# Effective therapeutic strategies against Pseudomonas aeruginosa and Burkholderia Cepacia complex infections

**Authors:** Noura A. M. Helmy, Ahmed F. Basyony, Sally T. K. Tohamy, Samar A. Zaki

PMC · DOI: 10.1038/s41598-025-26712-8 · Scientific Reports · 2025-11-23

## TL;DR

This study compares identification methods and antibiotic treatments for two bacteria that cause serious infections and are often misidentified.

## Contribution

The study introduces a more accurate PCR-based method for identifying Pseudomonas aeruginosa and Burkholderia cepacia complex.

## Key findings

- PCR amplification of the recA gene is more specific for identifying Bcc than conventional methods.
- P. aeruginosa is more susceptible to colistin and ceftazidime, while Bcc responds better to cotrimoxazole and minocycline.
- Combining NALC with meropenem or levofloxacin shows synergistic effects against both pathogens.

## Abstract

Pseudomonas aeruginosa and Burkholderia cepacia complex (Bcc) can cause serious nosocomial infections. The reported misidentification of Bcc as P. aeruginosa, besides the contrasting susceptibility patterns between these two pathogens, underscores the importance of accurate identification and the need to explore therapeutic approaches that could eradicate them both. Our study aimed to evaluate the susceptibilities of both pathogens to different antibiotics and test the effectiveness of different antimicrobial combinations. In addition, we compared conventional phenotypic and automated identification methods using the VITEK 2 system with PCR amplification and sequencing of recA gene to differentiate between P. aeruginosa and Bcc. Amplification by PCR of the recA gene showed high specificity in the identification of Bcc in comparison with conventional and automated phenotypic methods. Significant differences in susceptibility were observed with P. aeruginosa isolates having more susceptibility to colistin and ceftazidime, while Burkholderia isolates were more susceptible to cotrimoxazole and minocycline. Both P. aeruginosa and Burkholderia isolates tested were more susceptible to N-Acetyl-L-Cysteine (NALC) plus meropenem or levofloxacin, followed by gentamicin plus piperacillin/tazobactam. Synergistic effect of NALC plus meropenem or levofloxacin may help in the eradication of both pathogens to overcome the diagnostic challenges posed by the possible misidentification using conventional identification methods.

The online version contains supplementary material available at 10.1038/s41598-025-26712-8.

## Linked entities

- **Genes:** RAD51 (RAD51 recombinase) [NCBI Gene 5888]
- **Chemicals:** colistin (PubChem CID 5311054), ceftazidime (PubChem CID 5481173), cotrimoxazole (PubChem CID 358641), minocycline (PubChem CID 54675783), N-Acetyl-L-Cysteine (PubChem CID 12035), meropenem (PubChem CID 441130), levofloxacin (PubChem CID 149096), gentamicin (PubChem CID 3467), piperacillin/tazobactam (PubChem CID 461573)
- **Species:** Pseudomonas aeruginosa (taxon 287), Burkholderia cepacia complex (taxon 87882)

## Full-text entities

- **Diseases:** Pseudomonas aeruginosa (MESH:D011552), Burkholderia Cepacia complex infections (MESH:D019121), nosocomial infections (MESH:D003428)
- **Chemicals:** levofloxacin (MESH:D064704), gentamicin (MESH:D005839), cotrimoxazole (MESH:D015662), N-Acetyl-L-Cysteine (MESH:D000111), minocycline (MESH:D008911), ceftazidime (MESH:D002442), meropenem (MESH:D000077731), piperacillin/tazobactam (MESH:D000077725)
- **Species:** Burkholderia cepacia complex (species group) [taxon 87882], Pseudomonas aeruginosa (species) [taxon 287]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12644862/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12644862/full.md

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Source: https://tomesphere.com/paper/PMC12644862