Author

K. Plante

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Microbiology· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 3 Research Focus:cell type annotation· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1 Organism:virus· 1

Frequent Co-Authors

J. A. Plante· 3 shared V. D. Menachery· 3 shared D. H. Walker· 2 shared M. N. Vu· 2 shared A. Beall· 1 shared A. K. Overby· 1 shared A. L. Routh· 1 shared A. McLeland· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 32 mutual co-author links

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3 shared papersMicrobiology

J. A. Plante

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

SARS-CoV-2 hijacks fragile X mental retardation proteins for efficient infection

D. Garvanska, R. E. Alvarado, F. Mundt, E. Nilsson, J. Duel, F. Coscia, R. Lindqvist, K. Lokugamage, B. Johnson, J. A. Plante, D. R. Morris, M. N. Vu, L. Estes, A. McLeland, J. Walker, , J. Nilsson

This study identifies a novel interaction between SARS-CoV-2 NSP3 and FMRPs, showing that this interaction is critical for viral replication and disease progression.

bioRxiv · Sep 1, 2023 · PreprintMicrobiology

Nucleocapsid mutations in SARS-CoV-2 augment replication and pathogenesis.

B. A. Johnson, Y. Zhou, K. G. Lokugamage, M. N. Vu, N. E. Bopp, P. A. Crocquet-Valdes, B. Kalveram, C. Schindewolf, Y. Liu, D. Scharton, J. A. Plante, X. Xie, P. Aguilar, S. Weaver, P.-Y. Shi, , V. D. Menachery

This study shows that mutations in the SARS-CoV-2 nucleocapsid protein enhance viral replication and pathogenesis by increasing phosphorylation and resisting kinase inhibition.

PLOS Pathogens · Jun 21, 2022Peer-reviewedMicrobiology

Mucin 4 Protects Female Mice from Coronavirus Pathogenesis

J. A. Plante, K. Plante, L. Gralinski, A. Beall, M. T. Ferris, D. Bottomly, R. R. Green, S. McWeeney, M. T. Heise, R. S. Baric, V. D. Menachery

This study identifies Muc4 as a protective factor in female mice against SARS-CoV pathogenesis, showing sex-specific effects without altering viral titers.

bioRxiv · Feb 19, 2020 · PreprintMicrobiology