The coronavirus disease (COVID-19) is poised to become the largest pandemic on record since the 1918 flu pandemic. As of 17 December 2020, a total of 72.6 million cases of infections including over 1.6 million deaths have been confirmed in 220 countries/areas/territories due to the pandemic (WHO 2020a). Despite some earlier debate (Lewis 2020; Morawska and Milton 2020; WHO 2020b), airborne transmission has been recently recognized as an effective route of transmission of COVID-19. In a scientific brief issued on July 9, 2020, the World Health Organization (WHO) acknowledged that short-range airborne transmission of COVID-19 may exist in indoor settings with poor ventilation (WHO 2020b). On October 5, 2020, the U.S. Centers for Disease Control and Prevention (CDC) changed their stance and for the first time, acknowledged airborne transmission via small droplets and particles as an important route of virus spread in the current pandemic (CDC 2020).
According to an earlier definition by the WHO, airborne transmission is defined as the spread of droplet nuclei—the residue of dried respiratory aerosols (≤ 5 µm in diameter) that results from evaporation of droplets coughed or sneezed into the atmosphere or by aerosolization of infective material (WHO 2014). More recently, van Doremalen et al. (2020) tested the stability of SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2), the causation agent of the COVID-19 pandemic, on aerosols at 21–23 °C and 65% relative humidity. The study found that SARS-CoV-2 remained viable after 3 h and the infectious titer reduced from 103.5–102.7 TCID50 (median tissue culture infectious dose) per liter of air. Under similar environmental conditions (i.e., 23 ± 2 °C and 53 ± 11% relative humidity), Fears et al. (2020) further showed that SARS-CoV-2 viruses on respirable-size aerosols maintained their infectivity and virion integrity after 16 h.
The prolonged survival of SARS-CoV-2 on aerosol particles raised questions on whether atmospheric particles, including fine particulates in outdoor environments and indoor particle emissions could facilitate the dispersion, transport, and the persistence of the novel coronavirus (He and Han 2020; Mahabee-Gittens et al. 2020; Tang et al. 2020). In the latest public guidance, the CDC pointed out that COVID-19 can be spread by airborne transmission in enclosed spaces that have inadequate ventilation, where infectious small droplets and particles can remain suspended for minutes to hours in air and travel far from the sources (CDC 2020). Several recent studies have found strong positive correlations between atmospheric particulate levels and the local infection of COVID-19 as well as symptom aggravation in patients (Fig. 1). For instance, Yao et al. (2020) analyzed the relationship between particulate matter (PM) concentration and COVID-19 case fatality rates in 49 Chinese cities using Global Moran’s I and multivariate linear regression. The results showed that fatality rates increased by 0.24% with every 10 μg m−3 increase in the PM2.5 level (i.e., particulate matter in air that are 2.5 µm or less in diameter). Similar conclusions were drawn by Wu et al. (2020), who conducted a nationwide cross-sectional study in the United States and reported that an increase of 1.0 μg m−3 in PM2.5 correlated with an 8% increase in COVID-19 fatality rates. In an investigation in Milan metropolitan area, researchers investigated the potential association between the degree of accelerated diffusion, PM pollution, and morbidity of COVID-19. The study found that the local daily new cases were positively related with the PM, and proposed that outdoor atmospheric particulates may be possible routes of SARS-CoV-2 diffusion (Zoran et al. 2020). As the first evidence showing SARS-CoV-2 harboring on airborne particles, Setti et al. (2020b) found clusters of SARS-CoV-2 RNAs on atmospheric particulate matter in Bergamo, northern Italy, a region burdened with high atmospheric PM levels.
While considerable efforts have been expended on studying the potential implications of airborne particulates in outdoor atmosphere on COVID-19 transmission and symptom aggravation, indoor aerosols—fine particulate matter that is emitted by a common range of sources and human activities—represent an under-investigated route for harboring and transporting airborne pathogens, including SARS-CoV-2. Due to lockdowns, travel restrictions, and other human interventions, outdoor atmospheric particulates underwent significant decreases in many regions during COVID-19, and humans become more impacted by indoor particle emissions in their daily activities (Chauhan and Singh 2020; Li et al. 2017a; Wang et al. 2020; Wu et al. 2018). As a known cause of human respiratory diseases, these fine particulates can present a confounding factor in airborne transmission of COVID-19. An earlier estimate by Morawska et al. (2013) found that about 30% of human respiratory diseases caused by atmospheric particulates were associated with those generated from indoor sources. A multitude of indoor sources and human activities are known to generate fine particles, or aerosols, in indoor environments, and many of them have unique characteristics in physiochemical properties and aerodynamics in air. Given the fact that most people spend almost 90% of their time in indoor environments (Klepeis et al. 2001), the role of indoor aerosols in COVID-19 transmission should be scrutinized for effective infection prevention and control, especially in enclosed public settings with high user occupancy or foot traffic which may be high-risk settings for airborne transmission to effectuate. In this article, we aim to present a focused review on the sources and characteristics of common indoor aerosols and based on this information and the recent findings on COVID-19, we discussed their potential implications on COVID-19 transmission. Specifically, evidence and discussions are presented revolving the following topics: i) common sources and characteristics of indoor aerosols, from anthropogenic sources and activities; ii) human respiratory and immune systems impaired by particle inhalation; iii) association between exposure of indoor aerosol particles and the morbidity or mortality of COVID-19; and iv) whether common indoor aerosol particles can act as carriers of SARS-CoV-2.
Sources and characteristics of indoor aerosols
Understanding the roles and influence of indoor aerosols presents an urgent task in the ongoing scrutiny on the airborne transmission of SARS-CoV-2 in indoor environments, especially in enclosed public spaces where several large clustered outbreaks have been reported (Lewis 2020). To this end, a basic understanding of the sources and characteristics of indoor aerosols, in the context of airborne pathogens, is necessary. In recent discussions, several researchers postulated that particles generated by tobacco smoking and incense burning could facilitate the indoor transmission of SARS-CoV-2 (Amoatey et al. 2020; Mahabee-Gittens et al. 2020). In reality, there are many sources—mostly from human activities—that can generate or resuspend abundant quantities of aerosol particles in indoor air. These include activities involving combustion such as smoking, cooking, candles burning, incense burning, and mosquito coils burning, as well as non-burning sources such as vacuuming, laser printing. As shown in Table 1. large quantities of small particles, typically in the ultrafine range (< 100 nm), can be emitted from common indoor sources, resulting in relatively high mass or particle concentrations in simulated or real indoor environments.
With about 1 billion smokers around the world, tobacco smoking is one of the most common sources of indoor aerosol emissions. Secondhand smoke poses a major risk factor for indoor occupants, including children, pregnant women, and other non-smokers (Havey et al. 2009; Zhou et al. 2015). Without adequate natural ventilation, smoking can significantly elevate indoor aerosol concentrations in rooms and buildings. Connolly et al. (2009) evaluated indoor air quality in 128 Irish pubs in 15 countries, and found that the average concentration of PM2.5 in smoking-permitted pubs was 329 μg m−3, while that in the smoking-free pubs was equals to 23 μg m−3. A similar study was conducted by Hyland et al. (2008), where the authors measured PM2.5 levels in 1822 different workplaces including bars, restaurants, retail outlets, airports in 32 countries. The mean PM2.5 levels in smoking-permitted places were found to be 8.9 times higher than those measured at smoking-free venues. Semple et al. (2015) assessed fine particles levels in 110 Scottish homes. The median PM2.5 concentrations in households with smoking occupants were 31 μg m−3 which was approximately ten times greater than those in homes without smokers, suggesting that members of smoking homes were exposed to high concentrations of PM2.5, especially in those lacking ventilation.
Characteristics of aerosols from tobacco smoking have been studied under laboratory settings. By testing five brands of cigarettes, Wu et al. (2012) reported that the mean emission rate of ultrafine particles (UFPs) from smouldering cigarettes was 3.36 ± 0.24 × 1011 particles min−1, which was consistent with the source strength (3.76 × 1011 particles min−1) estimated by Afshari et al. (2005). The particle count median diameters of smoking particles were determined to be 102–113 nm. Similar results have also been reported on electronic cigarettes, also known as ‘e-cigarettes’. For instance, Fuoco et al. (2014) reported high particle number concentrations (4.39 ± 0.42 × 109 particles cm−3) in aerosol streams of electronic cigarettes, which were higher than the levels measured on traditional cigarettes under the same conditions. The number distribution mode of electronic cigarettes was in the 120–165 nm range. Volesky et al. (2018) measured the concentration of PM2.5 and ultrafine particles by testing three different e-cigarettes containing the same nicotine solution in a ~38 m3 office. The authors found that the mean PM2.5 concentration was elevated by 160- and 103-fold at 0.5 m and 1 m from the smoker, while the concentration of ultrafine particles increased by 5.2- and 3.0-fold, respectively. The maximum PM2.5 (174,160 μg m−3) and ultrafine particle concentration (284,260 particles cm−3) were observed at 0.5 m from the e-cigarette smoker.
In many indoor environments, cooking is recognized as a dominant source of indoor aerosols in terms of both particle count and mass (Vu and Harrison 2019). Wan et al. (2011) measured the PM2.5 levels during and after cooking activities in 12 naturally ventilated, smoking-free homes in Hong Kong. The average PM2.5 concentration increased to 160 μg m−3 in the kitchen and airborne particle generated from cooking dispersed quickly and resulted in a PM2.5 concentration of 60 μg m−3 in the living room. Meanwhile, particle number concentrations reached 105 particles cm−3 both in the kitchen and the living room, with their size distributions mainly in the sub-100 nm range. Kang et al. (2019) reported that rangehood systems cannot effectively reduce fine particle emissions during cooking activities, while combining rangehood use and natural ventilation reduced cooking particle concentrations, with the average particle decay rate constant increased to 9.1 h−1 from 2.9 h−1 when using the rangehood system alone. Depending on the fuel, cooking oil, food, and cooking method, the characteristics of particles emitted from cooking varied significantly. See and Balasubramanian (2006) investigated particle emissions from five different cooking methods including steaming, boiling, deep-frying, pan-frying, and stir-frying in a domestic kitchen. The study showed that in general cooking with oils generated much more particles than cooking with water. The highest particle number concentration was observed during deep-frying (6.0 × 105 particles cm−3), with a mean particle size of 20 nm. With respect to boiling and steaming, less particles were liberated from the cooking process, although particle number concentrations still exceeded 5.0 × 104 particles cm−3. Torkmahalleh et al. (2012) determined the emission fluxes (i.e., rates per unit area) of seven commercial cooking oils, namely, peanut, coconut, soybean, sunflower, corn, olive, and canola oils. The result showed that cooking with olive oil had the highest PM2.5 emission flux (5.7 × 106 μg min−1 m−2) and the peanut oil had the highest total particle number emission flux (3.8 × 1014 particles min−1 m−2).
Vacuum cleaners are commonly used in indoor environments to remove dusts and small debris from floors and surfaces. When operating, vacuum cleaners can also become significant sources of airborne particles for their ability to release or resuspend large amounts of small particles into the indoor air. In a study conducted by Knibbs et al. (2012), authors determined the maximum emission rate of 1.1 × 1011 particles min−1 for ultrafine particles by measuring the emissions from 21 vacuum cleaners, while the minimum emission rate still exceeded 106 particles min−1. Regarding larger particles (i.e., sizes in the range of 0.5–20 μm), their emission rates were measured between 4.0 × 104 to 1.2 × 109 particles min−1. The overall PM2.5 emission rates ranged from 2.4 × 10−1 to 5.4 × 103 μg min−1. Vu et al. (2017) reported a peak particle number concentration of 9.4 × 104 particles cm−3 in a naturally ventilated apartment during vacuum cleaning, where a unimodal number size distribution was observed with 98% of particles falling in the ultrafine range with a peak at 19.8 nm. On the particle mass concentration, the peak PM1.0, PM2.5 and PM10 levels were measured to be 1.5, 22.7 and 75.4 μg m−3, respectively. In a recent study, Vicente et al. (2020) investigated the emission rates from four common types of vacuum cleaners, namely, the washable filter bagless, wet, bagged, and HEPA (high-efficiency particulate air) filter equipped robot. Based on their results, the highest PM10 emission rates were observed with the operation of the bagged vacuum cleaner (207 ± 99.0 μg min−1), while similar emission rates were obtained from the wet and washable filter bagless vacuum cleaners (86.1 ± 16.9 μg min−1 and 75.4 ± 7.9 μg min−1). The number emission rates of particles in the size range of 8–322 nm varied from 5.3 × 1011 (washable filter bag less vacuum) to 2.1 × 1012 (wet vacuum) particles min−1. Notably, operating the HEPA filter equipped vacuum cleaner did not increase the particle mass (PM10) or number concentration when compared with the background levels.
With smoking becoming a prohibited activity in most office buildings, printer emission can be a main source of indoor aerosols in office environments. He et al. (2007) reported an average particle number concentration of 6.5 ± 8.2 × 103 particle cm−3 during the normal working periods in a 120-m2 open-plan office, which was much higher than the equivalent concentration at non-working time (1.2 ± 0.9 × 103 particles cm−3). Tang et al. (2012) assessed the indoor particulate matter level generated by laser printers in 63 German offices. To simulate worst case but realistic conditions commonly encountered in normal office rooms, the authors printed 500 pages in each office with ventilation system operating if available and found substantial releases of ultrafine particles (< 100 nm) during the printing phase. The median particle number concentrations were elevated from 6.5 × 103 particles cm−3 (standby phase) to 1.8 × 104 particles cm−3 (printing phase). The median particle mass concentrations (PM0.23–20) were 57 μg m−3 and 68 μg m−3 in the standby and printing phase, respectively. In the aforementioned study, He et al. (2007) investigated the particle characteristics generated by three laser printers in an experimental chamber. Conclusion was drawn that particle emission rates varied greatly with toner coverage and cartridge age, which ranged from 4.0 × 107 to 1.6 × 1011 particles min−1. Large numbers of ultrafine particles were emitted by all three types of printers, and the mean particle count median diameter was 76 ± 11 nm, 46 ± 9 nm, and 40 ± 4 nm, respectively. Koivisto et al. (2010) compared the particle emissions of two monochromes laser printers and a color laser printer in a flow-through chamber. The emission rates were measured to be 4.1 × 109 and 3.9 × 109 particles s−1 for the monochrome printers and 7.0 × 108 particles s−1 for the color printer. The geometric mean diameter of emission particles was larger for the color laser printer (79 nm) compared with the two monochrome laser printers (32 and 40 nm).
An overlooked source in recent studies and discussions (Kumar et al. 2013; Li et al. 2017c; Manigrasso et al. 2018), candle burning can be a substantial source of indoor particle emissions (Rogula-Kopiec et al. 2019). In the modern society, candles are no longer used primarily for lighting, but for esthetic and religious purposes such as meditation, memorials, and ceremonies, usually in indoor settings. Studies have shown that large quantities of fine particles are emitted during candle burning, mostly in the micron to submicron range. Afshari et al. (2005) characterized 13 different indoor particle sources in a 32-m3 chamber with a constant air exchange rate of 1.7 ± 0.1 h−1 with outside air. The study found that burning pure wax candles generated the highest concentration of ultrafine particles (2.4 × 105 particles cm−3) than smoking, frying meat, cooking with an electric stove, and all other sources of particle emission. Pagels et al. (2009) tested two representative tapered candles in a 21.6-m3 stainless steel chamber with an air exchange rate of 0.5 h−1. The authors found that the geometric mean diameter of the generated particles peaked at 20–30 nm during the steady-burn period, and at 270 ± 30 nm during the sooting-burn period. In a recent study, Wallace et al. (2019) measured the indoor ultrafine particles (2.3–64 nm) originated from burning candles in a residence. During the steady-burn stage, the mean emission rates of ultrafine particles were up to 7.2 × 1012 particles min−1, while the total particles number emission rate reached 1013 particles min−1 in the room. Particle emissions from candles varied greatly with different products. Derudi et al. (2014) reported that the total PMx emission was measured to be 7.0, 106, 272 μg g−1 for three Italian container candles constituted by different paraffin waxes. The authors further determined the air quality for the considered exposure scenario of a 30-m3 room with an air exchange rate of 0.5 h−1. With two candles of the same type burning simultaneously, the steady-state PM2.5 concentration was estimated to be 2.17, 26.4, and 97.8 μg m−3 in the well-mixed room environment, respectively.
Mosquito coil burning
Mosquito coils are widely used in Africa, Asia, and South America as an insect repellant in summer (Zhang et al. 2010). To achieve the desired effects, mosquito coils are often used in enclosed spaces and burned slowly through the night. Their typical patterns of use mean that users may be continuously exposed to high concentrations of indoor particulate matter for several hours in non-ventilated indoor environments. Liu et al. (2003) investigated several types of commonly used mosquito coils in China and Malaysia. The burning periods of those products ranged from 7 h to 11 h, and PM2.5 emission rates varied considerably for different mosquito coils between 51 ± 7 mg h−1 and 117 ± 14 mg h−1. The size distribution of mosquito coil combustion particles generally fell in the sub-micron range, mostly below 0.3 μm. Salvi et al. (2016) tested three types of mosquito coils in India in a room (5.7 m × 3 m × 2.4 m) with the doors and windows closed, and found that all of the three products emitted massive amounts of particles with a mean PM2.5 concentration of 1031 μg m−3. Wang et al. (2018) characterized the emissions from disc solid, electric liquid, and electric mat types of mosquito-repellent incenses in a large 60-m3 chamber under a ventilation rate of 3.0 m3 min−1. The highest PM2.5 emission rate was found on the disc solid type, which was 10-fold greater than the electric liquid type and five-fold higher than the electric mat type. Notably, Zhang et al. (2010) assessed the particle emissions from a ‘smokeless’ mosquito coil and compared them with four conventional mosquito coils. The results showed that the smokeless mosquito coil had lower emission rates in terms of both the mass of PM2.5 (12.6 ± 0.4 mg h−1) and the total number of particles (14.4 ± 3.0 × 109 particles h−1). With respect to conventional mosquito coils, the PM2.5 and total particle number emission rates were in the range of 62.8 ± 1.8 to 127 ± 2 mg h−1 and (43.4 ± 4.1) × 109 to (69.0 ± 7.3) × 109 particles h−1, respectively. The study also found that nearly all particles originated from burning mosquito coils were smaller than 0.35 μm.
From the far East to the West, incenses are commonly used in temples, churches, and in devotees’ residence (See et al. 2007; Yang et al. 2013). In the Arabian Peninsula, they are also used for improving scents or removing odors in homes (Cohen et al. 2013). As a visible source of particle emissions, burning incenses indoor often leads to substantial increases in particle concentrations in air (Hsueh et al. 2011). Weber (2006) reported that the PM10 and PM1.0 levels underwent a 6.9- and 9.1-time increase during incense burning in a German catholic church. Goel et al. (2017) reported high PM10 mass concentrations in an Indian temple with measurements up to 2184 μg m−3, where 99% of the released particles were PM2.5. Manoukian et al. (2013) reported that burning 0.5 g incense in 30 min could increase the number of ambient particles by 15 times from the background level in a 32.3-m3 rectangular-shaped chamber with an air exchange rate of 0.8 h−1. The particle concentration in air increased from 0.6 ± 0.3 × 104 particles cm−3 to 9.1 ± 0.2 × 104 particles cm−3, with an emission rate of 3.1 ± 0.3 × 1012 particles h−1 during this period and a unimodal size distribution centering at 125 ± 13 nm. Wang et al. (2006) characterized the particles released from incense burning in an 18-m3 stainless steel chamber with an air exchange rate of 0.5 h−1. The results showed that burning church incense generated the highest PM2.5 concentrations (up to 6025 μg m−3), while burning the traditional and aromatic incenses generated an average PM2.5 concentration of 1391 and 502 μg m−3, respectively. See et al. (2007) tested four different religious incense sticks used in eastern countries by Hindus, Buddhists, Taoists, and Shinto followers. The authors identified large numbers of fine particles emitted during incense burning with a magnitude of 1012–1013 particles g−1 and a particle size distribution peaked around 100 nm.
Implications of indoor aerosols on the COVID-19 pandemic
Human respiratory and immune systems impaired by particle inhalation
An early national survey in the United States showed that in general, people spent nearly 90% of their time in various indoor environments (Klepeis et al. 2001). The trend was reinforced in recent surveys that people increasingly adopted sedentary lifestyles by spending more time indoor (Gong et al. 2019; Yang et al. 2019). Since there are many common indoor sources that can emit substantial quantities of fine and ultrafine particles, which can remain suspended and accumulate in air, the wide adoption of sedentary lifestyles in the general population increases their likelihood of exposure to indoor aerosols, especially in enclosed spaces with inadequate ventilation.
The WHO estimated that as many as seven million people die each year due to exposure to fine particulate matter and associated diseases such as asthma, stroke, cardiovascular diseases, lung cancer, chronic obstructive pulmonary diseases, and respiratory infections, including pneumonia (WHO 2018). The mechanisms of airborne particle-induced adverse health effects are believed to mainly involve oxidative stress and inflammation. Oxidative stress mediated by airborne particles can be due to direct generation of reactive oxygen species (ROS) from the surface of particles containing metals, polycyclic aromatic hydrocarbons (PAHs), and so on. Meanwhile, mitochondria, cell membranes, phagosomes, and the endoplasmic reticulum also produce ROS after exposure to particulate matter. Studies showed that ROS could impair the structure and function of bio-macromolecules, including lipids, proteins, and DNAs (Feng et al. 2016; Moller et al. 2010). Excessive ROS may activate signaling pathways and further lead to cell apoptosis or necrosis (Azad et al. 2009). With respect to inflammation, the alveolar macrophages and airway/bronchial epithelial cells are the primary venues to process inhaled airborne particles, and both types of cells produce proinflammatory mediators upon exposure to particulate matter (Fujii et al. 2001; Miyata and van Eeden 2011). Moreover, alveolar macrophages and epithelial cells could interact, resulting in a synergistic increase in the production and secretion of proinflammatory mediators including GM-CSF and IL-6 (Fujii et al. 2002). The two cytokines can magnify local inflammatory responses or even lead to a systemic inflammatory response. Further, exposure to atmospheric particulates can also result in pathology changes in lung and respiratory tract, such as increased cell permeability, inflammatory cell infiltration, bronchial mucosal injury, and alveolar collapse (Liu et al. 2017a; Riva et al. 2011; Wang et al. 2015). To summarize, exposure to those indoor generated ultrafine particles could impair human respiratory tracts via oxidative stress and inflammatory response.
Exposure to respirable particles also impairs the host defense of the human respiratory system, which can lead to increased susceptibility to pathogen infections (Fig. 1). First, inhaled particles can impair the nasal and bronchial mucociliary system and result in low bacterial clearance, which often serves as the first line of host defense (Duan et al. 2013; Jia et al. 2019). Also, the tight junction of airway epithelial barrier can be impaired by oxidative stress, yielding increased permeability which allows invading pathogens to more easily pass through (Liu et al. 2019). Secondly, particle exposure can induce apoptosis and autophagy of lung epithelial cells and alveolar macrophages, and both play important roles in processing inhaled particles (Deng et al. 2013; Deng et al. 2014; Huang et al. 2004). In addition, studies showed that the dysfunctions of cytoskeletal in alveolar macrophages, impaired response of natural killer cells, and disrupted physical and immunological functions of pulmonary surfactants caused by particle exposure all hampered phagocytic defense reaction (Chen et al. 2016; Moeller et al. 2005). Last but not least, particle exposure changes the normal bacterial flora in the respiratory tract, which is an important part of the natural immune defense and prevents the invasion of pathogens or foreign substances through a variety of mechanisms (Yang et al. 2020). Overall, inhaling indoor aerosol particles could further damage the host defense and facilitate the intrusion of pathogens.
Increased COVID-19 morbidity and mortality due to exposure to indoor aerosol particles
Epidemiological studies on outpatient visits, respiratory emergency department visits and hospital admissions manifested a positive association between particle exposure and human respiratory infections (Li et al. 2017b; Strosnider et al. 2019; Xia et al. 2017). Similar conclusions were drawn from related animal models that exposure to particulate matter increased susceptibility to pulmonary infections (Liu et al. 2019; Zhao et al. 2014). It is worth noting that although positive correlations have been observed between outdoor atmospheric particulate matter and COVID-19 morbidity, knowledge on indoor aerosol particles and their implications on the susceptibility of COVID-19 infection and symptom aggravation in patients is limited in current literature. Depending on their sources of emission, indoor aerosol particles may have unique characteristics in terms of their chemical composition, size distribution, electrostatic charges, and aerodynamics, which not only affect their transport in air but their deposition and effects in human airways. Moreover, most indoor emission sources are in close proximity to human occupants in a confined environment, meaning that fresh and active particles may be inhaled by human shortly after their release, as opposed to the homogenous mixture of aged particles present in the open outdoor atmosphere.
As discussed earlier, particle emissions from common indoor sources may contain significant quantities of fine particulates, most of which fall in the sub-100 nm range (i.e., ultrafine particles) (Table 1). Compared with larger atmospheric particles, such as the PM10 and PM2.5, ultrafine particles not only can persist in air for longer periods (Fig. 2) but deposit in the deeper regions of the human airways (Fig. 3). Specifically, ultrafine particles with sizes around 20 nm showed the highest deposition rate in the alveolar region (up to 50%), which is consistent with the sizes of most particles released during candle burning (Pagels et al. 2009). Chen et al. (2016) predicted the fractional depositions of inhaled particles in the human respiratory tract during nose breathing (Fig. 3). Based on the results, most ultrafine particles generated from common indoor emission sources have the highest deposition efficiency in the deeper alveolar region rather than the tracheobronchial and nasopharyngeal regions. In a more recent study, Manigrasso et al. (2018) estimated that the total particle number doses emitted from common indoor sources were deposited in the head (15–17%), tracheobronchial (30–32%) and alveolar (51–56%) regions, with peak number doses reaching up to 1010 particles after a single respiratory act. The study suggested that large quantities of ultrafine particles can directly induce toxicity effects in the lung and even across the alveolar epithelium into the blood vessel.
It is difficult for the human respiratory system to clear ultrafine particles inhaled into deeper regions. Even after 24 h of inhalation, most ultrafine particles could remain deposited in the lung periphery and conducting airways (Moller et al. 2008). Compared with larger particles, these ultrafine particles usually have orders of magnitude higher surface areas absorbing air pollutants (oxidants, organic compounds, metals), which can induce more oxidative stress and inflammation and further impair the host defense system, causing higher morbidity and mortality in respiratory infections. With respect to COVID-19, exposure to airborne particles could elevate the expression of angiotensin-converting enzyme 2 (ACE2), the receptor of SARS-CoV-2 and responsible for its host cell entry (Hoffmann et al. 2020; Lin et al. 2018). Recent studies demonstrated that exposure to cigarette smoke particles upregulated the expression of ACE2 and increased the susceptibility of the host to COVID-19 infection (Brake et al. 2020; Smith et al. 2020).
Indoor aerosol exposure can also aggravate the symptoms of infection in COVID-19 patients. Mishra et al. (2020) reported that exposure to particulate matter could promote the replication of RNA viruses by suppressing the antiviral innate immune response. Zhou et al. (2020) conducted a comprehensive analysis of 30 immunological indicators in the blood of COVID-19 patients (n=33) and elucidated the key mechanism of severe pneumonia cytokine storm caused by SARS-CoV-2. The study showed that after SARS-CoV-2 infection, CD4+ T lymphocytes were quickly activated to become pathogenic T helper (Th) 1 cells and produced GM-CSF. The cytokine environment induced CD14+CD16+ inflammatory monocytes with a high expression of IL-6 and other inflammatory mediators, forming an inflammatory cytokine storm and causing severe immune damage to the lungs and other organs or even quick mortality. These echoed with findings in an earlier study where researchers found that exposure to particles increased the production of inflammatory cytokines including GM-CSF and IL-6 (Fujii et al. 2002). These findings provided mechanistic insights into the positive correlation between particle exposure and symptom aggravation of respiratory pathogen infection, which may explain the consistent trend of high fatality rates observed in COVID-19 patients in regions with air pollution (Paital and Agrawal 2020; Roviello and Roviello 2020; Wang et al. 2020; Wu et al. 2020; Yao et al. 2020). In summary, ultrafine particles released from common sources could deposit in the deeper lung region upon inhaling. Impaired host defense, upregulation of ACE2, and aggravated cytokine storm subsequently caused by these particles would increase the likelihood of COVID-19 infection and fatality.
Can indoor aerosol particles become effective airborne carriers of SARS-CoV-2?
Evidence on viruses, bacteria, and fungi recovered from atmospheric particles suggested that those could act as airborne carriers of human pathogens (Gast et al. 2004; Ryan et al. 2009; Yan et al. 2019; Zucker et al. 2000). Alonso et al. (2014) reported that porcine epidemic diarrhea virus (i.e., a Coronaviridae family member) harbored by airborne particles remained infectious after being transported over long distances, where genetic materials of the virus were detected in the downwind of infected swine farms at a distance of ten miles. Zhao et al. (2019) also reported that avian influenza viruses from infected poultry farms could spread across different states while being carried by fine particulate matter in air. Recently, researchers have postulated that atmospheric particulate matter may play an important role in SARS-CoV-2 transmission. In an early viewpoint, Qu et al. (2020) hypothesized that SARS-CoV-2 can adsorb onto air dusts or particulates and facilitate its long-distance transmission. Similar opinion was proposed by Prather et al. (2020) that viruses can attach to airborne dusts or other air pollutants which can facilitate their dissemination via increased dispersion and modified aerodynamic characteristics. Setti et al. (2020a) further proposed that SARS-CoV-2 may create clusters with atmospheric particles and subsequently enhance the dispersion and accumulation of the virus in air. Direct evidence on the presence of SARS-CoV-2 on airborne particles was reported by Setti et al. (2020b). The authors first detected the genetic materials of SARS-CoV-2 in atmospheric particulates in northern Italy, a region burdened with elevated levels of particulate matter in air and high mortality rates of COVID-19. Based on these findings, the authors suggested that SARS-CoV-2 could form clusters with PM10 present in the outdoor atmosphere.
Bioaerosols containing respiratory pathogens can be generated from the exhaling, talking, coughing, and sneezing of infected individuals, posing risks to co-occupants in enclosed indoor environments (Morawska and Milton 2020). Xu et al. (2017) reported a 107% increase in bioaerosol concentration in a 27-m3 enclosed experimental room after a 30-min presence of five adults without wearing face coverings. The average emission rate was determined to be 8.4 × 105 particles person−1 h−1 in the ‘no-mask’ scenario. When medical masks or N95 respirators were worn by the five occupants, bioaerosol increases were reduced to 31–81% under the same conditions. Buonanno et al. (2020) estimated the quantum emission rates of SARS-CoV-2 infected subjects, where a ‘quantum’ was defined as the dose of airborne droplet nuclei required to cause infection in 63% of susceptible individuals. The study estimated that the expiratory viral load of a virus-infected person when speaking and breathing were 320 and 10.5 quanta h−1, respectively. Droplets and droplet nuclei generated from human respiratory activities may also associate with airborne particles, including aerosol particles commonly found in indoor air. Some researchers recently postulated that aerosol particles originated from some indoor sources could become carriers for SARS-CoV-2. Mahabee-Gittens et al. (2020) underscored the possibility of SARS-CoV-2 virions (average diameter 100 nm) attaching to smoking particles with diameters of 0.2–0.5 μm emitted from e-cigarettes and combustible tobaccos, which may enhance the transmission of the novel coronavirus in smoking environments. Amoatey et al. (2020) highlighted the risk that airborne particles emitted from indoor incense burning may carry SARS-CoV-2 virus and promote the dissemination of COVID-19 in Middle East homes. However, no experimental data or evidence were supplied in those discussions to validate the hypotheses. Given the ubiquitous presence of indoor aerosol particles and the elevated risks of transmitting respiratory pathogens in enclosed environments, an effective transmission route mediated by those invisible agents—once we achieve a better understanding on their roles—would require urgent assessment and public attention in the ongoing pandemic with worsening situations and re-emergent outbreaks reported in countries and regions (Han et al. 2020; Sun and Han 2020; WHO 2020c).
Can indoor aerosol particles become effective carriers of SARS-CoV-2? There are a few important things to consider before we can answer this question. First, particles emitted from common indoor emission sources typically fell in the sub-micron range, where a large part of them are ultrafine (<100 nm) particles (Table 1). It is important to note that these particles are of comparable size or even smaller than the virion of the novel coronavirus (60–140 nm). While they may associate with other particles when suspended in air, it may be difficult for these tiny particles to become carrying substrates of the viruses. Adding to this argument, SARS-CoV-2 viruses rarely enter the air as single, isolated virions. Like other respiratory pathogens, they are contained in various sizes of electrolyte-containing droplets when expelled from mouth and nose. Most of the small-sized human respiratory droplets (e.g., <10 µm) would quickly evaporate into droplet nuclei, typically in less than 1.5 s, and the vast majority of droplets generated by human respiratory activities fall into this particular size range (Wei and Li 2015). Xu et al. (2017) reported that bioaerosols released from human breathing peaked at 1.5 μm, which was consistent with the results reported by Morawska et al. (2009). In the latter study, authors showed the bimodal distributions of droplets released from human breathing, speech, and mild coughing, with two prominent peaks shown at 1.8 μm and below 0.8 μm (Morawska et al. 2009). Droplets generated from human sneezing are often much larger in size. Han et al. (2013) found that the size distribution of sneeze droplets resembled a lognormal profile with a geometric mean size of 360 µm (unimodal distribution) and 74.4 μm (bimodal distribution). The components of human respiratory droplets are complicated. Apart from water and microorganisms, they contain electrolytes, sugars, enzymes, cells and remnants (Stadnytskyi et al. 2020). With the exception of large droplets which would quickly settle on the floor while evaporating (e.g., large sneezing droplets), most human respiratory droplets evaporate quickly to equilibrium sizes—which would depend on the humidity of the ambient air, initial droplet sizes and contents of droplets—or become droplet nuclei and stay airborne. It was estimated that the sizes of those droplet nuclei were typically about half of those of the original droplets (Liu et al. 2017b; Nicas et al. 2005). Meanwhile, limited studies pointed out that particles released from some indoor emission sources would undergo a coagulation process, reaching larger particle sizes although they still remained in the sub-micron range (Table 1). In those cases, the virus-laden droplet nuclei would still be significantly larger than those coagulated aerosol particles.
Given the fact that both the virus-laden droplet nuclei and indoor aerosol particles can suspend and accumulate in air for long periods of time (Fig. 2), they may form ‘clusters’ or ‘aggregates’ and subsequently alter the aerodynamic characteristics of their parent particles, causing either longer suspension or faster settlement via inertial impaction, electrostatic attraction, or repulsion (He and Han 2020; Yu 2014). Such coalescence clusters may protect the virus inside from radiation or toxic chemicals (Zuo et al. 2013). Setti et al. (2020a) pointed out that coalescence of droplet nuclei and aerosol particles is more likely to occur in environments with high relative humidity. In a set of experiments assessing bioaerosol emissions from human exhaled breath, Xu et al. (2017) consistently observed abnormal reductions in total particulate matter number concentrations during the increases in bioaerosol particles in air. Although no interpretation was offered in the study, a plausible explanation for this phenomenon is that bioaerosols generated from human activities formed aggregates with indoor particulate matter and reduced the total number of particulates suspended in air. It is unclear whether those coalescent particles settled on surfaces or objects, or remained suspended in air after getting better aerodynamic characteristics. Further evidence was found in aerosol sampling in commercial airplanes, health centers, and daycare centers during flu seasons, where large numbers of genome copies of influenza A virus (similar to SARS-CoV-2 in size) were detected in their indoor air (Fig. 4). Of these, 64% of viral genome copies were detected on airborne particles smaller than 2.5 μm, a size range allowing long periods of particle buoyancy in air (Yang et al. 2011). Unfortunately, in this study authors did not analyze the sources and characteristics of those virus-laden particles, and thus no conclusion could be drawn on whether the detected viruses in air were from virus-laden droplet nuclei or coalescent clusters formed by indoor aerosols, droplet nuclei, or both. In other words, while virus-laden droplets and droplet nuclei can interact with indoor aerosol particles, whether these interactions would facilitate the airborne transmission or the settlement of the virus and how they would affect the viability of the virus in common indoor environments are largely unknown. In the midst of a prolonging pandemic, these present some urgent questions for scientists and public health authorities on the airborne transmission of COVID-19 and other human respiratory pathogens.