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[Persistence of Newcastle disease virus in mouse cells]
Abstract:
The course of persistent infection in Newcastle disease virus (NDV)-infected mouse L cells (LNDV) was analysed. The production of infectious intra- and extracellular virus was markedly reduced (less than 10(1) PFU/ml), 30% of the cells produced virus-specific antigen. Analysis of the synthesis of 3H-nucleocapsid RNA in the LNDV system revealed predominance of low molecular weight RNAs. Virus-specific sequences were shown to be present in fraction of DNA extracted by Hirt's method. Only the "supernatant" Hirt's fraction was infectious. The possibility of the presence of virus-specific sequences in free unintegrated form is discussed.
Insights
Persistent Newcastle disease virus (NDV) infection in mouse cells showed significantly reduced infectious virus production. Virus-specific sequences were found in DNA, with infectious material present in the supernatant fraction.
Area of Science:
- Virology
- Molecular Biology
- Cell Biology
Background:
- Newcastle disease virus (NDV) can establish persistent infections in host cells.
- Understanding the mechanisms of persistent viral infections is crucial for developing therapeutic strategies.
Purpose of the Study:
- To analyze the characteristics of persistent Newcastle disease virus (NDV) infection in mouse L cells (LNDV).
- To investigate the state of viral genetic material and infectious virus production during persistent infection.
Main Methods:
- Infection of mouse L cells with NDV to establish persistent infection (LNDV).
- Quantification of infectious intra- and extracellular virus production.
- Analysis of viral antigen production using immunofluorescence.
- Detection and characterization of viral RNA synthesis.
- Extraction of DNA using Hirt's method to identify virus-specific sequences.
Main Results:
- Markedly reduced production of infectious NDV (less than 10(1) PFU/ml) in LNDV-infected cells.
- Approximately 30% of cells produced virus-specific antigen.
- Predominance of low molecular weight RNAs during NDV replication.
- Virus-specific DNA sequences were detected in Hirt's DNA fraction.
- Infectious viral material was exclusively found in the 'supernatant' Hirt's fraction.
Conclusions:
- Persistent NDV infection is characterized by significantly impaired infectious virus release.
- The presence of virus-specific sequences in the supernatant Hirt's fraction suggests the potential for free, unintegrated viral DNA.
- Further investigation is warranted to elucidate the role of unintegrated viral sequences in persistent NDV infections.