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Viability and infectivity of measles virus-infected nervous tissue frozen in cryoprotective medium
Applied Microbiology
|July 1, 1970
Abstract:
Measles virus-infected hamster brain tissue remained viable when frozen slowly in medium containing dimethyl sulfoxide. This procedure was essential for isolation of neurotropic measles virus from tissue specimens stored frozen.
Insights
Slowly freezing measles virus-infected hamster brain tissue with dimethyl sulfoxide preserved viability. This method is crucial for isolating neurotropic measles virus from frozen tissue samples.
Area of Science:
- Virology
- Neuroscience
- Cryobiology
Background:
- Measles virus can infect the central nervous system, leading to neurotropic complications.
- Preserving the viability of infected tissue is critical for isolating and studying neurotropic viruses.
Purpose of the Study:
- To determine an effective method for preserving measles virus-infected hamster brain tissue for subsequent viral isolation.
- To establish a reliable protocol for storing neurotropic measles virus specimens.
Main Methods:
- Hamster brain tissue infected with measles virus was subjected to slow-freezing.
- The cryoprotective medium used contained dimethyl sulfoxide (DMSO).
- Viability of the frozen tissue was assessed for neurotropic measles virus isolation.
Main Results:
- Slow freezing of infected brain tissue in medium with dimethyl sulfoxide maintained tissue viability.
- This cryopreservation technique proved essential for successful isolation of neurotropic measles virus.
Conclusions:
- Slow freezing with dimethyl sulfoxide is a viable method for preserving measles virus-infected brain tissue.
- This technique facilitates the isolation of neurotropic measles virus from frozen specimens, aiding further research.