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Published on: July 5, 2017
A carrier state of mumps virus in human conjunctiva cells. I. General characteristics
Abstract:
Mumps virus produced a carrier state in human conjunctiva cells that was maintained for more than 100 subcultures over a period of 3 years. Antiserum in the medium was not required. The virus had little apparent effect on the cells which grew at a rate similar to uninfected control cells. Mumps virus was regularly found in the culture medium at levels about 0.9 log higher than the cell-associated virus. When first tested after 30 subcultures, the virus was found to have lost its cytopathogenicity for cells ordinarily susceptible to mumps virus, but was identifiable as mumps virus by neutralization with specific antiserum. Use of fluorescein-labeled antiserum revealed that 80 to 95 per cent of cells in the carrier cultures contained mumps virus antigen. The antigen was concentrated in a few sharply circumscribed, discrete masses in the cell cytoplasm rather than in many granules throughout the cytoplasm as is characteristic of cell infection by cytopathogenic mumps virus. The carrier cultures were resistant to the destructive effect of a cytopathogenic line of mumps virus, but showed little resistance to the cytopathogenic effect of vesicular stomatitis, Sendai, or Newcastle disease viruses.
Insights
Mumps virus established a persistent carrier state in human conjunctiva cells. This non-cytopathic virus retained its identity but lost its cell-damaging ability, conferring resistance to superinfection.
Area of Science:
- Virology
- Cell Biology
- Immunology
Background:
- Mumps virus is a significant human pathogen.
- Understanding persistent viral infections is crucial for developing effective treatments.
- The interaction between viruses and host cells can lead to complex cellular states.
Purpose of the Study:
- To investigate the establishment and characteristics of a persistent mumps virus carrier state in human conjunctiva cells.
- To determine the biological and immunological properties of mumps virus in a long-term carrier culture.
- To assess the impact of the carrier state on cellular susceptibility to other viral infections.
Main Methods:
- Culturing human conjunctiva cells with mumps virus for over 100 subcultures (3 years).
- Monitoring viral presence in culture medium and cells.
- Assessing viral cytopathogenicity using susceptible cell lines.
- Identifying viral antigen within cells using fluorescein-labeled antiserum.
- Testing carrier cell resistance to superinfection with various viruses.
Main Results:
- A stable mumps virus carrier state was established in human conjunctiva cells, maintained for 3 years without antiserum.
- The carrier state virus lost its cytopathogenicity but remained identifiable by neutralization.
- 80-95% of carrier cells contained mumps virus antigen, localized in discrete cytoplasmic masses.
- Carrier cultures exhibited resistance to a cytopathogenic mumps virus strain but not to other paramyxoviruses.
Conclusions:
- Mumps virus can establish a long-term, non-cytopathic carrier state in human conjunctiva cells.
- This carrier state alters viral properties and confers cross-protection against homologous virus superinfection.
- The distinct intracellular antigen localization suggests unique viral-host interactions in carrier cells.
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