# Antibiotic Resistance, Biofilm Genes, and smeDEF Efflux Pump in Clinical Stenotrophomonas maltophilia Isolates From Iran

**Authors:** Haneen Fadhil Jasim, Nisreen Salah Majeed, Asmaa A. Salam, Rania Hameed Hamad, Yeganeh Behrouzi, Erta Rajabi, Razieh Shahbazi

PMC · DOI: 10.1002/mbo3.70222 · 2026-01-26

## TL;DR

This study analyzed antibiotic resistance and biofilm production in Stenotrophomonas maltophilia isolates from Iran, finding high susceptibility to some antibiotics but rising resistance and strong biofilm formation linked to specific genes.

## Contribution

The study provides new insights into the genetic and phenotypic factors contributing to antibiotic resistance and biofilm formation in clinical S. maltophilia isolates from Iran.

## Key findings

- Most isolates remained sensitive to trimethoprim/sulfamethoxazole, minocycline, and levofloxacin.
- TMP/SMX-resistant strains showed significantly higher expression of smeD and smeE genes.
- The rpfF gene was closely associated with strong biofilm formation in isolates.

## Abstract

Stenotrophomonas maltophilia is a nosocomial and opportunistic microorganism with increasing antibiotic resistance rates. This study aimed to assess its biofilm production capacity, antibiotic resistance distribution, and the prevalence of biofilm‐ and resistance‐related genes in clinical isolates. In this multiinstitutional study, 230 isolates were collected from hospitals across Iran between 2022 and 2024. Resistance trends were evaluated using disc diffusion and minimal inhibitory concentration E test methods, per Clinical and Laboratory Standards Institute guidelines. Crystal violet staining assessed biofilm production, while polymerase chain reaction (PCR) sequencing identified biofilm‐ and resistance‐related genes. Real‐time PCR was used to evaluate the relative expression of the smeD, smeE, and smeT genes, calibrated against TMP/SMX‐sensitive control strains. Susceptibility rates to trimethoprim/sulfamethoxazole (TMP/SMX), levofloxacin, and minocycline were 97.39%, 93.47%, and 93.04%, respectively. TMP/SMX‐resistant strains showed 19.8‐ and 16‐fold higher expression of smeD and smeE, compared with sensitive isolates. The spgM gene was detected in all isolates, and 93.04% (n = 214) were biofilm producers, with most showing moderate‐biofilm formation (n = 89, 38.70%). Additionally, the rpfF gene was closely associated with strong‐biofilm formation (p ≤ 0.05). The L2, L1, smqnr, sul2, and sul1 resistance genes were identified in 214 (93.04%), 181 (78.69%), 135 (58.7%), 136 (59.1%), and 127 (55.2%) isolates, respectively. Our findings demonstrate that most isolates remain sensitive to TMP/SMX, while resistance to alternative antibiotics is rising. Moreover, biofilm production appears significantly associated with the rpfF gene.

Iranian clinical Stenotrophomonas maltophilia isolates showed high susceptibility to trimethoprim/sulfamethoxazole, minocycline, and levofloxacin, but marked resistance to ceftazidime and ticarcillin‐clavulanate, alongside widespread biofilm production and resistance genes. Overexpressed smeDEF efflux pump and rpfF‐linked strong biofilms highlight emerging therapeutic challenges.

## Linked entities

- **Genes:** smeD (multidrug efflux RND transporter periplasmic adaptor subunit SmeD) [NCBI Gene 61474911], smeE (multidrug efflux RND transporter permease subunit SmeE) [NCBI Gene 61474912], smeT (efflux transporter SmeDEF transcriptional repressor SmeT) [NCBI Gene 64106195], rpfF (diffusible signal factor synthase RpfF) [NCBI Gene 46979989], PPFIBP1 (PPFIB scaffold protein 1) [NCBI Gene 8496], IGKV1-16 (immunoglobulin kappa variable 1-16) [NCBI Gene 28938], smqnr (SmQnr family pentapeptide repeat protein) [NCBI Gene 64103562], sul-2 (Sulfatase N-terminal domain-containing protein) [NCBI Gene 179194], sul-1 (Putative extracellular sulfatase Sulf-1 homolog) [NCBI Gene 180619]
- **Chemicals:** trimethoprim/sulfamethoxazole (PubChem CID 358641), levofloxacin (PubChem CID 149096), minocycline (PubChem CID 54675783), ceftazidime (PubChem CID 5481173)
- **Species:** Stenotrophomonas maltophilia (taxon 40324)

## Full-text entities

- **Genes:** smeT [NCBI Gene 93835038]
- **Diseases:** Stenotrophomonas maltophilia (MESH:C531821)
- **Chemicals:** levofloxacin (MESH:D064704), minocycline (MESH:D008911), TMP/SMX (MESH:D015662), sul1 (-)
- **Species:** Stenotrophomonas maltophilia (species) [taxon 40324]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12835191/full.md

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Source: https://tomesphere.com/paper/PMC12835191