Utilizing genomic analyses to investigate the first outbreak of vanA vancomycin-resistant Enterococcus in Australia with emergence of daptomycin non-susceptibility.
Adult
Aged
Aged, 80 and over
Anti-Bacterial Agents
/ pharmacology
Australia
/ epidemiology
Bacteremia
/ epidemiology
Bacterial Proteins
/ genetics
Carbon-Oxygen Ligases
/ genetics
Cross Infection
/ epidemiology
Daptomycin
/ pharmacology
Disease Outbreaks
Enterococcus faecium
/ drug effects
Female
Genomics
Genotype
Gram-Positive Bacterial Infections
/ blood
Humans
Linezolid
/ therapeutic use
Male
Microbial Sensitivity Tests
Middle Aged
Multilocus Sequence Typing
Oncology Service, Hospital
Treatment Outcome
Vancomycin
/ pharmacology
Vancomycin-Resistant Enterococci
/ drug effects
Whole Genome Sequencing
Vancomycin-resistant Enterococcus
daptomycin non-susceptible
outbreak
whole genome sequencing
Journal
Journal of medical microbiology
ISSN: 1473-5644
Titre abrégé: J Med Microbiol
Pays: England
ID NLM: 0224131
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
pubmed:
22
1
2019
medline:
20
3
2019
entrez:
22
1
2019
Statut:
ppublish
Résumé
The majority of vancomycin-resistant Enterococcus faecium (VREfm) in Australia is of the vanB genotype. An outbreak of vanA VREfm emerged in our haematology/oncology unit between November 2014 and May 2015. The first case of daptomycin non-susceptible E. faecium (DNSEfm) detected was a patient with vanA VREfm bacteraemia who showed clinical failure of daptomycin therapy, prompting microbiologic testing confirming daptomycin non-susceptibility. To describe the patient profiles, antibiotic susceptibility and genetic relatedness of vanA VREfm isolates in the outbreak. Chart review of vanA VREfm colonized and infected patients was undertaken to describe the demographics, clinical features and outcomes of therapy. Whole genome sequencing of vanA VREfm isolates involved in the outbreak was conducted to assess clonality. In total, 29 samples from 24 patients tested positive for vanA VREfm (21 screening swabs and 8 clinical isolates). Five isolates were DNSEfm (four patients colonized, one patient with bacteraemia), with only one patient exposed to daptomycin previously. In silico multi-locus sequence typing of the isolates identified 25/26 as ST203, and 1/26 as ST796. Comparative genomic analysis revealed limited core genome diversity amongst the ST203 isolates, consistent with an outbreak of a single clone of vanA VREfm. Here we describe an outbreak of vanA VREfm in a haematology/oncology unit. Genomic analysis supports transmission of an ST203 vanA VRE clone within this unit. Daptomycin non-susceptibility in 5/24 patients left linezolid as the only treatment option. Daptomycin susceptibility cannot be assumed in vanA VREfm isolates and confirmatory testing is recommended.
Identifiants
pubmed: 30663951
doi: 10.1099/jmm.0.000916
doi:
Substances chimiques
Anti-Bacterial Agents
0
Bacterial Proteins
0
VanA ligase, Bacteria
0
Vancomycin
6Q205EH1VU
Carbon-Oxygen Ligases
EC 6.1.-
Linezolid
ISQ9I6J12J
Daptomycin
NWQ5N31VKK
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM