Early SARS-CoV-2 Infection Events

Stable Identifier
R-HSA-9772572
Type
Pathway
Species
Homo sapiens
Related Species
Severe acute respiratory syndrome coronavirus 2
ReviewStatus
5/5
Locations in the PathwayBrowser
General
SVG |   | PPTX  | SBGN
Click the image above or here to open this pathway in the Pathway Browser
The initial steps of SARS-CoV-2 infection involve the specific binding of the coronavirus spike (S) protein to the cellular entry receptor, angiotensin-converting enzyme 2 (ACE2). The expression and tissue distribution of entry receptors consequently influence viral tropism and pathogenicity. Besides receptor binding, the proteolytic cleavage of coronavirus S proteins by host cell-derived proteases is essential to permit fusion. SARS-CoV has been shown to use the cell-surface serine protease TMPRSS2 for priming and entry, although the endosomal cysteine proteases cathepsin B (CatB) and CatL can also assist in this process. During the intracellular life cycle SARS-CoV-2 express and replicate their genomic RNA to produce full-length copies that are incorporated into newly produced viral particles. Coronaviruses possess remarkably large RNA genomes flanked by 5' and 3' untranslated regions that contain cis-acting secondary RNA structures essential for RNA synthesis. At the 5' end, the genomic RNA features two large open reading frames (ORFs; ORF1a and ORF1b) that occupy two-thirds of the capped and polyadenylated genome. Coronavirus S proteins are homotrimeric class I fusion glycoproteins that are divided into two functionally distinct parts (S1 and S2). The surface-exposed S1 contains the receptor-binding domain (RBD) that specifically engages the host cell receptor, thereby determining virus cell tropism and pathogenicity. Besides receptor binding, the proteolytic cleavage of coronavirus S proteins by host cell-derived proteases is essential to permit fusion. SARS-CoV has been shown to use the cell-surface serine protease TMPRSS2 for priming and entry, although the endosomal cysteine proteases cathepsin B (CatB) and CatL can also assist in this process The release of the coronavirus genome into the host cell cytoplasm upon entry marks the onset of a complex programme of viral gene expression, which is highly regulated in space and time. The translation of ORF1a and ORF1b from the genomic RNA produces two polyproteins, pp1a and pp1ab, respectively. ORF1a and ORF1b encode 15-16 non-structural proteins (nsp), of which 15 compose the viral replication and transcription complex (RTC) that includes, amongst others, RNA-processing and RNA-modifying enzymes and an RNA proofreading function necessary for maintaining the integrity of the >30kb coronavirus genome. The establishment of the viral RTC is crucial for virus replication The release of the coronavirus genome into the host cell cytoplasm upon entry marks the onset of a complex programme of viral gene expression, here divided into early and late.
Literature References
PubMed ID Title Journal Year
33116300 Coronavirus biology and replication: implications for SARS-CoV-2

Steiner, S, Thiel, V, V'kovski, P, Kratzel, A, Stalder, H

Nat Rev Microbiol 2021
12730501 The Genome sequence of the SARS-associated coronavirus

Artsob, H, Jones, S, Flick, R, Fernando, L, Smailus, DE, Cloutier, A, Brunham, RC, Bernard, K, Butterfield, YS, Schein, JE, Stroher, U, Asano, JK, Andonov, A, Plummer, F, Normand, S, Freeman, D, Bowness, D, Watson, B, Czub, M, Grolla, A, Barber, SA, Feldmann, H, Meyers, A, Yang, GS, Khattra, J, Gray, M, Petric, M, Booth, TF, Petrescu, AS, Krajden, M, Stott, JM, Marra, MA, Jones, SJ, Tyler, S, Kabani, A, Holt, RA, Coughlin, SM, Astell, CR, McDonald, H, Chan, SY, Li, Y, Robertson, AG, Griffith, OL, Siddiqui, A, Tipples, GA, Mayo, M, Montgomery, SB, Leach, SR, Pandoh, PK, Garbutt, M, Upton, C, Ward, D, Vogrig, R, Skowronski, DM, Brooks-Wilson, A, Girn, N, Roper, RL, Drebot, M, Bastien, N

Science 2003
Participants
Participates
Disease
Name Identifier Synonyms
COVID-19 DOID:0080600 2019 Novel Coronavirus (2019-nCoV), Wuhan seafood market pneumonia virus infection, 2019-nCoV infection, Wuhan coronavirus infection
Authored
Created
Cite Us!