Evidence map›Paper›PMID 41251486›Full record

ArticleThe Journal of infectious diseases2026

Detection of Carbapenem-Resistant Bacteria in Skilled Nursing Facility Wastewater.

Susanna Lenz, Subhasish Biswas, Ivy Terry, Lisa Tran-Basha, Amanda K Lyons, Tapati Mazumdar, Florence Whitehill, Alison Laufer Halpin, Lauren Franco, Maria Karlsson and 2 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Plasmid-borneOne health (Amsterdam, Netherlands) · 2026
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Susanna LenzCenters for Disease Control and Prevention, Division of Healthcare Quality Promotion (DHQP), Atlanta, Georgia, USA.ORCID 0009-0007-6660-4076
Subhasish BiswasTanaq Support Services, Anchorage, Alaska, USA.
Ivy TerryTanaq Support Services, Anchorage, Alaska, USA.
Lisa Tran-BashaCenters for Disease Control and Prevention, Division of Healthcare Quality Promotion (DHQP), Atlanta, Georgia, USA.
Amanda K LyonsCenters for Disease Control and Prevention, Division of Healthcare Quality Promotion (DHQP), Atlanta, Georgia, USA.ORCID 0000-0003-4312-2481
Tapati MazumdarTanaq Support Services, Anchorage, Alaska, USA.
Florence WhitehillCenters for Disease Control and Prevention, Division of Healthcare Quality Promotion (DHQP), Atlanta, Georgia, USA.ORCID 0000-0002-1047-2605
Alison Laufer HalpinCenters for Disease Control and Prevention, Division of Healthcare Quality Promotion (DHQP), Atlanta, Georgia, USA.ORCID 0000-0003-1643-1617
Lauren FrancoIndiana Department of Health, Clinical Microbiology Division, Indianapolis, Indiana, USA.
Maria KarlssonChenega Government Mission Solutions, LLC, Chesapeake, Virginia, USA.
Margaret WilliamsCenters for Disease Control and Prevention, Division of Healthcare Quality Promotion (DHQP), Atlanta, Georgia, USA.ORCID 0000-0003-3168-1286
Angela Coulliette-SalmondCenters for Disease Control and Prevention, Division of Healthcare Quality Promotion (DHQP), Atlanta, Georgia, USA.ORCID 0000-0003-0435-7595

Funding

CDC HHSIntramural CDC HHS CC999999Oak Ridge Institute for Science and EducationResearch Participation ProgramU.S. Department of Energy
6 · The paper itself

Abstract

backgroundWastewater surveillance at healthcare facilities for carbapenem-resistant (CR) bacteria harboring carbapenemase genes could result in earlier detection of circulating or emerging antimicrobial resistance (AR) threats. However, knowledge gaps exist regarding the CR bacterial community and carbapenemase genes present in facility wastewater and plumbing, which need to be addressed.

methodsWastewater effluent samples from three skilled nursing facilities (SNFs) (Georgia, USA) were collected weekly over six months. Selective chromogenic media were examined for their performance in screening the samples for targeted CR bacteria. Culture-dependent and culture-independent methods (ie, PCR) were applied to enriched wastewater samples (n = 73) to screen isolates and pooled samples for the most common carbapenemase genes circulating in the United States (blaKPC, blaNDM, blaVIM, blaOXA-48-like, and blaIMP), and method sensitivity was compared. Whole genome sequencing (WGS) was used to identify all AR genes present in isolates.

resultsBacteria (n = 209 isolates) were identified using MALDI-TOF and included >20 different genera. Clinically relevant (Acinetobacter baumannii complex, Enterobacter cloacae complex, Enterococcus faecium, Stenotrophomonas spp.) and environmental/opportunistic (Comamonas spp., Pandoraea spp., Pseudomonas putida group) CR bacteria were identified in each of the three SNFs. In Facility A and C, only blaKPC was detected in 9 (26.5%) of 34 and 14 (11.4%) of 123 recovered isolates, respectively. There were no PCR-positive results in Facility B. WGS confirmed the presence or absence of all genes screened by PCR (100% concordance).

conclusionsThese data provide a proof-of-concept and insights into CR bacteria present in healthcare facility wastewater using culture, PCR, and sequencing methods.

Indexed as

BacteriaCarbapenemsSkilled Nursing FacilitiesWastewaterAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesHumansMicrobial Sensitivity TestsWhole Genome SequencingAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseCarbapenemsWastewaterantimicrobial resistantculture and molecular method comparisonhealthcare facilityWastewater surveillancewhole genome sequencing

Identifiers

PMID41251486
PMCPMC13166048

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.