I interferon responses, modulate T cell proliferation and oxidative burst in macrophages, and inhibit viral transcriptional activators. Potential virally encoded selenoproteins have been identified by computational analysis in different viral genomes like HIV-1, Japanese encephalitis virus (JEV), and hepatitis C virus. This review discusses the role and the possible mechanisms of selenium, selenoproteins, and virally encoded selenoproteins in the pathogenicity of viral infections. Identification of potential selenoproteins in the COVID 19 genome by computational tools will give insights further into their role in the pathogenesis of viral infections.
在由SARS-CoV感染引起的严重急性呼吸综合征中,抗氧化防御系统已被证明遭到破坏。硒在减少因各种病毒感染而产生的活性氧(ROS)方面发挥着主要作用。硒蛋白酶对于对抗因ROS过度产生而导致的氧化应激至关重要。硒在抑制核因子κB(NF-κB)的激活方面也发挥作用,从而减轻炎症。在病毒感染中,还发现硒蛋白可抑制I型干扰素反应、调节巨噬细胞中的T细胞增殖和氧化爆发,并抑制病毒转录激活因子。通过计算分析已在不同病毒基因组(如HIV-1、日本脑炎病毒(JEV)和丙型肝炎病毒)中鉴定出潜在的病毒编码硒蛋白。本综述讨论了硒、硒蛋白和病毒编码硒蛋白在病毒感染致病性中的作用及可能机制。通过计算工具在新冠病毒基因组中鉴定潜在的硒蛋白将进一步深入了解它们在病毒感染发病机制中的作用。