key: cord-0929640-qm8nosf4 authors: Li, You; Wang, Xin; Nair, Harish title: Global Seasonality of Human Seasonal Coronaviruses: A Clue for Postpandemic Circulating Season of Severe Acute Respiratory Syndrome Coronavirus 2? date: 2020-07-21 journal: J Infect Dis DOI: 10.1093/infdis/jiaa436 sha: 1dddf95325e480568854cac2fe1dadcac26adc1d doc_id: 929640 cord_uid: qm8nosf4 BACKGROUND: The ongoing pandemic of coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) could recur as seasonal outbreaks, a circulating pattern observed among other preexisting human seasonal coronaviruses (sCoVs). However, little is known about seasonality of sCoVs on a global scale. METHODS: We conducted a systematic review of data on seasonality of sCoVs. We compared seasonality of sCoVs with influenza virus and respiratory syncytial virus. We modeled monthly activity of sCoVs using site-specific weather data. RESULTS: We included sCoV seasonality data in 40 sites from 21 countries. sCoVs were prevalent in winter months in most temperate sites except for China, whereas sCoVs tended to be less seasonal in China and in tropical sites. In temperate sites excluding China, 53.1% of annual sCoV cases (interquartile range [IQR], 34.6%–61.9%) occurred during influenza season and 49.6% (IQR, 30.2%–60.2%) of sCoV cases occurred during respiratory syncytial virus season. Low temperature combined with high relative humidity was associated with higher sCoV activity. CONCLUSIONS: This is the first study that provides an overview of the global seasonality of sCoVs. Our findings offer clues to the possible postpandemic circulating season of SARS-CoV-2 and add to the knowledge pool necessary for postpandemic preparedness for SARS-CoV-2. The novel human coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), that emerged in Wuhan, China in December 2019 has since spread worldwide [1] . SARS-CoV-2 has caused >3.6 million cases of coronavirus disease 2019 (COVID-19) and >250 000 deaths as of 6 May 2020 [2] . It remains unclear which trajectory the transmission of SARS-CoV-2 will follow after the initial pandemic wave. One of the speculations is that SARS-CoV-2 will adapt itself to a seasonal circulation like the 2009 influenza pandemic H1N1 virus, which was later found to circulate annually in the same season as other existing seasonal influenza strains [3] . For human coronaviruses, 4 known seasonal coronaviruses (sCoVs) have long been circulating in human populations, including 2 alphacoronaviruses (NL63 and 229E) and 2 betacoronaviruses (OC43 and HKU1). Therefore, it is possible that once endemic, SARS-CoV-2, a betacoronavirus, will follow the same seasonal patterns as the sCoVs. In a recent modeling study projecting the postpandemic transmission dynamics of SARS-CoV-2, Kissler and colleagues found that recurrent outbreaks of SARS-CoV-2 in the United States (US) would probably occur during wintertime, like the sCoVs, after the initial pandemic wave [4] . However, the seasonality of these long-circulating sCoVs is still unknown on a global scale. To this end, we conducted a systematic review on the global seasonality of human sCoVs. This systematic review is registered with the International Prospective Register of Systematic Reviews (PROSPERO; registration number CRD42020182629). We searched Medline (Ovid), Embase (Ovid), Global Health (Ovid), Web of Science, and 3 Chinese databases (China National Knowledge Infrastructure, Wanfang, and Chongqing VIP) for studies published between 1 January 1990 and 15 April 2020 that reported monthly or weekly activity of sCoVs (ie NL63, 229E, OC43, and HKU1). We also searched 2 preprint databases (medRxiv and bioRxiv) for preprints between 1 January 2020 and 15 April 2020. The detailed search strategy is shown in the Supplementary Appendix. Selection criteria were applied as follows: • Studies reporting data on laboratory-confirmed incidence of human infection of coronaviruses for at least 12 consecutive months (or 52 weeks equivalent); AND • Studies with stable testing practice throughout all years reported (eg, studies should be able to conduct coronavirus tests in both winter season and other seasons with In addition to the literature search, we also searched for online datasets that were eligible for our review, using the keywords "coronavirus*, " "surveillance, " and "seasonal*. " Two reviewers (Y. L. and X. W.) extracted the data from the literature, independently, using a template that was described elsewhere [5] . In brief, we collected general information from each study including site, country, data source, and test method. Geographical coordinates were extracted for the study site. For seasonality, we extracted monthly aggregated number of sCoV cases. We also extracted the monthly number of coronavirus cases by genus (ie, Alphacoronavirus and Betacoronavirus) and by species (ie, NL63, 229E, OC43, and HKU1). To compare the seasonality of sCoVs with other 2 common respiratory viruses, influenza virus and respiratory syncytial virus (RSV), we also extracted monthly aggregated number of influenza and RSV cases from each study, if available. For included studies where influenza virus and/or RSV seasonality was not available, we searched studies that reported data from the same or a nearby site from our previous work on influenza virus and RSV seasonality [5] . We also conducted quality assessment for each eligible study using a quality assessment form comprising 3 brief questions regarding data representativeness, test practice, and timely reporting as described elsewhere [5] . When 2 or more studies were available for a site, the study with the higher-quality score was retained with the rest being excluded and marked as duplicate data. We aggregated the number of positives by month across years for each site and calculated annual average percentage (AAP) as a measurement of the strength of virus activity by the formula below: where i denotes the month i and n denotes the number of cases. We plotted heat maps displaying the activity of sCoV, influenza virus, and RSV for each site sorted by latitude. To understand how the peak activity of each virus overlapped, we identified for each virus the top 3 months with highest AAP as the first step; we then calculated the cumulative AAP of another virus that occurred during these 3 months. For each site, we extracted meteorological data from the site's nearest weather station provided by the US National Centers for Environmental Information using R package GSODR [6] . We modeled monthly AAP of sCoV activity with meteorological predictors, including mean-centered temperature, relative humidity, and dew point, in a locally estimated scatterplot smoothing model as described elsewhere [5] . Details of the model are available in the Supplementary Appendix. In brief, we included 2 models based on the model selection results: 1 model with mean-centered dew point and relative humidity as predictors and the other with mean-centered temperature and relative humidity as predictors. Studies were eligible for this analysis if they reported >100 positive sCoV cases. We conducted 2 sets of models that excluded 2 temperate sites in China and included all sites, respectively. This was due to the observation that the sCoV seasonality in the temperate sites of China was less seasonal, different from the other temperate sites. We did not model sCoV activity by genus or by species due to the paucity of data. All data analyses were conducted using R software (version 3.5.2) [7] . All the data in the study are made available in Edinburgh DataShare [8] . We initially identified 2414 studies via our search; after excluding duplicates, we screened 1670 studies by title and abstract and screened 205 studies by full text. A total of 40 studies were included in the final analysis ( Figure 1 ). These studies represented 40 sites from 21 countries (Figure 2 and Supplementary Figure 1 ). The number of positive sCoVs ranged from 25 to 39 573 across sites. Polymerase chain reaction (PCR) was used to detect sCoV in all the studies. Six of the 40 studies focused on 1 or 2 particular sCoV species and therefore did not contribute to the results for the overall sCoVs (all species). Details on these studies and their quality assessment are in Supplementary Tables 1 and 2 . High activity of sCoVs, as measured by AAP, was observed in winter months in most temperate sites (Figure 3) , with the exception in China where sCoV activity tended to be year-round (Supplementary Figure 2) . No difference in study quality was observed between studies reporting sCoVs in China and other studies. More variations in sCoV activity were observed in the tropical sites. No difference in timing of season was observed between alphacoronaviruses and betacoronaviruses (Figures 4 and 5 ). In the temperate sites excluding China, 53.1% of the sCoV cases (interquartile range [IQR], 34.6%-61.9%) occurred during influenza season (defined by the top 3 months with highest AAP), and 49.6% of the sCoV cases (IQR, 30.2%-60.2%) occurred during RSV season. Less overlap was observed in the tropical sites as well as temperate sites in China between sCoV activity and influenza/RSV activity (20% during influenza season and 29% during RSV season; Supplementary Figure 3 ). A total of 17 studies with >100 positive sCoV cases were included in our model (including 2 sites from temperate China). Low temperature with higher relative humidity was found to be associated with higher proportion of sCoV cases; dew point was observed to have similar relationship with sCoV activity as temperature ( Figure 6 ). Similar results were found from the model excluding 2 temperate sites from China (Supplementary Figure 4) . At the time of writing, >180 countries have been affected by COVID-19 [2] , and it is timely and extremely important to understand the long-term future of SARS-CoV-2. Understanding of the global circulating season of sCoVs, the genetic relatives of SARS-CoV-2, might provide clues on the possible circulating season of SARS-CoV-2. In the present study, we described the month-by-month activity of sCoVs in 40 sites from 21 countries. We found that sCoVs occurred mainly in winter months in temperate sites except for China and was less seasonal in China and tropical sites. We highlighted a high proportion of co-circulating sCoV cases during influenza virus and RSV seasons, implicating the possibility RSV IFV sCoV 263 52 19 280 2056 239 248 58 51 216 87 39 573 388 98 117 133 1552 25 322 42 48 51 43 270 1924 160 293 38 87 46 32 30 34 28 691 86 213 540 211 994 49 232 509 541 16 575 376 11 610 102 767 307 549 254 171 755 5427 26 1707 803 236 393 149 34 9863 117 1859 194 84 548 889 4854 2358 61 53 16 633 705 3208 99 561 62 526 204 2780 64 4545 1270 80 180 415 620 122 2230 1362 120 2438 178 967 47 50 241 1002 75 1423 25 22 496 127 1215 32 141 364 of a substantial increase in the demand to healthcare system resources during wintertime. Our findings have important implications in the control and prevention of COVID-19. The global seasonality of sCoVs provides a clue for the possible circulating timing of SARS-CoV-2 after the initial pandemic. A modeling study reported that SARS-CoV-2 will likely enter into regular circulation starting from 2021 or 2022 in the US and synchronize with sCoVs, if immunity to SARS-CoV-2 is not permanent [4] . Although it is not entirely clear how long the immunity to SARS-CoV-2 could last, a recent study showed that most convalescent plasmas obtained from individuals who recover from COVID-19 do not contain high levels of neutralizing activity [9] ; of note, immunity to sCoV was reported to wane within 1 year [10] . We observed winter outbreaks similar for all species of sCoVs in the temperate sites, suggesting that the SARS-CoV-2 epidemics might occur in winter months in temperate regions. Interestingly, sCoV activity in the temperate sites of China was observed to be less seasonal, with high sCoV activity seen in summer, autumn, and winter. In the temperate sites excluding China, there was substantial overlap between sCoV activity and activity of influenza virus and RSV, with approximately 50% of annual sCoV cases occurring during influenza and RSV season. This would pose a big challenge to currently strained healthcare systems if SARS-CoV-2, which causes more severe illness than sCoVs, circulates in the same season as influenza virus and RSV, both of which represent substantial burdens in morbidity and mortality [11] [12] [13] . In addition, the seasonality of different species of sCoVs in our study provides important baseline data for epidemiology and modeling studies in understanding the interaction between SARS-CoV-2 and sCoVs; a recent study supported the cross-reactive T-cell recognition between sCoVs and SARS-CoV-2 [14] . However, it should be noted that the interpretation of our findings needs to be made in the context of several limitations in our study. First, although we found that seasonality of sCoVs did not differ by virus species, we could not rule out the possible scenario where SARS-CoV-2 adapts itself to a distinct circulating season from other sCoVs. This might be a result of competition between viruses, for example, the observed negative interaction between influenza A virus and rhinovirus [15] . Second, none of the included studies reported seasonality results of sCoVs by age group. Infectivity of sCoV is found to be higher in children [16] , whereas that of SARS-CoV-2 is higher in adults [17] . The seasonality results from those studies including all ages were consistently highly influenced by the pediatric group. Third, our findings are based on limited data, including only 20% (8/40) of studies reporting data in the tropics. Seasonality of sCoVs in the tropics is still largely unknown, especially in sub-Saharan Africa and in tropical America. Similarly, our model was mainly informed by the data from temperate sites (accounting for 88% [2/17] of data) and therefore, the model results should be interpreted with caution. Fourth, although most temperate sites excluding China showed winter outbreaks of sCoVs in our study, this finding should not be generalized to other temperate sites where sCoV seasonality was underreported (eg, Latin America). One of the lessons learned from the history of influenza pandemics is its transition from pandemic to seasonal circulation and the replacement of existing strain(s) with the pandemic strain. Although it is not clear how the existing sCoVs initially emerged or whether they had previously replaced any viruses, understanding the global seasonality of sCoVs would undoubtedly offer some clues on the possible postpandemic circulating season of SARS-CoV-2 and contribute to the knowledge pool for the postpandemic preparedness for SARS-CoV-2. not copyedited and are the sole responsibility of the authors, so questions or comments should be addressed to the corresponding author. World Health Organization. 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Clinical characteristics of coronavirus disease 2019 in China Author contributions. Y. L. conceptualized the study; Y. L. led the data collection with contributions from X. W; Y. L. led the data analysis and visualization; Y. L. led the data interpretation with input from X. W. and H. N.; Y. L. wrote the first draft of the report; and X. W. and H. N. reviewed the draft for intellectual content. All authors approved the final report.Potential conflicts of interest. Y. L. reports grants from the World Health Organization (WHO) and the Foundation for Influenza Epidemiology, outside the submitted work. H. N. reports grants from the Foundation for Influenza Epidemiology, the Innovative Medicines Initiative, the WHO, Sanofi, and the National Institute for Health Research, and personal fees from the Bill & Melinda Gates Foundation, Sanofi, Janssen, and AbbVie, outside the submitted work. X. W. reports no conflicts of interest.All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed. Supplementary materials are available at The Journal of Infectious Diseases online. Consisting of data provided by the authors to benefit the reader, the posted materials are