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Updated: Jun 23, 2026

Microfluidic Chip Fabrication and Method to Detect Influenza
Published on: March 26, 2013
Oligonucleotide microchip for subtyping of influenza A virus
Eugeny E Fesenko1, Dmitry E Kireyev, Dmitry A Gryadunov
1Laboratory of Biological Microchips, Engelhardt Institute of Molecular Biology of the Russian Academy of Sciences, Vavilov Str. 32, Moscow, Russia. fesenko@biochip.ru
Background:
Influenza A viruses are classified into subtypes depending on the antigenic properties of their two outer glycoproteins, hemagglutinin (HA) and neuraminidase (NA). Sixteen subtypes of HA and nine of NA are known. Lately, the circulation of some subtypes (H7N7, H5N1) has been closely watched because of the epidemiological threat they present.
Objectives:
This study assesses the potential of using gel-based microchip technology for fast and sensitive molecular subtyping of the influenza A virus.
Methods:
The method employs a microchip of 3D gel-based elements containing immobilized probes. Segments of the HA and NA genes are amplified using multiplex RT-PCR and then hybridized with the microchip.
Results:
The developed microchip was validated using a panel of 21 known reference strains of influenza virus. Selected strains represented different HA and NA subtypes derived from avian, swine and human hosts. The whole procedure takes 10 hours and enables one to identify 15 subtypes of HA and two subtypes of NA. Forty-one clinical samples isolated during the poultry fall in Novosibirsk (Russia, 2005) were successfully identified using the proposed technique. The sensitivity and specificity of the method were 76% and 100%, respectively, compared with the 'gold standard' techniques (virus isolation with following characterization by immunoassay).
Conclusions:
We conclude that the method of subtyping using gel-based microchips is a promising approach for fast detection and identification of influenza A, which may greatly improve its monitoring.
Insights
This study introduces a novel gel-based microchip technology for rapid and sensitive molecular subtyping of influenza A virus. The method efficiently identifies multiple hemagglutinin (HA) and neuraminidase (NA) subtypes, improving influenza A virus monitoring.
Area of Science:
- Virology
- Molecular Biology
- Biotechnology
Background:
- Influenza A viruses are classified by hemagglutinin (HA) and neuraminidase (NA) glycoproteins.
- Sixteen HA and nine NA subtypes are known, with some posing significant epidemiological threats.
- Accurate and rapid subtyping is crucial for monitoring influenza A virus circulation.
Purpose of the Study:
- To evaluate gel-based microchip technology for rapid and sensitive molecular subtyping of influenza A virus.
- To assess the potential of this technology for identifying diverse HA and NA subtypes.
- To determine the feasibility of this method for clinical and epidemiological surveillance.
Main Methods:
- Utilizes a microchip with 3D gel-based elements and immobilized probes.
- Employs multiplex reverse transcription polymerase chain reaction (RT-PCR) for gene amplification.
- Hybridizes amplified HA and NA gene segments to the microchip for subtyping.
Main Results:
- The developed microchip successfully identified 15 HA and 2 NA subtypes from 21 reference strains.
- The entire procedure is completed within 10 hours.
- Accurate identification of influenza A subtypes in 41 clinical samples was achieved with 76% sensitivity and 100% specificity.
Conclusions:
- Gel-based microchip technology offers a promising method for rapid influenza A virus detection and identification.
- This approach has the potential to significantly enhance influenza A virus surveillance efforts.
- The technology demonstrates high specificity and efficiency for molecular subtyping.
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