Abstract
The type II transmembrane serine proteases TMPRSS2 and HAT activate influenza viruses and the SARS-coronavirus (TMPRSS2) in cell culture and may play an important role in viral spread and pathogenesis in the infected host. However, it is at present largely unclear to what extent these proteases are expressed in viral target cells in human tissues. Here, we show that both HAT and TMPRSS2 are coexpressed with 2,6-linked sialic acids, the major receptor determinant of human influenza viruses, throughout the human respiratory tract. Similarly, coexpression of ACE2, the SARS-coronavirus receptor, and TMPRSS2 was frequently found in the upper and lower aerodigestive tract, with the exception of the vocal folds, epiglottis and trachea. Finally, activation of influenza virus was conserved between human, avian and porcine TMPRSS2, suggesting that this protease might activate influenza virus in reservoir-, intermediate- and human hosts. In sum, our results show that TMPRSS2 and HAT are expressed by important influenza and SARS-coronavirus target cells and could thus support viral spread in the human host.
Highlights
Influenza viruses and the SARS-coronavirus (SARS-CoV) are highly transmissible respiratory viruses which pose a serious threat to human health
We examined if TMPRSS2 of mouse origin facilitates HA proteolysis, since mice are commonly used as a model system for influenza virus spread and pathogenesis
Our observations suggest that TMPRSS2 can support influenza virus spread in species integral to the influenza zoonosis, and that mice are suitable models to study the role of TMPRSS2, TMPRSS4 and HAT in viral spread and pathogenesis
Summary
Influenza viruses and the SARS-coronavirus (SARS-CoV) are highly transmissible respiratory viruses which pose a serious threat to human health. The severe acute respiratory syndrome coronavirus (SARS-CoV), which causes a novel lung disease, SARS, emerged in 2002 and spread to 26 countries in 2003, with 774 fatal infections [2]. Both SARS-CoV and influenza viruses circulate in animal reservoirs, water fowl (influenza) and bats (SARS-CoV) [3,4]. SARS-S and influenza HA bind to host cell receptors, ACE2 (SARS-CoV) [5] and 2,6-linked sialic acid on membrane proteins or lipids (human influenza viruses) [6], and mediate the fusion of the viral membrane with a host cell membrane. Viral components are released into the host cell and can subvert the synthetic capabilities of the host cell for production and release of progeny particles
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