ACE2 and Furin Expressions in Oral Epithelial Cells Possibly Facilitate COVID-19 Infection via Respiratory and Fecal–Oral Routes

Frontiers in Medicine

article

Mei Zhong¹  Jian-ming Chen¹  Jiangyong Huang¹  Learn-Han Lee²  Cui-ling Qi³  Linhu Ge¹  Lijing Wang¹  Bingpeng Lin¹  Janak L. Pathak¹  Hongbin Gao⁵  Andrew J. Young⁶  Xinhong Wang¹  Chang Liu⁷  Kaibin Wu¹  Mingxiao Liu¹ 

[1] Guangzhou Key Laboratory of Basic and Applied Research of Oral Regenerative Medicine, Affiliated Stomatology Hospital of Guangzhou Medical University;Novel Bacteria and Drug Discovery Research Group (NBDD), Microbiome and Bioresource Research Strength (MBRS), Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia;School of Life Science and Biopharmaceutics, Vascular Biology Research Institute, Guangdong Pharmaceutical University;Institute of Oral Disease, Guangzhou Medical University;Key Laboratory of Guangdong Laboratory Animals, Guangdong Laboratory Animals Monitoring Institute;United States;Stomatology School of Ji'nan University

关键词: COVID-19;    SARS-CoV-2;    ACE2 (angiotensin converting enzyme-2);    Furin;    oral mucosa;    single cell RNA seq;   

DOI  :  10.3389/fmed.2020.580796

学科分类：社会科学、人文和艺术（综合）

来源: Frontiers

【 摘 要 】

Background: Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that mainly transfers from human to human via respiratory and gastrointestinal routes. The S-glycoprotein in the virus is the key factor for the entry of SARS-CoV-2 into the cell, which contains two functional domains: S1 is an angiotensin-converting enzyme 2 (ACE2) receptor binding domain, and S2 is necessary for fusion of the coronavirus and cell membranes. Moreover, it has been reported that ACE2 is likely to be the receptor for SARS-CoV-2. In addition, mRNA level expression of Furin enzyme and ACE2 receptor had been reported in airway epithelia, cardiac tissue, and enteric canals. However, the expression patterns of ACE2 and Furin in different cell types of oral tissues are still unclear. Methods: In order to investigate the potential infective channel of the new coronavirus via the oropharyngeal cavity, we analyze the expression of ACE2 and Furin in human oral mucosa using the public single-cell sequence datasets. Furthermore, immunohistochemistry was performed in mucosal tissue from different oral anatomical sites to confirm the expression of ACE2 and Furin at the protein level. Results: The bioinformatics results indicated the differential expression of ACE2 and Furin on epithelial cells from different oral anatomical sites. Immunohistochemistry results revealed that both the ACE2-positive and Furin-positive cells in the target tissues were mainly positioned in the epithelial layers, partly expressed in fibroblasts, further confirming the bioinformatics results. Conclusions: Based on these findings, we speculated that SARS-CoV-2 could invade oral mucosal cells through two possible routes: binding to the ACE2 receptor and fusion with cell membrane activated by Furin protease. Our results indicated that oral mucosa tissues are susceptible to SARS-CoV-2 that could facilitate COVID-19 infection via respiratory and fecal–oral routes.

【 授权许可】

CC BY