Analyses of spike protein from first deposited sequences of SARS-CoV2 from West Bengal, India [version 1; peer review: 2 approved, 1 approved with reservations]

India has recently started sequencing SARS-CoV2 genome from clinical isolates. Currently only few sequences are available from three states in India. Kerala was the first state to deposit complete sequence from two isolates followed by one from Gujarat. On April 27, 2020, the first five sequences fr...

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Main Authors: Feroza Begum, Debica Mukherjee, Dluya Thagriki, Sandeepan Das, Prem Prakash Tripathi, Arup Kumar Banerjee, Upasana Ray
Format: Article
Language:English
Published: F1000 Research Ltd 2020-05-01
Series:F1000Research
Online Access:https://f1000research.com/articles/9-371/v1
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spelling doaj-abd01f784fdc4247b0a897633e0198442020-11-25T03:42:14ZengF1000 Research LtdF1000Research2046-14022020-05-01910.12688/f1000research.23805.126268Analyses of spike protein from first deposited sequences of SARS-CoV2 from West Bengal, India [version 1; peer review: 2 approved, 1 approved with reservations]Feroza Begum0Debica Mukherjee1Dluya Thagriki2Sandeepan Das3Prem Prakash Tripathi4Arup Kumar Banerjee5Upasana Ray6CSIR-Indian Institute of Chemical Biology, Kolkata, West Bengal, 700032, IndiaCSIR-Indian Institute of Chemical Biology, Kolkata, West Bengal, 700032, IndiaCSIR-Indian Institute of Chemical Biology, Kolkata, West Bengal, 700032, IndiaCSIR-Indian Institute of Chemical Biology, Kolkata, West Bengal, 700032, IndiaCSIR-Indian Institute of Chemical Biology, Kolkata, West Bengal, 700032, IndiaDepartment of Biochemistry, North Bengal Medical College and Hospital, Sushrutanagar, West Bengal, 734012, IndiaCSIR-Indian Institute of Chemical Biology, Kolkata, West Bengal, 700032, IndiaIndia has recently started sequencing SARS-CoV2 genome from clinical isolates. Currently only few sequences are available from three states in India. Kerala was the first state to deposit complete sequence from two isolates followed by one from Gujarat. On April 27, 2020, the first five sequences from the state of West Bengal (Eastern India) were deposited on GISAID, a global initiative for sharing avian flu data. In this study, we have analysed the spike protein sequences from all five isolates and also compared their similarities or differences with other sequences reported in India and with isolates of Wuhan origin. We report one unique mutation at position 723 and another at 1124 in the S2 domain of spike protein of the isolates from West Bengal only.  There was one mutation downstream of the receptor binding domain at position 614 in S1 domain which was common with the sequence from Gujarat (a state of western India).  Mutation in the S2 domain showed changes in the secondary structure of the spike protein at region of the mutation. We also studied molecular dynamics using normal mode analyses and found that this mutation decreases the flexibility of S2 domain.  Since both S1 and S2 are important in receptor binding followed by entry in the host cells, such mutations may define the affinity or avidity of receptor binding.https://f1000research.com/articles/9-371/v1
collection DOAJ
language English
format Article
sources DOAJ
author Feroza Begum
Debica Mukherjee
Dluya Thagriki
Sandeepan Das
Prem Prakash Tripathi
Arup Kumar Banerjee
Upasana Ray
spellingShingle Feroza Begum
Debica Mukherjee
Dluya Thagriki
Sandeepan Das
Prem Prakash Tripathi
Arup Kumar Banerjee
Upasana Ray
Analyses of spike protein from first deposited sequences of SARS-CoV2 from West Bengal, India [version 1; peer review: 2 approved, 1 approved with reservations]
F1000Research
author_facet Feroza Begum
Debica Mukherjee
Dluya Thagriki
Sandeepan Das
Prem Prakash Tripathi
Arup Kumar Banerjee
Upasana Ray
author_sort Feroza Begum
title Analyses of spike protein from first deposited sequences of SARS-CoV2 from West Bengal, India [version 1; peer review: 2 approved, 1 approved with reservations]
title_short Analyses of spike protein from first deposited sequences of SARS-CoV2 from West Bengal, India [version 1; peer review: 2 approved, 1 approved with reservations]
title_full Analyses of spike protein from first deposited sequences of SARS-CoV2 from West Bengal, India [version 1; peer review: 2 approved, 1 approved with reservations]
title_fullStr Analyses of spike protein from first deposited sequences of SARS-CoV2 from West Bengal, India [version 1; peer review: 2 approved, 1 approved with reservations]
title_full_unstemmed Analyses of spike protein from first deposited sequences of SARS-CoV2 from West Bengal, India [version 1; peer review: 2 approved, 1 approved with reservations]
title_sort analyses of spike protein from first deposited sequences of sars-cov2 from west bengal, india [version 1; peer review: 2 approved, 1 approved with reservations]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2020-05-01
description India has recently started sequencing SARS-CoV2 genome from clinical isolates. Currently only few sequences are available from three states in India. Kerala was the first state to deposit complete sequence from two isolates followed by one from Gujarat. On April 27, 2020, the first five sequences from the state of West Bengal (Eastern India) were deposited on GISAID, a global initiative for sharing avian flu data. In this study, we have analysed the spike protein sequences from all five isolates and also compared their similarities or differences with other sequences reported in India and with isolates of Wuhan origin. We report one unique mutation at position 723 and another at 1124 in the S2 domain of spike protein of the isolates from West Bengal only.  There was one mutation downstream of the receptor binding domain at position 614 in S1 domain which was common with the sequence from Gujarat (a state of western India).  Mutation in the S2 domain showed changes in the secondary structure of the spike protein at region of the mutation. We also studied molecular dynamics using normal mode analyses and found that this mutation decreases the flexibility of S2 domain.  Since both S1 and S2 are important in receptor binding followed by entry in the host cells, such mutations may define the affinity or avidity of receptor binding.
url https://f1000research.com/articles/9-371/v1
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