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Updated: Jan 21, 2026

Animal Model of Implant-Associated Infections in Mice
Published on: June 27, 2025
MTOR involved in bacterial elimination against Trueperella pyogenes infection based on mice model by transcriptome
Ting Huang1, Kai Cui2, Xuhao Song2
1Antibiotics Research and Re-evaluation Key Laboratory of Sichuan Province, SichuanIndustrial Institute of Antibiotics, Chengdu University, Chengdu, China; Key Laboratory of Bio-resources and Eco-environment (Ministry of Education), College of Life Sciences, Sichuan University, Chengdu, China.
Abstract:
Trueperella pyogenes is an importantly opportunistic and commensal pathogen that causes suppurative lesions of most economically important livestock. To understand the molecular mechanism underlying the infection by T. pyogenes, we carried out a large-scale transcriptome sequencing of mice livers intraperitoneally infected with T. pyogenes using RNA-sequencing. A total of 47 G clean bases were obtained and 136 differentially expressed genes were detected between the control and the infection groups in the liver transcriptomes. Additionally, we found that the expression of a key autophagy regulator, mTOR (mechanistic target of rapamycin) was significantly up-regulated in the infection groups. Mechanistically, T. pyogenes infection induced the expression of mTOR and subsequently inhibited the autophagy of host cell. Blocking autophagy with inhibitor 3-methyladenine (3-MA) or silencing autophagy-related gene 7 (Atg7) reduced the effect of bacterial elimination. Interestingly, inhibition of mTOR induced autophagy and reduced T. pyogenes viability in RAW264.7 murine macrophages. The silencing mTOR regulated oxidation and cytokines (interleukin-1β, IL-6 and tumor necrosis factro-α) against T. pyogenes in macrophages and significantly protected mice from T. pyogenes challenge. These findings indicate that mTOR is a novel functional regulator in autophagy-mediated T. pyogenes elimination and will be useful to further knowledge on the development of effective therapeutic strategy to control T. pyogenes-related diseases.
Insights
Trueperella pyogenes infection up-regulates mechanistic target of rapamycin (mTOR), inhibiting autophagy. Inhibiting mTOR boosts autophagy, reducing bacterial load and protecting mice, revealing mTOR as a therapeutic target for T. pyogenes infections.
Area of Science:
- Microbiology
- Immunology
- Molecular Biology
Background:
- Trueperella pyogenes is an opportunistic pathogen causing suppurative lesions in livestock.
- Understanding T. pyogenes infection mechanisms is crucial for developing treatments.
Purpose of the Study:
- To elucidate the molecular mechanisms of T. pyogenes infection using transcriptomic analysis.
- To investigate the role of mechanistic target of rapamycin (mTOR) in T. pyogenes pathogenesis and host defense.
Main Methods:
- Large-scale transcriptome sequencing (RNA-sequencing) of infected mouse livers.
- Analysis of gene expression changes, focusing on autophagy regulators like mTOR.
- Experimental manipulation of mTOR and autophagy pathways in macrophages and mice.
Main Results:
- T. pyogenes infection significantly up-regulated mTOR expression in mouse livers.
- mTOR up-regulation inhibited host cell autophagy, aiding bacterial survival.
- Inhibition of mTOR promoted autophagy, reduced T. pyogenes viability, and protected mice from infection.
Conclusions:
- mTOR is a key regulator of autophagy-mediated elimination of T. pyogenes.
- Targeting the mTOR-autophagy pathway offers a potential therapeutic strategy against T. pyogenes infections.
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