Affiliation:
1. School of Science and Technology, Örebro University, Fakultetsgatan 1, SE 701 82 Örebro, Sweden
2. Saint-Gobain SWEDEN AB, SCANSPAC, Kemivägen 7, SE 705 97 Glanshammar, Sweden
3. Saint-Gobain Recherche, 39 Quai Lucien Lefranc, FR-93303 Aubervilliers Cedex, France
Abstract
Biocide resistance poses a significant challenge in industrial processes, with bacteria like Pseudomonas oleovorans exhibiting intrinsic resistance to traditional antimicrobial agents. In this study, the impact of biocide exposure on the metabolome of two P. oleovorans strains, namely, P. oleovorans P4A, isolated from contaminated coating material, and P. oleovorans 1045 reference strain, were investigated. The strains were exposed to 2-Methylisothiazol-3(2H)-one (MI) MIT, 1,2-Benzisothiazol-3(2H)-one (BIT), and 5-chloro-2-methyl-isothiazol-3-one (CMIT) at two different sub-inhibitory concentrations and the lipids and polar and semipolar metabolites were analyzed by ultra-high performance liquid chromatography quadrupole time-of-flight mass spectrometry UPLC–Q–TOF/MS. Exposure to the BIT biocide induced significant metabolic modifications in P. oleovorans. Notable changes were observed in lipid and metabolite profiles, particularly in phospholipids, amino acid metabolism, and pathways related to stress response and adaptation. The 1045 strain showed more pronounced metabolic alterations than the P4A strain, suggesting potential implications for lipid, amino acid metabolism, energy metabolism, and stress adaptation. Improving our understanding of how different substances interact with bacteria is crucial for making antimicrobial chemicals more effective and addressing the challenges of resistance. We observed that different biocides trigged significantly different metabolic responses in these strains. Our study shows that metabolomics can be used as a tool for the investigation of metabolic mechanisms underlying biocide resistance, and thus in the development of targeted biocides. This in turn can have implications in combating biocide resistance in bacteria such as P. oleovorans.
Reference74 articles.
1. Williams, T.M. (2006, January 12–16). The Mechanism of Action of Isothiazolone Biocide. Proceedings of the CORROSION 2006, San Diego, CA, USA.
2. Luz, G.V.S., Sousa, B.A.S.M., Guedes, A.V., Barreto, C.C., and Brasil, L.M. (2018). Biocides Used as Additives to Biodiesels and Their Risks to the Environment and Public Health: A Review. Molecules, 23.
3. Kim, J., and Choi, J. (2023). Trans- and Multigenerational Effects of Isothiazolinone Biocide CMIT/MIT on Genotoxicity and Epigenotoxicity in Daphnia magna. Toxics, 11.
4. Methylisothiazolinone contact allergy: A review;Lundov;Br. J. Dermatol.,2011
5. Contact dermatitis to methylisothiazolinone;Scherrer;An. Bras. Dermatol.,2015