# Environmental surveillance of bacteria in a new intensive care unit using plate sweeps

**Authors:** Aasha McMurray-Jones, Kirsten Spann, Prasad K. D. V. Yarlagadda, Jeremy Fernando, Leah W. Roberts

PMC · DOI: 10.1099/mgen.0.001597 · Microbial Genomics · 2026-01-13

## TL;DR

This study used plate sweeps to monitor bacteria in a new ICU, finding changes in microbial communities and antibiotic resistance after patient introduction.

## Contribution

The study introduces plate sweeps as a cost-effective method for environmental bacterial surveillance in hospitals.

## Key findings

- Post-patient ICU samples showed different bacterial species compared to pre-patient samples.
- Post-patient samples had increased antimicrobial resistance genes, including resistance to fosfomycin, quinolones, and beta-lactams.
- Cluster analysis identified 17 possible transmission links, highlighting communal bathrooms as key transmission areas.

## Abstract

The hospital environment plays a critical role in the transmission of infectious diseases. Surveillance methods often rely on selective enrichment or deep metagenomic sequencing, which both have significant drawbacks in terms of community resolution and cost. Plate sweeps provide a practical moderate approach to cultivate a wide range of bacteria, capturing more diversity than a single colony pick without high sequencing costs. Here, we use this approach to characterize a newly built hospital intensive care unit (ICU) in Queensland, Australia. Between November 2023 and February 2024, we sampled 78 sites within an 8-bed private hospital ICU pre- and post-patient introduction to the environment. Samples were enriched on non-selective media before DNA was extracted from whole plate sweeps and sequenced using Illumina. We assessed species, antimicrobial resistance (AMR) genes, virulence genes and transmission across all samples and between the pre- and post-patient samples using Kraken2, AbritAMR and Tracs. While the rate of positive microbial growth within the ICU environment did not change significantly pre- and post-patient introduction, the post-patient microbiome consisted of largely different bacterial species; of 22 genera identified, only 3 genera were represented at both timepoints. Post-patient samples were enriched in AMR genes, including resistance to fosfomycin, quinolones and beta-lactams. Common genera identified post-patient were Pseudomonas, Delftia and Stenotrophomonas, often associated with areas of plumbing. Cluster analysis identified 17 possible transmission links from a single timepoint, highlighting several areas in the ICU (e.g. communal bathrooms) as key areas for transmission. We demonstrate the utility of plate sweeps as a means of economical non-selective environmental surveillance and highlight their ability to identify hotspots of transmission within a hospital ward that could be targeted by infection control prior to an outbreak of a more serious pathogen.

## Linked entities

- **Genes:** ACKR5 (atypical chemokine receptor 5) [NCBI Gene 11318]
- **Chemicals:** fosfomycin (PubChem CID 441029), quinolones (PubChem CID 6038), beta-lactams (PubChem CID 136721)
- **Species:** Pseudomonas (taxon 286), Delftia (taxon 80865), Stenotrophomonas (taxon 40323)

## Full-text entities

- **Genes:** SRPRA (SRP receptor subunit alpha) [NCBI Gene 6734] {aka DP, SRPR, Sralpha}, smeF [NCBI Gene 93835035]
- **Diseases:** sepsis (MESH:D018805), infectious (MESH:D003141), respiratory failure (MESH:D012131), AMR (MESH:D060467), infection (MESH:D007239), HAIs (MESH:D003428), GTDB (MESH:D042822), opportunistic infections (MESH:D009894)
- **Chemicals:** Nickel (MESH:D009532), cephalosporins (MESH:D002511), iron (MESH:D007501), fosfomycin (MESH:D005578), NA (MESH:D012964), Arsenite (MESH:C015001), toluene (MESH:D014050), Horse Blood agar (-), aminoglycoside (MESH:D000617), carbapenems (MESH:D015780), quinolone (MESH:D015363), beta-lactams (MESH:D047090), tellurite (MESH:C026660), kanamycin (MESH:D007612), fluoroquinolones (MESH:D024841), silver (MESH:D012834), tigecycline (MESH:D000078304), agar (MESH:D000362), copper (MESH:D003300), mercury (MESH:D008628), copB (MESH:C039178), methicillin (MESH:D008712), azithromycin (MESH:D017963)
- **Species:** Delftia (genus) [taxon 80865], Enterobacter hormaechei (CDC Enteric Group 75, species) [taxon 158836], Staphylococcus aureus (species) [taxon 1280], Pantoea sp. (species) [taxon 69393], Klebsiella sp. (species) [taxon 576], Delftia sp. (species) [taxon 1886637], aureus [taxon 46170], Pseudomonas sp. (species) [taxon 306], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mycobacteriales (order) [taxon 85007], Raoultella [taxon 160674], Acinetobacter (genus) [taxon 469], Klebsiella michiganensis (species) [taxon 1134687], Brevundimonas (genus) [taxon 41275], Pantoea agglomerans (species) [taxon 549], Stenotrophomonas maltophilia (species) [taxon 40324], Pseudomonas aeruginosa (species) [taxon 287], Homo sapiens (human, species) [taxon 9606], Pseudomonas juntendi (species) [taxon 2666183], Staphylococcus sp. (species) [taxon 29387], Enterococcus faecium (species) [taxon 1352], Mycobacterium tuberculosis (species) [taxon 1773], Stenotrophomonas (genus) [taxon 40323], Klebsiella pneumoniae (species) [taxon 573], Paenibacillus urinalis (species) [taxon 521520], Klebsiella planticola (species) [taxon 575], Aerococcus (genus) [taxon 1375], Escherichia coli (E. coli, species) [taxon 562], Pseudomonas (RNA similarity group I, genus) [taxon 286], Serratia (genus) [taxon 613]
- **Mutations:** rs214

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12799223/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12799223/full.md

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Source: https://tomesphere.com/paper/PMC12799223