pubmed-article:16081909 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C0949920 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C0015733 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C2347026 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C0370003 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C0205102 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C0035668 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C1555029 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C0205332 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C1442989 | lld:lifeskim |
pubmed-article:16081909 | lifeskim:mentions | umls-concept:C2587213 | lld:lifeskim |
pubmed-article:16081909 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:16081909 | pubmed:dateCreated | 2005-8-5 | lld:pubmed |
pubmed-article:16081909 | pubmed:abstractText | We developed a nested reverse transcription-PCR (nRT-PCR) for the detection of noroviruses in stools, using random primers for RT, the JV12/JV13 primer pair in the first round of nPCR, and a set of nine inner primers for the second, comprising the reverse sequences of primers SR46, SR48, SR50, and SR52, and five novel oligonucleotide sequences (113-1, 113-2, 115-1, 115-2, and 115-3). The specificity of the nRT-PCR was confirmed by testing 61 stools containing enteric viruses other than noroviruses. In comparative assays on either stools or RNA dilutions from two genogroup I and three genogroup II (GII) norovirus-positive samples, nRT-PCR was always at least as sensitive as RT-PCR and Southern hybridization. With some of the samples tested, the increase in sensitivity was 10-fold or higher. For GII viruses, the detectable range of nRT-PCR was estimated to be 8.4 x 10(4) to 2 RNA viral particles. When used on 85 stools from pediatric patients with acute gastroenteritis negative for viruses by electron microscopy and cell culture, the nRT-PCR detected norovirus in 19 samples (22.3%), while it failed to detect one reference RT-PCR-positive sample containing a Desert Shield strain. Sixteen of the 19 nRT-PCR-positive samples gave concordant results with reference RT-PCR and Southern hybridization, and all with sequence analysis. Partial sequencing of the polymerase region revealed that from January to April 2000 all GII strains except two (Rotterdam- and Leeds-like viruses) formed a tight cluster related to Hawaii virus. The nRT-PCR described could prove suitable for large epidemiological studies and for specialized clinical laboratories performing routine molecular testing. | lld:pubmed |
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pubmed-article:16081909 | pubmed:language | eng | lld:pubmed |
pubmed-article:16081909 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16081909 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16081909 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16081909 | pubmed:month | Aug | lld:pubmed |
pubmed-article:16081909 | pubmed:issn | 0095-1137 | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:CalderaroAdri... | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:DettoriGiusep... | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:ChezziCarloC | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:RuggeriFranco... | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:BoscoSimonaS | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:ArcangelettiM... | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:MediciMaria... | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:MartinelliMon... | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:De... | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:PinardiFederi... | lld:pubmed |
pubmed-article:16081909 | pubmed:author | pubmed-author:AbelliLaura... | lld:pubmed |
pubmed-article:16081909 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16081909 | pubmed:volume | 43 | lld:pubmed |
pubmed-article:16081909 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16081909 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16081909 | pubmed:pagination | 3772-8 | lld:pubmed |
pubmed-article:16081909 | pubmed:dateRevised | 2010-9-21 | lld:pubmed |
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pubmed-article:16081909 | pubmed:year | 2005 | lld:pubmed |
pubmed-article:16081909 | pubmed:articleTitle | Broadly reactive nested reverse transcription-PCR using an internal RNA standard control for detection of noroviruses in stool samples. | lld:pubmed |
pubmed-article:16081909 | pubmed:affiliation | Section of Microbiology, Department of Pathology and Laboratory Medicine, University of Parma, Viale Antonio Gramsci, 14, 43100 Parma, Italy. mariacristina.medici@unipr.it | lld:pubmed |
pubmed-article:16081909 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16081909 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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