2002
DOI: 10.1080/003130201201117909
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Laboratory diagnosis of influenza virus infection

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Cited by 38 publications
(8 citation statements)
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“…Direct immunofluorescence was performed using cells from nose and throat swabs spotted on glass slides. The cells were acetone-fixed and stained with fluorescein-conjugated monoclonal antibodies (Chemicon International, Temecula, CA, USA) against influenza A and B and other respiratory viruses (adenoviruses, parainfluenzaviruses and respiratory syncytial virus) [20]. Nucleic acid testing was performed using a nested reverse transcriptase polymerase chain reaction for influenza A and B on RNA extracted from the nose and throat samples using the High Pure viral RNA kit (Roche Diagnostics GmbH, Mannheim, Germany) according to the manufacturer's instructions [21].…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Direct immunofluorescence was performed using cells from nose and throat swabs spotted on glass slides. The cells were acetone-fixed and stained with fluorescein-conjugated monoclonal antibodies (Chemicon International, Temecula, CA, USA) against influenza A and B and other respiratory viruses (adenoviruses, parainfluenzaviruses and respiratory syncytial virus) [20]. Nucleic acid testing was performed using a nested reverse transcriptase polymerase chain reaction for influenza A and B on RNA extracted from the nose and throat samples using the High Pure viral RNA kit (Roche Diagnostics GmbH, Mannheim, Germany) according to the manufacturer's instructions [21].…”
Section: Methodsmentioning
confidence: 99%
“…Influenza A- and influenza B-specific complement fixing antibody titres were determined on acute and convalescent sera in parallel, with definitive influenza recorded if there was a four-fold or greater rise in titres [20].…”
Section: Methodsmentioning
confidence: 99%
“…Influenza testing included the following: 1) point-of-care tests (POCTs) performed either on site or in the laboratory (Quickvue A & B; Quidel, San Diego, CA, USA, or BinaxNOW Influenza A & B, Binax, Scarborough, ME, USA), 2) antigen detection using type-specific indirect fluorescent antibodies (IFA) (Chemicon, Millipore, Billerica, MA, USA, or Bartels, Immunodiagnostic Supplies Inc., Bellevue, WA, USA); 3) validated in-house type- and subtype-specific nucleic acid testing (NAT) by using PCR that targeted the matrix, nonstructural, and hemagglutinin region of the influenza virus genome; and 4) virus culture using MDCK cells ( 13 ). IFA and NAT were the preferred diagnostic methods.…”
Section: Methodsmentioning
confidence: 99%
“…*Case definition outbreak values were subsequently used in the Markov model and are similar to previous published case definition ranges of between 44 and 87% [28], [29], [30], [31], [32].†The “gold standard” was defined as isolation of influenza virus by culture and/or detection of virus by PCR 1 The calculated laboratory testing values were subsequently used in the Markov model and are similar to published PCR, IFA and POCT sensitivities of 90 to 100% [13], [33], [34], [35]; 60 to 100% [12], [36], [37] and 50 to 95% [38], [39], [40] respectively.…”
Section: Methodsmentioning
confidence: 62%
“…All positive IFA samples were inoculated into Madin-Darby Canine Kidney (MDCK) cell lines with cultured viral identification confirmed by IFA. Following the outbreak, virus detection was conducted on all samples by polymerase chain reaction (PCR) targeting the matrix region of the influenza virus genome [12], [13]. Testing was performed on the stored respiratory specimen aliquots (at −80°C) following nucleic acid extraction with a commercial assay (Roche® High Pure, Mannheim, Germany).…”
Section: Methodsmentioning
confidence: 99%