Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/31296
Title: Pseudomonas aeruginosa clinical isolates can encode plastic-degrading enzymes that allow survival on plastic and augment biofilm formation
Authors: Howard, SA
de Dios, R
Maslova, E
Myridakis, A
Miller, TH
McCarthy, RR
Keywords: Pseudomonas aeruginosa;pathogenicity;biofilm;polyesterase;plastic degradation;CP: microbiology
Issue Date: 7-May-2025
Publisher: Elsevier
Citation: Howard, S.A. et al. (2025) 'Pseudomonas aeruginosa clinical isolates can encode plastic-degrading enzymes that allow survival on plastic and augment biofilm formation', Cell Reports, 0 (ahead of print), 115650, pp. 1 - 20 + 17 supplementary pp. (37). doi: 10.1016/j.celrep.2025.115650.
Abstract: Multiple bacteria encoding plastic-degrading enzymes have been isolated from the environment. Given the widespread use of plastic in healthcare, we hypothesized that bacterial clinical isolates may also degrade plastic. This could render plastic-containing medical devices susceptible to degradation and failure and potentially offer these pathogens a growth-sustaining substrate, enabling them to persist in the hospital-built environment. Here, we mined the genomes of prevalent pathogens and identified several species encoding enzymes with homology to known plastic-degrading enzymes. We identify a clinical isolate of Pseudomonas aeruginosa that encodes an enzyme that enables it to degrade a medically relevant plastic, polycaprolactone (PCL), by 78% in 7 days. Furthermore, this degradation enables the bacterium to utilize PCL as its sole carbon source. We also demonstrate that encoding plastic-degrading enzymes can enhance biofilm formation and pathogenicity. Given the central role of plastic in healthcare, screening nosocomial bacteria for plastic-degrading capacity should be an important future consideration.
Description: Data and code availability: • RNA-seq data have been deposited at the National Centre for Biotechnology Information Gene Expression Omnibus public database and are publicly available as of the date of publication. Accession numbers are listed in the key resources table. • This paper does not report original code. • Any additional information required to reanalyze the data reported in this work paper is available from the lead contact upon request.
Materials availability: The materials that support the findings of this study are available from the corresponding author upon reasonable request. Please contact the lead contact for additional information.
Acknowledgements: We thank Prof. Stephan Heeb for kindly providing the clinical isolate P. aeruginosa PA-W23 and the British Society for Antimicrobial Chemotherapy for providing the BSAC Bacteraemia Resistance Surveillance Programme P. aeruginosa collection. We would like to thank Prof. Alain Filloux for the gift of the different secretion mutants and Dr. Luke Allsopp for retrieving them. We thank the Brunel University Experimental Techniques Centre for SEM support.
Declaration of interests: Brunel University London has a priority patent and PCT filings covering the manipulation of biofilm levels to enhance plastic degradation.
URI: https://bura.brunel.ac.uk/handle/2438/31296
DOI: https://doi.org/10.1016/j.celrep.2025.115650
ISSN: 2639-1856
Other Identifiers: ORCiD: Sophie A. Howard https://orcid.org/0000-0003-0291-911X
ORCiD: Rubén de Dios https://orcid.org/0000-0001-6704-9149
ORCiD: Antonis Myridakis https://orcid.org/0000-0003-1690-6651
ORCiD: Thomas H. Miller https://orcid.org/0000-0003-2206-7663
ORCiD: Ronan R. McCarthy https://orcid.org/0000-0002-7480-6352
Article number: 115650
Appears in Collections:The Experimental Techniques Centre
Dept of Life Sciences Research Papers

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