Evidence map›Paper›PMID 36298650›Full record

ArticleViruses2022

Origin of New Lineages by Recombination and Mutation in Avian Infectious Bronchitis Virus from South America.

Ana Marandino, Ariel Vagnozzi, Gonzalo Tomás, Claudia Techera, Rocío Gerez, Martín Hernández, Joaquín Williman, Mauricio Realpe, Gonzalo Greif, Yanina Panzera and 1 more

Abstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Avian infectious bronchitis virus (AIBV) review by continent.Frontiers in cellular and infection microbiology · 2024
    Review
  7. Article
  8. Review
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

11 authors.

Ana MarandinoSección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo 11400, Uruguay.
Ariel VagnozziInstituto de Virología, CICVyA, INTA-Castelar, Castelar 1712, Buenos Aires, Argentina.
Gonzalo TomásSección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo 11400, Uruguay.
Claudia TecheraSección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo 11400, Uruguay.
Rocío GerezInstituto de Virología, CICVyA, INTA-Castelar, Castelar 1712, Buenos Aires, Argentina.
Martín HernándezSección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo 11400, Uruguay.
Joaquín WillimanSección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo 11400, Uruguay.
Mauricio RealpeCentro Universitario de Ciencias Biológicas y Agropecuarias, Universidad de Guadalajara, Jalisco 44214, Mexico.ORCID 0000-0001-9271-3865
Gonzalo GreifUnidad de Biología Molecular, Instituto Pasteur de Montevideo, Montevideo 11400, Uruguay.ORCID 0000-0002-6769-3249
Yanina PanzeraSección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo 11400, Uruguay.
Ruben PérezSección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo 11400, Uruguay.ORCID 0000-0003-4961-4743

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gammacoronavirus avian infectious bronchitis virus (IBV) is a highly contagious respiratory pathogen of primary economic importance to the global poultry industry. Two IBV lineages (GI-11 and GI-16) have been widely circulating for decades in South America. GI-11 is endemic to South America, and the GI-16 is globally distributed. We obtained full-length IBV genomes from Argentine and Uruguayan farms using Illumina sequencing. Genomes of the GI-11 and GI-16 lineages from Argentina and Uruguay differ in part of the spike coding region. The remaining genome regions are similar to the Chinese and Italian strains of the GI-16 lineage that emerged in Asia or Europe in the 1970s. Our findings support that the indigenous GI-11 strains recombine extensively with the invasive GI-16 strains. During the recombination process, GI-11 acquired most of the sequences of the GI-16, retaining the original S1 sequence. GI-11 strains with recombinant genomes are circulating forms that underwent further local evolution. The current IBV scenario in South America includes the GI-16 lineage, recombinant GI-11 strains sharing high similarity with GI-16 outside S1, and Brazilian GI-11 strains with a divergent genomic background. There is also sporadic recombinant in the GI-11 and GI-16 lineages among vaccine and field strains. Our findings exemplified the ability of IBV to generate emergent lineage by using the S gene in different genomic backgrounds. This unique example of recombinational microevolution underscores the genomic plasticity of IBV in South America.

Indexed as

Coronavirus InfectionsInfectious bronchitis virusPoultry DiseasesAnimalsBrazilChickensMutationPhylogenyRecombination, Geneticgenomic evolutioninfectious bronchitis viruslineagerecombinationSouth America

Identifiers

PMID36298650
PMCPMC9609748

What OpenQuestion holds

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LicenceCC BY
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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.