Molecular Epidemiology of a Vancomycin-Intermediate Heteroresistant Staphylococcus epidermidis Outbreak in a Neonatal Intensive Care Unit. 2016

Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
Department of Epidemiology and Biostatistics, McGill University, Montreal, QC, Canada.

Coagulase-negative staphylococci (CoNS) have become the leading cause of bloodstream infections (BSIs) in intensive care units (ICUs), particularly in premature neonates. Vancomycin-intermediate heteroresistant CoNS (hVICoNS) have been identified as sources of BSIs worldwide, and their potential to emerge as significant pathogens in the neonatal ICU (NICU) remains uncertain. This study describes the molecular epidemiology of an outbreak of vancomycin-heteroresistant (hV) Staphylococcus epidermidis central-line-associated BSI (CLABSI) in a single tertiary care NICU and compares it to a second tertiary care NICU that had not been associated with an outbreak. Between November 2009 and April 2014, 119 S. epidermidis CLABSIs were identified in two tertiary care NICUs in Quebec, Canada. Decreased vancomycin susceptibility was identified in about 88% of all collected strains using Etest methods. However, discrepancies were found according to the Etest and population analysis profiling-area under the concentration-time curve (PAP-AUC) methods used. All strains were susceptible to linezolid, and a few isolates were nonsusceptible to daptomycin. Great genetic diversity was observed within the collection, with 31 pulsed-field gel electrophoresis (PFGE) patterns identified. The outbreak strains were all determined to be heteroresistant to vancomycin and were polyclonal. The study identified two major clones, PFGE patterns E and G, which were found in both NICUs across the 5-year study period. This suggests the persistence of highly successful clones that are well adapted to the hospital environment. hV S. epidermidis seems more common than currently realized in the NICU, and certain hV S. epidermidis clones can become endemic to the NICU. The reservoirs for these clones remain unknown at this time, and identification of the reservoirs is needed to better understand the impact of hV S. epidermidis in the NICU and to inform infection prevention strategies. In addition, there is a need to investigate and validate hV determination protocols for different species of CoNS.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D007363 Intensive Care Units, Neonatal Hospital units providing continuing surveillance and care to acutely ill newborn infants. Neonatal Intensive Care Unit,Neonatal Intensive Care Units,Newborn Intensive Care Unit,Newborn Intensive Care Units,ICU, Neonatal,Neonatal ICU,Newborn ICU,Newborn Intensive Care Units (NICU),ICU, Newborn,ICUs, Neonatal,ICUs, Newborn,Neonatal ICUs,Newborn ICUs
D008297 Male Males
D008826 Microbial Sensitivity Tests Any tests that demonstrate the relative efficacy of different chemotherapeutic agents against specific microorganisms (i.e., bacteria, fungi, viruses). Bacterial Sensitivity Tests,Drug Sensitivity Assay, Microbial,Minimum Inhibitory Concentration,Antibacterial Susceptibility Breakpoint Determination,Antibiogram,Antimicrobial Susceptibility Breakpoint Determination,Bacterial Sensitivity Test,Breakpoint Determination, Antibacterial Susceptibility,Breakpoint Determination, Antimicrobial Susceptibility,Fungal Drug Sensitivity Tests,Fungus Drug Sensitivity Tests,Sensitivity Test, Bacterial,Sensitivity Tests, Bacterial,Test, Bacterial Sensitivity,Tests, Bacterial Sensitivity,Viral Drug Sensitivity Tests,Virus Drug Sensitivity Tests,Antibiograms,Concentration, Minimum Inhibitory,Concentrations, Minimum Inhibitory,Inhibitory Concentration, Minimum,Inhibitory Concentrations, Minimum,Microbial Sensitivity Test,Minimum Inhibitory Concentrations,Sensitivity Test, Microbial,Sensitivity Tests, Microbial,Test, Microbial Sensitivity,Tests, Microbial Sensitivity
D011792 Quebec A province of eastern Canada. Its capital is Quebec. The region belonged to France from 1627 to 1763 when it was lost to the British. The name is from the Algonquian quilibek meaning the place where waters narrow, referring to the gradually narrowing channel of the St. Lawrence or to the narrows of the river at Cape Diamond. (From Webster's New Geographical Dictionary, 1988, p993 & Room, Brewer's Dictionary of Names, 1992, p440)
D004196 Disease Outbreaks Sudden increase in the incidence of a disease. The concept includes EPIDEMICS and PANDEMICS. Outbreaks,Infectious Disease Outbreaks,Disease Outbreak,Disease Outbreak, Infectious,Disease Outbreaks, Infectious,Infectious Disease Outbreak,Outbreak, Disease,Outbreak, Infectious Disease,Outbreaks, Disease,Outbreaks, Infectious Disease
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D013203 Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. Infections, Staphylococcal,Staphylococcus aureus Infection,Staphylococcal Infection,Staphylococcus aureus Infections

Related Publications

Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
January 2015, The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases,
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
October 1995, The Journal of hospital infection,
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
January 2017, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica,
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
May 2000, Journal of clinical microbiology,
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
October 2013, American journal of infection control,
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
June 2007, Pathology,
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
June 2023, Iranian journal of microbiology,
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
January 2020, Journal of medical microbiology,
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
February 1995, Journal of chemotherapy (Florence, Italy),
Jasmine Chong, and Caroline Quach, and Ana C Blanchard, and Philippe Guillaume Poliquin, and George R Golding, and Céline Laferrière, and Simon Lévesque
October 2001, Infection control and hospital epidemiology,
Copied contents to your clipboard!