<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Marandino A</submitter><funding>Comisión Sectorial de Investigación Científica</funding><funding>Programa de Desarrollo de las Ciencias Básicas</funding><funding>Fondo Conjunto de Cooperación México-Uruguay</funding><pagination>2095</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9609748</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(10)</volume><pubmed_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.</pubmed_abstract><journal>Viruses</journal><pubmed_title>Origin of New Lineages by Recombination and Mutation in Avian Infectious Bronchitis Virus from South America.</pubmed_title><pmcid>PMC9609748</pmcid><funding_grant_id>FMV_3_2018_1_148439</funding_grant_id><pubmed_authors>Techera C</pubmed_authors><pubmed_authors>Gerez R</pubmed_authors><pubmed_authors>Realpe M</pubmed_authors><pubmed_authors>Marandino A</pubmed_authors><pubmed_authors>Panzera Y</pubmed_authors><pubmed_authors>Perez R</pubmed_authors><pubmed_authors>Vagnozzi A</pubmed_authors><pubmed_authors>Tomas G</pubmed_authors><pubmed_authors>Hernandez M</pubmed_authors><pubmed_authors>Williman J</pubmed_authors><pubmed_authors>Greif G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Origin of New Lineages by Recombination and Mutation in Avian Infectious Bronchitis Virus from South America.</name><description>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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-04-08T11:41:12.121Z</modification><creation>2025-04-06T21:03:44.996Z</creation></dates><accession>S-EPMC9609748</accession><cross_references><pubmed>36298650</pubmed><doi>10.3390/v14102095</doi></cross_references></HashMap>