Author

Jordan Anderson-Daniels

Vanderbilt University Medical CenterORCID 0000-0002-9275-4330Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Microbiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Organism:mouse· 2 Organism:human· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

Laura J. StevensiD· 2 shared Mark R. DenisoniD· 2 shared Nicholas S. HeatoniD· 2 shared Xiaotao LuiD· 2 shared Boyd L. YountiD· 1 shared Brook E. HeatoniD· 1 shared Cameron NguyeniD· 1 shared Camryn Pajon· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersMicrobiology

Laura J. StevensORCID

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2 papers

Recent·Most cited

Loss of nsp14-exonuclease activity impairs the replication, proofreading, fitness and pathogenesis of SARS-CoV-2

Jordan Anderson-Daniels, Meghan V. Diefenbacher, Boyd L. Yount, Rita M. Meganck, Longping V. Tse, Kaitlyn N. Burke, Hector A. Miranda, D. Trevor Scobey, Xiaotao Lu, Laura J. Stevens, Kenneth H. Dinnon, Nathaniel S. Chapman, Camryn Pajon, John M. Powers, Cameron Nguyen, , Timothy Patrick Sheahan

This study shows that SARS-CoV-2 with impaired nsp14-exonuclease activity has reduced replication, fitness, and pathogenesis, but remains viable in some conditions.

mBio · May 6, 2026Peer-reviewedMicrobiology

The coronavirus nsp14 exoribonuclease interface with the cofactor nsp10 is essential for efficient virus replication and enzymatic activity.

Samantha L. Grimes, Brook E. Heaton, Mackenzie L. Anderson, Katie Burke, Laura J. Stevens, Xiaotao Lu, Nicholas S. Heaton, Mark R. Denison, Jordan Anderson-Daniels

This study shows that the nsp14-nsp10 interaction is essential for coronavirus replication and enzymatic activity, with specific interface residues critical for function.

Journal of Virology · Jan 10, 2025Peer-reviewedMicrobiology