Department of Pharmacology in Dentistry, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.
J Periodontol. 2021 Jul;92(7):35-43. doi: 10.1002/JPER.20-0623. Epub 2021 Jan 12.
Type 2 diabetes and periodontitis predispose to a higher risk of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Recent studies show upregulation of innate immuno-regulatory microRNA-146a and -155 in oral fluids of patients with type 2 diabetes as well as of patients with periodontitis. The aim was to investigate whether upregulation of these microRNAs may relate to patient susceptibility to the infection via modulation of SARS-CoV-2 cellular entry factors expression.
Due to limited experimental feasibility and health risks in Coronavirus Disease 2019, bioinformatic analyses combining with system biology were used as initial investigation of interaction between microRNA-146 and -155 and genes encoding SARS-CoV-2 entry factors.
SARS-CoV-2 cellular entry factors are expressed in salivary glands and masticatory mucosa (tongue) at different expression levels, comparable with those measured in lungs and tonsil. MicroRNA-146 and -155 are widely involved in the regulation of SARS-CoV-2 oral cellular entry factors and may enhance expression of ACE2 and modulate genes involved in host immunity.
Diabetes- and periodontitis-induced increase in microRNA-146a and -155 in oral cavity is predicted to upregulate angiotensin-converting enzyme 2 expression, essential SARS-CoV-2 entry receptors, and modulate host antiviral response. As it could suggest increased infectivity of diabetes and periodontitis patients, additional protective measures for periodontists are recommended.
2 型糖尿病和牙周炎使严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染的风险更高。最近的研究表明,2 型糖尿病患者和牙周炎患者的口腔液中先天免疫调节 microRNA-146a 和 -155 上调。目的是研究这些 microRNA 的上调是否可能通过调节 SARS-CoV-2 细胞进入因子的表达与患者对感染的易感性有关。
由于在 2019 年冠状病毒疾病中实验可行性和健康风险有限,因此使用生物信息学分析结合系统生物学作为 microRNA-146 和 -155 与编码 SARS-CoV-2 进入因子的基因之间相互作用的初步研究。
SARS-CoV-2 细胞进入因子在唾液腺和咀嚼黏膜(舌头)中以不同的表达水平表达,与肺部和扁桃体中测量的表达水平相当。microRNA-146 和 -155 广泛参与 SARS-CoV-2 口腔细胞进入因子的调节,可能增强 ACE2 的表达,并调节参与宿主免疫的基因。
口腔中糖尿病和牙周炎诱导的 microRNA-146a 和 -155 增加预计会上调血管紧张素转换酶 2 表达,这是 SARS-CoV-2 进入受体的必需物质,并调节宿主抗病毒反应。由于这可能表明糖尿病和牙周炎患者的感染性增加,建议牙周病学家采取额外的保护措施。