Table 2 Summary of sampling parameters, molecular analysis methods, and results on the detection, quantification, and viability of SARS-CoV-2 RNA in air samples
Reference | Air sampler | Volume of air sampled | Duration of sampling | Air flow rate | Type of filters | Samples storage conditions | Other parameters | Internal standards: (Recovery) | Genes analysed | Definition of positive sample | LoD and LoQ | Positivity rate in filters (positive samples/total air samples) | Viral RNA load, range: (minimum-maximum) | SARS-CoV-2 viability |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cai et al.82 | Dry-filter air sampler | 12 m3 ** | 1 h | 200 L/min | Electret filters (5 mm) | Stored at −20°C and analysed within 3 days of collection | Not mentioned | Not reported | ORF1ab | Ct ≤ 38 | Not clear | 0% (0/15) | No quantification | Not studied |
Cheng et al.83 | Sartorious MD8 | 1 m3 | 20 min | 50 L/min | Gelatine (80 mm) filter | Not clear | Not mentioned | Not reported | RdRp | Not clear | Not clear | 0% (0/6) | No quantification | Not studied |
Chia et al.84 | NIOSH connected to either SKC AirCheck TOUCH Pumps or SKC pumps. SKC 37 mm cassettes connected to SKC pumps | 5.04 m3 (NIOSH) and 1.2 m3 (cassettes) | 4 h | 3.5 L/min (NIOSH) and 5 L/min (cassettes) | PTFE (37 mm) filter * | Storage at 4 °C, transport to the analysis laboratory, pretreatment and storage at -80 °C | Not mentioned | Not reported | E and ORF1ab | Amplification in at least one assay | Not clear | 0% (0/4). Detection in other matrices that are not filters. | No quantification | Not studied |
Conway-Morris et al.85 | (NIOSH) BC 251 2-stage cyclone aerosol samplers. Samplers ≥2 m from patients. | 1.26 m3 | 6 h | 3.5 L/min | PTFE (37 mm) filter * | Pretreatment of samples and storage at -80 °C | Not mentioned | Not reported | Not clear | Not clear | Not clear | 0% (0/73). Detection in other matrices that are not filters. | No quantification | Not studied |
Declementi et al.86 | SKC Flite pumps | 5.1 m3 ** | 340 min | 15 L/min | PTFE (47 mm) filter | Transfer of the samples to 4 °C and analysis in the subsequent 3 h | Not mentioned | Not reported | Not clear | Not clear | Not clear | 0% (0/8) | No quantification | Not studied |
Kim et al.87 | MD8 Airport Portable Air Sampler (Sartorius). Air was sampled 2 m from the patient | 1 m3 | 20 min ** | 50 L/min | Gelatine filter | Not clear | Not mentioned | Not reported | RdRp and E | Ct ≤ 35 (positive); Ct > 40 (negative); Ct 35–40 (Indeterminate). | Not clear | 0% (0/52) | No quantification | Not studied |
Lane et al.88 | NIOSH connected a PCXR-4, SKC pump. 102-152 cm above the floor | 1.26 m3 ** | 6 h | 3.5 L/min | PTFE (37 mm) filter * | Storage at −80 °C | Not mentioned | Not reported | (N1, N2, N3) or (N1, E) | Ct < 40 | 10 viral copies/mL | 0% (0/176) | No quantification | Not studied |
Lei et al.89 | A two-stage cyclonic bioaerosol sampler NIOSH. The equipment is placed at a height of 1.3 m and 1 m from the patient | 0.84 m3 ** | 4 h | 3.5 L/min | PTFE filter * | Not clear | Temperature, relative humidity, and CO2 | Not reported | Orf1 and N | Not clear | Not clear | 0%, the number of filter samples is not clear. Detection in other matrices that are not filters. | No quantification | Not studied |
Moore et al.90 | MD8 air sampler. Samplers located near to patients ( < 1 m) | 0,5 m3 | 10 min | 50 L/min | Gelatine filter * | Storage at −80 °C | Temperature and relative humidity | Not reported | RdRp, E, N, Orf1ab | Sample positive: both replicates amplified. “Suspect”: one replicate amplified. | Not clear | 0% (0/34). Detection in other matrices that are not filters. | No quantification in filters. Quantification in other matrices that are not filters | Not studied |
Morioka et al.91 | MD8 airscan sampling device (Sartorius) | 1 m3 ** | 20 min | 50 L/min | Gelatine (80 mm) filter | Pretreatment after sample collection. Storage −80 °C until extraction. | Not mentioned | Not reported | N | Not clear | Not clear | 0% (0/4) | No quantification | Not studied |
Nakamura et al.92 | MD8 airscan (Sartorius). Samplers on the floor about 1.5–2 m from the patient’s head. | 1 m3 ** | 20 min | 50 L/min | Gelatine (80 mm) filter | Pretreatment after sample collection. Storage −80 °C until extraction. | Not mentioned | Not reported | N | Not clear | Not clear | 0% (0/11) | No quantification | Not studied |
Ong et al.93 | SKC Universal pumps (with 37-mm filter cassettes) in the room and a Sartorius MD8 microbiological sampler outside the room | 1.2 m3 (SKC) and 1.5 m3 (MD8) ** | 4 h (SKC) and 15 min (MD8) | 5 L/min (SKC) and 100 L/min (MD8) | PTFE (37 mm) filter (SKC) and gelatine filter (MD8) | Storage at −80 °C until PCR | Not mentioned | Not reported | E | Strong positive: low Ct ( ≤ 32). Weak positive: high Ct ( > 32). | Not clear | 0% (0/5) | No quantification | Not studied |
Perrone et al.94 | ACD-200 Bobcat dry-filter air sampler | Not clear | Not clear | 200 L/min | Dry electret filter (52 mm) | Analysis hours after collection | Not mentioned | Not reported | Not clear | Not clear | Not clear | 0% (0/17) | No quantification | Not studied |
Song et al.95 | Derenda PNS 16T-3.1 (automatic sampling system) | 1.5 m3 ** | 1.5 h | 16,7 L/min | Membrane filter (46 mm) | Storage −80 °C until extraction. | Not mentioned | Not reported | RdRp and N | Not clear | Not clear | 0% (0/42) | No quantification | Not studied |
Zhang et al.96 | Air Virus collection equipment (NingBo iGene TecTM) | 1 m3 ** | 10 min | 100 L/min | Gelatine filter | Samples analysed within 24 hours of collection | Not mentioned | Not reported | ORF1ab | Ct ≤ 38 | LoD 100 copies/mL | 0% (0/24) | No quantification | Not studied |
Ang et al.25 | SASS 3100 air samplers. 0.9–3 m of distance to the patient | 24 and 72 m3 ** | 8 h | 50 and 150 L/min | SASS bioaerosol filter (polyester) (44 mm) | Storage at −80 °C | Not mentioned | Not reported | E and N | Not clear | 1.3-2.2 copies/m3 | 72% (13/18) | No quantification | Not show conclusive evidence for successful viral culture. |
Baboli et al.26 | SKC universal air sampling pumps. 1–3 m from patient beds. The samplers operated at a height of 1.5 to 1.8 m above the ground. | 0.12 m3 ** | 30 min | 4 L/min | PTFE (37 mm) filter | Stored at 4 °C until arrival at the analysis laboratory and then frozen at −70 °C until extraction. | Temperature and relative humidity | Not reported | RdRp and N | Ct ≤ 40 | Not clear | 22% (2/9) | No quantification | Not studied |
Barbieri et al.27 | SILENT air sampler. | 14.4 m3 | 24 h | 10 L/min | Quartz filter | Not clear | Not mentioned | Not reported | RdRp | Ct < 40 | Not clear | 80% (4/5), positive in at least one replicate | No quantification | Not studied |
Bazzazpour et al.28 | AV1000 air sampler (collects PM2.5). Positioned 1–2 m above floor, 0.8–2 m from individuals. | 2.9-5.9 m3 | 1-2 h | 30-58 L/min | PTFE (90 mm) filter | Transport to the laboratory at 4 °C. Pretreatment of samples and storage at −80 °C | Temperature, relative humidity and other records | Infectious ronchitis virus (IBV) for extraction efficiency (Recovery 25%) | N and ORF1ab | Not clear | Not clear | 36% (13/36) | No quantification | Not studied |
Ben-Shmuel et al.29 | MD8 air sampler (Sartorius) | 1 m3 | 20 min | 50 L/min | Gelatine filter | Samples were transported at 4–8 °C and processed within 2–3 hours of collection. | Not mentioned | Not reported | E | Not clear | Not clear | 38% (3/8) | No quantification | No viable virus was recovered from any of the samples in Vero-E6 cell cultures. |
Binder et al.30 | NIOSH sampler. 1.5 m from the ground; 1-3.2 m from the patient’s head. | 0.84 m3 | 4 h | 3.5 L/min | PTFE filter * | Not clear | Not mentioned | Not reported | N1 and N2 | Ct < 40 (positive for two genes) | 3.31 (N1) and 2.93 (N2) copies/reaction | 2% (3/195) | No quantification | The culture of the virus in cells from the positive air samples was negative |
Dubey et al.31 | Total suspended particulate (TSP) air sampler. 1–3 m distance from patients. | 0.9, 1 and 1.62 m3 ** | 1 h | 1.5, 16.7 and 27 L/min | PVDF (47 mm) filter | Not clear | Not mentioned | Not reported | E and RdRp | Ct < 35 for two genes | Not clear | 43% (17/126) | No quantification | Not studied |
Ge et al.32 | NIOSH bioaerosol sampler (BC251) with air pumps (XR5000, SKC) | 0.105 m3 ** | 30 min | 3.5 L/min | Not clear | Transport on ice to laboratory | Not mentioned | Not reported | N | Ct < 40 | Not clear | 9% (1/11) | No quantification | Not studied |
Ghaffari et al.33 | ESPS LVM Model (Fanpava) | 24.04 m3 | 24 h | 16.7 L/min | PTFE filter | Transport to the laboratory at 4 °C. Storage at −80 °C | Temperature, relative humidity, PM2.5, PM10 and TSP | Not reported | N and RdRp | Not clear | Not clear | 13% (2/16) | No quantification | Not studied |
Gohli et al.34 | SASS 3100 samplers. Inlet at face level, 45° downward. Positioned 1, 2, and 4 m from subjects | 4.5 m3 | 15 min | 300 L/min | Electret filters | Transported to the laboratory in ice bags and stored at -80 °C until further processing | Not mentioned | Not reported | RdRp and ORF1b | Ct < 45 | 2.2 copies /L of air (LoD) | 22% (19/87) | No quantification | The cell culture assay was negative for all samples. |
Hadavi et al.35 | SKC personal sampling pumps: cassette filter holder. Height: 1.5 m, distance: 1.5–2 m from patient bed | 1.5 m3 | 1 h | 25 L/min | PTFE (47 mm) filter | Stored at 4 °C until arrival at the laboratory and then frozen at -30 °C until extraction | Not mentioned | Not reported | RdRp and S | Not clear | Not clear | 9% (2/23) | No quantification | Not studied |
Huang et al.36 | A Sartorius AirPort MD8 air sampler | 1 m3 | 20 min | 50 L/min | Gelatine (80 mm) filter | Not clear | Not mentioned | Not reported | Not clear | Not clear | LoD: 10 copies/ml in gelatin suspension | 2% (19/838) | No quantification | Not studied |
Kotwa et al.37 | GilAir Plus personal pump: 3-piece cassette and NIOSH. Positioned 1 m and 2 m from patient head | 0.42 m3 ** | 2 h | 3.5 L/min | PTFE (37 mm), polycarbonate (37 mm) and gelatine (25 mm) filters | Transport in coolers. Pretreatment after sample collection. Storage -80 °C until extraction. | Not mentioned | Not reported | E and UTR | Ct < 40 | Not clear | 2% (3/146) | No quantification | Virus cultures negative for air |
Lane et al. (2)38 | NIOSH sampler. 1-1.5 m from the ground; 0.3-3 m from the patient’s head | 1.26 m3 ** | 6 h | 3.5 L/min | PTFE (37 mm) filter * | Storage at -80 °C | Not mentioned | Not reported | (N1, N2) or (N2, E) | Ct < 40 | 1-5 copies/µL | 1% (1/192) | No quantification | Not studied |
López et al.39 | A vacuum pump was used | 1.73 m3 ** | 3 h | 9.6 L/min | Not clear | Not clear | Not mentioned | Not reported | E | Not clear | Not clear | 30% (3/10) | No quantification | Not studied |
Mouchtourri et al.40 | Sartorius Airport MD8 | 0.5 m3 | 10 min | 50 L/min | Gelatine (80 mm) filter | Not clear | Not mentioned | Not reported | Not clear | Not clear | Not clear | 8% (1/12) | No quantification | Not studied |
Nissen et al.41 | HEPA filters of the ventilation system. 3 filter samples (3 × 3 cm) were randomly cut with sterilized scissors | Not clear | Not clear | Ventilation airflow: 2.27–3.48 m3/s | HEPA filter | Storage at 4 °C until analysis up to 72 hours later | Not mentioned | Not reported | N and E | Not clear | Not clear | 62% (8/13) | No quantification | No significant Potential cytopathic effect (CPE) |
Razzini et al.42 | MD8 Airport Portable Air Sampler. 1.5 m above the floor | 2 m3 | 40 min | 50 L/min | Gelatine filter | Transport between 2 and 8 °C to the laboratory | Not mentioned | Not reported | Not clear | Ct < 38 | Not clear | 40% (2/5) | No quantification | Not studied |
Sousan et al.43 | Filter cassettes (SKC), Button sampler (SKC) and AerosolSense sampler (ThermoFisher Scientific) | 7.2 m3 (Filter cassetes); 5.76 m3 (Button); 288 m3(AerosolSense) ** | 24 h | 5 L/min (Filter cassetes); 4 L/min (Button); 200 L/min (AerosolSense) | PTFE, PVC and gelatine filters * | Storage at -20 °C and analysis in 10 days | Not mentioned | Not reported | N1 and N2 | Not clear | Not clear | 7% (11/163) | No quantification | Not studied |
Stern et al.44 | Cascade impactor: 3 sizes: >10.0 μm, 2.5–10.0 μm, <2.5 μm. Inlets at breathing-zone height | Not clear | 72 h | Not clear | Not clear | Not clear | Not mentioned | Not reported | N1 and N2 | Ct ≤ 40 | Not clear | 6% (31/510) | No quantification | Not studied |
Tan et al.45 | The air samplers were placed less than one meter from the patient’s head and in clean areas | 0.3 m3 ** | 1 h | 5 L/min | Membrane filter | Samples were immediately transported on ice to the laboratory for analysis | Not mentioned | Not reported | ORF1ab | Not clear | Not clear | 3% (1/29) | No quantification | Not studied |
Amato-Lourenço et al.46 | MiniVol sampler (Air Metrics). The samplings were carried out at a height of 1.25 m | 2.4 m3 ** | 8 h | 5 L/min | Polycarbonate (47 mm) filter | Storage at -20 °C | Temperature and relative humidity | Not reported | N and E | Ct < 40 | Not clear | E: 73% (24/33), N: 15% (5/33) | E: 1,294-262,500 genomic units/m³, N: 12.45-718.83 | Not studied |
Barberá-Riera et al.47 | Derenda | 55 m3 | 24 h | 38 L/min | Quartz (47 mm) filter | Stored at −20 °C until analysis | Temperature, relative humidity and CO2 | Mengovirus for extraction efficiency (Recovery 51% ± 22%) | N1, N2 and E | Ct < 40 (at least 1 positive of 3 target genes) | Not clear | 11% (5/44) | 1.9-13.5 gc/m3 | Not studied |
Feng et al.48 | NIOSH. heigh 1,2 m. 2 m away the bed | 0.105 m3 | 30 min | 3.5 L/min | PTFE filter * | Not clear | Not mentioned | Not reported | Not clear | Ct < 40 | Not clear | 8% (1/12) | 1,112 copies/m3 | Not studied |
Gregorio et al.49 | A small vacuum pump connected to a 37 mmdisposable cassette. Sampler positioned at a height of 1.2 m | 0.6, 2.4 and 4.8 m3 ** | 2 h, 8 h and 16 h | 5 L/min | PTFE (37 mm) filter | Not clear | Temperature, relative humidity, CO2, total volatile organic compounds and particulate matter (PM1.0, PM2.5 and PM10) | Not reported | N1 and N3 | Ct < 38 | Not clear | 30% (9/30) | 6,800-285,000 copies/m3 | Not studied |
Groma et al.50 | An in-house built May-type cascade impactor | 9.6 m3 | 8 h | 20 L/min | Gelatine filter | Analysis of samples between 12 and 72 h after filter collection | Not mentioned | Not reported | N2 | Not clear | LoQ 10 copies/sample (1.04 copies/m3) | 36% (90/252) | 0.9-184 copies/m³ | Not studied |
Horve et al.51 | Air handling units filters (ventilation ducts). Samples were collected using swabs on an air filter | Not clear | Not clear | Not clear | Not clear | Not clear | Not mentioned | Not reported | S | Not clear | LoD of 2.22 gene copies/µL | 25% (14/56) | 3.2-49 copies/µL of reaction | Not studied |
Nor et al.52 | Low Volumen Sampler (LVS) (MINIVOL) | 14.4 m3 ** | 48 h | 5 L/min | Glass microfiber filter | Storage at -80 °C | PM2.5 | Not reported | N1 | Not clear | Not clear | 50% (2/4) | 10-74 copies/µL | Not studied |
Oksanen et al.53 | 3 sampling equipment by filter-based or impaction: 1. A Dekati PM10 cascade impactor (model PMS-420); 2. A sampler Button with a Gilian 5000 air sampling pump; 3. A Dekati eFilter | 3,6 m3 (Dekati), 0.09 m3 (Button) and 0.85 m3 (eFilter) ** | 2-4 h (Dekati), 13-31 min (Button) and 30 min (eFilter) | 20 L/min (Dekati), 4 L/min min (Button) and 28.3 L/min (eFilter) | Cellulose acetate membrane (25 mm) and 40-mm filter for the backup (Dekati); gelatine or mixed cellulose ester (MCE) (25 mm) (Button); gelatine (47 mm) filter (eFilter) * | Not clear | PM | Not reported | N1 | Results positive: both qRT-PCR < 40 Ct, or one qRT-PCR < 38 Ct. | between 5 and 50 copies/reaction for N1 gene | 9% (5/55) | 1.04 × 103 -2.05 × 107 copies/ml of sample | All air samples were cultured, but no viable viruses were observed. |
Santarpia et al.54 | Sartorius Airport MD8 sampler. Additional personal air samples were collected using SKC button samplers and Air Chek pumps. At least 1 meter from the patient | 0.75 m3 | 15 min (MD8) | 50 L/min (MD8) and 4 L/min (personal air samples) | Gelatine filter (80 mm for MD8 and 25 mm for personal air samples) | Not clear | Not mentioned | Not reported | E | Not clear | Minimum detection: 1e¯1 copies/µL, 39–44 cycles. | 66% (23/35) | 2,080-48,220 copies/m3 | Infectivity: extremely low. Virus culture not confirmed due to low concentrations. |
Santarpia et al.55 | NIOSH BC251 sampler | 0.105 m3 ** | 30 min | 3.5 L/min | Gelatine (37 mm) filter * | Not clear | Aerosol concentrations and size distributions | Not reported | E | Not clear | Not clear | 100% (6/6) | 1.01× 106 -9.69× 106 copies/m3 | 3 samples out of 18 showed viral growth in cells. |
Stein et al.56 | 3 sampling equipment: 1. An AerosolSense 2900 sampler; 2. BC-251 (NIOSH) 2-stage cyclone samplers with vacuum supplied by an Airchek pump (Model 224-44XR, SKC); 3. Button Samplers (SKC) with vacuum supplied by an Airchek XR5000 pump (SKC) | 0.63 m3–1,440 m3 | 3.5 h–120 h | 200 L/min (AerosolSense); 3 L/min (BC-251); 5 L/min (Button) | Gelatine (25 mm) filter | Not clear | Not mentioned | Not reported | E | Ct < 39 | Minimum detectable concentration: 1241 copies/mL | 13% (7/53) | 2-17,140 copies/m3 | Not studied |
Stern et al.57 | Micro-environmental cascade impactor of own design. Located 48 to 56 inches above the floor | 14 m3 | 48 h | 5 L/min | Polyurethane foam impaction substrates (large and coarse particles) and glass fiber (37 mm) filter (fine particles) | Sending samples on ice to the laboratory for analysis | Not mentioned | Not reported | N | Ct < 40.85 (corresponded to one copy number) | Not clear | 9% (8/90) | 5-51 copies/m3 | Not studied |
Young et al.58 | Ultrasonic personal aerosol samplers | 0.96 m3 ** | 8 h | 2 L/m | PTFE (37 mm) filter | Filters were frozen at -80 °C for 1–5 months prior to processing | Not mentioned | Not reported | N1 | Ct < 38 | LoD: 536 (N1), 443 (N2) and 63 (E) copies | 4% (14/336) | 66-212,429 gc/m3 | Not studied |
Conte et al.101 | An automatic sequential low-volume sampler (Skypost PM-TCR Tecora), a low-volume sampler (Zambelli Explorer pump) and an in-house built manual TSP sampler operating at low-volume | 6.2-29.7 m3 | 12 h | 38.3 L/min (Skypost PM-TCR Tecora), 61.7 L/min (Zambelli Explorer pump) and 13.4 L/min (in-house built manual TSP sampler) | Quartz (47 mm) filter | Storage at -25 °C or -80 °C | Not mentioned | Mengovirus for extraction efficiency (Recovery 54% ± 13%) | RdRp, N and E | Ct ≤ 40 for at least one gene (RdRp or N) | 2 copies/μl for all genes (RT-PCR) and 0.58 copies/μL (ddPCR) | 0% (0/69) | No quantification | Not studied |
de Man et al.59 | A Nilfisk household vacuum cleaner which has a high-efficiency particulate air (HEPA) filter on the air outlet. Air sampling in homes was done 10 cm from the mouth. Air sampling in UCI was done 50 cm from patients | 1.21 m3 ** | 2.5 min | 483 L/min | Surgical face mask was used as a sample filter | Not clear | Not mentioned | Not reported | E and RdRp | Not clear | Not clear | Healthcare settings: 24% (4/17) (hospital); residential: 71% (29/41) | No quantification | Not studied |
Moharir et al.60 | AirPort MD8 air sampler (Sartorius) | 1 m3 | 20 min | 50 L/min | Gelatine filter | Not clear | Not mentioned | Not reported | E, N and ORF1ab | Not clear | Not clear | Healthcare settings: 38% (30/80) (hospital); residential: 43% (15/35) | No quantification | A positive virus culture was established in 1 of the 3 samples that were analysed |
Habibi et al.61 | The samples were collected using a custom-made sampling device | 3.6 m3 | 2 h | 30 L/min | Not clear | Not clear | Not mentioned | Not reported | Not clear | Not clear | Not clear | Healthcare settings: 46% (6/13) (hospitals); Educational settings: 0% (0/2) (institute for Scientific Research) | Healthcare settings: 12-98 copies/m³ (hospitals) | Not studied |
Kušan et al.62 | NanoMOUDI R122 cascade impactor | m3 ** | 2-7 days | 30 L/min | Aluminium foils | Immediate analysis upon receipt of samples | Not mentioned | Not reported | Orf1 and S | Ct < 40 | Not clear | Healthcare settings: 48% (74/154) (hospital); Residential: 14% (2/14) | Healthcare settings: 0.1-9.5 copies/m3 (hospital); Residential: 0.12-0.56 copies/m3 | Not studied |
Alfaro et al.5 | Derenda low volume samplers (PM2.5 inlet): samplers at 1 m above ground, away from doors, windows, and ventilation units. | 55,2 m3 | 24 h | 38.3 L/min | Quartz (47 mm) filter | The filters were stored at −2 °C until analysis | Not mentioned | Mengovirus for extraction efficiency (Recovery 58% ± 38%) | N1, N2, E | Ct < 40 (at least one positive of the three target genes) | LoD and LoQ for N1, N2, and E was 2.70 gc/m3, 5.41 gc/m3, and 2.70 gc/m3, respectively. | Healthcare settings: 9% (20/139); socio-health settings: 15% (13/85); educational settings: 4% (11/273) | Healthcare settings: 4.3-504 gc/m3; socio-health settings: 5.4-77 gc/m3; educational settings: 3.1-14 gc/m3 | Not studied |
Mallach et al.63 | Ultrasonic Personal Air Samplers (UPAS) | 1.92 m3 | 16 h | 2 L/min | Gelatine filter * | Storage at 4 °C until analysis | Not mentioned | Not reported | E and N | Samples with Ct <36: RNA positive. Ct >36: positive if E and N genes ≤40. E protein concentrations more reliable than N protein. | Not clear | Healthcare settings: 9% (9/95) (hospital); Socio-health settings: 20% (3/15) (long-term care rooms); Other indoor settings: 13% (1/8) (prisons) | Healthcare settings: 64–288 copies/m3 (hospital); Socio-health settings: 93–11,940 copies/m3 (long-term care rooms); Other indoor settings: 395 copies/m3 (prisons) | Viable virus after 16 hours of sampling |
Barberá-Riera et al.10 | Personal pump Casella Apex2 Plus Air connected to a PALL 1119 polycarbonate in-line filter holder | 1.35 m3–5.76 m3 | 7,5 - 24,7 h | 4 L/m (quartz filters) and 2 L/m (PTFE filters) | PTFE (47 mm) and quartz (47 mm) filters | Filters were stored 24 h at 4 °C until analyis | Not mentioned | Mengovirus for extraction efficiency (Recovery 37 ± 23%) | N1, N2 and E | Ct < 40 (at least one positive of the three target genes) | Not clear | Socio-health settings: 79% (11/14); transport settings: 100% (3/3); other indoor settings (residential): 100% (1/1) | Socio-health settings: ND-19,525 gc/m3; transport settings: ND-1,233 gc/m3; other indoor settings (residential): 829-14,642 gc/m3 | Not studied |
Dumont-Leblond et al.97 | IOM Multidust sampler (SKC) connected to a portable pump Gillian Air 5. At least 1.5 m above the floor and 2 meters from residents | 0.72 m3 | 4 h | 3 L/min | Gelatine filter | Filters were eluted on the day of sampling and stored at −80 ˚C until RNA extraction. | Not mentioned | Not reported | ORF1b | Ct < 40 | Not clear | 0% (0/31) | No quantification | Viral culture was negative for all samples |
Correia et al.64 | Styrene filter cassette SKC (TSP) connected a Leland Legacy Personal Sample Pump and an AirChek XR5000 Pump. Size segregated aerosol samples were collected using a miniature cascade impactor (Sioutas impactor, SKC) | 0,08-11.88 m3 | 15-1320 min | TSP (5 L/m) and size segregated (9 L/m) | Gelatine (25 or 37 mm) filters | Analysis within 4 h of sample collection | Not mentioned | Not reported | E | Not clear | Not clear | 5% (2/37) | No quantification | In the viral viability analyses, the replication of SARS-CoV-2 in the host cells was not confirmed |
Linde et al.65 | NIOSH BC 251 and Conical Inhalable dust Sampler (CIS), both connected to a Gilian GilAir 5 pump. Heigh 1,5 m | 1.26 m3 | 6 h | 3.5 L/min | PTFE (37 mm) filter * | Transport at 4 °C to the laboratory. Storage at 4 °C in the laboratory until analysis in 24 h | Not mentioned | Not reported | RdRp and E | Ct < 40 (detection of both genes) | Not clear | 20% (2/10) | No quantification | Cytopathic effects were observed in an active air sample, but did not correspond to the smallest fraction (filter) |
Di Carlo et al.102 | Constant flow sampler (AMS Analitica model HE BASIC PLUS) | 18.7 m3 | 6.5 h | 24 L/min | Gelatine filter | The samples were sent immediately after collection to the laboratory for analysis | Not mentioned | Not reported | ORF1ab, N and S | Ct < 37 for at least two genes | Not clear | 0% (0/14) | No quantification | Not studied |
Yamagishi et al.98 | MD8, Sartorius | 1 m3 ** | 20 min | 50 L/min | Gelatine filter | The samples were stored for at least 14 days at -80 °C | Not mentioned | Not reported | Not clear | Not clear | Not clear | 0% (0/7) | No quantification | Not studied |
Hadei et al.66 | AV1000 sampler and SKC pump (Universal PCXR4). The samplers were placed at the height of 0.9–1.6 m above the ground | 1.27–3.5 m3 (AV1000) and 0.2–0.24 m3 (SKC) | 1–1.5 h | 40 L/min (AV1000) and 3.5 L/min (SKC) | PTFE (AV1000) and glass fiber (SKC) filters | Transport at 4 °C to the laboratory. Pretreatment of samples and stored at -80°C until analysis. | Temperature | Infectious Bronchitis Virus (IBV) for extraction efficiency. (Recovery 20%) | N and ORF1ab | Not clear | Not clear | Transport settings: 67% (10/15); other indoor settings (residential): 62% (8/13) | No quantification | Not studied |
Mortazavi et al.67 | Sensidyne Gilian BDX-II Abatement air sampling pump with 47 mm filter cassettes | 0.027 m3 | 90 min | 0.3 L/min | PTFE (47 mm) filter | Transportation of the samples at 4 °C to the laboratory and then they are analysed | PM1, PM2.5, and PM10 | Not reported | Not clear | Not clear | Not clear | 10% (3/30) | No quantification | Not studied |
Lednicky et al.17 | Sioutas personal cascade impactor sampler (PCIS) with a Leland Legacy (SKC) pump. 3 feet from face | 0.14 m3 | 15 min | 9 L/min | PTFE filter | Pretreatment 30 min after sample collection. Storage -80 °C until extraction | Not mentioned | Not reported | N | Not clear | Not clear | 80% (4/5) | 1.2 × 103 -7.8 × 103 genome equivalents/m3 | Not studied |
Moreno et al.68 | Personal Environmental Monitor (PEM) with Leland pump equipment | 5.2-6.2 m3 | 9-10 h | 10 L/min | PTFE (47 mm) filter | Not clear | Not mentioned | Not reported | IP2, IP4 and E | 2–3 positive targets: high virus contamination. 1 positive target: weak contamination | Not clear | 25% (3/12) | 1.4-23.4 cg/m3 | Not studied |
Vass et al.99 | NIOSH bioaerosol samplers (Model BC-251). 1.5 m above the floor | 0.54 m3 ** | 3 h | 3 L/min | PTFE (37 mm) filter * | Transport on dry ice and storage at −80 °C | Not mentioned | Not reported | N2 | Not clear | Not clear | 0% (0/2). Detection in other matrices that are not filters. | No quantification in filters. Quantification in other matrices that are not filters | They observe viable using non–filter-based samplers |
Vass et al.100 | NIOSH (BC-251 model) connected a Airheck pump (224-PCXR4) | 0.63 m3 ** | 3 h | 3,5 L/min | PTFE (37 mm) filter * | Storage at −80 °C | Temperature and relative humidity | Not reported | N2 | Not clear | Not clear | 0% (0/22). Detection in other matrices that are not filters. | No quantification in filters. Quantification in other matrices that are not filters | They observe viable virus using non–filter-based samplers |
Laumbach et al.69 | Leland Legacy pump (SKC) with an open-face filter holder | 14.4 m3 | 24 h | 10 L/min | PTFE filter | Not clear | Not mentioned | Not reported | N, S and ORF1ab | Ct < 37 | Not clear | 70% (14/20) | No quantification | Not studied |
Shankar et al.70 | Airchek sampler pump or Escort ELF pump with an inline air sampler that traps particles, a NIOSH 2-stage cyclone sampler (BC-251), and a Sioutas personal cascade impactor sampler with Leland Legacy pump | 0.27, 0.36, 0.54 and 0.81 m3 | 90, 120 and 180 min | 3 L/min (Airchek sampler and NIOSH), 9 L/min (Sioutas) | PTFE (25 or 37 mm) filter | Pretreatment 30 min after sampling. Storage −80 °C until extraction | Not mentioned | Not reported | RdRp and N | Not clear | Not clear | 31% (5/16) | 9.9 × 108- 3× 1011 genome equivalents/m3 | Not studied |
Del Real et al.71 | Indoor: Personal PM samplers connected to a particle impactor and a cassette for a non-segregated. Portable pump: placed ~1.5 m above ground.Outdoor: A gravimetric air sampler (Dekati PM10 Impactor) | Indoor: 0.71-4.68 m3 Outdoor: 43.2 m3 | Indoor: 4-26 h Outdoor: 24 h | Indoor: 3 L/min Outdoor: 30 L/min | Indoor: PTFE filter Outdoor: Polycarbonate and PTFE filters | Pretreatment after sample collection. Storage -80 °C until extraction | Not mentioned | Not reported | N1 and N2 | Ct < 40 (when N1 and N2 genes are positive) | The lowest concentration of RNA was 0.04 ng/µL | Healthcare settings: 2% (1/44) (hospital); Educational settings: 0% (0/42) (university); Outdoor: 0% (0/5) | Healthcare settings: 15 ng/μL (hospital); Outdoor: No quantification | Not studied |
Passos et al.72 | Indoor: Different air samplers: CRIFFER with a styrene filter cassette (SKN); AIRIDEAL 3 P; MD8; 821 T connected to an adapted acrylic collector Outdoor: HANDI-VOL (high-volume); HVS (high-volume) | Indoor: 0.12-800 m3 Outdoor: 7.1-4500 m3 | Variable: From a few minutes to over 7 days | Indoor: 2.5 L/min (Criffer); 18 L/min (821 T); 150 L/min (HANDI-VOL) Outdoor: 1130 L/min | Indoor: Gelatine filter (MD8), Cellulose nitrate membrane, PTFE and quartz microfiber filters Outdoor: Quartz filter | Samples sent immediately to the laboratory or refrigerated at 4 °C until receipt in the laboratory. | Temperature, relative humidity and atmospheric pressure | Not reported | N1 and N2 | Ct < 40 (positive for two genes) | Not clear | Healthcare settings: 9% (3/33) (hospital); Outdoor: 0% (0/10) | Healthcare settings: 0.14-34.3 genomic units/m3 (hospital); Outdoor: No quantification | Not studied |
Grimalt et al.73 | Aircheck XR5000 pump (SKC) with a SureSeal Cassette Blanks composed of three 37 mm diameter styrene clear pieces. 1.5 m above ground. In the COVID-19 patient rooms it was located 2 m away from the beds (indoor). | 1.08 m3 | 4 h | 4.5 L/min | PTFE (37 mm) filter | Not clear | Not mentioned | The 77b fragment of the Equine Arteritis virus as internal control of the extraction (Recovery 100%) | E | Ct < 44.25 | Not clear | Healthcare settings: 72% (31/43) (hospital); Outdoor: 25% (1/4) | Healthcare settings: 700-6200 copies/m3 (hospital); Outdoor: 290 copies/m3 | Not studied |
Liu et al.74 | Indoor: Styrene filter cassettes (SKC) with a portable pump (APEX2, Casella) and miniature cascade impactor (Sioutas Impactor, SKC). The sampling inlet: 1.5 m above floor Outdoor: Styrene filter cassettes (SKC) a portable pump (APEX2, Casella). | Indoor: 1.3–10.8 m3 ** Outdoor: 1.5 - 5 m3 ** | Indoor: 4.3–20 h Outdoor: 5–16.7 h | Indoor: 5.0 L/min (APEX2, Casella); 9.0 L/min (Sioutas Impactor, SKC) Outdoor: 5 L/min | Gelatine filter | All samples were processed immediately in the laboratory | Not mentioned | Not reported | ORF1ab and N | Not clear | ddPCR LLoD:ORF1ab: 2.18 copies;N: 0.42 copies per 20 µl reaction | Healthcare settings: 64% (16/25) (hospital); Outdoor: 38% (3/8) | Healthcare settings: 1-42 copies/m3 (hospital); Outdoor: <3-11 copies/m3 | Not studied |
Stern et al. (2)75 | Custom-designed Harvard Micro-Environmental Cascade Impactors: 3 distinct size fractions: fine ( ≤ 2.5 μm), coarse (2.5–10 μm), and large ( ≥ 10 μm) | 14.4 m3 | 48 h | 5 L/min | Polyurethane foam (PUF) substrate (2 first stages) and glass fiber (37 mm) filter (last stage) | Storage at 4 °C and shipping on ice to the analysis laboratory | Not mentioned | Not reported | N | Ct < 39 | Not clear | Healthcare settings: 6% (8/125); Outdoor: 10% (5/51) | Healthcare settings: 25 copies/m3 (maximum concentration); Outdoor: 17 copies/m3 (maximum concentration) | Not studied |
de Rooij et al.76 | Indoor: Stationary air sampling (Gilian GilAir 5 pumps) and personal air sampling were conducted for PM10 (PEM sampling heads (MSP 90)). Inhalable dust sampling (GSP, Gesamtstaubprobenahme) Outdoor: Stationary air sampling for PM10. Harvard impactors (Air Diagnostics and Engineering Inc.) and GSP sampling heads connected to a Gilian GilAir 5 pump (Sensidyne) | Indoor: 1.26-1.92 m3 Outdoor: 43-72 m3 (Harvard) and 15-25 m3 (GSP) | Indoor: 6-8 h Outdoor: 3–7 days | Indoor: 3.5 L/min (GSP) and 4 L/min (MSP90) Outdoor: 10 L/min (Harvard) and 3.5 L/min (GSP) | PTFE (37 mm) filter | Transport at 4 °C, stored at -80 °C in the lab, and sent on dry ice to another lab for analysis. | Not mentioned | Not reported | E | Not clear | Not clear | Indoor: 20% (13/66) Outdoor: 15% (11/72) | Indoor: 2,400-4,900 copies/m3 Outdoor: 110-4,800 copies/m3 | Viability testing on the two air samples was unsuccessful. |
Chirizzi et al.103 | Low volume aerosol sampler (PM10) (Skypost PM-TCR Tecora and SWAM 5a Dual Channel Monitor-FAI Instruments). Size-segregated samples were collected with a r MOUDI cascade impactor | 110 m3 (PM10) and 250 m3 (MOUDI) | 48 h (PM10) and 144 h (MOUDI) | 38,3 L/min (PM10 samples) and 30 L/min (Size-segregated samples) | Quartz filter | Filters were frozen at -25 °C until analysis up to 4 days. | Not mentioned | Mengovirus for extraction efficiency (Recovery 49 ± 5%) | RdRp and E | Not clear | LoD 10 copies/µL (RT-PCR) and 0,625 copies/µL (ddPCR) | 0% (0/60) | No quantification | Not studied |
Linillos et al.104 | MCV high volume samplers were collocated with different inlets (Digitel DHA-80) for sampling the PM10, PM2.5 and PM1 specific size fractions | 525–720 m3 ** | 17.5–24 h | 500 L/min | Quartz (150 mm) filter | Not clear | Real-time monitoring of PM10 y PM2,5 and PM1. Meteorological parameters were recorded. | Not reported | N1and N2 | Ct < 35 for N1 and N2 | 0% (0/18) | No quantification | Not studied | |
Pivato et al.105 | PM (PM10, PM2.5) samples were collected with a low-volume sampling | 55.2 m3 ** | 24 h | 38.3 L/min | Quartz (47 mm) filter | Samples for up to 6 days at 20°C and then stored at -20 °C until analysis | Filter gravimetry | Synthetic SARS-CoV-2 armored RNA for extraction efficiency (Recovery not mentioned) | N and Orf1b-14nsp | Ct < 40 | LoD 1.2 copies/m3 | 0% (0/44) | No quantification | Not studied |
Setti et al.77 | A low-volume gravimetric air sampler | 55 m3 | 24 h | 36.3 L/min | Quartz filter | Not clear | Temperature, relative humidity and irradiance | Not reported | E, N and RdRp | Not clear | Not clear | 59% (20/34), for at least one of the three marker genes | No quantification | Not studied |
Amato-Lourenço et al. (2)78 | TSP samples were collected using a Handi-vol sampler. The samplings were carried out at a height of 1.25 m. | 4.32 m3 ** | 24 h | 3 L/min | Fibreglass (110 mm) filter | The filters were stored at −20 °C until analysis | Filter gravimetry, weather data, including the temperature (°C) and relative humidity (%), were obtained from the station closest to the sampling points | Not reported | E and N1 | Ct < 40 | Not clear | E: 58% (22/38); N1: 16% (6/38) | E: 4.3-218 genomic units/TSP; N1: 17-157 genomic units/TSP | Not studied |
Kayalar et al.79 | SKC Filter Pack Sampler, Dichotomous PM Sampler, High Volume Air Sampler, Low Vol Stack Filter Unit, Zambelli PM Sampler and High Vol Cascade Impactor | 7.2-1422 m3 | 24 h | Not clear | Glass fiber, PTFE and nucleopore polycarbonate filters | The filters were stored at −20 °C until analysis | Downloaded air quality data and meteorological data | Not reported | N1 and RdRp | Ct < 37 for two genes | Not clear | 10% (20/203) | <0.2-23 copies/m3 | Not studied |
Pivato et al.80 | Two sampling devices: a low-volumetric rate (LVR; 23–54 m3/sample) sampler and a high-volumetric rate sampler (HVR) | 23-54 m3 (LVR) 248-534 m3 (HVR) | 24 h (LVR) and not mentioned for HVR | 38.3 L/min (LVR) and not mentioned for HVR | Quartz (47 mm) (LVR) and PTFE (142 mm) (HVR) filters | Samples for up to 6 days at 20°C and then stored at -20 °C until analysis (LVR) and he filters were stored at −20 °C until analysis (HVR) | Meteorological conditions were registered by the weather station closest | Mengovirus for extraction efficiency (Recovery 0.8%) | Orf1b nsp14 | Ct < 40 | LoD 0.41 gc/µL and LoQ 3,71 gc/µL | 63% (24/38) | 0.3-4.2 copies/m3 | Not studied |
Tao et al.81 | Fine particle samples (PM2.5) and coarse particle samples (PM10) were collected using high-volume samplers (Digitel DA-80H) | 720 m3 ** | 24 h | 500 L/min | Quartz filter | The filters were stored at −80 °C until analysis | The data of environmental factors were downloaded (O3, nitrogen dioxide (NO2), SO2, carbon monoxide (CO), PM10, PM2.5, temperature, etc.) | Not reported | ORF1ab | Not clear | Not clear | SARS-CoV-2 was detected in PM10 and PM2.5 samples, but the number of samples is not specified | 10^0 copies/m3 - 10^3.1 copies/m3 + 1 | Not studied |