Evidence map›Paper›PMID 35219552›Full record

ArticleDiagnostic microbiology and infectious disease2022

Y380Q novel mutation in receptor-binding domain of SARS-CoV-2 spike protein together with C379W interfere in the neutralizing antibodies interaction.

Ivaine Tais Sauthier Sartor, Fernanda Hammes Varela, Mariana Rost Meireles, Luciane Beatriz Kern, Thaís Raupp Azevedo, Gabriela Luchiari Tumioto Giannini, Mariana Soares da Silva, Meriane Demoliner, Juliana Schons Gularte, Paula Rodrigues de Almeida and 13 more

Open access · greenAbstract read
In one paragraph

Article in Diagnostic microbiology and infectious disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Impact of rhinovirus on hospitalization during the COVID-19 pandemic: A prospective cohort study.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2022
    Article
  3. Review
  4. Chimera X Interface to Enhance Understanding in Biochemistry and Immunology.Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 5 institutions in 1 country.

Ivaine Tais Sauthier SartorSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil. Electronic address: ivaine.sartor@hmv.org.br.
Fernanda Hammes VarelaSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil; School of Medicine, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil. Electronic address: fernanda.varela@hmv.org.br.
Mariana Rost MeirelesGenetics Department, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Luciane Beatriz KernSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil.
Thaís Raupp AzevedoSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil.
Gabriela Luchiari Tumioto GianniniLaboratory of Genetics and Molecular Biology, Hospital Moinhos de Vento, Porto Alegre, Brazil.
Mariana Soares da SilvaLaboratory of Molecular Microbiology, Universidade FEEVALE, Novo Hamburgo, Brazil.
Meriane DemolinerLaboratory of Molecular Microbiology, Universidade FEEVALE, Novo Hamburgo, Brazil.
Juliana Schons GularteLaboratory of Molecular Microbiology, Universidade FEEVALE, Novo Hamburgo, Brazil.
Paula Rodrigues de AlmeidaLaboratory of Molecular Microbiology, Universidade FEEVALE, Novo Hamburgo, Brazil.
Juliane Deise FleckLaboratory of Molecular Microbiology, Universidade FEEVALE, Novo Hamburgo, Brazil.
Gabriela Oliveira ZavagliaSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil.
Ingrid Rodrigues FernandesSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil.
Caroline Nespolo de DavidSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil.
Amanda Paz SantosSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil.
Walquiria Aparecida Ferreira de AlmeidaGeneral Coordination, National Immunization Program, Brazilian Ministry of Health, Brasilia, Brazil.
Victor Bertollo Gomes PortoGeneral Coordination, National Immunization Program, Brazilian Ministry of Health, Brasilia, Brazil.
Marcelo Comerlato ScottaSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil; School of Medicine, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil.
Gustavo Fioravanti VieiraGenetics Department, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil; Post-Graduation Program in Health and Human Development, Universidade La Salle, Canoas, Brazil.
Fernando Rosado SpilkiLaboratory of Molecular Microbiology, Universidade FEEVALE, Novo Hamburgo, Brazil.
Renato T SteinSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil; School of Medicine, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil.
Márcia Polese-BonattoSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil. Electronic address: marcia.bonatto@hmv.org.br.
COVIDa study groupSocial Responsibility, Hospital Moinhos de Vento, Porto Alegre, Brazil.
Hospital Moinhos de Vento · BRUniversidade Feevale · BRPontifícia Universidade Católica do Rio Grande do Sul · BRMinistério da Saúde · BRUniversidade Federal do Rio Grande do Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to describe the SARS-CoV-2 lineages circulating early pandemic among samples with S gene dropout and characterize the receptor-binding domain (RBD) of viral spike protein. Adults and children older than 2 months with signs and symptoms of COVID-19 were prospectively enrolled from May to October in Porto Alegre, Brazil. All participants performed RT-PCR assay, and samples with S gene dropout and cycle threshold < 30 were submitted to high-throughput sequencing (HTS). 484 out of 1,557 participants tested positive for SARS-CoV-2. The S gene dropout was detected in 7.4% (36/484) and a peak was observed in August. The B.1.1.28, B.1.91 and B.1.1.33 lineages were circulating in early pandemic. The RBD novel mutation (Y380Q) was found in one sample occurring simultaneously with C379W and V395A, and the B.1.91 lineage in the spike protein. The Y380Q and C379W may interfere with the binding of neutralizing antibodies (CR3022, EY6A, H014, S304).

Indexed as

COVID-19Spike Glycoprotein, CoronavirusAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralChildHumansInfantMutationProtein BindingSARS-CoV-2Antibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralCR3022Spike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19Novel mutationRBDSARS-CoV-2Variants

Identifiers

PMID35219552
PMCPMC8761118
OpenAlexW4221089743

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.