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Frontiers of Environmental Science & Engineering

ISSN 2095-2201

ISSN 2095-221X(Online)

CN 10-1013/X

Postal Subscription Code 80-973

2018 Impact Factor: 3.883

Front. Environ. Sci. Eng.    2024, Vol. 18 Issue (7) : 85    https://doi.org/10.1007/s11783-024-1845-y
Rapid monitoring of indoor airborne influenza and coronavirus with high air flowrate electrostatic sampling and PCR analysis
Sanggwon An1, Sangsoo Choi1, Hyeong Rae Kim2, Jungho Hwang1()
1. School of Mechanical Engineering, Yonsei University, Seoul 02876, Republic of Korea
2. Gas Metrology Group, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, Republic of Korea
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Abstract

● Electrostatic virus sampler was designed and evaluated in a pandemic scenario and real indoor field environment.

● Airborne virus was gently sampled with high aerosol sampling performance.

● Viral samples detectable for PCR were produced within 40 min.

The World Health Organization has raised concerns about the possibility of airborne transmission in enclosed and poorly ventilated areas. Therefore, rapid monitoring of airborne viruses is necessary in multi-use facilities with dense population. Accordingly, an electrostatic air sampler (250 L/min) was developed in this work to obtain indoor viral aerosol samples for analysis via the Polymerase Chain Reaction (PCR). Aerosol tests with H1N1 and HCoV-229E were performed to evaluate the sample collection efficiency. PCR analysis, along with another aerosol test, was conducted to evaluate the recovery of the virus particles collected by the sampler. In laboratory tests, our electrostatic sampler obtained viral samples that were detectable by PCR under the simulated viral pandemic scenario (3000 RNA copies per cubic meter of air) within 40 min. The resulting cycle threshold (Ct) values were 35.07 and 37.1 for H1N1 and HCoV-229E, respectively. After the performance evaluation in the laboratory, field tests were conducted in a university classroom from October 28 to December 2, 2022. Influenza A and HCoV-229E were detected in two air samples, and the corresponding Ct values were 35.3 and 36.8. These PCR results are similar to those obtained from laboratory tests, considering the simulated viral pandemic scenario.

Keywords Airborne virus      Electrostatic sampler      Rapid monitoring      Indoor environment      Field test     
Corresponding Author(s): Jungho Hwang   
Issue Date: 08 April 2024
 Cite this article:   
Sanggwon An,Sangsoo Choi,Hyeong Rae Kim, et al. Rapid monitoring of indoor airborne influenza and coronavirus with high air flowrate electrostatic sampling and PCR analysis[J]. Front. Environ. Sci. Eng., 2024, 18(7): 85.
 URL:  
https://academic.hep.com.cn/fese/EN/10.1007/s11783-024-1845-y
https://academic.hep.com.cn/fese/EN/Y2024/V18/I7/85
Fig.1  Electrostatic virus samplers (A) Kim et al. (2021) (B) This study.
Fig.2  Experimental setup for evaluation of virus sampling performance (A) Our electrostatic sampler−one pass test (B) Comparison with SKC BioSampler−one pass test (C) Comparison with SKC BioSampler−8 m3 chamber test.
Fig.3  Performance of our electrostatic sampler (A) Electrical currents with various applied voltages (B) Collection efficiency of our sampler for H1N1 under various air flow rates and applied voltages (w/o desalting process) (C) Collection efficiency of our electrostatic sampler for NaCl aerosols under various applied voltages (250 L/min air flow rate) (D) Collection efficiency for HCoV-229E and MS2 at 250 L/min (w/o desalting process) (E) Effect of desalting process on the collection efficiencies for H1N1 virus at 250 L/min (F) Recovery rates for H1N1 and human coronavirus 229E (HCoV-229E) (one-pass test, w/o desalting process).
Fig.4  Comparison between our electrostatic sampler and the SKC BioSampler for virus detection performance. (A) Real-time qRT-PCR analysis for our sampler and SKC BioSampler (one-pass test, w/o desalting process) (B) Real-time qRT-PCR analysis for our sampler and SKC BioSampler (one-pass test, w/ desalting process) (C) Plaque assay results for our sampler and SKC BioSampler (chamber test, w/ desalting process).
Sampler Sampling time (min) Cycle number
H1N1 HCoV-229E
24000 RNA copies/m3 12000 RNA copies/m3 6000 RNA copies/m3 24000 RNA copies/m3 12000 RNA copies/m3 6000 RNA copies/m3
Our sampler (250 LPM) 40 32.34 33.26 34.54 33.96 35.24 36.37
Original sampler (100 LPM) 40 35.49 36.62 N·D 36.30 37.90 N·D
SKC BioSampler 40 N·D N·D N·D N·D N·D N·D
60 N·D N·D N·D N·D N·D N·D
120 N·D N·D N·D N·D N·D N·D
180 N·D N·D N·D N·D N·D N·D
360 36.83 N·D N·D 38.54 N·D N·D
Tab.1  Comparison test results between our sampler, original sampler (Kim et al., 2021), and SKC BioSampler
Fig.5  Comparison between our electrostatic sampler, original electrostatic sampler, and the SKC BioSampler for virus detection performance (A) Real-time qRT-PCR analysis for our electrostatic sampler and original electrostatic sampler (B) Real-time qRT-PCR analysis for our electrostatic sampler and SKC BioSampler.
Fig.6  qRT-PCR analysis for virus particles collected using an aerosol-to-hydrosol approach of our electrostatic sampler in real pandemic scenario.
Fig.7  Field test in classroom of Yonsei University using our electrostatic sampler. (A) photograph of airborne virus sampling in classroom of the Yonsei University (B) Real-time qRT-PCR analysis for air samples collected at 2022/11/04 (13:30~15:30) (C) Real-time qRT-PCR analysis for air samples collected at 2022/11/04 (16:00–18:00).
Date Time Detected virus species
2022/10/28 13:30–15:30 N·D
16:00–18:00 N·D
2022/11/04 13:30–15:30 Influenza A (Ct = 36.5)
16:00–18:00 Influenza A (Ct = 35.3)HCoV-229E (Ct = 36.8)
2022/11/11 13:30–15:30 N·D
16:00–18:00 N·D
2022/11/18 13:30–15:30 N·D
16:00–18:00 N·D
2022/12/02 13:30–15:30 N·D
16:00– 8:00 N·D
Tab.2  Real-time qRT-PCR results for collected virus samples in field tests
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