Overwhelming mutations or SNPs of SARS-CoV-2: A point of caution

•Mutation studies hits cause for the superior infectious rate of SARS-CoV-2.•SARS-CoV-2 is evolving rapidly with number of mutations and SNPs.•Mutations were found in the ACE2 binding region of SARS-CoV-2 spike glycoprotein.•ORF1ab, ORF8 and spike glycoprotein regions of SARS-CoV-2 are highly mutate...

Full description

Saved in:
Bibliographic Details
Published inGene Vol. 752; p. 144792
Main Author Vankadari, Naveen
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 20.08.2020
Subjects
Online AccessGet full text

Cover

Loading…
Abstract •Mutation studies hits cause for the superior infectious rate of SARS-CoV-2.•SARS-CoV-2 is evolving rapidly with number of mutations and SNPs.•Mutations were found in the ACE2 binding region of SARS-CoV-2 spike glycoprotein.•ORF1ab, ORF8 and spike glycoprotein regions of SARS-CoV-2 are highly mutated.•Overwhelming mutations or SNPs of SARS-CoV-2 alerts drug treatment options. The morbidity of SARS-CoV-2 (COVID-19) is reaching 3 Million landmark causing and a serious public health concern globally and it is enigmatic how several antiviral and antibody treatments were not effective in the different period across the globe. With the drastic increasing number of positive cases around the world WHO raised the importance in the assessment of the risk of spread and understanding genetic modifications that could have occurred in the SARS-CoV-2. Using all available deep sequencing data of complete genome from all over the world (NCBI repository), we identified several hundreds of point mutations or SNPs in SARS-CoV-2 all across the genome. This could be the cause for the constant change and differed virulence with an increase in mortality and morbidity. Among the 12 different countries (one sequence from each country) with complete genome sequencing data, we noted the 47 key point mutations or SNPs located along the entire genome that might have impact in the virulence and response to different antivirals against SARS-CoV-2. In this regard, key viral proteins of spike glycoprotein, Nsp1, RdRp and the ORF8 region got heavily mutated within these 3 months via person-to-person passage. We also discuss what could be the possible cause of this rapid mutation in the SARS-CoV-2.
AbstractList • Mutation studies hits cause for the superior infectious rate of SARS-CoV-2. • SARS-CoV-2 is evolving rapidly with number of mutations and SNPs. • Mutations were found in the ACE2 binding region of SARS-CoV-2 spike glycoprotein. • ORF1ab, ORF8 and spike glycoprotein regions of SARS-CoV-2 are highly mutated. • Overwhelming mutations or SNPs of SARS-CoV-2 alerts drug treatment options. The morbidity of SARS-CoV-2 (COVID-19) is reaching 3 Million landmark causing and a serious public health concern globally and it is enigmatic how several antiviral and antibody treatments were not effective in the different period across the globe. With the drastic increasing number of positive cases around the world WHO raised the importance in the assessment of the risk of spread and understanding genetic modifications that could have occurred in the SARS-CoV-2. Using all available deep sequencing data of complete genome from all over the world (NCBI repository), we identified several hundreds of point mutations or SNPs in SARS-CoV-2 all across the genome. This could be the cause for the constant change and differed virulence with an increase in mortality and morbidity. Among the 12 different countries (one sequence from each country) with complete genome sequencing data, we noted the 47 key point mutations or SNPs located along the entire genome that might have impact in the virulence and response to different antivirals against SARS-CoV-2. In this regard, key viral proteins of spike glycoprotein, Nsp1, RdRp and the ORF8 region got heavily mutated within these 3 months via person-to-person passage. We also discuss what could be the possible cause of this rapid mutation in the SARS-CoV-2.
The morbidity of SARS-CoV-2 (COVID-19) is reaching 3 Million landmark causing and a serious public health concern globally and it is enigmatic how several antiviral and antibody treatments were not effective in the different period across the globe. With the drastic increasing number of positive cases around the world WHO raised the importance in the assessment of the risk of spread and understanding genetic modifications that could have occurred in the SARS-CoV-2. Using all available deep sequencing data of complete genome from all over the world (NCBI repository), we identified several hundreds of point mutations or SNPs in SARS-CoV-2 all across the genome. This could be the cause for the constant change and differed virulence with an increase in mortality and morbidity. Among the 12 different countries (one sequence from each country) with complete genome sequencing data, we noted the 47 key point mutations or SNPs located along the entire genome that might have impact in the virulence and response to different antivirals against SARS-CoV-2. In this regard, key viral proteins of spike glycoprotein, Nsp1, RdRp and the ORF8 region got heavily mutated within these 3 months via person-to-person passage. We also discuss what could be the possible cause of this rapid mutation in the SARS-CoV-2.
•Mutation studies hits cause for the superior infectious rate of SARS-CoV-2.•SARS-CoV-2 is evolving rapidly with number of mutations and SNPs.•Mutations were found in the ACE2 binding region of SARS-CoV-2 spike glycoprotein.•ORF1ab, ORF8 and spike glycoprotein regions of SARS-CoV-2 are highly mutated.•Overwhelming mutations or SNPs of SARS-CoV-2 alerts drug treatment options. The morbidity of SARS-CoV-2 (COVID-19) is reaching 3 Million landmark causing and a serious public health concern globally and it is enigmatic how several antiviral and antibody treatments were not effective in the different period across the globe. With the drastic increasing number of positive cases around the world WHO raised the importance in the assessment of the risk of spread and understanding genetic modifications that could have occurred in the SARS-CoV-2. Using all available deep sequencing data of complete genome from all over the world (NCBI repository), we identified several hundreds of point mutations or SNPs in SARS-CoV-2 all across the genome. This could be the cause for the constant change and differed virulence with an increase in mortality and morbidity. Among the 12 different countries (one sequence from each country) with complete genome sequencing data, we noted the 47 key point mutations or SNPs located along the entire genome that might have impact in the virulence and response to different antivirals against SARS-CoV-2. In this regard, key viral proteins of spike glycoprotein, Nsp1, RdRp and the ORF8 region got heavily mutated within these 3 months via person-to-person passage. We also discuss what could be the possible cause of this rapid mutation in the SARS-CoV-2.
ArticleNumber 144792
Author Vankadari, Naveen
Author_xml – sequence: 1
  givenname: Naveen
  orcidid: 0000-0001-9363-080X
  surname: Vankadari
  fullname: Vankadari, Naveen
  email: Naveen.vankadari@monash.edu
  organization: Monash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32445924$$D View this record in MEDLINE/PubMed
BookMark eNp9kE1LAzEQhoMo2qp_wIPs0cvWJJv9iIhYil8gKla9hjQ7W1N2k5rsVvz3ZqmKXpzLwMz7vsk8Q7RprAGEDggeEUyy48VoDgZGFNMwYCzndAMNSJHzGOOk2EQDnORFTAjhO2jo_QKHSlO6jXYSyljKKRug8_sVuPdXqBtt5lHTtbLV1vjIumh69xB6FU3Hj9N4Yl9iehKNo6XVpu3HSna9dA9tVbL2sP_Vd9Hz5cXT5Dq-vb-6mYxvY8XStI1llhJc4RnwMgNZ5bScqYpmnLEKk0ImjBdMSUgZpiSXvMRppvJKkmDjPAm1i87Wuctu1kCpwLRO1mLpdCPdh7BSi78bo1_F3K5EThMe7g4BR18Bzr514FvRaK-grqUB23lBGc4SXCSsl9K1VDnrvYPq5xmCRY9eLESPXvToxRp9MB3-_uCP5Zt1EJyuBRAwrTQ44ZUGo6DUDlQrSqv_y_8Eu8uVNQ
CitedBy_id crossref_primary_10_3390_biology11121786
crossref_primary_10_1007_s00203_021_02527_9
crossref_primary_10_1016_j_nmni_2022_100955
crossref_primary_10_1177_00368504211026119
crossref_primary_10_1007_s12250_021_00384_w
crossref_primary_10_1080_07391102_2023_2228919
crossref_primary_10_1007_s10555_022_10019_5
crossref_primary_10_1021_acs_jpclett_0c01698
crossref_primary_10_1093_cid_ciaa1474
crossref_primary_10_1021_acs_jpclett_2c00967
crossref_primary_10_1002_jmv_27477
crossref_primary_10_1016_j_gene_2021_145843
crossref_primary_10_29132_ijpas_793377
crossref_primary_10_3390_biology9060141
crossref_primary_10_1080_07391102_2022_2079562
crossref_primary_10_1128_msystems_00035_22
crossref_primary_10_1016_j_dsx_2020_06_067
crossref_primary_10_1371_journal_pone_0241163
crossref_primary_10_1128_mBio_00788_21
crossref_primary_10_1093_bib_bbab025
crossref_primary_10_3390_genes12060826
crossref_primary_10_1016_j_molstruc_2021_131879
crossref_primary_10_3389_fvets_2021_644414
crossref_primary_10_1038_s41598_023_29206_7
crossref_primary_10_1177_11769343211003079
crossref_primary_10_1016_j_diagmicrobio_2022_115718
crossref_primary_10_1089_jicm_2022_0554
crossref_primary_10_1038_s41598_020_78965_0
crossref_primary_10_1021_acs_jpclett_0c02818
crossref_primary_10_1016_j_imbio_2021_152130
crossref_primary_10_1134_S1022795421080056
Cites_doi 10.1186/s13643-019-1011-y
10.1128/JVI.00694-10
10.1016/S0140-6736(20)30183-5
10.1128/JVI.01048-15
10.1080/22221751.2020.1719902
10.1080/22221751.2020.1739565
10.1016/j.gene.2004.12.033
10.1016/S1473-3099(20)30243-7
10.1128/JVI.01031-17
10.1128/JVI.02472-07
10.1038/s41591-020-0820-9
10.1016/j.antiviral.2020.104742
10.1126/science.abb2507
ContentType Journal Article
Copyright 2020 Elsevier B.V.
Copyright © 2020 Elsevier B.V. All rights reserved.
2020 Elsevier B.V. All rights reserved. 2020 Elsevier B.V.
Copyright_xml – notice: 2020 Elsevier B.V.
– notice: Copyright © 2020 Elsevier B.V. All rights reserved.
– notice: 2020 Elsevier B.V. All rights reserved. 2020 Elsevier B.V.
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
5PM
DOI 10.1016/j.gene.2020.144792
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
MEDLINE - Academic
DatabaseTitleList
MEDLINE

Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Engineering
Anatomy & Physiology
Biology
EISSN 1879-0038
EndPage 144792
ExternalDocumentID 10_1016_j_gene_2020_144792
32445924
S0378111920304613
Genre Letter
Correspondence
GeographicLocations Americas
Asia
Europe
GeographicLocations_xml – name: Americas
– name: Europe
– name: Asia
GroupedDBID ---
--K
--M
-~X
.~1
0R~
1B1
1RT
1~.
1~5
4.4
457
4G.
5GY
5VS
7-5
71M
8P~
9JM
AABNK
AACTN
AAEDT
AAEDW
AAIAV
AAIKJ
AAKOC
AALRI
AAOAW
AAQFI
AAXUO
ABFNM
ABFRF
ABGSF
ABJNI
ABLJU
ABMAC
ABUDA
ABYKQ
ACDAQ
ACGFO
ACGFS
ACIUM
ACNCT
ACRLP
ADBBV
ADEZE
ADUVX
AEBSH
AEFWE
AEHWI
AEKER
AENEX
AFKWA
AFTJW
AFXIZ
AGHFR
AGUBO
AGYEJ
AHHHB
AIEXJ
AIKHN
AITUG
AJOXV
ALMA_UNASSIGNED_HOLDINGS
AMFUW
AMRAJ
AXJTR
BKOJK
BLXMC
CS3
DOVZS
DU5
EBS
EFJIC
EFLBG
EO8
EO9
EP2
EP3
F5P
FDB
FIRID
FNPLU
FYGXN
G-Q
GBLVA
IHE
J1W
KOM
LX3
M41
MO0
N9A
O-L
O9-
OAUVE
OZT
P-8
P-9
P2P
PC.
Q38
ROL
RPZ
SCC
SDF
SDG
SDP
SES
SPCBC
SSU
SSZ
T5K
WH7
ZA5
~G-
AAHBH
AAXKI
AKRWK
CGR
CUY
CVF
ECM
EIF
NPM
RIG
.55
.GJ
0SF
29H
53G
AAQXK
AAYXX
ABEFU
ABXDB
ADIYS
ADMUD
ADVLN
AFJKZ
AGRDE
AI.
ASPBG
AVWKF
AZFZN
CITATION
EJD
FEDTE
FGOYB
G-2
G8K
HLW
HVGLF
HZ~
MVM
R2-
SBG
SEW
VH1
WUQ
X7M
XOL
XPP
Y6R
ZGI
~KM
7X8
5PM
ID FETCH-LOGICAL-c455t-a6510f0be9d6eaf72dbcf26944f018a34984cae540217a9d056c7fa1651993333
IEDL.DBID AIKHN
ISSN 0378-1119
IngestDate Tue Sep 17 21:07:46 EDT 2024
Fri Oct 25 11:48:51 EDT 2024
Thu Sep 26 17:22:49 EDT 2024
Sat Sep 28 08:25:29 EDT 2024
Fri Feb 23 02:47:23 EST 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords COVID-19
ACE2
Nsp1
Coronavirus
SNP
Rdrp
NCBI
Evolution
CD26
Sequence
Genome
WHO
Language English
License Copyright © 2020 Elsevier B.V. All rights reserved.
Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c455t-a6510f0be9d6eaf72dbcf26944f018a34984cae540217a9d056c7fa1651993333
Notes SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ORCID 0000-0001-9363-080X
OpenAccessLink https://pubmed.ncbi.nlm.nih.gov/PMC7239005
PMID 32445924
PQID 2406308345
PQPubID 23479
PageCount 1
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_7239005
proquest_miscellaneous_2406308345
crossref_primary_10_1016_j_gene_2020_144792
pubmed_primary_32445924
elsevier_sciencedirect_doi_10_1016_j_gene_2020_144792
PublicationCentury 2000
PublicationDate 2020-08-20
PublicationDateYYYYMMDD 2020-08-20
PublicationDate_xml – month: 08
  year: 2020
  text: 2020-08-20
  day: 20
PublicationDecade 2020
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Gene
PublicationTitleAlternate Gene
PublicationYear 2020
Publisher Elsevier B.V
Publisher_xml – name: Elsevier B.V
References Wrapp (b0030) 2020; 367
Manrubia (b0060) 2005; 347
Miller (b0040) 2020; 16
Verity (b0005) 2020
Huang (b0010) 2020; 395
Puty (b0015) 2019; 8
Sanjuan (b0070) 2010; 84
Narayanan (b0035) 2008; 82
Peck, Lauring (b0065) 2018; 92
Chan (b0050) 2020; 9
Andersen (b0020) 2020; 26
Lau (b0055) 2015; 89
Vankadari, Wilce (b0025) 2020; 9
Coutard (b0045) 2020; 176
Verity (10.1016/j.gene.2020.144792_b0005) 2020
Coutard (10.1016/j.gene.2020.144792_b0045) 2020; 176
Puty (10.1016/j.gene.2020.144792_b0015) 2019; 8
Wrapp (10.1016/j.gene.2020.144792_b0030) 2020; 367
Manrubia (10.1016/j.gene.2020.144792_b0060) 2005; 347
Chan (10.1016/j.gene.2020.144792_b0050) 2020; 9
Sanjuan (10.1016/j.gene.2020.144792_b0070) 2010; 84
Andersen (10.1016/j.gene.2020.144792_b0020) 2020; 26
Huang (10.1016/j.gene.2020.144792_b0010) 2020; 395
Narayanan (10.1016/j.gene.2020.144792_b0035) 2008; 82
Peck (10.1016/j.gene.2020.144792_b0065) 2018; 92
Lau (10.1016/j.gene.2020.144792_b0055) 2015; 89
Miller (10.1016/j.gene.2020.144792_b0040) 2020; 16
Vankadari (10.1016/j.gene.2020.144792_b0025) 2020; 9
References_xml – volume: 347
  start-page: 273
  year: 2005
  end-page: 282
  ident: b0060
  article-title: High mutation rates, bottlenecks, and robustness of RNA viral quasispecies
  publication-title: Gene
  contributor:
    fullname: Manrubia
– volume: 84
  start-page: 9733
  year: 2010
  end-page: 9748
  ident: b0070
  article-title: Viral mutation rates
  publication-title: J. Virol.
  contributor:
    fullname: Sanjuan
– year: 2020
  ident: b0005
  article-title: Estimates of the severity of coronavirus disease 2019: a model-based analysis
  publication-title: Lancet Infect. Dis.
  contributor:
    fullname: Verity
– volume: 9
  start-page: 221
  year: 2020
  end-page: 236
  ident: b0050
  article-title: Genomic characterization of the 2019 novel human-pathogenic coronavirus isolated from a patient with atypical pneumonia after visiting Wuhan
  publication-title: Emerg. Microbes Infect.
  contributor:
    fullname: Chan
– volume: 26
  start-page: 450
  year: 2020
  end-page: 452
  ident: b0020
  article-title: The proximal origin of SARS-CoV-2
  publication-title: Nat. Med.
  contributor:
    fullname: Andersen
– volume: 9
  start-page: 601
  year: 2020
  end-page: 604
  ident: b0025
  article-title: Emerging WuHan (COVID-19) coronavirus: glycan shield and structure prediction of spike glycoprotein and its interaction with human CD26
  publication-title: Emerg. Microbes Infect.
  contributor:
    fullname: Wilce
– volume: 176
  year: 2020
  ident: b0045
  article-title: The spike glycoprotein of the new coronavirus 2019-nCoV contains a furin-like cleavage site absent in CoV of the same clade
  publication-title: Antiviral Res.
  contributor:
    fullname: Coutard
– volume: 92
  start-page: 1031
  year: 2018
  end-page: 1117
  ident: b0065
  article-title: Complexities of viral mutation rates
  publication-title: J. Virol.
  contributor:
    fullname: Lauring
– volume: 82
  start-page: 4471
  year: 2008
  end-page: 4479
  ident: b0035
  article-title: Severe acute respiratory syndrome coronavirus nsp1 suppresses host gene expression, including that of type I interferon, in infected cells
  publication-title: J. Virol.
  contributor:
    fullname: Narayanan
– volume: 16
  start-page: 94
  year: 2020
  ident: b0040
  article-title: Systemic expression of a viral RdRP protects against retrovirus infection and disease
  publication-title: J. Virol.
  contributor:
    fullname: Miller
– volume: 89
  start-page: 10532
  year: 2015
  end-page: 10547
  ident: b0055
  article-title: Severe acute respiratory syndrome (SARS) coronavirus ORF8 protein is acquired from SARS-related coronavirus from greater horseshoe bats through recombination
  publication-title: J. Virol.
  contributor:
    fullname: Lau
– volume: 367
  start-page: 1260
  year: 2020
  end-page: 1263
  ident: b0030
  article-title: Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation
  publication-title: Science
  contributor:
    fullname: Wrapp
– volume: 8
  start-page: 109
  year: 2019
  ident: b0015
  article-title: Evaluation of the impact of single-nucleotide polymorphisms on treatment response, survival and toxicity with cytarabine and anthracyclines in patients with acute myeloid leukaemia: a systematic review protocol
  publication-title: Syst. Rev.
  contributor:
    fullname: Puty
– volume: 395
  start-page: 497
  year: 2020
  end-page: 506
  ident: b0010
  article-title: Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China
  publication-title: Lancet
  contributor:
    fullname: Huang
– volume: 8
  start-page: 109
  issue: 1
  year: 2019
  ident: 10.1016/j.gene.2020.144792_b0015
  article-title: Evaluation of the impact of single-nucleotide polymorphisms on treatment response, survival and toxicity with cytarabine and anthracyclines in patients with acute myeloid leukaemia: a systematic review protocol
  publication-title: Syst. Rev.
  doi: 10.1186/s13643-019-1011-y
  contributor:
    fullname: Puty
– volume: 84
  start-page: 9733
  issue: 19
  year: 2010
  ident: 10.1016/j.gene.2020.144792_b0070
  article-title: Viral mutation rates
  publication-title: J. Virol.
  doi: 10.1128/JVI.00694-10
  contributor:
    fullname: Sanjuan
– volume: 395
  start-page: 497
  issue: 10223
  year: 2020
  ident: 10.1016/j.gene.2020.144792_b0010
  article-title: Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China
  publication-title: Lancet
  doi: 10.1016/S0140-6736(20)30183-5
  contributor:
    fullname: Huang
– volume: 89
  start-page: 10532
  issue: 20
  year: 2015
  ident: 10.1016/j.gene.2020.144792_b0055
  article-title: Severe acute respiratory syndrome (SARS) coronavirus ORF8 protein is acquired from SARS-related coronavirus from greater horseshoe bats through recombination
  publication-title: J. Virol.
  doi: 10.1128/JVI.01048-15
  contributor:
    fullname: Lau
– volume: 9
  start-page: 221
  issue: 1
  year: 2020
  ident: 10.1016/j.gene.2020.144792_b0050
  article-title: Genomic characterization of the 2019 novel human-pathogenic coronavirus isolated from a patient with atypical pneumonia after visiting Wuhan
  publication-title: Emerg. Microbes Infect.
  doi: 10.1080/22221751.2020.1719902
  contributor:
    fullname: Chan
– volume: 9
  start-page: 601
  issue: 1
  year: 2020
  ident: 10.1016/j.gene.2020.144792_b0025
  article-title: Emerging WuHan (COVID-19) coronavirus: glycan shield and structure prediction of spike glycoprotein and its interaction with human CD26
  publication-title: Emerg. Microbes Infect.
  doi: 10.1080/22221751.2020.1739565
  contributor:
    fullname: Vankadari
– volume: 347
  start-page: 273
  issue: 2
  year: 2005
  ident: 10.1016/j.gene.2020.144792_b0060
  article-title: High mutation rates, bottlenecks, and robustness of RNA viral quasispecies
  publication-title: Gene
  doi: 10.1016/j.gene.2004.12.033
  contributor:
    fullname: Manrubia
– year: 2020
  ident: 10.1016/j.gene.2020.144792_b0005
  article-title: Estimates of the severity of coronavirus disease 2019: a model-based analysis
  publication-title: Lancet Infect. Dis.
  doi: 10.1016/S1473-3099(20)30243-7
  contributor:
    fullname: Verity
– volume: 92
  start-page: 1031
  issue: 14
  year: 2018
  ident: 10.1016/j.gene.2020.144792_b0065
  article-title: Complexities of viral mutation rates
  publication-title: J. Virol.
  doi: 10.1128/JVI.01031-17
  contributor:
    fullname: Peck
– volume: 82
  start-page: 4471
  issue: 9
  year: 2008
  ident: 10.1016/j.gene.2020.144792_b0035
  article-title: Severe acute respiratory syndrome coronavirus nsp1 suppresses host gene expression, including that of type I interferon, in infected cells
  publication-title: J. Virol.
  doi: 10.1128/JVI.02472-07
  contributor:
    fullname: Narayanan
– volume: 26
  start-page: 450
  year: 2020
  ident: 10.1016/j.gene.2020.144792_b0020
  article-title: The proximal origin of SARS-CoV-2
  publication-title: Nat. Med.
  doi: 10.1038/s41591-020-0820-9
  contributor:
    fullname: Andersen
– volume: 16
  start-page: 94
  issue: 9
  year: 2020
  ident: 10.1016/j.gene.2020.144792_b0040
  article-title: Systemic expression of a viral RdRP protects against retrovirus infection and disease
  publication-title: J. Virol.
  contributor:
    fullname: Miller
– volume: 176
  year: 2020
  ident: 10.1016/j.gene.2020.144792_b0045
  article-title: The spike glycoprotein of the new coronavirus 2019-nCoV contains a furin-like cleavage site absent in CoV of the same clade
  publication-title: Antiviral Res.
  doi: 10.1016/j.antiviral.2020.104742
  contributor:
    fullname: Coutard
– volume: 367
  start-page: 1260
  issue: 6483
  year: 2020
  ident: 10.1016/j.gene.2020.144792_b0030
  article-title: Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation
  publication-title: Science
  doi: 10.1126/science.abb2507
  contributor:
    fullname: Wrapp
SSID ssj0000552
Score 2.532516
Snippet •Mutation studies hits cause for the superior infectious rate of SARS-CoV-2.•SARS-CoV-2 is evolving rapidly with number of mutations and SNPs.•Mutations were...
The morbidity of SARS-CoV-2 (COVID-19) is reaching 3 Million landmark causing and a serious public health concern globally and it is enigmatic how several...
• Mutation studies hits cause for the superior infectious rate of SARS-CoV-2. • SARS-CoV-2 is evolving rapidly with number of mutations and SNPs. • Mutations...
SourceID pubmedcentral
proquest
crossref
pubmed
elsevier
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 144792
SubjectTerms Americas - epidemiology
Asia - epidemiology
Betacoronavirus - genetics
Coronavirus
Coronavirus Infections - epidemiology
Coronavirus Infections - virology
COVID-19
Drug Resistance, Viral
Europe - epidemiology
Evolution
Genome
Genome, Viral
Humans
Pandemics
Phylogeny
Pneumonia, Viral - epidemiology
Pneumonia, Viral - virology
Point Mutation
Polymorphism, Single Nucleotide
SARS-CoV-2
Sequence
Spike Glycoprotein, Coronavirus - genetics
Viral Proteins - classification
Viral Proteins - genetics
Title Overwhelming mutations or SNPs of SARS-CoV-2: A point of caution
URI https://dx.doi.org/10.1016/j.gene.2020.144792
https://www.ncbi.nlm.nih.gov/pubmed/32445924
https://search.proquest.com/docview/2406308345
https://pubmed.ncbi.nlm.nih.gov/PMC7239005
Volume 752
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NT9swFH_iQ0jbATFgrAyQkRCXKTT1R9JwIlRDBURBFBA3y3EcUUSTCtoDF_72PccJUKbtQA5J7MSS9b78s_3eM8CO0lb9EuppgTeuw8yLdGK8KNUsC7Thujx57qwXdK_5ya24nYFOHQtj3Sor2-9semmtq5pmRc3maDBo9n1moyQRobis4WwW5nE4oija8_Hxabf3ZpCFcJsJdsKEDarYGefmhWyy2TKpb7c5w4j-a3z6G39-dKN8Ny4dLcFiBShJ7Pr8DWZMvgwrcY6T6eEz2SWli2e5dr4MC4f129d3eQhX4ODcukffmYchFslw4rbnn0jxSPq9C3xmpB9f9r1OcePRfRKTUTHIx7Zaq1JwV-H66PdVp-tVRyt4mgsx9lSAupj5iYnSwKgspGmiMxvUyjO_1VaMR22ulUE4h1MWFaUIk5CNqoXNENDg9R3m8iI3P4AwtBKBUKjLBtFNELUNExr5zRRLA0pbDfhVE1SOXAYNWbuW3UtLfmnJLx35GyBqmsspOZBo4v_bbrtmkEQFsbseKjfF5ElayMIQaHLRgDXHsNd-IJrkAmegDQinWPn6g02-Pf0lH9yVSbhDyiKUrPVP9vcnfLEluzpN_Q2YGz9OzCbCm3GyBbN7L62tSoj_AHq59uI
link.rule.ids 230,315,783,787,888,4510,24129,27937,27938,45598,45692
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwED-NTQh4QGPjo8A2I6G9oNDUH0nDE6XaVPZR0LqhvlmO42hFNKm29oEX_nbu4mSsTNvD8pAPx5asu_P5d77zGeC9sTT8Uh5YhTdp4zxIbOqCJLMij6yTtjp57ngYDc7kwViNV6Df7IWhsMpa93udXmnruqRdU7M9m0zao1DQLklEKD5ruHgAa5LSjaNQf_zzL84jVMq7Eshcwur1zhkf5IVMolyZPCQnZ5zw22anm-jz_yDKa7PS_jo8reEk6_keP4MVV2zAZq9AU3r6m-2yKsCzWjnfgIdfmrcn17IQbsLnbxQcfe5-TfGTTRfeOX_Jygs2Gn7HZ85GvZNR0C9_BPwT67FZOSnmVGxNJbbP4Wx_77Q_COqDFQKLFJoHJsKRmIepS7LImTzmWWpz2tIq87DTNUImXWmNQzCHBotJMgRJyETTwWYIZ_B6AatFWbhXwATqiEgZHMkOsU2UdJ1QFrktjMgizjst-NAQVM98_gzdBJb91ER-TeTXnvwtUA3N9ZIUaFTwd7Z71zBI4_Agn4cpXLm41ARYBMJMqVrw0jPsqh-IJaVC-7MF8RIrrypQ6u3lP8XkvErBHXORoGS9vmd_d-DR4PT4SB99HR6-gcf0h9apefgWVucXC7eFQGeebleC_BezEPe7
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Overwhelming+mutations+or+SNPs+of+SARS-CoV-2%3A+A+point+of+caution&rft.jtitle=Gene&rft.au=Vankadari%2C+Naveen&rft.date=2020-08-20&rft.eissn=1879-0038&rft.volume=752&rft.spage=144792&rft_id=info:doi/10.1016%2Fj.gene.2020.144792&rft_id=info%3Apmid%2F32445924&rft.externalDocID=32445924
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0378-1119&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0378-1119&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0378-1119&client=summon