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Aerosol transmission of influenza A virus: a review of new studies

Raymond=20 Tellier1,2,*

¹
Provincial Laboratory for Public Health of Alberta, Calgary
, Canada
²
Department of Microbiology and Infectious Diseases
, University of Calgary,=20
Calgary
, Canada

*r.tellier{at}provlab.ab.ca

Abstract

Over the past few = years, prompted by pandemic preparedness initiatives, the debate over the modes of transmission of influenza has been rekindled and several reviews have appeared. Arguments supporting an important role for aerosol transmission that were reviewed included prolonged = survival of the virus in aerosol suspensions, demonstration of the low infectious dose required = for aerosol transmission in human volunteers, and clinical and epidemiological observations were disentanglements of large droplets and aerosol transmission was possible. Since these reviews = were=20 published, several new = studies have been done and generated new data.=20 These include direct demonstration=20 of the presence of influenza viruses in aerosolized droplets from the = tidal breathing of infected persons and in the air of an emergency department; the establishment of the guinea pig model for influenza transmission, where it was shown that aerosol transmission is important and probably modulated by temperature and humidity; the demonstration of some genetic determinants of airborne transmission of influenza viruses as assessed using the ferret model; = and mathematical modelling studies that strongly support the aerosol route. These recent results = and their implication for infection control of influenza are discussed in this review. =

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1. Introduction

Concerns about = an influenza pandemic have been recently rekindled by the = emergence=20 in southeast Asia=20 of highly pathogenic strains of avian influenza A (H5N1) with pandemic potential. These concerns have been vindicated by the emergence of a=20 pandemic caused by a new influenza A(H1N1) virus of swine origin, the full impact of which remains unclear at the time of the writing of this article.

In turn, these concerns have=20 generated a renewed interest in the study = of the transmission modes of influenza not only for a better understanding of the pathogenesis of the disease but also for the rational design of infection-control strategies. Three modes of transmission have been postulated, which are not mutually exclusive: aerosol transmission, transmission by large droplets and self-inoculation of the nasal=20 mucosa by contaminated hands. The mode of transmission that, arguably, has the greatest impact for infection control is aerosol transmission since it requires = specialized personal protective equipment (PPE), e.g. = N95=20 respirators, and procedures.

There is considerable support=20 in the scientific literature = for a contribution of aerosol transmission to the spread of influenza A, which has been reviewed elsewhere (Tellier=20 2006). Briefly, supportive evidences include the prolonged = persistence of infectivity in aerosolized influenza A virus at low humidity, the transmission to volunteers of influenza by aerosols, reproducing the full = spectrum of disease, at doses much smaller than the doses required by intranasal=20 drop inoculation (which = mimics large droplet transmission), and the interruption of transmission of influenza by blocking the aerosol route through UV irradiation of upper room air. In addition, whereas intranasal=20 zanamivir prophylaxis protected against intranasal=20 drop inoculation in the = laboratory, it is ineffective against natural transmission; in contrast, zanamivir prophylaxis by inhalation was effective.

Over the past few = years many new studies have been published which lend = further support=20 to the hypothesis that aerosol transmission plays an important role in the spread of influenza. These new studies and their implications are reviewed here.

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2. Definition of aerosols

Fundamentally, aerosols are suspensions in air (or in a gas) of solid or liquid particles small enough that they will remain airborne for a prolonged period of time because of their low settling velocity. The = settling=20 velocity in still air can be calculated using Stokes' law (Hinds=20 1999); for example, a 3 m fall takes 4 min for a 20 =C2=B5m particle (aerodynamic diameter), 17 min for 10 =C2=B5m = and 67 min for 5 =C2=B5m.

When studying bioaerosols=20 generated by human subjects, it is important to distinguish between the = initial diameter of particles and the diameter after evaporation of water in ambient air; the resulting desiccated particles are termed =E2=80=98droplet = nuclei=E2=80=99; for particles with an initial diameter <20 =C2=B5m the evaporation occurs in <1 s (Nicas et al. 2005; Xie=20 et al. 2007) = and the diameter shrinks to a little less than half the initial diameter (Nicas et al. 2005).

Another = important consideration for the pathogenesis of infectious diseases acquired by aerosols is the penetration of the respiratory tract. Particles of 5 =C2=B5m or less have a significant penetration into the respiratory tract all the way to the alveolar region (30% penetration for 5 =C2=B5m particles); penetration into the alveolar region rapidly diminishes beyond 5 =C2=B5m, = but=20 significant penetration into the tracheobronchial region still occurs for particles in the 5=E2=80=9310 = =C2=B5m range (for 10 =C2=B5m, 50% = penetration) but diminishes rapidly after that. At 20 =C2=B5m and beyond there is essentially no penetration below the trachea (Hinds=20 1999). Of course, = penetration is not the same thing as deposition and only a fraction of the penetrating particles will be deposited, the = remainder being exhaled back (Yu=20 & Diu 1983). All = these=20 considerations likely = explain why aerosols are defined differently by various authors. There is essential agreement that particles with an aerodynamic diameter of 5 =C2=B5m or less are aerosols, whereas particles >20 =C2=B5m would be = large droplets. Some authors define aerosols as =E2=89=A410 =C2=B5m or even = =E2=89=A420 =C2=B5m (Knight=20 1973; Treanor 2005); particles between 5 and 15 to 20 =C2=B5m have also been termed = =E2=80=98intermediate=E2=80=99 (Couch=20 et al. 1966; = all values refer to the aerodynamic diameter; for bioaerosols, they refer to the aerodynamic diameter after evaporation). When reviewing the = literature, it is therefore important to verify the size of the particles being studied and the authors' definitions.

The issue of = long-range transmission has been contentious. Because aerosols settle very slowly in = still air, they are easily carried over long distance by turbulences and air currents, and this may potentially cause long-distance infections. Certainly, the demonstration of long-range infection implies aerosol transmission. The converse, = however, is not=20 necessarily true; aerosol particles are rapidly diluted, and are removed by ventilation; the infectious risk is = critically affected by parameters such as the infectious dose, the amount of infectious particles aerosolized at the source, and the rate of biological decay of the infectious agent. For influenza, a quick =E2=80=98back of the envelope=E2=80=99 type of calculation suggests that even for patients with a high viral load the amount of viruses aerosolized in a single sneeze is in fact quite small and would be rapidly diluted as the aerosol disperses; yet, because the infectious dose by aerosol is so small, the infectious risk in = proximity of the patient would be significant (Tellier=20 2007). It should also be = pointed=20 out that a low frequency of long-range transmission can be extremely difficult to = demonstrate (or rule out), especially if the disease considered is widely prevalent in the community (as is typically the case with influenza). For example, long-range transmission of smallpox could be unequivocally demonstrated only during a hospital outbreak at a=20 time when the disease had long been eradicated from the community (Gellfand & Posch 1971). =

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3. Direct detection of = influenza viruses in bioaerosols from patients

Generation of a=20 large number of aerosol particles by coughing or sneezing = has been documented for a long time (reviewed in Nicas et al. 2005). A recent study (Yang et al. 2007) confirmed yet = again the generation of a=20 large number of aerosol particles, and showed a significant heterogeneity between = individuals in the amount and size distribution of aerosols. Recently, the technique = of Schlieren photography has been used to visualized the aerosols emitted by coughing (Tang & Settles 2008). It is = often less appreciated that exhalation during normal breathing also produces aerosol particles. A recent study (Edwards et al. 2004) has confirmed the production of aerosol size particles by normal breathing, and confirmed that the size of the majority of the particles exhaled by mouth is 1 =C2=B5m or less. = This is=20 explained by the fact that aerosol particles from normal breathing are generated in the lower respiratory tract (LRT), and the larger particles tend to be retained through impaction or deposition. Another remarkable finding is that there is considerable heterogeneity in aerosol production between = individuals, consistently over time (Edwards et al. 2004). Although coughing and sneezing produce more aerosols per breathing manoeuvre than normal breathing, since normal breathing is continuous it would account for a significant fraction of the bioaerosols produced over the course = of a=20 day (Fiegel=20 et al. 2006). =

Direct measurement of influenza viruses in aerosols produced by cough or = sneezing has not been reported in the = literature. This is in part because of the significant experimental difficulties in working with = bioaerosols, including the low = concentration of particles and, in the case of influenza virus, the relative insensitivity of virus detection by culture methods, = the=20 lability of the viruses and potential inactivation caused by the aerosol-sampling methodology. It should be = noted=20 however that in the laboratory setting, infectivity measurements of aerosolized influenza viruses could be reliably predicted from the infectious = titre=20 of the viral culture fluid used to generate aerosols, over several orders of magnitude (Alford et al. 1966). The development = of sensitive detection assays based on reverse transcriptase=E2=80=93polymerase chain reaction (RT=E2=80=93PCR) now permits = much more=20 sensitive detection of = viral particles. Using this methodology, = Fabian and colleagues (Fabian et al. 2008) have recently directly detected = influenza virus RNA in aerosol particles generated by normal breathing in patients with influenza and collected through an oronasal=20 facemask. Patients were selected on the basis of symptoms and a positive rapid detection test for influenza (given the relative insensitivity of these tests, in all likelihood these patients had a=20 high viral load). Out of 12 patients subjected to analysis, four had detectable influenza virus RNA in exhaled breath (three with influenza A, one with influenza B); as measured by quantitative RT=E2=80=93PCR, one patient with influenza A exhaled 20 RNA copies per minute, the three = others=20 exhaled less than 3.2 RNA copies per minute. Evaluation of the size distribution of the particles showed that 87 per cent of the exhaled particles had a=20 diameter of less than 1 =C2=B5m, with less than 0.1 per cent larger than 5 =C2=B5m (Fabian et al. 2008).

An important limitation of such a study is that RT=E2=80=93PCR cannot establish the infectivity of the viral particles detected; one must make inferences based on other studies that looked at the biological decay of aerosolized influenza viruses (e.g. Hemmes=20 et al. 1960,1962).=20 Based on their RT=E2=80=93PCR = assay and the influenza virus stock they used for calibration, Fabian et al. (2008) established a ratio of 300 copies per tissue culture = infectious=20 50 per cent (TCID₅₀), which is well within previously = published=20 estimates of 100=E2=80=93350 or 650 (van Elden et al. 2001; Wei=20 et al. 2007). = This would=20 translate, for the highest producer in = the study,=20 to a rate of 4 TCID₅₀ = h^=E2=88=921 in=20 exhaled breath; the human infection dose 50 per cent=20 (HID₅₀) by aerosol = inoculation (using particles of 1=E2=80=933 =C2=B5m) has previously been measured as between 0.6 and 3 TCID₅₀ (Alford et al. 1966).

Another = significant recent observation on the occurrence of naturally produced influenza bioaerosols is the report of Blachere and colleagues (Blachere et al. 2009) of the detection of aerosolized influenza viruses in a hospital emergency department. Aerosol samples were collected over the = course of 4=E2=80=935 h, during the month = of February, using aerosol sampling that allowed for size fractionation. Samples were analysed with a quantitative RT=E2=80=93PCR method. The = authors reported the detection = of influenza A RNA in 14 samples; the largest amounts of RNA recovered were equivalent to 15 532 TCID₅₀ = in the=20 fraction of particles greater than 4 =C2=B5m, and 13 426 TCID₅₀ in the = fraction of particles in the 1=E2=80=934 =C2=B5m = range (Blachere et al. 2009). The description = of the method for quantitative measurements in this study is = imprecise, with=20 the unfortunate = =E2=80=98assumption that 1 TCID₅₀ is = equivalent to one viral RNA copy=E2=80=99. However, a careful reading of the previous study by this = group, which=20 describes in detail their = quantitative RT=E2=80=93PCR assay, reveals that the quantitative PCR was in fact calibrated in TCID₅₀ by using = serial dilution of a=20 virus preparation quantitated in TCID₅₀ = ml^=E2=88=921 (Blachere et al. 2007). The viral preparation used was the live attenuated vaccine, Flumist, containing = 10^6.5=E2=80=9310^7.5=20 TCID₅₀ ml^=E2=88=921; the authors assumed 10⁷ = TCID₅₀=20 ml^=E2=88=921 in their calculation and therefore the amounts reported in Blachere et al. (2009) may have to be adjusted (upward or downward, by a factor of at most 10^0.5 or approx. 3.16-fold), but even so = remain impressive when compared with the HID₅₀ by = aerosol (Alford et al. 1966). As was the case with the study of Fabian et al. (2008) above, detection by RT=E2=80=93PCR = alone does not imply infectivity, = but it is=20 noteworthy that on the days where samples were obtained, the relative humidity (RH) was 30 =C2=B1 3.3 per cent (Blachere et al. 2009), well under the = 40 per=20 cent threshold below which aerosolized=20 influenza virus infectivity decays slowly (Hemmes=20 et al. 1960). =

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4. Observations from = animal infections with influenza

One of the most = interesting=20 recent developments in the field has=20 been the establishment of the guinea pig model for influenza transmission by the group of Palese and co-workers (Lowen=20 et al. 2006). It = was shown that guinea pigs are readily infected by human strains of influenza A virus, without prior viral adaptation, that the virus replicates in both the upper and lower RT, and that the virus is readily transmitted between guinea pigs. The infection can be asymptomatic or not, depending largely on the strain of guinea pig used; Hartley strain guinea pigs were asymptomatic, whereas strain 13 animals displayed weight loss, hair loss, lethargy and hypotermia (Lowen=20 et al. 2006). = However, in=20 another study by the same group, strain 13 animals were also asymptomatic (Mubareka et al. 2009). Importantly, coughing and sneezing do not occur.

In their initial = study Lowen=20 et al. demonstrated several instances of influenza transmission between guinea pigs, including when the source = animal and the contact were in different cages separated by 91 cm (Lowen=20 et al. 2006). It = may be argued that transmission over such a distance rules out large droplet transmission and therefore would have to be ascribed to aerosol transmission. In many infection control guidelines = for influenza, it is stated that large droplets do not travel farther than 3 ft (=E2=80=98the three-feet = rule=E2=80=99), although this was not rigorously demonstrated. Xie et al. recently performed an analysis of dispersion of respiratory droplets (Xie=20 et al. 2007); in = their=20 model, they assumed that respiratory droplets behave like droplets of 0.9 per cent NaCl in water. Respiratory droplets initially all move forward with the exhaled air jet; very large droplets leave the jet quickly and fall on the ground; = =E2=80=98intermediate size=E2=80=99 large droplets leaving the jet desiccate in ambient air (partially or completely, depending on = their size);=20 and small droplets completely desiccate within the jet. They calculated that, using a horizontal jet emitted at a=20 height of 2 m, at an RH of 50 per cent, the horizontal distance travelled by particles of initial diameter of 30=E2=80=9350 =C2=B5m is less = than a=20 metre if the initial velocity = of the jet is 1 m = s^=E2=88=921 (typical of normal breathing), and more than 6 m if the initial jet velocity is 50 m = s^=E2=88=921=20 (typical of sneezing); larger particles travel less far because they fall on the ground quickly, and smaller particles desiccate into aerosol-size particles. Increase in RH decreases the horizontal distance travelled by non-aerosol droplets, and conversely (Xie=20 et al. 2007). In = the=20 guinea pig experiments = described above, obviously the height at which the jet was emitted was considerably lower than 2 m, and they do not sneeze or cough = when infected=20 with influenza; it would = therefore=20 appear that 91 cm is too far to be explained by large droplets transmission. Two missing measurements prevent a definitive conclusion: the RH for = those=20 experiments was not = specified; it=20 was noted that transmission followed the airflow direction but the velocity = of the airflow was not stated (Lowen=20 et al. 2006). = Again using the guinea pig model, the same group described recently a stronger experimental evidence for aerosol transmission when they documented = instances of transmission with the cage of the contact animal above the cage of the source animal at a=20 distance of 80 or 107 cm (Mubareka et al. 2009). Another important observation in this study is that different influenza strains differ considerably in their capacity for aerosol transmission.

Palese and colleagues also used their guinea pig model to study the effects = of temperature and RH on transmission in two additional studies (Lowen et al. 2007,=20 2008)=20 where they compared contact transmission and airborne transmission. Of note in these two studies airborne transmission was assessed with the source and contact guinea pigs in two different cages side by side; this short = distance makes it impossible to rule out = a contribution from large droplets. Indeed, the authors explicitly stated that they used the term = =E2=80=98aerosol=E2=80=99 to encompass both large droplets and droplet nuclei. They showed = that airborne transmission (large droplets and/or droplet nuclei) was enhanced at low temperature (5=C2=B0C) and that high temperature (30=C2=B0C) interrupted airborne transmission at all values of RH. At 20=C2=B0C, transmission was highly efficient at an RH of 20 and 35 per cent, low at 50 per cent, efficient again at 65 per cent and absent at 80 per cent. The authors tentatively attributed the effect of low temperature to the increased viral load observed in the animals at this temperature (Lowen=20 et al. 2007), = but proposed=20 no explanation for the effect of high temperature, which interestingly enough = did not=20 interfere with contact transmission between animals in the same cage (Lowen=20 et al. 2008). = As the authors noted, the effect of RH is reminiscent on studies = of infectivity decay in influenza virus aerosols. Hemmes and colleagues, using aerosols in the 5=E2=80=936 =C2=B5m = range, showed that the biological decay of aerosolized influenza is low at RH < 40 per cent, but rapidly increases with RH (Hemmes et al. 1960,=20 1962).=20 However, Schaffer et = al. did observe a biphasic effect of RH, with the greatest stability at an RH of 20 per cent, the greatest decay at 50=E2=80=9360 per cent, and a return to moderate stability at greater RH; unfortunately, they did not state the size of the particles in their aerosols (Schaffer et al. 1976).

Using the ferret model, Van=20 Hoeven and colleagues showed that not all influenza strains are capable of =E2=80=98airborne transmission=E2=80=99, by which = they meant large droplets and/or aerosols, as their experimental set-up did not allow for the distinction (Van Hoeven et al. 2009); it should be = noted,=20 however, that aerosol transmission of influenza between ferrets was demonstrated a long time ago (Andrewes & Glover 1941). = An avian influenza strain was shown to be incapable of transmission between ferrets, by = either=20 direct contact (co-caged animals) or large droplets and/or aerosols. By reverse genetics, the = HA and NA genes from the 1918 A(H1N1) pandemic strain were substituted to those of the original virus (thereby changing the sialic acid receptor affinity), which resulted in direct = contact transmission between ferrets, but = still not=20 by large droplets/aerosols. The latter was finally achieved by the subsequent addition of the PB2 gene from the = 1918 A(H1N1) virus. The impact of the PB2 gene is = presumably mediated through higher replication rate in the cells of the respiratory tract. Using the guinea pig model, Steel and colleagues also showed how mutations in the PB2 gene = allow for efficient transmission, including through the = large droplet and/or aerosol route (Steel=20 et al. 2009). = Another example of strain differences in their capacity for large droplets and/or aerosol transmission is provided by the = study of Bouvier et al. using the guinea pig model. They showed that oseltamivir resistance in an A(H3N2) strain modifies its transmission efficacy. The wild-type transmitted efficiently by both = contact and large droplets/aerosols, but introduction of a=20 single or two amino acids mutation conferring oseltamivir resistance significantly decreased or completely interrupted, = respectively,=20 droplet transmission while = contact transmission was unaffected (Bouvier=20 et al. 2008). In = a similar manner, Sorrell et al. have shown that re-assortant influenza viruses carrying the surface proteins of avian A(H9N2) on a backbone of human A(H3N2) (which therefore included = a PB2 gene well adapted to mammalian hosts) could be rapidly adapted to ferrets. The authors observed ferret-to-ferret = transmission by direct contact, and between ferrets in adjacent cages, thereby demonstrating transmission by aerosol and/or large droplets (Sorrell=20 et al. 2009). =

Also using the = ferret model,=20 Munster et al. = compared experimental infections with the seasonal A(H1N1) and the swine origin A(H1N1) currently responsible for = an ongoing pandemic; from the point of view of transmission, again using an experimental set-up with adjacent cages, they showed that both strains were equally proficient in aerosol and/or large droplet transmission (Munster=20 et al. 2009). In = contrast however, Maines et al. (2009), who also compared seasonal A(H1N1) with the swine origin A(H1N1), found that the latter was less proficient at aerosol/large droplet transmission (six of nine contacts infected, compared with three of three for seasonal A(H1N1); Maines et al. 2009).

As a last example involving animal transmission, a recent outbreak of equine influenza A(H3) in Queensland, Australia=20 offered a unique opportunity to study the = spread of the virus in a region of the world where it was previously absent (Davis et al. 2009). The cluster = of equine influenza started at a=20 quarantine facility and eventually involved 437 other premises, = 81 per cent=20 of which were not contiguous = to a premise with cases. Distances between non-contiguous = premises were=20 often several kilometres (most within 5 km but = there=20 was one instance of a=20 13 km separation). Strict quarantines and a standstill were put in place at the onset of the outbreak, precluding transfer of horses between premises in the = region.=20 Transfer of fomites between premises was pre-empted by extensive = media and publicity campaigns; surveillance reports showed that compliance was high. The authors further note that the observed geographic spread was consistent with the = predominant direction of wind patterns at the time (Davis et al. 2009). All in all, an outbreak with several instances of transmission consistent with and suggestive of aerosol transmission which, as the authors note in their discussion, = has been implicated before in equine influenza transmission. In fact, experimental transmission of equine influenza to horses has been shown to be more reliably achieved by aerosol inoculation than by intranasal=20 instillation (Mumford=20 et al. 1990). =

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5. Mathematical modelling

As mathematical models for infectious diseases become increasingly sophisticated, it is only natural that they would be brought to bear on the problem of influenza transmission.

Recognizing that = aerosol, large droplets and self-inoculation by contaminated hands are not mutually exclusive, Nicas and Sun built a Markov chain model incorporating these three modes of transmission and identifying several parameters that would need to be measured experimentally in order to use the model for = a specific pathogen. For purposes of illustration they ascribed values to several parameters for a hypothetical pathogen and showed that for that pathogen, if a healthcare worker spent 15 min at the bedside of a=20 patient without coughing or = sneezing=20 events, the probability of infection by self-inoculation with contaminated hands was 0.029 and by aerosols in the room air was 8.3 =C3=97 = 10^=E2=88=926 (taking 5 =C2=B5m particles as =E2=80=98representative=E2=80=99). Coughing within = 0.6 m of the healthcare worker is associated with a probability of infection of 0.14 by large droplets; for a 15 min stay in the room, estimating the probability of coughing and of the proximity at any given time, the probability of transmission by large droplets originating in a cough is 0.021. A similar treatment for aerosols shows, for a 15 min visit, a probability of 4.5 =C3=97 = 10^=E2=88=924 (Nicas & Sun 2006). Of course, these probabilities depend critically on the values ascribed to the parameters; for example, the infectivity parameter =CE=B1, calculated from the HID₅₀, is = assumed to be the same for all routes. But as the authors themselves point out, influenza A virus is a counterexample since the HID₅₀ by = aerosol is about 100 times less than by large droplets, as reviewed (Tellier=20 2006).

Similarly, Atkinson and Wein built a model of multiple modes of transmission, based on an infinite set of differential equations, and estimated parameters using the available literature and various hypotheses (Atkinson & Wein 2008). In = a household transmission model, initially omitting transmission at close range, a comparison of transmission through hands contaminated by fomites and transmission by aerosols showed aerosol transmission to be dominant. The authors also presented a detailed analysis of the transmission of influenza by a cough or a sneeze at close range (60 cm) from an infected patient with a peak shedding of 2.88 =C3=97 10⁷ = TCID₅₀,=20 with 99 per cent of shedding = occurring=20 in sneezes and 1 per cent in = cough. The=20 authors separately analysed the infection probability from inhalation of particles <20 =C2=B5m, of particles between 20 and 200 =C2=B5m, and from droplets landing directly on the mucosa because of their trajectory. A first analysis shows that for a cough, the probability of infection is 0.244 with the = greatest contribution from particles of 20=E2=80=93200 =C2=B5m (transmission fraction of 0.91); for a sneeze the probability would be 0.9999 with = equal contribution from particles <20 =C2=B5m, from = particles between 20 and 200 =C2=B5m, and from droplets landing directly (assuming that the contact person is breathing in at the time of the cough or sneeze). The authors proposed a different analysis where the distribution of particles in the cone-shaped cloud caused by coughing or sneezing is = uneven=20 because of the different stopping distances of different size particles. With this analysis, the probability for a cough is 0.011 and for a sneeze 0.981, all caused by direct deposition (Atkinson & Wein 2008). The = stopping=20 distance is the maximum distance travelled by an aerosol particle in still air for a given initial speed (Hinds=20 1999). The application of this concept in Atkinson & Wein (2008) = appears incorrect, since following = a cough or a sneeze particles are carried by a jet of air, and in fact bioaeorosols from the respiratory tract are created by air jets over the airway lining fluid (Fiegel=20 et al. 2006). = The use=20 of stopping distance for particles in a jet of air is more relevant when the jet changes direction, in the context = of an analysis of impaction (Hinds=20 1999). For the horizontal = distance travelled by particles expelled from the = respiratory tract, the analysis of Xie=20 et al. (2007), = reviewed=20 above, appears more convincing.

Both Nicas & Sun (2006) and Atkinson & Wein (2008) = calculated the aerosolized infectious agents in coughs and sneezes from published studies = of particles distribution in coughs = and sneezes and from measured infectious titres in nasal=20 washing. While this appears adequate for sneezing, it may be an underestimate for cough. The fluid aerosolized in a cough comes in part from the LRT; in a patient with an LRT infection with influenza, it may well be that the concentration of virus is greater in the fluid lining the LRT = than the nasal=20 mucosa; to my knowledge this = has not been measured, but in humans and in mice the surface ratio of epithelial surfaces between the LRT and the nasal=20 mucosa is roughly 1000, = whereas the ratio of the volumes of fluid and mucous lining the epithelium in = the LRT=20 and nasal=20 mucosa is approximately 9 (Ito=20 et al. 2003). =

In a recently = published=20 study, Nicas and Best provided a mathematical analysis of the risk of influenza infection by hand-to-face contact. This mode of infection, which has been documented for some = respiratory viruses, has been deemed plausible since Bean et al. (1982) demonstrated the persistence of influenza virus infectivity on hard non-porous surfaces for 24=E2=80=9348 h, = theoretically allowing for hand contamination and infection by self-inoculation. One problem with that proposed route of infection is that the same study also showed that on the hands, the infectivity titre of a=20 suspension of influenza A viruses drops by two to three logs = within 5=20 min (Bean et al. 1982); similarly, Schurmann and co-workers documented a decay of three logs on the hands within 12 min (Schurmann & Eggers 1983); thus = the=20 interval for self-inoculation is relatively short. Nicas and Best made a systematic analysis of this possible mode of transmission, including a measurement of the frequency of hand-to-face contact by videotaping volunteers for several hours, and estimating other relevant parameters from the literature. As an example using influenza A virus, for a 30 min exposure in an environment with contaminated surfaces, followed by a 30 min decay period before hand-to-face contact, the probability of infection is estimated at 0.00 011 (Nicas & Best 2008). Of course, as the authors noted, the estimate of several parameters remains uncertain. For example, the infectivity parameter =CE=B1 was estimated from a study of experimental infection by nasal=20 instillation in volunteers = that was one of the first successful reports = of reliable infection by nasal=20 instillation, but which used = doses in=20 the range of 790=E2=80=9310 000 = TCID₅₀, which are larger than the more recent estimates of HID₅₀ by nasal=20 instillation, namely 127 TCID₅₀ and 320 TCID₅₀ (Couch = et al. 1971,=20 1974).=20 Taking HID₅₀ as 127 TCID₅₀, one = can re-calculate =CE=B1 =3D 5.46 =C3=97 = 10^=E2=88=923 and the probability of infection in the scenario above is 0.01, still rather low. Thus it appears unlikely that in most circumstances hand-to-face contact is a major route of transmission for influenza (Nicas & Best 2008).

Shaman and Kohn re-examined the experimental data=20 of several studies to question whether RH = is in=20 fact a better parameter to predict infectivity = persistence=20 of aerosolized influenza than absolute humidity (Shaman=20 & Kohn 2009). Hemmes et al. concluded that RH was a=20 determining factor based on the sharp transition at about 40 per cent RH for the values of the death rate constant when plotted against RH (Hemmes et al. 1960,=20 1962).=20 Analysing the data=20 from experiments on transmission of influenza between guinea pigs (Lowen et al. 2007,=20 2008),=20 Shaman and Kohn showed a better statistical correlation with vapour pressure compared with RH; a similar re-analysis of the data=20 from Harper (1961) on infectivity = decay in aerosolized influenza viruses also showed a better correlation using vapour pressure (Shaman=20 & Kohn 2009). When considering aerosol transmission, the latter is the strongest argument put forth by Shaman=20 and Kohn (even though Harper did not state the size of the aerosols studied) since, as noted by Lowen and colleagues, and as reviewed above, the experimental set-up in these guinea pig studies did not allow for the contributions of aerosol and large droplets to be disentangled. Other studies reviewed were = found to=20 be consistent with the notion that=20 vapour pressure was a=20 better parameter, although it is unclear what contributions the cited studies = by=20 Mitchell et al. = could bring=20 since they were all conducted = at a=20 temperature of 70=C2=B0F and an RH of 75 per cent (Mitchell=20 et al. 1968; Mitchell=20 & Guerin 1972).

The questions raised in this=20 study are however important from a fundamental point of view, as the biochemistry of the effect of humidity on aerosolized influenza viruses (or other enveloped viruses for that matter) remains incompletely understood. = Furthermore,=20 Shaman and Kohn, noting the agreement between several studies that low humidity is associated with prolonged infectivity = persistence=20 of aerosolized influenza virus but that the decay accelerates at higher humidity, suggest that humidification measures for infection control may be warranted (Shaman=20 & Kohn 2009). Other engineering measures would be expected to = interfere with=20 aerosol transmission of influenza, starting of course with adequate ventilation and mechanical ventilation (Liao et al. 2005; Qian et al. 2006; Furuya 2007; Bolashikov & Melikov 2009; Gao et al. 2009). Recently, = interest in=20 upper room air UV irradiation has been rekindled (McDevitt=20 et al. 2008); it = is=20 interesting to note that 50 = per cent RH=20 is considered optimal for = this method,=20 whereas RH above 75 per cent significantly decreases its performance (Bolashikov & Melikov 2009). = Other=20 methods of engineering = control include=20 induct UV irradiation, filtration and more speculative methods such as photocatalytic oxidation, desiccant rotor and plasmacluster ions (Bolashikov & Melikov 2009). =

Previous=20 Section Next=20 Section

6. Discussion

Increasing = evidences point=20 towards a role for aerosol transmission in the spread of influenza, at least over short distance where exposure to both aerosol and large droplets occurs. In most = settings where=20 there is adequate ventilation, long-range transmission does not appear to occur frequently. This = distinction=20 of =E2=80=98short-range aerosol transmission=E2=80=99 is not merely = academic; aerosolized particles would readily penetrate or circumvent ordinary surgical masks, and penetration of aerosolized influenza viruses into the LRT where they = can initiate infection would account well for the association of aerosol transmission and severe disease.

The recent results reviewed here include direct detection = of aerosolized influenza virus (albeit by RT=E2=80=93PCR) in patients' exhaled breath and in the ambient air of an emergency department room; the demonstration of aerosol transmission between guinea pigs of human influenza strain; and mathematical modelling studies predicting = an important contribution of aerosol transmission, whereas a=20 rigorous mathematical analysis of transmission by hand-to-face contact suggests that it plays but a minor role.

Studies using guinea pig=20 models have further confirmed = the=20 effect of temperature and humidity on influenza transmission by respiratory droplets, although the experimental setting was such that the role of aerosol and large droplets could not be = disentangled; the authors made a very good case that the relative contribution of different modes of transmission may be different depending on the = setting=20 (including temperature and humidity). These studies, and the physical properties of aerosols, suggest that in addition to PPE, several engineering control methods = implemented in=20 hospitals and other institutions could be = beneficial.

Studies using the guinea pig=20 model and the ferret model = have demonstrated differences between strains in their capacity for droplets (aerosols and/or large droplets) transmission, including genetic = characterization of some required mutations. This exciting development = is=20 expected, as our knowledge = increases, to allow for better prediction of the pandemic potential of new influenza strains.

The accumulating evidence for an important contribution of the aerosol route in the transmission of influenza implies that infection-control protocols must = take it into account, and especially during a pandemic. As an additional consideration, it may well be that aerosol transmission is responsible for the = most=20 severe cases of disease involving viral infection of the LRT. Whereas engineering control methods = are useful, and indeed necessary, to prevent long-range infections, they would be = of little help to healthcare workers in close proximity = of a=20 patient to provide care. Precautions should include the use = of an N95 respirator (or better) when appropriate, including in close proximity = of an infected patient.

Finally, a note on the heterogeneity of patients' contagiousness. It was already well established that not all patients have the same viral load (Murphy=20 et al. 1973); = this=20 heterogeneity is now compounded by the demonstration of heterogeneity between subjects = of the size distribution and quantity of aerosol particles generated in coughing and sneezing, and during normal breathing. This heterogeneity must be = remembered=20 when establishing = infection-control=20 protocols, and taken into account for mathematical modelling (Lloyd-Smith=20 et al. 2005; Pourbohloul=20 et al. 2005). =

Previous=20 Section Next=20 Section

Acknowledgements

The opinions expressed in this article are those of the author and do not necessarily reflect the opinions of the institutions with which he = is affiliated.

Previous=20 Section Next=20 Section

Footnotes

One contribution to a=20 Theme Supplement =E2=80=98Airborne transmission of disease in hospitals=E2=80=99.
- Received July 20, 2009.
- Accepted=20 August 24, 2009.=20

Previous=20 Section

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Published=20 online before print September = 22,=20 2009, doi: 10.1098/=E2=80=8Brsif.2009.0302.focus=20 rsif20090302=20

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Abstract
1.=20 Introduction
2.=20 Definition of aerosols
3.=20 Direct detection of influenza viruses in bioaerosols from = patients
4.=20 Observations from animal infections with influenza
5.=20 Mathematical modelling
6.=20 Discussion
Acknowledgements
Footnotes
References

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Online ISSN: 1742-5662 | Co= pyright =C2=A9=20 The Royal Society 2009

Aerosol transmission of influenza A virus: a review of new studies

Abstract

1. Introduction

2. Definition of aerosols

3. Direct detection of = influenza viruses in bioaerosols from patients

4. Observations from = animal infections with influenza

5. Mathematical modelling

6. Discussion

Acknowledgements

Footnotes

References

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