Spike substitution T813S increases Sarbecovirus fusogenicity by enhancing the usage of TMPRSS2

PLoS Pathog. 2023 May 17;19(5):e1011123. doi: 10.1371/journal.ppat.1011123. eCollection 2023 May.

Abstract

SARS-CoV Spike (S) protein shares considerable homology with SARS-CoV-2 S, especially in the conserved S2 subunit (S2). S protein mediates coronavirus receptor binding and membrane fusion, and the latter activity can greatly influence coronavirus infection. We observed that SARS-CoV S is less effective in inducing membrane fusion compared with SARS-CoV-2 S. We identify that S813T mutation is sufficient in S2 interfering with the cleavage of SARS-CoV-2 S by TMPRSS2, reducing spike fusogenicity and pseudoparticle entry. Conversely, the mutation of T813S in SARS-CoV S increased fusion ability and viral replication. Our data suggested that residue 813 in the S was critical for the proteolytic activation, and the change from threonine to serine at 813 position might be an evolutionary feature adopted by SARS-2-related viruses. This finding deepened the understanding of Spike fusogenicity and could provide a new perspective for exploring Sarbecovirus' evolution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • COVID-19*
  • Humans
  • Proteolysis
  • SARS-CoV-2 / genetics
  • SARS-CoV-2 / metabolism
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism
  • Severe acute respiratory syndrome-related coronavirus* / genetics
  • Spike Glycoprotein, Coronavirus / metabolism
  • Virus Internalization
  • Virus Replication

Substances

  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2
  • TMPRSS2 protein, human
  • Serine Endopeptidases

Grants and funding

This project was funded by the National Key R&D Program of China (grant number: 2022YFC2304204 to YQC); the National Natural Science Foundation of China (32000648 to YM); the National Natural Science Foundation of China (NO. 92169104, 31970881, 82150204,32171192, 31971161 and 31900546); Shenzhen Science and Technology Program (Grant No. RCJC20210706092009004, JSGG20200225152008136 and JCYJ20190807154603596 to YQC, JCYJ20200109142438111 and GXWD20201231165807008 to YM, KQTD20200820145822023 to MS). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.