tetano
Editor, Senior Moderator
J Virol Methods. 2018 May 2;257:79-84. doi: 10.1016/j.jviromet.2018.05.001. [Epub ahead of print]
[h=1]Development and evaluation of a real-time RT-PCR assay for detection of a novel avian influenza A (H5N6) virus.[/h] Zhang R[SUP]1[/SUP], Yao D[SUP]1[/SUP], Chen J[SUP]1[/SUP], Ye W[SUP]1[/SUP], Ou X[SUP]1[/SUP], Chen T[SUP]1[/SUP], Sun B[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] As of Aug 25, 2017, 17 incidences of human infection and 6 deaths due to the novel H5N6 virus have been reported in China. Genetic analysis of the viral genome revealed that this reassortant virus is highly pathogenic to poultry, and that the virus has a risk of transmission to humans. Accordingly, the development of a rapid, sensitive, and specific molecular diagnostic assay is critical for public health. In this study, a real-time reverse-transcription PCR (RT-PCR) assay was developed to specifically detect the novel H5N6 virus, with primer pairs targeting the hemagglutinin and neuraminidase gene sequences of this virus. RNA was extracted from throat swab specimens from patients with influenza-like illness (ILIs), and environmental samples were collected from live poultry markets (LPMs) for H5N6 virus detection by real-time RT-PCR. The method was demonstrated to enable specific detection of the avian H5N6 virus, with no cross-reactivity with seasonal influenza viruses (H1N1, H1N1 pdm09, H3N2 or B); H5N1, H7N9, H9N2 viruses; or other human respiratory viruses. The detection limit of the assay was 1.0 ? 10[SUP]1[/SUP] copies per reaction for N6 and 1.0 ? 10[SUP]2[/SUP] copies per reaction for H5 assays. The assay is a powerful tool for rapid, sensitive, and specific detection of H5N6 virus infection in specimens derived from humans, animals, and the environment.
[h=4]KEYWORDS:[/h] Avian influenza; Detection; H5N6; Real-time RT-PCR
PMID: 29729298 DOI: 10.1016/j.jviromet.2018.05.001
[h=1]Development and evaluation of a real-time RT-PCR assay for detection of a novel avian influenza A (H5N6) virus.[/h] Zhang R[SUP]1[/SUP], Yao D[SUP]1[/SUP], Chen J[SUP]1[/SUP], Ye W[SUP]1[/SUP], Ou X[SUP]1[/SUP], Chen T[SUP]1[/SUP], Sun B[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] As of Aug 25, 2017, 17 incidences of human infection and 6 deaths due to the novel H5N6 virus have been reported in China. Genetic analysis of the viral genome revealed that this reassortant virus is highly pathogenic to poultry, and that the virus has a risk of transmission to humans. Accordingly, the development of a rapid, sensitive, and specific molecular diagnostic assay is critical for public health. In this study, a real-time reverse-transcription PCR (RT-PCR) assay was developed to specifically detect the novel H5N6 virus, with primer pairs targeting the hemagglutinin and neuraminidase gene sequences of this virus. RNA was extracted from throat swab specimens from patients with influenza-like illness (ILIs), and environmental samples were collected from live poultry markets (LPMs) for H5N6 virus detection by real-time RT-PCR. The method was demonstrated to enable specific detection of the avian H5N6 virus, with no cross-reactivity with seasonal influenza viruses (H1N1, H1N1 pdm09, H3N2 or B); H5N1, H7N9, H9N2 viruses; or other human respiratory viruses. The detection limit of the assay was 1.0 ? 10[SUP]1[/SUP] copies per reaction for N6 and 1.0 ? 10[SUP]2[/SUP] copies per reaction for H5 assays. The assay is a powerful tool for rapid, sensitive, and specific detection of H5N6 virus infection in specimens derived from humans, animals, and the environment.
[h=4]KEYWORDS:[/h] Avian influenza; Detection; H5N6; Real-time RT-PCR
PMID: 29729298 DOI: 10.1016/j.jviromet.2018.05.001