Evidence map›Paper›PMID 36851091›Full record

ArticleVaccines2023

Incipient Parallel Evolution of SARS-CoV-2 Deltacron Variant in South Brazil.

Fernando Hayashi Sant'Anna, Tiago Finger Andreis, Richard Steiner Salvato, Ana Paula Muterle Varela, Juliana Comerlato, Tatiana Schäffer Gregianini, Regina Bones Barcellos, Fernanda Marques de Souza Godinho, Paola Cristina Resende, Gabriel da Luz Wallau and 14 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

24 authors at 6 institutions in 2 countries.

Fernando Hayashi Sant'AnnaHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Tiago Finger AndreisHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Richard Steiner SalvatoCentro de Desenvolvimento Científico e Tecnológico, Centro Estadual de Vigilância em Saúde, Secretaria Estadual da Saúde do Rio Grande do Sul (CDCT/CEVS/SES-RS), Porto Alegre 90450-190, RS, Brazil.ORCID 0000-0002-5701-9437
Ana Paula Muterle VarelaHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Juliana ComerlatoHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Tatiana Schäffer GregianiniLaboratório Central de Saúde Pública, Centro Estadual de Vigilância em Saúde, Secretaria Estadual da Saúde do Rio Grande do Sul (LACEN/CEVS/SES-RS), Porto Alegre 90450-190, RS, Brazil.ORCID 0000-0002-9912-9060
Regina Bones BarcellosCentro de Desenvolvimento Científico e Tecnológico, Centro Estadual de Vigilância em Saúde, Secretaria Estadual da Saúde do Rio Grande do Sul (CDCT/CEVS/SES-RS), Porto Alegre 90450-190, RS, Brazil.
Fernanda Marques de Souza GodinhoCentro de Desenvolvimento Científico e Tecnológico, Centro Estadual de Vigilância em Saúde, Secretaria Estadual da Saúde do Rio Grande do Sul (CDCT/CEVS/SES-RS), Porto Alegre 90450-190, RS, Brazil.ORCID 0000-0002-2211-192X
Paola Cristina ResendeLaboratory of Respiratory Viruses and Measles, Oswaldo Cruz Institute (IOC), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro 21040-900, RJ, Brazil.
Gabriel da Luz WallauDepartamento de Entomologia e Núcleo de Bioinformática, Instituto Aggeu Magalhães, Fundação Oswaldo Cruz Pernambuco (FIOCRUZ-PE), Recife 50740-465, PE, Brazil.ORCID 0000-0002-1419-5713
Thaís Regina Y CastroDepartamento de Análises Clínicas, Universidade Federal de Santa Maria, Santa Maria 97105-900, RS, Brazil.ORCID 0000-0003-4553-4455
Bruna Campestrini CasarinDepartamento de Análises Clínicas, Universidade Federal de Santa Maria, Santa Maria 97105-900, RS, Brazil.ORCID 0000-0003-0414-8240
Andressa de Almeida VieiraDepartamento de Análises Clínicas, Universidade Federal de Santa Maria, Santa Maria 97105-900, RS, Brazil.ORCID 0000-0003-1322-9288
Alexandre Vargas SchwarzboldDepartamento de Análises Clínicas, Universidade Federal de Santa Maria, Santa Maria 97105-900, RS, Brazil.ORCID 0000-0002-5535-6288
Priscila de Arruda TrindadeDepartamento de Análises Clínicas, Universidade Federal de Santa Maria, Santa Maria 97105-900, RS, Brazil.ORCID 0000-0002-3454-9654
Gabriela Luchiari Tumioto GianniniHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Luana FreeseHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Giovana BristotHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Carolina Serpa BrasilHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Bruna de Oliveira RochaHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Paloma Bortolini MartinsHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Francine Hehn de OliveiraHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.
Cock van OosterhoutSchool of Environmental Sciences, University of East Anglia, Norwich Research Park, Norwich NR4 7TJ, UK.ORCID 0000-0002-5653-738X
Eliana WendlandHospital Moinhos de Vento, Porto Alegre 90035-000, RS, Brazil.ORCID 0000-0001-6356-6413
Hospital Moinhos de Vento · BRUniversidade Federal de Santa Maria · BRFundação Estadual de Produção e Pesquisa em Saúde · BRFundação Oswaldo Cruz · BRUniversidade Federal de Ciências da Saúde de Porto Alegre · BRUniversity of East Anglia · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the coexistence of multiple lineages and increased international travel, recombination and gene flow are likely to become increasingly important in the adaptive evolution of SARS-CoV-2. These processes could result in genetic introgression and the incipient parallel evolution of multiple recombinant lineages. However, identifying recombinant lineages is challenging, and the true extent of recombinant evolution in SARS-CoV-2 may be underestimated. This study describes the first SARS-CoV-2 Deltacron recombinant case identified in Brazil. We demonstrate that the recombination breakpoint is at the beginning of the Spike gene. The 5' genome portion (circa 22 kb) resembles the AY.101 (Delta), and the 3' genome portion (circa 8 kb nucleotides) is most similar to the BA.1.1 (Omicron). Furthermore, evolutionary genomic analyses indicate that the new strain emerged after a single recombination event between lineages of diverse geographical locations in December 2021 in South Brazil. This Deltacron, AYBA-RS, is one of the dozens of recombinants described in 2022. The submission of only four sequences in the GISAID database suggests that this lineage had a minor epidemiological impact. However, the recent emergence of this and other Deltacron recombinant lineages (XD, XF, and XS) suggests that gene flow and recombination may play an increasingly important role in the COVID-19 pandemic. We explain the evolutionary and population genetic theory that supports this assertion, concluding that this stresses the need for continued genomic surveillance. This monitoring is vital for countries where multiple variants are present, as well as for countries that receive significant inbound international travel.

Indexed as

adaptive landscapeAYBA-RSBrazilCOVID-19Deltacrongene flowgenetic introgressionrecombinantrecombinationSARS-CoV-2 genomessevere acute respiratory syndrome coronavirus 2

Identifiers

PMID36851091
PMCPMC9961971
OpenAlexW4317426350

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.