Sensitivity to Neutralizing Antibodies and Resistance to Type I Interferons in SARS-CoV-2 R.1 Lineage Variants, Canada.
COVID-19
Canada
N501Y spike
SARS-CoV-2
VoC
VuM
coronavirus disease
neutralizing antibodies
respiratory infections
severe acute respiratory syndrome coronavirus 2
type I interferons
variant under monitoring
variants of concern
viruses
zoonoses
Journal
Emerging infectious diseases
ISSN: 1080-6059
Titre abrégé: Emerg Infect Dis
Pays: United States
ID NLM: 9508155
Informations de publication
Date de publication:
07 2023
07 2023
Historique:
medline:
23
6
2023
pubmed:
13
6
2023
entrez:
12
6
2023
Statut:
ppublish
Résumé
Isolating and characterizing emerging SARS-CoV-2 variants is key to understanding virus pathogenesis. In this study, we isolated samples of the SARS-CoV-2 R.1 lineage, categorized as a variant under monitoring by the World Health Organization, and evaluated their sensitivity to neutralizing antibodies and type I interferons. We used convalescent serum samples from persons in Canada infected either with ancestral virus (wave 1) or the B.1.1.7 (Alpha) variant of concern (wave 3) for testing neutralization sensitivity. The R.1 isolates were potently neutralized by both the wave 1 and wave 3 convalescent serum samples, unlike the B.1.351 (Beta) variant of concern. Of note, the R.1 variant was significantly more resistant to type I interferons (IFN-α/β) than was the ancestral isolate. Our study demonstrates that the R.1 variant retained sensitivity to neutralizing antibodies but evolved resistance to type I interferons. This critical driving force will influence the trajectory of the pandemic.
Identifiants
pubmed: 37308158
doi: 10.3201/eid2907.230198
pmc: PMC10310370
doi:
Substances chimiques
Interferon Type I
0
Antibodies, Neutralizing
0
Antibodies, Viral
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1386-1396Subventions
Organisme : CIHR
ID : 439999
Pays : Canada
Références
iScience. 2021 May 21;24(5):102477
pubmed: 33937724
PLoS Pathog. 2020 Jul 29;16(7):e1008737
pubmed: 32726355
Med. 2022 Jun 10;3(6):422-432.e3
pubmed: 35437520
Emerg Infect Dis. 2020 Sep;26(9):2054-2063
pubmed: 32558639
Proc Natl Acad Sci U S A. 2022 Aug 9;119(32):e2203760119
pubmed: 35867811
Nature. 2021 May;593(7857):142-146
pubmed: 33780970
Nature. 2022 Feb;602(7896):294-299
pubmed: 34818667
Nat Rev Microbiol. 2021 Jul;19(7):409-424
pubmed: 34075212
Nature. 2021 Apr;592(7854):438-443
pubmed: 33690265
Nat Rev Microbiol. 2022 May;20(5):270-284
pubmed: 35354968
China CDC Wkly. 2021 Dec 3;3(49):1049-1051
pubmed: 34934514
Science. 2020 Oct 23;370(6515):
pubmed: 32972995
J Mol Biol. 2021 Jul 23;433(15):167058
pubmed: 34023401
Nat Rev Genet. 2021 Dec;22(12):757-773
pubmed: 34535792
Cytokine. 2013 Sep;63(3):219-24
pubmed: 23800788
Science. 2020 Sep 25;369(6511):1603-1607
pubmed: 32732280
Infect Control Hosp Epidemiol. 2021 Nov;42(11):1340-1344
pubmed: 33436122
Nat Med. 2021 May;27(5):917-924
pubmed: 33772244
J Clin Microbiol. 2021 Sep 20;59(10):e0052721
pubmed: 34288726
JAMA. 2021 Sep 28;326(12):1145-1146
pubmed: 34424275
FEBS Lett. 2021 May;595(10):1454-1461
pubmed: 33728680
Glob Chall. 2017 Jan 10;1(1):33-46
pubmed: 31565258
Nat Immunol. 2022 Feb;23(2):165-176
pubmed: 35105981
Cell Host Microbe. 2021 Jul 14;29(7):1052-1062
pubmed: 34022154
ACS Chem Biol. 2021 Apr 16;16(4):642-650
pubmed: 33787221
mBio. 2022 Oct 26;13(5):e0214122
pubmed: 35997285
Nat Rev Microbiol. 2023 Mar;21(3):162-177
pubmed: 36653446
J Virol. 2022 Jan 12;96(1):e0111021
pubmed: 34668774
Nature. 2021 May;593(7857):130-135
pubmed: 33684923
Sci Rep. 2022 Feb 8;12(1):2114
pubmed: 35136161
Lancet Microbe. 2020 May;1(1):e14-e23
pubmed: 32835326
J Infect Dis. 2022 Mar 2;225(5):768-776
pubmed: 34850051
Cell Host Microbe. 2021 Apr 14;29(4):508-515
pubmed: 33789086