BMC Complementary Medicine and Therapies· 2026Q1
Baicalein in combination with ceftazidime-avibactam exhibits synergism against carbapenem-resistant Acinetobacter baumannii in vitro
- 0citations
- Q1SCImago
- 2026year
Short summary
Combining baicalein (BCL) with ceftazidime-avibactam (CZA) demonstrates synergistic killing of carbapenem-resistant Acinetobacter baumannii (CRAB), inhibiting biofilm formation and modulating key metabolic and resistance pathways.
AI-generated from the title and abstract; the full text is not read.
Key points
- Baicalein (BCL) combined with ceftazidime-avibactam (CZA) showed synergistic activity against 20 CRAB clinical strains (FICI=0.5).
- The CZA+BCL combination significantly inhibited CRAB biofilm formation (P < 0.05).
- Transcriptomic analysis identified 100 differentially expressed genes, enriched in sulfur and butanoate metabolism.
- Key mechanisms include modulation of iron metabolism, MFS transporters, and a negative correlation between AbsR25 and MFS-transporter expression (r = -0.689).
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract Background The escalating global threat of carbapenem-resistant Acinetobacter baumannii (CRAB), classified by the WHO as a critical priority pathogen, underscores the urgent need for innovative therapeutic strategies. Traditional antibiotics face diminishing efficacy due to rapid resistance evolution, necessitating exploration of adjuvant therapies. Baicalein (BCL), a flavonoid from Scutellaria baicalensis, exhibits broad antimicrobial and resistance-modulating properties. This study aims to evaluate the synergistic effects and mechanisms of BCL combined with ceftazidime-avibactam (CAZ/AVI, CZA) against CRAB to address therapeutic gaps in managing these infections. Methods Twenty CRAB clinical strains from a tertiary hospital were characterized using multi-locus sequence typing (MLST). Synergy between CZA and BCL was assessed via checkerboard assays (fractional inhibitory concentration index, FICI), time-kill kinetics, and biofilm inhibition assays. Transcriptomic profiling (RNA-seq) was performed to identify differentially expressed genes associated with synergistic effect. The change of sRNA and mRNA expression was validated by quantitative reverse transcription-PCR. Results MLST revealed two dominant sequence types: ST208 and ST195. Checkerboard assays demonstrated significant synergism between CZA (8/4 µg/mL) and BCL (16 µg/mL), with a FICI of 0.5. Biofilm formation was significantly inhibited by the combination ( P < 0.05). Transcriptomic analysis identified 100 common DEGs across treatment groups, enriched in sulfur metabolism, butanoate metabolism, and amino acid degradation pathways. Notably, iron metabolism genes and major facilitator superfamily (MFS) transporters were differentially regulated by changing the concentration of BCL in drug combination. A negative correlation was observed between AbsR25 and MFS-transporter ( r = -0.689, P < 0.001). Conclusion The combination of CZA and BCL exerts potent synergistic antibacterial and anti-biofilm activities against CRAB, with putative mechanisms involving the modulation of efflux pumps, iron homeostasis, and key metabolic pathways. The study not only establishes BCL as a promising adjuvant in the fight against CRAB infections, but also provides a molecular basis for optimizing combinatorial therapeutic regimens.
The authors' abstract, as published at the source. BMC Complementary Medicine and Therapies, 2026 · DOI ↗
Continue with a free account
Ask the paper: 3 free questions a day about this paper; save it, get its citation, new summaries every day for your field. Takeaways are Premium.
Continue free on the webSign in with Google or Apple; no card needed. You come back to this paper.
On your phone:
Molecular MedicineBiochemistry, Genetics and Molecular Biology