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dc.contributor.author
Gonzalez Espinosa, Francisco Eduardo  
dc.contributor.author
Di Pilato, Vincenzo  
dc.contributor.author
Magariños, Francisco  
dc.contributor.author
Di Conza, José Alejandro  
dc.contributor.author
Rossolini, Gian Maria  
dc.contributor.author
Gutkind, Gabriel Osvaldo  
dc.contributor.author
Radice, Marcela Alejandra  
dc.contributor.author
Cejas, Daniela  
dc.date.available
2024-07-03T15:32:23Z  
dc.date.issued
2024-06  
dc.identifier.citation
Gonzalez Espinosa, Francisco Eduardo; Di Pilato, Vincenzo; Magariños, Francisco; Di Conza, José Alejandro; Rossolini, Gian Maria; et al.; Genomic characterization of carbapenemase-producing Klebsiella pneumoniae ST307 revealed multiple introductions in Buenos Aires, Argentina; Elsevier; Journal of Global Antimicrobial Resistance; 37; 6-2024; 176-178  
dc.identifier.issn
2213-7165  
dc.identifier.uri
http://hdl.handle.net/11336/238961  
dc.description.abstract
Objectives: To describe at genomic level nine carbapenemase-producing Klebsiella pneumoniae ST307 (Kp-ST307) clinical isolates recovered in Buenos Aires during 2017 to 2021, investigating their resistome, virulome, and phylogeny.Methods: Antimicrobial susceptibility was determined according to Clinical and Laboratory Standards Intitute (CLSI). Genomic DNA was sequenced by Illumina MiSeq and analysed using SPAdes, PROKKA, and Kleborate. Phylogeny of 355 randomly selected Kp-ST307 genomes and those from nine local isolates was inferred by a maximum-likelihood approach. The tree was visualized using Microreact.Results: Besides resistance to ß-lactams and fluoroquinolones, six out of nine Kp-ST307 werealso resistant to ceftazidime/avibactam (CZA). This difficult-to-treat resvistance phenotype was mediated by blaSHV-28 and GyrA - 83I /P arC - 80I mutations in addition to carbapenemase coding genes. Among CZA susceptible isolates, two of them harboured blaKPC-3 while the other harboured blaKPC-2 + blaCTX-M-15. Regarding CZA-resistant isolates, three harboured blaKPC-3 + blaNDM-1 + blaCMY-6 , two carried blaKPC-2 + blaNDM-5 + blaCTX-M-15 , and blaNDM-5 + blaCTX-M-15 were detected in the remaining isolate. Furthermore, five colistin-resistant isolates presented a nonsense mutation in mgrB. Global Kp-ST307 isolates were distributed in two deep-branching lineages while local isolates were set in the main clade of the phylogenetic tree. The five isolates from the same hospital, harbouring blaKPC-3 or blaKPC-3 + blaNDM-1 + blaCMY-6 , clustered in a monophyletic subclade with Italian isolates. Also, an isolate harbouring blaKPC-2 + blaNDM-5 + blaCTX-M-15 recovered in another hospital was closed to this group. The remaining local Kp-ST307 were grouped in other subclades containing isolates of diverse geographical origin.Conclusion: The inferred resistome was consistent with the resistant phenotype. Phylogeny suggested multiple introduction events in our region and a single major introduction in one hospital followed by local spread.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
KLEBSIELLA PNEUMONIAE  
dc.subject
NDM  
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KPC  
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ST307  
dc.subject.classification
Enfermedades Infecciosas  
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Ciencias de la Salud  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Genomic characterization of carbapenemase-producing Klebsiella pneumoniae ST307 revealed multiple introductions in Buenos Aires, Argentina  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2024-06-24T13:11:52Z  
dc.journal.volume
37  
dc.journal.pagination
176-178  
dc.journal.pais
Reino Unido  
dc.description.fil
Fil: Gonzalez Espinosa, Francisco Eduardo. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Investigaciones en Bacteriología y Virología Molecular; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Di Pilato, Vincenzo. University Of Genoa; Italia  
dc.description.fil
Fil: Magariños, Francisco. Gobierno de la Ciudad de Buenos Aires. Hospital de Agudos "D. F. Santojanni"; Argentina  
dc.description.fil
Fil: Di Conza, José Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Investigaciones en Bacteriología y Virología Molecular; Argentina  
dc.description.fil
Fil: Rossolini, Gian Maria. University Of Florence; Italia  
dc.description.fil
Fil: Gutkind, Gabriel Osvaldo. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Investigaciones en Bacteriología y Virología Molecular; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Radice, Marcela Alejandra. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Investigaciones en Bacteriología y Virología Molecular; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Cejas, Daniela. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Investigaciones en Bacteriología y Virología Molecular; Argentina  
dc.journal.title
Journal of Global Antimicrobial Resistance  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S2213716524000699  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.jgar.2024.03.017