# Insulin Affects Biological Behaviours of Pseudomonas aeruginosa

**Authors:** Defne Gümüş, Fatma Kalaycı-Yüksek, Mine Anğ-Küçüker

PMC · DOI: 10.3390/ph19020300 · Pharmaceuticals · 2026-02-11

## TL;DR

This study shows that insulin influences the behavior of Pseudomonas aeruginosa, affecting its growth, biofilm formation, and virulence.

## Contribution

The study reveals that insulin modulates Pseudomonas aeruginosa virulence through multiple mechanisms.

## Key findings

- All insulin concentrations increased bacterial growth.
- Insulin reduced biofilm production, motility, and haemolytic activity.
- 200 µU/mL insulin decreased bacterial virulence in an animal model.

## Abstract

Background: It is well known that host factors are capable of regulating microbial behaviours such as growth, metabolic pathways, virulence properties, and antimicrobial susceptibilities. In this respect, the present study aimed to investigate the relationship between insulin and various virulence properties of Pseudomonas aeruginosa ATCC 27853. Methods: Growth alterations, biofilm formation, motility, haemolytic activity, and pigment production (pyocyanin and pyoverdine) were determined in the presence/absence of three different insulin concentrations (10 µU/mL –20 µU/mL –200 µU/mL) under in vitro conditions. In addition, changes in bacterial virulence were evaluated in an in vivo animal (Caenorhabditis elegans) model. Alterations in growth, haemolytic activity, and pigment production were investigated spectrophotometrically. Biofilm formation was examined using the crystal violet well-plate assay. A soft agar plate method was used to detect swimming motility. Results: According to the results, all three insulin concentrations enhanced the bacterial growth. On the other hand, biofilm production, swimming motility, and haemolytic activity decreased in the presence of all insulin concentrations. Pyocyanin production was shown to be increased in the presence of only 10 µU/mL of insulin, but pyoverdine production did not change. In vivo animal survival rates showed that 200 µU/mL of insulin decreased bacterial virulence. Conclusions: This research demonstrates that P. aeruginosa can sense and respond to mammalian hormones (insulin), which can modulate microbial virulence through diverse mechanisms, providing new insights that may be relevant to infection dynamics.

## Linked entities

- **Chemicals:** insulin (PubChem CID 70678557), pyocyanin (PubChem CID 6817), pyoverdine (PubChem CID 5289234)
- **Species:** Pseudomonas aeruginosa (taxon 287), Caenorhabditis elegans (taxon 6239)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** inflammatory cytokines (MESH:D000080424), tissue damage (MESH:D017695), neuropathy (MESH:D009422), bloodstream infections (MESH:D018805), Chronic foot ulcers (MESH:D016523), death (MESH:D003643), P. aeruginosa infections (MESH:D011552), diabetic foot wounds (MESH:D017719), toxicity (MESH:D064420), diabetic wound infections (MESH:D014946), insulin resistance (MESH:D007333), infection (MESH:D007239), myocardial infarction (MESH:D009203), haemolytic (MESH:D006463), stroke (MESH:D020521), dead (MESH:D001926), organ dysfunction (MESH:D009102), blindness (MESH:D001766), burn (MESH:D002056), haemolysis (MESH:D006461), ventilator-associated pneumonia (MESH:D053717), inflammation (MESH:D007249), lung infections (MESH:D012141), injury to (MESH:D014947), critically (MESH:D016638), cystic fibrosis (MESH:D003550), renal failure (MESH:D051437), multiple (MESH:D009104), diabetes (MESH:D003920)
- **Chemicals:** lipids (MESH:D008055), LPS (MESH:D008070), chloroform (MESH:D002725), glucose (MESH:D005947), gangliosides (MESH:D005732), Broth (-), crystal violet (MESH:D005840), fluoroquinolones (MESH:D024841), amikacin (MESH:D000583), heme (MESH:D006418), Pyoverdine (MESH:C042453), latex (MESH:D007840), iron (MESH:D007501), ceftazidime (MESH:D002442), Pyocyanin (MESH:D011710), ethanol (MESH:D000431), HCl (MESH:D006851), SDS (MESH:D012967), sugars (MESH:D000073893), piperacillin (MESH:D010878), mannose (MESH:D008358), methanol (MESH:D000432), agar (MESH:D000362), polysaccharides (MESH:D011134)
- **Species:** Neurospora crassa (species) [taxon 5141], Burkholderia pseudomallei (species) [taxon 28450], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Enterococcus faecalis (species) [taxon 1351], C. elegans [taxon 328850], Escherichia coli (E. coli, species) [taxon 562], Momordica charantia (balsam pear, species) [taxon 3673], Caenorhabditis elegans (species) [taxon 6239], Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** N2 — Mus musculus (Mouse), Mouse neuroblastoma, Cancer cell line (CVCL_0470)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943400/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943400/full.md

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Source: https://tomesphere.com/paper/PMC12943400