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Evaluation of the Reveal® rapid AST system to assess the susceptibility of Pseudomonas aeruginosa from blood cultures

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Abstract

This study was set up to assess the performance of the Reveal® rapid AST system to determine the drug susceptibility of Pseudomonas aeruginosa strains directly from blood cultures. Two hundred fully sequenced clinical P. aeruginosa strains were selected for the evaluation, of which 26.5% (n = 53) produced transferable β-lactamases, and 2.0 to 33.0% had susceptibility levels close to the EUCAST 2021 breakpoints of 11 commonly used antipseudomonal antibiotics. The Reveal® AST system was run with a commercial MIC microplate designed for fast-growing Gram-negative bacilli (Microscan Neg MDR MIC 1), and was compared to the manually operated GN6F MIC microdilution panel from Thermo Fisher, as a comparator method. The Reveal® AST system provided MIC results for the 11 antipseudomonal antibiotics tested within a mean time to result of 6 h 22 min. By comparison with the GN6F panel, the overall rates of categorical agreement (CA), very major errors (VME), major errors (ME), and minor errors (mE for meropenem only) were 96.1%, 1.6%, 4.2%, and 0.6%, respectively. The Specific Reveal® AST system appears to be a reliable and fast technology to determine the susceptibility of P. aeruginosa to antibiotics, including those with resistance levels near categorical breakpoints, directly from blood cultures.

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Data availability

All the data are available on request from the corresponding author (PP). Complementary information is provided as supplemental material (Table S1).

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Acknowledgements

The authors thank Martin Rottman for reviewing the manuscript.

Funding

DF, MB, and KJ are public officials whose salaries were supported by the Centre Hospitalier Universitaire of Besançon, France. Specific Diagnostics (LR, PR, PS) provided the material and reagents necessary for the study, as well as the funds to hire JC as laboratory technician.

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Authors

Contributions

As follows: study design (PP, DF, KJ, LR, PS), bacterial collections (DF, KJ, PP), experimental work (JC, MB, DF), data analysis (DF, PP), draft preparation (PP, DF, KJ).

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Correspondence to P. Plésiat.

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Ethics approval

This in vitro study did not require specific ethical review or consent.

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Informed consent was obtained from all individual participants included in the study.

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Informed consent was obtained from all individual participants included in the study.

Conflict of interest

The authors JC, DF, MB, KJ, and PP declare to have no specific conflicts of interest. LR, PR, and PS belonged to the staff of Specific Diagnostics at the time of experiments. They did not interfere with the process of data production or their interpretation.

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Couchot, J., Fournier, D., Bour, M. et al. Evaluation of the Reveal® rapid AST system to assess the susceptibility of Pseudomonas aeruginosa from blood cultures. Eur J Clin Microbiol Infect Dis 42, 359–363 (2023). https://doi.org/10.1007/s10096-023-04556-2

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  • DOI: https://doi.org/10.1007/s10096-023-04556-2

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