SARS-CoV-2 uses metabotropic glutamate receptor subtype 2 as an internalization factor to infect cells

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) uses angiotensin-converting enzyme 2 (ACE2) as a binding receptor to enter cells via clathrin-mediated endocytosis (CME). However, receptors involved in other steps of SARS-CoV-2 infection remain largely unknown. Here, we found that metabotropic glutamate receptor subtype 2 (mGluR2) is an internalization factor for SARS-CoV-2. Our results show that mGluR2 directly interacts with the SARS-CoV-2 spike protein and that knockdown of mGluR2 decreases internalization of SARS-CoV-2 but not cell binding. Further, mGluR2 is uncovered to cooperate with ACE2 to facilitate SARS-CoV-2 internalization through CME and mGluR2 knockout in mice abolished SARS-CoV-2 infection in the nasal turbinates and significantly reduced viral infection in the lungs. Notably, mGluR2 is also important for SARS-CoV spike protein- and Middle East respiratory syndrome coronavirus spike protein-mediated internalization. Thus, our study identifies a novel internalization factor used by SARS-CoV-2 and opens a new door for antiviral development against coronavirus infection.

Automated summary

mGluR2 has been identified as an internalization factor for SARS-CoV-2, facilitating viral entry into cells. It cooperates with ACE2 to promote virus internalization through clathrin-mediated endocytosis, and its knockout in mice significantly reduces viral infection in the nasal turbinates and lungs. mGluR2 is also important for the internalization of other coronaviruses, suggesting it may be a potential target for antiviral development.