Related Experiment Video
Updated: Jul 19, 2025

Improved Enzyme Protection Assay to Study Staphylococcus aureus Internalization and Intracellular Efficacy of Antimicrobial Compounds
Published on: September 8, 2021
Antibacterial Activity and Mechanism of Canagliflozin against Methicillin-Resistant Staphylococcus aureus
Siyao Gu1,2,3,4, Bing Fan4, Fang Wan1,3
1State Key Laboratory of Chemical Oncogenomics, Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Abstract:
Diabetic foot infection (DFI) is a common complication in diabetes patients, with foot infections being the leading cause of amputations. Staphylococcus aureus is frequently found in diabetic foot infections, of which methicillin-resistant Staphylococcus aureus (MRSA) has become a major clinical and epidemiological challenge. Since MRSA strains are resistant to most β-lactam antibiotics, and also partially resistant to other antibiotics, treatment is difficult and costly. The emergence of drug-resistant bacteria often arises from overuse or misuse of antibiotics. Clinically, canagliflozin is commonly used for the treatment of type 2 diabetes. On this basis, we investigated the antibacterial activity and mechanism of canagliflozin against MRSA, with the aim to discover novel functions of canagliflozin and provide new insights for the treatment of MRSA. Using the microbroth dilution method to determine the half maximal inhibitory concentration of drugs, we found that canagliflozin not only can inhibit the growth of methicillin-sensitive Staphylococcus aureus (MSSA) but also exhibits antibacterial activity against MRSA. The IC50 values, at approximately 56.01 μM and 57.60 μM, were almost the same. At 12 h, canagliflozin showed a significant antibacterial effect against MRSA at and above 30 μM. In addition, its combined use with penicillin achieved better antibacterial effects, which were increased by about three times. Additive antibacterial activity (FICI = 0.69) was found between penicillin and canagliflozin, which was better than that of doxycycline and canagliflozin (FICI = 0.95). Canagliflozin also affected bacterial metabolic markers, such as glucose, ATP, and lactic acid. The results of crystal violet staining indicate that canagliflozin disrupted the formation of bacterial biofilm. Our electron microscopy results showed that canagliflozin distorted the bacterial cell wall. The results of RT-PCR suggest that canagliflozin down-regulated the expressions of biofilm-related gene (clfA, cna, agrC, mgrA, hld) and methicillin-resistance gene (mecA), which was related to MRSA. Molecular docking also indicated that canagliflozin affected some interesting targets of MRSA, such as the sarA, crtM and fnbA proteins. In conclusion, canagliflozin exhibits antibacterial activity against MRSA by affecting bacterial metabolism, inhibiting its biofilm formation, distorting the bacterial cell wall, and altering the gene expression of biofilm formation and its virulence. Our study reveals the antibacterial activity of canagliflozin against MRSA, providing a new reference for treating diabetic foot infections.
Insights
Canagliflozin shows antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA), a common cause of diabetic foot infections. This drug impacts bacterial metabolism, biofilm formation, and cell walls, offering new treatment possibilities.
Area of Science:
- Microbiology
- Pharmacology
- Infectious Diseases
Background:
- Diabetic foot infections (DFI) are a leading cause of amputations in diabetes patients.
- Methicillin-resistant Staphylococcus aureus (MRSA) presents a significant challenge due to antibiotic resistance.
- Effective treatments for MRSA, particularly in DFI, are urgently needed.
Purpose of the Study:
- To investigate the antibacterial activity of canagliflozin against MRSA.
- To elucidate the mechanism of action of canagliflozin against MRSA.
- To explore potential new therapeutic applications for canagliflozin in treating MRSA infections.
Main Methods:
- Microbroth dilution to determine half maximal inhibitory concentration (IC50).
- Assays for bacterial metabolism, biofilm formation (crystal violet staining), and cell wall integrity (electron microscopy).
- RT-PCR for gene expression analysis and molecular docking for target identification.
Main Results:
- Canagliflozin inhibited both methicillin-sensitive Staphylococcus aureus (MSSA) and MRSA growth (IC50 ≈ 56-57 μM).
- Canagliflozin demonstrated significant antibacterial effects against MRSA at concentrations ≥ 30 μM and showed additive effects with penicillin.
- The drug disrupted MRSA metabolism, inhibited biofilm formation, distorted cell walls, and down-regulated key virulence and resistance genes (e.g., mecA).
Conclusions:
- Canagliflozin possesses direct antibacterial activity against MRSA.
- Its mechanisms involve metabolic disruption, biofilm inhibition, cell wall damage, and modulation of gene expression.
- Canagliflozin represents a potential therapeutic agent for MRSA infections, including diabetic foot infections.
Related Concept Videos
Gene Regulation in Microbial Communities: Quorum Sensing
Antimicrobial Effectiveness
Combined Effects of Drugs: Synergism
Such synergistic combinations...

