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Evaluation of the ability to form biofilms in KPC-producing and ESBL-producing Klebsiella pneumoniae isolated from clinical samples

datacite.subject.fosCiências Médicas::Ciências da Saúde
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorSabença, Carolina
dc.contributor.authorCosta, Eliana
dc.contributor.authorSousa, Sara
dc.contributor.authorBarros, Lillian
dc.contributor.authorOliveira, Ana
dc.contributor.authorRamos, Sónia
dc.contributor.authorIgrejas, Gilberto
dc.contributor.authorTorres, Carmen
dc.contributor.authorPoeta, Patrícia
dc.date.accessioned2026-02-20T17:03:15Z
dc.date.available2026-02-20T17:03:15Z
dc.date.issued2023-07
dc.description.abstractThe appearance of Klebsiella pneumoniae strains producing extended-spectrum β-lactamase (ESBL), and carbapenemase (KPC) has turned into a significant public health issue. ESBL- and KPC-producing K. pneumoniae’s ability to form biofilms is a significant concern as it can promote the spread of antibiotic resistance and prolong infections in healthcare facilities. A total of 45 K. pneumoniae strains were isolated from human infections. Antibiograms were performed for 17 antibiotics, ESBL production was tested by Etest ESBL PM/PML, a rapid test was used to detect KPC carbapenemases, and resistance genes were detected by PCR. Biofilm production was detected by the microtiter plate method. A total of 73% of multidrug resistance was found, with the highest resistance rates to ampicillin, trimethoprim–sulfamethoxazole, cefotaxime, amoxicillin-clavulanic acid, and aztreonam. Simultaneously, the most effective antibiotics were tetracycline and amikacin. blaCTX-M, blaTEM, blaSHV, aac(3)-II, aadA1, tetA, cmlA, catA, gyrA, gyrB, parC, sul1, sul2, sul3, blaKPC, blaOXA, and blaPER genes were detected. Biofilm production showed that 80% of K. pneumoniae strains were biofilm producers. Most ESBL- and KPC-producing isolates were weak biofilm producers (40.0% and 60.0%, respectively). There was no correlation between the ability to form stronger biofilms and the presence of ESBL and KPC enzymes in K. pneumoniae isolates.eng
dc.identifier.citationSabença C, Costa E, Sousa S, Barros L, Oliveira A, Ramos S, Igrejas G, Torres C, Poeta P. Evaluation of the Ability to Form Biofilms in KPC-Producing and ESBL-Producing Klebsiella pneumoniae Isolated from Clinical Samples. Antibiotics. 2023; 12(7):1143. https://doi.org/10.3390/antibiotics12071143
dc.identifier.doi10.3390/antibiotics12071143
dc.identifier.issn2079-6382
dc.identifier.urihttp://hdl.handle.net/10400.26/61812
dc.language.isoeng
dc.peerreviewedyes
dc.publisherMDPI
dc.relation.hasversionhttps://doi.org/10.3390/antibiotics12071143
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectKlebsiella pneumoniae
dc.subjectextended-spectrum β-lactamase (ESBL)
dc.subjectKlebsiella pneumoniae carbapenemase (KPC)
dc.subjectbiofilm
dc.subjectantimicrobial resistance
dc.titleEvaluation of the ability to form biofilms in KPC-producing and ESBL-producing Klebsiella pneumoniae isolated from clinical sampleseng
dc.typecontribution to journal
dspace.entity.typePublication
oaire.citation.issue7
oaire.citation.startPage1143
oaire.citation.titleAntibiotics
oaire.citation.volume12
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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