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dc.contributor.authorSchramm, Sareda T. J.-
dc.contributor.authorPlace, Kori-
dc.contributor.authorMontaña, Sabrina-
dc.contributor.authorAlmuzara, Marisa-
dc.contributor.authorFung, Sammie-
dc.contributor.authorFernandez, Jennifer S.-
dc.contributor.authorTuttobene, Marisel R.-
dc.contributor.authorGolic, Adrián-
dc.contributor.authorAltilio, Matías-
dc.contributor.authorTraglia, German M.-
dc.contributor.authorVay, Carlos-
dc.contributor.authorMussi, Maria Alejandra-
dc.contributor.authorIriarte, Andres-
dc.contributor.authorRamirez, Maria Soledad-
dc.date.accessioned2026-06-23T12:01:57Z-
dc.date.available2026-06-23T12:01:57Z-
dc.date.issued2019-
dc.identifier.citationSCHRAMM, STJ., PLACE, K., MONTAÑA, S., y otros. Genetic and Phenotypic Features of a Novel Acinetobacter Species, Strain A47, Isolated From the Clinical Setting. Front Microbiol [en línea] 2019, 10. DOI: 10.3389/fmicb.2019.01375es
dc.identifier.urihttps://hdl.handle.net/20.500.12008/55661-
dc.description.abstractIn 2014, a novel species of Acinetobacter, strain A47, determined to be hospital acquired was recovered from a single patient soft tissue sample following a traumatic accident. The complexity of the Acinetobacter genus has been established, and every year novel species are identified. However, specific features and virulence factors that allow members of this genus to be successful pathogens are not well understood. Utilizing both genomic and phenotypic approaches, we identified distinct features and potential virulence factors of the A47 strain to understand its pathobiology. In silico analyses confirmed the uniqueness of this strain and other comparative and sequence analyses were used to study the evolution of relevant features identified in this isolate. The A47 genome was further analyzed for genes associated with virulence and genes involved in type IV pili (T4P) biogenesis, hemolysis, type VI secretion system (T6SS), and novel antibiotic resistance determinants were identified. A47 exhibited natural transformation with both genomic and plasmid DNA. It was able to form biofilms on different surfaces, to cause hemolysis of sheep and rabbit erythrocytes, and to kill competitor bacteria. Additionally, surface structures with non-uniform length were visualized with scanning electron microscopy and proposed as pili-like structures. Furthermore, the A47 genome revealed the presence of two putative BLUF type photoreceptors, and phenotypic assays confirmed the modulation by light of different virulence traits. Taken together, these results provide insight into the pathobiology of A47, which exhibits multiple virulence factors, natural transformation, and the ability to sense and respond to light, which may contribute to the success of an A47 as a hospital dwelling pathogen.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenes
dc.relation.ispartofFront Microbiol. 10, 2019es
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.subjectAcinetobacter spp.es
dc.subjectbiofilmes
dc.subjectantibiotic resistancees
dc.subjectvirulence traitses
dc.subjectnatural transformationes
dc.titleGenetic and Phenotypic Features of a Novel Acinetobacter Species, Strain A47, Isolated From the Clinical Settinges
dc.typeArtículoes
dc.contributor.filiacionSchramm Sareda T. J., California State University Fullerton (Estados Unidos). Department of Biological Science-
dc.contributor.filiacionPlace Kori, California State University Fullerton (Estados Unidos). Department of Biological Science-
dc.contributor.filiacionMontaña Sabrina, Universidad de Buenos Aires (UBA-CONICET) (Argentina). Instituto de Microbiología y Parasitología Médica. Facultad de Medicina-
dc.contributor.filiacionAlmuzara Marisa, Universidad de Buenos Aires (Argentina). Facultad de Farmacia y Bioquímica. Hosp. de Clínicas José de San Martín. Departamento de Bioquímica Clínica. Laboratorio de Bacteriología Clínica-
dc.contributor.filiacionFung Sammie, California State University Fullerton (Estados Unidos). Department of Biological Science-
dc.contributor.filiacionFernandez Jennifer S., California State University Fullerton (Estados Unidos). Department of Biological Science-
dc.contributor.filiacionTuttobene Marisel R., Centro de Estudios Fotosintéticos y Bioquímicos (CEFOBI– CONICET) (Argentina)-
dc.contributor.filiacionGolic Adrián, Centro de Estudios Fotosintéticos y Bioquímicos (CEFOBI– CONICET) (Argentina)-
dc.contributor.filiacionAltilio Matías, Centro de Estudios Fotosintéticos y Bioquímicos (CEFOBI– CONICET) (Argentina)-
dc.contributor.filiacionTraglia German M., Universidad de Buenos Aires (Argentina). Facultad de Farmacia y Bioquímica. Hosp. de Clínicas José de San Martín. Departamento de Bioquímica Clínica. Laboratorio de Bacteriología Clínica-
dc.contributor.filiacionVay Carlos, Universidad de Buenos Aires (Argentina). Facultad de Farmacia y Bioquímica. Hosp. de Clínicas José de San Martín. Departamento de Bioquímica Clínica. Laboratorio de Bacteriología Clínica-
dc.contributor.filiacionMussi Maria Alejandra, Centro de Estudios Fotosintéticos y Bioquímicos (CEFOBI– CONICET) (Argentina)-
dc.contributor.filiacionIriarte Andres, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico. Laboratorio de Biología Computacional-
dc.contributor.filiacionRamirez Maria Soledad, California State University Fullerton (Estados Unidos). Department of Biological Science-
dc.rights.licenceLicencia Creative Commons Atribución (CC - By 4.0)es
dc.identifier.doi10.3389/fmicb.2019.01375-
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