tetano
Editor, Senior Moderator
Proc Natl Acad Sci U S A
. 2026 Jul 7;123(27):e2601806123.
doi: 10.1073/pnas.2601806123. Epub 2026 Jun 29.
Evaluation of a proposed link between the SARS-CoV-2 furin cleavage site and mouse-adapted MERS-coronavirus MA30
Sarah M Metzger[SUP] 1 [/SUP], Terry C Jones[SUP] 1 2 [/SUP], Jenny I J Meier[SUP] 1 [/SUP], Anja Richter[SUP] 1 [/SUP], Mark-Christian Klassen[SUP] 3 [/SUP], Ruth Olmer[SUP] 3 [/SUP], Nicolai Diegmüller[SUP] 1 [/SUP], Kim C Heimsch[SUP] 1 [/SUP], Christian Drosten[SUP] 1 4 5 [/SUP]
Affiliations
The origin of the polybasic furin cleavage site (FCS) of SARS-CoV-2 remains a central question in debates on the emergence of COVID-19. One hypothesis proposes a genetic relationship between the SARS-CoV-2 S1/S2 motif RRAR and the RRVR sequence found in the mouse-adapted MERS-CoV strain MERS-MA30. Here, we combined large-scale bioinformatic analysis with experimental virology to evaluate this scenario. Analysis of over 17 million SARS-CoV-2 genomes revealed that the S:684V substitution corresponding to RRVR occurred repeatedly but only sporadically, never became phylogenetically basal, and showed limited geographic and temporal spread. Using reverse genetics, we generated SARS-CoV-2 variants encoding RRVR and demonstrated that S:684V consistently reduced viral entry efficiency and competitive fitness in multiple cell systems, including human respiratory epithelial cultures. RRVR variants did not evolve toward RRAR but instead accumulated alternative substitutions. These findings do not support an evolutionary relationship between MERS-MA30 and the SARS-CoV-2 FCS.
Keywords: MERS-CoV; SARS-CoV-2; pandemic origins.
. 2026 Jul 7;123(27):e2601806123.
doi: 10.1073/pnas.2601806123. Epub 2026 Jun 29.
Evaluation of a proposed link between the SARS-CoV-2 furin cleavage site and mouse-adapted MERS-coronavirus MA30
Sarah M Metzger[SUP] 1 [/SUP], Terry C Jones[SUP] 1 2 [/SUP], Jenny I J Meier[SUP] 1 [/SUP], Anja Richter[SUP] 1 [/SUP], Mark-Christian Klassen[SUP] 3 [/SUP], Ruth Olmer[SUP] 3 [/SUP], Nicolai Diegmüller[SUP] 1 [/SUP], Kim C Heimsch[SUP] 1 [/SUP], Christian Drosten[SUP] 1 4 5 [/SUP]
Affiliations
- PMID: 42372164
- DOI: 10.1073/pnas.2601806123
The origin of the polybasic furin cleavage site (FCS) of SARS-CoV-2 remains a central question in debates on the emergence of COVID-19. One hypothesis proposes a genetic relationship between the SARS-CoV-2 S1/S2 motif RRAR and the RRVR sequence found in the mouse-adapted MERS-CoV strain MERS-MA30. Here, we combined large-scale bioinformatic analysis with experimental virology to evaluate this scenario. Analysis of over 17 million SARS-CoV-2 genomes revealed that the S:684V substitution corresponding to RRVR occurred repeatedly but only sporadically, never became phylogenetically basal, and showed limited geographic and temporal spread. Using reverse genetics, we generated SARS-CoV-2 variants encoding RRVR and demonstrated that S:684V consistently reduced viral entry efficiency and competitive fitness in multiple cell systems, including human respiratory epithelial cultures. RRVR variants did not evolve toward RRAR but instead accumulated alternative substitutions. These findings do not support an evolutionary relationship between MERS-MA30 and the SARS-CoV-2 FCS.
Keywords: MERS-CoV; SARS-CoV-2; pandemic origins.