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Published on: December 21, 2011
Taurine attenuates OTA-promoted PCV2 replication through blocking ROS-dependent autophagy via inhibiting AMPK/mTOR
Nianhui Zhai1, Hong Wang1, Ying Chen1
1College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, Jiangsu Province, China; Institute of Nutritional and Metabolic Disorders in Domestic Animals and Fowls, Nanjing Agricultural University, Nanjing, 210095, Jiangsu Province, China.
Abstract:
Previous research found that ochratoxin A (OTA) could promote PCV2 replication by inducing autophagy. The aim of this study is to evaluate the effect of dietary amino acid derivative taurine on OTA-promoted PCV2 replication and explore the underlying mechanism. The results showed that taurine could inhibit OTA-promoted PCV2 replication in PK-15 cells. The effect of taurine could be mediated by its ability to attenuate ROS level and block OTA-promoted autophagy. Indeed, induction of autophagy by rapamycin could suppress the inhibitory effect of taurine on OTA-promoted PCV2 replication. Furthermore, taurine supplementation inhibited 5'AMP-activated protein kinase (AMPK) and activated mammalian target of rapamycin (mTOR). Activation of AMPK by acadesine (AICAR) could suppress the effect of taurine. In conclusion, taurine treatment suppresses autophagy by regulating the ROS/AMPK/mTOR signaling axis, thereby inhibiting OTA-promoted PCV2 replication. These findings provide the rationale for the use of taurine as an intervention against PCV2 infection.
Insights
Taurine inhibits ochratoxin A-induced PCV2 replication by blocking autophagy via the ROS/AMPK/mTOR pathway. This study supports taurine as a potential intervention for PCV2 infections.
Area of Science:
- Veterinary Virology
- Toxicology
- Cellular Biology
Background:
- Ochratoxin A (OTA) promotes Porcine circovirus type 2 (PCV2) replication by inducing autophagy.
- Understanding the mechanisms behind OTA's effects is crucial for developing interventions.
Purpose of the Study:
- To evaluate the effect of taurine on OTA-promoted PCV2 replication.
- To elucidate the underlying molecular mechanisms of taurine's action.
Main Methods:
- In vitro study using PK-15 cells.
- Assessment of PCV2 replication, reactive oxygen species (ROS) levels, and autophagy.
- Analysis of the AMPK/mTOR signaling pathway.
Main Results:
- Taurine inhibited OTA-induced PCV2 replication in PK-15 cells.
- Taurine attenuated ROS levels and blocked OTA-induced autophagy.
- Taurine regulated the ROS/AMPK/mTOR signaling axis, suppressing autophagy.
Conclusions:
- Taurine suppresses autophagy by modulating the ROS/AMPK/mTOR pathway, thereby inhibiting OTA-promoted PCV2 replication.
- Taurine shows promise as a dietary intervention against PCV2 infection.
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