1966
DOI: 10.1128/mmbr.30.1.152-176.1966
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Multiplication of measles virus in cell cultures.

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1966
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Cited by 22 publications
(9 citation statements)
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“…Both facts suggest a difference in growth pattern between SSPE virus and measles virus in culture that should be examined further. The other growth properties, such as thermolability of the SSPE virus and the lack of effect of actinomycin D on virus production, are similar to that reported for measles virus (19).…”
Section: Discussionsupporting
confidence: 77%
See 1 more Smart Citation
“…Both facts suggest a difference in growth pattern between SSPE virus and measles virus in culture that should be examined further. The other growth properties, such as thermolability of the SSPE virus and the lack of effect of actinomycin D on virus production, are similar to that reported for measles virus (19).…”
Section: Discussionsupporting
confidence: 77%
“…The growth properties of the LEC strain SSPE virus in CV-1 cells differ from the in vitro growth properties of measles virus in two respects. First, the SSPE virus-infected cells undergo cytopathic changes culminating in their destruction within 48 hr after infection, whereas measles virus-infected cells were able to maintain cell integrity for a much longer time (19,22). Secondly, the titer of extracellular virus of SSPE-infected cultures never attains the high infections titer attained by measles virus infections (19,22).…”
Section: Discussionmentioning
confidence: 99%
“…Shortly thereafter, it was reported that the virus could also replicate in established cell lines and chicken embryos (100,231), and plaque assay systems were developed (152,371). It has subsequently been shown that measles virus can be grown in a variety of primary and continuous cell lines, although the best results are obtained with cells of human and simian origin (225).…”
Section: Virus-cell Interactionsmentioning
confidence: 99%
“…The availability of systems for growing relatively large amounts of some paramyxoviruses [Newcastle disease virus (NDV), Sendai virus, and simian virsus 5] in large part accounts for the fact that most of what is presently known about paramyxovirus structure and replication comes from work with these viruses (1,18,27). The much poorer growth, especially in cell culture systems, of paramyxoviruses more pertinent to human disease probably explains the paucity of data on their structure and replication (6,21). It is important to learn more about these neglected paramyxoviruses not only because of their relevance to medicine but because the biological significance of phenomena like the synthesis of single-stranded ribonucleic acid (RNA) species complementary to virus genomes in infected cells (2,3,16) "incomplete" or defective visions containing viral genome fragments (20) may not be fully understood until it is known how general they are among the paramyxovirus group.…”
mentioning
confidence: 99%