Please use this identifier to cite or link to this item: https://doi.org/10.3389/fcimb.2017.00515
Title: Klebsiella pneumoniae in Singapore: Hypervirulent infections and the carbapenemase threat
Authors: Chew, K.L
Lin, R.T.P 
Teo, J.W.P
Keywords: beta lactamase AmpC
carbapenem
carbapenemase
colistin
extended spectrum beta lactamase
antiinfective agent
bacterial protein
beta lactamase
carbapenemase
antibiotic prophylaxis
antibiotic resistance
antibiotic sensitivity
bacterial virulence
controlled study
cystitis
endophthalmitis
enzyme activity
gene expression
hospital infection
human
infection control
Klebsiella pneumoniae
liver abscess
sepsis
Short Survey
Singapore
analysis
beta-lactam resistance
classification
disease management
enzymology
genetics
incidence
isolation and purification
Klebsiella infection
Klebsiella pneumoniae
microbiology
plasmid
Anti-Bacterial Agents
Bacterial Proteins
beta-Lactam Resistance
beta-Lactamases
Disease Management
Humans
Incidence
Klebsiella Infections
Klebsiella pneumoniae
Plasmids
Singapore
Issue Date: 2017
Publisher: Frontiers Media S.A.
Citation: Chew, 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
Rights: Attribution 4.0 International
Abstract: Klebsiella 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.
Source Title: Frontiers in Cellular and Infection Microbiology
URI: https://scholarbank.nus.edu.sg/handle/10635/183472
ISSN: 2235-2988
DOI: 10.3389/fcimb.2017.00515
Rights: Attribution 4.0 International
Appears in Collections:Staff Publications
Elements

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_3389_fcimb_2017_00515.pdf450.53 kBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons