# Synergistic Antimicrobial Effects of Baicalin Combined with Kanamycin Against MRSA: Underlying Mechanisms and Diminished Colonization on Lettuce

**Authors:** Xin Meng, Zhiyun Yu, Chao Ning, Mingtong Sun, Mengna Kang, Haiyong Guo

PMC · DOI: 10.3390/ph18101458 · Pharmaceuticals · 2025-09-28

## TL;DR

Baicalin combined with kanamycin effectively fights MRSA infections by disrupting cell structures and reducing biofilm formation, with potential applications in agriculture.

## Contribution

The study reveals the synergistic mechanism of baicalin and kanamycin against MRSA, including cell membrane disruption and biofilm inhibition.

## Key findings

- The BA/KM combination reduced MRSA biofilm formation by 77.85% and cell metabolic activity by 42.93%.
- The combination suppressed staphyloxanthin synthesis and downregulated agrA and agrC genes.
- MRSA colonization on lettuce was reduced by 0.88 log CFU/cm², comparable to hydrogen peroxide.

## Abstract

Background: The treatment of methicillin-resistant Staphylococcus aureus (MRSA) infections is extremely challenging due to its antibiotic resistance, and the combination of plant active ingredients with antibiotics represents a potential strategy to address this issue. Methods: We determined the combinatorial relationship between baicalin (BA) and kanamycin (KM) using the checkerboard dilution method. The antibacterial activity of the baicalin–kanamycin (BA/KM) combination was evaluated through growth curve determination assays and scanning electron microscopy (SEM). The effects of the BA/KM combination on the cell membrane and cell wall of MRSA were analyzed using reactive oxygen species (ROS) detection assays, intracellular protein leakage experiments, alkaline phosphatase (AKP) activity assays, laser scanning confocal microscopy (LSCM) observations, and molecular docking simulations. The antibiofilm activity and related mechanisms of the BA/KM combination were elucidated via crystal violet staining, MTT assay, phenol-sulfuric acid method, congo red staining, staphyloxanthin determination assays, and quantitative real-time polymerase chain reaction (qPCR). The safety of the BA/KM combination was assessed through hemolytic activity analysis, and its anti-MRSA efficacy was evaluated on lettuce. Results: BA/KM combination showed a synergistic antibacterial effect on MRSA USA300. Mechanistic studies revealed that BA may interact with amino acid residues of peptidoglycan synthetase PBP2a to hinder peptidoglycan synthesis, thereby facilitating KM penetration through the cell wall. Subsequently, BA binds to amino acid residues of the membrane transporter NorA, leading to disruption of cell membrane homeostasis and enhancing KM’s ability to induce intracellular ROS accumulation in MRSA. Furthermore, the BA/KM combination reduced MRSA biofilm formation by 77.85% and decreased the metabolic activity of biofilm cells by 42.93% through inhibiting the synthesis of biofilm components EPS and PIA. Additionally, this combination suppressed the synthesis of staphyloxanthin and downregulated the expression of agrA and agrC genes. When 1/8 MIC BA was combined with 1/4 MIC KM, the count of MRSA on lettuce surfaces was reduced by 0.88 log CFU/cm2, an effect comparable to that of 0.2% (v/v) hydrogen peroxide. Conclusions: According to these findings, the BA/KM combination may offer a promising option for enhancing antibacterial efficacy through synergism, reducing antibiotic usage concentrations, and limiting MRSA transmission in fresh agricultural products.

## Linked entities

- **Genes:** pbp2a (penicillin-binding protein PBP2A) [NCBI Gene 8154155], norA (multidrug efflux MFS transporter NorA) [NCBI Gene 3616737], agrA (quorum-sensing response regulator AgrA) [NCBI Gene 3617361], agrC (quorum-sensing sensor histidine kinase AgrC) [NCBI Gene 3617362]
- **Chemicals:** baicalin (PubChem CID 64982), kanamycin (PubChem CID 6032), staphyloxanthin (PubChem CID 56928085), hydrogen peroxide (PubChem CID 784)
- **Diseases:** MRSA (MONDO:0100073)
- **Species:** Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Genes:** AKP [NCBI Gene 28379728]
- **Diseases:** MRSA (MESH:D013203), infections (MESH:D007239)
- **Chemicals:** KM (MESH:D007612), sulfuric acid (MESH:C033158), staphyloxanthin (MESH:C031841), BA (MESH:C038044), PIA (MESH:C047235), methicillin (MESH:D008712), phenol (MESH:D019800), congo red (MESH:D003224), crystal violet (MESH:D005840), EPS (MESH:C100219), hydrogen peroxide (MESH:D006861), ROS (MESH:D017382), MTT (MESH:C070243)
- **Cell lines:** USA300 — Homo sapiens (Human), Parkinson disease, Induced pluripotent stem cell (CVCL_C952)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12567461/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12567461/full.md

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Source: https://tomesphere.com/paper/PMC12567461