Full-genome sequences of the first two SARS-CoV-2 viruses from India

Background & objectives: Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India, suspected cases were screened for SARS-CoV-2 as per the advisory of the Ministry of Health and Family Welfare. The objective of this study was...

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Published inIndian journal of medical research (New Delhi, India : 1994) Vol. 151; no. 2; pp. 200 - 209
Main Authors Yadav, Pragya, Potdar, Varsha, Choudhary, Manohar, Nyayanit, Dimpal, Agrawal, Megha, Jadhav, Santosh, Majumdar, Triparna, Shete-Aich, Anita, Basu, Atanu, Abraham, Priya, Cherian, Sarah
Format Journal Article
LanguageEnglish
Published India Wolters Kluwer India Pvt. Ltd 01.02.2020
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Abstract Background & objectives: Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India, suspected cases were screened for SARS-CoV-2 as per the advisory of the Ministry of Health and Family Welfare. The objective of this study was to characterize SARS-CoV-2 sequences from three identified positive cases as on February 29, 2020. Methods: Throat swab/nasal swab specimens for a total of 881 suspected cases were screened by E gene and confirmed by RdRp (1), RdRp (2) and N gene real-time reverse transcription-polymerase chain reactions and next-generation sequencing. Phylogenetic analysis, molecular characterization and prediction of B- and T-cell epitopes for Indian SARS-CoV-2 sequences were undertaken. Results: Three cases with a travel history from Wuhan, China, were confirmed positive for SARS-CoV-2. Almost complete (29,851 nucleotides) genomes of case 1, case 3 and a fragmented genome for case 2 were obtained. The sequences of Indian SARS-CoV-2 though not identical showed high (~99.98%) identity with Wuhan seafood market pneumonia virus (accession number: NC 045512). Phylogenetic analysis showed that the Indian sequences belonged to different clusters. Predicted linear B-cell epitopes were found to be concentrated in the S1 domain of spike protein, and a conformational epitope was identified in the receptor-binding domain. The predicted T-cell epitopes showed broad human leucocyte antigen allele coverage of A and B supertypes predominant in the Indian population. Interpretation & conclusions: The two SARS-CoV-2 sequences obtained from India represent two different introductions into the country. The genetic heterogeneity is as noted globally. The identified B- and T-cell epitopes may be considered suitable for future experiments towards the design of vaccines and diagnostics. Continuous monitoring and analysis of the sequences of new cases from India and the other affected countries would be vital to understand the genetic evolution and rates of substitution of the SARS-CoV-2.
AbstractList Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India, suspected cases were screened for SARS-CoV-2 as per the advisory of the Ministry of Health and Family Welfare. The objective of this study was to characterize SARS-CoV-2 sequences from three identified positive cases as on February 29, 2020.Background & objectivesSince December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India, suspected cases were screened for SARS-CoV-2 as per the advisory of the Ministry of Health and Family Welfare. The objective of this study was to characterize SARS-CoV-2 sequences from three identified positive cases as on February 29, 2020.Throat swab/nasal swab specimens for a total of 881 suspected cases were screened by E gene and confirmed by RdRp (1), RdRp (2) and N gene real-time reverse transcription-polymerase chain reactions and next-generation sequencing. Phylogenetic analysis, molecular characterization and prediction of B- and T-cell epitopes for Indian SARS-CoV-2 sequences were undertaken.MethodsThroat swab/nasal swab specimens for a total of 881 suspected cases were screened by E gene and confirmed by RdRp (1), RdRp (2) and N gene real-time reverse transcription-polymerase chain reactions and next-generation sequencing. Phylogenetic analysis, molecular characterization and prediction of B- and T-cell epitopes for Indian SARS-CoV-2 sequences were undertaken.Three cases with a travel history from Wuhan, China, were confirmed positive for SARS-CoV-2. Almost complete (29,851 nucleotides) genomes of case 1, case 3 and a fragmented genome for case 2 were obtained. The sequences of Indian SARS-CoV-2 though not identical showed high (~99.98%) identity with Wuhan seafood market pneumonia virus (accession number: NC 045512). Phylogenetic analysis showed that the Indian sequences belonged to different clusters. Predicted linear B-cell epitopes were found to be concentrated in the S1 domain of spike protein, and a conformational epitope was identified in the receptor-binding domain. The predicted T-cell epitopes showed broad human leucocyte antigen allele coverage of A and B supertypes predominant in the Indian population.ResultsThree cases with a travel history from Wuhan, China, were confirmed positive for SARS-CoV-2. Almost complete (29,851 nucleotides) genomes of case 1, case 3 and a fragmented genome for case 2 were obtained. The sequences of Indian SARS-CoV-2 though not identical showed high (~99.98%) identity with Wuhan seafood market pneumonia virus (accession number: NC 045512). Phylogenetic analysis showed that the Indian sequences belonged to different clusters. Predicted linear B-cell epitopes were found to be concentrated in the S1 domain of spike protein, and a conformational epitope was identified in the receptor-binding domain. The predicted T-cell epitopes showed broad human leucocyte antigen allele coverage of A and B supertypes predominant in the Indian population.The two SARS-CoV-2 sequences obtained from India represent two different introductions into the country. The genetic heterogeneity is as noted globally. The identified B- and T-cell epitopes may be considered suitable for future experiments towards the design of vaccines and diagnostics. Continuous monitoring and analysis of the sequences of new cases from India and the other affected countries would be vital to understand the genetic evolution and rates of substitution of the SARS-CoV-2.Interpretation & conclusionsThe two SARS-CoV-2 sequences obtained from India represent two different introductions into the country. The genetic heterogeneity is as noted globally. The identified B- and T-cell epitopes may be considered suitable for future experiments towards the design of vaccines and diagnostics. Continuous monitoring and analysis of the sequences of new cases from India and the other affected countries would be vital to understand the genetic evolution and rates of substitution of the SARS-CoV-2.
Background & objectives: Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India, suspected cases were screened for SARS-CoV-2 as per the advisory of the Ministry of Health and Family Welfare. The objective of this study was to characterize SARS-CoV-2 sequences from three identified positive cases as on February 29, 2020. Methods: Throat swab/nasal swab specimens for a total of 881 suspected cases were screened by E gene and confirmed by RdRp (1), RdRp (2) and N gene real-time reverse transcription-polymerase chain reactions and next-generation sequencing. Phylogenetic analysis, molecular characterization and prediction of B- and T-cell epitopes for Indian SARS-CoV-2 sequences were undertaken. Results: Three cases with a travel history from Wuhan, China, were confirmed positive for SARS-CoV-2. Almost complete (29,851 nucleotides) genomes of case 1, case 3 and a fragmented genome for case 2 were obtained. The sequences of Indian SARS-CoV-2 though not identical showed high (~99.98%) identity with Wuhan seafood market pneumonia virus (accession number: NC 045512). Phylogenetic analysis showed that the Indian sequences belonged to different clusters. Predicted linear B-cell epitopes were found to be concentrated in the S1 domain of spike protein, and a conformational epitope was identified in the receptor-binding domain. The predicted T-cell epitopes showed broad human leucocyte antigen allele coverage of A and B supertypes predominant in the Indian population. Interpretation & conclusions: The two SARS-CoV-2 sequences obtained from India represent two different introductions into the country. The genetic heterogeneity is as noted globally. The identified B- and T-cell epitopes may be considered suitable for future experiments towards the design of vaccines and diagnostics. Continuous monitoring and analysis of the sequences of new cases from India and the other affected countries would be vital to understand the genetic evolution and rates of substitution of the SARS-CoV-2.
Background & objectives: Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India, suspected cases were screened for SARS-CoV-2 as per the advisory of the Ministry of Health and Family Welfare. The objective of this study was to characterize SARS-CoV-2 sequences from three identified positive cases as on February 29, 2020. Methods: Throat swab/nasal swab specimens for a total of 881 suspected cases were screened by E gene and confirmed by RdRp (1), RdRp (2) and N gene real-time reverse transcription-polymerase chain reactions and next-generation sequencing. Phylogenetic analysis, molecular characterization and prediction of B- and T-cell epitopes for Indian SARS-CoV-2 sequences were undertaken. Results: Three cases with a travel history from Wuhan, China, were confirmed positive for SARS-CoV-2. Almost complete (29,851 nucleotides) genomes of case 1, case 3 and a fragmented genome for case 2 were obtained. The sequences of Indian SARS-CoV-2 though not identical showed high (~99.98%) identity with Wuhan seafood market pneumonia virus (accession number: NC 045512). Phylogenetic analysis showed that the Indian sequences belonged to different clusters. Predicted linear B-cell epitopes were found to be concentrated in the S1 domain of spike protein, and a conformational epitope was identified in the receptor-binding domain. The predicted T-cell epitopes showed broad human leucocyte antigen allele coverage of A and B supertypes predominant in the Indian population. Interpretation & conclusions: The two SARS-CoV-2 sequences obtained from India represent two different introductions into the country. The genetic heterogeneity is as noted globally. The identified B- and T-cell epitopes may be considered suitable for future experiments towards the design of vaccines and diagnostics. Continuous monitoring and analysis of the sequences of new cases from India and the other affected countries would be vital to understand the genetic evolution and rates of substitution of the SARS-CoV-2.
Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India, suspected cases were screened for SARS-CoV-2 as per the advisory of the Ministry of Health and Family Welfare. The objective of this study was to characterize SARS-CoV-2 sequences from three identified positive cases as on February 29, 2020. Throat swab/nasal swab specimens for a total of 881 suspected cases were screened by E gene and confirmed by RdRp (1), RdRp (2) and N gene real-time reverse transcription-polymerase chain reactions and next-generation sequencing. Phylogenetic analysis, molecular characterization and prediction of B- and T-cell epitopes for Indian SARS-CoV-2 sequences were undertaken. Three cases with a travel history from Wuhan, China, were confirmed positive for SARS-CoV-2. Almost complete (29,851 nucleotides) genomes of case 1, case 3 and a fragmented genome for case 2 were obtained. The sequences of Indian SARS-CoV-2 though not identical showed high (~99.98%) identity with Wuhan seafood market pneumonia virus (accession number: NC 045512). Phylogenetic analysis showed that the Indian sequences belonged to different clusters. Predicted linear B-cell epitopes were found to be concentrated in the S1 domain of spike protein, and a conformational epitope was identified in the receptor-binding domain. The predicted T-cell epitopes showed broad human leucocyte antigen allele coverage of A and B supertypes predominant in the Indian population. The two SARS-CoV-2 sequences obtained from India represent two different introductions into the country. The genetic heterogeneity is as noted globally. The identified B- and T-cell epitopes may be considered suitable for future experiments towards the design of vaccines and diagnostics. Continuous monitoring and analysis of the sequences of new cases from India and the other affected countries would be vital to understand the genetic evolution and rates of substitution of the SARS-CoV-2.
Audience Academic
Author Potdar, Varsha
Yadav, Pragya
Nyayanit, Dimpal
Agrawal, Megha
Choudhary, Manohar
Jadhav, Santosh
Basu, Atanu
Shete-Aich, Anita
Cherian, Sarah
Abraham, Priya
Majumdar, Triparna
AuthorAffiliation 4 Bioinformatics & Data Management Group, ICMR-National Institute of Virology, Pune, Maharashtra, India
3 Electron Microscopy, ICMR-National Institute of Virology, Pune, Maharashtra, India
1 Maximum Containment Laboratory, ICMR-National Institute of Virology, Pune, Maharashtra, India
2 Influenza Group, ICMR-National Institute of Virology, Pune, Maharashtra, India
ICMR-National Institute of Virology, Pune, Maharashtra, India
AuthorAffiliation_xml – name: 1 Maximum Containment Laboratory, ICMR-National Institute of Virology, Pune, Maharashtra, India
– name: 3 Electron Microscopy, ICMR-National Institute of Virology, Pune, Maharashtra, India
– name: 2 Influenza Group, ICMR-National Institute of Virology, Pune, Maharashtra, India
– name: ICMR-National Institute of Virology, Pune, Maharashtra, India
– name: 4 Bioinformatics & Data Management Group, ICMR-National Institute of Virology, Pune, Maharashtra, India
Author_xml – sequence: 1
  givenname: Pragya
  surname: Yadav
  fullname: Yadav, Pragya
  organization: Maximum Containment Laboratory, ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 2
  givenname: Varsha
  surname: Potdar
  fullname: Potdar, Varsha
  organization: Influenza Group, ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 3
  givenname: Manohar
  surname: Choudhary
  fullname: Choudhary, Manohar
  organization: Influenza Group, ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 4
  givenname: Dimpal
  surname: Nyayanit
  fullname: Nyayanit, Dimpal
  organization: Maximum Containment Laboratory, ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 5
  givenname: Megha
  surname: Agrawal
  fullname: Agrawal, Megha
  organization: Bioinformatics & Data Management Group, ICMR-National Institute of Virology, Pune, Maharashtra
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  givenname: Santosh
  surname: Jadhav
  fullname: Jadhav, Santosh
  organization: Bioinformatics & Data Management Group, ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 7
  givenname: Triparna
  surname: Majumdar
  fullname: Majumdar, Triparna
  organization: Maximum Containment Laboratory, ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 8
  givenname: Anita
  surname: Shete-Aich
  fullname: Shete-Aich, Anita
  organization: Maximum Containment Laboratory, ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 9
  givenname: Atanu
  surname: Basu
  fullname: Basu, Atanu
  organization: Electron Microscopy & ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 10
  givenname: Priya
  surname: Abraham
  fullname: Abraham, Priya
  organization: ICMR-National Institute of Virology, Pune, Maharashtra
– sequence: 11
  givenname: Sarah
  surname: Cherian
  fullname: Cherian, Sarah
  organization: Bioinformatics & Data Management Group, ICMR-National Institute of Virology, Pune, Maharashtra
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32242873$$D View this record in MEDLINE/PubMed
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Issue 2
Keywords genomes
Epitope
next-generation sequencing
severe acute respiratory syndrome coronavirus 2
real-time reverse transcription-polymerase chain reaction
phylogeny
Kerala
India
Language English
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Snippet Background & objectives: Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India,...
Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has globally affected 195 countries. In India, suspected cases were screened...
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SubjectTerms Betacoronavirus - genetics
Coronavirus Infections
Coronaviruses
COVID-19
Epitopes, B-Lymphocyte - genetics
Epitopes, T-Lymphocyte - genetics
Genome, Viral
Genomics
Humans
India
Laboratories
Middle East respiratory syndrome
Models, Molecular
Original
Pandemics
Phylogeny
Pneumonia, Viral
Protein Structure, Tertiary
Reverse Transcriptase Polymerase Chain Reaction
RNA, Viral - genetics
SARS-CoV-2
Severe acute respiratory syndrome
Severe acute respiratory syndrome coronavirus 2
Spike Glycoprotein, Coronavirus - genetics
Viruses
Whole genome sequencing
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Title Full-genome sequences of the first two SARS-CoV-2 viruses from India
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