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Pathophysiology
Last updated: 2021 Dec 8
Total hit(s): 13
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Original Article
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The loss of neutralising activity against the pseudovirus
B.1.351
was comparable to the loss of neutralising activity against the live
B.1.351
virus.
These diverse findings support previous studies that pseudovirus neutralisation does not always accurately replicate live viral neutralisation.
✍
33532778
(
bioRxiv
)
PMID
33532778
Date of Publishing
: 2021 Jan 26
Title
Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7
Author(s) name
Wang P, Nair MS et al.
Journal
bioRxiv
Impact factor
- n/a -
Citation count
: 1
Date of Entry
2021 Dec 8
×
NLM format
Wang P, Nair MS, Liu L, Iketani S, Luo Y, Guo Y, Wang M, Yu J, Zhang B, Kwong PD, Graham BS, Mascola JR, Chang JY, Yin MT, Sobieszczyk M, Kyratsous CA, Shapiro L, Sheng Z, Huang Y, Ho DD. Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7. bioRxiv. 2021 Feb 12:2021.01.25.428137. PMID:33532778
Eight convalescent patient samples showed a decrease of >2.5-fold in neutralizing activity against B.1.1.78 pseudovirus.
These diverse findings support previous studies that pseudovirus neutralisation does not always accurately replicate live viral neutralisation.
✍
33532778
(
bioRxiv
)
PMID
33532778
Date of Publishing
: 2021 Jan 26
Title
Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7
Author(s) name
Wang P, Nair MS et al.
Journal
bioRxiv
Impact factor
- n/a -
Citation count
: 1
Date of Entry
2021 Dec 8
×
NLM format
Wang P, Nair MS, Liu L, Iketani S, Luo Y, Guo Y, Wang M, Yu J, Zhang B, Kwong PD, Graham BS, Mascola JR, Chang JY, Yin MT, Sobieszczyk M, Kyratsous CA, Shapiro L, Sheng Z, Huang Y, Ho DD. Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7. bioRxiv. 2021 Feb 12:2021.01.25.428137. PMID:33532778
The post-vaccination sera had significantly stronger neutralizing activity than the pre-vaccination sera. In thepre-vaccination sera, however, the 50% neutralisation titres (NT50) for the wild type Wuhan-Hu-1 strain were higher than that of the SARS-CoV-2variants
(Alpha,
Beta,
Delta)
.
The results of the two assays, RVPN and MSD ACE2 inhibition for VOCs were substantially consistent, with r=0.8587, according to a Spearman correlation analysis.
✍
Pre-print
(
medRXiv
)
Title
Vaccination of COVID-19 Convalescent Plasma Donors Increases Binding and Neutralizing Antibodies Against SARS-CoV-2 Variants
Impact factor
N/A
Date of Entry
2021 Dec 8
The viral infectivity of the
Lambda
variant was found to be considerably higher than the parental strain
(D614G)
. However, the infectivity of the Lambda
S
derivative
(Lambda+
deletion
mutation) had no significant difference to that of the Lambda
S
variant, indicating that the 7-amino-acid
deletion
in the NTD does not affect viral infection.
The substitution in the L452 of SARS-CoV-2 S protein is a common feature in the Lambda, Delta and Epsilon variants (L452Q mutation in Lambda variant and L452R mutation in the Delta and Epsilon variants). The study has also demonstrated that the L452Q mutation increases viral infectivity. Therefore, this strongly suppports the hypothesis that the relatively higher infectivity of the Lambda, Delta and Epsilon variants is due to the L452Q/R mutation.
✍
Pre-print
(
bioRXiv
)
Title
SARS-CoV-2 Lambda variant exhibits higher infectivity and immune resistance
Impact factor
N/A
Date of Entry
2021 Dec 15
The
mutation
P681R greatly improved furin's efficiency to cleave the spike peptide, indicating that the arginine
substitution
is responsible for the B.1.617 lineage spike protein's enhanced cleavage. This might play a role in increased transmissibility and pathogenicity.
This study speculates that the higher transmissibility of these SARS-CoV-2 variants is due to increased S1/S2 cleavage found in B.1.617 and B.1.1.7 lineages. Therefore, they must be closely monitored for any early signs of faster transmission or increased pathogenesis.
✍
Pre-print
(
bioRXiv
)
Title
The SARS-CoV-2 variants associated with infections in India, B.1.617, show enhanced spike cleavage by furin
Impact factor
N/A
Date of Entry
2021 Nov 2
The D614G
mutation
was introduced into Spike-pseudotyped lentivirus and complete SARS-CoV-2 virus via site-directed mutagenesis. The
D614G
mutant was shown to be up to 8-fold more effective at infecting cells than wild-type. The Spike variants did not differ significantly in terms of
ACE2
receptor
binding,
but the G614 variant is more resistant to proteolytic cleavage in vitro and in human cells than the D614. This could have an impact on the efficacy of immunizations based on spikes.
The G614 variant was found to be ~2.5 fold more resistant to cleavage in the host cell than the D614 variant in cells expressing Spike by transient transfection. Virions with the G614 variant were seen to have less Spike cleavage compared to the D614 variant. No significant difference between Spike D614 and Spike G614 incorporation into pseudotyped lentiviral particles was observed.
✍
32587969 (33570490)
(
bioRxiv
)
PMID
32587969 (33570490)
Date of Publishing
: 2020 Jun 15
Title
The Spike D614G mutation increases SARS-CoV-2 infection of multiple human cell types
Author(s) name
Daniloski Z, Guo X, Sanjana NE.
Journal
bioRxiv
Impact factor
N/A
Citation count
: 2
Date of Entry
2021 Sep 13
×
NLM format
Daniloski Z, Guo X, Sanjana NE. The Spike D614G mutation increases SARS-CoV-2 infection of multiple human cell types. bioRxiv. . PMID:32587969 (33570490)
The in vitro studies on primate endothelial kidney cells (BGM) and human
lung
adenocarcinoma cells (Calu-3) indicated comparable replication kinetics with the wild-type but a significant difference was observed between cell lines for each strain.
After infection with WT and ORF6 variants, Interferon-stimulated genes were upregulated, the latter inducing overexpression of 9 genes coding for inflammatory cytokines in the NF-kB pathway, including CCL2/MCP1, PTX3, and TNF, for which high plasma levels is associated with severe COVID-19.
✍
33399033
(
Emerg Microbes Infect
)
PMID
33399033
Date of Publishing
: 2021 Jan 5
Title
Characterization of SARS-CoV-2 ORF6 deletion variants detected in a nosocomial cluster 1 during routine genomic surveillance, Lyon, France
Author(s) name
Quéromès G, Destras G et al.
Journal
Emerg Microbes Infect
Impact factor
5.84
Citation count
: 20
Date of Entry
2021 Aug 6
×
NLM format
Quéromès G, Destras G, Bal A, Regue H, Burfin G, Brun S, Fanget R, Morfin F, Valette M, Trouillet-Assant S, Lina B, Frobert E, Josset L. Characterization of SARS-CoV-2 ORF6 deletion variants detected in a nosocomial cluster 1 during routine genomic surveillance, Lyon, France. Emerg Microbes Infect. 2021 Dec;10(1):167-177. PMID:33399033
Growth curves for GLA1 (N439/D614G) or GLA2 (N439K/D614G) virus isolates were assessed in Vero E6 cells with
ACE2
and
TMPRSS2
overexpression. No significant growth amongst the isolates were observed indicating that N439K
mutation
played no role in viral growth.
✍
33621484
(
Cell
)
PMID
33621484
Date of Publishing
: 2021 Jan 28
Title
Circulating SARS-CoV-2 spike N439K variants maintain fitness while evading antibody-mediated immunity
Author(s) name
Thomson EC, Rosen LE et al.
Journal
Cell
Impact factor
27.35
Citation count
: 259
Date of Entry
2021 Aug 6
×
NLM format
Thomson EC, Rosen LE, Shepherd JG, Spreafico R, da Silva Filipe A, Wojcechowskyj JA, Davis C, Piccoli L, Pascall DJ, Dillen J, Lytras S, Czudnochowski N, Shah R, Meury M, Jesudason N, De Marco A, Li K, Bassi J, O'Toole A, Pinto D, Colquhoun RM, Culap K, Jackson B, Zatta F, Rambaut A, Jaconi S, Sreenu VB, Nix J, Zhang I, Jarrett RF, Glass WG, Beltramello M, Nomikou K, Pizzuto M, Tong L, Cameroni E, Croll TI, Johnson N, Di Iulio J, Wickenhagen A, Ceschi A, Harbison AM, Mair D, Ferrari P, Smollett K, Sallusto F, Carmichael S, Garzoni C, Nichols J, Galli M, Hughes J, Riva A, Ho A, Schiuma M, Semple MG, Openshaw PJM, Fadda E, Baillie JK, Chodera JD; ISARIC4C Investigators; COVID-19 Genomics UK (COG-UK) Consortium, Rihn SJ, Lycett SJ, Virgin HW, Telenti A, Corti D, Robertson DL, Snell G. Circulating SARS-CoV-2 spike N439K variants maintain fitness while evading antibody-mediated immunity. Cell. 2021 Mar 4;184(5):1171-1187.e20. PMID:33621484
The L452R
mutation
increases viral replication in VeroE6/TMPRSS2 cells.
✍
Pre-print
(
bioRXiv
)
Title
An emerging SARS-CoV-2 mutant evading cellular immunity and increasing viral infectivity
Impact factor
N/A
Date of Entry
2021 Aug 6
Pseudovirus with L452R
mutation
showed higher infectivity in 293T cells (6.7- to 22.5-fold increase) and HAO cell line (5.8- to 14.7-fold increase) than
D614G-
Pseudovirus but slightly lower infectivity than
N501Y-
Pseudovirus.
N501Y mutation was known to increase pseudovirus entry owing to its higher infectivity levels compared to D614G mutation.
✍
33991487
(
Cell
)
PMID
33991487
Date of Publishing
: 2021 Jun 24
Title
Transmission, infectivity, and neutralization of a spike L452R SARS-CoV-2 variant
Author(s) name
Deng X, Garcia-Knight MA et al.
Journal
Cell
Impact factor
27.35
Citation count
: 162
Date of Entry
2021 Jul 2
×
NLM format
Deng X, Garcia-Knight MA, Khalid MM, Servellita V, Wang C, Morris MK, Sotomayor-González A, Glasner DR, Reyes KR, Gliwa AS, Reddy NP, Sanchez San Martin C, Federman S, Cheng J, Balcerek J, Taylor J, Streithorst JA, Miller S, Sreekumar B, Chen PY, Schulze-Gahmen U, Taha TY, Hayashi JM, Simoneau CR, Kumar GR, McMahon S, Lidsky PV, Xiao Y, Hemarajata P, Green NM, Espinosa A, Kath C, Haw M, Bell J, Hacker JK, Hanson C, Wadford DA, Anaya C, Ferguson D, Frankino PA, Shivram H, Lareau LF, Wyman SK, Ott M, Andino R, Chiu CY. Transmission, infectivity, and neutralization of a spike L452R SARS-CoV-2 variant. Cell. 2021 Jun 24;184(13):3426-3437.e8. PMID:33991487
A comparative cohort study was conducted on COVID 19 samples from two different variants Daxing
B.1.1.7
and Shunyi B.1.470, to determine the clinical freatures of
B.1.1.7
variant. 7 clinical features
-fever,
C-reactive protein, d-dimmer,
serum
Amyloid A, creative kinase,
CD4+
T
lymphocyte
and ground glass opacity was more in the Daxing group (B.1.1.7) when compared to the Shunyi B.1.470 group
Limitations of this study are - 1. Small sample size of the two groups and 2. Clinical feature of B.1.1.7 variant was not compared with SARS-COV2 variant other than B.1.470.
✍
Pre-print
(
medRXiv
)
Date of Publishing
2021 May 08
Title
COVID-19 cases from the first local outbreak of SARS-CoV-2 B.1.1.7 variant in China presented more serious clinical features: a prospective, comparative cohort study
Impact factor
N/A
Date of Entry
2021 Jul 2
N440K variant of SARS CoV2, one of the prevalent strains found in
India
during the second wave of pandemic, produced 10 times and 1000 fold higher infectious viral titers than A2a (prevalent) and A3i (less prevalent) strains respectively. The results were obtained when Caco2 and Calu-3 cell cultures were infected with 0.1 MOI of the three variants and supernatant was collected after 24, 48 and 72 hours post-infection.
No correlation was found between the RNA content and infectivity of the strain.Owing to the fact that the variant with high reproducibility was least infectious, the importance of measuring infectious viral titres instead of RT-qPCR assays in comparative studies is highlighted. Sequencing of the samples will provide more insight in the mechanism of rapid spread of N440K variant.
✍
Pre-print
(
bioRXiv
)
Title
N440K variant of SARS-CoV-2 has Higher Infectious Fitness
Impact factor
N/A
Date of Entry
2021 Jul 2
A222V mutations in the spike region do not lead to very large increases in the spike-pseudotyped lentiviruses but show a 1.3-fold higher titer than the wild type. However, the 20E (EU1) variant does not gain any transmission advantage over the variant with the D614G
mutation.
Lentiviral particles pseudotyped with the D614G spike mutation showed very large titers, which seem to have increased the transmission fitness of the SARS-CoV-2 variant.
✍
Pre-print
(
medRXiv
)
Title
Emergence and spread of a SARS-CoV-2 variant through Europe in the summer of 2020
Impact factor
N/A
Date of Entry
2021 Jul 2