The Coronavirus superfamily (Coronaviridae) includes several human pathogens with large RNA-encoded genomes, e.g., influenza, common cold, and viral encephalitis, which are classified into alpha-, beta- and gamma-coronavirus families with further division into Lineages A, B, and C. COVID-19 is classed as a Lineage B beta-coronavirus with high similarity to SARS-CoV, thus it'-s recentl renaming to SARS-CoV-2 (1). Although the first members of the beta-coronavirus family were recorded in the 1960’s, the family’s rate of new virulent human pathogens has increased rapidly over the past 20 years, now numbering six in total with the latest ones having the familiar pseudonyms SARS (Severe Acute Respiratory Syndrome, 2002), HKU (HongKong, 2005), MERS (Middle East Respiratory Syndrome, 2012), and now COVID-19 / SARS-CoV-2. Their emergence is linked to increased density of human and animal populations which has enhanced zoonotic transmission rates (2).
Here, we describe the four stages of virus “life” cycle with respect to its interaction with the cytoskeleton.
The first stage of infection for Coronaviridae is Spike (S) protein-mediated attachment to the cell surface via the Spike (S) protein to neuramidic acid moieties (acidic carbohydrates with nine carbon atoms) or heparan sulphate (3). This infectious strategy is very effective because there are many types of these docking molecules on all mammalian cell surfaces which creates high redundancy for plasma membrane attachment. After binding, the virus particles actively rearrange the cytoskeleton by regulating the FAK/Cofilin/Rac/Cdc42 pathway (4). Lv et al. showed temporal fluctuations in filopodia, lamellipodia, and stress fiber proportions after administering coronavirus PHEV to mouse brain neuronal (N2a) cells in vitro. Interestingly, within 5 min, stress fibers were largely depleted, whereas filopodia dominated the detectable F-actin content, producing 80% of the total fluorescent phalloidin signal (4). Between 20-40 min, lamelopodia emerged as an equal co-player, and finally at 60 min, proportions returned to near normal levels, i.e., 60% of the signal was stress fibers. Although this is a macroscopic observation, it indicates on a nanometer scale that virions may create a local environment that regulates their own individual cellular entry. In another report, Owczarek et al. administered coronavirus OC43 to human colorectal adenocarcinoma (HCT-8) cells to study the method of invagination, vesical excision, and function of F-actin (5). Clathrin-dependent endocytosis, caveolae- dependent invagination, and pinocytosis were all implicated in redundant virion entry mechanisms. And dynamin, a large GTPase, was necessary for vesical excision and entry (5). Similar studies of viral entry were described by Milewska et al. with active endocytosis or mass action entry of virions through other mechanisms, e.g., caveolae- dependent invagination or pinocytosis, with the infection rate being dependent on the viral loading of the cell surface (6). Cellular entry also packages the virion in a vesicle that is transported close to the nucleus (5).
Bottom: HCT-8 cells treated or untreated with PHEV coronavirus for 5 min, cells were fixed and stained with Acti-stain 488 (green, Cytoskeleton), anti-PHEV coat protein (red) and DNA (blue, Hoescht). Top - Infected with coronavirus, bottom - Un-infected. Note high level of staining on the periphery of the cell in the infected samples indicating lamellipodia and filopodia (narrow spikes). Compared to the un-infected cell which indicate a high level of cytosplasmic stianing indicating stress fibers. (Kindly provided by Prof. Wenqi He, from Lv et al. 2019).
In the second stage, several studies have implicated both actin and tubulin components are complementary cytoskeleton components of intracellular transport. Owczarek et al. probed the function of F-actin in intracellular localization; interestingly, jasplakinolide, a cell permeable F-actin stabilizing compound, inhibited viral entry of plasma membrane bound virions, whereas cytochalsin D, an F-actin depolymerizing compound, did not inhibit viral entry but did disrupt the normal localization of virions from peri-nuclear to cytoplasmic areas (5). In contrast, Rüdiger et al. used a spin-down format to show preferential tubulin isoform binding of virions. Coronavirus Spike protein C-terminal peptide (S-protein) bound to several beta-tubulin isoforms in a coronavirus strain-specific manner (7). A scrambled peptide showed the binding was not due to random ionic charge interaction. Thus, intracellular transport of virions utilizes multiple cytoskeletal structural proteins to navigate through and localize to specific areas within the cell (see Figure Top Right).
The third stage is, assembly and maturation. After transport to the perinuclear region, coronavirus RNA exudes from the vesicle and virion capsule and enters the nucleus for reverse transcription and replication. The DNA replicon is subsequently transcribed back into RNA and this exits the nucleus into the Golgi/ER/microtubule organizing center (8). Initially, the nucleocapsid (N) protein binds to an RNA copy and binds to vesicle membranes (8,9), and further maturation occurs with N and E proteins which are required for assembly of the basic virus-like particle (VLP). If Spike (S) protein is co-expressed, then this is incorporated into the virus particle (8). In concert with several cytoskeleton and membrane regulator proteins, e.g., HDAC6, ubiquitin, and Rab GTPases aid assembly by concentrating packaging components (10). It is unknown which one of these predominates for COVID-19 / SARS-CoV-2.
The fourth stage is, egress. The genetic fusion of the coronavirus nucleocapsid or spike proteins with GFP permits tracking of non-infective virus particles by fluorescent microscopy. Using this technique, Siu et al. monitored SARS-CoV egress and, found vesicles that fused into multi-particle conglomerates (8). The transport was sensitive to Brefeldin A, which indicates that the secretory pathway was being used. Other studies have found nocodazole was effective at inhibiting virion transport to the plasma membrane (10, 11), indicating that microtubules are an essential component of egress. Rab11 is implicated in binding to KHC for microtubule transport and then binds to myosin to help transverse the peripheal actin matrix and egress from the cell.
In summary, coronavirus has highly redundant mechanisms of plasma membrane attachment and invagination to enter the cell. Subsequently, both actin, tubulin, and their chemo-mechanical motors dynein, kinesin and myosin cytoskeleton components are required for intracellular transport to the correct location for replication. After reverse transcription and transcription, positive strand RNA is packaged on a scaffold of Golgi/ER/microtubule complexes. The vesicle- encased virions track along microtubules before fusing with the plasma membrane and escaping the cell. Many of the methods in coronavirus research use reagents such as fluorescent phalloidins, microtubule and actin spin-down kits, dynein, kinesin proteins, and Rac and Cdc42 activation assays that are present in the Cytoskeleton catalog and noted below in the tables. There are many un-answered questions in coronavirus research; for example, how do the virions regulate the cytoskeleton through the plasma membrane interactions to coordinate their entry? Can a single virion enter the cell on its own? What is the significance of using actin and microtubule cytoskeletons for different functions? How does the virus evade the immune system for so long compared to influenza and the common cold? Answering these questions will undoubtedly lead to greater knowledge and possible pharmacological breakthroughs in the future.
Reference & Source information: https://www.cytoskeleton.com/
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