# Genomic screening of eight antibiotic-resistant Pseudomonas isolated from rainbow trout (Oncorhynchus mykiss)

**Authors:** Kenny Oberlé, Gaëlle Bednarek, Claude Rispe, Ségolène Calvez

PMC · DOI: 10.1099/acmi.0.001029.v3 · Access Microbiology · 2026-02-11

## TL;DR

This study explores antibiotic resistance in Pseudomonas bacteria from rainbow trout, revealing resistance genes and their potential spread.

## Contribution

The study identifies mobile genetic elements harboring resistance genes in Pseudomonas from aquaculture systems.

## Key findings

- Resistance genes tet(Y), sul2, and floR were found on mobile elements in Pseudomonas isolates.
- Mutations in PhoP/Q and absence of pmrA/B systems were linked to colistin resistance.
- LPS-modifying genes associated with colistin resistance were detected in resistant isolates.

## Abstract

Open aquaculture systems represent a strategic environment for the study of antibiotic resistance dynamics, given the interactions between bacteria from humans, animals and the environment. The genomic investigation of eight Pseudomonas isolated from rainbow trout in a previous study demonstrated that non-wild-type and resistance phenotypes to several antibiotics (oxytetracycline, sulphonamides and florfenicol) were predominantly attributable to the presence of related genes [tet(Y), sul2 and floR]. Phylogenetic analyses revealed that several species of Pseudomonas iridis harboured these genes on mobile genetic elements, including integrative conjugative elements (ICE) on the chromosome or plasmids with a high degree of sequence similarity (>99%) between the genetic structures. Furthermore, comparisons between isolates with low and high MIC values to colistin showed mutations in the amino acid sequences of the PhoP/Q two-component system and a lack of the pmrA/B system. A wide diversity of known LPS-modifying genes involved in colistin resistance was also detected in resistant isolates. This study provided insights into the dynamics of antibiotic resistance in aquaculture systems. It demonstrated the presence of genes located on an ICE inserted into a chromosome or plasmid in P. iridis, which was isolated from healthy rainbow trout in different farms within the same watershed. Our study raises questions about the ability of environmental Pseudomonas bacteria to spread their antibiotic resistance genes to other bacterial species that are of interest in terms of human or animal surveillance.

## Linked entities

- **Genes:** sul-2 (Sulfatase N-terminal domain-containing protein) [NCBI Gene 179194], floR (chloramphenicol/florfenicol efflux MFS transporter FloR) [NCBI Gene 57334229]
- **Chemicals:** oxytetracycline (PubChem CID 54675779), florfenicol (PubChem CID 114811), colistin (PubChem CID 5311054)
- **Species:** Pseudomonas (taxon 286), Pseudomonas iridis (taxon 2710587), Oncorhynchus mykiss (taxon 8022)

## Full-text entities

- **Chemicals:** LPS (MESH:D008070), oxytetracycline (MESH:D010118), sulphonamides (MESH:D013449), florfenicol (MESH:C035534)
- **Species:** Pseudomonas iridis (species) [taxon 2710587], Homo sapiens (human, species) [taxon 9606], Oncorhynchus mykiss (rainbow trout, species) [taxon 8022]

## Full text

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## Figures

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## References

88 references — full list in the complete paper: https://tomesphere.com/paper/PMC12893666/full.md

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Source: https://tomesphere.com/paper/PMC12893666