Related Experiment Videos
Evidence for early nuclear antigens in cytomegalovirus-infected cells
The Journal of General Virology
|August 1, 1976
Abstract:
Human cytomegalovirus (CMV) induces nuclear antigens resembling the Epstein-Barr nuclear antigen (EBNA) as early as 3 h after infection. These early antigens can be detected only with the anti-complement immunofluorescence staining (ACIF) technique. Synthesis of these new antigens is not influenced by cytosine arabinoside (ara-C).
Insights
Human cytomegalovirus (CMV) infection rapidly produces early nuclear antigens, detectable via anti-complement immunofluorescence staining (ACIF). Their synthesis is independent of cytosine arabinoside (ara-C) treatment.
Area of Science:
- Virology
- Immunology
- Cell Biology
Background:
- Human cytomegalovirus (CMV) is a significant human pathogen.
- Early viral antigen expression is crucial for understanding viral replication cycles.
- Epstein-Barr nuclear antigen (EBNA) is a well-characterized viral nuclear antigen.
Purpose of the Study:
- To investigate the early induction of nuclear antigens by human cytomegalovirus (CMV).
- To characterize the detection methods for these early CMV-induced antigens.
- To determine the influence of cytosine arabinoside (ara-C) on the synthesis of these antigens.
Main Methods:
- Infection of human cells with CMV.
- Detection of viral nuclear antigens using the anti-complement immunofluorescence staining (ACIF) technique.
- Treatment with cytosine arabinoside (ara-C) to assess its effect on antigen synthesis.
Main Results:
- CMV induces nuclear antigens as early as 3 hours post-infection.
- These early antigens are detectable exclusively by the ACIF technique.
- The synthesis of these newly identified antigens is not inhibited by ara-C.
Conclusions:
- CMV expresses distinct early nuclear antigens shortly after infection.
- The ACIF method is essential for identifying these specific CMV-early antigens.
- Viral antigen synthesis in early CMV infection is resistant to ara-C.