Evidence map›Paper›PMID 40790577›Full record

ArticleBMC oral health2025

Pseudomonas aeruginosa in dental unit waterlines: an emerging threat of virulence genes in healthcare-associated infections.

Maryam Shafipour, Niloufar Emrani, Ali Shahryari

Abstract read
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Article in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Maryam ShafipourDepartment of Environmental Health Engineering, School of Health, Golestan University of Medical Science, Gorgan, Iran.
Niloufar EmraniDepartment of Pediatric Dentistry, School of Dentistry, Golestan University of Medical Sciences, Gorgan, Iran.
Ali ShahryariDepartment of Environmental Health Engineering, School of Health, Golestan University of Medical Science, Gorgan, Iran. dr.shahryari@goums.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPseudomonas aeruginosa is a leading cause of healthcare-associated infections (HAIs), especially in dental environments. In this study, we examine the prevalence of virulence factors in P. aeruginosa isolated from dental chair unit (DCU) water, aiming to evaluate the hygienic status of dental unit waterlines (DUWLs).

methodsA total of 100 water samples were collected from DCU and the urban water supply at the Dental Faculty of Gorgan, Iran. The samples were cultured in Mueller-Hinton Broth, and DNA was extracted. Molecular identification was performed using gyrB-specific primers, with five isolates confirmed by Sanger sequencing and BLAST analysis. P. aeruginosa was detected in 95 samples. The prevalence of virulence genes (exoS,algD, toxA, and lasB) was assessed via multiplex PCR.

resultsAmong 95 isolates, 72.63% (69/95) harbored all four genes, with lasB and algD each present in 97.1%, toxA in 95.65%, and exoS in 78.26%. Gene frequencies varied across sites: urban water inlet (12.5%), dental handpiece (83.87%), air-water syringe (75.67%), and water nozzle (81.25%). All five clinical isolates harbored silent mutations in gyrB (C→T132, T→C144, and A→T 111) that preserved the wild-type gyrB amino acid sequence. As all mutations were silent (C→T132, T→C144, A→T111), no structural alterations were observed in the gyrB protein.

conclusionThese findings highlight that DUWLs act as reservoirs for P. aeruginosa strains harboring multiple virulence genes associated with biofilm formation. Targeted strategies are urgently needed to disrupt both bacterial growth and gene expression, which could help reduce antibiotic resistance and improve infection control in dental care.

Indexed as

Cross InfectionDental EquipmentPseudomonas aeruginosaVirulence FactorsWater MicrobiologyEquipment ContaminationGenes, BacterialHumansIranPseudomonas InfectionsVirulenceWater SupplyVirulence FactorsDental unit waterlinesPseudomonas aeruginosaVirulence factorsWaterborne infection

Identifiers

PMID40790577
PMCPMC12337419

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