An official website of the United States government
The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before
sharing sensitive information, make sure you’re on a federal
government site.
The site is secure.
The https:// ensures that you are connecting to the
official website and that any information you provide is encrypted
and transmitted securely.
To address the expression pattern of the SARS-CoV-2 receptor ACE2 and the viral priming protease TMPRSS2 in the respiratory tract, this study investigated RNA sequencing transcriptome profiling of samples of airway and oral mucosa. As shown, ACE2 has medium levels of expression in both small airway epithelium and masticatory mucosa, and high levels of expression in nasal epithelium. The expression of ACE2 is low in mucosal-associated invariant T (MAIT) cells and cannot be detected in alveolar macrophages. TMPRSS2 is highly expressed in small airway epithelium and nasal epithelium and has lower expression in masticatory mucosa. Our results provide the molecular basis that the nasal mucosa is the most susceptible locus in the respiratory tract for SARS-CoV-2 infection and consequently for subsequent droplet transmission and should be the focus for protection against SARS-CoV-2 infection.
The authors declare that they have no competing interests.
Figures
Figure 1
The expression of SARS-CoV-2 entry…
Figure 1
The expression of SARS-CoV-2 entry genes. ( a ) Established SARS-CoV-2 entry genes, …
Figure 1
The expression of SARS-CoV-2 entry genes. (a) Established SARS-CoV-2 entry genes, ACE2 and TMPRSS2, in five different types of samples. The difference between ACE2 and TMPRSS2 in the small airway epithelium is highly significant (p = 1.00 × 10-12). In the nasal epithelium, the expression of ACE2 is significantly higher than that in small airway epithelium (p = 6.92 × 10−4), alveolar macrophages (p = 5.02 × 10−4), MAIT (p = 0.016), and masticatory mucosa (p = 5.48 × 10−7); the expression of TMPRSS2 is lower than that in small airway epithelium (p = 5.20 × 10−3), but higher than in alveolar macrophages (p = 2.98 × 10−3), MAIT (p = 0.040), and masticatory mucosa (p = 1.40 × 10−5). (b) The expression of ACE and possible SARS-CoV-2 alternative entry genes, BSG, DPP4, and FURIN. Y-axis represents normalized FPKM values by the average of relative levels of 6 HKGs. The boxplot produced by the IBM SPSS Statistics Version 23 shows the mean, the first quartile and the third quartile, and the 95% confidence interval (CI). FPKM: fragments per kilobase of transcript per million mapped reads.
Wu Z., McGoogan J.M. Characteristics of and Important Lessons from the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases from the Chinese Center for Disease Control and Prevention. JAMA. 2020;323:1239–1242. doi: 10.1001/jama.2020.2648.
-
DOI
-
PubMed
Lu R., Zhao X., Li J., Niu P., Yang B., Wu H., Wang W., Song H., Huang B., Zhu N. Genomic characterisation and epidemiology of 2019 novel coronavirus: Implications for virus origins and receptor binding. Lancet. 2020;395:565–574. doi: 10.1016/S0140-6736(20)30251-8.
-
DOI
-
PMC
-
PubMed
Ferrario C.M., Ahmad S., Nagata S., Simington S.W., Varagic J., Kon N., Dell’italia L.J. An evolving story of angiotensin-II-forming pathways in rodents and humans. Clin. Sci. 2014;126:461–469. doi: 10.1042/CS20130400.
-
DOI
-
PMC
-
PubMed
Li W., Moore M.J., Vasilieva N., Sui J., Wong S.K., Berne M.A., Somasundaran M., Sullivan J.L., Luzuriaga K., Greenough T.C. Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus. Nature. 2003;426:450–454. doi: 10.1038/nature02145.
-
DOI
-
PMC
-
PubMed
Liu Y., Gayle A.A., Wilder-Smith A., Rocklöv J. The reproductive number of COVID-19 is higher compared to SARS coronavirus. J. Travel Med. 2020;27:taaa021. doi: 10.1093/jtm/taaa021.
-
DOI
-
PMC
-
PubMed