Please use this identifier to cite or link to this item: https://doi.org/10.3389/fcimb.2017.00515
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dc.titleKlebsiella pneumoniae in Singapore: Hypervirulent infections and the carbapenemase threat
dc.contributor.authorChew, K.L
dc.contributor.authorLin, R.T.P
dc.contributor.authorTeo, J.W.P
dc.date.accessioned2020-11-17T04:33:44Z
dc.date.available2020-11-17T04:33:44Z
dc.date.issued2017
dc.identifier.citationChew, K.L, Lin, R.T.P, Teo, J.W.P (2017). Klebsiella pneumoniae in Singapore: Hypervirulent infections and the carbapenemase threat. Frontiers in Cellular and Infection Microbiology 7 (DEC) : 515. ScholarBank@NUS Repository. https://doi.org/10.3389/fcimb.2017.00515
dc.identifier.issn2235-2988
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/183472
dc.description.abstractKlebsiella pneumoniae remains a major pathogen responsible for localized infections such as cystitis and pneumonia, and disseminated infections that may result in severe sepsis and death. Invasive disease such as liver abscesses and endogenous endophthalmitis are associated with capsular serotypes K1 and K2. These infections require a prolonged course of antimicrobial treatment which has evolved over the years from inpatient treatment to outpatient parenteral antibiotic therapy. The emergence of plasmid-mediated resistance began with extended-spectrum β-lactamases (ESBLs) and AmpC β-lactamases. This was followed by carbapenemase genes and now plasmid transmissible colistin resistance (mcr), thus limiting viable treatment options. Plasmid-mediated carbapenemase production in Singapore was first reported in 1996. Carbapenemase production has since become the predominant mechanism of carbapenem resistance and incidence rates continue to increase over time. Although carbapenemases can occur in all Enterobacteriaceae, K. pneumoniae are the most common carrier of carbapenemase genes. Alternative treatment options are urgently required before the simplest infections, let alone invasive infections are left potentially untreatable. Clinical management requires guidance from robust laboratory testing methods to optimize patient outcomes. We explore past and present trends in treatment of K. pneumoniae infections, and discuss future treatment options and gaps in knowledge for further study. © 2017 Chew, Lin and Teo.
dc.publisherFrontiers Media S.A.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectbeta lactamase AmpC
dc.subjectcarbapenem
dc.subjectcarbapenemase
dc.subjectcolistin
dc.subjectextended spectrum beta lactamase
dc.subjectantiinfective agent
dc.subjectbacterial protein
dc.subjectbeta lactamase
dc.subjectcarbapenemase
dc.subjectantibiotic prophylaxis
dc.subjectantibiotic resistance
dc.subjectantibiotic sensitivity
dc.subjectbacterial virulence
dc.subjectcontrolled study
dc.subjectcystitis
dc.subjectendophthalmitis
dc.subjectenzyme activity
dc.subjectgene expression
dc.subjecthospital infection
dc.subjecthuman
dc.subjectinfection control
dc.subjectKlebsiella pneumoniae
dc.subjectliver abscess
dc.subjectsepsis
dc.subjectShort Survey
dc.subjectSingapore
dc.subjectanalysis
dc.subjectbeta-lactam resistance
dc.subjectclassification
dc.subjectdisease management
dc.subjectenzymology
dc.subjectgenetics
dc.subjectincidence
dc.subjectisolation and purification
dc.subjectKlebsiella infection
dc.subjectKlebsiella pneumoniae
dc.subjectmicrobiology
dc.subjectplasmid
dc.subjectAnti-Bacterial Agents
dc.subjectBacterial Proteins
dc.subjectbeta-Lactam Resistance
dc.subjectbeta-Lactamases
dc.subjectDisease Management
dc.subjectHumans
dc.subjectIncidence
dc.subjectKlebsiella Infections
dc.subjectKlebsiella pneumoniae
dc.subjectPlasmids
dc.subjectSingapore
dc.typeOthers
dc.contributor.departmentPATHOLOGY
dc.description.doi10.3389/fcimb.2017.00515
dc.description.sourcetitleFrontiers in Cellular and Infection Microbiology
dc.description.volume7
dc.description.issueDEC
dc.description.page515
dc.published.statePublished
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