tetano
Editor, Senior Moderator
Sci Rep. 2017 Oct 18;7(1):13455. doi: 10.1038/s41598-017-13768-4.
[h=1]Development of a multiplex probe combination-based one-step real-time reverse transcription-PCR for NA subtype typing of avian influenza virus.[/h] Sun Z[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Qin T[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Meng F[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Chen S[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Peng D[SUP]4,[/SUP][SUP]5,[/SUP][SUP]6[/SUP], Liu X[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Nine influenza virus neuraminidase (NA) subtypes have been identified in poultry and wild birds. Few methods are available for rapid and simple NA subtyping. Here we developed a multiplex probe combination-based one-step real-time reverse transcriptase PCR (rRT-PCR) to detect nine avian influenza virus NA subtypes. Nine primer-probe pairs were assigned to three groups based on the different fluorescent dyes of the probes (FAM, HEX, or Texas Red). Each probe detected only one NA subtype, without cross reactivity. The detection limit was less than 100 EID[SUB]50[/SUB] or 100 copies of cDNA per reaction. Data obtained using this method with allantoic fluid samples isolated from live bird markets and H9N2-infected chickens correlated well with data obtained using virus isolation and sequencing, but was more sensitive. This new method provides a specific and sensitive alternative to conventional NA-subtyping methods.
PMID: 29044197 DOI: 10.1038/s41598-017-13768-4
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[h=1]Development of a multiplex probe combination-based one-step real-time reverse transcription-PCR for NA subtype typing of avian influenza virus.[/h] Sun Z[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Qin T[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Meng F[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Chen S[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Peng D[SUP]4,[/SUP][SUP]5,[/SUP][SUP]6[/SUP], Liu X[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Nine influenza virus neuraminidase (NA) subtypes have been identified in poultry and wild birds. Few methods are available for rapid and simple NA subtyping. Here we developed a multiplex probe combination-based one-step real-time reverse transcriptase PCR (rRT-PCR) to detect nine avian influenza virus NA subtypes. Nine primer-probe pairs were assigned to three groups based on the different fluorescent dyes of the probes (FAM, HEX, or Texas Red). Each probe detected only one NA subtype, without cross reactivity. The detection limit was less than 100 EID[SUB]50[/SUB] or 100 copies of cDNA per reaction. Data obtained using this method with allantoic fluid samples isolated from live bird markets and H9N2-infected chickens correlated well with data obtained using virus isolation and sequencing, but was more sensitive. This new method provides a specific and sensitive alternative to conventional NA-subtyping methods.
PMID: 29044197 DOI: 10.1038/s41598-017-13768-4
Free full text