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Luteolin Showed a Resistance Elimination Effect on Gentamicin by Decreasing MATE mRNA Expression in Trueperella
Dexian Zhang1, Xiang Gao1, Xuejiao Song1
1Key Laboratory of Zoonosis of Liaoning Province, College of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang, P.R. China.
Abstract:
Trueperella pyogenes is a common inhabitant of mucosal surfaces in animals and causes a variety of infections, including endometritis, mastitis, and liver abscessation, in dairy cows. Many antimicrobial agents are used for treatment of infections caused by T. pyogenes; however, antibiotic resistance has recently become a serious problem. The objective of this study was to characterize the effect of the efflux pump-encoding multidrug and toxic compound extrusion (MATE) gene on antibiotic resistance in T. pyogenes isolates from cows with signs of endometritis. As a compound from plants, luteolin showed antimicrobial activities in Escherichia coli and Staphylococcus aureus; therefore, we also investigated whether luteolin can eliminate antibiotic resistance. We constructed a MATE deletion mutant in BM-H06-3 to identify the function of MATE in antibiotic resistance. MATE mRNA expression was measured to identify the mechanism of luteolin in gentamicin resistance elimination effect in T. pyogenes. The T. pyogenes isolate BM-H06-3 became susceptible to gentamicin, amikacin, streptomycin, erythromycin, and roxithromycin after MATE deletion. No synergistic effect between luteolin and gentamicin was observed in eight isolates, which were randomly selected from 34 T. pyogenes isolates, but the isolates became susceptible to gentamicin after luteolin treatment at a subinhibitory concentration (1/4 minimum inhibitory concentration [MIC]) for 36 hr. Furthermore, luteolin can decrease MATE mRNA expression after luteolin treatment at a subinhibitory concentration (1/4 MIC). We found that the MATE gene was involved in antibiotic resistance and that luteolin induces a resistance elimination effect in T. pyogenes. Therefore, luteolin may be a potential agent to inhibit efflux pumps in multidrug-resistant T. pyogenes.
Insights
The multidrug and toxic compound extrusion (MATE) gene contributes to antibiotic resistance in Trueperella pyogenes. Luteolin, a plant compound, can eliminate this resistance by reducing MATE gene expression.
Area of Science:
- Veterinary Microbiology
- Antimicrobial Resistance
- Molecular Biology
Background:
- Trueperella pyogenes causes significant infections in dairy cows, including endometritis and mastitis.
- Increasing antibiotic resistance in T. pyogenes necessitates novel treatment strategies.
- Efflux pumps, like those encoded by the MATE gene, are a key mechanism of multidrug resistance.
Purpose of the Study:
- To investigate the role of the multidrug and toxic compound extrusion (MATE) gene in antibiotic resistance in T. pyogenes.
- To evaluate the potential of luteolin, a plant-derived compound, in overcoming antibiotic resistance in T. pyogenes.
- To elucidate the mechanism by which luteolin affects antibiotic resistance.
Main Methods:
- Construction of a MATE deletion mutant in T. pyogenes isolate BM-H06-3.
- Assessment of antibiotic susceptibility before and after MATE gene deletion.
- Measurement of MATE mRNA expression following luteolin treatment.
- Evaluation of luteolin's effect on antibiotic resistance in T. pyogenes isolates.
Main Results:
- Deletion of the MATE gene rendered T. pyogenes susceptible to multiple antibiotics, including gentamicin, amikacin, streptomycin, erythromycin, and roxithromycin.
- Luteolin treatment at subinhibitory concentrations (1/4 MIC) restored susceptibility to gentamicin in T. pyogenes isolates.
- Luteolin significantly decreased MATE mRNA expression, indicating inhibition of the efflux pump.
Conclusions:
- The MATE gene plays a crucial role in conferring multidrug resistance in Trueperella pyogenes.
- Luteolin demonstrates a resistance-eliminating effect against T. pyogenes, likely by downregulating MATE gene expression.
- Luteolin holds potential as an adjuvant therapy to combat multidrug-resistant T. pyogenes infections by inhibiting efflux pumps.
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