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Porcine IFI30 inhibits PRRSV proliferation and host cell apoptosis in vitro
Jia Guo1, Mengjiao Zhou1, Xin Liu1
1College of Animal Science, Jilin University, Xi An Road 5333, Changchun, Jilin 130062, PR China.
Abstract:
Interferon-gamma-inducible protein 30 (IFI30) is an IFN-γ-inducible protein that is involved in MHC class II-restricted antigen processing and MHC class I-restricted cross-presentation pathways of adaptive immunity. The present study aimed to investigate the effects of porcine IFI30 expression on PRRSV proliferation in host cells. MARC-145 cells and pig Sertoli (ST) cells were infected with PRRSV after transfection with porcine IFI30 expression vectors and an empty vector. PRRSV copy numbers were analyzed by absolute real-time quantitative PCR, and the results showed that porcine IFI30 expression could significantly inhibit PRRSV transcription. Western blot analysis also determined that IFI30 expression could reduce the production of PRRSV M protein. Flow cytometric analysis indicated that the apoptosis of MARC-145 cells, which are non-porcine but highly permissive to PRRSV cells, was significantly decreased in the IFI30 expression group. In porcine ST cells, apoptosis was significantly increased in IFI30 knockdown cells but not in IFI30-overexpressing cells (**p < 0.01). In conclusion, porcine IFI30 expression may inhibit PRRSV proliferation and host cell apoptosis in vitro.
Insights
Porcine interferon-gamma-inducible protein 30 (IFI30) expression inhibits Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) transcription and M protein production. IFI30 also modulates host cell apoptosis in PRRSV-infected cells.
Area of Science:
- Immunology
- Virology
- Cell Biology
Background:
- Interferon-gamma-inducible protein 30 (IFI30) is crucial for antigen processing in adaptive immunity.
- Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) poses a significant threat to swine health and the global pork industry.
- Understanding host-pathogen interactions is key to developing effective antiviral strategies.
Purpose of the Study:
- To investigate the role of porcine IFI30 in regulating PRRSV proliferation.
- To determine the impact of IFI30 expression on PRRSV transcription and protein production.
- To assess the effect of IFI30 on host cell apoptosis during PRRSV infection.
Main Methods:
- Transfection of MARC-145 and pig Sertoli (ST) cells with porcine IFI30 expression vectors.
- PRRSV infection of transfected cells.
- Absolute real-time quantitative PCR to quantify PRRSV copy numbers.
- Western blot analysis for PRRSV M protein detection.
- Flow cytometry to assess host cell apoptosis.
Main Results:
- Porcine IFI30 expression significantly inhibited PRRSV transcription.
- IFI30 expression reduced the production of PRRSV M protein.
- IFI30 expression decreased apoptosis in MARC-145 cells.
- IFI30 knockdown increased apoptosis in porcine ST cells, while overexpression did not.
Conclusions:
- Porcine IFI30 expression demonstrates an inhibitory effect on PRRSV proliferation in vitro.
- IFI30 plays a role in modulating host cell apoptosis in response to PRRSV infection.
- These findings suggest IFI30 as a potential target for controlling PRRSV.
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