Sarah A. Kuehne
Characterization of the impact of rpoB mutations on the in vitro and in vivo competitive fitness of Clostridium difficile and susceptibility to fidaxomicin
Kuehne, Sarah A.; Dempster, Andrew W.; Collery, Mark M.; Joshi, Nimitray; Jowett, Jamie; Kelly, Michelle L.; Cave, Rory; Longshaw, Chris M.; Minton, Nigel P.
Authors
Andrew W. Dempster
Mark M. Collery
Nimitray Joshi
Jamie Jowett
Michelle L. Kelly
Rory Cave
Chris M. Longshaw
Professor NIGEL MINTON NIGEL.MINTON@NOTTINGHAM.AC.UK
Professor of Applied Molecular Microbiology
Abstract
Objectives
To establish the role of specific, non-synonymous SNPs in the RNA polymerase β subunit (rpoB) gene in reducing the susceptibility of Clostridium difficile to fidaxomicin and to explore the potential in vivo significance of rpoB mutant strains.
Methods
Allelic exchange was used to introduce three different SNPs into the rpoB gene of an erythromycin-resistant derivative (CRG20291) of C. difficile R20291. The genome sequences of the created mutants were determined and each mutant analysed with respect to growth and sporulation rates, toxin A/B production and cytotoxicity against Vero cells, and in competition assays. Their comparative virulence and colonization ability was also assessed in a hamster infection model.
Results
The MIC of fidaxomicin displayed by three mutants CRG20291-TA, CRG20291-TG and CRG20291-GT was substantially increased (>32, 8 and 2 mg/L, respectively) relative to that of the parent strain (0.25 mg/L). Genome sequencing established that the intended mutagenic substitutions in rpoB were the only changes present. Relative to CRG20291, all mutants had attenuated growth, were outcompeted by the parental strain, had lower sporulation and toxin A/B production capacities, and displayed diminished cytotoxicity. In a hamster model, virulence of all three mutants was significantly reduced compared with the progenitor strain, whereas the degree of caecum colonization was unaltered.
Conclusions
Our study demonstrates that particular SNPs in rpoB lead to reduced fidaxomicin susceptibility. These mutations were associated with a fitness cost in vitro and reduced virulence in vivo.
Citation
Kuehne, S. A., Dempster, A. W., Collery, M. M., Joshi, N., Jowett, J., Kelly, M. L., …Minton, N. P. (2018). Characterization of the impact of rpoB mutations on the in vitro and in vivo competitive fitness of Clostridium difficile and susceptibility to fidaxomicin. Journal of Antimicrobial Chemotherapy, 73(4), 973-980. https://doi.org/10.1093/jac/dkx486
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 25, 2017 |
Online Publication Date | Dec 15, 2017 |
Publication Date | Apr 1, 2018 |
Deposit Date | Apr 30, 2019 |
Publicly Available Date | May 17, 2019 |
Journal | Journal of Antimicrobial Chemotherapy |
Print ISSN | 0305-7453 |
Electronic ISSN | 1460-2091 |
Publisher | Oxford University Press |
Peer Reviewed | Peer Reviewed |
Volume | 73 |
Issue | 4 |
Pages | 973-980 |
DOI | https://doi.org/10.1093/jac/dkx486 |
Public URL | https://nottingham-repository.worktribe.com/output/1854088 |
Publisher URL | https://academic.oup.com/jac/article/73/4/973/4748886 |
Contract Date | May 17, 2019 |
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Publisher Licence URL
https://creativecommons.org/licenses/by-nc/4.0/
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