First report and whole-genome sequencing of Pseudochrobactrum saccharolyticum in Latin America

dc.creatorPereira, Carine Rodrigues
dc.creatorSousa, Thiago de Jesus
dc.creatorSilva, Alessandra Lima da
dc.creatorSantos, Roselane Gonçalves dos
dc.creatorMinharro, Sílvia
dc.creatorCustodio, Dirceia Aparecida Costa
dc.creatorPickard, Derek J.
dc.creatorO'Callaghan, David
dc.creatorFoster, Jeffrey T.
dc.creatorSoares, Siomar de Castro
dc.creatorRamos, Rommel Thiago Juca
dc.creatorGóes Neto, Aristoteles
dc.creatorCosta, Mateus Matiuzzi da
dc.creatorLage, Andrey Pereira
dc.creatorAzevedo, Vasco
dc.creatorDorneles, Elaine Maria Seles
dc.date.accessioned2023-07-03T19:39:56Z
dc.date.available2023-07-03T19:39:56Z
dc.date.issued2023
dc.description.abstractThe Brucellaceae family comprises microorganisms similar both phenotypically and genotypically, making it difficult to identify the etiological agent of these infections. This study reports the first isolation, identification, and characterization of Pseudochrobactrum saccharolyticum (strain 115) from Latin America. Strain 115 was isolated in 2007 from a bovine in Brazil and was initially classified as Brucella spp. by classical microbiological tests and bcsp31 PCR. The antimicrobial susceptibility of strain 115 was tested against drugs used to treat human brucellosis by minimal inhibitory concentration test. Subsequently, the whole genome of the strain was sequenced, assembled, and characterized. Phylogenetic trees built from 16S rRNA and recA gene sequences enabled the classification of strain 115 as Pseudochrobactrum spp. Phylogenomic analysis using Single Nucleotide Polymorphisms and Average Nucleotide Identity allowed the classification of the strain as P. saccharolyticum. Additionally, a Tetra Correlation Search identified one related genome from the same species, which was compared with strain 115 by analyzing genomic islands. This is the first identification and whole-genome sequence of P. saccharolyticum in Latin America and highlights a challenge in the diagnosis of bovine brucellosis, which could be solved by including the sequencing of 16S rRNA and recA genes in routine diagnostics.pt_BR
dc.identifier.citationPEREIRA, C. R. et al. First report and whole-genome sequencing of Pseudochrobactrum saccharolyticum in Latin America. Microbes and Infection, Paris, v. 25, n. 1/2, Jan./Feb. 2023. DOI: https://doi.org/10.1016/j.micinf.2022.105018.pt_BR
dc.identifier.urihttps://repositorio.ufla.br//handle/1/58036
dc.identifier.urihttps://doi.org/10.1016/j.micinf.2022.105018pt_BR
dc.languageen_USpt_BR
dc.publisherElsevierpt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceMicrobes and Infectionpt_BR
dc.subjectBrucellaceaept_BR
dc.subjectPhylogeneticpt_BR
dc.subjectAntimicrobial resistancept_BR
dc.subjectFilogenéticapt_BR
dc.subjectResistência antimicrobianapt_BR
dc.subjectSequenciamento de genomapt_BR
dc.titleFirst report and whole-genome sequencing of Pseudochrobactrum saccharolyticum in Latin Americapt_BR
dc.typeArtigopt_BR

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