Circadian clocks control the function of our immune system, virus replication and the severity of infections. Our daily rhythms also regulate the pharmacokinetics and efficacy of several therapeutics. Consequently, better understanding of the effects of circadian biology on SARS-CoV-2 infection would improve the clinical management of COVID-19.
The world is still in the throes of a coronavirus outbreak known as coronavirus disease 2019 (COVID-19), which caused more than half a million deaths worldwide within just a few months. Circadian rhythms have a profound impact on human health, because they have a central role in coordinating daily physiological processes, including the functions of innate and adaptive immunity. Circadian clock disruption in hosts leads to increased pathogen replication and dissemination, which indicates that the severity of acute infections could be markedly influenced by circadian rhythms.
Humans are more susceptible to infections at certain times of the day, because the function of our defence systems follows a daily rhythmic pattern1. We have previously demonstrated that the time of day of virus infection critically affects disease progression following herpes and influenza A virus infections2. Study of the ‘clock–infection biology’ in viral diseases, which intends to decipher the complex relationships between circadian timekeeping, host immunity and host–virus interactions, is a relatively new concept3. This emerging field holds great potential to unravel the complex pathogenesis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and may help to improve therapy against this novel pathogen, as well as inform public health policy.
Infection severity could be regulated by the clock
Viruses entirely depend on host-cell machineries for their replication and dissemination. Circadian rhythms regulate diverse types of systemic viral infections, including those of influenza A virus, herpes viruses, flavivirus and vesicular stomatitis virus3. Disruption of our circadian clock favours rapid virus replication and dissemination, which may subsequently lead to a severe form of infection2. Although no direct evidence of circadian control of SARS-CoV-2 infection has been reported, circadian regulation in other respiratory viruses (such as influenza A) and the circadian nature of our immune responses accentuate the urgent need for studying clock–infection biology in COVID-19.
The pathophysiology of SARS-CoV-2 infection and its severe complications are not well understood. Host responses in COVID-19, specifically the uncontrolled aggressive inflammatory response that can lead to multi-organ failure, strongly modulate disease severity. Notably, the expression and/or activity of virtually all the components of our innate and adaptive immune system, and thus of inflammatory immune responses, follow robust circadian rhythms1. Therefore, it would be highly informative to investigate the circadian aspects of SARS-CoV-2 pathophysiology and host responses against this pathogen. Moreover, boosting the activity of circadian immunity factors could help to manage COVID-19, as circadian clocks provide a competitive advantage to the host.
We anticipate that COVID-19 severity also depends on when in the day–night cycle SARS-CoV-2 infection occurs, as the battle between virus replication and its neutralization by the host immune system depends on the circadian activity phase of the host. Whether the severity of COVID-19 is influenced by the time of virus infection could be easily tested using human cell lines or mouse models of SARS-CoV-2 infection, in which the animals or cells need to be inoculated with the same dose of pathogen 12 h apart, that is, during the ‘resting’ and ‘active’ phases. In such studies, a comparative analysis of the wild-type animals and core clock mutant animals would be essential to elucidate the specific roles of circadian clocks in regulating SARS-CoV-2 replication and in the progression of the infection.
Dosing time could improve therapeutic efficacy
Circadian clocks regulate the pharmacokinetics and efficacy of many therapeutics, as several drug targets and the proteins involved in drug transport and metabolism exhibit daily rhythmic expression in our bodies4. Consequently, another critical aspect of COVID-19 management will be to understand the dosing-time dependency of drugs that inhibit SARS-CoV-2 in vitro or that elicit any clinical improvement in the infected patients. Drugs with shorter half-lives (~6 hours or less) are substantially influenced by dosing time, and most drugs with moderate half-lives (8 to 15 hours) also exhibit dosing time dependency4. In addition to drugs, dosing time can also regulate the efficacy of viral vaccines, as time of day influences the magnitude of the antibody response generated in our bodies post-vaccination. Notably, vaccination against the influenza virus A/H1N1 and B strains was found to be more effective when administered in the morning compared with the afternoon5.
At present, there is no established, effective therapy for SARS-CoV-2 infection, and the available treatments are mainly supportive. However, a recent study has demonstrated clinical improvement in severe cases of COVID-19 following a 10-day course treatment with remdesivir (GS-5734)6. Remdesivir has a very short plasma half-life in non-human primates and mice. Similarly, many other potential antiviral drugs have poor plasma stability and short half-lives, leading to inadequate effectiveness against the rapid and persistent viral expansion.
Assessment of the most effective dosing time in the context of dynamic host–pathogen interactions may dramatically improve the efficacy of drugs and vaccines. Consequently, circadian rhythms should be considered when designing and dosing candidate drugs and vaccinations against SARS-CoV-2, in order to obtain the best possible clinical outcomes.
The clocks of pathogenicity and treatment
SARS-CoV-2 infection results in dysregulation of several essential physiological processes in the host, including diverse metabolic pathways, protein synthesis, macrophage function, cellular oxidant detoxification, apoptosis and platelet degranulation7,8. In addition, SARS-CoV-2 infection activates inflammatory responses, interleukin signalling and the complement cascade7. Intriguingly, almost all of these physiological processes are tightly regulated by the circadian clock machinery.
Recent systems-level studies have defined many host factors and physiological pathways as potential therapeutic targets for COVID-197,9. A recently published study identified 332 human proteins that interact with SARS-CoV-2 proteins using affinity-purification mass spectrometry9. We examined the possible circadian rhythms of expression of the mouse orthologues of these 332 SARS-CoV-2-interacting host factors using our recently published mouse circadian transcriptome data10. Importantly, we observed that the expression of 30% of these host factors shows circadian oscillation (Supplementary Fig. 1a). Furthermore, using the Circadian Expression Profiles Database (CircaDB), we evaluated the daily expression profiles of the SARS-CoV-2 interacting host factors that are targeted by existing FDA-approved drugs or by clinical or preclinical compounds. Notably, we have found that the expression profiles of most of these potential drug targets exhibit robust 24-hour oscillation in at least one organ or tissue in mammalian systems (Supplementary Fig. 1b). Taken together, these findings strongly support our view of the pressing need to better understand how the circadian clock affects SARS-CoV-2 infection to achieve optimal clinical management of COVID-19.
Based on our current knowledge of the crosstalk between the circadian clocks and viral infections, it is apparent that we are more vulnerable to certain respiratory viruses during the early morning. We now need to determine empirically whether COVID-19 is also more severe at certain times of the day. If so, an infection during that specific time of the day might spread faster and affect our immune system more severely than at other times. Emerging evidence suggests that people with a disrupted circadian clock owing to old age, working night shifts, jet lag or irregular sleeping and eating habits have a less vigorous immune system and thereby could be more susceptible to such viral respiratory diseases. These simple considerations could help us to control outbreaks of this pandemic and possibly of future pandemics by defining the most suitable working (or staying at home) hours and maintaining a healthy body and circadian clock to reduce the chance of infection and rapid transmission. At a population level, such ‘temporal’ social interventions, alongside the conventional ‘spatial’ social distancing, could help abate the spread of SARS-CoV-2.
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The authors declare no competing interests.
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Ray, S., Reddy, A.B. COVID-19 management in light of the circadian clock. Nat Rev Mol Cell Biol 21, 494–495 (2020). https://doi.org/10.1038/s41580-020-0275-3
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