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J Virol Methods. 2014 Nov 22;212C:76-79. doi: 10.1016/j.jviromet.2014.10.019. [Epub ahead of print]
Quantitative RT-PCR evaluation of a rapid influenza antigen test for efficient diagnosis of influenza virus infection.
Tsushima Y1, Uno N2, Sasaki D1, Morinaga Y3, Hasegawa H3, Yanagihara K3.
Author information
Abstract
Influenza virus infection is diagnosed in most cases using a rapid influenza antigen diagnostic test (RIDT). However, false-negative results are a major concern. By contrast, the nucleic acid amplification test offers high sensitivity and therefore can aid the interpretation of negative RIDT results. In this study, influenza viral loads were quantified with quantitative reverse transcription-polymerase chain reaction (qRT-PCR) using viral suspensions left over after RIDT, and the performance of both methods was evaluated. qRT-PCR detected as few as 103copies/mL of influenza viruses A and B, whereas RIDT showed negative results for viral loads less than 107 and 105copies/mL of influenza viruses A and B, respectively. These results indicate that small quantities of the virus that cause false-negative RIDT results can be detected efficiently with qRT-PCR follow-up. In addition, influenza A virus subtype was determined using qRT-PCR.
Copyright ? 2014 Elsevier B.V. All rights reserved.
KEYWORDS:
Influenza virus; Quantitative RT-PCR; Rapid influenza antigen detection test
PMID:
25449113
[PubMed - as supplied by publisher]
Quantitative RT-PCR evaluation of a rapid influenza antigen test for efficient diagnosis of influenza virus infection.
Tsushima Y1, Uno N2, Sasaki D1, Morinaga Y3, Hasegawa H3, Yanagihara K3.
Author information
Abstract
Influenza virus infection is diagnosed in most cases using a rapid influenza antigen diagnostic test (RIDT). However, false-negative results are a major concern. By contrast, the nucleic acid amplification test offers high sensitivity and therefore can aid the interpretation of negative RIDT results. In this study, influenza viral loads were quantified with quantitative reverse transcription-polymerase chain reaction (qRT-PCR) using viral suspensions left over after RIDT, and the performance of both methods was evaluated. qRT-PCR detected as few as 103copies/mL of influenza viruses A and B, whereas RIDT showed negative results for viral loads less than 107 and 105copies/mL of influenza viruses A and B, respectively. These results indicate that small quantities of the virus that cause false-negative RIDT results can be detected efficiently with qRT-PCR follow-up. In addition, influenza A virus subtype was determined using qRT-PCR.
Copyright ? 2014 Elsevier B.V. All rights reserved.
KEYWORDS:
Influenza virus; Quantitative RT-PCR; Rapid influenza antigen detection test
PMID:
25449113
[PubMed - as supplied by publisher]
