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For the betacoronaviruses MHV and SARS-CoV, ExoN was reported to promote the fidelity of genome replication, presumably by mediating a form of proofreading. For these viruses, ExoN knockout mutants are viable while displaying an increased mutation frequency. Strikingly, we have now established that the equivalent ExoN knockout mutants of two other betacoronaviruses, MERS-CoV and SARS-CoV-2, are nonviable, suggesting an additional and critical ExoN function in their replication. This is remarkable in light of the very limited genetic distance between SARS-CoV and SARS-CoV-2, which is highlighted, for example, by 95% amino acid sequence identity in their nsp14 sequences. For (recombinant) MERS-CoV nsp14, both its enzymatic activities were evaluated using newly developed\n                    <jats:italic>in vitro<\/jats:italic>\n                    assays that can be used to characterize these key replicative enzymes in more detail and explore their potential as target for antiviral drug development.\n                  <\/jats:p>","DOI":"10.1128\/jvi.01246-20","type":"journal-article","created":{"date-parts":[[2020,9,16]],"date-time":"2020-09-16T11:03:29Z","timestamp":1600254209000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":239,"title":["The Enzymatic Activity of the nsp14 Exoribonuclease Is Critical for Replication of MERS-CoV and SARS-CoV-2"],"prefix":"10.1128","volume":"94","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3577-4909","authenticated-orcid":false,"given":"Natacha S.","family":"Ogando","sequence":"first","affiliation":[{"name":"Molecular Virology Laboratory, 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