Oligonucleotide mapping of viral ribonucleic acid as an aid in identifying laboratory contaminants of influenza virus
Identifieur interne : 002356 ( Main/Exploration ); précédent : 002355; suivant : 002357Oligonucleotide mapping of viral ribonucleic acid as an aid in identifying laboratory contaminants of influenza virus
Auteurs : N. J. Cox ; S. Nakajima ; R. Black ; A. P. KendalSource :
- Diagnostic Microbiology & Infectious Disease [ 0732-8893 ] ; 1986.
English descriptors
- Teeft :
- Antigenic properties, Clinical specimens, Diagnostic specimens, Disease control, Embryonated eggs, First dimension, Genetic identity, Genetic relatedness, High growth, Hospital laboratory, Human population, Human services, Infectious diseases, Influenza, Influenza virus, Influenza viruses, Kendal, Laboratory contaminants, Laboratory contamination, Laboratory passage, Laboratory records, Laboratory stock, Laboratory stock strain, Laboratory strain, Laboratory strains, Oligonucleotide, Oligonucleotide mapping, Oligonucleotide maps, Palese, Polynucleotide kinase, Public health, Public health service, Recombinant, Reference analysis, Reference strain, Reference strains, Second dimension, Serologic evidence, Serum samples, Serum specimens, Standard laboratory strain, Standard laboratory strains, Standard strains, Swine virus, Total virion, University virology laboratory, Variant subpopulation, Virus, Virus isolation, Virus strains, World health organization.
Abstract
Abstract: Influenza viruses that were suspected to be laboratory contaminants of clinical specimens because they had antigenic properties identical to standard laboratory strains were examined by T1 oligonucleotide mapping of virion ribonucleic acid. For the three instances reported herein involving thirteen viruses, it was concluded that laboratory contamination had occurred, since 1) in each instance, a standard laboratory strain that had been used in the clinical laboratory before the isolation, had an oligonucleotide map that was either identical to or very similar to those of the “isolates,” 2) there was no evidence of spread of these viruses, and 3) in cases where serum samples were available, no serologic evidence existed of infection by these virus strains.
Url:
DOI: 10.1016/0732-8893(86)90102-1
Affiliations:
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J." last="Cox">N. J. Cox</name></author><author><name sortKey="Nakajima, S" sort="Nakajima, S" uniqKey="Nakajima S" first="S." last="Nakajima">S. Nakajima</name></author><author><name sortKey="Black, R" sort="Black, R" uniqKey="Black R" first="R." last="Black">R. Black</name></author><author><name sortKey="Kendal, A P" sort="Kendal, A P" uniqKey="Kendal A" first="A. P." last="Kendal">A. P. Kendal</name></author></analytic><monogr></monogr><series><title level="j">Diagnostic Microbiology & Infectious Disease</title><title level="j" type="abbrev">DMB</title><idno type="ISSN">0732-8893</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1986">1986</date><biblScope unit="volume">4</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="231">231</biblScope><biblScope unit="page" to="239">239</biblScope></imprint><idno type="ISSN">0732-8893</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0732-8893</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Antigenic properties</term><term>Clinical specimens</term><term>Diagnostic specimens</term><term>Disease control</term><term>Embryonated eggs</term><term>First dimension</term><term>Genetic identity</term><term>Genetic relatedness</term><term>High growth</term><term>Hospital laboratory</term><term>Human population</term><term>Human services</term><term>Infectious diseases</term><term>Influenza</term><term>Influenza virus</term><term>Influenza viruses</term><term>Kendal</term><term>Laboratory contaminants</term><term>Laboratory contamination</term><term>Laboratory passage</term><term>Laboratory records</term><term>Laboratory stock</term><term>Laboratory stock strain</term><term>Laboratory strain</term><term>Laboratory strains</term><term>Oligonucleotide</term><term>Oligonucleotide mapping</term><term>Oligonucleotide maps</term><term>Palese</term><term>Polynucleotide kinase</term><term>Public health</term><term>Public health service</term><term>Recombinant</term><term>Reference analysis</term><term>Reference strain</term><term>Reference strains</term><term>Second dimension</term><term>Serologic evidence</term><term>Serum samples</term><term>Serum specimens</term><term>Standard laboratory strain</term><term>Standard laboratory strains</term><term>Standard strains</term><term>Swine virus</term><term>Total virion</term><term>University virology laboratory</term><term>Variant subpopulation</term><term>Virus</term><term>Virus isolation</term><term>Virus strains</term><term>World health organization</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: Influenza viruses that were suspected to be laboratory contaminants of clinical specimens because they had antigenic properties identical to standard laboratory strains were examined by T1 oligonucleotide mapping of virion ribonucleic acid. For the three instances reported herein involving thirteen viruses, it was concluded that laboratory contamination had occurred, since 1) in each instance, a standard laboratory strain that had been used in the clinical laboratory before the isolation, had an oligonucleotide map that was either identical to or very similar to those of the “isolates,” 2) there was no evidence of spread of these viruses, and 3) in cases where serum samples were available, no serologic evidence existed of infection by these virus strains.</div></front></TEI><affiliations><list></list><tree><noCountry><name sortKey="Black, R" sort="Black, R" uniqKey="Black R" first="R." last="Black">R. Black</name><name sortKey="Cox, N J" sort="Cox, N J" uniqKey="Cox N" first="N. J." last="Cox">N. J. Cox</name><name sortKey="Kendal, A P" sort="Kendal, A P" uniqKey="Kendal A" first="A. P." last="Kendal">A. P. Kendal</name><name sortKey="Nakajima, S" sort="Nakajima, S" uniqKey="Nakajima S" first="S." last="Nakajima">S. Nakajima</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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