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Molecular epidemiology of carbapenemase resistant Klebsiella pneumoniae

dc.contributor.authorJones-Dias, Daniela
dc.contributor.authorCaniça, Manuela
dc.contributor.authorManageiro, Vera
dc.date.accessioned2017-03-06T12:18:41Z
dc.date.available2017-03-06T12:18:41Z
dc.date.issued2016
dc.description.abstractCarbapenem-resistant Klebsiella pneumoniae have emerged as a class of pathogens that pose a significant threat to patients admitted to healthcare facilities. This phenotype is mostly due to the production of carbapenemases, which constitute the group of β-lactamases capable of hydrolysing all β-lactam antibiotics, including carbapenems. However, the successful worldwide dissemination of carbapenem resistant K. pneumoniae has been linked to the emergence of a specific type of carbapenemase: KPC (K. pneumoniae carbapenemase). Although this carbapenemase has been identified in several sequence-types (STs), the pandemic seems to be mainly driven by the spread of KPC-producing K. pneumoniae from ST258. Apart from the triumph of the clonal spread, there is a considerable variability in the number of mobile genetic elements that KPC-producing K. pneumoniae might harbour, and that contribute to the mobilization and transference of the KPC-encoding gene (blaKPC). This transmission can be mediated by different molecular mechanisms that include the mobilization of minor genetic elements and the horizontal transfer of different conjugative plasmids. Tn4401 transposon is highly involved in the horizontal dissemination of blaKPC. This transposon can even assume different isoforms that, in turn, may become associated with multiple blaKPC-bearing plasmids. Although many plasmids have been linked to the dissemination of blaKPC gene, the incompatibility groups enclosing Tn4401 seem to be predominant. In K. pneumoniae, other carbapenem resistance determinants have been identified throughout the years but none has disseminated to the extent of KPC. Its spread and success seems to be multifactorial with virulence factors, antibiotic resistance determinants and mobile genetic elements playing major roles. Only the early detection of these factors may ease their establishment worldwide and prevent their emergence in non endemic countries.pt_PT
dc.description.sponsorshipFCTpt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationIn: Shelton C. (ed). Superbugs - Clostridium difficile and Klebsiella pneumoniae: Recognition, Prevention and Treatment. Hauppauge NY: Nova Science Publishers, 2016. pp. 57-72pt_PT
dc.identifier.isbn978-1-63484-412-3
dc.identifier.urihttp://hdl.handle.net/10400.18/4484
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherNova Science Publishers, Incpt_PT
dc.relation.ispartofAllergies and Infectious Diseases
dc.relation.publisherversionhttps://www.novapublishers.com/catalog/product_info.php?products_id=59169pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.subjectAntibiotic Resistancept_PT
dc.subjectCarbapenemasept_PT
dc.subjectKlebsiella Pneumoniaept_PT
dc.subjectInfectious Diseasespt_PT
dc.subjectResistência aos Antimicrobianospt_PT
dc.titleMolecular epidemiology of carbapenemase resistant Klebsiella pneumoniaept_PT
dc.typebook part
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/PEst-OE%2FAGR%2FUI0211%2F2014/PT
oaire.citation.endPage72pt_PT
oaire.citation.startPage57pt_PT
oaire.citation.titleSuperbugs - Clostridium difficile and Klebsiella pneumoniae: Recognition, Prevention and Treatmentpt_PT
oaire.fundingStream5876
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typebookPartpt_PT
relation.isProjectOfPublicationd3e4188b-642e-4ad7-9a4d-aeea65a89449
relation.isProjectOfPublication.latestForDiscoveryd3e4188b-642e-4ad7-9a4d-aeea65a89449

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