Purpose
Colistin represents one of the last treatment options for infections caused by multi-drug resistant (MDR)
Enterobacterales
. The emergence of a plasmid-mediated mobile colistin resistance-1 (
mcr-1
) gene has raised serious concerns about its potential dissemination among bacteria.
Methods
In this study, we evaluated the chromogenic medium, CHROMID
®
Colistin Resistance (COLR) agar, for the rapid detection of colistin-resistant
Enterobacterales
using broth microdilution (BMD) as a reference method. We also attempted to detect
mcr-1
,
−2
,
−3
,
−4
, and
−5
genes, as well as the insertion sequence IS
Apl1
via polymerase chain reaction (PCR), followed by sequencing of
mcr
gene(s).
Results
Among the 100 studied
Enterobacterales
isolates, 53% of them were colistin-resistant, with higher rate among
Klebsiella pneumoniae
(75%) as compared to
Escherichia coli
(44.4%). The COLR agar showed 83.2% sensitivity and 97.9% specificity for the detection of colistin resistance. Among colistin-resistant isolates,
mcr-1
gene was only detected in four (7.5%)
E. coli
isolates. The IS
Apl1
was not found among
mcr-1
positive isolates. Sequencing of
mcr-1
gene revealed nucleotide sequence homogeneity with the wild-type
mcr-1
gene in BLAST.
Conclusion
The COLR agar is a promising phenotypic method for the detection of colistin-resistant
Enterobacterales
. Multiplex PCR followed by sequencing can be used for
mcr
genes’ detection and characterization.