Production of Venezuelan equine encephalitis virus in cells grown on artificial capillaries.
Abstract: Primary cell cultures, a continuous cell line, and a diploid cell line were grown on an artificial capillary system. The cells were subsequently infected with Venezuelan equine encephalitis virus, and viral replication was studied. Extracellular fluids harvested from this system contained high titers of virus and were relatively free of cell debris.
Publication Date: 1978-02-01 PubMed ID: 637540PubMed Central: PMC242848DOI: 10.1128/aem.35.2.431-434.1978Google Scholar: Lookup
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Summary
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The research article discusses how a deadly virus, known as the Venezuelan equine encephalitis virus, is produced in cells that are grown on an artificial capillary system. The researchers examine how the virus replicates within these cells and evaluate the level of viral presence in the extracellular fluids.
Study Design
- The scientists utilized three different types of cells for this experiment. These included primary cell cultures, a continuous cell line, and a diploid cell line. These cells were specifically grown on an artificial capillary system.
- The chosen cells were thereafter infected with the Venezuelan equine encephalitis virus. The primary aim here was to understand and analyze the virus’s replication procedure within these cells.
Viral Replication Observation
- After the infection process, viral replication was thoroughly investigated. This study was crucial for understanding how the virus proliferates within the cell environment and how it impacts the cells’ structure and functioning.
- The study of viral replication is significant in disease research, as it provides insight into how infections spread and how they could potentially be controlled or treated.
Analysis of Extracellular Fluids
- Following the investigation into viral replication, the researchers examined the extracellular fluids that were harvested from the system. This was to measure the degree of the virus’s presence in these fluids.
- Interesting observations were made. The extracellular fluids contained high titers (concentrations) of the virus, indicating that the virus had not only replicated within the cells, but also managed to permeate the cell membranes and enter the surrounding fluids.
- Another key observation was that these fluids were relatively free of cell debris. This might suggest that the virus was able to enter the extracellular fluids without causing significant damage to the cells’ structure. This aspect may have great implications for the understanding of the virus’s survival and propagation capabilities.
Cite This Article
APA
Johnson AD, Eddy GA, Gangemi JD, Ramsburg HH, Metzger JF.
(1978).
Production of Venezuelan equine encephalitis virus in cells grown on artificial capillaries.
Appl Environ Microbiol, 35(2), 431-434.
https://doi.org/10.1128/aem.35.2.431-434.1978 Publication
Researcher Affiliations
MeSH Terms
- Cell Line
- Cells, Cultured
- Encephalitis Virus, Venezuelan Equine / growth & development
- Virus Cultivation / instrumentation
- Virus Cultivation / methods
References
This article includes 6 references
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- Wolf CF, Munkelt BE. Bilirubin conjugation by an artificial liver composed of cultured cells and synthetic capillaries.. Trans Am Soc Artif Intern Organs 1975;21:16-27.
- Knazek RA, Kohler PO, Gullino PM. Hormone production by cells grown in vitro on artificial capillaries.. Exp Cell Res 1974 Mar 15;84(1):251-4.
- Chick WL, Like AA, Lauris V, Galletti PM, Richardson PD, Panol G, Mix TW, Colton CK. A hybird artifical pancreas.. Trans Am Soc Artif Intern Organs 1975;21:8-15.
- Cole FE Jr, Pedersen CE Jr, Robinson DM, Eddy GA. Improved method for production of attenuated Venezuelan equine encephalomyelitis (TC-83 strain) vaccine.. J Clin Microbiol 1976 Apr;3(4):460-2.
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