| Literature DB >> 34306118 |
L Guo1,2, Z Yang3, L Zhang4, S Wang3, T Bai3,4, Y Xiang1, E Long1,3,4.
Abstract
Environmental factors such as temperature and relative humidity can affect the inactivation and transmission of coronaviruses. By reviewing medical experiments on virus survival and virus transmission between infected and susceptible species in different temperature and humidity conditions, this study explores the influence of temperature and relative humidity on the survival and transmission of viruses, and provides suggestions, with experimental evidence, for the environmental control measures of Coronavirus Disease 2019. The results indicated that (1) virus viability and infectivity is increased at a low temperature of 5 ℃ and reduced at higher temperatures. (2) Virus survival and transmission is highly efficient in a dry environment with low relative humidity, and also in a wet environment with high relative humidity, and it is minimal at intermediate relative humidity. Therefore, in indoor environments, the lack of heating in winter or overventilation, leading to low indoor temperature, can help virus survival and help susceptible people being infected. On the contrary, modulating the indoor relative humidity at an intermediate level is conducive to curb epidemic outbreaks. © Islamic Azad University (IAU) 2021.Entities:
Keywords: Coronavirus Disease 2019; Environmental control strategies; Relative humidity; Temperature; Virus infectivity; Virus survival
Year: 2021 PMID: 34306118 PMCID: PMC8286163 DOI: 10.1007/s13762-021-03495-9
Source DB: PubMed Journal: Int J Environ Sci Technol (Tehran) ISSN: 1735-1472 Impact factor: 2.860
Survival of virus on surfaces
| References | Test virus | Viral titer | Substrate | T | RH | Results |
|---|---|---|---|---|---|---|
| Lin and Marr ( | MS2 phage and Φ6 phage | 1010 to 1011 pfu·ml−1 | Polystyrene cell culture plate | 22 ℃ | 23–100% 7 working conditions | Both viruses had high relative survival at low and high RH |
| Prussin et al. ( | Phi6 phage | 108 to 1010pfu·ml−1 | Cell culture plate | 14 °C; 19 °C; 22 °C; 25 °C; 28 °C; 31 °C; 34 °C; 37 °C; 40 °C | 23–98% 7 working conditions | Viral infectivity decreases exponentially with increasing temperature. When RH is moderate, the infectivity decreases significantly |
| Yang et al. ( | IAV | 1.78 × 108 TCID50·ml−1 | Cell culture plate | 20–24 °C | 17.5–98.9 9 working conditions | The survival rate of influenza virus was highest when the RH was close to 100% or less than 50% |
| Chan et al. ( | SARS-CoV | 107 TCID50·ml−1 | Plastic plates | 28 °C; 33 °C; 38 °C 80 °C; | 89%; > 95% | High RH and high temperature have certain inactivation effect on SARS-CoV |
| Casanova et al. ( | TGEV | 106 to 107MPN·ml−1 | Stainless steel | 4 °C; 20 °C; 40 °C | 20%; 50%; 80% | High temperature inactivates the virus to a certain extent; the inactivation rate of the virus is higher under moderate RH |
| MHV | 106 to 107MPN·ml−1 | 4 °C; 20 °C;40 °C | 20%; 50%; 80% | |||
| Duan et al. ( | SARS-CoV | 3.33 × 106 TCID50·ml−1 | Materials in household and in nature | 4 °C; 20 °C; 37 °C; 56 °C; 67 °C; 75 °C | Uncontrolled | The infectivity of SARS-CoV decreases with increasing temperature |
| Riddell et al. ( | SARS-CoV-2 | 4.97 × 107·ml−1 | Stainless steel, Polymer note, Paper note, Glass, Cotton, Vinyl | 20 °C; 30 °C; 40 °C | Uncontrolled | High temperature decreases the half-life and initial viral loads of SARS-CoV-2 on different surfaces |
| Kratzel et al. ( | SARS-CoV-2/München-1.1/2020/929 | 1.58 × 107 TCID50·ml−1 | Metal discs | 4 °C; Room temper-ature; 30 °C | Uncontrolled | The recovered virus titers had only minimal decline at 30 °C and a larger variability at 4 °C |
| Bearden and Casanova ( | Φ6 phage | 107 PFU | Plastic toy | 22 ℃ | 40%; 60% | Inactivation was approximately 2log10 after 24 h at 60% RH and 6.8log10 at 10 h at 40% RH |
Fig. 1Ambient temperature affects the survival of viruses on surfaces
Fig. 2RH affects the survival of viruses on surfaces
Survival of aerosolized virus in the air
| References | Test virus | Initial concentration | Aerosolization space | T | RH | Results |
|---|---|---|---|---|---|---|
| Lin and Marr ( | MS2 phage and Φ6 phage | 1010 to 1011 pfu·ml−1 | 27L aluminum rotating drum | 22 °C | 23–100% 7 working conditions | Viruses survived well in RHs below 33% and 100% |
| Pyankov et al. ( | MERS-CoV | 6.1 ± 0.23 lg·ml−1 | Rotating aerosol chamber | 25 °C | 79% | In hot, dry air, the virus decays more strongly |
| 38 °C | 24% | |||||
| de la Noue et al. ( | MNV | 106.2 pfu·ml−1 | Sealed aerosolization boxes | 25 °C | 10–100% 5 working conditions | Moderate RH facilitates viral inactivation and reduces viral infectivity |
9 °C 25 °C | 10–100% 5 working conditions | Low temperature is more suitable for virus survival | ||||
| Noti et al. ( | H1N1 | 4.5 × 103 total virus·l−1 | 23m3 aerosolization chamber | 20 °C | 7–73% 7 working conditions | High RH reduces the infectivity of influenza viruses |
| 20 °C | 20%, 45% | At moderate humidity, viruses in aerosols rapidly lose infectivity after coughing | ||||
| van Doremalen, Bushmaker, and Munster ( | MERS-CoV | 106 TCID50·ml−1 | An aerosolization chamber | 20 °C | 40%, 70% | MERS-CoV virus aerosols are very stable at low relative humidity |
| Zhao et al. ( | Gumbro | 6 to 7log10 EID50·ml−1 | 1.4m3 aerosolization chamber | 10 °C 20 °C 30 °C | 40%, 70% | Long-range transmission of airborne viruses is more likely at 20 °C than at 10 °C or 30 °C |
| Harper ( | Vaccinia virus | 5 × 107pfu·ml−1 | 75L rotating stainless steel drum | (1) 11 °C (2) 22 °C (3) 32 °C | (1) 20%, 50%, 83%; (2) 18%, 50%, 83%; (3) 18%, 50%, 82% | Most viruses survive well at low temperatures The lower the relative humidity, the better the survival of most viruses, the opposite is true for poliovirus |
| Influenza virus | 1 × 107 MP 50·ml−1 | (1) 7 °C (2) 22 °C (3) 32 °C | (1) 24%, 51%, 82%; (2) 21%, 35%, 50%, 65%, 81%; (3) 30%, 50%, 81% | |||
| Venezuelan equine encephalom-yelitis virus | 1 × 1010 MIPLD 50·ml−1 | (1) 9 °C (2) 22 °C (3) 32 °C | (1) 19%, 48%, 86%; (2) 21%, 50%, 82%; (3) 19%, 48%, 83% | |||
| Poliomyeli-tis virus | 5 × 108 pfu·ml−1 | 22 °C | 20.5% 35% 50% 65% 80% | |||
| Hemmes et al. ( | Influenza virus | 2 × 103 to 2 × 104 ID50·l−1 | 4m3 aerosolization chamber | 10 °C 20 °C 30 °C | < 50%; > 50% | Viral mortality increases with relative humidity |
| Poliomyelitis virus | 2–8 × 107 pfu·ml−1 | Viral mortality decreases with increasing relative humidity | ||||
| Smither et al. ( | SARS-CoV-2 England-2 | 1 × 106 TCID50·ml−1 | 40L Goldberg drum | 19–22 °C | 40–60%; 68–88% | In tissue culture media, SARS-CoV-2 England-2 is more stable at medium RH compared to higher RH |
Fig. 3Temperature affects the survival of aerosolized virus
Fig. 4RH affects the survival of aerosolized virus
Infectivity of virus in animal models
| References | Test virus | Viral titer | Animal(s) | Contact method | T | RH (%) | Results |
|---|---|---|---|---|---|---|---|
| Gustin et al. ( | PN99 | 103.8 to 105.5 pfu·ml−1 | Ferrets | Aerosolized virus | 5 °C | 70 | Infectivity 33.3% |
| 23 °C | 30 | Infectivity 66.7% | |||||
| 50 | Infectivity 33.3% | ||||||
| 70 | Infectivity 66.7% | ||||||
| IN11 | 5 °C | 70 | Infectivity 0% | ||||
| 23 °C | 30 | Infectivity 100% | |||||
| 50 | Infectivity 0% | ||||||
| 70 | Infectivity 66.7% | ||||||
| Lowen et al. ( | PN99 | 103 pfu·ml−1 | Guinea pigs | Cage to cage | 30 °C | 20 50 65 80 | Infectivity 0% |
| Housed in one cage | 30 °C | 20 | Infectivity 100% | ||||
| 50 | Infectivity 100% | ||||||
| 80 | Infectivity 75% | ||||||
| 20 °C | 20 | Infectivity 100% | |||||
| Lowen ( | PN99 | 103 pfu·ml−1 | Guinea pigs | Cage to cage | 5 °C | 35 | Infectivity 100% |
| 50 | Infectivity 75–100% | ||||||
| 65 | Infectivity 50% | ||||||
| 80 | Infectivity 50% | ||||||
| 20 °C | 20 | Infectivity 75–100% | |||||
| 35 | Infectivity 100% | ||||||
| 50 | Infectivity 25% | ||||||
| 65 | Infectivity 75% | ||||||
| 80 | Infectivity 0% | ||||||
| 30 °C | 35 | Infectivity 0% | |||||
| Lester ( | Influenza A-PR8 strain | 0.82–0.85gm | Mice | aerosolized virus | 23 °C | 23 | Mortality 100% |
| 30 | Mortality 100% | ||||||
| 40 | Mortality 95% | ||||||
| 45 | Mortality 22.5% | ||||||
| 50 | Mortality 22.5% | ||||||
| 55 | Mortality 22.5% | ||||||
| 60 | Mortality 22.5% | ||||||
| 65 | Mortality 42.5% | ||||||
| 70 | Mortality 75% | ||||||
| 80 | Mortality 100% |
Fig. 5Temperature affects the infectivity of virus in animal models
Fig. 6RH affects the infectivity of virus in animal models