Bloodstream Infections caused by Klebsiella pneumoniae and Serratia marcescens isolates co-harboring NDM-1 and KPC-2.
Taniela Marli BesDebora NaganoRoberta MartinsAna Paula MarchiLauro Perdigão-NetoHermes HigashinoGladys PradoThais GuimaraesAnna S LevinSilvia CostaPublished in: Annals of clinical microbiology and antimicrobials (2021)
Carbapenem-resistant Enterobacteriaceae are a worldwide health problem and isolates carrying both blaKPC-2 and blaNDM-1 are unusual. Here we describe the microbiological and clinical characteristics of five cases of bloodstream infections (BSI) caused by carbapenem-resistant Klebsiella pneumoniae and Serratia marcescens having both blaKPC-2 and blaNDM-1. Of the five blood samples, three are from hematopoietic stem cell transplantation patients, one from a renal transplant patient, and one from a surgical patient. All patients lived in low-income neighbourhoods and had no travel history. Despite antibiotic treatment, four out of five patients died. The phenotypic susceptibility assays showed that meropenem with the addition of either EDTA, phenylboronic acid (PBA), or both, increased the zone of inhibition in comparison to meropenem alone. Molecular tests showed the presence of blaKPC-2 and blaNDM-1 genes. K. pneumoniae isolates were assigned to ST258 or ST340 by whole genome sequencing. This case-series showed a high mortality among patients with BSI caused by Enterobacteriae harbouring both carbapenemases. The detection of carbapenemase-producing isolates carrying both blaKPC-2 and blaNDM-1 remains a challenge when using only phenotypic assays. Microbiology laboratories must be alert for K. pneumoniae isolates producing both KPC-2 and NDM-1.
Keyphrases
- klebsiella pneumoniae
- multidrug resistant
- escherichia coli
- end stage renal disease
- newly diagnosed
- gram negative
- chronic kidney disease
- prognostic factors
- healthcare
- type diabetes
- drug resistant
- peritoneal dialysis
- mental health
- gene expression
- public health
- case report
- genome wide
- risk assessment
- acute myeloid leukemia
- single molecule
- cystic fibrosis
- pseudomonas aeruginosa
- high throughput
- dna methylation