key: cord-0042822-t0cw7l2a
authors: Kumar, Swatantra; Nyodu, Rajni; Maurya, Vimal K.; Saxena, Shailendra K.
title: Morphology, Genome Organization, Replication, and Pathogenesis of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)
date: 2020-04-30
journal: Coronavirus Disease 2019 (COVID-19)
DOI: 10.1007/978-981-15-4814-7_3
sha: ff3a1e08a2a0a848d8711ee88db34a9197daea6c
doc_id: 42822
cord_uid: t0cw7l2a

SARS-CoV-2 is a single-stranded RNA virus of ~30 kb genome size which belongs to genus Coronavirus and family Coronaviridae. SARS-CoV-2 has recently emerged and has been declared as a pandemic by the World Health Organization. Genomic characterization of SARS-CoV-2 has shown that it is of zoonotic origin. The structure of SARS-CoV-2 is found to be similar to SARS-CoV with virion size ranging from 70 to 90 nm. Spike, membrane, and envelope surface viral proteins of coronavirus are embedded in host membrane-derived lipid bilayer encapsulating the helical nucleocapsid comprising viral RNA. The genome comprises of 6–11 open reading frames (ORFs) with 5′ and 3′ flanking untranslated regions (UTRs). Sequence variation among SARS-CoV-2 and SARS-CoV revealed no significant difference in ORFs and nsps. The nsps includes two viral cysteine proteases including papain-like protease (nsp3), chymotrypsin-like, 3C-like, or main protease (nsp5), RNA-dependent RNA polymerase (nsp12), helicase (nsp13), and others likely to be involved in the transcription and replication of SARS-CoV-2. The structure of spike glycoprotein structure of SARS-CoV-2 resembles that of the spike protein of SARS-CoV with an root-mean-square deviation (RMSD) of 3.8 Å. Like SARS-CoV, SARS-CoV-2 uses the ACE2 receptor for internalization and TMPRSS2 serine proteases for S protein priming. Histopathological investigation of tissues from SARS-CoV-2 infected patients showed virus-induced cytopathic effect with signs of acute respiratory distress syndrome in lung cells. This chapter discusses about the morphology, genome organization, replication, and pathogenesis of SARS-CoV-2 that may help us understand the disease that may leads to identification of effective antiviral drugs and vaccines.

Coronaviruses (CoVs) are enveloped single-stranded positive sense RNA viruses that belong to the family Coronaviridae. On the basis of genomic organization and phylogenetic relationship, coronaviruses have been classified into the subfamily Coronavirinae that consists of four genera Alphacoronavirus (αCoV), Betacoronavirus (βCoV), Gammacoronavirus (γCoV), and Deltacoronavirus (δCoV) (Cui et al. 2019) . Evolutionary trend analysis of coronaviruses has revealed that αCoV and βCoV originated from bats and rodents, while γCoV and δCoV were found to have originated from avian species (Ge et al. 2017) . The ability of CoVs to cross the species barrier has resulted in some of the pathogenic CoVs. HKU1, NL63, OC43, and 229E CoVs are associated with mild symptoms in humans, whereas severe acute respiratory syndrome CoV (SARS-CoV) and Middle East respiratory syndrome CoV (MERS-CoV) are known to cause severe disease (Fehr and Perlman 2015) . In 2002 In -2003 , SARS-CoV emerged in China with 8000 clinical cases and 800 deaths. Since 2012, MERS-CoV has caused persistent epidemics in the Arabian Peninsula. Both the viruses have been found to originate from bats and then transmitted into intermediate mammalian host civets in the case of SARS-CoV and camels in the case of MERS-CoV and eventually infected humans (Song et al. 2019) .

SARS-CoV-2 has been declared as a pandemic, with 1,844,683 confirmed cases and 117,021 deaths globally by 14th April 2020 (World Health Organization 2020). To characterize the novel coronavirus, bronchoalveolar lavage fluid and throat swabs were collected from nine patients who had visited the Wuhan seafood market during the initial outbreak. Special pathogen-free human airway epithelial (HAE) cells were used for virus isolation. The collected samples were inoculated into the HAE cells through the apical surfaces. HAE cells were monitored for cytopathic effects and supernatant was collected to perform RT-PCR assays. Apical samples were collected for next generation sequencing after three passages. The whole-genome sequences of SARS-CoV-2 were generated by a combination of Sanger, Illumina, and Oxford nanopore sequencing (Lu et al. 2020) . Phylogenetic analysis has revealed that bats might be at the source of SARS-CoV-2 (Andersen et al. 2020) . Additionally, some studies have suggested that the origin of SARS-CoV-2 is associated with pangolins Shereen et al. 2020) . To decipher the mechanism of replication and development of effective preventive and therapeutic strategies, understanding the structure of SARS-CoV-2, genome organization, and replication is crucial. Therefore this chapter focuses on the morphology and structure, genomic organization, and replication cycle of SARS-CoV-2.

SARS-CoV-2 isolated from nasopharyngeal and oropharyngeal samples were inoculated on the vero cells. In order to identify SARS-CoV-2, inoculated cells were prefixed using 2% paraformaldehyde and 2.5% glutaraldehyde, and transmission electron microscopy was performed. The structure of SARS-CoV-2 observed by examining infected cells after 3 days post infection. Electron microscopy revealed the coronavirus-specific morphology of SARS-CoV-2 with virus particle sizes ranging from 70 to 90 nm observed under a wide variety of intracellular organelles, most specifically in vesicles (Park et al. 2020 ). Due to high sequence similarity, the structure of SARS-CoV-2 is speculated to be the same as SARS-CoV (Kumar et al. 2020) . The surface viral protein spike, membrane, and envelope of coronavirus are embedded in host membrane-derived lipid bilayer encapsulating the helical nucleocapsid comprising viral RNA ( Fig. 3 .1) (Finlay et al. 2004 ). The structure of spike ) and protease of SARS-CoV-2 (Zhang et al. 2020) has been resolved, which provides an opportunity to develop a newer class of drugs for treatment of COVID-19. 

The size of coronavirus genome is in the range of 26 to 32 kb and comprise 6-11 open reading frames (ORFs) encoding 9680 amino acid polyproteins ). The first ORF comprises approximately 67% of the genome that encodes 16 nonstructural proteins (nsps), whereas the remaining ORFs encode for accessory and structural proteins. The genome of SARS-CoV-2 lacks the hemagglutininesterase gene. However, it comprises two flanking untranslated regions (UTRs) at 5 0 end of 265 and 3 0 end of 358 nucleotides. Sequence variation among SARS-CoV-2 and SARS-CoV revealed no significant difference in ORFs and nsps. The nsps includes two viral cysteine proteases including papain-like protease (nsp3), chymotrypsin-like, 3C-like, or main protease (nsp5), RNA-dependent RNA polymerase (nsp12), helicase (nsp13), and others likely to be involved in the transcription and replication of SARS-CoV-2 (Chan et al. 2020 ). In addition to nsps, four major structural proteins are spike surface glycoprotein (S), membrane, nucleocapsid protein (N), envelope (E) and accessory proteins encoded by ORFs. N-terminal glycosylated ectodomain is present at the N-terminal end of M protein that comprises of three transmembrane domains (TM) and a long C-terminal CT domain ( Fig. 3.2) .

The M and E proteins are required for virus morphogenesis, assembly, and budding, whereas S glycoprotein is a fusion viral protein comprising two subunits S1 and S2. The S1 subunit, which shares 70% sequence identity with bat SARS-like CoVs and human SARS-CoV, comprises signal peptide, N-terminal domain (NTD), and receptor-binding domain (RBD) (Walls et al. 2020 ). Most of the differences were found in the external subdomain that is primarily responsible for interaction of spike with the ACE2 receptor. The ectodomain of spike protein (1-1208 amino acid residues) was cloned, expressed and crystallize to solve the spike glycoprotein structure of SARS-CoV-2. The structure of spike glycoprotein structure of SARS-CoV-2 resembles the spike protein of SARS-CoV with an RMSD of 3.8 Å. The The first ORF comprises of approximately 67% of the genome that encodes 16 nonstructural proteins (nsps), whereas the remaining ORFs encode for accessory and structural proteins. The nsps includes two viral cysteine proteases, including papain-like protease (nsp3), chymotrypsin-like, 3C-like, or main protease (nsp5), RNA-dependent RNA polymerase (nsp12), helicase (nsp13), and others likely to be involved in the transcription and replication of SARS-CoV-2. In addition to nsps, the genome encodes for four major structural proteins including spike surface glycoprotein (S), membrane, nucleocapsid protein (N), envelope (E) and accessory proteins like ORFs study also reveals that the receptor-binding region (RBD) exhibited the highest structural divergence (Wrapp et al. 2020) . The S2 subunit that shares 99% sequence identity with bat SARS-like CoVs and human SARS-CoV comprises two heptad repeat regions known as HR-N and HR-C, which form the coiled-coil structures surrounded by the protein ectodomain. The S protein has been found to exhibit a furin cleavage site (PRRARS'V) at the interface between S1 and S2 subunits that is processed during the biogenesis (Coutard et al. 2020 ).

Entry of coronaviruses into host target cells depends on the binding of spike glycoprotein to the cellular receptor and priming of S protein by host cell proteases. Like SARS-CoV, SARS-CoV-2 uses the ACE2 receptor for internalization and TMPRSS2 serine proteases for S protein priming (Hoffmann et al. 2020 ). Similar to SARS-CoV, the extrapulmonary spread of SARS-CoV-2 may be seen due to the widespread tissue expression of the ACE2 receptor. In addition, studies revealed that the spike protein of SARS-CoV-2 exhibits 10-20 times higher affinity as compared to that of SARS-CoV (Wrapp et al. 2020) . Binding of spike protein to the ACE2 receptor results in conformational changes in spike protein that leads to the fusion of viral envelop protein with host cell membrane following entry via endosomal pathway (Coutard et al. 2020; Matsuyama and Taguchi 2009 ). This event is followed by the release of viral RNA into the host cytoplasm that undergoes translation and generates replicase polyproteins pp1a and pp1b that further cleaved by virus encoded proteinases into small proteins. The replication of coronavirus involves ribosomal frame shifting during the translation process and generates both genomic and multiple copies of subgenomic RNA species by discontinuous transcription that encodes for relevant viral proteins. Assembly of virion takes place via interaction of viral RNA and protein at endoplasmic reticulum (ER) and Golgi complex. These virions are subsequently released out of the cells via vesicles (Fig. 3. 3) (Hoffmann et al. 2020 ).

The pathological findings of SARS-CoV-2 infected patients highly resemble that of SARS-CoV and MERS-CoV infected patients. Flow cytometric analysis of peripheral blood samples showed significant reduction of CD4 and CD8 T cell counts, and their status was found to be hyperactivated as higher proportion of dual positive (HLA-DR and CD38) was seen. Rapid progression of pneumonia was seen in chest X-ray images with some differences between the right and left lung. Histopathological investigation of lung, liver, and heart tissue was performed. Lung biopsy showed cellular fibromyxoid exudates with bilateral diffuse alveolar damage. The right lung showed prominent desquamation of pneumocytes and formation of hyaline membrane, indicating signs of acute respiratory distress syndrome (ARDS), whereas the left lung showed pulmonary edema with formation of hyaline membrane ). In addition, both lungs were found to exhibit interstitial mononuclear patchy inflammatory infiltrates dominated specifically by lymphocytes (Tian et al. 2020 ). The intra-alveolar spaces were characterized by multinucleated syncytial cells with atypical enlarged pneumocytes showing virus-induced cytopathic effect. Liver biopsy of patients infected with SARS-CoV-2 showed moderate microvesicular steatosis and mild portal and lobular activity, suggesting that injury might have been caused by the virus or drug induced. A few interstitial mononuclear inflammatory infiltrates were observed in the heart tissue. These pathological changes may provide new insights into the pathogenesis of pneumonia induced by SARS-CoV-2 that may help clinicians to effectively deal with COVID-19 patients.

Phylogenetic analysis revealed that SARS-CoV-2 might have originated from bats or pangolins. Structural investigations of virus-infected cells reveal the coronavirusspecific morphology of SARS-CoV-2 and the size of the virus (70-90 nm). The size of SARS-CoV-2 genome ranges from 26 to 32 kb and comprises 6-11 ORFs which lacks hemagglutinin-esterase gene. However, it comprises of 5 0 and 3 0 flanking untranslated regions (UTRs). The spike glycoprotein structure of SARS-CoV-2 resembles the spike protein of SARS-CoV with an RMSD of 3.8 Å. Like SARS-CoV, SARS-CoV-2 uses the ACE2 receptor for internalization and TMPRSS2 serine proteases for S protein priming. Histopathological investigation of tissues from SARS-CoV-2 infected patients showed virus-induced cytopathic effect with signs of acute respiratory distress syndrome in lung cells.

SARS-CoV-2 has recently emerged and has been declared as a pandemic by the World Health Organization. Based on the genomic sequences submitted to NCBI database, the scientific community has analyzed the samples and suggested preventive and therapeutic strategies. Therefore, investigation of genomic diversity in the collected specimens from around the globe needs to be conducted in order to design common, effective therapies and vaccines. In addition, genomic characterization helps us accurately identify the origin and evolution of the virus. Deciphering the mechanism of SARS-CoV-2 replication in various cell-based models may help us understand the pathogenesis and identify specific targets to develop effective antiviral drugs.

The proximal origin of SARS-CoV-2

Genomic characterization of the 2019 novel human-pathogenic coronavirus isolated from a patient with atypical pneumonia after visiting Wuhan

The spike glycoprotein of the new coronavirus 2019-nCoV contains a furin-like cleavage site absent in CoV of the same clade

Origin and evolution of pathogenic coronaviruses

Coronaviruses: an overview of their replication and pathogenesis

Rapid response research to emerging infectious diseases: lessons from SARS

Detection of alpha-and betacoronaviruses in rodents from Yunnan, China

The origin, transmission and clinical therapies on coronavirus disease 2019 (COVID-19) outbreakan update on the status

SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor

Structural, glycosylation and antigenic variation between 2019 novel coronavirus (2019-nCoV) and SARS coronavirus (SARS-CoV)

Evolutionary history, potential intermediate animal host, and cross-species analyses of SARS-CoV-2

Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding

Two-step conformational changes in a coronavirus envelope glycoprotein mediated by receptor binding and proteolysis

Virus isolation from the first patient with SARS-CoV-2 in Korea

COVID-19 infection: origin, transmission, and characteristics of human coronaviruses

From SARS to MERS, thrusting coronaviruses into the spotlight

Pulmonary pathology of early-phase 2019 novel coronavirus (COVID-19) pneumonia in two patients with lung cancer

Veesler D (2020) Structure, function, and antigenicity of the SARS-CoV-2 spike glycoprotein

World Health Organization (2020) Coronavirus disease 2019 (COVID-19) situation report-85. World Health Organization

Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation

Pathological findings of COVID-19 associated with acute respiratory distress syndrome

Structural basis for the recognition of the SARS-CoV-2 by full-length human ACE2

Crystal structure of SARS-CoV-2 main protease provides a basis for design of improved α-ketoamide inhibitors

Acknowledgments The authors are grateful to the Vice Chancellor, King George's Medical University (KGMU), Lucknow, India, for the encouragement of this work. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.