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Mechanistic theory predicts the effects of temperature and humidity on inactivation of SARS-CoV-2 and other enveloped viruses
Abstract
Ambient temperature and humidity strongly affect inactivation rates of enveloped viruses, but a mechanistic, quantitative theory of these effects has been elusive. We measure the stability of SARS-CoV-2 on an inert surface at nine temperature and humidity conditions and develop a mechanistic model to explain and predict how temperature and humidity alter virus inactivation. We find SARS-CoV-2 survives longest at low temperatures and extreme relative humidities (RH); median estimated virus half-life is >24 hr at 10°C and 40% RH, but ∼1.5 hr at 27°C and 65% RH. Our mechanistic model uses fundamental chemistry to explain why inactivation rate increases with increased temperature and shows a U-shaped dependence on RH. The model accurately predicts existing measurements of five different human coronaviruses, suggesting that shared mechanisms may affect stability for many viruses. The results indicate scenarios of high transmission risk, point to mitigation strategies, and advance the mechanistic study of virus transmission.
Introduction
For viruses to transmit from one host to the next, virus particles must remain infectious in the period between release from the transmitting host and uptake by the recipient host. Virus environmental stability thus determines the potential for surface (fomite) transmission and for mid-to-long range transmission through the air. Empirical evidence suggests that virus environmental stability depends strongly on ambient temperature and humidity, particularly for enveloped viruses; examples among enveloped viruses that infect humans include influenza viruses (Marr et al., 2019), endemic human coronaviruses (Ijaz et al., 1985), and the zoonotic coronaviruses SARS-CoV-1 (Chan et al., 2011) and MERS-CoV (van Doremalen et al., 2013).
In late 2019, a new zoonotic coronavirus now called SARS-CoV-2 emerged; it has since caused a global pandemic (COVID-19) and is poised to become an endemic human pathogen. Many countries in the Northern Hemisphere experienced a substantial uptick in transmission with the arrival of their late autumn and winter. Epidemiologists had anticipated such a seasonal increase (Neher et al., 2020; Kissler et al., 2020) based on observations from other enveloped respiratory viruses, such as endemic human coronaviruses (Monto et al., 2020) and influenza viruses (Lofgren et al., 2007). These viruses spread more readily in temperate zone winters than in temperate zone summers. SARS-CoV-2 has also displayed epidemic dynamics shaped by superspreading events, in which one person transmits to many others (Furuse et al., 2020; Kain et al., 2021); the related SARS-CoV-1 virus was likewise characterized by superspreading (Lloyd-Smith et al., 2005).
Virus transmission is governed by many factors, among them properties of the virus and properties of the host population. But anticipating seasonal changes in transmission and preventing superspreading events both require an understanding of virus persistence in the environment, since ambient conditions can facilitate or impede virus spread. Empirical evidence suggests that SARS-CoV-2, like other enveloped viruses, varies in its environmental stability as a function of temperature and humidity (Biryukov et al., 2020; Matson et al., 2020), but the joint effect of these two factors remains unclear.
Moreover, despite years of research on virus environmental stability, there do not exist mechanistically motivated quantitative models for virus inactivation as a function of both temperature and humidity. Existing predictive models for the environmental stability of SARS-CoV-2 (Biryukov et al., 2020; Guillier et al., 2020) and other viruses (Posada et al., 2010) are phenomenological regression models that do not model the underlying biochemical mechanisms of inactivation. This limits both our insight into the underlying inactivation process and our ability to generalize from any given experiment to unobserved conditions, or to real-world settings. A lack of quantitative, mechanistic models also makes it difficult to determine which environmental factors are most important, for instance whether absolute humidity (Shaman et al., 2010) or relative humidity (Marr et al., 2019) best explains influenza inactivation and seasonality.
We measured the environmental stability of SARS-CoV-2 virus particles (virions) suspended in cell culture medium and deposited onto a polypropylene plastic surface at nine environmental conditions: three relative humidities (RH; 40%, 65%, and 85%) at each of three temperatures (10°C, 22°C, and 27°C). We first quantified viable (infectious) virus titer over time and estimated virus decay rates and corresponding half-lives in each condition using a simple Bayesian regression model (see Materials and methods). We quantified the evaporation of the suspension medium and compared virus stability during the sample evaporation phase—while substantial water loss was ongoing—to virus stability after a quasi-equilibrium phase was reached—when further evaporation was not evident over the timescale of the experiment.
We then created a mechanistic biochemical model of virus inactivation kinetics, drawing upon existing hypotheses for how temperature and humidity affect the inactivation chemistry of virus particles in microdroplets (Marr et al., 2019; Lin and Marr, 2020). We fit this mechanistic model to our SARS-CoV-2 data, and used it to predict observations from other human coronaviruses and other studies of SARS-CoV-2, and to extrapolate our SARS-CoV-2 results to unobserved temperature and humidity conditions.
Our mechanistic model is based on a simple premise: virus inactivation in the environment is a chemical reaction and so obeys the laws of chemical kinetics. Reactions proceed faster at higher temperatures and higher solute concentrations. Solutes will be more concentrated when there is more evaporation; this occurs when the ambient relative humidity is lower. But below a threshold relative humidity, the efflorescence relative humidity (ERH), droplets may crystallize; this is also expected to change reaction kinetics. These principles apply across reactions. We do not need to know the exact identities and concentrations of non-virus reactants (e.g. amino acids, electrolytes, etc.) involved to make mechanistic predictions about how the inactivation reaction rate will vary with temperature and humidity.
Our model encodes these principles. We estimated its three central parameters from our data.
Results
Empirical patterns of virus decay
Our data suggest that SARS-CoV-2 environmental persistence could vary meaningfully across the range of temperatures and humidities encountered in daily life, with posterior median [95% credible interval] half-lives as long as 27 hr [20, 39] (10°C, 40% RH) and as short as 1.5 hr [1.1, 2.1] (27°C, 65% RH), once droplets reach quasi-equilibrium with the ambient air conditions (Figure 1b, Appendix 1—table 1).
(a) Example of medium evaporation and virus inactivation as a function of time since deposition; experiments at 22°C and 65% RH shown. Inactivation proceeds in two phases: an evaporation phase during which water mass is lost from the sample to evaporation and a quasi-equilibrium phase once the sample mass has plateaued. Light blue vertical line shows posterior median estimated time that quasi-equilibrium was reached. Top plot: medium evaporation. Dots show measured masses. Square shows measured final (quasi-equilibrium) mass; plotted at 24 hr for readability. Lines are 10 random draws from the posterior for the evaporation rate; horizontal section of line reflects the reaching of quasi-equilibrium (measured final mass). See figure supplements for all conditions. Bottom plot: virus inactivation. Points show posterior median estimated titers in log10 TCID50/mL for each sample; lines show 95% credible intervals. Black dotted line shows the approximate single-replicate limit of detection (LOD) of the assay: 100.5TCID50/mL media. Three samples collected at each time-point. Lines are 10 random draws per measurement from the posterior distribution for the inactivation rates, estimated by a simple regression model (see Materials and methods). (b) Measured virus half-lives. Violin plots show posterior distribution of estimated half-lives, plotted on a logarithmic scale. Dots show posterior median value. Color indicates temperature. Measurements at 40%, 65%, and 85% RH reflect decay kinetics once the deposited solution has reached quasi-equilibrium with the ambient air. Estimated half-lives for the evaporation phase that occurs prior to quasi-equilibrium are plotted to the right, since conditions during this phase are mainly dilute, and thus analogous to high RH quasi-equilibrium conditions. See figure supplements for plots showing the fit of the regression used to estimate half-lives to the titer data. (c) Schematic of hypothesized effects of temperature and relative humidity on duration of virus viability. Virus half-lives are longer at lower temperatures, regardless of humidity, because inactivation reaction kinetics proceed more slowly. Relative humidity affects virus half-life by determining quasi-equilibrium solute concentration in the droplet containing the virus. Above the efflorescence relative humidity (ERH), solutes are concentrated by evaporation. The lower the ambient humidity, the more water evaporates, the more concentration occurs, and the faster inactivation reactions proceed. Below the ERH, solutes effloresce, forming crystals. Half-lives are thus not particularly sensitive to changes in sub-ERH relative humidity, and half-lives even slightly below the ERH may be substantially longer than half-lives slightly above it.
Figure 1—figure supplement 1.
Fit of the regression model used to estimate half-lives to evaporation phase (pre-drying) SARS-CoV-2 titer data, according to method described in Empirical virus decay estimation (see Equation 44). We model evaporation phase decay of infectious virus at temperature as exponential at a rate ; this decay rate can therefore be estimated by fitting a line to the time series of estimated log10 virus titers. Points show posterior median estimated titers in log10 TCID50/mL for each sample; lines show 95% credible intervals. Black dotted line shows the approximate single-replicate limit of detection (LOD) of the assay: 100.5 TCID50/mL media. Three samples collected at each time-point. x-axis shows time since sample deposition. Lines are truncated at the estimated time quasi-equilibrium was reached. Lines are random draws (10 per sample) from the joint posterior distribution of the initial sample virus concentration and the estimated decay rate; the distribution of lines gives an estimate of the uncertainty in the decay rate and the variability of the initial titer for each experiment.
Figure 1—figure supplement 2.
Fit of the regression model used to estimate half-lives to quasi-equilibrium (post-drying) SARS-CoV-2 titer data, according to method described in Empirical virus decay estimation (see Equation 44). We model quasi-equilibrium decay of infectious virus in environmental condition as exponential at a rate ; this decay rate can therefore be estimated by fitting a line to the time series of estimated log10 virus titers. Points show posterior median estimated titers in log10 TCID50/mL for each sample; lines show 95% credible intervals. Time-points with no positive wells for any replicate are plotted as triangles at the approximate single-replicate limit of detection (LOD) of the assay—denoted by a black dotted line at 100.5 TCID50/mL media—to indicate that a range of sub-LOD values are plausible. Three samples collected at each time-point. x-axis shows time since quasi-equilibrium was reached, as measured in evaporation experiments. Lines are random draws (10 per sample) from the joint posterior distribution of the initial sample virus concentration and the estimated decay rate; the distribution of lines gives an estimate of the uncertainty in the decay rate and the variability of the initial titer for each experiment.
Figure 1—figure supplement 3.
Evaporation of supplemented Dulbecco’s Modified Eagle Medium (DMEM) as a function of temperature and humidity. Dots show measured masses. Square shows measured final (quasi-equilibrium) mass; actual measurement times for final masses were upon removal of sample from chamber, but for readability they are plotted at 24 hr for all experiments. Lines are 100 random draws from the posterior distribution for the evaporation rate; horizontal section of line reflects the reaching of quasi-equilibrium (measured final mass). Transition point between evaporation phase and quasi-equilibrium phase inferred from data (see Modeling of medium evaporation and Evaporation model fitting). Note that final mass measurement is more accurate than time series measurements (see Materials and methods, Evaporation experiment).
Minimal virus decay occurred during the evaporation phase (Figure 1a, Figure 1—figure supplement 1), when excess water was present. Estimated half-lives were long but exact values were highly uncertain, as the small amount of absolute virus inactivation during the brief evaporation phases, combined with the noise involved in sampling and titration, limits our inferential capacity. Posterior median half-lives during the evaporation phase were 42 hr [11, 330] at 10°C, 12 hr [4.5, 160] at 22°C, and 5.8 hr [2.1, 130] at 27°C (Table 1).
Table 1.
Estimated half-lives are reported as posterior median and the middle 95% credible interval.
| T (°C) | RH (%) | Median half-life (h) | 2.5 % | 97.5 % | |
|---|---|---|---|---|---|
| Quasi-equilibrium phase | 10 | 40 | 26.55 | 20.28 | 38.75 |
| 10 | 65 | 14.22 | 12.17 | 17.16 | |
| 10 | 85 | 13.78 | 10.67 | 19.70 | |
| 22 | 40 | 6.43 | 5.52 | 7.56 | |
| 22 | 65 | 2.41 | 2.03 | 2.88 | |
| 22 | 85 | 7.50 | 6.22 | 9.24 | |
| 27 | 40 | 3.43 | 2.91 | 4.12 | |
| 27 | 65 | 1.52 | 1.05 | 2.14 | |
| 27 | 85 | 2.79 | 2.12 | 3.78 | |
| Evaporation phase | 10 | 42.08 | 10.97 | 334.34 | |
| 22 | 12.18 | 4.47 | 163.58 | ||
| 27 | 5.76 | 2.14 | 125.85 |
Overall, virus decay became markedly faster as temperature increased for all humidities, with decay at 27°C roughly five to ten times faster than decay at 10°C. Across temperatures, virus decay was relatively rapid at 65% RH and tended to be slower either at lower (40%) or higher (85%) humidities, or when excess water was present during the evaporation phase (Figure 1b, Table 1).
Mechanistic model for temperature and humidity effects
Many viruses, including SARS-CoV-2, exhibit exponential decay on surfaces and in aerosols (Marr et al., 2019; van Doremalen et al., 2020; Biryukov et al., 2020). We drew upon chemical principles of droplet evaporation and virus inactivation (Figure 1c) to create a minimal mechanistic model incorporating the effects of both temperature and relative humidity on exponential decay rates.
We model virus inactivation at quasi-equilibrium on inert surfaces as a chemical reaction with first-order reaction kinetics; that is, the quantity of virus is the limiting reactant of the rate-determining step. This reflects the empirical pattern of exponential decay and is consistent with the fact that virions will be numerically rare in microdroplets compared to other reactants.
We characterize the temperature dependence of this reaction with the Arrhenius equation, which describes a reaction rate (here the virus inactivation rate ) as a function of an activation energy , an asymptotic high-temperature reaction rate , the universal gas constant , and the absolute temperature :
Prior work has found Arrhenius-like temperature dependence for virus inactivation on surfaces and in aerosols for many viruses (Adams, 1949), including human coronaviruses (Yap et al., 2020).
Mechanistic principles of virus inactivation as a function of humidity have been more elusive. Recent work has suggested that relative humidity affects virus inactivation by controlling evaporation and thus governing the solute concentrations in a droplet containing virions (Marr et al., 2019; Lin and Marr, 2020). In more humid environments, evaporation is slower and more water remains when quasi-equilibrium is reached. In less humid environments, evaporation is faster and little or no water remains (Figure 1c).
When released from infected hosts, virions are found in host bodily fluids, and virus inactivation experiments are typically conducted in cell culture medium. Both solutions contain amino acids and electrolytes, in particular sodium chloride (NaCl) (Cavaliere et al., 1989; Dulbecco and Freeman, 1959). Prior work has found that higher quasi-equilibrium solute concentrations are associated with faster virus inactivation rates (Yang and Marr, 2012; Yang et al., 2012). The simplest explanation for this is that the measured solute concentration is a direct proxy for the concentration of the reactants governing the inactivation reaction. Thus, ambient humidity affects the reaction rate by setting the quasi-equilibrium concentrations of the reactants that induce inactivation of the virus.
The exact quasi-equilibrium state reached will depend on the solutes present, since different solutes depress vapor pressure to different degrees. In electrolyte solutions like bodily fluids or cell culture media, efflorescence is also important. Below a threshold ambient humidity—the efflorescence relative humidity (ERH)—electrolytes effloresce out of solution, forming a crystal (Figure 1c). Below the ERH, the reaction no longer occurs in solution, and so inactivation may be slower. The non-monotonic (‘U-shaped’) dependence of virus inactivation on relative humidity, observed in our data (Figure 1a) and elsewhere in the literature (Yang et al., 2012; Benbough, 1971; Prussin et al., 2018; Webb et al., 1963), including for coronaviruses (Casanova et al., 2010; Songer, 1967), could be explained by this regime shift around the ERH (Figure 1c).
During the evaporation phase prior to quasi-equilibrium, reactants are less concentrated and decay is expected to be slower, as observed from our data (Figure 1a,b). If small initial droplet sizes are used—as in real-world depositions (predominantly < 10 µL; Johnson et al., 2011; Johnson et al., 2013; Thompson et al., 2013) and in some experiments—evaporative quasi-equilibration should be near instant, and so inactivation should follow the kinetics at quasi-equilibrium. Larger droplets, such as those used in our experiments, will take more time to equilibrate (depending on temperature and humidity); this allows us to distinguish the quasi-equilibrium phase from the evaporation phase.
We partition inactivation at quasi-equilibrium into two humidity regimes, effloresced and solution, according to whether the ambient RH is below the ERH (effloresced) or above (solution). In either case, we approximate virus inactivation as a first-order reaction with inactivation rate or , respectively. Based on observations of NaCl solutions at room temperature and atmospheric pressure (Mikhailov et al., 2004), we use an ERH of 45%. This means that 40% RH experiments are in the effloresced regime and 65% and 85% RH experiments are in the solution regime.
We model the effloresced and solution inactivation rates and using two Arrhenius equations with a shared activation energy but distinct asymptotic high-temperature reaction rates and . In solution conditions, we further modulate by a quasi-equilibrium ‘concentration factor’ , which quantifies how concentrated the solution has become at quasi-equilibrium relative to its initial state .
Given our assumption of first-order kinetics, an n-fold increase in the non-virion reactant concentrations should translate directly into an n-fold increase in the inactivation rate. Lower relative humidity leads to higher quasi-equilibrium concentration and thus increases virus inactivation rate, until the ERH is reached. Below the ERH, inactivation rates may again be low due to crystallization, depending on . We do not force the relationship between RH and inactivation rate to be continuous at the ERH; there may be a discontinuity (see Appendix, Interpretation of the transition in inactivation rate at the ERH, for a discussion).
We estimated , , and from our data, constraining all to be positive. We treated evaporation phase data as governed by , with a dynamic value of the concentration factor (Appendix, Modeling of virus decay dynamics during the evaporation phase). We computed the quasi-equilibrium concentration factor by fitting a theoretically-motivated curve to our evaporation data (Figure 2—figure supplement 1).
The relationship between RH and quasi-equilibrium concentration factor depends on complex evaporative kinetics that will vary among media. For this reason, we do not attempt to predict it from first principles, but instead measure it directly and use the fitted curve to extrapolate to unmeasured RH conditions. We use this approach for the results presented in the main text; we refer to it as the ‘main model’.
To check robustness of the main model results, we also estimated a version of the model without this theoretical curve–using only directly-measured equilibrium concentration factors. This model (referred to as the ‘directly-measured concentration model’) yielded similar results to the main model; see Appendix, Mechanistic model versions for details.
We also considered a four-parameter variant of the model with distinct activation energies below the ERH () and above (), placing the same prior on each. This accounts for the possibility that the rate-determining step of the inactivation reaction might be distinct in the two regimes. The estimated activation energies were very similar below and above the ERH (Appendix 1—figure 1). This suggests that the rate-determining reaction step—and thus the activation energy—is the same in both regimes. Accordingly, we report estimates from the three-parameter model with a shared . We provide additional details and interpretation of our mechanistic inactivation modeling in the Appendix; see Mechanistic inactivation model interpretation and Mechanistic model estimation.
Model fitting and prediction of unobserved conditions
Our dataset comprises nine experimental conditions, each with seven time-points that span the evaporation and quasi-equilibrium phases. We sought to explain the virus inactivation rates across this entire dataset using our mechanistic model with just three free parameters: the activation energy and the asymptotic high-temperature reaction rates under effloresced and solution conditions, and . The mechanistic function used and the constraint on the parameters to be positive means that inactivation rate must increase with temperature and with increasing solute concentration. Remarkably, the fit of the mechanistic model (Figure 2) is nearly as good as that of the simple regression, in which we estimate independent exponential decay rates for each condition to measure virus half-life (Figure 1—figure supplement 2, see Appendix, Simple regression model). Mechanistic model parameter estimates are given in Figure 2—figure supplement 2 and Appendix 1—table 1.
Points show posterior median estimated titers in log10 TCID50/mL for each sample; lines show 95% credible intervals. Time-points with no positive wells for any replicate are plotted as triangles at the approximate single-replicate limit of detection (LOD) of the assay—denoted by a black dotted line at 100.5TCID50/mL media—to indicate that a range of sub-LOD values are plausible. Three samples collected at each time-point. x-axis shows time since quasi-equilibrium was reached, as measured in evaporation experiments. Lines are random draws (10 per sample) from the joint posterior distribution of the initial sample virus concentration and the mechanistic model predicted decay rate; the distribution of lines gives an estimate of the uncertainty in the decay rate and the variability of the initial titer for each experiment. See Figure 2—figure supplement 4 for a visualization of the mechanistic model fit using directly-measured concentration, rather with a curve estimating the humidity/concentration relationship.
Figure 2—figure supplement 1.
Fitted curve estimating concentration factor at quasi-equilibrium a function of relative humidity. Points show estimates for quasi-equilibrium concentration factor based on empirically measured masses from the evaporation experiments (Figure 1—figure supplement 3) and the estimated initial solute mass fraction. Estimates shown for each temperature (point color) and ambient RH (x-axis value). Vertical lines around the points show a 68% (thick) and 95% (thin) credible interval. Blue curves show model predictions for concentration factor given parameters , (see Solute concentration factor, Equation 12), and the initial solute mass fraction, all estimated jointly alongside mechanistic model parameters and evaporation rates. Each curve is an independent draw from the joint posterior distribution of the parameters, thus giving a sense of the distribution of possible curves; 100 curves plotted. Vertical dashed line shows the efflorescence relative humidity, 45%.
Figure 2—figure supplement 2.
Posterior distributions for key mechanistic model parameters. Main model fit (with fitted curve relating RH to concentration factor) shown at left, directly-measured concentration factor model fit shown at right. Distributions are visualized as quantile dotplots (Kale et al., 2020); 100 representative dots are shown for each parameter. Black circle below shows posterior median, bars show 68% (thick) and 95% (thin) credible intervals. For and , parameter values are plotted on a logarithmic scale. See Appendix 1—table 1 and Appendix 1—table 2 for posterior medians and 95% credible intervals; see Code and data availability for code to reproduce full set of posterior samples.
Figure 2—figure supplement 3.
Comparison of directly-measured half-lives (left) with those predicted by the mechanistic model, either with a fitted curve relating RH to concentration (center), as in the main text, or using directly-measured concentration factors (right). Violin plots show posterior distribution of estimated half-lives, plotted on a logarithmic scale. Dots show posterior median value. Color indicates temperature. Measurements at 40%, 65%, and 85% RH reflect decay kinetics once the deposited solution has reached quasi-equilibrium with the ambient air.
Figure 2—figure supplement 4.
Estimated titers and fit of the directly-measured concentration mechanistic model for SARS-CoV-2 stability on polypropylene at quasi-equilibrium (concentration factor taken from evaporation experiments, rather than from a fitted curve that relates RH to concentration). Points show posterior median estimated titers in log10 TCID50/mL for each sample; lines show 95% credible intervals. Time-points with no positive wells for any replicate are plotted as triangles at the approximate single-replicate limit of detection (LOD) of the assay—denoted by a black dotted line at 100.5 TCID50/mL media—to indicate that a range of sub-LOD values are plausible. Three samples collected at each time-point. x-axis shows time since quasi-equilibrium was reached, as measured in evaporation experiments. Lines are random draws (10 per sample) from the joint posterior distribution of the initial sample virus concentration and the mechanistic model predicted decay rate; the distribution of lines gives an estimate of the uncertainty in the decay rate and the variability of the initial titer for each experiment.
Figure 2—figure supplement 5.
Estimated titers and main mechanistic model fit for SARS-CoV-2 stability on polypropylene during the evaporation phase. Points show posterior median estimated titers in log10 TCID50/mL for each sample; lines show 95% credible intervals. Black dotted line shows the approximate single-replicate limit of detection (LOD) of the assay: 100.5 TCID50/mL media. Three samples collected at each time-point. x-axis shows time since sample deposition. Lines are truncated at the estimated time quasi-equilibrium was reached. Lines are random draws (10 per sample) from the joint posterior distribution of the initial sample virus concentration and the mechanistic model predicted decay rate; the distribution of lines gives an estimate of the uncertainty in the decay rate and the variability of the initial titer for each experiment.
Figure 2—figure supplement 6.
Estimated titers and fit of the directly-measured concentration mechanistic model for SARS-CoV-2 stability on polypropylene during the evaporation phase (concentration factor taken from evaporation experiments, rather than from a fitted curve that relates RH to concentration). Points show posterior median estimated titers in log10 TCID50/mL for each sample; lines show 95% credible intervals. Black dotted line shows the approximate single-replicate limit of detection (LOD) of the assay: 100.5 TCID50/mL media. Three samples collected at each time-point. x-axis shows time since sample deposition. Lines are truncated at the estimated time quasi-equilibrium was reached. Lines are random draws (10 per sample) from the joint posterior distribution of the initial sample virus concentration and the mechanistic model predicted decay rate; the distribution of lines gives an estimate of the uncertainty in the decay rate and the variability of the initial titer for each experiment.
We used the mechanistic model to predict SARS-CoV-2 half-life for unobserved temperature and humidity conditions from 0°C to 40°C, and from 0% to 100% RH. We chose these ranges to reflect environments encountered by human beings in daily life. We did not extrapolate to temperatures below 0°C since inactivation kinetics may be different when fluid containing the virus freezes. The exact freezing points of suspension medium and human fluids at sea level will depend on solute concentration, but will typically be below the 0°C freezing point of pure water.
Median predicted SARS-CoV-2 half-life varies by more than three orders of magnitude, from less than half an hour at 40°C just above the modeled approximate ERH, to more than a month at 0°C and 100% RH (Figure 3a,c). We find good qualitative agreement between model predictions and model-free estimates from our data, including long half-lives prior to quasi-equilibrium. The U-shaped effect of humidity on virus half-life is readily explained by the regime-shift at the ERH (Figure 3a). In particular, half-lives become extremely long at cold temperatures and in very dilute solutions, which are expected at high RH (Figure 3a,b). Of note, the worst agreement between mechanistic model predictions and (independent) simple regression estimates is found at 10°C and 85% RH (Figure 3a). This is partially explained by the fact that the empirical quasi-equilibrium concentration reached under those conditions was higher than our model prediction based on RH (Figure 2—figure supplement 1). Accordingly, the half-life prediction for 10°C and 85% RH based on directly-measured concentrations is superior to the prediction based on an extrapolation from the relative humidity (Figure 2—figure supplement 3).
(a) Predicted half-life as a function of relative humidity. Points show posterior median for measured half-lives, estimated without the mechanistic model (simple regression estimate for each temperature/humidity combination), lines show a 68% (thick) and 95% (thin) credible interval. Dashed line shows the ERH. Estimated evaporation phase half-lives are plotted at the right. Colored lines show predicted half-lives as a function of humidity at five temperatures: 0°C, 10°C, 22°C, 27°C, and 40°C. One hundred100 random draws from the posterior distribution are shown at each temperature to visualize uncertainty. Line and point colors indicate temperature. (b) Predicted half-life above the ERH as a function of quasi-equilibrium concentration factor. Points and lines as in a, but only solution (above ERH) conditions are shown. (c) Heatmap showing posterior median predicted half-lives as a function of temperature and relative humidity. Posterior median estimated half-lives for human coronaviruses from our study and from the literature plotted on top using the same color map (see also Appendix 1—table 3 and Figure 3—figure supplement 1). Shape indicates virus; measurements from our own group are shown slightly larger with a slightly thicker outline. Points of identical temperature and humidity are nudged slightly to avoid direct overplotting. (d) Relative within-study mechanistic model predictions (x-axis, see Appendix, Relative predictions) compared to simple regression measurements (y-axis) for human coronavirus half-lives. Points show posterior median for measured (horizontal) or predicted (vertical) half-lives and lines show a 68% (thick) and 95% (thin) credible interval. Shape indicates virus; datapoints come from studies in the literature for which there were measurements at at least two temperature and/or humidity conditions for the same virus and experimental material (e.g. plastic, steel, bulk medium).
Figure 3—source data 1.
Predicted and measured half-lives (posterior medians and credible intervals) for within-study relative predictions shown in d.Figure 3—figure supplement 1.
Mechanistic model predictions compared to half-lives estimated directly from data via simple regression. All inactivation studies in which both temperature and relative humidity were reported are included. (a) Half-life as a function of relative humidity at different temperatures. Colored lines show predicted half-life as a function of relative humidity (x-axis value) and temperature (color) according to the main model fit. 100 random draws from the posterior distribution are plotted for each of 20 evenly spaced temperatures between 0 and 40°C. Gray line shows the efflorescence relative humidity (ERH) assumed in the model, 45%. Points show posterior median for measured half-lives for human coronaviruses. Measurements included come from this study (Table 1), from our meta-analysis of the literature (Appendix 1—table 3), and from SARS-CoV-1 and MERS-CoV data collected by our group (Appendix 1—table 4). (b) Half-lives predicted from the mechanistic model (x-axis) compared to independent estimates (y-axis), for the same observations plotted in a. In both panels, half-life estimates are simple regression estimates (i.e. no mechanistic model; fitting of independent exponential decay rates to each condition). Shape indicates virus; in a, measurements from our own group are shown slightly larger. Black lines show a 68% (thick) and 95% (thin) credible interval for posterior estimates. Note that three SARS-CoV-2 points from a particular study (Harbourt et al., 2020) show consistently longer-than-predicted half-lives, and all MERS-CoV points show shorter-than-predicted half-lives. In both instances, our mechanistic model makes accurate relative predictions for these data once calibrated to a reference half-life within the same study (Figure 3d). Taken together, this indicates that there can be experiment- and/or virus- specific effects on absolute half-lives while the general mechanism remains: hotter, more concentrated solutions produce faster virus inactivation.
Figure 3—figure supplement 1—source data 1.
Predicted and measured half-lives (posterior medians and credible intervals) for absolute predictions shown in c and in Figure 3—figure supplement 1.As a stronger test of our model’s validity, we used our estimated and values to make out-of-sample predictions of the half-lives of five human coronaviruses reported from independent studies: four betacoronaviruses (SARS-CoV-2, SARS-CoV-1, MERS-CoV and HCoV-OC43) and one alphacoronavirus (HCoV-229E). We compiled data on the environmental stability of those viruses under conditions ranging from 4°C to 95°C, from 30% to 80% RH, and on a range of surfaces or bulk media, and computed empirical (regression) estimates of virus half-lives (Appendix 1—table 3). We also included data on stability of SARS-CoV-1 (van Doremalen et al., 2020) and MERS-CoV (same method as in van Doremalen et al., 2020) collected by our group during previous studies (Appendix 1—table 4).
Where both temperature and RH were available, we compared these model-free estimates to predictions based on the mechanistic model parameterized with our SARS-CoV-2 data (Figure 3c, Figure 3—figure supplement 1). We found striking agreement for half-life estimates both above and below the ERH, and for temperatures ranging from 4°C to 37°C.
To include a broader range of conditions in our out-of-sample model testing, we used our model to predict half-lives observed in all comparable studies by extrapolating from a reference half-life in each study. Predicted half-lives matched observations well across five orders of magnitude (Figure 3d), despite spanning five virus species and despite important heterogeneities in the data collection process (see Appendix, Meta-analysis of human coronavirus half-lives). The two conspicuous outliers, where SARS-CoV-2 half-lives were measured to be substantially shorter than our prediction, correspond to samples exposed to high heat in closed vials (Chin et al., 2020; Chin, 2020, personal communication) which is known to accelerate virus inactivation (Gamble et al., 2021).
Discussion
Combining novel data, mathematical modeling, and a meta-analysis of existing literature, we have developed a unified, mechanistic framework to quantify the joint effects of temperature and humidity on virus stability. In particular, our model provides a mechanism for the non-linear and non-monotonic relationship between relative humidity and virus stability previously observed for numerous enveloped viruses (Yang and Marr, 2012; Casanova et al., 2010; Songer, 1967), but not previously reported for SARS-CoV-2. Our work documents and explains the strong dependence of SARS-CoV-2 stability on environmental temperature and relative humidity, and accurately predicts half-lives for five coronavirus species in conditions from 4°C to 95°C, and from 30% to 80% RH and in bulk solution.
Our findings have direct implications for the epidemiology and control of SARS-CoV-2 and other enveloped viruses. The majority of SARS-CoV-2 clusters have been linked to indoor settings (Leclerc et al., 2020), suggesting that virus stability in indoor environmental conditions may be an important determinant of superspreading risk. Our results provide a mechanistic explanation for the many observed SARS-CoV-2 superspreading events in cool indoor environments such as food processing plants (Dyal, 2020; Günther et al., 2020; Pokora et al., 2020) and hockey rinks (Atrubin et al., 2020; McNabb and Ries, 2020), where the typical air temperature is around 10°C, or in dry indoor environments such as long-distance flights (Khanh et al., 2020; Jayaweera et al., 2020). Conversely, our results imply that the relative rarity of outdoor SARS-CoV-2 transmission clusters is not readily explained by temperature and humidity effects, since these conditions outdoors during temperate zone winters should be favorable for the virus. Instead, increased ventilation (Prather et al., 2020) and UV light inactivation (Ratnesar-Shumate et al., 2020) may be more important than the effects of temperature and humidity outdoors. In contrast, typical climate-controlled conditions indoors (moderate temperature and low humidity) are favorable for virus stability, and specialized conditions such as those found in food processing plants even more so. Our results highlight the importance of proper personal protective equipment and improved ventilation for protecting workers, particularly in cold indoor settings, and the general transmission risks associated with indoor gatherings.
The effects of temperature and humidity we observe in our data and model are relevant both to fomite and to airborne transmission. Prior work has shown that virus decay as a function of RH is similar in droplets on surfaces and suspended aerosols (Lin and Marr, 2020; Kormuth et al., 2018). Numerous studies of smaller deposited droplets (Prussin et al., 2018) or aerosols (Benbough, 1971; Yang et al., 2012; Ijaz et al., 1985) have reported similar qualitative patterns to those we report, with increased decay rates at high temperatures and a U-shaped effect of RH. Furthermore, surface stability can matter for aerosol transmission risk, since small particles containing infectious virions can be re-suspended from surfaces and inhaled (Asadi et al., 2020). Re-suspension is further enhanced by procedures such as high-pressure washing, which is common in food processing plants. While the relative contributions of aerosol and fomite transmission to the epidemiology of SARS-CoV-2 continue to be investigated (Ong et al., 2020; Cai et al., 2020), our results indicate that cold situations present elevated transmission risks for either mode, especially if air is either dry or very humid. It has been speculated, for instance, that chilled or frozen foods might allow for rare but impactful long-range fomite transmission (Han et al., 2020). Our results show that this is conceivable, as there is good empirical and mechanistic support for prolonged virus viability at very low temperatures.
Environmental stability is not the only mechanism by which temperature and humidity affect respiratory virus transmission. Very hot or cold conditions outdoors can lead people to spend more time indoors, where transmission risks are heightened due to poor ventilation. Low-humidity environments can dry out human airways and thus impair defenses against respiratory viruses (Kudo et al., 2019). Ambient humidity also determines the size distribution of aerosols in the environment, again by affecting evaporation rates. Smaller aerosols settle to the ground more slowly (Marr et al., 2019), which could facilitate transmission.
At low RH, humidity effects on inactivation, immunity, and settling may compound each other: all increase transmission risk. At high RH, reduced inactivation could promote transmission, but improved immune defenses and faster settling could hinder it, so the net effect on transmission is less clear.
Still, temperate zone winters increase transmission of many respiratory viruses (Lofgren et al., 2007). Individuals spend increased time indoors in heated buildings. Ventilation is often poor, as windows are kept closed to make heating efficient. Air in heated buildings is typically very dry; this improves virus stability and weakens immune defenses. Policymakers should consider ventilating and humidifying essential indoor spaces to reduce transmission risk. Other mitigation measures such as indoor masking may likewise be even more crucial during winter. Indoor spaces in which individuals cannot be masked, such as bars and restaurants, remain particular cause for concern.
Several analyses have projected that SARS-CoV-2 transmission will likewise be faster in temperate zone winters (Neher et al., 2020; Kissler et al., 2020; Baker et al., 2020). Major seasonal or climate-mediated mitigation of SARS-CoV-2 spread was not evident during the northern hemisphere’s spring and summer (Carlson et al., 2020; Poirier et al., 2020). This was expected, since population susceptibility and epidemic control measures can be more important than seasonality in an early pandemic context (Baker et al., 2020). Thus, the fact that temperate zone summers did not eliminate transmission should not have led to false confidence that temperate zone winters would not promote it. Winter surges in cases, hospitalizations, and deaths across the northern hemisphere may have been driven in part by behavioral, immunological, or virological seasonality.
Our work has implications for the study of virus environmental stability and seasonality more broadly. Whether absolute or relative humidity is more important for influenza stability has been a matter of debate (Shaman et al., 2010; Marr et al., 2019). The answer has proved elusive because it is difficult to disentangle the effects of humidity from those of temperature. Our mechanistic model permits principled dis-aggregation of those effects, and reveals a strong effect of relative humidity even after accounting for the effects of temperature.
There may thus exist general principles that govern virus inactivation across enveloped viruses, and perhaps even more broadly. Similar empirical patterns of temperature and humidity dependence to what we measured, and modeled, for SARS-CoV-2 have been observed for other important viruses. In particular, the U-shaped dependence of inactivation on RH has been reported for animal coronaviruses (Songer, 1967; Casanova et al., 2010), as well as for influenza viruses, paramyxoviruses, rhabdoviruses, and retroviruses (Yang et al., 2012; Benbough, 1971; Prussin et al., 2018; Webb et al., 1963), suggesting the existence of a shared mechanism for the effect of humidity across enveloped RNA viruses. Some enveloped DNA viruses such as herpesviruses and poxviruses (Songer, 1967; Webb et al., 1963) and some encapsulated viruses such as polioviruses (de Jong and Winkler, 1968; Songer, 1967) also show similar empirical behavior. Experiments have found that heat treatment of viruses reduces infectivity principally by degrading surface proteins (Wigginton et al., 2012), lending further support to a chemical model of environmental virus inactivation.
Individual enveloped viruses may be more or less stable than SARS-CoV-2 while still obeying our model’s basic principle: increased heat and concentration lead to faster inactivation. The values of model parameters (, , ) may change while the mechanistic model itself remains valid. The data from our own group and from the literature on MERS-CoV is suggestive in this regard: our model predictions using SARS-CoV-2 parameters slightly overestimate the stability of MERS-CoV, but correctly predict the pattern of temperature and humidity effects (Figure 3—figure supplement 1).
Similarly, it is striking that our model for Arrhenius-like temperature dependence works well with a single estimated activation energy across the effloresced and solution regimes for our SARS-CoV-2 experiments and for experiments on a range of coronaviruses conducted in different conditions by other investigators. This suggests that the rate-limiting step in coronavirus inactivation may not necessarily depend on the exact inactivating reactant. We propose one simple potential mechanism for how this could be so: if inactivation depends on disruption of the virion once it has formed a complex with some inactivating reactant, the activation energy for that disruption event could depend mainly on the chemical properties of the virion itself (see Appendix, Interpretation of the single activation energy).
We discuss additional practical implications for the empirical study of virus environmental stability in the Appendix (Methodological implications for experimental studies on virus stability).
Despite years of research on virus stability as a function of temperature and humidity and plausible hypotheses about the underlying chemistry, proposed mechanisms have lacked explicit quantitative support. By encoding the underlying chemistry into a mathematical model and estimating parameters using modern computational techniques, we provide such support, with critical insights for the control of an ongoing pandemic. Our empirical results provide mechanistic insight into transmission risks associated with cold and climate-controlled indoor settings, while our modeling work allows for explicit quantitative comparison of the aerosol and fomite risks in different environments, and suggests that simple, general mechanisms govern the viability of enveloped viruses: hotter, more concentrated solutions are favorable to chemical reactions—and therefore unfavorable to viruses.
Materials and methods
Laboratory experiments
Viruses and titration
We used SARS-CoV-2 strain HCoV-19 nCoV-WA1-2020 (MN985325.1; Holshue et al., 2020) for this study. We quantified viable virus by end-point titration on Vero E6 cells as described previously (Fischer et al., 2020; van Doremalen et al., 2020), and inferred posterior distributions for titers and exponential decay rates directly from raw titration data using Bayesian statistical models (see Statistical analyses and mathematical modeling, below).
Virus stability experiment
We measured virus stability on polypropylene (ePlastics, reference PRONAT.030X24X47S/M) as previously described (van Doremalen et al., 2020). We prepared a solution of Dulbecco’s Modified Eagle Medium (DMEM, a common cell culture medium) supplemented with 2 mM L-glutamine, 2% fetal bovine serum, and 100 units/mL penicillin/streptomycin, and containing 105 TCID50/mL SARS-CoV-2. Polypropylene disks were autoclaved for decontamination prior to the experiment. We then placed 50 μL aliquots of this SARS-CoV-2 suspension onto the polypropylene disks under nine environmental conditions: three RH (40%, 65%, and 85%) at each of three temperatures (10°C, 22°C, and 27°C). These controlled environmental conditions were produced in incubators (MMM Group CLIMACELL and Caron model 6040) with protection from UV-B or UV-C exposure. We prepared 216 disks corresponding to three replicates per eight post-deposition time-points (0, 1, 4, 8, and 24 hr, then daily for 4 days) for the nine conditions. At each time-point, samples were collected by rinsing the disks with 1 mL of DMEM and stored at −80°C until titration.
Evaporation experiment
We measured the evaporation kinetics of suspension medium under the same temperature and humidity conditions as the virus stability experiments. We placed 50 μL aliquots of supplemented DMEM onto polypropylene disks in a Electro-Tech Systems 5518 environmental chamber. The polypropylene disks were rinsed three times 1M sulfuric acid, ethanol and DI H2O respectively before use. We measured medium mass every 5 min for up to 20 hr or until a quasi-equilibrium was reached using a micro-balance (Sartorius MSE3.6P-000-DM, readability 0.0010 mg). The chamber of the micro-balance was half-opened to keep air circulating with the environmental chamber. The flow entering the balance chamber decreased the balance accuracy to around 0.01 mg. We measured initial droplet mass () and final droplet mass () under closed-chamber conditions to increase accuracy.
Statistical analyses and mathematical modeling
We quantified the stability of SARS-CoV-2 under different conditions by estimating the decay rates of viable virus titers. We inferred individual titers using a Bayesian model we have previously described (Gamble et al., 2021). Briefly, the model treats titration well infection as a Poisson single-hit process. We inferred raw exponential decay rates by modifying a previously-described simple regression model (Gamble et al., 2021) to account for the evaporation phase. See the Appendix (Empirical virus decay estimation) for model description.
We estimated parameters of our mechanistic models by predicting titers based on those models and then applying the same Poisson single-hit observation process to estimate parameters from the data. See Appendix (Mechanistic model estimation) for a complete description, including model priors.
We estimated evaporation rates and corresponding drying times by modeling mass loss for each environmental condition as linear in time at a rate until the final mass was reached. See Appendix (Modeling of medium evaporation and Evaporation model fitting) for a full description, including model priors.
We drew posterior samples using Stan (Stan Development Team, 2018), which implements a No-U-Turn Sampler (a form of Markov Chain Monte Carlo), via its R interface RStan (Stan Development Team, 2016). We inferred all parameters jointly (e.g. evaporation parameters and mechanistic model parameters were inferred in light of each other).
Meta-analysis
To test the validity of our model beyond the measured environmental conditions (i.e. beyond 10–27°C and 40–85% RH), we compiled data from 11 published studies on human coronaviruses, including SARS-CoV-2, SARS-CoV-1, MERS-CoV, HCoV-OC43, and HCoV-299E, under 17 temperature-RH conditions. We generated estimates of half-lives and uncertainties (Appendix 1—table 3) and compared those estimates to the half-lives predicted by the mechanistic model parametrized from our SARS-CoV-2 data. As data on evaporation kinetics were not available, we estimated a unique half-life for each experimental condition, covering both the evaporation and quasi-equilibrium phases. As virus decay during the evaporation phase is expected to be minimal, and the evaporation phase to be short, the estimated half-life can be used as a proxy for the quasi-equilibrium half-life. The complete data selection, extraction and analysis process is detailed in the Appendix (Meta-analysis of human coronavirus half-lives).
We also included data from SARS-CoV-1 and MERS-CoV collected by our group during previous studies (van Doremalen et al., 2020). Those data were collected at 22°C and 40% RH on polypropylene using the protocol described previously (van Doremalen et al., 2020) and similar to the one used to collect the SARS-CoV-2 data. SARS-CoV-1 strain Tor2 (AY274119.3) (Marra et al., 2003) and MERS-CoV strain HCoV-EMC/2012 (Zaki et al., 2012) were used for these experiments. We calculated half-lives for evaporation and quasi-equilibrium phases using the same analysis pipeline used for SARS-CoV-2 (Appendix, Empirical virus decay estimation). These data were used only for out-of-sample prediction testing. We used the obtained evaporation phase half-lives as proxies for the half-life at 100% RH, as with SARS-CoV-2. See Appendix for a figure showing model fits (Appendix 1—figure 23) and a table of estimated half-lives (Appendix 1—table 4).
Visualization
We created plots in R using ggplot2 (Wickham, 2016), ggdist (Kay, 2020a), and tidybayes (Kay, 2020b), and created original schematics using BioRender.com.
Acknowledgements
We thank eLife editors W Garrett and CB Ogbunu and two anonymous reviewers for valuable comments on the manuscript. This research was supported by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH). DHM was supported by the US National Science Foundation (CCF 1917819). JOL-S and AG were supported by the Defense Advanced Research Projects Agency DARPA PREEMPT #D18AC00031 and the UCLA AIDS Institute and Charity Treks, and JOL-S was supported by the US National Science Foundation (DEB-1557022), the Strategic Environmental Research and Development Program (SERDP, RC‐2635) of the US QH, LCM, and PJV were supported by the US National Science Foundation (CBET-1705653, CBET-2029911). The content of the article does not necessarily reflect the position or the policy of the US government, and no official endorsement should be inferred.
Appendix 1
Funding Statement
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Contributor Information
Wendy S Garrett, Harvard T.H. Chan School of Public Health, United States.
C Brandon Ogbunugafor, Yale University, United States.
Funding Information
This paper was supported by the following grants:
- National Science Foundation CCF 1917819 to Dylan H Morris.
- Defense Advanced Research Projects Agency D18AC00031 to Amandine Gamble, James O Lloyd-Smith.
- UCLA AIDS Institute and Charity Treks to Amandine Gamble, James O Lloyd-Smith.
- National Institute of Allergy and Infectious Diseases Intramural Research Program to Kwe Claude Yinda, Trenton Bushmaker, Robert J Fischer, M Jeremiah Matson, Neeltje Van Doremalen, Vincent J Munster.
- National Science Foundation DEB-1557022 to James O Lloyd-Smith.
- Strategic Environmental Research and Development Program RC‐2635 to James O Lloyd-Smith.
- National Science Foundation CBET-1705653 to Qishen Huang, Peter J Vikesland, Linsey C Marr.
- National Science Foundation CBET-2029911 to Qishen Huang, Peter J Vikesland, Linsey C Marr.
Additional information
Competing interests
No competing interests declared.
Author contributions
Conceptualization, Software, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing - original draft, Writing - review and editing, Led development of mechanistic model.
Conceptualization, Investigation, Methodology, Writing - original draft, Writing - review and editing, Led empirical measurement work.
Conceptualization, Data curation, Formal analysis, Validation, Investigation, Methodology, Writing - original draft, Writing - review and editing, Led meta-analysis.
Formal analysis, Investigation, Methodology, Writing - review and editing.
Investigation, Writing - review and editing.
Investigation, Writing - review and editing.
Investigation, Writing - review and editing.
Investigation, Writing - review and editing.
Investigation, Methodology, Writing - review and editing.
Formal analysis, Supervision, Funding acquisition, Validation, Methodology, Writing - review and editing.
Formal analysis, Supervision, Funding acquisition, Validation, Methodology, Writing - review and editing.
Conceptualization, Resources, Methodology, Project administration, Writing - review and editing.
Conceptualization, Formal analysis, Supervision, Funding acquisition, Validation, Investigation, Writing - original draft, Writing - review and editing.
Data availability
All code and data needed to reproduce results and figures is archived on Github (https://github.com/dylanhmorris/sars-cov-2-temp-humidity/; copy archived at https://archive.softwareheritage.org/swh:1:rev:d80dd0132be738753f1a77c99ce280219dc5afba) and on Zenodo (https://doi.org/10.5281/zenodo.4093264), and licensed for reuse, with appropriate attribution/citation, under a BSD 3-Clause Revised License. This includes all original data generated in the experiments and all data collected and used for meta-analysis.
The following dataset was generated:
Morris DH. 2021. Code and data for Mechanistic theory predicts the effects of temperature and humidity on inactivation of SARS-CoV-2 and other enveloped viruses. Zenodo. [CrossRef]
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Decision letter
Acceptance summary:
The study offered a provocative, highly technical, and courageously cross-disciplinary approach to understanding environmental survival in viruses, including SARS-CoV-2. We applaud the rigor and care in the work, and thank you for submitting it to eLife. There is little doubt that this will be a very worthy and meaningful contribution to the literature. Even further, this work may transcend the COVID-19 pandemic, and serve as grand example of how one can rigorously integrate fields like biophysics with epidemiology.
Decision letter after peer review:
Thank you for submitting your article "Mechanistic theory predicts the effects of temperature and humidity on inactivation of SARS-CoV-2 and other enveloped viruses" for consideration by eLife. Your article has been reviewed by 2 peer reviewers, one of whom is a member of our Board of Reviewing Editors, and the evaluation has been overseen by a Senior Editor.
Please address the changes as outlined by the reviewers below, as they will make for an improved manuscript. We encourage the authors to address them, and more broadly, make this article as clear as possible. Both reviewers provided some insight into this, and strongly encourage the authors to pay close attention to this.
Reviewer #1:
In this manuscript, Morris and colleagues offer a mechanistic model, featuring chemistry and physics details, that explain the effects of temperature and humidity.
I found this manuscript to be highly relevant for any virus, but given the context-the COVID-19 pandemic-I find the results to be timely, relevant, and fantastically well conducted. The interaction between the epidemiological knowledge and biophysical precision is clear, and the implications are also very clear. The manuscript is well-written and organized.
I believe that this manuscript should be published, would make a worthy contribution to great body of SARS-CoV-2 and extended COVID-19 literature.
The recommended changes have to do with subtle editorial points, and efforts to make this work as clear as possible.
1. Figure 1: I believe that the authors should check the labels. I could be wrong, but I believe the labels in the captions are wrong.
2. Equations:
The interaction between the text and the appendix could be improved, and I challenge the authors to better integrate this information. The authors should read the equations from the perspective of the reader: can the reader fully grasp the flow of information from the equations as provided. I am of a mixed opinion on this, but given the overall excellence of the manuscript, I encourage the authors to make this work as clear and digestible as possible, as it has the potential to be a defining piece of literature.
Reviewer #2:
This is a very well-done and thorough analysis of SARS-CoV-2 decay rates, with new theory and models being developed that also apply to other viruses. The methodology is solid, the analyses extensive, and the authors fully achieve their goal of further understanding the decay characteristics of SARS-CoV-2 and other viruses in the environment. The main novel contribution is the detailed mechanistic model relating decay rates to temperature and relative humidity. I believe this is a major contribution toward better understanding and predicting environmental virus decay dynamics.
I consider this paper perfectly suited for eLife. Overall, I think another pass-through the main manuscript with an eye to making it as easy and stand-alone to follow as possible for the 'casual reader/browser' would be useful.
Author response
Reviewer #1:
In this manuscript, Morris and colleagues offer a mechanistic model, featuring chemistry and physics details, that explain the effects of temperature and humidity.
I found this manuscript to be highly relevant for any virus, but given the context-the COVID-19 pandemic-I find the results to be timely, relevant, and fantastically well conducted. The interaction between the epidemiological knowledge and biophysical precision is clear, and the implications are also very clear. The manuscript is well-written and organized.
I believe that this manuscript should be published, would make a worthy contribution to great body of SARS-CoV-2 and extended COVID-19 literature.
The recommended changes have to do with subtle editorial points, and efforts to make this work as clear as possible.
1. Figure 1: I believe that the authors should check the labels. I could be wrong, but I believe the labels in the captions are wrong.
2. Equations:
The interaction between the text and the appendix could be improved, and I challenge the authors to better integrate this information. The authors should read the equations from the perspective of the reader: can the reader fully grasp the flow of information from the equations as provided. I am of a mixed opinion on this, but given the overall excellence of the manuscript, I encourage the authors to make this work as clear and digestible as possible, as it has the potential to be a defining piece of literature.
We have revised the manuscript in light of the decision comments, with the aim of improving readability and clarity. Edits include collating supplementary figures as figure supplements to the main figures, where appropriate, nudging points in figures to avoid overplotting and improve readability, and clarifying distinctions between the different measurements and model fits used.




































