4.7 Article

Genome Sequencing Identifies Previously Unrecognized Klebsiella pneumoniae Outbreaks in Neonatal Intensive Care Units in the Philippines

期刊

CLINICAL INFECTIOUS DISEASES
卷 73, 期 -, 页码 S316-S324

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OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciab776

关键词

antimicrobial resistance; K. pneumoniae; outbreak detection; whole genome sequencing

资金

  1. Official Development Assistance (ODA) funding from the National Institute for Health Research (Wellcome Trust) [206194]
  2. National Institute for Health Research using Official Development Assistance (ODA)

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A survey on Klebsiella pneumoniae isolates in the Philippines found prevalent antibiotic resistance mechanisms including bla(CTX-M-15) and bla(NDM-1). Whole-genome sequencing identified an epidemic plasmid carrying bla(NDM-1) and uncovered three previously unrecognized outbreaks, highlighting the utility of WGS in outbreak detection and public health.
Background. Klebsiella pneumoniae is a critically important pathogen in the Philippines. Isolates are commonly resistant to at least 2 classes of antibiotics, yet mechanisms and spread of its resistance are not well studied. Methods. A retrospective sequencing survey was performed on carbapenem-, extended spectrum beta-lactam-, and cephalosporin-resistant Klebsiella pneumoniae isolated at 20 antimicrobial resistance (AMR) surveillance sentinel sites from 2015 through 2017. We characterized 259 isolates using biochemical methods, antimicrobial susceptibility testing, and whole-genome sequencing (WGS). Known AMR mechanisms were identified. Potential outbreaks were investigated by detecting clusters from epidemiologic, phenotypic, and genome-derived data. Results. Prevalent AMR mechanisms detected include bla(CTX-M-15) (76.8%) and bla(NDM-1) (37.5%). An epidemic IncFII(Yp) plasmid carrying bla(NDM-1) was also detected in 46 isolates from 6 sentinel sites and 14 different sequence types (STs). This plasmid was also identified as the main vehicle of carbapenem resistance in 2 previously unrecognized local outbreaks of ST348 and ST283 at 2 different sentinel sites. A third local outbreak of ST397 was also identified but without the IncFII(Yp) plasmid. Isolates in each outbreak site showed identical STs and K- and O-loci, and similar resistance profiles and AMR genes. All outbreak isolates were collected from blood of children aged < 1 year. Conclusion. WGS provided a better understanding of the epidemiology of multidrug resistant Klebsiella in the Philippines, which was not possible with only phenotypic and epidemiologic data. The identification of 3 previously unrecognized Klebsiella outbreaks highlights the utility of WGS in outbreak detection, as well as its importance in public health and in implementing infection control programs.

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