Source:http://linkedlifedata.com/resource/pubmed/id/16540179
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2006-5-2
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pubmed:abstractText |
The similarity of symptoms produced by tick-borne encephalitis (TBE) and Japanese encephalitis (JE) and the high degree of cross-reactivity between TBE and JE viruses by serological tests make the development of a differential diagnostic test a priority. In this study, recombinant prM/E proteins of TBE virus strain Oshima 5-10 expressed in mammalian cells resulted in the release of subviral particles (SPs) into the culture medium. Using the SPs as antigens, enzyme-linked immunosorbent assay (ELISA) systems were developed to detect TBE virus-specific IgM and IgG antibodies, designated SP-IgG and SP-IgM ELISAs, respectively. Of 83 serum samples from encephalitis patients in Khabarovsk, Russia, which were positive with the neutralization test (NT), 82 were positive by the SP-IgG ELISA, for a sensitivity of 98.8%, which was higher than that of a commercial ELISA kit. All 12 NT-negative samples were also negative by the SP-IgG ELISA (specificity, 100%). Of 17 patient samples that were NT-positive, 16 (94.1%) were positive by the SP-IgM ELISA. Of 15 paired serum samples that yielded equivocal results by NT, 11 had positive results with the SP-IgM ELISA, indicating a diagnosis of TBE infection. The SP-IgG and SP-IgM ELISAs showed no cross-reactivity with antibodies to the JE virus. The results indicate that these ELISAs will be useful for the detection of TBE-specific antibodies.
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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/Antibodies, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin M,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Envelope Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/glycoprotein E, Flavivirus,
http://linkedlifedata.com/resource/pubmed/chemical/prM protein, Flavivirus
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0166-0934
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
134
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
55-60
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16540179-Animals,
pubmed-meshheading:16540179-Antibodies, Viral,
pubmed-meshheading:16540179-Antigens, Viral,
pubmed-meshheading:16540179-Cell Line,
pubmed-meshheading:16540179-Cricetinae,
pubmed-meshheading:16540179-Encephalitis, Tick-Borne,
pubmed-meshheading:16540179-Encephalitis Viruses, Tick-Borne,
pubmed-meshheading:16540179-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:16540179-Humans,
pubmed-meshheading:16540179-Immunoglobulin G,
pubmed-meshheading:16540179-Immunoglobulin M,
pubmed-meshheading:16540179-Sensitivity and Specificity,
pubmed-meshheading:16540179-Serologic Tests,
pubmed-meshheading:16540179-Viral Envelope Proteins
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pubmed:year |
2006
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pubmed:articleTitle |
Development of an enzyme-linked immunosorbent assay for serological diagnosis of tick-borne encephalitis using subviral particles.
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pubmed:affiliation |
Laboratory of Public Health, Department of Environmental Veterinary Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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