Insights on Epidemiology, Pathogenesis, Diagnosis and Possible Treatment of COVID-19 Infection

Abstract

The sudden outbreak of the novel coronavirus infection (COVID-19, SARS-CoV-2 virus) is posing a significant threat by affecting millions of people across the globe showing mild to severe symptoms of pneumonia and acute respiratory distress. The absence of precise information on primary transmission, diagnosis, prognosis, and therapeutics for patients with COVID-19 makes prevention and control tough. In the current scenario, only supportive treatment is available, which in turn possess a biggest challenge for scientists to develop specific drugs and vaccines for COVID-19. Further, India, with the second largest populated country and fluctuating climatic conditions quarterly, has high vulnerability towards COVID-19 infection. Thus, this highlights the importance of a better understanding of the COVID-19 infection, pathology, diagnosis and its treatment. The present review article has been intended to discuss the COVID-19 biology, mechanism of infection in humans with primary effects on pregnancy, the nervous system, diabetes, and cardiovascular disease. The article will also discuss the drug repurposing strategy as an alternative line of treatment and clinical practices recommended by the World Health Organization and other government agencies and represent the COVID-19 scenario with the Indian context.

Introduction

Recently in December 2019, patients were presented with symptoms of fever or dry cough having either usual or reduced count of white blood cells from Wuhan city of China. They were classified as bearing ‘Fever of Unknown Origin’ along with pneumonia [1]. Later on, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) was identified as a causative agent, potentially having human-to-human transmission [1]. The World Health Organization (WHO) declared ‘Public Health Emergency of International Concern’ at the outbreak of infection induced by COVID-19 on 30th January 2020. On 12th January 2020, WHO termed the virus as ‘2019 novel coronavirus’ (2019‐nCoV), and subsequently on 11th February 2020, the disease was designated as ‘coronavirus disease’ (COVID‐19). The genome analyses of SARS-CoV-2 have shown the evolution of these viruses into L- and S-types [2]. The prevalence of S-type (~ 30%) is reported to be less than that of L-type (~ 70%). Further, the S-type is evolutionarily older and less aggressive, while the L-type, being more contagious, showed higher frequency during the early stages of the COVID outbreak in Wuhan. Nonetheless, its frequency declined gradually. However, this decline was soon followed up by a second wave which has affected several countries, however, India battles a devastating COVID surge since April 2021.

Coronavirus (CoVs)

Coronaviruses are a group of varied and large-enveloped viruses enclosing non-segmented and positive-sense single-stranded RNA. They have been observed to cause enteric and respiratory diseases. Besides, they also affect the liver and neurological system with varying severity among animals and humans [3]. Human corona virus subtypes like HCoV-HKU1, HCoV-229E, HCoV-NL63, and HCoV-OC43 lead to mild respiratory sickness [4]. However, the worldwide spread of two novel corona viruses, namely SARS-CoV and the Middle East Respiratory Syndrome CoV (MERS-CoV) in the last 20 years has attracted global attention due to their high lethal potential. More than 8,000 people with around a 10% mortality rate worldwide have died due to widespread SARS-CoV infection. However, the MERS-CoV was infested in around 857 patients with a high death rate (35%) [5]. A recent outbreak of SARS-CoV-2 in China has rapidly spread throughout the world. Genome analysis revealed that, like SARS-CoV and MERS-CoV, the SARS-CoV-2 also falls in the same beta-corona virus (βCoV) clade and shows high homology with SARS-CoV [6]. Consequently, SARS-CoV-2 shares analogous pneumonia pathogenesis as instigated by SARS-CoV or MERS-CoV-infected cases, and its entrance into the human host cells has been recognized utilizing a similar receptor as SARS-CoV. Since most CoVs have almost the same viral structure and infection pathway, observations related to mechanisms of infections may also be applicable for SARS-CoV-2 [7].

The SARS-Cov-2

SARS-CoV-2 belongs to Sarbecovirus subgenus of the genus Beta-coronavirus [6]. It possesses 29.9 kb long RNA consisting of 5’ untranslated region (5’ UTR), replicase gene, S gene (for Spike protein), E gene (for envelope protein), M gene (for Membrane protein), N gene (for Nucleocapsid protein) and 3’ poly (A) UTR with unknown open reading frames [8]. It is surrounded by an envelope and spikes with spherical, oval, or pleomorphic shapes of 60–140 nm diameters. Although SARS-CoV-2 has distinct gene sequences from other corona viruses, it exhibits high sequence identity (80.26%) to the human SARS-CoV genome [7]. As per WHO, it appears as a chimera of coronavirus of a bat and of an unknown origin. Nevertheless, snakes are considered a possible source for SARS-CoV-2 after comparing with other animals. Another research group reported that Chinese chrysanthemum-headed bats are closely related to SARS-CoV-2 and transmission to humans could have started from bats [9]. However, the SARS-CoV-2 transitional animal host is still under investigation.

Route of Infection of SARS-CoV-2 in Humans

The envelope spike (S) protein has been observed to shape host tropism and transmission capacity. It also facilitates receptor binding and membrane fusion. Structural analysis revealed two domains (S1 domain and S2 domain) of S protein. The S1 domain facilitates binding to the receptor, whereas the S2 domain aids in fusion of the virus with the cell membrane. Like SARS-CoV, the SARS-CoV-2 also employs an angiotensin-converting enzyme 2 (ACE-2) receptors for entering into the host cells [10]. The ACE-2 has high expression in the lungs alveolar cells, the upper epithelial cells in the esophagus, and absorptive enterocytes cells of the ileum and colon. This indicates that along with the respiratory system, the digestive system could also act as a probable route of entry for SARS-CoV-2 [6]. The binding of SARS-CoV-2 to its receptor promotes the expression of ACE-2 that leads to alveolar cell damage that in turn activates a sequence of lethal reactions leading to death. As compared to European and American populations, the expression level of ACE-2 was observed significantly higher in the Asian populations and that too in males than females. The differential expression pattern of ACE-2 may form the basis of high rates of infection in Asian male population [11]. However, cases in Europe and America may have additional sensitivity or genetic predisposition.

Moreover, SARS-CoV-2 with its widespread potential and causing many infections has gained the potential to mutate, and several variants have hit the world with high rates. These variants based on the type of mutations may vary in the type of transmission (spread more or less) and severity. In the UK, a new variant of the virus known as B.1.1.7 emerged rapidly, with several other mutations. There was another variant of this virus that was found in South Africa and shared some of the mutations with B.1.1.7. This variant of SARS-CoV-2 is named B.1.351. Another variant known as P.1 was identified in Brazil. Some of these variants and their mutations spread more quickly and may be associated with an increased risk of death. The centers for disease control and prevention (CDC) with weblink (https://www.cdc.gov/coronavirus/2019-ncov/science/science-briefs/scientific-brief-emerging-variants.html) in association with a wide array of partners worldwide, is providing data and information on these variants which can be used by public health professionals, researchers, and companies for public welfare.

Epidemiology, Clinical Features and Pathological Conditions of COVID-19 Infection

COVID-19 has caused a global pandemic (WHO Media Briefing held on 11th March 2020). The global reports have suggested that the individuals infected with SARS-CoV-2 had an average age of 59 years, among them males represent 56% of cases. The median incubation period for the virus was observed to be around 5 days. Also, the proportion of male-to-female mortality was observed to be high (3:1) with 75 years as the median age. Further, the median time between the onsets of symptoms to death is reported as 14 days that vary for patients with ≥ 70 years of age (11.5 days) from the subjects aging < 70 years (20 days) [12]. About half of the patients contracting COVID-19 infection were seen to have other diseased conditions, mainly hypertension, diabetes, or cardiovascular disease. With regard to children of age less than 15 years, comparatively, a smaller number of cases has been reported. Also, the clinical course was generally milder in children than adults infected with COVID-19 [6].

The COVID-19-infected patients showed fever with dry cough and fatigue as common clinical symptoms. Some patients were presented with upper respiratory symptoms, gastrointestinal symptoms such as vomiting, diarrhea and abdominal discomfort [5–7], and they were categorized into mild, severe, and critical medical conditions. The patients with mild symptoms were reported to have non-pneumonia or mild pneumonia. In severe conditions, observations suggest that oxygen saturation and partial pressure ratio of oxygen in arteries to inspire oxygen fraction decrease, whereas lung infiltrates may increase within a short span of 24–48 h [5]. The laboratory observation showed lymphopenia (low levels of lymphocytes) in the blood as a cardinal feature of COVID-19. Apart from this, the elevated levels of lactate dehydrogenase and creatinine kinase relate to abnormal myocardial zymograms. The patients also showed altered liver function with increased levels of alanine or aspartate aminotransferase [13]. Also, the levels of interleukins (IL10, IL9, IL8, IL7, IL1B, and IL1RA), granulocyte–macrophage colony-stimulating factor (GMCSF), granulocyte colony-stimulating factor (GCSF), fibroblast growth factor (FGF), interferon gamma-induced protein 10 (IP10), interferon-gamma (IFN-γ), macrophage inflammatory protein 1 alpha and beta (MIP1A, MIP1B), monocyte chemoattractant protein 1 (MCP1), platelet-derived growth factor (PDGF), vascular endothelial growth factor (VEGF), and tumor necrosis factor alpha (TNFα) concentrations were reported up in COVID-19 patients compared to healthy adults. They also noticed that plasma concentrations of TNFα and interleukins (MIP1A, IP10, MCP1, GCSF, IL10, IL2, and IL7) were higher in patients admitted in the intensive care unit (ICU) indicating damage to the host lung due to the production of chemokines and cytokines upon the initiation of the immune response to COVID19 infection [14]. The reactome analysis (https://reactome.org), a high throughput in silico approach, was done in a subset of COVID-19 clinical data. The upregulated proteins predicted 25 biological pathways that may be affected in the COVID19 infected patients (Fig. 1). These pathways are related to the signaling of interleukin and cytokines, the inflammasome pathway, and chemokine receptors. The ATF4 activates genes in response to endoplasmic reticulum (ER) stress, regulation of gene expression by hypoxia inducing factor (HIF), VEGF-ligand receptor interaction, and dimerization, Dectin-1 signaling, cell recruitment (pro-inflammatory response). Further extensive studies are needed to identify specific molecular targets and trace critical molecular pathways to better understand the transmission and pathogenic nature of this pandemic infection.

Fig. 1.

In silico analysis of proteins through neural networks (Reactome analysis, https://reactome.org) indicates COVID19 infection may trigger innate and adaptive immune response, leading to activation of signaling pathways and signal transduction mechanisms

The radiologic display observed using chest computed tomography (CT) scans of SARS-CoV-2 infected patients revealed patchy ground glass opacities (GGO) with condensation in the middle and outer zone of the lungs. Based on chest CT scans, four stages of abnormalities were observed in patients. The GGO appears in the lower lobes of either one or both the lungs in the early stage. In progressive stages, GGO appear bilateral, diffused and condensed in more than two lobes. However, diffuse GGO and compact consolidation developed more dominant in peak stage, whereas widespread GGO and condensation was progressively absorbed in the last or absorption stage [5, 14].

The lung biopsy reports of a few patients showed bilateral diffuse alveolar destruction with cellular fibromyxoid dislodge and interstitial mononuclear inflammatory penetration mainly by lymphocytes [5]. The SARS-CoV2 viral cytopathic-like changes, i.e., multinucleated syncytial cells with unusually magnified pneumocytes identified in the intra-alveolar spaces, were similar to observation among patients infected with MERS-CoV and SARS-CoV. Further, liver tissue showed adequate microvascular steatosis, mild lobular, portal activity and heart tissue showed few interstitial mononuclear inflammatory infiltrates [14].

Effect of COVID 19 Infection on Pregnancy

The literature on the outcomes of COVID-19 infection during pregnancy is gradually building up. In two reports describing 18 pregnancies with COVID-19 where all were infected in the third trimester, the clinical findings were similar to those in non-pregnant adults. Fetal distress and preterm delivery were observed in a few cases. Out of all, two pregnancies were cesarean deliveries, and SARS-CoV-2 was negative on all babies tested. Based on these limited reports, and the available data from other respiratory pathogens such as SARS and influenza, it is unknown whether pregnant women with COVID-19 experience more severe disease [15]. Further, another study on 141 COVID-19 positive subjects also indicates a similar finding where no vertical transmission of COVID-19 infection nor its effect on maternal and fetal outcome was observed. [16]. However, further case studies and follow-ups of patients are of utmost importance to the large number of pregnant women affected with COVID-19 infection throughout the world to understand the probable effect of COVID-19 on the neonate and maternal health.

Effect of COVID 19 on Nervous System

Research and clinical data suggest that headache, weakness, dizziness, altered consciousness, hyposmia, encephalitis, neuropathy, seizure, demyelination, and stroke are some of the common symptoms in COVID-19 patients [17]. Further, agitation, confusion, enhanced tendon reflexes, clonus, olfactory and gustatory dysfunction are also observed in COVID-19 patients who require intensive care [18] CT scan and MRI reports in patients have also shown endothelial dysfunction and formation of clots in the brain and in multiple organs [19]. It has been proposed that COVID-19 infection may spread through the cribriform plate and olfactory bulb and dissemination via trans-synaptic transfer [17]. However, further studies are needed to identify how COVID-19 disease progression starts in the brain. The altered blood-brain barrier also recruits virus particles in the brain which can further cause neuronal toxicity [20]. Increased cytokine storms in COVID-19 patients also cause alteration in blood-brain barrier leading to penetration of peripheral immune cells in the brain results in seizures and encephalopathy-like conditions [21]. It will be interesting to investigate whether COVID19 spreads across the brain or got localized at a specific brain region. Likewise, COVID-19 related neurological pathologies should also be investigated mainly in the asymptomatic infection population. Like any other neurovirulent virus, COVID19 may also affect brain-specific immunity and cross the blood–brain barrier or reach directly to the brain through the olfactory bulb (Fig. 2). The microglia are innate immune cells of the brain, perform regular immunological surveillance of the brain and regulate brain immunity. Thus, microglia may be having a protective function coordinating the innate immune response like other microorganisms, however, the above-mentioned underlying mechanisms still remain unclear.

Fig. 2.

Diagrammatic representation showing possible site of entry of COVID19 infection, either directly from the nose through the olfactory bulb into the brain or directly into the lungs and then migrate through the peripheral nervous system into the brain. Further, the underlying mechanism of whether microglia will be neuroprotective in nature if COVID19 virus enters through the olfactory bulb or it will initiate neuroinflammation cascade still remains elusive. The status of neurons and astrocytes at the site of virus entry remains unknown till date

Effect of COVID 19 on Individuals Having Diabetes and Cardiovascular Disease

Diabetic individuals are at greater risk of infections and are highly prone to influenza and pneumonia-like MERS CoV, SARS CoV, and Pandemic Influenza A 2009 (H1N1). It is suggested that the presence of medical conditions like diabetes and cardiovascular disease with SARS-CoV2 infection can increase the mortality risk in the population [22]. It has been hypothesized that pneumonia can potentially cause a low level of oxygen in the blood due to gas exchange obstruction, which will adversely affect the cell metabolism, increase anaerobic fermentation, intracellular acidosis, and oxygen free radicals which will further damage the phospholipid bilayer of the cell membrane [23]. At the same time, calcium ions influx due to hypoxia can damage cardiac muscle cells. In such stress conditions and due to medication, the release of neurotransmitters mainly catecholamines, in an excess amount can cause myocardial damage. It is also suggested that cardiac diseases, hypertension, or diabetic patients are prone to severe COVID-19 infection when treated with ACE2-increasing drugs [24]. Thus, ACE inhibitors or ARBs (angiotensin II type-I receptor blockers) have been proposed to modulate ACE2 medications in such patients. Further, based on patients with COVID-19 studies, Chen et al., 2020 proposed that COVID-19 can significantly affect the heart function and lead to myocardial injury [25].

Diagnosis of COVID-19

The general approaches to detect COVID-19 are molecular and serological tests. Currently, the standard diagnostic test for SARS-CoV-2 infection using samples taken from the respiratory tract by PCR techniques such as RT-PCR, RT-insulated isothermal PCR, RT-LAMP, and single-step rRT-PCR assay based on specific TaqMan probes. The whole genome sequencing may also be carried out on positive samples to aid understanding of transmission and mutations. In comparison, molecular tests (RT-PCR) have shown higher sensitivity than serological (ELISA) tests. For improving the sensitivity of the test, an additional sensitive molecular marker, i.e., N gene, has been incorporated into nested PCR [26]. Further, CT scan has also been considered the most reliable method to identify and validate COVID19 infection in patients. However, efforts are still going on in the direction of using NGS (Next Generation Sequencing) and CRISPR (Clustered Regularly Inter Spaced Palindromic Repeats) Technology as Point-of-Care diagnostic tools [27] to detect COVID-19 infection even at the early stage in a minimum possible testing time with high sensitivity.

Drug Repurposing Strategies for COVID-19

James Black, Nobel laureate, excellently quoted that “The most fruitful basis of the discovery of a new drug is to start with an old drug.” [28]. Thus, the concept of Drug repurposing, which is also coined as Drug repositioning or Drug reprofiling developed and helped bring new therapies to the world (Table 1). Drug repurposing is basically defined as the reapplication of the approved drugs or failed drugs to target new indication(s). Three R’s (Repositioning, Reprofiling, and Repurposing) strategy has served as an important part of the drug development process of pharmaceutical business for the last few decades. It helps to adjust or develop multiple applications of an active molecule. The advantage of using the existing drugs is that they have known pharmacokinetics, pharmacodynamics, clinical history, and safety profile data for human use. Thus, repurposing may reduce early testing and clinical trials and dramatic dropping development times and cost.

Table 1.

Some of the classic examples of repurposed drugs

Drug	Original indication	Repurposed indication
Thalidomide	Sedative	Leprosy and Multiple myeloma
Ropinirole	Parkinson's disease	Restless legs syndrome, sexual dysfunction induced by selective serotonin reuptake inhibitor (SSRI)
Pregabalin and Gabapentin	Anti‐epileptics	Neuropathic pain and anxiety disorders
Minoxidil	Anti‐hypertensive agent	Topical treatment for hair re‐growth
Methotrexate	Chemotherapy drug	Autoimmune disorders including arthritis
Gemcitabine	Anti-viral	Anticancer
Raloxifene	Breast cancer	Osteoporosis
Buproprion	Depression	Smoking cessation
Dapoxetine	Analgesia	Premature ejaculation
Dapsone (DDS)	Antileprosy drug	Antimalarial
Fluxetine	Depression	Premenstrual dysphoria disorder (PMDD)
Doxepin	Antidepressant	Antipruritic
Bimatoprost	Glaucoma	Eyelash growth

Papapetropoulos and Szabo [31], Insa [32]

The repurposing strategy has highlighted many other potential candidates also such as leronlimab, a CCR5 antagonist with the potential for multiple therapeutic indications, and galidesivir, a nucleoside RNA polymerase inhibitor, favipiravir, darunavir, immunoglobulins, arbidol hydrochloride combined with interferon atomization and others [7] (Table 2). In another study, open label non-randomized clinical trials showed that hydroxychloroquine treatment significantly reduce the viral load in COVID-19 patients, where providing azithromycin along with hydroxychloroquine enhanced its anti-viral effect [29]. However, the efficacy and safety of hydroxychloroquine is still under investigation. Another protease inhibitor, lopinavir/ritonavir, conventionally used for HIV-1 treatment, have shown potential to act on SARS-CoV-2 and is advised to the high-risk group of COVID-19 pneumonia in the Korean population. The controlled clinical trials suggest no effect of lopinavir/ritonavir on COVID-19 [30]. The BCG vaccination has also been proposed as an alternative treatment strategy in reducing COVID19 infection mortality rate. Recently, the compassionate use of anti-viral drug Remdesivir (RDV) has been suggested to be effective in severe COVID-19 infected individuals. However, COVID19 specific drug is still under investigation.

Table 2.

List of drugs considered potential to repurpose for COVID-19 infection treatment

Drug	Action mode	Mechanism	Target disease
Chloroquine phosphate	9-aminoquinolin	Immunomodulating, autophagy inhibitors, raising endosomal pH	Malaria, autoimmune disease
Remdesivir	Nucleotide analog	Post entry interference with virus	SARS, MERS
Lopinavir/Ritonavir	Protease inhibitor	Inhibits HIV-1 protease for protein cleavage	HIV/AIDS, SARS, MERS
Ribavirin	Synthetic guanosine nucleoside	Interfering with the synthesis of viral mRNA	HCV, SARS, MERS
Favipiravir	Viral RNA polymerase inhibitor	Acts on genetic copying of virus, prevents its reproduction without affecting nucleic acid synthesis of host cell	Ebola, H1N1 Influenza
Nitazoxanide	Antiprotozoal agent	Modulating growth and proliferation of microbes like protozoa, helminths, virus and bacteria	Human/anima coronavirus
Ganciclovir	Nucleoside analog	Inhibitor of herpesvirus family including cytomegalovirus	AIDS-associated cytomegalovirus infections
Nafamostat	Synthetic serine protease inhibitor	Reduces release of cathepsin B, anticoagulant activity	Ebola, MERS, Influenza
Oseltamivir	Neuraminidase inhibitor	Prevents viral replication and infectivity by inhibiting viral neuraminidase	Influenza viruses A
Darunavir	Antiretroviral protease inhibitor	Inhibiting of HIV-1 protease and blocks the cleavage of HIC gag-pol polyprotein	HIV/AIDS
IFN-beta	Anti-inflammatory agent	Reduces antigen presentation and T-cell proliferation	Hepatitis, Ebola

Guo et al. [7]

Apart from hunting for the drug against COVID-19, scientists across the world have tried and come up with another possibility to protect individuals from COVID-19 infection, i.e., through immunization. COVID-19 specific vaccine has been developed in different parts of the world and a vaccination drive has been started. However, the efficacy of vaccines developed needs to be improved for which further research is underway. Till now, 1,011,457,859 vaccine doses have been administered to individuals globally, according to WHO data indicating that we have to go a long way to immunize and protect our population with COVID-19. Therefore, the identification and development of COVID-19 specific drugs are of utmost importance for treatment purposes.

COVID-19 Infection in India

Humans serve as hosts to the number of respiratory viruses. Respiratory transmission from human to human is one of the preliminary causes of viral infections including measles and COVID-19. Due to the large population size (approximately 1.38 billion) Indians live closer so that it is easier for pathogens to jump from one host to another via air or surface transmission. Their reservoir is also facilitated due to the 4 climatological seasons of about three months each.

The first case of COVID-19 in India was detected on 30th January 2020. Soon after, quarantine centers were established and admitted for monitoring for citizens from traveling to China and other parts of the world (Source: PIB Daily Bulletin on COVID-19 matters, Government of India, https://pib.gov.in/newsite/bulletinn.aspx). Due to proactive measures of complete lockdown and monitoring, the spread of infection came under control as compared to other countries [4] (Fig. 4). Meanwhile, based on the whole genome sequence of the first Indian COVID19 case, gene-specific in vitro transcribed RNA for all the gene targets, i.e., N, E and RdRp, as an in-house positive control for laboratory diagnosis of SARS-CoV-2 by the National Institute of Virology, Indian Council of Medical Research, Pune, India. The genome sequences of Indian SARS-CoV-2 showed approximately 99.98% similarity with that of (Accession number: NC 045,512) but belong to different clusters in phylogenetic analysis. Due to the non-availability of any specific treatment for COVID-19, lopinavir/ritonavir combination therapy and remdesivir have been approved for COVID-19 under restricted public health emergency by Central Drugs Standard Control and Indian Regulatory Authority. Recently, the second wave of COVID-19 infection in India has caused tremendous damage to the life of people, therefore setting up a new pandemic rate worldwide. As per WHO data, there have been 19,164,969 confirmed cases with 211,853 deaths from 3rd January 2020 to 1st May 2021. The spread of new variants with the potential of causing severe damage has been one of the reasons for this widespread use. Some of the common symptoms being observed in infected people include fever, headache, cough and breathlessness. Moreover, the young population appears to be most affected by this second wave. Additionally, there have been double and triple mutant strains which are still evolving further to evade the human immune response. Thus, as a prevention measure, a large vaccination drive has started and till date 147,727,054 vaccine doses have been administered among individuals with above age group of 45 and above. Vaccines including Covaxin, AstraZeneca and Sputnik, which are some of the vaccines being approved by WHO against COVID-19, which may provide a high degree of protection against getting seriously ill and dying from the disease although no vaccine is 100% protective. Moreover, it will take longer time to vaccinate the whole Indian population.

Conclusion

COVID-19 infection is causing major public health problems across the globe. Apart from severe respiratory illness, COVID-19 infection seems to affect multiple organs. Some drugs have shown promising results, however, novel standard treatment regimes and potent interventions are the need of the hour. Rapid immunization at the large scale at the global level is urgently required to boost our immune response against COVID-19 infection. These comprehensive studies, genomic data, epidemiology data, and clinical details positively support a novel and comprehensive diagnosis and treatment options in upcoming days to beat COVID-19.

Author’s Contributions

SKM conceptualized the manuscript. SKM, AB and PS wrote the manuscript. SKM, AB and RM reviewed and edited the manuscript. All authors approved the manuscript before submission.

Funding

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

Declarations

Conflict of Interest

SKM, AB, PS, and RM declare no conflict of interest.