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Published on: August 9, 2013
IFITM proteins inhibit the late step of feline foamy virus replication
1Department of Systems Biotechnology, Chung-Ang University, Ansung, Republic of Korea.
Abstract:
Interferon-induced transmembrane (IFITM) proteins as host restriction factors are known to inhibit the replication of several viruses. In this study, transient IFITM expression vectors were used to investigate whether IFITMs inhibit feline foamy viral (FFV) replication and which step of viral replication is inhibited. In our studies, viral production was significantly reduced when cells were infected with FFV at almost same times such as -3, 0, or 3 h post-transfection with IFITM vector. However viral production was not reduced even though cells were infected with FFV at 3 or 6 days post-transfection when production of IFITM proteins was maximized. Considering that IFITM expression was maximized at 3 days post-transfection, the stage of viral replication inhibited by IFITM appears to be the late step of viral replication. Moreover, the viral Gag proteins detected in the virus-infected cell lysates were proportionally correlated with viral titer of the culture supernatants. Therefore, it is likely that IFITMs can restrict production of FFV at the late step of viral replication.
Insights
Interferon-induced transmembrane (IFITM) proteins restrict feline foamy virus (FFV) replication. IFITMs inhibit FFV late-stage replication, reducing viral production and Gag protein levels.
Area of Science:
- Virology
- Cell Biology
- Immunology
Background:
- Interferon-induced transmembrane (IFITM) proteins are known host restriction factors.
- IFITMs inhibit the replication of various viruses.
- The role of IFITMs in feline foamy viral (FFV) replication is not well understood.
Purpose of the Study:
- To investigate whether IFITM proteins inhibit FFV replication.
- To determine the specific stage of the FFV replication cycle inhibited by IFITMs.
Main Methods:
- Transient IFITM expression vectors were utilized.
- Cells were infected with FFV at various time points relative to IFITM transfection.
- Viral production and Gag protein levels were quantified.
Main Results:
- Viral production was significantly reduced when FFV infection occurred shortly after IFITM transfection.
- IFITM expression did not inhibit viral production when maximized at later time points post-transfection.
- Viral Gag protein levels correlated with viral titers, suggesting late-stage inhibition.
Conclusions:
- IFITM proteins restrict FFV replication.
- IFITMs appear to inhibit a late step in the FFV replication cycle.
- IFITM-mediated restriction involves the inhibition of viral production and Gag protein accumulation.
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