# Carriage of multiple resistance genes by community and hospital isolates of Stenotrophomonas maltophilia resistant to the first-line drug of choice in Nigeria

**Authors:** David Olusoga Ogbolu, Oyebode Armstrong Terry Alli, Adeolu Sunday Oluremi, Deborah Iyanu Ojebode, Yetunde Temilola Ogunjimi, Mark Alexander Webber

PMC · DOI: 10.11604/pamj.2024.49.125.21124 · The Pan African Medical Journal · 2024-12-18

## TL;DR

This study found that Stenotrophomonas maltophilia isolates from Nigeria carry multiple drug resistance genes, making treatment difficult.

## Contribution

The study identifies multiple resistance genes and plasmids in S. maltophilia isolates from both hospital and community settings in Nigeria.

## Key findings

- All isolates showed multidrug resistance and carried multiple antimicrobial resistance genes.
- Common resistance genes included oqxB, bla1_3, aph(3), cmlB1, sul, and dfrA variants.
- Multiple plasmids like ColBS512, ColMG828, and IncR were identified in the isolates.

## Abstract

Stenotrophomonas maltophilia (S. maltophilia) has emerged as an important nosocomial pathogen and causes life-threatening infections among the vulnerable, and occasionally in immunocompetent individuals. We examined the mechanisms of multidrug resistance in S. maltophilia isolated from sick and healthy individuals in Nigeria. Susceptibility testing and genome sequencing revealed multidrug resistance and carriage of multiple antimicrobial resistance genes in all isolates. Genes encoding resistance to fluoroquinolones, beta-lactams, aminoglycosides, chloramphenicol, sulphonamide and trimethoprim including oqxB, bla1_3, aph(3), cmlB1, sul and dfrA, variants were found in all the isolates. Genome analysis revealed multiple plasmids were present in the strains including ColBS512, ColMG828, and IncR plasmids. Resistance to multiple drugs compromises the treatment option for S. maltophilia limiting a potential treatment option that can cause serious nosocomial infections.

## Linked entities

- **Genes:** oqxB (multidrug efflux RND transporter permease subunit OqxB) [NCBI Gene 23847048], sul (dihydropteroate synthases) [NCBI Gene 987081], dfrA (dihydrofolate reductase) [NCBI Gene 887777]
- **Chemicals:** beta-lactams (PubChem CID 136721), chloramphenicol (PubChem CID 5959), sulphonamide (PubChem CID 5333), trimethoprim (PubChem CID 5578)
- **Species:** Stenotrophomonas maltophilia (taxon 40324)

## Full-text entities

- **Diseases:** Stenotrophomonas maltophilia (MESH:C531821), infections (MESH:D007239), nosocomial infections (MESH:D003428)
- **Chemicals:** trimethoprim (MESH:D014295), chloramphenicol (MESH:D002701), aminoglycosides (MESH:D000617), fluoroquinolones (MESH:D024841), sulphonamide (MESH:D013449), beta-lactams (MESH:D047090)
- **Species:** Stenotrophomonas maltophilia (species) [taxon 40324]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11971824/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11971824/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC11971824/full.md

---
Source: https://tomesphere.com/paper/PMC11971824