Development of selective medium for IMP-type carbapenemase-producing Enterobacteriaceae in stool specimens

BMC Infect Dis. 2017 Mar 24;17(1):229. doi: 10.1186/s12879-017-2312-1.

Abstract

Background: Identification of carbapenemase-producing Enterobacteriaceae (CPE) in faecal specimens is challenging. This fact is particularly critical because low-level carbapenem-resistant organisms such as IMP-producing CPE are most prevalent in Japan. We developed a modified selective medium more suitable for IMP-type CPE.

Methods: Fifteen reference CPE strains producing different types of β-lactamases were used to evaluate the commercially available CHROMagar KPC and chromID CARBA as well as the newly prepared MC-ECC medium (CHROMagar ECC supplemented with meropenem, cloxacillin, and ZnSO4) and M-ECC medium (CHROMagar ECC supplemented with meropenem and ZnSO4). A total of 1035 clinical samples were then examined to detect CPE using chromID CARBA and M-ECC medium.

Results: All tested strains producing NDM-, KPC-, and OXA-48-carbapenemases were successfully cultured in the media employed. Although most of the IMP-positive strains did not grow in CHROMagar KPC, chromID CARBA, or MC-ECC, all tested strains grew on M-ECC. When faecal samples were applied to the media, M-ECC medium allowed the best growth of IMP-type CPE with a significantly higher sensitivity (99.3%) than that of chromID CARBA (13.9%).

Conclusions: M-ECC medium was determined as the most favourable selective medium for the detection of IMP-type CPE as well as other types of CPE.

Keywords: Carbapenemase-producing Enterobacteriaceae; Faecal specimens; IMP; Selective culture medium.

MeSH terms

  • Bacterial Proteins*
  • Bacterial Typing Techniques / methods*
  • Culture Media*
  • Enterobacteriaceae Infections* / diagnosis
  • Enterobacteriaceae Infections* / microbiology
  • Enterobacteriaceae* / enzymology
  • Enterobacteriaceae* / isolation & purification
  • Enterobacteriaceae* / metabolism
  • Feces / microbiology
  • Humans
  • Inosine Monophosphate / metabolism*
  • beta-Lactamases*

Substances

  • Bacterial Proteins
  • Culture Media
  • Inosine Monophosphate
  • beta-Lactamases
  • carbapenemase