Author

D. J. Bennison

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 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Assay:proteomics· 3 Organism:bacteria (other)· 2 Research Focus:host-pathogen & immune response· 2 Research Focus:protein folding & dynamics· 2 Research Focus:cell signaling & trafficking· 1 Organism:E. coli· 1 Organism:mouse· 1

Frequent Co-Authors

A. Crespo-Puig· 2 shared A. R. Shenoy· 2 shared R. M. Corrigan· 2 shared V. Mishra· 2 shared A. Dejoux· 1 shared A. J. Choi· 1 shared A. Wood· 1 shared C. McCarthy· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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2 shared papersMicrobiology

A. Crespo-Puig

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Aminoglycoside heteroresistance in Enterobacter cloacae is driven by the cell envelope stress response.

A. J. Choi, D. J. Bennison, E. Kulkarni, H. Sun, H. Li, J. Bradshaw, H. W. Yeap, N. Lim, V. Mishra, A. Crespo-Puig, F. Davies, S. Sriskandan, A. R. Shenoy

This study identifies the CpxRA cell envelope stress response as the driver of aminoglycoside heteroresistance in E. cloacae, showing its role in transient resistance and MIC elevation.

bioRxiv · Oct 11, 2023 · PreprintMicrobiology

IL-1β turnover by TRIP12 and AREL1 ubiquitin ligases and UBE2L3 limits inflammation

V. Mishra, A. Crespo-Puig, C. McCarthy, T. Masonou, I. Glegola-Madejska, A. Dejoux, G. Dow, M. J. G. Eldridge, L. H. Marinelli, M. Meng, S. Wang, D. J. Bennison, A. R. Shenoy

This study identifies UBE2L3, TRIP12, and AREL1 as ubiquitin ligases that regulate pro-IL-1β turnover, limiting inflammation by reducing precursor availability.

bioRxiv · Sep 14, 2022Immunology

(p)ppGpp inhibits 70S ribosome formation in Staphylococcus aureus by impeding GTPase-ribosome interactions

D. J. Bennison, J. A. Nakamoto, T. D. Craggs, P. Milon, J. B. Rafferty, R. M. Corrigan

This study shows (p)ppGpp inhibits 70S ribosome formation in Staphylococcus aureus by reducing RA-GTPase-ribosome interactions through inducing the OFF-state conformation.

bioRxiv · Jan 19, 2021 · PreprintMicrobiology

The (p)ppGpp-binding GTPase Era promotes rRNA processing and cold shock survival in Staphylococcus aureus

A. Wood, S. E. Irving, D. J. Bennison, R. M. Corrigan

This study identifies Era as a GTPase that facilitates rRNA processing and cold shock survival in S. aureus by interacting with other proteins involved in ribosome biogenesis.

bioRxiv · May 2, 2019Microbiology