Annual congress report
Published: 2022-04-26
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New endemic and pandemic pathologies with interhuman airborne transmission through ear, nose and throat anatomical sites

Clinic of infectious Diseases, University of Bari, Aldo Moro, Bari, Italy
Infection Control & Infectious Disease Service, University Hospital Campus Bio-Medico, Rome, Italy
SARS MERS SARS-CoV-2 COVID-19 H1N1 RSV pandemic health system

Abstract

The current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has once again stigmatised the importance of airborne pathogens and their clinical, social and public health impact. Respiratory viruses are transmitted between individuals when the pathogen is released from the upper airways or from the lower respiratory tract of an infected individual. Airborne transmission is defined as the inhalation of the infectious aerosol, named droplet nuclei which size is smaller than 5 mm and that can be inhaled at a distance up to 2 metres. This route of transmission is relevant for viral respiratory pathogens, including severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome (MERS)-CoV, influenza virus, human rhinovirus, respiratory syncytial virus (RSV) and other respiratory virus families that differ in viral and genomic structures, susceptibility of a population to the infection, severity, transmissibility, ways of transmission and seasonal recurrence. Human respiratory viruses generally infect cells of the upper respiratory tract, eliciting respiratory signs and symptoms, sometimes without the possibility to differentiate them clinically. As seen by the current Coronavirus Disease 2019 (COVID-19) pandemic, human respiratory viruses can substantially contribute to increased morbidity and mortality, economic losses and, eventually, social disruption. In this article, we describe the structural, clinical and transmission aspects of the main respiratory viruses responsible for endemic, epidemic and pandemic infections.

Introduction

The current SARS-CoV-2 pandemic has once again stigmatised the importance of airborne pathogens and their clinical, social and public health impact. Respiratory viruses are transmitted between individuals when the pathogen is released from the upper airways or from the lower respiratory tract of an infected individual 1. Actually, pathogen droplets released from respiratory events are the primary means of dispersion and transmission of organisms that colonise or/and infect the upper airways. During breathing, talking, singing, shouting, coughing and sneezing, individuals harbouring pathogens in the upper airways may produce small saliva particles (droplets) and aerosols containing those pathogens 2-4. Airborne transmission is defined as the inhalation of the infectious aerosol, named droplet nuclei which size is smaller than 5 mm and which can be inhaled at a distance of up to 2 metres. This way of transmission is relevant for viral respiratory pathogens, including severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome (MERS)-CoV, influenza virus, human rhinovirus, respiratory syncytial virus (RSV) and other respiratory virus families that differ in viral and genomic structures, susceptibility of the populations to the infection, severity, transmissibility, ways of transmission and seasonal recurrence.

These human respiratory viruses generally infect cells of the upper respiratory tract, eliciting respiratory signs and symptoms, sometimes without the possibility to differentiate them clinically. As seen by the current COVID-19 pandemic, human respiratory viruses can substantially contribute to increase morbidity and mortality, economic losses and, eventually, social disruption 5.

Methods

To carry out this narrative review we searched PubMed, Scopus, Google Scholar, EMBASE, Cochrane Library, and WHO websites from 1950 to January 2022 to identify articles discussing structural, clinical and transmission aspects of the main respiratory viruses responsible for endemic, epidemic and pandemic infections.

The chain of transmission for pathogens transmitted through the airborne route: the case of COVID-19

Predicting changes in the spread of COVID-19 requires understanding of the interaction between natural processes, such as host immunity, and interventions such as physical distancing. A framework for natural processes is provided by the coevolution of hosts and viruses. Although it is early in the co-evolutionary history of SARS-CoV-2 and the human host, complementary theoretical insights into the dynamics of host-pathogen interactions are becoming relevant, e.g., the possibility of endemic equilibria 6.

Drivers of disease dynamics can be conceptualised as a sequence of rings in a chain of infection which, in turn, relates to the life cycle of the pathogen and present different opportunities for intervention. The first link in the chain of infection is the pathogen itself. SARS-CoV-2 is an RNA virus, with the potential for high rates of mutation and recombination and therefore a high diversity of genotypes 7. Mutations may contribute to enhancement of viral proliferation and infection as well as escape from host immune attack 8.

The chain of infection can be interrupted at the point of the reservoir, including other hosts (primary, intermediate) and the wider environment. Currently there is no evidence of animal reservoirs for SARS-CoV-2, and therefore no ongoing transfer to humans, other than from the original hypothesised primary host (bats) in China. SARS-CoV-2 can survive in the abiotic environment with half-lives of up to nine days, depending on the nature of the substrate and the temperature 9. Coronaviruses can persist in aqueous solutions for several weeks, again with a strong inverse correlation with temperature 10. Various disinfectants are effective at inactivating the virus and therefore the abiotic environment is a potential target for disruption of COVID-19 dynamics 11.

The third ring is represented by the transfer of the virus between human hosts, which has been the main target of control measures, including use of masks, reduction of social activities, contact tracing, quarantine and physical/social distancing. As with other viruses transmitted through the respiratory route, SARS-CoV-2 is primarily transmitted by droplets, airborne route and contact with contaminated surfaces and fomites (which in turn relate to the properties of the abiotic environment), and by aerosol formation during invasive respiratory procedures. Some concern has been raised by the respiratory shedding of virus which peaks at the end of the first week after infection, just before and as symptoms are developing 12. Although testing of convalescent COVID-19 patients has provided evidence for persistent RNA shedding, there is no suggestion of chronic carriers of SARS-CoV-2.

The last ring of the chain of infection is represented by the characteristics of the susceptible human host. Host determinants are an important ring in the chain of transmission for infectors and infectees. Indeed, for infectors, tissue and cellular tropism for virus replication can be important determinants for contagiousness and transmission of respiratory viruses. Whereas SARS-CoV replicates mainly in epithelial cells of the alveoli, SARS-CoV-2 replicates predominantly in upper respiratory ways and in the bronchial epithelium, thus explaining its more efficient transmission 13. The Omicron variant of SARS-CoV-2 appears to be more efficient in transmission because tropism for the epithelial cells of the otolaryngological anatomic sites seems higher than for the Wuhan and Delta variants 14. As a consequence, host nasal or throat viral shedding is an important determinant for contagiousness and transmission.

For influenza A virus, however, otolaryngological site viral shedding alone seems does not completely explain household transmission 15. Other factors have been hypothesised, including the presence of superspreaders, and presymptomatic shedding. For SARS-CoV-2, levels of viral shedding seem to be similar between presymptomatic and symptomatic infected individuals, thus determining a silent presymptomatic transmission and a consistent fraction of infected individuals from asymptomatic COVID-19 individuals 16,17.

Another important point is the fact that pre-existing immunity and vaccination can “modulate” viral shedding from infectors 18-20. In the recent forth wave of the COVID-19 pandemic, highly sustained by Omicron, boostering by a third vaccine administration can partly explain the higher rate of asymptomatic or paucisymptomatic SARS-CoV-2 infected individuals, who manifest only congestion, runny nose and sore throat. Passive immunisation in early infected COVID-19 patients has been shown to decrease the rate of hospitalisation for COVID-19 in acute and intensive care units 21. Similarly, new antivirals have been introduced in clinical practice to decrease the viral load in early infected individuals 22. Fully vaccination coverage, new vaccines and monoclonal antibodies targeted against new variants are probably the main steps to reduce the burden of susceptible hosts.

From the side of infectees, tissue-specific expression of viral receptors angiotensin-converting enzyme 2 (ACE-2) 23 or glycosylation and glycan expression in the upper and lower respiratory tract may determine not only the most prevalent clinical manifestations, but also may affect contagiousness, as the case of virus-laden aerosols infecting predominantly the nasal cavity 23.

Human genetic factors can also influence susceptibility to SARS-COV-2, including effects via blood group, HLA genotypes and fibroblasts. The major genetic risk factor for severe SARS-CoV-2 infection and hospitalisation seems to be related to variations on human chromosome 3. Finally, the role of innate immunity against COVID-19 is under study, since exposure to microbial signals and to cytokines trains myelomonocytic cells with enhanced effector function against microbial agents.

Below we describe the structural, clinical and transmission aspects of the main respiratory viruses responsible for endemic, epidemic and pandemic infections.

Coronaviruses

Coronaviruses (CoVs), enveloped positive-sense RNA viruses, were isolated for the first time in 1960 as disease-causing agents in humans. There are four genera (alpha, beta, gamma, and delta), with alpha and beta receiving the most attention due to their propensity to cross animal-human boundaries and to cause relevant human diseases.

There are seven known beta human Coronaviruses (HCoVs), including Severe Acute Respiratory Syndrome (SARS)-CoV (SARS-CoV), Middle East Respiratory Syndrome (MERS)-CoV (MERS-CoV), SARS-CoV hCoV-HKU1, and hCoV-OC43, as well as hCoV-NL63 and hCoV-229E from the genus alfa.

The coronaviruses hCoV-HKU1, hCoV-OC43, hCoV-NL63 and hCoV-229E cause asymptomatic or moderate respiratory and gastrointestinal infections, accounting for 5-30% of common colds 24. However, attention to this family of viruses only began with the first global outbreak caused by the SARS-CoV in 2002. To date, only three highly pathogenic and lethal hCoVs are known, namely SARS-CoV, MERS-CoV and SARS-CoV-2 25. In this section we will summarise structural, transmission and clinical findings of this family of viruses.

SARS and MERS

SARS was the first new disease of the 21st century of global interest. The virus was first identified in Foshan, Guangdong Province, China, in mid-November 2002. However, only in February 2003 did the virus spread to Hong Kong, and through international air travel it rapidly spread worldwide 26.

The association of the first SARS-CoV patients with wild animal markets in Guangdong strengthens the hypothesis that SARS-CoV emerged from wild animals (including palm civets) sold at these markets 27. To confirm this, a CoV strain with a homology similarity of almost 99.9% was isolated from palm civets at wild animal markets able to pass their hosts to humans causing human-to-human transmission 28. Also, as epidemiological criteria supporting this hypothesis, almost 80% of SARS-CoV patients claimed to have had contact with palm civets during the sporadic occurrence in Guangdong 29. Furthermore, other authors found that farmed palm civets were free of SARS-CoV, while those sold in animal markets showed high IgG levels for SARS CoV 30. This corroborates the role of palm civets in the origin of disease.

SARS-CoV is both contagious and virulent. Moreover, due to its incubation period of up to 10 days, it can be spread worldwide by asymptomatic carriers travelling worldwide with no symptoms 31. By the end of the pandemic in June 2004, there were 8422 cases worldwide with 916 deaths (11% mortality rate) 32. In Table I, we summarise the main findings.

The virus is spread from person to person through droplets produced by coughing and sneezing. In addition, infection can spread through contact with contaminated droplets on surfaces 33. Fortunately, numerous studies have shown that regularly used disinfectants such as Clorox, 75% ethanol and fixatives such as formaldehyde and paraformaldehyde cause the virus to lose its infectivity 34.

In September 2012, eight years after the first SARS-CoV outbreak, a new Coronavirus classified as MERS-CoV (Middle East Respiratory Syndrome) was identified in Saudi Arabia 35. The first MERS cases were reported in Jordan in April 2012, but it was confirmed only later 36. So far, all MERS infections have been linked to travel or stays in or around the Arabian Peninsula. Most MERS-CoV cases have been reported in Middle Eastern countries, including Saudi Arabia, the United Arab Emirates, Qatar, Oman, Kuwait and Iran 35.

There were 2578 laboratory-confirmed cases of Middle East respiratory syndrome (MERS) from 2012 to 2018. Larger outbreaks occurred in South Korea in 2015 and Saudi Arabia in 2018, with fatality rates of 34.3% in both cases 37.

MERS-CoV is a zoonotic virus that infects people through direct or indirect contact with ill dromedary camels, according to several studies 35,37. MERS-CoV has been confirmed in dromedaries in the Middle East, Africa and South Asia 38. The virus’s origins are unknown, although based on the examination of multiple viral genomes, it is thought to have originated in bats and been transferred to camels at some point in the distant past.

Both SARS and MERS have an average incubation period of 5-days, and 95% of patients who develop symptoms within 13 days after exposure. In both infections, cough, asthenia, headache, fever, cold, cough and myalgia are common symptoms 39,40. Also, diagnostic confirmation with a nasopharyngeal molecular swab with real-time Polymerase Chain Reaction (RT-PCR) can be facilitated by accurate history, which enhances the possibility of infection 41,42. MERS patients have a higher radiological involvement (90-100%) than SARS patients (60-10%). This is linked to a higher need for intensive care and a higher incidence of acute respiratory distress syndrome (ARDS) in MERS patients than with SARS 43,44. The fatality rate for MERS, which is around 34%, is consistently higher than the 9.6% mortality rate for SARS.

Diabetes, hypertension, renal failure and neoplasia are among the comorbidities that worsen the condition in both SARS and MERS patients. Furthermore, different studies have revealed that older age and male sex are risk factors of poor outcome for both diseases 43,44.

Furthermore, follow-up studies on SARS and MERS patients have showed that long-term sequalae occur in nearly 20-60% of individuals with asthenia, chronic tiredness, reduced lung function and worse quality of life at two years after infection 44-46. Anxiety, post-traumatic stress disorder and impaired performance at work are also reported in 20% of MERS and SARS patients 47,48.

SARS-CoV-2

The SARS-CoV-2 pandemic began when a significant number of atypical pneumonias were reported in December 2019 in Wuhan, China 49. Within weeks, a new coronavirus was isolated: SARS-CoV-2. After only few months, the virus had spread to 114 countries and on March 11th, 2020, the WHO declared SARS-CoV-2 as a global pandemic 50. To date, exactly 2 years after the start of the pandemic, more than 390 million cases with more than 5.7 million deaths are reported 51. No country in the world is virus free, with significant direct and indirect impact on mortality and control of other communicable and non-communicable diseases, due to a major impact on health services, with outpatient services severely disrupted 52,53.

SASR-CoV-2 is a single-stranded RNA virus with positive polarity (28-32 kb). The virus has four structural proteins: Spike (protein S), which allows the virus to bind to the membranes of the host cells, Envelope (protein E) and Membrane (protein M) combine to form the Nucleocapsid (protein N) capsid, which holds the genome. The S-glycoprotein is what determines the virus’ specificity for respiratory epithelial cells; in fact, it is known that SARS-CoV-2 can bind the ACE-2 receptor, which is expressed by cells in the capillaries of the lungs 54,55.

The specific origin of the new coronavirus is unclear, and no theory has been ruled out. A possible zoonotic aetiology has been postulated by several ideas proposed in early investigations (such as SARS and MERS) 56. In particular, Bungarus multicinctus, a highly venomous snake trafficked in the Wuhan wet market, was suspected by several scientists to be the source of the disease. Since most of the first affected people worked in that market, it was suspected that an early strain of the virus had arrived and spread to the province and adjacent territories. However, another zoonotic option might be the Malaysian pangolin, which is also sold in the Wuhan market 57-59.

It is known that SARS-CoV-2 has more of an indirect cytotoxic action than direct cytotoxicity. In fact, the action of the virus is decoded in this triple activity:

  1. cytokine storm: dysregulated or overactive immune responses can cause significant systemic damage. In the patient’s lung tissue and peripheral blood, mononuclear cells such as neutrophils and monocytes release high amounts of pro-inflammatory cytokines such as interleukin-6, interleukin-1 and tumour necrosis factor, which are linked to disease severity and death 60,61;
  2. hypoxaemic respiratory failure: some of the distinctive clinical features found in individuals with COVID-19 include the direct cytotoxic effects of the virus and the virus-induced reduction in surfactant levels, resulting in atelectasis. The pulmonary derangement of the disease is characterised by hypoxaemia, which occurs without any indication of respiratory distress (‘silent hypoxemia’) 62;
  3. COVID-19-related hypercoagulability: the cytokine storm and virus-induced endothelial dysfunction work together in this process with a significant risk of thrombosis in lungs or extrapulmonary areas 63,64.
  4. SARS CoV-2 has a 5-day incubation period, like SARS-CoV and MERS, with clinical features ranging from asymptomatic to severe patterns, where interstitial pneumonia evolves into ARDS causing high mortality 65. Currently, the mortality rate is of about 4%, but the global scenario for this disease is changing with the start of the vaccination campaign in December 2020 66 and the appearance of new virus variants.

Going beyond the acute phase, there is increasing evidence about long COVID syndrome, with symptoms related to COVID-19 persistent for 12 weeks after the acute infection episode. In particular, asthenia, myalgia, reduced working capacity can persist in 30-60% of cases 67. Also, anxiety and depression related to previous SARS-CoV-2 infection appear to be frequent 68.

In addition, multiple variants of the Wuhan type (Alpha, Delta, Gamma, Mu, Zeta, Omicron, and many more) have been identified in the last two years of the pandemic 69,70, which has an influence on both clinical management and global health policy, which we will not address in this paper.

H1N1

H1N1 influenza was first isolated in military troops during the 1918-1919 pandemic in the United States. One third of the world’s population was affected, around 50 million people died globally, of whom about 675,000 in the United States 71. Subsequent outbreaks of H1N1 swine flu were recorded in the United States in 1976 and more recently in April 2009, when a reassortant triple strain of influenza (H1N1) caused 2000 deaths in Mexico 72.

Influenza viruses are very unstable RNA viruses and can be found in wild animals as reservoirs, allowing genetic mutations and reassortments 73. Currently circulating in humans as seasonal influenza, H1N1 and H3N2 74 are subtypes of influenza A that originated in birds and pigs 75.

Until 1979, these strains had been the only one present in Europe isolated from pig farms and with a clear lineage relationship to the 1918 pandemic virus 75. Subsequently, since the 1980s, new strains of H1N1 swine influenza have been isolated, such as the H1avN1 virus, showing rapid and persistent adaptation in mammals 76. Subsequent viral reassortments led to the development of different genotypes such as H1N2 (H1huN2) with a higher capacity for gene reassortment and spreading 77.

Crucial for the pathogenesis of the virus is the HA protein, which is capable of drift and anti-hygienic shifts due to the flexibility of the viral RNA-dependent RNA polymerase 78. Indeed, previous pandemics are thought to have been caused by changes in the HA protein, including reassortments and mutations between animals and humans. Clinically, influenza has a short incubation period of about 2 days (range, 1-5 days). The clinical presentation may range from moderate to severe patterns, with fever, cough, bacterial overinfection and, in severe circumstances, acute respiratory distress syndrome (ARDS) and acute respiratory failure 79.

The H1N1 virus is now a common human flu virus with low mortality rate (0.03-0.8%), which is related to comorbidities and age of patients 80. The use of the 2009 H1N1 influenza virus vaccine has recently been approved, with positive implications for pandemic containment, patient outcomes and maintenance of healthcare systems 81.

Respiratory syncytial virus, RSV

The human respiratory syncytial virus (RSV) is an enveloped, non-segmented negative-strand RNA virus of family Paramyxoviridae able to cause respiratory tract infections especially in children with a seasonality between December and February and between April and May 82,83. It was first isolated in chimpanzees in 1955 and subsequently in infants with severe pulmonary disease 83.

The clinical presentation varies from mild infection of the upper respiratory tract or otitis media to severe and life-threatening involvement of the lower respiratory tract 84. The most common form in infants is bronchiolitis, with a hospitalisation rate of about 3%. Preterm delivery, chronic lung disease of prematurity, low birth weight, Down syndrome together with other chromosomal abnormalities, and neuromuscular dysfunction are also risk factors for RSV-related hospitalisation or worsening of the condition and admission to the critical care unit 85. RSV symptoms peak around day 5 and usually improve after 7-10 days. Due to the prolonged recovery of the ciliated cells, the cough may last for up to four weeks 86. The diagnosis of acute bronchiolitis is clinical and microbiological based on presentation with typical respiratory signs and symptoms, which may be accompanied by lethargy, irritability and poor nutrition. Nasopharyngeal washes or tracheal secretions are better specimens for confirming RSV than nasal swabs, although nasal swabs are the most widely used due to their convenience. Because of the short timeframe (less than 30 minutes), low cost and objective end point, enzyme immunoassay is the quick detection test most used. A chest X-ray may show a radiological image of pneumonia, with enhancement of the bronchial pattern. In addition, especially in children admitted to intensive care, concomitant battery overinfection is frequent. The mortality rate is low, below 0.5/0.8%, but with higher mortality in low-income countries due to the scarcity of resources and neonatal intensive care 87,88.

Conclusions and recommendations

In the last 20 years we have experienced three different Coronavirus pandemics with progressively greater spread and impact on life and health systems, and learned to live with RSV and H1N1 epidemics.

Some reflections can be drawn from this:

  1. training on epidemic preparedness and response must be an integral part of the educational and cultural background of health workers in order to always be prepared for what is no longer a sporadic or episodic event;
  2. a One Health approach, with high respect for nature and animals, is the basis for the prevention of infectious diseases. Deforestation, the use of exotic animals as food or medicine and intensive animal husbandry may be at the root of current pandemics and responsible for future ones;
  3. the indirect impact on other diseases cannot be neglected. Health systems must have plan to avoid disruption of diagnostic and therapeutic pathways;
  4. team working should be central in the health section. Respiratory pathogens require a strong co-operation of different specialists: infectious diseases specialists, microbiologists, ENT specialists, pulmonologists and epidemiologists. Only thinking system-wide and working together will it be possible to tackle current and future pandemics;
  5. vaccination is proving to be one of the most successful strategies in the fight against SARS-CoV-2. Allowing vaccination worldwide, including in low-income countries, is necessary for justice but also to avoid the emergence of new variants;
  6. development of therapeutic strategies is a key pillar to improve the outcome of our patients;
  7. developing cost-effective point-of-care tests can be crucial for widespread diagnosis in remote areas, more investments are needed on this field;
  8. long-term effects on patients and healthcare personnel must be constantly monitored;
  9. strengthening networks of molecular genomics laboratories worldwide is indispensable for nipping future epidemics in the bud.

Conflict of interest statement

The authors declare no conflict of interest.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Authors’ contributions

FDG and NP conceived the idea. Both authors reviewed the literature, drafted the manuscript, critically revised, and approved the final version before submission. Both authors have read and agreed to the published version of the manuscript.

Ethical consideration

The research was conducted ethically, with all study procedures being performed in accordance with the requirments of the World Medical Association’s Declaration of Helsinki.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Figures and tables

SARS-CoV MERS SARS-CoV-2 RSV H1N1
First isolation 16 November 2002, Foshan, China 4 April 2012, Zarqa, Jordan 7 December 2019, Wuhan, China 1955, United States 1918, United States
Family Betacoronavirus, lineage B Betacoronavirus, lineage C Betacoronavirus, lineage B Paramyxoviridae Orthomyxoviridae
Host receptor ACE2 DPP4 or CD26 ACE2 CX3CR1 Sialic acid
Reservoir and origin Palm civets Dromedary camels Unclear Chimpanzees Pigs
Genome RNA RNA RNA RNA RNA
Mode of transmission Respiratory droplet, Contact Respiratory droplet, Contact Respiratory droplet, Contact Respiratory Respiratory droplet, Contact
Mortality rate 9.6% 34.3% 4.4% < 1% 0.03-0.8%
Diagnosis rRT-PCR rRT-PCR rRT-PCR EIA rRT-PCR
Blood test results Lymphopenia and leukopenia Lymphopenia, thrombocytopenia Lymphopenia, thrombocytopenia, leukopenia, LDH Lymphopenia, AST, ALT, PCR Lymphocytosis and leukopenia
Long sequalae Yes Yes Yes No No
Vaccine No No Yes No Yes
Table I.Main characteristics of SARS-CoV, MERS, SARS-CoV2, VRS and H1N1.

References

  1. Wang CC, Prather KA, Sznitman J. Airborne transmission of respiratory viruses. Science. 2021; 373:eabd9149. DOI
  2. Morawska L, Johnson GR, Ristovski ZD. Size distribution and sites of origin of droplets expelled from the human respiratory tract during expiratory activities. J Aerosol Sci. 2009; 40:256-269. DOI
  3. Johnson GR, Morawska L, Ristovski ZD. Modality of human expired aerosol size distributions. J Aerosol Sci. 2011; 42:839-851. DOI
  4. Scheuch G. Breathing is enough: for the spread of influenza virus and SARS-CoV-2 by breathing only. J Aerosol Med Pulm Drug Deliv. 2020; 33:230-234. DOI
  5. EUROSTAT.Publisher Full Text
  6. Khajanchi S, Sarkar K. Forecasting the daily and cumulative number of cases for the COVID-19 pandemic in India. Chaos. 2020; 30:071101. DOI
  7. Denison MR, Graham RL, Donaldson EF. Coronaviruses: an RNA proofreading machine regulates replication fidelity and diversity. RNA Biol. 2011; 8:270-279. DOI
  8. Toyoshima Y, Nemoto K, Matsumoto S. SARS-CoV-2 genomic variations associated with mortality rate of COVID-19. J Hum Genet. 2020; 65:1075-1082. DOI
  9. Riddell S, Goldie S, Hill A. The effect of temperature on persistence of SARS-CoV-2 on common surfaces. Virol J. 2020; 17:145. DOI
  10. 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 Emerg Dis. 2021; 68:296-312. DOI
  11. Kampf G, Todt D, Pfaender S. Persistence of coronaviruses on inanimate surfaces and their inactivation with biocidal agents. J Hosp Infect. 2020; 104:246-251. DOI
  12. Beeching NJ, Fletcher TE, Beadsworth BJ. COVID-19: testing times. BMJ. 2020; 369:m1403. DOI
  13. Hui KPY, Cheung MC, Perera RAPM. Tropism, replication competence, and innate immune responses of the coronavirus SARS-CoV-2 in human respiratory tract and conjunctiva: an analysis in ex-vivo and in-vitro cultures. Lancet Respir Med. 2020; 8:687-695. DOI
  14. Shuai H, Chan JFW, Hu B. Attenuated replication and pathogenicity of SARS-CoV-2 B.1.1.529 Omicron. Nature. 2022; 603:693-699. DOI
  15. Tsang TK, Cowling BJ, Fang VJ. Influenza a virus shedding and Infectivity in households. J Infect Dis. 2015; 212:1420-1428. DOI
  16. Cevik M, Tate M, Lloyd O. SARS-CoV-2, SARS-CoV, and MERS-CoV viral load dynamics, duration of viral shedding, and infectiousness: a systematic review and meta-analysis. Lancet Microbe. 2021; 2:e13-e22. DOI
  17. Chen X, Huang Z, Wang J. Ratio of asymptomatic COVID-19 cases among ascertained SARS-CoV-2 infections in different regions and population groups in 2020: a systematic review and meta-analysis including 130 123 infections from 241 studies. BMJ Open. 2021; 11:e049752. DOI
  18. Leung NHL, Chu DKW, Shiu EYC. Respiratory virus shedding in exhaled breath and efficacy of face masks. Nat Med. 2020; 26:676-680. DOI
  19. Maier HE, Nachbagauer R, Kuan G. Pre-existing antineuraminidase antibodies are associated with shortened duration of Influenza A(H1N1)pdm virus shedding and illness in naturally infected adults. Clin Infect Dis. 2020; 70:2290-2297. DOI
  20. Yan J, Grantham M, Pantelic J. Infectious virus in exhaled breath of symptomatic seasonal influenza cases from a college community. Proc Natl Acad Sci U S A. 2018; 115:1081-1086. DOI
  21. Kreuzberger N, Hirsch C, Chai KL. SARS-CoV-2-neutralising monoclonal antibodies for treatment of COVID-19. Cochrane Database Syst Rev. 2021; 9:CD013825. DOI
  22. Soriano V, de-Mendoza C, Edagwa B. Oral antivirals for the prevention and treatment of SARS-CoV-2 infection. AIDS Rev. 2022; 24:41-49. DOI
  23. Hou YJ, Okuda K, Edwards CE. SARS-CoV-2 reverse genetics reveals a variable infection gradient in the respiratory tract. Cell. 2020; 182:429-446.e14. DOI
  24. Fehr AR, Perlman S. Coronaviruses: an overview of their replication and pathogenesis. Methods Mol Biol. 2015; 1282:1-23. DOI
  25. Weiss SR, Navas-Martin S. Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus. Microbiol Mol Biol Rev. 2005; 69:635-664. DOI
  26. Chan-Yeung M, Xu RH. SARS: epidemiology. Respirology. 2003; 8:S9-S14. DOI
  27. Zhu Z, Lian X, Su X. From SARS and MERS to COVID-19: a brief summary and comparison of severe acute respiratory infections caused by three highly pathogenic human coronaviruses. Respir Res. 2020; 21:224. DOI
  28. World Health Organization. First data on stability and resistance of SARS coronavirus compiled by members of WHP laboratory network.Publisher Full Text
  29. Hui DSC, Zumla A. Severe acute respiratory syndrome: historical, epidemiologic, and clinical features. Infect Dis Clin North Am. 2019; 33:869-889. DOI
  30. Lessler J, Reich NG, Brookmeyer R. Incubation periods of acute respiratory viral infections: a systematic review. Lancet Infect Dis. 2009; 9:291-300. DOI
  31. Perlman S, Netland J. Coronaviruses post-SARS: update on replication and pathogenesis. Nat Rev Microbiol. 2009; 7:439-450. DOI
  32. Di Gennaro F, Marotta C, Locantore P. Malaria and COVID-19: common and different findings. Trop Med Infect Dis. 2020; 5:141. DOI
  33. Knoops K, Kikkert M, Worm SH. SARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulum. PLoS Biol. 2008; 6:e226. DOI
  34. Snijder EJ, Bredenbeek PJ, Dobbe JC. Unique and conserved features of genome and proteome of SARS-coronavirus, an early split-off from the coronavirus group 2 lineage. J Mol Biol. 2003; 331:991-1004. DOI
  35. Zaki AM, van Boheemen S, Bestebroer TM. Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia. N Engl J Med. 2012; 367:1814-1820. DOI
  36. Hijawi B, Abdallat M, Sayaydeh A. Novel coronavirus infections in Jordan, April 2012: epidemiological findings from a retrospective investigation. East Mediterr Health J. 2013; 19:S12-S18.
  37. WHO. Coronavirus infections: disease outbreak news. 2020. Publisher Full Text
  38. Korea Centers for Disease Control and Prevention. Middle East respiratory syndrome coronavirus outbreak in the Republic of Korea, 2015. Osong Public Health Res Perspect. 2015; 6:269-278. DOI
  39. Quaglio G, Tognon F, Finos L. Impact of Ebola outbreak on reproductive health services in a rural district of Sierra Leone: a prospective observational study. BMJ Open. 2019; 9:e029093. DOI
  40. Zhou P, Yang XL, Wang XG. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature. 2020; 579:270-273. DOI
  41. de Wit E, van Doremalen N, Falzarano D. SARS and MERS: recent insights into emerging coronaviruses. Nat Rev Microbiol. 2016; 14:523-534. DOI
  42. Grant R, Malik MR, Elkholy A. A review of asymptomatic and subclinical Middle East respiratory syndrome Coronavirus infections. Epidemiol Rev. 2019; 41:69-81. DOI
  43. Rabaan AA, Al-Ahmed SH, Sah R. MERS-CoV: epidemiology, molecular dynamics, therapeutics, and future challenges. Ann Clin Microbiol Antimicrob. 2021; 20:8. DOI
  44. Zhang P, Li J, Liu H. Long-term bone and lung consequences associated with hospital-acquired severe acute respiratory syndrome: a 15-year follow-up from a prospective cohort study. Bone Res. 2020; 8:8. DOI
  45. Hui DS, Memish ZA, Zumla A. Severe acute respiratory syndrome vs. the Middle East respiratory syndrome. Curr Opin Pulm Med. 2014; 20:233-241. DOI
  46. O’Sullivan O. Long-term sequelae following previous coronavirus epidemics. Clin Med (Lond). 2021; 21:e68-e70. DOI
  47. Ngai JC, Ko FW, Ng SS. The long-term impact of severe acute respiratory syndrome on pulmonary function, exercise capacity and health status. Respirology. 2010; 15:543-550. DOI
  48. Park HY, Park WB, Lee SH. Posttraumatic stress disorder and depression of survivors 12 months after the outbreak of Middle East respiratory syndrome in South Korea. BMC Public Health. 2020; 20:605. DOI
  49. Di Gennaro F, Pizzol D, Marotta C. Coronavirus diseases (COVID-19) current status and future perspectives: a narrative review. Int J Environ Res Public Health. 2020; 17:2690. DOI
  50. Phan T. Novel coronavirus: from discovery to clinical diagnostics. Infect Genet Evol. 2020; 79:104211. DOI
  51. World Health Organisation. WHO Coronavirus (COVID-19) dashboard.Publisher Full Text
  52. Moynihan R, Sanders S, Michaleff ZA. Impact of COVID-19 pandemic on utilisation of healthcare services: a systematic review. BMJ Open. 2021; 11:e045343. DOI
  53. Di Gennaro F, Gualano G, Timelli L. Increase in tuberculosis diagnostic delay during first wave of the COVID-19 pandemic: data from an Italian infectious disease referral hospital. Antibiotics (Basel). 2021; 10:272. DOI
  54. Satarker S, Nampoothiri M. Structural proteins in severe acute respiratory syndrome Coronavirus-2. Arch Med Res. 2020; 51:482-491. DOI
  55. Yadav R, Chaudhary JK, Jain N. Role of structural and non-structural proteins and therapeutic targets of SARS-CoV-2 for COVID-55. Cells. 2021; 10:821. DOI
  56. Petrosillo N, Viceconte G, Ergonul O. COVID-19, SARS and MERS: are they closely related?. Clin Microbiol Infect. 2020; 26:729-734. DOI
  57. Holmes EC, Goldstein SA, Rasmussen AL. The origins of SARS-CoV-2: a critical review. Cell. 2021; 184:4848-4856. DOI
  58. Boni MF, Lemey P, Jiang X. Evolutionary origins of the SARS-CoV-2 sarbecovirus lineage responsible for the COVID-19 pandemic. Nat Microbiol. 2020; 5:1408-1417. DOI
  59. Centers for Disease Control and Prevention (CDC). Prevalence of IgG antibody to SARS-associated coronavirus in animal traders – Guangdong Province, China, 2003. MMWR Morb Mortal Wkly Rep. 2003; 52:986-987.
  60. Di Gennaro F, Marotta C, Storto M. SARS-CoV-2 Transmission and outcome in neuro-rehabilitation patients hospitalized at neuroscience hospital in Italy. Mediterr J Hematol Infect Dis. 2020; 12:e2020063. DOI
  61. Lu R, Zhao X, Li J. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet. 2020; 395:565-574. DOI
  62. Dhont S, Derom E, Van Braeckel E. The pathophysiology of ‘happy’ hypoxemia in COVID-19. Respir Res. 2020; 21:198. DOI
  63. Rico-Mesa JS, Rosas D, Ahmadian-Tehrani A. The role of anticoagulation in COVID-19-induced hypercoagulability. Curr Cardiol Rep. 2020; 22:53. DOI
  64. Di Castelnuovo A, Costanzo S, Antinori A. Heparin in COVID-19 patients is associated with reduced in-hospital mortality: the multicenter Italian CORIST study. Thromb Haemost. 2021; 121:1054-1065. DOI
  65. SeyedAlinaghi S, Mirzapour P, Dadras O. Characterization of SARS-CoV-2 different variants and related morbidity and mortality: a systematic review. Eur J Med Res. 2021; 26:51. DOI
  66. COVID-19 RISk and Treatments (CORIST) Collaboration. RAAS inhibitors are not associated with mortality in COVID-19 patients: findings from an observational multicenter study in Italy and a meta-analysis of 19 studies. Vascul Pharmacol. 2020; 135:106805. DOI
  67. Crook H, Raza S, Nowell J. Long covid-mechanisms, risk factors, and management. BMJ. 2021; 374:n1648. DOI
  68. Huang C, Huang L, Wang Y. 6-month consequences of COVID-19 in patients discharged from hospital: a cohort study. Lancet. 2021; 397:220-232. DOI
  69. Choi JY, Smith DM. SARS-CoV-2 variants of concern. Yonsei Med J. 2021; 62:961-968. DOI
  70. Mondi A, Lorenzini P, Castilletti C. Risk and predictive factors of prolonged viral RNA shedding in upper respiratory specimens in a large cohort of COVID-19 patients admitted to an Italian reference hospital. Int J Infect Dis. 2021; 105:532-539. DOI
  71. Jester B, Uyeki TM, Jernigan DB. Historical and clinical aspects of the 1918 H1N1 pandemic in the United States. Virology. 2019; 527:32-37. DOI
  72. Franco-Paredes C, Hernandez-Ramos I, Del Rio C. H1N1 influenza pandemics: comparing the events of 2009 in Mexico with those of 1976 and 1918-1919. Arch Med Res. 2009; 40:669-672. DOI
  73. Michaelis M, Doerr HW, Cinatl JJr. An influenza A H1N1 virus revival – pandemic H1N1/09 virus. Infection. 2009; 37:381-389. DOI
  74. Peacey M, Hall RJ, Sonnberg S. Pandemic (H1N1) 2009 and Seasonal Influenza A (H1N1) co-infection, New Zealand, 2009. Emerg Infect Dis. 2010; 16:1618-1620.
  75. Sriwilaijaroen N, Suzuki Y. Molecular basis of the structure and function of H1 hemagglutinin of influenza virus. Proc Jpn Acad Ser B Phys Biol Sci. 2012; 88:226-249. DOI
  76. Le Goffic R, Bouguyon E, Chevalier C. Influenza A virus protein PB1-F2 exacerbates IFN-beta expression of human respiratory epithelial cells. J Immunol. 2010; 185:4812-4823. DOI
  77. Wise HM, Foeglein A, Sun J. A complicated message: identification of a novel PB1-related protein translated from influenza A virus segment 2 mRNA. J Virol. 2009; 83:8021-8031. DOI
  78. Wise HM, Barbezange C, Jagger BW. Overlapping signals for translational regulation and packaging of influenza A virus segment 2. Nucleic Acids Res. 2011; 39:7775-7790. DOI
  79. Cunha BA. Swine Influenza (H1N1) pneumonia: clinical considerations. Infect Dis Clin North Am. 2010; 24:203-228. DOI
  80. Thompson WW, Shay DK, Weintraub E. Mortality associated with influenza and respiratory syncytial virus in the United States. JAMA. 2003; 289:179-186. DOI
  81. Borse RH, Shrestha SS, Fiore AE. Effects of vaccine program against pandemic influenza A(H1N1) virus, United States, 2009-2010. Emerg Infect Dis. 2013; 19:439-448. DOI
  82. Borchers AT, Chang C, Gershwin ME. Respiratory syncytial virus – a comprehensive review. Clin Rev Allergy Immunol. 2013; 45:331-379. DOI
  83. Schweitzer JW, Justice NA. Respiratory syncytial virus infection. StatPearls Publishing: Treasure Island (FL); 2021.
  84. Johnson SM, McNally BA, Ioannidis I. Respiratory syncytial virus uses CX3CR1 as a receptor on primary human airway epithelial cultures. PLoS Pathog. 2015; 11:e1005318. DOI
  85. Glezen WP, Paredes A, Allison JE. Risk of respiratory syncytial virus infection for infants from low-income families in relationship to age, sex, ethnic group, and maternal antibody level. J Pediatr. 1981; 98:708-715. DOI
  86. Lu G, Gonzalez R, Guo L. Large-scale seroprevalence analysis of human metapneumovirus and human respiratory syncytial virus infections in Beijing, China. Virol J. 2011; 8:62. DOI
  87. Henderson FW, Collier AM, Clyde WA. Respiratory-syncytial-virus infections, reinfections and immunity. A prospective, longitudinal study in young children. N Engl J Med. 1979; 300:530-534.
  88. Nair H, Nokes DJ, Gessner BD. Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis. Lancet. 2010; 375:1545-1555. DOI

Affiliations

Francesco Di Gennaro

Clinic of infectious Diseases, University of Bari, Aldo Moro, Bari, Italy

Nicola Petrosillo

Infection Control & Infectious Disease Service, University Hospital Campus Bio-Medico, Rome, Italy

Copyright

© Società Italiana di Otorinolaringoiatria e chirurgia cervico facciale , 2022

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