[Identification of influenza virus type A by solid-phase radioimmunological analysis].
Identifieur interne : 000511 ( PubMed/Corpus ); précédent : 000510; suivant : 000512[Identification of influenza virus type A by solid-phase radioimmunological analysis].
Auteurs : T V Ignat'Eva ; G N Trushinskaia ; E I IsaevaSource :
- Voprosy virusologii [ 0507-4088 ]
English descriptors
- KwdEn :
- Animals, Chick Embryo, Evaluation Studies as Topic, Hemagglutination Inhibition Tests, Hemagglutinins, Viral (analysis), Immune Sera (isolation & purification), Immunoglobulin G (analysis), Influenza A virus (immunology), Influenza A virus (isolation & purification), Rabbits, Radioimmunoassay (methods), Virus Cultivation.
- MESH :
- chemical , analysis : Hemagglutinins, Viral, Immunoglobulin G.
- chemical , isolation & purification : Immune Sera.
- immunology : Influenza A virus.
- isolation & purification : Influenza A virus.
- methods : Radioimmunoassay.
- Animals, Chick Embryo, Evaluation Studies as Topic, Hemagglutination Inhibition Tests, Rabbits, Virus Cultivation.
Abstract
High sensitivity and specificity of solid-phase radioimmunoassay (SPRIA) in identification of influenza A (H1N1 and H2N2) viruses in the infected allantoic culture were demonstrated. Mixtures of influenza hyperimmune sera free from antibodies to host cell antigens and antineuraminidase antibodies were used as active test sera. The test serum a-H1N1 consisted of antisera to A/FmI/47, A/Netherlands/36/56, and A/USSR/090/77 strains; it detected practically all tested variants of H1N1 virus isolated in 1947-1982 in allantoic cultures containing virus-specific protein in amounts of 1.4 to 0.7 ng/ml. For the detection of H2N2 subtype viruses (1957-1967), a mixture of antisera to A/Singapore/1/57, A/Leningrad/2/63, A/Gorkiy/62/65, and A/Tokyo/3/67 viruses was used. This test serum could detect H2N2 virus in the allantoic fluid containing 0.7-035 ng/ml of virus protein.
PubMed: 3993004
Links to Exploration step
pubmed:3993004Le document en format XML
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<author><name sortKey="Ignat Eva, T V" sort="Ignat Eva, T V" uniqKey="Ignat Eva T" first="T V" last="Ignat'Eva">T V Ignat'Eva</name>
</author>
<author><name sortKey="Trushinskaia, G N" sort="Trushinskaia, G N" uniqKey="Trushinskaia G" first="G N" last="Trushinskaia">G N Trushinskaia</name>
</author>
<author><name sortKey="Isaeva, E I" sort="Isaeva, E I" uniqKey="Isaeva E" first="E I" last="Isaeva">E I Isaeva</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="????"><PubDate><MedlineDate>1985 Jan-Feb</MedlineDate>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">[Identification of influenza virus type A by solid-phase radioimmunological analysis].</title>
<author><name sortKey="Ignat Eva, T V" sort="Ignat Eva, T V" uniqKey="Ignat Eva T" first="T V" last="Ignat'Eva">T V Ignat'Eva</name>
</author>
<author><name sortKey="Trushinskaia, G N" sort="Trushinskaia, G N" uniqKey="Trushinskaia G" first="G N" last="Trushinskaia">G N Trushinskaia</name>
</author>
<author><name sortKey="Isaeva, E I" sort="Isaeva, E I" uniqKey="Isaeva E" first="E I" last="Isaeva">E I Isaeva</name>
</author>
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<series><title level="j">Voprosy virusologii</title>
<idno type="ISSN">0507-4088</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Chick Embryo</term>
<term>Evaluation Studies as Topic</term>
<term>Hemagglutination Inhibition Tests</term>
<term>Hemagglutinins, Viral (analysis)</term>
<term>Immune Sera (isolation & purification)</term>
<term>Immunoglobulin G (analysis)</term>
<term>Influenza A virus (immunology)</term>
<term>Influenza A virus (isolation & purification)</term>
<term>Rabbits</term>
<term>Radioimmunoassay (methods)</term>
<term>Virus Cultivation</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Hemagglutinins, Viral</term>
<term>Immunoglobulin G</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Immune Sera</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Influenza A virus</term>
</keywords>
<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Influenza A virus</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Radioimmunoassay</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Chick Embryo</term>
<term>Evaluation Studies as Topic</term>
<term>Hemagglutination Inhibition Tests</term>
<term>Rabbits</term>
<term>Virus Cultivation</term>
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<front><div type="abstract" xml:lang="en">High sensitivity and specificity of solid-phase radioimmunoassay (SPRIA) in identification of influenza A (H1N1 and H2N2) viruses in the infected allantoic culture were demonstrated. Mixtures of influenza hyperimmune sera free from antibodies to host cell antigens and antineuraminidase antibodies were used as active test sera. The test serum a-H1N1 consisted of antisera to A/FmI/47, A/Netherlands/36/56, and A/USSR/090/77 strains; it detected practically all tested variants of H1N1 virus isolated in 1947-1982 in allantoic cultures containing virus-specific protein in amounts of 1.4 to 0.7 ng/ml. For the detection of H2N2 subtype viruses (1957-1967), a mixture of antisera to A/Singapore/1/57, A/Leningrad/2/63, A/Gorkiy/62/65, and A/Tokyo/3/67 viruses was used. This test serum could detect H2N2 virus in the allantoic fluid containing 0.7-035 ng/ml of virus protein.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">3993004</PMID>
<DateCompleted><Year>1985</Year>
<Month>06</Month>
<Day>14</Day>
</DateCompleted>
<DateRevised><Year>2016</Year>
<Month>11</Month>
<Day>09</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0507-4088</ISSN>
<JournalIssue CitedMedium="Print"><Volume>30</Volume>
<Issue>1</Issue>
<PubDate><MedlineDate>1985 Jan-Feb</MedlineDate>
</PubDate>
</JournalIssue>
<Title>Voprosy virusologii</Title>
<ISOAbbreviation>Vopr. Virusol.</ISOAbbreviation>
</Journal>
<ArticleTitle>[Identification of influenza virus type A by solid-phase radioimmunological analysis].</ArticleTitle>
<Pagination><MedlinePgn>53-7</MedlinePgn>
</Pagination>
<Abstract><AbstractText>High sensitivity and specificity of solid-phase radioimmunoassay (SPRIA) in identification of influenza A (H1N1 and H2N2) viruses in the infected allantoic culture were demonstrated. Mixtures of influenza hyperimmune sera free from antibodies to host cell antigens and antineuraminidase antibodies were used as active test sera. The test serum a-H1N1 consisted of antisera to A/FmI/47, A/Netherlands/36/56, and A/USSR/090/77 strains; it detected practically all tested variants of H1N1 virus isolated in 1947-1982 in allantoic cultures containing virus-specific protein in amounts of 1.4 to 0.7 ng/ml. For the detection of H2N2 subtype viruses (1957-1967), a mixture of antisera to A/Singapore/1/57, A/Leningrad/2/63, A/Gorkiy/62/65, and A/Tokyo/3/67 viruses was used. This test serum could detect H2N2 virus in the allantoic fluid containing 0.7-035 ng/ml of virus protein.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ignat'eva</LastName>
<ForeName>T V</ForeName>
<Initials>TV</Initials>
</Author>
<Author ValidYN="Y"><LastName>Trushinskaia</LastName>
<ForeName>G N</ForeName>
<Initials>GN</Initials>
</Author>
<Author ValidYN="Y"><LastName>Isaeva</LastName>
<ForeName>E I</ForeName>
<Initials>EI</Initials>
</Author>
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<Language>rus</Language>
<PublicationTypeList><PublicationType UI="D004740">English Abstract</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<VernacularTitle>Identifikatsiia virusa grippa tipa A metodom tverdofazovogo radioimmunologicheskogo analiza.</VernacularTitle>
</Article>
<MedlineJournalInfo><Country>Russia (Federation)</Country>
<MedlineTA>Vopr Virusol</MedlineTA>
<NlmUniqueID>0417337</NlmUniqueID>
<ISSNLinking>0507-4088</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D006389">Hemagglutinins, Viral</NameOfSubstance>
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<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D007106">Immune Sera</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D007074">Immunoglobulin G</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002642" MajorTopicYN="N">Chick Embryo</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005069" MajorTopicYN="N">Evaluation Studies as Topic</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006385" MajorTopicYN="N">Hemagglutination Inhibition Tests</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006389" MajorTopicYN="N">Hemagglutinins, Viral</DescriptorName>
<QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007106" MajorTopicYN="N">Immune Sera</DescriptorName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007074" MajorTopicYN="N">Immunoglobulin G</DescriptorName>
<QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009980" MajorTopicYN="N">Influenza A virus</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011817" MajorTopicYN="N">Rabbits</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011863" MajorTopicYN="N">Radioimmunoassay</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014776" MajorTopicYN="N">Virus Cultivation</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1985</Year>
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