4.7 Article

High air flow-rate electrostatic sampler for the rapid monitoring of airborne coronavirus and influenza viruses

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 412, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2021.125219

Keywords

Airborne virus; Electrostatic air sampler; Viral recovery; Enrichment capacity; Rapid monitoring

Funding

  1. Technology Innovation ProgramIndustrial Technology Alchemist Project - Ministry of Trade, Industry and Energy, Korea (MOTIE, Korea) [20012215]
  2. Korea Evaluation Institute of Industrial Technology (KEIT) [20012215] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Efficient and nondestructive collection of airborne virus particles is essential for monitoring airborne viruses, with a high air flow rate required for quick sample collection. The introduction of a high air flowrate electrostatic sampler allows for continuous collection of virus aerosols in liquid, making it suitable for real-time qRT-PCR detection. A 20-minute air sampling period is sufficient for producing a sample suitable for use in a viral epidemic scenario.
Capturing virus aerosols in a small volume of liquid is essential when monitoring airborne viruses. As such, aerosol-to-hydrosol enrichment is required to produce a detectable viral sample for real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) assays. To meet this requirement, the efficient and nondestructive collection of airborne virus particles is needed, while the incoming air flow rate should be sufficiently high to quickly collect a large number of virus particles. To achieve this, we introduced a high air flowrate electrostatic sampler (HAFES) that collected virus aerosols (human coronavirus 229E, influenza A virus subtypes H1N1 and H3N2, and bacteriophage MS2) in a continuously flowing liquid. Viral collection efficiency was evaluated using aerosol particle counts, while viral recovery rates were assessed using real-time qRT-PCR and plaque assays. An air sampling period of 20 min was sufficient to produce a sample suitable for use in realtime qRT-PCR in a viral epidemic scenario.

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