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Mechanism by which fiber antigen inhibits multiplication of type 5 adenovirus

Journal of Virology
|August 1, 1967
PubMed

Insights

Type 5 adenovirus fiber antigen significantly inhibits viral multiplication and blocks host cell biosynthesis. Hexon antigen showed no such effects, indicating fiber antigen

Area of Science:

  • Virology
  • Molecular Biology
  • Cell Biology

Background:

  • Adenovirus infections pose a significant public health challenge.
  • Understanding viral replication mechanisms is crucial for developing antiviral therapies.

Purpose of the Study:

  • To investigate the inhibitory effects of type 5 adenovirus fiber antigen on viral multiplication and host cell biosynthesis.
  • To compare the effects of fiber antigen with hexon antigen on adenovirus replication.

Main Methods:

  • Purified type 5 adenovirus fiber antigen was added to KB cell cultures.
  • Viral multiplication, adsorption, and deoxyribonucleic acid (DNA) liberation were assessed.
  • Biosynthesis of DNA, ribonucleic acid (RNA), and protein was monitored.
  • Cell-association of antigens and induction of interferon-like substances were evaluated.

Main Results:

  • Fiber antigen inhibited type 5 adenovirus multiplication by 50% at 35 µg/10^6 cells.
  • Fiber antigen reduced virion adsorption at high multiplicity but not at low multiplicity.
  • Viral DNA liberation was unaffected by fiber antigen.
  • Fiber antigen blocked host cell DNA, RNA, and protein biosynthesis 20-25 hours post-addition.
  • Hexon antigen showed no inhibitory effects and did not attach to cells.
  • Fiber antigen's effects were not mediated by an interferon-like substance.

Conclusions:

  • Type 5 adenovirus fiber antigen possesses potent antiviral activity by inhibiting viral multiplication and host cell macromolecular synthesis.
  • Fiber antigen's mechanism of action involves interference with viral replication and host cell processes.
  • Hexon antigen does not exhibit antiviral properties.
  • Fiber antigen represents a potential target for antiviral drug development against adenovirus infections.

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