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Differential metabolism between biofilm and suspended Pseudomonas aeruginosa cultures in bovine synovial fluid by 2D NMR-based metabolomics

Differential metabolism between biofilm and suspended Pseudomonas aeruginosa cultures in bovine synovial fluid by 2D NMR-based metabolomics
Differential metabolism between biofilm and suspended Pseudomonas aeruginosa cultures in bovine synovial fluid by 2D NMR-based metabolomics

Total joint arthroplasty is a common surgical procedure resulting in improved quality of life; however, a leading cause of surgery failure is infection. Periprosthetic joint infections often involve biofilms, making treatment challenging. The metabolic state of pathogens in the joint space and mechanism of their tolerance to antibiotics and host defenses are not well understood. Thus, there is a critical need for increased understanding of the physiological state of pathogens in the joint space for development of improved treatment strategies toward better patient outcomes. Here, we present a quantitative, untargeted NMR-based metabolomics strategy for Pseudomonas aeruginosa suspended culture and biofilm phenotypes grown in bovine synovial fluid as a model system. Significant differences in metabolic pathways were found between the suspended culture and biofilm phenotypes including creatine, glutathione, alanine, and choline metabolism and the tricarboxylic acid cycle. We also identified 21 unique metabolites with the presence of P. aeruginosa in synovial fluid and one uniquely present with the biofilm phenotype in synovial fluid. If translatable in vivo, these unique metabolite and pathway differences have the potential for further development to serve as targets for P. aeruginosa and biofilm control in synovial fluid.

2045-2322
Leggett, Abigail
d76c4acc-46f8-4579-b2ed-2fa27ec82187
Li, Da-Wei
9be6a5e1-b1d4-43da-a77d-3ad8ce5e64c4
Bruschweiler-Li, Lei
7e7b4a89-5034-4a27-88a0-d15dcf7c6850
Sullivan, Anne
2fc4e087-c92c-405d-9071-18d5873b4cbd
Stoodley, Paul
08614665-92a9-4466-806e-20c6daeb483f
Brüschweiler, Rafael
3d5b7892-306b-4cae-9d0e-9328ea60926f
Leggett, Abigail
d76c4acc-46f8-4579-b2ed-2fa27ec82187
Li, Da-Wei
9be6a5e1-b1d4-43da-a77d-3ad8ce5e64c4
Bruschweiler-Li, Lei
7e7b4a89-5034-4a27-88a0-d15dcf7c6850
Sullivan, Anne
2fc4e087-c92c-405d-9071-18d5873b4cbd
Stoodley, Paul
08614665-92a9-4466-806e-20c6daeb483f
Brüschweiler, Rafael
3d5b7892-306b-4cae-9d0e-9328ea60926f

Leggett, Abigail, Li, Da-Wei, Bruschweiler-Li, Lei, Sullivan, Anne, Stoodley, Paul and Brüschweiler, Rafael (2022) Differential metabolism between biofilm and suspended Pseudomonas aeruginosa cultures in bovine synovial fluid by 2D NMR-based metabolomics. Scientific Reports, 12 (1), [17317]. (doi:10.1038/s41598-022-22127-x).

Record type: Article

Abstract

Total joint arthroplasty is a common surgical procedure resulting in improved quality of life; however, a leading cause of surgery failure is infection. Periprosthetic joint infections often involve biofilms, making treatment challenging. The metabolic state of pathogens in the joint space and mechanism of their tolerance to antibiotics and host defenses are not well understood. Thus, there is a critical need for increased understanding of the physiological state of pathogens in the joint space for development of improved treatment strategies toward better patient outcomes. Here, we present a quantitative, untargeted NMR-based metabolomics strategy for Pseudomonas aeruginosa suspended culture and biofilm phenotypes grown in bovine synovial fluid as a model system. Significant differences in metabolic pathways were found between the suspended culture and biofilm phenotypes including creatine, glutathione, alanine, and choline metabolism and the tricarboxylic acid cycle. We also identified 21 unique metabolites with the presence of P. aeruginosa in synovial fluid and one uniquely present with the biofilm phenotype in synovial fluid. If translatable in vivo, these unique metabolite and pathway differences have the potential for further development to serve as targets for P. aeruginosa and biofilm control in synovial fluid.

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Accepted/In Press date: 10 October 2022
Published date: 15 October 2022
Additional Information: Funding Information: This work was supported by the National Institutes of Health [Grants R01GM124436 (to P.S.) and R35GM139482 (to R.B.)] and by the Pilot Program Funding from the Department of Microbial Infection and Immunity in the College of Medicine at OSU. All NMR experiments were performed at the CCIC NMR facility at The Ohio State University. Publisher Copyright: © 2022, The Author(s).

Identifiers

Local EPrints ID: 471477
URI: http://eprints.soton.ac.uk/id/eprint/471477
ISSN: 2045-2322
PURE UUID: 9f66fce8-1e51-4638-aeca-c28c5dbfcfd9
ORCID for Paul Stoodley: ORCID iD orcid.org/0000-0001-6069-273X

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Date deposited: 08 Nov 2022 19:09
Last modified: 17 Mar 2024 03:18

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Contributors

Author: Abigail Leggett
Author: Da-Wei Li
Author: Lei Bruschweiler-Li
Author: Anne Sullivan
Author: Paul Stoodley ORCID iD
Author: Rafael Brüschweiler

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