Evidence map›Paper›PMID 40623962›Full record

ArticleEnvironmental microbiology2025

High Prevalence of Plasmid-Mediated Quinolone Resistance in Salmonella enterica Serovars Isolated From Surface Water.

Daniel F M Monte, Alan Douglas de Lima Rocha, Mateus Lacerda Pereira Lemos, Laiorayne Araújo de Lima, Julia Memrava Cabrera, Nádyra Jerônimo da Silva, Xinyang Huang, Zhao Chen, Eric W Brown, Marc W Allard and 4 more

Abstract read
In one paragraph

Article in Environmental microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Genomic Epidemiology ofChina CDC weekly · 2026
    Article
  3. Review
  4. Article
  5. 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

14 authors.

Daniel F M MonteDepartment of Population Health and Pathobiology, North Carolina State University, College of Veterinary Medicine, Raleigh, North Carolina, USA.ORCID https://orcid.org/0000-0003-3787-1988
Alan Douglas de Lima RochaDepartmento de Zootecnia, Centro de Ciências Agrárias, Universidade Federal da Paraíba (CCA/UFPB), Areia, Paraíba, Brazil.ORCID https://orcid.org/0009-0009-6494-7846
Mateus Lacerda Pereira LemosDepartmento de Zootecnia, Centro de Ciências Agrárias, Universidade Federal da Paraíba (CCA/UFPB), Areia, Paraíba, Brazil.ORCID https://orcid.org/0000-0002-2006-1826
Laiorayne Araújo de LimaDepartmento de Zootecnia, Centro de Ciências Agrárias, Universidade Federal da Paraíba (CCA/UFPB), Areia, Paraíba, Brazil.ORCID https://orcid.org/0000-0002-7212-3021
Julia Memrava CabreraSao Paulo State University (Unesp), School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-1774-7592
Nádyra Jerônimo da SilvaDepartmento de Zootecnia, Centro de Ciências Agrárias, Universidade Federal da Paraíba (CCA/UFPB), Areia, Paraíba, Brazil.ORCID https://orcid.org/0000-0002-2688-3521
Xinyang HuangUS Food and Drug Administration, Human Foods Program, Office of Laboratory Operations and Applied Science, College Park, Maryland, USA.ORCID https://orcid.org/0000-0002-6100-377X
Zhao ChenUS Food and Drug Administration, Human Foods Program, Office of Laboratory Operations and Applied Science, College Park, Maryland, USA.ORCID https://orcid.org/0000-0002-1784-167X
Eric W BrownUS Food and Drug Administration, Human Foods Program, Office of Laboratory Operations and Applied Science, College Park, Maryland, USA.ORCID https://orcid.org/0009-0002-9197-8057
Marc W AllardUS Food and Drug Administration, Human Foods Program, Office of Laboratory Operations and Applied Science, College Park, Maryland, USA.ORCID https://orcid.org/0000-0001-8841-8847
Rebecca L BellUS Food and Drug Administration, Human Foods Program, Office of Laboratory Operations and Applied Science, College Park, Maryland, USA.ORCID https://orcid.org/0000-0002-7469-1946
Magaly ToroJoint Institute for Food Safety and Applied Nutrition (JIFSAN), University of Maryland, College Park, College Park, Maryland, USA.ORCID https://orcid.org/0000-0002-6280-2215
Jianghong MengUS Food and Drug Administration, Human Foods Program, Office of Laboratory Operations and Applied Science, College Park, Maryland, USA.ORCID https://orcid.org/0000-0002-8623-6764
Celso José Bruno de OliveiraDepartmento de Zootecnia, Centro de Ciências Agrárias, Universidade Federal da Paraíba (CCA/UFPB), Areia, Paraíba, Brazil.ORCID https://orcid.org/0000-0002-7761-0697

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 3136678/2020-0Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 420755/2023-3Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Finance Code 001FDA HHS U01 FD001418Financiadora de Estudo e Projetos (FINEP)Fundação de Apoio à Pesquisa do Estado da Paraíba (FAPESQ) 88887.898770/2023-00U.S. Department of Health and Human Services U01FDU001418
6 · The paper itself

Abstract

Considering the increasing reports of Salmonella enterica strains resistant to quinolones, antimicrobials frequently employed as therapeutic agents globally, our goal was to investigate the occurrence of plasmid-mediated quinolone resistance (PMQR) determinants in S. enterica recovered from natural surface waters in Paraíba state, Brazil. Water samples (n = 230) were collected monthly in triplicate using modified Moore swabs from 29 sampling sites belonging to 10 large dams. After conventional microbial isolation, representative isolates (n = 938) were submitted to whole genome sequencing, assembly and annotation. Antimicrobial resistance genes (ARGs) were identified, and core genome multilocus sequence typing (cgMLST) was used to infer phylogenetic relationships. Among recovered S. enterica, 130 (13.9%) isolates harboured PMQR determinants; 124 (95.4%) harboured qnrB19, while 6 (4.6%) harboured qnrS1. Multiple other ARGs associated with resistance to aminoglycosides, β-lactams, sulphonamides, tetracyclines and fosfomycin were identified. The diversity of ARGs and plasmids suggests a highly complex resistance landscape. Phylogenetic analysis revealed clustering by serovar and sequence type but not by resistance profile or geographic origin. The absence of association between phylogeny and ARGs highlights the potential role of horizontal gene transfer in disseminating resistance genes in water. Our findings reinforce the importance of antimicrobial resistance surveillance in surface waters.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialFresh WaterPlasmidsQuinolonesSalmonella entericaBrazilMicrobial Sensitivity TestsMultilocus Sequence TypingPhylogenyPrevalenceSerogroupWhole Genome SequencingAnti-Bacterial AgentsQuinolonesantimicrobial‐resistanceenvironmental watergenomic analysis

Identifiers

PMID40623962
PMCPMC12234413

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.