Evidence map›Paper›PMID 40760424›Full record

ArticleBMC microbiology2025

Phenotypic and genotypic characterization of antimicrobial resistance in Enterococcus spp. Isolated from the skin microbiota of channel catfish (Ictalurus punctatus) in Southeastern United States.

Yesutor K Soku, Jaelyn Reeves, Faith W Kadzviti, Temesgen Samuel, Abdelrahman Mohamed

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Yesutor K SokuDepartment of Pathobiology, College of Veterinary Medicine, Tuskegee University, Tuskegee, AL, 36088, USA. ysoku9133@tuskegee.edu.
Jaelyn ReevesDepartment of Pathobiology, College of Veterinary Medicine, Tuskegee University, Tuskegee, AL, 36088, USA.
Faith W KadzvitiDepartment of Pathobiology, College of Veterinary Medicine, Tuskegee University, Tuskegee, AL, 36088, USA.
Temesgen SamuelDepartment of Pathobiology, College of Veterinary Medicine, Tuskegee University, Tuskegee, AL, 36088, USA.
Abdelrahman MohamedDepartment of Pathobiology, College of Veterinary Medicine, Tuskegee University, Tuskegee, AL, 36088, USA. amohamed@tuskegee.edu.

Funding

DHHS/HRSA D34HP00001-35-00USDA/NIFA NI24AHDRXXXXG067
6 · The paper itself

Abstract

backgroundAquaculture systems may contribute to the emergence and persistence of antimicrobial-resistant (AMR) bacteria, posing risks to animal, environmental, and human health. This study characterized the phenotypic and genotypic antimicrobial resistance profiles of Enterococcus spp. isolated from the skin microbiota of 125 channel catfish (Ictalurus punctatus) harvested from two earthen ponds in Alabama, USA.

methodsSkin swabs from the body of channel catfish were enriched in Enterococcosel broth and cultured on Enterococcosel agar at 28 °C for 24 h. Isolates were confirmed using Biolog Gen III and VITEK

results36% of isolates exhibited multidrug resistance (resistance to ≥ 3 antimicrobial classes), with the highest resistance rates observed for ampicillin (44.8%), rifampicin (42.4%), and tetracycline (38.4%). The most prevalent resistance genes were aac(6')-Iid (65.7%), aac(6')-Ii (22.9%), efmA, and msr(C) (20.0% each). Plasmid replicons rep1 and repUS15 frequently co-occurred with resistance genes. Biofilm-associated genes, including efaA, fsrA, fsrB, sprE, ebpABC, ace, and scm, were commonly detected. Multivariate analyses (PERMANOVA, PCA) revealed no significant species-level differences in resistance burden or biofilm gene carriage, indicating similar resistance and virulence gene carriage across species in this dataset.

conclusionsThe skin microbiota of pond-raised catfish harbors antimicrobial-resistant Enterococcus spp. with mobile resistance elements and biofilm-associated virulence factors, suggesting a potential role in AMR persistence within aquaculture settings. These findings support the need for targeted AMR surveillance in fish-associated microbiota as part of integrated One Health strategies.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialEnterococcusIctaluridaeMicrobiotaSkinAlabamaAnimalsAquacultureDrug Resistance, Multiple, BacterialGenotypeMicrobial Sensitivity TestsPhenotypeSkin MicrobiomeWhole Genome SequencingAnti-Bacterial AgentsAntimicrobial resistanceAquacultureBiofilmEnterococcusMultidrug resistancePlasmid repliconResistomeSkin microbiotaWhole-genome sequencing

Identifiers

PMID40760424
PMCPMC12323147

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.