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Turkish Journal of Medical Sciences logoLink to Turkish Journal of Medical Sciences
. 2021 Dec 17;51(7):3253–3261. doi: 10.3906/sag-2110-153

Epidemiology of COVID-19: What changed in one year?

Cemal BULUT 1,*, Yasuyuki KATO 2
PMCID: PMC8771048  PMID: 34844297

Abstract

A coronavirus brought the first pandemic attack of this century as a flu virus did a hundred years ago. This greatest pandemic of the century brings us new opportunities to understand and explore the dynamics of a contagious disease. Nearly two years later, we are still collecting the evidence to understand the disease. Some basic epidemiological properties are still urgently needed. Not only the origin of the virus but also Ro value, possible transmission routes, epidemiologic curves, case fatality rates, seasonality, severity and mortality risk factor, effects on the risk groups, differences between countries and so on still require strong evidence prior to making final suggestions. In this review, we tried to evaluate the epidemiological evidence to scrutinize where exactly we are in this pandemic.

Keywords: COVID-19, epidemiology, pandemic

1. Introduction

A coronavirus brought the first pandemic attack of this century as a flu virus did a hundred years ago. Nowadays, this greatest pandemic of the century greatly opens up new opportunities for our lives to understand and explore the dynamics of a contagious disease in detail. Almost two years later, we are still collecting the evidence to clearly comprehend the disease. With this respect, some basic epidemiological properties are still questioned due to several unknown parameters in this area. In these cases, scientific findings should be supported and augmented theoretically and experimentally during/after the pandemic. In this study, we aim to evaluate epidemiological evidence to obviously elucidate where exactly we are in this pandemic.

2. Origin of the virus

It is well-known that bats are reservoirs of coronaviruses. It is interesting to note here that most of these viruses are unknown to us and their number might be 1200–6000 [1]. A study focusing on the evolutionary origin of SARS-CoV reported four novel SARS-CoV-2–related viruses. Another result of this report was that high diversity of bat coronaviruses could be placed in a small area [2].

Even though reported new bat viruses highly related to SARS-CoV or SARS-CoV-2 in China and neighboring countries strengthen the theory of zoonotic origin [3], similarity between SARS-CoV-2 and viruses studied at the Wuhan Institute of Virology does not remove the questions about a laboratory leak incident, as reported elsewhere [4,5].

According to the WHO report about the origin of SARS-CoV-2 virus, for introduction of virus, possible-to-likely pathway is direct zoonotic spillover. Keep in mind that the existence of an intermediate animal host for this introduction had been considered likely to very likely pathway. Furthermore, possibility of a laboratory escape from a laboratory working with animal coronavirus had been reckoned as extremely unlikely pathway [6].

3. Ro and Rt value of COVID-19

Basic reproduction number (Ro) as an indicator of the transmissibility of a virus is utilized frequently. Ro of COVID-19 was quite different among countries. It is well-known that its value was 3.2 in China whilst it was 2.2 in western European countries [7]. In a mathematic modeling, Ro values in Turkey and Japan were 1.71 and 4.3, respectively [8]. In a metaanalysis, the pooled global Ro was found to be 4.08 [9]. Stated simply, the estimated summary reproductive number was 2.87 (95% CI, 2.39–3.44) [10]. As for time-varying reproduction number (Rt), it is the value for the population which was not completely susceptible and not fully adopted some prevention or control measures. In a study, upon evaluating Rt values for 160 countries, it can be expressed that this value was nearly 10 at the beginning of pandemic [11].

4. Incubation period

Incubation period of COVID-19 was 5.7 days according to a systematic review result [12]. This period could be as short as 3.1 days and could be long as 12.1 days. It can be seen that incubation period was a bit shorter than one year before report [13,14]. The surprising result in [20] was that the incubation period in men could be about 3.2 days longer than in women. This period seems to be different in several countries [12].

5. Epidemic curves of COVID-19

As of June 21, according to WHO data, COVID 19 has been confirmed as the cause of a total of 180,518,201 cases and 3,918,120 deaths. Many areas of the world have experienced four series of waves of epidemic (see Figure 1 for details). For some countries such as Iran and Japan, each wave was bigger than previous ones, while for others such as Turkey and United Kingdom the amplitudes of waves were getting low, as seen in Figure 2.

Figure 1.

Figure 1

New daily case and death numbers all over the world.

Figure 2.

Figure 2

New daily case numbers of some countries from different parts of the world.

These epidemic curves have been partly formed by strong restriction rules and preparedness of the health care systems. Surprisingly, its shapes were also quite different in the Western and the Eastern parts of the world. It is obviously seen in Figure 3 that whilst in Europe, big and devastating waves occurred during the first year of the pandemic, eastern Asian countries saw the highest numbers of case and death during the second year of the disease.

Figure 3.

Figure 3

Epidemic curves of some European and Asian country and waves of outbreak.

Different scenarios such as progression rate, mortality, and Ro values were noted for each country, and each country developed their own new normal rules to overcome the pandemic. It seems that progression of pandemic was affected not only by governments’ political and economic decisions or accessibility to health care, but also by seasonality, weather condition, vaccination status, and many different specified or unspecified factors.

6. Transmission routes

6.1. Respiratory routes

As other respiratory pathogens, SARS-CoV-2 spreads mainly by respiratory secretion produced by cough, sneeze, and talk. In spite of the fact that person-to-person contact is the major route of transmission, various sizes of contaminated air particles seem to be involved [15]. It is widely accepted that SARS-CoV-2 virus is primarily spread by large droplets (>5 µL). Nevertheless, more scientific evidence has been available supporting that smaller particles transmit the virus and airborne transmission can occur [16]. Although live viruses were isolated from surface and air samples, their half-live was around 6 h [17]. Additionally, Ro value of SARS-CoV-2 is very low as compared to other airborne transmitted viruses. More importantly, another exact fact is that aerosol generating procedures could lead to aerosol transmission and could be problematic in hospital settings [17].

6.2. Direct contact

The presence of SARS-CoV-2 in the environment and contamination of the surface have been recognized as a possible mode of transmission of COVID-19. This environmental contamination could be a problem especially in health care settings [18]. It seems that durability of SARS-CoV-2 on different materials is a bit shorter than other coronaviruses [19]. Environmental contamination could be as high as 54%–69% of the contact surfaces, with SARS-CoV-2 loads ranging from 28.1 to 132.7 gene copies per cm2 [20]. Though environmental contamination serves as a possible route transmission, the contribution of this type of transmission remains unclear [18].

6.3. Vertical routes (mother to children)

It is well-known that maternal SARS-CoV-2 infection could increase the risk of some respiratory disorders and could cause some other morbidities in neonates [21]. However, vertical transmission had not been demonstrated as a transmission route [22]. Anecdotal detection of SARS-CoV-2 in the fetal site of placenta by using different methods had brought a possibility of transplacental transmission and fetal infection [23]. The probability of vertical transmission is not as high enough as it was at the beginning of the pandemic [24-26].

6.4. Oral–fecal routes

Although the detection rate of SARS-CoV-2 RNA in fecal samples is high, the isolation rate of viable viruses seems low. In a study from China, serial stool sampling showed that viral shedding was directly related to disease severity and it could be as long as 5 weeks [27]. This study also reported a successful isolation of SARS-CoV-2 in 2 samples collected (when?). Another important point was more than 2/3 of the patients had positive fecal RNA after pharyngeal swabs became negative [28]. Some other reports suggested that environmental sampling of sewage water revealed the presence of SARS-CoV-2 and relevant community outbreaks of COVID-19 [29]. These reports raises a new possibility that oral–fecal transmission of SARS-CoV-2 could occur like the outbreak of SARS in Amoi Garden occurred through the sewage system in 2003 [30].

7. Asymptomatic carriage/infection

According to a metaanalysis, up to half of COVID patients could be asymptomatic. The rate of this condition could be higher among female and children [31]. It is interesting to note that an earlier metaanalysis showed that asymptomatic infection rate was as low as 16% [32]. Results of another metaanalysis indicated that these asymptomatic cases could transmit the virus for a longer period and could have subclinical lung injuries [33]. Nonetheless, some other studies emphasized the need for a standard asymptomatic infection definition [34]. It is heartening to note that these metaanalyses also showed the need of early recognition, better surveillance, and effective preventive strategies to control COVID-19 disease in population [32-36].

8. Superspreaders

The possibility of infecting a large number of patients has become an attractive topic of COVID-19. Patients who infect a large number of susceptible people are accepted as superspreaders. Characteristics of superspreaders remain unclear. Predisposing conditions like environmental conditions, large gatherings, ineffective ventilation systems, unwise use of personnel protective equipment, poor hygiene are among possibilities, but these questions have not been properly answered yet [37]. Recent reports from different countries have showed that 10%–20% of the cases were responsible for 80% of transmission [38], which suggests that superspreading events occur more commonly than previously thought.

9. Reinfection

Emergence of antigenic variation is a challenge for control of respiratory viruses [39]. Coronaviruses has become an example of these challenges. In spite of the fact that SARS-CoV-2 generates enough B cell and T cell response to control the disease, lack of long-term immunity is an accepted reality for coronavirus-related immunity [40]. New evidence exhibits that immunity could not wane for a year at least [41]. A review showed that reinfection rate was very low (0.0%–1.1%) and there was no evidence of increasing risk of infection over time [42]. Another clear fact was that reinfection rate was higher in younger patients, and generally, disease severity was not increased in the second course [43,44]. However, we need more detail about if these results are due to viral reactivation, reinfection, or false test results [43].

10. Seasonality of COVID-19

In general, all respiratory viruses have seasonal cycles [45]. These cycles are formed both by environmental factors and human behavior. Newly discovered SARS-CoV and SARS-CoV-2 infections also started in winter months. In addition, some reports support the seasonal nature of SARS-CoV-2 [46,47]. However, it cannot be pointed out that climatic parameters such as temperature or humidity alone play a central role during the pandemic [48]. Therefore, it is important to point that countries should focus on health policies rather than weather variable to control the pandemic.

11. Mortality, how deadly COVID-19 is?

The overall case fatality of COVID-19 was 2.1% at the end of August 2021 World Health Organization (2021). COVID-19 Weekly Epidemiological Update, Edition 55, published 31 August 2021 https://www.who.int/publications/m/item/weekly-epidemiological-update-on-covid-19---31-august-2021 [Access data:01.09.2021]. Nevertheless, this rate was 6.3 on the April 2020 World Health Organization (2020). Coronavirus disease 2019 (COVID-19). Situation Report – 84. https://www.who.int/docs/default-9 source/coronaviruse/situation-reports/20200413-sitrep-84-covid-19.pdf?sfvrsn=44f511ab_2 [Access data:14.07.2021] . Herein, it seems that the mortality rates have shown great differences among patient groups and between countries. Case fatality rates in several countries are presented in Figure 4, which shows different case fatality rates observed at different phases of the pandemic.

Figure 4.

Figure 4

Epidemic curves of some European and Asian country and waves of outbreak.

It is noticed that mortality rates of COVID-19 vary widely in different countries. Generally speaking, at the end of August 2021, this number fell in the range of 0.46 and 9.24. Crude mortality rates of some countries whose case number is greater than a hundred thousand are listed in Table 1.

Table 1.

Crude mortality rates of some countries (August 2021).

Name Cases, cumulative total Deaths, cumulative total Crude mortality rates %
Peru 2,142,153 197,879 9.24
Mexico 3,225,073 253,155 7.85
Ecuador 498,678 32,087 6.43
China 122,744 5676 4.62
Tunisia 642,788 22,609 3.52
Zimbabwe 123,001 4293 3.49
Indonesia 4,008,166 128,252 3.2
South Africa 2,698,605 79,584 2.95
Italy 4,488,779 128,795 2.87
Brazil 20,570,891 574,527 2.79
Namibia 123,861 3345 2.7
Russian Federation 6,785,374 177,614 2.62
Viet Nam 358,456 8666 2.42
Germany 3,877,612 92,022 2.37
Chile 1,634,394 36,688 2.24
Pakistan 1,127,584 25,003 2.22
Iran 4,715,771 102,648 2.18
Argentina 5,133,831 110,352 2.15
The United Kingdom 6,524,585 131,680 2.02
Kenya 229,628 4528 1.97
France 6,448,367 112,180 1.74
Spain 4,794,352 83,337 1.74
United States of America 37,588,957 623,900 1.66
India 32,474,773 435,110 1.34
Japan 1,318,346 15,663 1.19
Iraq 1,832,240 20,262 1.11
Republic of Korea 239,287 2228 0.93
Malaysia 1,572,765 14,342 0.91
Thailand 1,083,951 9788 0.9
Turkey 6,234,520 54,765 0.88
Cuba 592,619 4618 0.78
Israel 1,005,511 6864 0.68

Table 2 summarizes and compares the changes on mortality rates of selected countries during the pandemic. To explain in more detail, it can be stated that, as given in Table 2, an interesting result was that while some countries that had higher mortality rates in the first months of the pandemic, a decline in the rate was observed in later phases of the pandemic. Another interesting point was that some countries with higher mortality rates in the early months of the pandemic recorded a decline in the rate at the later stages of the pandemic (Table 2).

Table 2.

Changes on mortality rates of selected countries during the pandemic.

Countries June 30, 2020 December 31, 2020 March 31, 2021 August 15, 2021
Bangladesh 1.3 1.5 1.5 1.7
Brazil 4.3 2.6 2.5 2.8
Canada 8.3 2.7 2.3 1.8
France 18.9 2.5 2.0 1.7
Germany 4.6 1.8 2.7 2.4
India 3.0 1.4 1.3 1.3
Indonesia 5.1 3.0 2.7 3.1
Iran 4.7 4.6 3.3 2.2
Iraq 3.9 2.2 1.7 1.1
Italy 14.5 3.5 3.1 2.9
Japan 5.2 1.5 1.9 1.3
Mexico 12.3 8.9 9.1 8.0
Pakistan 2.1 2.1 2.2 2.2
Peru 3.3 3.7 9.3 9.3
Republic of Korea 2.2 1.4 3.4 3.0
South Africa 1.8 2.7 1.7 1.0
Spain 11.4 2.7 2.3 1.8
Turkey 2.6 1.5 1.0 0.9
United Kingdom 14.0 3.1 2.9 2.1
United States of America 5.0 1.8 1.8 1.7

12. Risk factors for mortality and severe diseases

Now, many risk factors for mortality and severe disease have been clearly defined. According to metaanalyses, some chronic comorbidities, demographic variables and laboratory findings are identified as risk factors for higher mortality.

Chronic comorbidities, complications, and demographic variables including acute kidney injury, COPD, diabetes, hypertension, cerebrovascular disease, cancer, increased D-dimer, male sex, older age, current smoking, and obesity are clinical risk factors for a fatal outcome associated with COVID-19 [49-51]. Another finding of the metaanalyses was that there was considerable variety in the prevalence of comorbidities, and severe disease and mortality in different geographic regions. While the prevalence of comorbidities was highest in the US studies, the proportion of severe disease of COVID-19 was highest in Asian studies and the mortality was highest in the European and Latin American countries [52].

Potential genetic host factors like HLA-C*04:01, HLA-A*01:01, HLA-A*02:01, and HLA-A*03:01 have been identified as having an important role in immune defense against COVID-19 [53,54].

Prognostic score, a combination of variables like age, comorbidity, CD4+ T cell count, C-reactive protein (CRP), D-dimer, lactate dehydrogenase, cardiac troponin I, have been developed to predict the progression to severe illness and death in COVID-19 patients [55,56]. These scores should be applied carefully to different situations and countries.

13. Conclusion

We have achieved better understanding of the epidemiology of COVID-19 in the past 2 years. However, we still do not know when this pandemic will finally end. We need to create more evidence and make further scientific progress to understand, to explore, and to pass on the future generations what exactly happened during this pandemic and how we acted to control it.

References

  1. Anthony SJ Johnson CK Greig DJ Kramer S Che X Global patterns in coronavirus diversity. Virus Evolution. 2017;3 doi: 10.1093/ve/vex012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Zhou H Ji J Chen X Bi Y Li J Identification of novel bat coronaviruses sheds light on the evolutionary origins of SARS-CoV-2 and related viruses. Cell. 2021;184:4380–4391. doi: 10.1016/j.cell.2021.06.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Holmes EC Goldstein SA Rasmussen AL Robertson DL Crits-Christoph A The origins of SARS-CoV-2: A critical review. Cell. 2021;184:4848–4856. doi: 10.1016/j.cell.2021.08.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Burki T. The origin of SARS-CoV-2. Lancet Infectious Diseases. 2020;20:1018–1019. doi: 10.1016/S1473-3099(20)30641-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Knight D. Bioweapons and the History of Laboratory Leaks. Southern Medical Journal. 2021;114:465–467. doi: 10.14423/SMJ.0000000000001283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Part. Joint China 6. WHO-convened Global Study of Origins of SARS-CoV-2. February 2021. Joint Report 30 March. 2021;14:January–January. [Google Scholar]
  7. Locatelli I Trächsel B Rousson V Estimating the basic reproduction number for COVID-19 in Western Europe. PLoS One. 2021;16 doi: 10.1371/journal.pone.0248731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Niu Y Rui J Wang Q Zhang W Chen Z Containing the Transmission of COVID-19: A Modeling Study in 160 Countries. Frontier Medicine (Lausanne) 2021;8:701836–701836. doi: 10.3389/fmed.2021.701836. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Yu CJ Wang ZX Xu Y Hu MX Chen K Assessment of basic reproductive number for COVID-19 at global level: A meta-analysis. Medicine (Baltimore) 2021;100 doi: 10.1097/MD.0000000000025837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Billah MA Miah MM Khan MN Reproductive number of coronavirus: A systematic review and meta-analysis based on global level evidence. PLoS One. 2020;15 doi: 10.1371/journal.pone.0242128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Niu Y Rui J Wang Q Zhang W Chen Z Containing the Transmission of COVID-19: A Modeling Study in 160 Countries. Frontier Medicine (Lausanne) 2021;8:701836–701836. doi: 10.3389/fmed.2021.701836. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Wassie GT Azene AG Bantie GM Dessie G Aragaw AM A Systematic Review and Meta-Analysis. Incubation Period of Severe Acute Respiratory Syndrome Novel Coronavirus 2 that Causes Coronavirus Disease. 2019;93:100607–100607. doi: 10.1016/j.curtheres.2020.100607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Wang Y Wang Y Chen Y Qin Q. Unique epidemiological and clinical features of the emerging 2019 novel coronavirus pneumonia (COVID-19) implicate special control measures. Journal of Medical Virology. 2020;92:568–576. doi: 10.1002/jmv.25748. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Lai CC Shih TP Ko WC Tang HJ Hsueh PR Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and coronavirus disease-2019 (COVID-19): The epidemic and the challenges. International Journal of Antimicrobial Agents. 2020;55:105924–105924. doi: 10.1016/j.ijantimicag.2020.105924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Meyerowitz EA Richterman A Gandhi RT Sax PE Transmission of SARS-CoV-2: A Review of Viral, Host, and Environmental Factors. Annals of Internal Medicine. 2021;174:69–79. doi: 10.7326/M20-5008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Greenhalgh T Jimenez JL Prather KA Tufekci Z Fisman D Ten scientific reasons in support of airborne transmission of SARS-CoV-2. 2021;397:1603–1605. doi: 10.1016/S0140-6736(21)00869-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. van Doremalen N Bushmaker T Morris DH Holbrook MG Gamble A Aerosol and Surface Stability of SARS-CoV-2 as Compared with SARS-CoV-1. New England Journal of Medicine. 2020;382:1564–1567. doi: 10.1056/NEJMc2004973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kanamori H Weber DJ Rutala WA Role of the Healthcare Surface Environment in Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Transmission and Potential Control Measures. Clinical Infectious Diseases. 2021;72:2052–2061. doi: 10.1093/cid/ciaa1467. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Aboubakr HA Sharafeldin TA Goyal SM Stability of SARS-CoV-2 and other coronaviruses in the environment and on common touch surfaces and the influence of climatic conditions: A review. Transbound Emerging Diseases. 2021;68:296–312. doi: 10.1111/tbed.13707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Amoah ID Pillay L Deepnarian N Awolusi O Pillay K Detection of SARS-CoV-2 RNA on contact surfaces within shared sanitation facilities. International Journal of Hygiene and Environmental Health. 2021;236:113807–113807. doi: 10.1016/j.ijheh.2021.113807. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Norman M Navér L Söderling J Ahlberg M Hervius Askling Association of Maternal SARS-CoV-2 Infection in Pregnancy with Neonatal Outcomes. Journal of the American. 2021;325:2076–2086. doi: 10.1001/jama.2021.5775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Oliveira KF Oliveira JF Wernet M Paschoini MC Ruiz MT English Vertical transmission and COVID-19: a scoping review. Revista Brasileira de Enfermagem. 2021;10:0034–0034. doi: 10.1590/0034-7167-2020-0849. [DOI] [PubMed] [Google Scholar]
  23. Schwartz D.A. Dhaliwal A Coronavirus Diseases in Pregnant Women, the Placenta, Fetus, and Neonate. In: Rezaei N. (eds) Coronavirus Disease - COVID-19. Advances in Experimental Medicine and Biology. 2021;1318:223–242. doi: 10.1007/978-3-030-63761-3_14. [DOI] [PubMed] [Google Scholar]
  24. Fan C Lei D Fang C Li C Wang M We Worry? Clinical Infectious Diseases Should Perinatal Transmission of 2019 Coronavirus Disease-Associated Severe Acute Respiratory Syndrome Coronavirus. 2021;2:862–864. doi: 10.1093/cid/ciaa226. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Halici-Ozturk F Ocal FD Aydin S Tanacan A Ayhan SG Investigating the risk of maternal-fetal transmission of SARS-CoV-2 in early pregnancy. Placenta. 2021;106:25–29. doi: 10.1016/j.placenta.2021.02.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Tolu LB Ezeh A Feyissa GT Vertical transmission of Severe Acute Respiratory Syndrome Coronavirus 2: A scoping review. PLoS One. 2021;16 doi: 10.1371/journal.pone.0250196. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Zhang Y Chen C Song Y Zhu S Wang D Excretion of SARS-CoV-2 through faecal specimens. Emerging Microbes and Infection. 2020;9:2501–2508. doi: 10.1080/22221751.2020.1844551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Cuicchi D Lazzarotto T Poggioli G Fecal-oral transmission of SARS-CoV-2: review of laboratory-confirmed virus in gastrointestinal system. International Journal of Colorectal Disease. 2021;36:437–444. doi: 10.1007/s00384-020-03785-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Dhama K Patel SK Yatoo MI Tiwari R Sharun K SARS-CoV-2 existence in sewage and wastewater: A global public health concern? Journal of Environmental Management. 2021;280:111825–111825. doi: 10.1016/j.jenvman.2020.111825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Meng XJ Liang TJ SARS-CoV-2 Infection in the Gastrointestinal Tract: Fecal-Oral Route of Transmission for COVID- 2021;160:1467–1469. doi: 10.1053/j.gastro.2021.01.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Syangtan G Bista S Dawadi P Rayamajhee B Shrestha LB Asymptomatic SARS-CoV-2 Carriers: A Systematic Review and Meta-Analysis. Frontiers in Public Health. 2021;8:587374–587374. doi: 10.3389/fpubh.2020.587374. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. He J Guo Y Mao R A systematic review and meta-analysis. Proportion of asymptomatic coronavirus disease. 2019;93:820–830. doi: 10.1002/jmv.26326. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Oran DP Topol EJ Prevalence of Asymptomatic SARS-CoV-2 Infection : A Narrative Review. Annals of Internal Medicine. 2020;173:362–367. doi: 10.7326/M20-3012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Cevik M Bogoch II Carson G D’Ortenzio E Kuppalli K. Prevalence of Asymptomatic SARS-CoV-2 Infection. Annals of Internal Medicine. 2021;174:283–284. doi: 10.7326/L20-1283. [DOI] [PubMed] [Google Scholar]
  35. Kronbichler A Kresse D Yoon S Lee KH Effenberger M Asymptomatic patients as a source of COVID-19 infections: A systematic review and meta-analysis. International Journal of Infectious Diseases. 2020;98:180–186. doi: 10.1016/j.ijid.2020.06.052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Stadler RN Maurer L Aguilar-Bultet L Franzeck F Ruchti C Systematic screening on admission for SARS-CoV-2 to detect asymptomatic infections. Antimicrobial Resistance and Infection Control. 2021;10:44–44. doi: 10.1186/s13756-021-00912-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Majra D Benson J Pitts J Stebbing J SARS-CoV-2 (COVID-19) superspreader events. Journal of Infection. 2021;82:36–40. doi: 10.1016/j.jinf.2020.11.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Althouse BM Wenger EA Miller JC Scarpino SV Allard A Superspreading events in the transmission dynamics of SARS-CoV-2: Opportunities for interventions and control. PLoS Biology. 2020;18 doi: 10.1371/journal.pbio.3000897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Siggins MK Thwaites RS Openshaw PJM Respiratory Other Durability of Immunity to SARS-CoV-2. Trends in Microbiology. 2021;29:648–662. doi: 10.1016/j.tim.2021.03.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Cromer D Juno JA Khoury D Reynaldi A Wheatley AK Prospects for durable immune control of SARS-CoV-2 and prevention of reinfection. Nature Reviews Immunology. 2021;21:395–404. doi: 10.1038/s41577-021-00550-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Vitale J Mumoli N Clerici P De Paschale M Evangelista I Assessment of SARS-CoV-2 Reinfection 1 Year After Primary Infection in a Population in Lombardy, Italy. JAMA Internal Medicine. 2021;10 doi: 10.1001/jamainternmed.2021.2959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Murchu O Byrne E Carty P De Gascun PG Keogan C Quantifying the risk of SARS-CoV-2 reinfection over time. Reviews in Medical Virology. 2021;10 doi: 10.1002/rmv.2260. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Piri SM Edalatfar M Shool S Jalalian MN Tavakolpour S. A systematic review on the recurrence of SARS-CoV-2 virus: frequency, risk factors, and possible explanations. Infectious Diseases (Lond) 2021;53:315–324. doi: 10.1080/23744235.2020.1871066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Abu-Raddad LJ Chemaitelly H Malek JA Ahmed AA Mohamoud YA Assessment of the risk of SARS-CoV-2 reinfection in an intense re-exposure setting. Clinical Infectious Diseases. 2020;10 doi: 10.1093/cid/ciaa1846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Li Y Wang X Nair H. Global Seasonality of Human Seasonal Coronaviruses: A Clue for Postpandemic Circulating Season of Severe Acute Respiratory Syndrome Coronavirus 2? Journal of Infectious Diseases. 2020;222:1090–1097. doi: 10.1093/infdis/jiaa436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Scafetta N. Distribution of the SARS-CoV-2 Pandemic and Its Monthly Forecast Based on Seasonal Climate Patterns. International Journal of Environmental Research and Public Health. 2020;17:3493–3493. doi: 10.3390/ijerph17103493. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Zheng HL Guo ZL Wang ML Yang C An SY Effects of climate variables on the transmission of COVID-19: a systematic review of 62 ecological studies. Environmental Science and Pollution Research International. 2021;10:1–18. doi: 10.1007/s11356-021-15929-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Paraskevis D Kostaki EG Alygizakis N Thomaidis NS Cartalis C A review of the impact of weather and climate variables to COVID-19: In the absence of public health measures high temperatures cannot probably mitigate outbreaks. The Science of the Total Environonment. 2021;768:144578–144578. doi: 10.1016/j.scitotenv.2020.144578. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Dessie ZG Zewotir T Mortality-related risk factors of COVID-19: a systematic review and meta-analysis of 42 studies and 423,117 patients. BMC Infectious Diseases. 2021;21:855–855. doi: 10.1186/s12879-021-06536-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Ssentongo P Ssentongo AE Heilbrunn ES Ba DM Chinchilli VM Association of cardiovascular disease and 10 other pre-existing comorbidities with COVID-19 mortality: A systematic review and meta-analysis. PLoS One. 2020;15 doi: 10.1371/journal.pone.0238215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Wu Y Li H Zhang Z Liang W Zhang T Risk factors for mortality of coronavirus disease 2019 (COVID-19) patients during the early outbreak of COVID-19: a systematic review and meta-analysis. Annals of Palliatiave Medicine. 2021;10:5069–5083. doi: 10.21037/apm-20-2557. [DOI] [PubMed] [Google Scholar]
  52. Thakur B Dubey P Benitez J Torres JP Reddy S A systematic review and meta-analysis of geographic differences in comorbidities and associated severity and mortality among individuals with COVID-19. 2021;11:8562–8562. doi: 10.1038/s41598-021-88130-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Weiner J Suwalski P Holtgrewe M Rakitko A Thibeault C Medicine EClinical Increased risk of severe clinical course of COVID-19 in carriers. 2021 Sep. 2021;04:01–01. doi: 10.1016/j.eclinm.2021.101099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Shkurnikov M Nersisyan S Jankevic T Galatenko A Gordeev I Association of HLA Class I Genotypes With Severity of Coronavirus Disease-19. Frontiers in Immunolology. 2021;12:641900–641900. doi: 10.3389/fimmu.2021.641900. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Xu W Huang C Fei L Li W Xie X A Novel Prediction Model of COVID-19 Progression: A Retrospective Cohort Study. Infectious Diseases and Therapy. 2021;10:1491–1504. doi: 10.1007/s40121-021-00460-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Moriyama M Hugentobler WJ Iwasaki A Seasonality of Respiratory Viral Infections. Annualal Review of Virology. 2020;7:83–101. doi: 10.1146/annurev-virology-012420-022445. [DOI] [PubMed] [Google Scholar]

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