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dc.contributor.authorPons, M.J.
dc.contributor.authorMarí-Almirall, M.
dc.contributor.authorYmaña, B.
dc.contributor.authorMoya-Salazar, J.
dc.contributor.authorMuñoz, L.
dc.contributor.authorSauñe, S.
dc.contributor.authorSalazar-Hernández, R.
dc.contributor.authorVila, J.
dc.contributor.authorRoca, I.
dc.date.accessioned2025-10-31T18:36:48Z
dc.date.available2025-10-31T18:36:48Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/20.500.12805/5455
dc.description.abstractThe aim of this study was to characterize carbapenem-resistant Klebsiella pneumoniae (CR-Kp) isolates recovered from adults and children with severe bacteremia in a Peruvian Hospital in June 2018. Antimicrobial susceptibility was determined by disc/gradient diffusion and broth microdilution when necessary. Antibiotic resistance mechanisms were evaluated by PCR and DNA sequencing. Clonal relatedness was assessed using pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). Plasmid typing was performed with a PCR-based method. Thirty CR-Kp isolates were recovered in June 2018. All isolates were non-susceptible to all β-lactams, ciprofloxacin, gentamicin and trimethoprim-sulfamethoxazole, while mostly remaining susceptible to colistin, tigecycline, levofloxacin and amikacin. All isolates carried the bla<inf>NDM-1</inf> gene and were extended spectrum β-lactamase (ESBL) producers. PFGE showed four different pulsotypes although all isolates but two belonged to the ST348 sequence type, previously reported in Portugal. bla<inf>NDM-1</inf> was located in an IncFIB-M conjugative plasmid. To our knowledge, this is the first report of an New Delhi metallo-β-lactamase (NDM)-producing K. pneumoniae recovered from both children and adults in Lima, Peru, as well as the first time that the outbreak strain ST348 is reported in Peru and is associated with NDM. Studies providing epidemiological and molecular data on CR-Kp in Peru are essential to monitor their dissemination and prevent further spread.en_US
dc.description.sponsorshipFunding: This study was supported by Plan Nacional de I+D+i 2013–2016, Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Investigación Cooperativa, Ministerio de Economía y Competitividad, Spanish Network for Research in Infectious Diseases (REIPI RD16/0016/0010); the 2017 call for Strategic Action on Health (PI17/01932), co-financed by European Development Regional Fund “A way to achieve Europe” and the operative program Intelligent Growth 2014–2020; and grant 2017 SGR 0809 from the Departament d’Universitats, Recerca i Societat de la Informació, of the Generalitat de Catalunya. M.J.P. was supported by “Becas Iberoamérica Movilización. Jóvenes Profesores e Investigadores. Santander Universidades-2018” and internal funds of the Universidad Científica del Sur. M.M.-A. was supported by grant FPU 14/06357, from the Spanish Ministry of Education, Culture and Sports. I.R. was supported by the Department of Health, Generalitat de Catalunya, grant SLT002/16/00349. We also acknowledge support from the Spanish Ministry of Science, Innovation and Universities through the “Centro de Excelencia Severo Ochoa 2019–2023” Program (CEX2018-000806-S), and support from the Generalitat de Catalunya through the CERCA Program”.
dc.formatapplication/pdf
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofurn:issn:2076-2607
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectSDG 3en_US
dc.subjectAntibiotic Resistance Mechanisms in Clinical Infectionsen_US
dc.subjectCarbapenem Resistance Mechanisms in Klebsiella Pneumoniaeen_US
dc.titleSpread of st348 klebsiella pneumoniae producing NDM-1 in a peruvian hospitalen_US
dc.typehttps://purl.org/coar/resource_type/c_2df8fbb1
dc.identifier.doihttps://doi.org/10.3390/microorganisms8091392
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#5.00.00
dc.type.otherResearch article
dc.identifier.journalMicroorganisms
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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