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RESEARCH PRODUCT

Contamination of a hospital plumbing system by persister cells of a copper-tolerant high-risk clone of Pseudomonas aeruginosa

Xavier BertrandAlexandre MeunierAudrey JeanvoineDidier HocquetBenoît ValotHélène Puja

subject

Environmental EngineeringMultidrug tolerance0208 environmental biotechnology02 engineering and technology010501 environmental sciencesmedicine.disease_cause01 natural sciencesMicrobiologyAgar platechemistry.chemical_compoundGenomic islandmedicinePseudomonas syringaeHumansWaste Management and DisposalPathogen0105 earth and related environmental sciencesWater Science and TechnologyCivil and Structural EngineeringOne healthbiologyPersistersPseudomonas aeruginosaEcological Modelingbiology.organism_classificationPollutionPremises plumbingPseudomonas putidaHospitals020801 environmental engineering3. Good healthR2a agar[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryPseudomonas aeruginosaFranceSanitary EngineeringCopper

description

Abstract Background Pseudomonas aeruginosa (PA) is an important opportunistic pathogen that thrives best in the distal elements of plumbing and waste-water systems. Although nosocomial outbreaks of PA have been associated with water sources, the role of the plumbing system of healthcare premises as a reservoir for this pathogen is still unclear. Materials and methods We collected water samples from 12 technical areas, distant from any medical activity, in a teaching hospital in France once a week for 11 weeks. We used a method that resuscitates persister cells because of the nutrient-poor conditions and the presence of inhibitors (e.g. chlorine and copper ions). Briefly, water was sampled in sterile bottles containing 100 μM of the copper-ion chelating agent diethyldithiocarbamate (DDTC). A portion of the samples was immediately filtered through 0.45-μm membranes, deposited on R2A agar plates, and incubated seven days at 22 °C (following European recommendations). The remaining water was incubated 14 days at 22 °C and then filtered and cultured on R2A, blood-, or cetrimide-containing agar plates. PA isolates were identified by MS MALDI-TOF, genotyped by PFGE and WGS, and tested for survival in a 150 μg/L copper (II) sulphate solution. Results Although the 12 water sampling points always tested negative with the recommended method, 67% were positive at least once for PA with the adapted method (i.e. with DDTC). The 14 PA persister isolates found throughout the plumbing system were clonal and belong to the high-risk clone ST308. Their genome harbours a 37-kb genomic island (GI-7) containing 13 genes linked to copper resistance. ST308 survived better in the copper solution than comparators that did not harbour GI-7 (P. aeruginosa strains PAO1, PA14, and ST235). The deletion of GI-7 in ST308 abrogated its tolerance to copper. The GI-7 nucleotide sequence shares 98% and 72% identity with sequences from the environmental species Pseudomonas putida and the phytopathogenic species Pseudomonas syringae, respectively. Conclusion We report the contamination of the plumbing system of a healthcare premises by persister cells of the high-risk clone P. aeruginosa ST308. New recommendations for the monitoring of water contamination should consider persister cells. The genomic island GI-7, which confers tolerance to copper, probably originates from Pseudomonas species found in copper-contaminated soils and plants. Agricultural practices may have an unexpected consequence, allowing copper-tolerant pathogens to survive in the hospital environment and contaminate fragile patients.

10.1016/j.watres.2019.04.011https://hal.archives-ouvertes.fr/hal-02315692/file/S004313541930315X.pdf