key: cord-0754305-wrqw5zv1
authors: Mulpuru, Viswajit; Mishra, Nidhi
title: Immunoinformatic based identification of cytotoxic T lymphocyte epitopes from the Indian isolate of SARS-CoV-2
date: 2021-02-25
journal: Sci Rep
DOI: 10.1038/s41598-021-83949-9
sha: 5c2156da2c8165aac39675db8534fb3a98c93ea7
doc_id: 754305
cord_uid: wrqw5zv1

The Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has turned into a pandemic with about thirty million confirmed cases worldwide as of September 2020. Being an airborne infection, it can be catastrophic to populous countries like India. This study sets to identify potential cytotoxic T lymphocyte (CTL) epitopes in the SARS-CoV-2 Indian isolate which can act as an effective vaccine epitope candidate for the majority of the Indian population. The immunogenicity and the foreignness of the epitopes towards the human body have to be studied to further confirm their candidacy. The top-scoring epitopes were subjected to molecular docking studies to study their interactions with the corresponding human leukocyte antigen (HLA) system. The CTL epitopes were observed to bind at the peptide-binding groove of the corresponding HLA system, indicating their potency as an epitope candidate. The candidacy was further analyzed using sequence conservation studies and molecular dynamics simulation. The identified epitopes can be subjected to further studies for the development of the SARS-CoV-2 vaccine.

Prediction of cytotoxic T cell epitopes for the Indian population. NetCTLpan version 1.1 3 was used to predict the CTL epitopes across the proteins coded by the SARS-CoV-2 Indian isolate. NetCTLpan uses a neural network to predict TAP-transporter binding and C terminal cleavage predictions in addition to HLA binding prediction. Considering the HLA supertype variation across populations, we predicted the epitopes only for those HLA supertypes which constitute the majority of human leukocyte antigen (HLA) distribution in the Indian population keeping cutoffs and parameters of NetCTLpan as default. The study on the evolution of HLA-A and HLA-B polymorphisms reveals that HLA A3, B7, and B44 are the major HLAs present in the Indian population 4 with HLA A3 constituting HLA-A type in 47 percent of the Indian population and HLA B7, B44 constituting HLA-B type in 30 percent and 28 percent of the Indian population respectively.

Prediction of epitope immunogenicity. Although the binding affinities of the peptides towards HLA help in predicting the epitopes, the immunogenicity plays an important role in the immune response. All the predicted epitopes were subjected to the Immune Epitope Database (IEDB) immunogenicity tool 5, 6 to predict their immunogenicity score. IEDB immunogenicity tool relies on physicochemical properties such as side chain composition, amino acid position to predict the immunogenicity of the peptide sequence.

Identification of unique epitopes. As the healthy human body majorly shows immune response only towards foreign antigens except under certain conditions such as autoimmune disorders, it is of great importance to consider only those epitopes which are foreign to the human body as a potential vaccine epitope candidate. To identify the vaccine epitope candidates that are foreign to the human body, all the epitopes that show positive immunogenicity are subjected to the Multiple Peptide Match tool 7 against human reference proteome with Proteome ID UP000005640. The Peptide Match tool is a search engine based on Apache Lucene and is designed to quickly retrieve all occurrences of the given query peptides from a reference or specified proteome. Docking studies. The top two percent of the foreign epitopes based on immunogenicity scores were selected.

To further confirm the candidacy of the foreign epitopes for vaccine development, these epitopes were subjected to molecular docking studies to confirm their interactions with the specified HLA at the peptide-binding groove considering PDB IDs 6O9C, 6AT5, and 3KPS for the structures of HLA-A3, HLA-B7, HLA-B44 respectively. This molecular docking study was performed using HPEPDOCK Server 8 . The docking was performed without specifying the binding site residues to investigate if the studied epitopes would bind at the peptide-binding groove without any lead. The interaction diagrams are generated using LigPlot+ 9 .

Conserved nature of the selected epitopes. To check the conserved nature of the selected epitopes from Indian isolates of the virus, The SARS-CoV-2 genomic sequences isolated in the Indian region were obtained from GISAID 10 and aligned using the MAFFT sequence alignment server 11 . All the 2084 genomic sequences as of 15 September 2020 were downloaded from the EpiCoV repository of the GISAID. Later, the alignment was translated using the standard genetic code and the locations containing the epitopes were extracted from the alignment. The extracted alignment was subjected to WebLogo 12 to generate sequence logos for visualizing their conserved nature in the Indian isolates.

To study the stability of the HLA-epitope interactions, the structures from the docking studies were subjected to all-atom molecular dynamics simulations to explore their stability and conformational flexibility using CHARMM36 all-atom force field 13 and GROMACS (Version 2018.2) 14 . The complex was solvated using TIP3P explicit water molecules and in-house ad hoc scripts were used to neutralize, minimize, and equilibrate using GROMACS. The neutralization was performed using Cl− and Na+ ions as needed while the minimization was performed using the steepest descent algorithm until the maximum force is less than 10.0 kJ/mol. The system was equilibrated using NPT conserved ensemble under constant pressure and temperature of 1 Bar and 300 K respectively. Further, the molecular dynamics simulations of 50 ns were performed using the leapfrog algorithm with an integration time step of 2 fs. The generated trajectories were analyzed using GROMACS analysis utilities to derive results. The graphs showing the root mean square deviation (RSMD) between the initial and the simulated structure, the change in coulombic interaction energies between HLA and epitope over the simulation time, and the change in the number of hydrogen bonds formed between HLA and epitope are plotted to determine the stability of the HLA-epitope complex. 15, 16 . The MHC class I are also known to be ubiquitous while MHC class II molecules are known to be present only on select antigen-presenting cells 17 . There are also instances of viruses inhibiting MHC class II antigen presentation 18 .

The IEDB immunogenicity tool was used to calculate the immunogenicity of the epitopes as it plays an important role in examining the immune response. IEDB immunogenicity tool returned 139 epitopes with positive scores. The data showing the immunogenicity score of the epitopes are shown in Supplementary Table S2 online.

All the epitopes with positive immunogenicity scores are subjected to the Multiple Peptide Match tool to identify the epitopes that are foreign to the human body. It was observed that all the epitopes that showed positive scores for immunogenicity calculations were foreign to the human proteome. The peptide matching step was performed on the sequence dataset 'UniProtKB release 2020_01 plus isoforms |SwissProt| Isoform' with the target organism set as 'Homo sapiens [9606]' . The output log had stated that 0 out of 139 unique peptides had matches in 0 protein(s) found in 0 organism(s) confirming their foreignness to the human body. Ultimately, to select the promising epitopes, the NetCTLpan score and immunogenicity score were employed. The NetCTLpan score was used to filter the highly likely CTL epitopes by eliminating the epitopes with a negative NetCTLpan score. The remaining epitopes were sorted based on their immunogenicity score to identify the top epitope candidates.

Although there were many peptide-based vaccines against various infections in different phases of development, none of these have either been concluded or had their sequence data directly available. So, we have considered an epitope from protein Superoxide Dismutase of Mycobacterium tuberculosis that showed promising results in human subjects as a control epitope in this study 19 . The control epitope and the top five vaccine epitope candidates amounting to the top two percent of the total 253 epitopes as predicted by the above steps along with their epitope prediction score by NetCTLpan and immunogenicity score are given in Table 1 .

The top three vaccine epitope candidates based on their immunogenicity score are subjected to molecular docking studies using HPEPDOCK Server. Although the top two percent of the predicted epitopes were selected for docking studies, coincidentally the top three selected epitopes were against different HLAs covering all the HLAs from the study. So, the docking studies were performed only for the best epitope candidate for each HLA. The interaction diagrams revealed that the peptide epitopes bind to the peptide-binding groove even though they were subjected to blind docking. Thus, confirming their vaccine candidacy. To visualize the equivalent interactions between the reference and the epitope towards the corresponding HLA, the interaction plots of the docked epitopes and the references are shown in Figs. 1, 2, and 3 by superposing the reference peptide-HLA interaction plot (foreground) onto the epitope-HLA interaction plot (background) where the peptide molecule already bound to the HLA in the PDB structure file is considered as the reference. The equivalent interactions between the reference peptide available in the PDB file and the studied epitope are circled in red to facilitate identification. The hydrogen bonds are represented by a green dotted line along with their distance while the non-bonded interactions (salt bridges and hydrophobic interactions) are represented by a red dotted line. The residues from different loops of the heavy chain are represented by different shades of green. Chains A and B are the chains corresponding to the protein while the chain C is the epitope. The two-dimensional interaction diagrams tracing the whole backbone of the studied epitopes are shown in Fig. 4 . The three-dimensional representation of the interactions between the identified epitope and the corresponding HLA is also shown in Fig. 4 with hydrogen bonds in cyan and nonbonded interactions in dot surfaces. The epitope residues are represented in magenta either by balls or intra-residue bonds.

As it is observed that the Interactions between the identified epitopes are similar to that of the reference peptides, the conserved nature of the selected epitopes was studied and the sequence logos as generated by WebLogo is shown in Fig. 5 showing their probability of occurrence. From the sequence logos, we conclude that the identified epitopes are highly conserved in the Indian isolates of the virus.

To check the HLA-epitope stability of the conserved epitopes, a molecular dynamics simulation of 50 ns was performed. The RMSD plot as shown in Fig. 6 suggests that the docked HLA-epitope complexes are highly stable with an average RMSD of 0.2 nm, 0.19 nm, and 0.16 nm for HLA-A*03-epitope, HLA-B*07-epitope, and www.nature.com/scientificreports/ www.nature.com/scientificreports/ HLA-B*44-epitope complexes respectively. The RMSD plots of the reference complexes are studied as control and these complexes are also found to be stable throughout the simulation time as shown in Supplementary  Fig. S1 online. Further, the short-range coulombic interaction and hydrogen bonding between the epitope and the HLA were analyzed to reveal the interaction stability of the epitope towards the corresponding HLA. The interaction plots as shown in Fig. 7 further confirm that the epitopes form a stable complex with strong bonding with the corresponding HLA.

While identifying the potential vaccine epitopes from SARS-CoV-2, this study considers all the epitopes that are not an identical subsequence to the human proteome as a foreign sequence. This could lead to the epitopes showing immune camouflaging that is generally seen in pathogens as an immune evasion strategy. This immune evasion is achieved by adopting amino acid configurations recognized by autologous regulatory T cells of the hosts which are known for their immune-modulating capabilities 20 . Apart from immune camouflaging, crossreactivity of the T cells is also a major concern where the TCR recognizes more than one peptide-MHC complex. Although cross-reactivity is an essential feature of the immune system for biological robustness, in this case where only completely identical peptide sequences are filtered out to identify the epitope candidates, the autologous peptides could also be identified for an immune response especially in the case of an engineered TCR 21, 22 .

The identified epitopes could be further subjected to in-vitro and in-vivo analysis after considering the limitations. Although epitopes play an important role in immune response, epitopes alone are not sufficient to develop vaccines as they cannot stimulate the immune system sufficiently. So, adjuvants such as biopolymers and nanoparticles are used besides an epitope in developing a peptide-based vaccine prototype for high immune response. These peptide-based vaccine prototypes should be further tested on a cell line for their physiological, biological, and chemical effects leading to cytotoxicity using in-vitro cytotoxicity assays such as in-vitro titration of live organisms, enzyme-linked immunosorbent assay (ELISA), and in-vitro antigen-quantification tests. The promising prototypes could be further subjected to in-vivo studies using animal testing techniques to identify the immunogenic prototype through immunization of laboratory animals and titration of immune sera to measure their antibody response. In-vivo serology analysis methods can be used to measure antibodies in blood samples employing techniques such as enzyme-linked immunosorbent assay (ELISA) and a multiplex assay that could analyze multiple antigens simultaneously before proceeding to further clinical phase studies 23 .

Over the last few months, there have been various studies on the identification of immunogenic epitopes from SARS-CoV-2 using computational techniques. But, these studies focus on a particular viral protein 24-26 , identifying epitopes from SARS-CoV which shows high sequence similarity along with sequence conservation to SARS-CoV-2 27 or considering viral sequences from diverse geographical regions 28 . Unlike the other studies, our analysis primarily targets the Indian population where an infectious disease could escalate very rapidly. We have also analyzed the conserved nature of the identified epitopes along with their interaction stability towards the HLAs at the peptide-binding groove considering a known bound peptide as a reference. This could significantly increase the predictability in an in-vivo environment.

Designing a vaccine is of top priority in the time of a pandemic. In this study, we attempted to identify potential CTL epitopes from the SARS-CoV-2 Indian isolate for the Indian population using a bioinformatics approach.

The list of CTL epitopes was predicted using the NetCTLPan server which considers HLA binding affinity, TAP transport efficiency, and C-terminal cleavage to identify the epitopes. Further, Immunogenicity scores were calculated using the IEDB immunogenicity tool to identify the potential vaccine epitope candidates. The epitopes www.nature.com/scientificreports/ with positive immunogenic scores are subjected to peptide matching against the human proteome to check their foreignness to the human body. These unique immunogenic epitopes were further docked with their respective HLA molecule to study their interactions with the HLA molecule. The docking studies revealed that all the studied epitopes bind at the peptide-binding site of the HLA confirming their epitope candidacy. The identified epitopes were checked for their sequence conservation in the viral isolates from India and the HLA-epitope complexes were subjected to molecular dynamics simulation studies to analyze their interaction stability. The epitopes were observed to be highly conserved and the interactions between the HLA and the epitopes were seen to be very stable, further confirming their potency in vaccine development. The epitopes identified in this study can be further subjected to in-vitro and in-vivo studies to design a vaccine against the dreadful SARS-CoV-2. www.nature.com/scientificreports/ Data availability

Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: A retrospective cohort study

Immune responses to viruses

NetCTLpan: Pan-specific MHC class I pathway epitope predictions

HLA supertype variation across populations: new insights into the role of natural selection in the evolution of HLA-A and HLA-B polymorphisms

Properties of MHC class I presented peptides that enhance immunogenicity

The immune epitope database (IEDB): 2018 update

The protein information resource (PIR)

HPEPDOCK: A web server for blind peptide-protein docking based on a hierarchical algorithm

Multiple ligand-protein interaction diagrams for drug discovery

Data, disease and diplomacy: GISAID's innovative contribution to global health

The EMBL-EBI search and sequence analysis tools APIs in 2019

A sequence logo generator

CHARMM36 all-atom additive protein force field: Validation based on comparison to NMR data

GROMACS: High performance molecular simulations through multi-level parallelism from laptops to supercomputers

MHC class I molecules exacerbate viral infection by disrupting type I interferon signaling

Most viral peptides displayed by class I MHC on infected cells are immunogenic

Present yourself! By MHC class I and MHC class II molecules

Viral inhibition of MHC class II antigen presentation

HLA-A2-restricted CD8+-cytotoxic-T-cell responses to novel epitopes in Mycobacterium tuberculosis superoxide dismutase, alanine dehydrogenase, and glutamine synthetase

Immune camouflage: Relevance to vaccines and human immunology

Identification of a titin-derived HLA-A1-presented peptide as a cross-reactive target for engineered MAGE A3-directed T cells

Cross-reactivity of T cells and its role in the immune system

New generation peptide-based vaccine prototype

Development of epitope-based peptide vaccine against novel coronavirus 2019 (SARS-COV-2): Immunoinformatics approach

Bioinformatics analysis of epitope-based vaccine design against the novel SARS-CoV-2

A candidate multi-epitope vaccine against SARS-CoV-2

A sequence homology and bioinformatic approach can predict candidate targets for immune responses to SARS-CoV-2

Anti-COVID-19 multi-epitope vaccine designs employing global viral genome sequences

All the datasets generated and/or analyzed during the current study are either available in the figshare repository https ://doi.org/10.6084/m9.figsh are.12106 737 or are included in this published article (and its Supplementary Information files). GenBank ID of the genome: MT050493.1. PDB ID for the structure of HLA-A3: 6O9C. PDB ID for the structure of HLA-B7: 6AT5. PDB ID for the structure of HLA-B44: 3KPS.Received: 3 April 2020; Accepted: 19 January 2021

The research work was carried out in the laboratory of Bioinformatics, Department of Applied Sciences, Indian Institute of Information Technology Allahabad, Prayagraj-India. The molecular dynamics simulation results reported in this work were performed on the Central Computing Facility of IIITA, Prayagraj. V.M. is thankful to the Ministry of Education, Govt. of India, for the fellowship to pursue a doctoral degree.

The authors declare no competing interests.