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dc.contributor.authorShin, Gi Yoon-
dc.contributor.authorDe Armas, Stefanie-
dc.contributor.authorGalván, Guillermo A.-
dc.contributor.authorSiri, María I.-
dc.contributor.authorRojas, Mariah-
dc.contributor.authorVinatzer, Boris A.-
dc.contributor.authorAsselin, Jo Ann E.-
dc.contributor.authorStodghill, Paul-
dc.contributor.authorZhao, Mei-
dc.contributor.authorDutta, Bhabesh-
dc.contributor.authorTambong, James-
dc.contributor.authorKvitko, Brian H.-
dc.date.accessioned2026-07-24T15:00:14Z-
dc.date.available2026-07-24T15:00:14Z-
dc.date.issued2026-
dc.identifier.citationShin, G., De Armas, S., Galván, G. y otros. "Comparative genomics of Pantoea allii lineages and distribution of ecologically relevant traits". Microbial Genomics [en línea], v. 12, n°2, 2026. -- e001624. 17 p.es
dc.identifier.urihttps://hdl.handle.net/20.500.12008/56217-
dc.description.abstractPantoea allii, one of four Pantoea species known to cause onion centre rot, is infrequently isolated from onion compared to its closely related onion-pathogenic species in the same genus. To better understand the genomic diversity and genetic determinants of pathogenicity in this species, we analysed a collection of 38 P. allii strains isolated from 2 primary ecological niches, plants and rainwater, across North and South American and African continents using comparative genomics and phylogenetic approaches. Core-genome phylogeny, average nucleotide identity and gene presence–absence analyses revealed three genetically distinct lineages. All strains harboured conserved biosynthetic gene clusters (BGCs) for quorum sensing, carotenoid production, siderophores and thiopeptides. In contrast, two phosphonate BGCs, key determinants of onion pathogenicity, exhibited lineage-specific distributions. Onion-associated strains from lineages 1 and 2 carried the Halophos BGC responsible for onion tissue necrosis and also encoded the alt gene cluster that confers tolerance to thiosulfinates. Lineage 3 strains, isolated from both onion and rainwater, either lacked a phosphonate BGC entirely or possessed the HiVir phosphonate BGC. In addition, lineage 3 strains lacked the alt cluster altogether. The localization of these virulence genes in the genome varied, with Halophos integrated in the chromosome, HiVir encoded on the conserved Large Pantoea Plasmid, and alt located on small, variable plasmids (plasmid B). The type IV secretion system (T4SS) and type VI secretion system (T6SS) showed variable genomic architectures, with plasmid-borne T4SSs and two chromosomal T6SS loci differing in conservation and gene content. Additionally, conserved Pantailocin phage islands were detected in most genomes. Overall, this study reveals that while core metabolic and competitive traits are conserved across P. allii, virulence-associated loci display lineage-specific distribution, reflecting ecological differentiation and evolutionary plasticity within the species.es
dc.format.extent17 p.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenes
dc.publisherMicrobiology Societyes
dc.relation.isformatofPDFes
dc.relation.ispartofMicrobial Genomics, v. 12, n°2, 2026. -- e001624es
dc.rightsLas obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)es
dc.subjectPatógenoses
dc.subjectGenómicaes
dc.subjectCebollaes
dc.subjectEnfermedades de las plantases
dc.titleComparative genomics of Pantoea allii lineages and distribution of ecologically relevant traitses
dc.typeArtículoes
dc.contributor.filiacionShin Gi Yoon, University of California Davis (USA). Department of Plant Pathology-
dc.contributor.filiacionDe Armas Stefanie, Universidad de la República (Uruguay). Facultad de Química. Laboratorio de Microbiología Molecular-
dc.contributor.filiacionGalván Guillermo A., Universidad de la República (Uruguay). Facultad de Agronomía. Departamento de Producción Vegetal (CRS)-
dc.contributor.filiacionSiri María I., Universidad de la República (Uruguay). Facultad de Química. Laboratorio de Microbiología Molecular-
dc.contributor.filiacionRojas Mariah, Virginia Tech School of Plant and Environmental Sciences (USA)-
dc.contributor.filiacionVinatzer Boris A., Virginia Tech School of Plant and Environmental Sciences (USA)-
dc.contributor.filiacionAsselin Jo Ann E., United States Department of Agriculture (USA). Agricultural Research Service. Robert W. Holley Center for Agriculture and Health. Emerging Pests and Pathogens Research Unit; Cornell University (USA). School of Integrated Plant Science. Plant Pathology & Plant-Microbe Biology Section-
dc.contributor.filiacionStodghill Paul, United States Department of Agriculture (USA). Agricultural Research Service. Robert W. Holley Center for Agriculture and Health. Emerging Pests and Pathogens Research Unit; Cornell University (USA). School of Integrated Plant Science. Plant Pathology & Plant-Microbe Biology Section-
dc.contributor.filiacionZhao Mei, China Agricultural University (China). College of Plant Protection. Department of Plant Pathology-
dc.contributor.filiacionDutta Bhabesh, University of Georgia (USA). Department of Plant Pathology-
dc.contributor.filiacionTambong James, Agriculture and Agri-Food Canada (Canada). Ottawa Research and Development Centre-
dc.contributor.filiacionKvitko Brian H., University of Georgia (USA). Department of Plant Pathology-
dc.rights.licenceLicencia Creative Commons Atribución (CC - By 4.0)es
dc.identifier.doi10.1099/mgen.0.001624-
Aparece en las colecciones: Publicaciones académicas y científicas - Facultad de Química

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