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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1994-6-22
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S70786,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S70787,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S70788,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S70789,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S70790
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pubmed:abstractText |
Group I and II hepatitis C virus genotypes were determined by a newly developed serological genotyping assay. This assay detected antibodies against group-specific recombinant proteins in the putative NS4 protein region (amino acid no. 1676-1760) by an enzyme-linked immunosorbent assay. This region of the hepatitis C virus peptide has many group-specific amino acids; fewer than 50% of these amino acids are identical between groups I and II. Genotypes determined by the serological genotyping assay were compared with those determined by a method in which the polymerase chain reaction was used in 91 chronic hepatitis patients. The group-specific polymerase chain reaction was performed within the genome region corresponding to the putative NS5 protein, where the group II hepatitis C virus genome is 57 nucleotides longer than that of group I. Among 91 chronic hepatitis C patients who had positive results in the second-generation hepatitis C virus antibody (core and NS3 region) assay, hepatitis C virus RNA was detected in 80 patients by polymerase chain reaction in the 5' untranslated region and in 78 patients by this group-specific polymerase chain reaction. As a result, in 76 of 91 patients (84%) genotypes determined by the serological genotyping assay showed complete agreement with those determined by the group-specific polymerase chain reaction, and none of the patients revealed a group opposite to that of hepatitis C virus genotype. The detection rate of the serological genotyping assay (89 of 91; 98%) was even higher than that of the polymerase chain reaction assay (78 of 91; 86%).(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/Hepatitis Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/Hepatitis C Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Nonstructural Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0270-9139
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1347-53
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7514558-Adult,
pubmed-meshheading:7514558-Aged,
pubmed-meshheading:7514558-Amino Acid Sequence,
pubmed-meshheading:7514558-Antigens, Viral,
pubmed-meshheading:7514558-Base Sequence,
pubmed-meshheading:7514558-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:7514558-Epitopes,
pubmed-meshheading:7514558-Female,
pubmed-meshheading:7514558-Genotype,
pubmed-meshheading:7514558-Hepacivirus,
pubmed-meshheading:7514558-Hepatitis Antibodies,
pubmed-meshheading:7514558-Hepatitis C,
pubmed-meshheading:7514558-Hepatitis C Antibodies,
pubmed-meshheading:7514558-Humans,
pubmed-meshheading:7514558-Male,
pubmed-meshheading:7514558-Middle Aged,
pubmed-meshheading:7514558-Molecular Sequence Data,
pubmed-meshheading:7514558-Polymerase Chain Reaction,
pubmed-meshheading:7514558-Recombinant Proteins,
pubmed-meshheading:7514558-Sensitivity and Specificity,
pubmed-meshheading:7514558-Viral Nonstructural Proteins
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pubmed:year |
1994
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pubmed:articleTitle |
Significance of specific antibody assay for genotyping of hepatitis C virus.
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pubmed:affiliation |
Liver Unit, Tokyo Metropolitan Komagome Hospital, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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