Immune escape facilitation by mutations of epitope residues in RdRp of SARS-CoV-2.

Mutations drive viral evolution and genome variability that causes viruses to escape host immunity and to develop drug resistance. SARS-CoV-2 has considerably higher mutation rate. SARS-CoV-2 possesses a RNA dependent RNA polymerase (RdRp) which helps to replicate its genome. The mutation P323L in RdRp is associated with the loss of a particular epitope (321-327) from this protein. We consider the effects of mutations in some of the epitope region including the naturally occurring mutation P323L on the structure of the epitope and their interface with paratope using all-atom molecular dynamics (MD) simulation studies. We observe that the mutations cause conformational changes in the epitope region by opening up the region associated with increase in the radius of gyration and intramolecular hydrogen bonds, making the region less accessible. Moreover, we study the conformational stability of the epitope region and epitope:paratope interface under the mutation from the fluctuations in the dihedral angles. We observe that the mutation renders the epitope and the epitope:paratope interface unstable compared to the corresponding wild type ones. Thus, the mutations may help in escaping antibody mediated immunity of the hostCommunicated by Ramaswamy H. Sarma.

Microscopic model on indoor propagation of respiratory droplets.

Indoor propagation of airborne diseases is yet poorly understood. Here, we theoretically study a microscopic model based on the motions of virus particles in a respiratory microdroplet, responsible for airborne transmission of diseases, to understand their indoor propagation. The virus particles are driven by a driving force that mimics force due to gushing of air by devices like indoor air conditioning along with the gravity. A viral particle within the droplet experiences viscous drag due to the droplet medium, force due to interfacial tension at the droplet boundary, the thermal forces and mutual interaction forces with the other viral particles. We use Brownian Dynamics (BD) simulations and scaling arguments to study the motion of the droplet, given by that of the center of mass of the viral assembly. The BD simulations show that in presence of the gravity force alone, the time the droplet takes to reach the ground level, defined by the gravitational potential energy being zero, from a vertical height H,tf∼γ-0.1 dependence, where γ is the interfacial tension. In presence of the driving force of magnitude F0 and duration τ0, the horizontal propagation length, Ymax from the source increase linearly with τ0, where the slope is steeper for larger F0. Our scaling analysis explains qualitatively well the simulation observations and show long-distance transmission of airborne respiratory droplets in the indoor conditions due to F0 ∼ nano-dyne.

Effect on the conformations of the spike protein of SARS-CoV-2 due to mutation.

The spike protein of SARS-CoV-2 mediates receptor binding and cell entry and is the key immunogenic target for virus neutralization and the present attention of many vaccine layouts. It exhibits significant conformational flexibility. We study the structural fluctuations of spike protein among the most common mutations that appeared in the variant of concerns (VOC). We report the thermodynamics of conformational changes in mutant spike protein with respect to the wild-type from the distributions of the dihedral angles obtained from the equilibrium configurations generated via all-atom molecular dynamics simulations. We find that the mutation causes the increase in distance between the N-terminal domain and receptor binding domain, leading to an obtuse angle cosine θ distribution in the trimeric structure in spike protein. Thus, an increase in open state is conferred to the more infectious variants of SARS-CoV-2. The thermodynamically destabilized and disordered residues of receptor binding motif among the mutant variants of spike protein are proposed to serve as better binding sites for the host factor. We identify a short stretch of region connecting the N-terminal domain and receptor binding domain forming a linker loop where many residues undergo stabilization in the open state compared to the closed one.

Non-synonymous mutations of SARS-CoV-2 leads epitope loss and segregates its variants.

The non-synonymous mutations of SARS-CoV-2 isolated from across the world have been identified during the last few months. The surface glycoprotein spike of SARS-CoV-2 forms the most important hotspot for amino acid alterations followed by the ORF1a/ORF1ab poly-proteins. It is evident that the D614G mutation in spike glycoprotein and P4715L in RdRp is the important determinant of SARS-CoV-2 evolution since its emergence. P4715L in RdRp, G251V in ORF3a and S1498F of Nsp3 is associated with the epitope loss that may influence pathogenesis caused by antibody escape variants. The phylogenomics distinguished the ancestral viral samples from China and most part of Asia, isolated since the initial outbreak and the later evolved variants isolated from Europe and Americas. The evolved variants have been found to predominant globally with the loss of epitopes from its proteins. These have implications for SARS-CoV-2 transmission, pathogenesis and immune interventions.