Background
Carbapenem-resistant
Klebsiella pneumoniae
(CRKP) infection has attracted worldwide concern and became a serious challenge for clinical treatment. The aims of this study were to evaluate the molecular characteristics and risk factors for CRKP infection.
Methods
All the CRKP strains were screened for antimicrobial resistance genes, virulence genes, and integron by polymerase chain reaction (PCR). Plasmid typing was performed by plasmid conjugation assay and PCR-based replicon typing (PBRT). The genetic environments of
bla
KPC-2
and
bla
NDM-1
were analyzed by using overlapping PCR and molecular typing was performed by multi-locus sequence typing (MLST). Risk factors for CRKP infection were analyzed by logistic regression model.
Results
All the 66 CRKP isolates were multidrug-resistant, but all of them were susceptible to tigecycline and polymyxin B. Among the CRKP isolates, 42
bla
KPC-2
-positive strains were identified carrying IncFII plasmids. Meanwhile, 24
bla
NDM
-positive strains were found on lncX3 plasmids, including 20
bla
NDM-1
isolates and 4
bla
NDM-5
isolates. Most of CRKP isolates contained several virulence genes and the class I integron (
intl1
). The genetic environments of
bla
KPC-2
and
bla
NDM-1
revealed that the conserved regions (
tnpA-tnpR
-IS
kpn8-bla
KPC-2
) and (
bla
NDM-1
-
ble
MBL
-trpF-tat
) were associated with the dissemination of KPC-2 and NDM-1. ST11 was the most common type in this work. Hematological disease, tracheal cannula, and use of β-lactams and β-lactamase inhibitor combination were identified as independent risk factors for CRKP infection.
Conclusion
This study established the resistance pattern, molecular characteristics, clonal relatedness, and risk factors of CRKP infection. The findings of the novel strain that co-harboring
bla
NDM-5
and
bla
IMP-4,
and the novel ST4495 indicated that the brand-new types have spread in Southwest China, emphasizing the prevent and control the further dissemination of CRKP isolates are highly needed.