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Protocols for Investigating the Host-tissue Distribution, Transmission-mode, and Effect on the Host Fitness of a Densovirus in the Cotton Bollworm
Published on: April 12, 2017
Some energy relations in a host-virus system
Abstract:
It was found that DNP (2,4-dinitrophenol) will inhibit completely the propagation of influenza virus in chorioallantoic membrane. This reagent did not permanently alter those metabolic processes required for the synthesis of virus and at the concentrations employed demonstrated no virucidal effects. In minced preparations of chorioallantoic membrane DNP was shown to have a pronounced stimulatory effect upon ATPase (adenosinetriphosphatase). When DNP was used with intact tissues, an excellent correlation was found between the inhibition of viral propagation and the stimulation of respiration and release of phosphate. Concentrations of DNP which permitted a twofold increase in the endogenous respiration of intact membranes allowed little or no viral synthesis. It is concluded that the energy required for viral synthesis derives from the oxidative phosphorylative activity of the host tissue.
Insights
2,4-dinitrophenol (DNP) completely inhibits influenza virus propagation without damaging host cells. Viral synthesis energy is derived from the host tissue's oxidative phosphorylation, as shown by DNP
Area of Science:
- Virology
- Cellular Metabolism
- Biochemistry
Background:
- Influenza virus propagation relies on host cell metabolic processes.
- Understanding the energy sources for viral synthesis is crucial for antiviral development.
Purpose of the Study:
- To investigate the effect of 2,4-dinitrophenol (DNP) on influenza virus propagation.
- To determine the metabolic pathways involved in viral synthesis.
Main Methods:
- Using chorioallantoic membranes infected with influenza virus.
- Assessing viral propagation inhibition by DNP.
- Measuring ATPase activity, respiration, and phosphate release in response to DNP.
Main Results:
- DNP completely inhibited influenza virus propagation in chorioallantoic membranes.
- DNP stimulated ATPase activity and respiration in host tissues.
- Viral synthesis correlated inversely with host cell respiration and phosphate release.
Conclusions:
- The energy required for influenza viral synthesis is supplied by the host tissue's oxidative phosphorylation.
- DNP inhibits viral propagation by interfering with host cell energy production, not by direct virucidal effects.
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