Antibacterial efficacy and mechanism of action of VTC3-knockout Saccharomyces cerevisiae against multidrug- resistant pathogenic bacteria
4 affiliations
- 1School of Medical Technology, Xuzhou Medical University, Xuzhou
- 2Suqian Zhongwu Hospital, Suqian
- 3Department of Genetics, Xuzhou Medical University, Xuzhou
- 4Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Department of Microbial and Biochemical Pharmacy, School of Pharmacy, Xuzhou Medical University, Xuzhou
Abstract
Introduction: Multidrug-resistant (MDR) bacterial infections are a global public health crisis, and traditional antibiotic therapies are becoming increasingly ineffective. Probiotics represent a promising strategy in this context.
Methods: In this study, we examined the antibacterial activity and mechanism of action of Saccharomyces cerevisiae with VTC3 gene knockout ( VTC3- KO).
Results: Growth curves, biofilm formation, antibacterial spectrum, and coculture experiments demonstrated that VTC3- KO S. cerevisiae effectively inhibited the growth of pathogens and significantly suppressed the biofilm formation of Escherichia coli , Staphylococcus aureus , and Klebsiella pneumoniae . Moreover, VTC3- KO S. cerevisiae exhibited tolerance to the gastrointestinal environment, with enhanced auto and coaggregation with pathogens. In in vivo culture of Galleria mellonella and in a mouse infection model, VTC3- KO S. cerevisiae significantly improved host survival, alleviated intestinal tissue damage, and reduced inflammatory cell infiltration.
Discussion: Mechanistic studies suggest that the observed antimicrobial effect may be attributable to the production of acidic substances. These findings demonstrate that VTC3- KO S. cerevisiae possesses dual antibacterial and probiotic functions, providing a sustainable alternative to traditional antibiotics for treating MDR infections.
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BibTeX
@article{yang2026antibacterial,
title = {{Antibacterial efficacy and mechanism of action of VTC3-knockout Saccharomyces cerevisiae against multidrug- resistant pathogenic bacteria}},
author = {Weibao Yang and Mengkun Li and Yu Zhang and Kan Hu and Bingjie Lu and Ailin Yuan and Zuobin Zhu and Ying Li},
journal = {Frontiers in Microbiology},
year = {2026},
month = oct,
doi = {10.3389/fmicb.2026.1937861},
url = {https://www.frontiersin.org/articles/10.3389/fmicb.2026.1937861/full},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Antibacterial efficacy and mechanism of action of VTC3-knockout Saccharomyces cerevisiae against multidrug- resistant pathogenic bacteria
AU - Weibao Yang
AU - Mengkun Li
AU - Yu Zhang
AU - Kan Hu
AU - Bingjie Lu
AU - Ailin Yuan
AU - Zuobin Zhu
AU - Ying Li
PY - 2026
DA - 2026/10/21
JO - Frontiers in Microbiology
DO - 10.3389/fmicb.2026.1937861
UR - https://www.frontiersin.org/articles/10.3389/fmicb.2026.1937861/full
AB - Introduction: Multidrug-resistant (MDR) bacterial infections are a global public health crisis, and traditional antibiotic therapies are becoming increasingly ineffective. Probiotics represent a promising strategy in this context. Methods: In this study, we examined the antibacterial activity and mechanism of action of Saccharomyces cerevisiae with VTC3 gene knockout ( VTC3- KO). Results: Growth curves, biofilm formation, antibacterial spectrum, and coculture experiments demonstrated that VTC3- KO S. cerevisiae effectively inhibited the growth of pathogens and significantly suppressed the biofilm formation of Escherichia coli , Staphylococcus aureus , and Klebsiella pneumoniae . Moreover, VTC3- KO S. cerevisiae exhibited tolerance to the gastrointestinal environment, with enhanced auto and coaggregation with pathogens. In in vivo culture of Galleria mellonella and in a mouse infection model, VTC3- KO S. cerevisiae significantly improved host survival, alleviated intestinal tissue damage, and reduced inflammatory cell infiltration. Discussion: Mechanistic studies suggest that the observed antimicrobial effect may be attributable to the production of acidic substances. These findings demonstrate that VTC3- KO S. cerevisiae possesses dual antibacterial and probiotic functions, providing a sustainable alternative to traditional antibiotics for treating MDR infections.
SN - 1664-302X
ER -