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Viral Concentration Determination Through Plaque Assays: Using Traditional and Novel Overlay Systems
Published on: November 4, 2014
Plaque formation with influenza viruses in dog kidney cells
The Journal of General Virology
|October 1, 1976
Abstract:
Infectious influenza and parainfluenza viruses were produced as plaql passages of egg-grown viruses in MDCK monolayers. Virus titres of 10(6) to 10(11) p.f.u./ml were obtained for several A and B strains of influenza and parainfluenza viruses.
Insights
Researchers successfully produced infectious influenza and parainfluenza viruses in MDCK cell cultures. High virus titers, up to 10(11) p.f.u./ml, were achieved for multiple strains, aiding virology research.
Area of Science:
- Virology
- Cell Biology
- Infectious Diseases
Background:
- Influenza and parainfluenza viruses are significant respiratory pathogens.
- Efficient production of these viruses is crucial for research and vaccine development.
- Previous methods for virus propagation have limitations.
Purpose of the Study:
- To establish a reliable method for producing high-titer infectious influenza and parainfluenza viruses.
- To optimize virus yield in a cell culture system.
Main Methods:
- Egg-grown influenza and parainfluenza viruses were used as initial inocula.
- Viruses were propagated through multiple passages in Madin-Darby Canine Kidney (MDCK) cell monolayers.
- Virus titers were quantified using plaque-forming units (p.f.u.).
Main Results:
- Infectious influenza and parainfluenza viruses were successfully produced.
- High virus titers ranging from 10(6) to 10(11) p.f.u./ml were achieved.
- The method proved effective for multiple strains of influenza A and B, and parainfluenza viruses.
Conclusions:
- MDCK cell culture provides an effective platform for high-yield production of influenza and parainfluenza viruses.
- This method facilitates the generation of sufficient viral material for various research applications.
- The established protocol supports the advancement of studies on influenza and parainfluenza pathogenesis and control.

