Clonal replacement of epidemic KPC-producing Klebsiella pneumoniae in a hospital in China
© The Author(s). 2017
Received: 19 October 2016
Accepted: 16 May 2017
Published: 23 May 2017
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© The Author(s). 2017
Received: 19 October 2016
Accepted: 16 May 2017
Published: 23 May 2017
Klebsiella pneumoniae is a frequent nosocomial pathogen causing difficult-to-treat infections worldwide. The prevalence of Klebsiella pneumoniae carbapenemase (KPC)-producing Klebsiella pneumoniae (KPC-KP) is increasing in China. The aim of this study was to investigate the molecular epidemiology of KPC-KP in a nosocomial outbreak.
Fifty-four KPC-KP isolates were consecutively collected between November 2013 and August 2014 during a KPC-KP outbreak in a tertiary care hospital in Beijing, China. Antimicrobial susceptibility was determined by agar dilution. Carbapenemase, extended-spectrum β–lactamase, 16S rRNA methylase, AmpC β-lactamase, and plasmid-mediated quinolone resistance determinants were detected by PCR amplification. The genetic relatedness of isolates was analyzed by pulsed-field gel electrophoresis and multi-locus sequence typing.
All isolates belonged to ST11 except one isolate which was identified as a new sequence type (ST2040). PFGE profile of genomic DNA revealed seven clusters, of which cluster A and C dominated the KPC-KP outbreak and cluster A was replaced by cluster C during the outbreak. PFGE of genomic DNA, S1-PFGE of plasmids, replicon typing, and drug resistant characteristics showed that clonal spread occurred during the outbreak. When compared with isolates within cluster A, all isolates in cluster C harbored rmtB and showed higher level of resistance to cefepime, amikacin, tobramycin, and tigecycline.
We reported a nosocomial outbreak of KPC-KP with clonal replacement and a new sequence type (ST2040) of KP. High degree of awareness and surveillance of KPC-KP should be given to avoid potential outbreaks, especially in ICU wards.
Carbapenem-resistant Klebsiella pneumoniae (KP) has spread worldwide and become a major public health threat in health care facilities , and the mortality could reach up to 40–50% . According to an antimicrobial resistance surveillance networks in China (CHINET), the rate of carbapenem-resistant KP escalated from 0.7% in 2006 to 10% in 2013 , which is mainly due to the rapid dissemination of Klebsiella pneumoniae carbapenemase (KPC)-producing Klebsiella pneumoniae (KPC-KP) . The bla KPC gene can be disseminated by both clonal spread and horizontal plasmid transfer . In China, KPC-KP was firstly identified in 2007 . Since then, this pathogen has been identified in several provinces and ST11 has been demonstrated to be the dominant clone [4, 7–16]. Nosocomial outbreaks of KPC-KP were also described previously [14, 17, 18]. However, clonal replacement of epidemic KPC-KP has not been reported in China or abroad.
Here, we reported a nosocomial outbreak of KPC-KP with clonal replacement in our hospital, which involved 54 consecutive patients and mainly occurred in ICU wards. The drug resistance and epidemiologic features of KPC-KP were also described.
All Carbapenem-resistant KP strains, which were collected between November 2013 and August 2014 in this study, were isolated from different clinical wards of our tertiary care hospital with 1500 beds. Species were identified by the Vitek 2 system, followed by 16S rDNA sequencing. Crude mortality was defined as death during hospitalization. Infection-related mortality was defined as death only as a direct consequence of KPC-KP infection during hospitalization. A KPC-KP outbreak was defined as two or more laboratory-confirmed patients that were temporally related, epidemiologically linked, and infected by the same KP variant.
Isolates exhibiting resistance to at least one of the carbapenems (imipenem or ertapenem) were evaluated for the presence of bla KPC by PCR and sequencing as described previously [19, 20]. All of the KPC-positive isolates were subjected to PCR amplification and sequencing for the presence of carbapenemase genes (bla GES, bla SME, bla IMI, bla BIC, bla NDM, bla IMP, bla VIM, bla SIM, and bla SPM) [19, 20], extended-spectrum β–lactamase genes (bla TEM, bla SHV, bla CTX-M, and bla OXA-48-like) [21–23], 16S rRNA methylase genes (armA, rmtA, rmtB, rmtC, rmtD, rmtE, and npmA) [24, 25], AmpC β-lactamase genes (bla ACC, bla FOX, bla MOX, bla DHA, bla CIT /bla SPM, and bla EBC) , and plasmid-mediated quinolone resistance (PMQR) genes (qnrA, qnrB, qnrC, qnrS, qepA, acc(6′)-Ib-cr, oqxA, and oqxB) .
Susceptibility tests were performed using the Vitek 2 system and the AST-GN card. MICs of various antimicrobials were determined by agar dilution method and results were interpreted according to the criteria recommended by CLSI (2014) .
The clonal relatedness of KP isolates were analyzed by PFGE as described previously . Prepared genomic DNA was digested using XbaI restriction enzyme on all clinical isolates. The banding patterns were analyzed by the BioNumerics software. The genetic similarity was calculated by dice coefficients and dendrograms were constructed by the unweighted pair group of arithmetic average. The analysis parameters were based on 1.5% tolerance values. Clusters were defined as DNA patterns sharing ≥85% similarity. Plasmid profiling was performed by PFGE of total bacteria genome DNA cut with nuclease S1.
Genotyping was further determined by MLST analysis. Standard DNA amplification and sequencing of seven housekeeping genes (gapA, infB, mdh, pgi, phoE, rpoB, and tonB) were performed as described previously . The allele sequences and sequence types (ST) were identified at http://bigsdb.web.pasteur.fr/klebsiella/klebsiella.html.
To determine the plasmid incompatibility groups (F, FIA, FIB, FIC, HI1, HI2, I1-Ic, L/M, N, P, W, T, A/C, K, B/O, X, Y, and FII), PBRT were carried out in all isolates as described previously .
The conjugation experiments were performed by using azide-resistant E.coli J53 as the recipient strain. Cultures of donor and recipient cells in logarithmic phase (0.5 ml of each) were added to 4 ml of fresh Luria-Bertani broth and were incubated overnight without shaking. The transconjugants were selected on Mueller-Hinton agar plates containing 100 μg/ml ampicillin and 300 μg/ml sodium-azide. Antibiotic resistance genes and replicon typing were performed as described previously in this study.
All statistical analysis were performed using the SPSS software package version 20.0. Continuous variables (age and Charlson score) were summarized as medians and were compared using non-parametric Mann-Whitney U test. Categorical variables were summarized as percentages and were compared using the pearson chi-square test. A p-value of less than 0.05 was considered statistically significant.
A total of 54 non-duplicate KPC-KP isolates were included in this study. All patients, where the 54 isolates were isolated from, were identified as clinical infections based on the isolation of KPC-KP from clinical samples and medical diagnosis established by physicians according to the clinical manifestations and the antibacterial effects. The predominant type of samples from which KPC isolates were isolated was sputum (n = 41, 75.9%), followed by bronchoalveolar lavage fluid (n = 5, 9.3%), blood (n = 4, 7.4%), secretions (n = 2, 3.7%), urine (n = 1, 1.9%), and peritoneal fluid (n = 1, 1.9%). Of note, 77.8% (42/54) of isolates were isolated from patients in two ICU wards (ICU-1, respiratory medicine department; ICU-2, department of critical care medicine), and remaining 22.2% (12/54) of isolates were isolated from other seven medical wards. Specifically, the ICU-1 ward (with 14 beds) and ICU-2 ward (with 12 beds) belonged to two departments and were located in two different buildings with a distance of about 100 m. There were no intercommunications of patients, staffs, and medical instruments between the two ICU wards. Patients in the two ICU wards were scattered in patient rooms or beds.
Among the 54 KPC-KP (bla KPC-2), 1.9% (1/54) carried bla SHV-11, 48.1% (26/54) carried bla SHV-11 and bla TEM-1, and the remaining 50% (27/54) carried bla TEM-1 , bla SHV (bla SHV-1, bla SHV-2, bla SHV-11 and bla SHV-12), and bla CTX (bla CTX-M-3 and bla CTX-M-14). Among rmtB-positive KPC-KP (RP-KP) isolates (n = 20), 45.0% (9/20) of isolates carried qnrS and 50.0% (10/20) of isolates carried qnrS and acc(6′)-Ib-cr. However, among rmtB-negative KPC-KP (RN-KP) isolates (n = 34), only 5.9% (2/34) of isolates carried acc(6′)-Ib-cr and 8.8% (3/34) of isolates carried qnrS and acc(6′)-Ib-cr. Resistance genes encoding class B carbapenemase (bla NDM, bla SIM, bla IMP, bla VIM, and bla SPM) and AmpC β–lactamase (bla ACC, bla FOX, bla MOX, bla DHA, bla CIT /bla SPM, and bla EBC) were not detected in any of the isolates.
PBRT revealed that 55.6% (30/54) and 37.0% (20/54) of KP isolates contained IncFIIAs and IncFII, respectively. Specifically, 96.3% (26/27) of isolates in cluster A contained IncFIIAs, and 100% (20/20) of isolates in cluster C contained IncFII. After sequencing, the IncFIIAs confirmed in this study was identified as a new subtype of IncFII, which was characterized with low nucleotide identity (90%) when compared with the IncFIIAs replicon of Salmonella virulence plasmids.
Five predominant isolates (KPN-01, KPN-16, KPN-34, KPN-60, and KPN-69) in cluster A and 11 predominant isolates (KPN-50, KPN-66, KPN-70, KPN-71, KPN-73, KPN-75, KPN-79, KPN-84, KPN-87, KPN-88, and KPN-89) in cluster C were used in conjugation experiments. Of the 16 tested isolates, only one isolate (KPN-69) in cluster A and four isolates (KPN-50, KPN-66, KPN-70, and KPN-88) in cluster C yielded transconjugants. As for replicon type, IncFIIAs and IncFII were confirmed in transconjugants (IncFIIAs: KPN-69; IncFII: KPN-50 and KPN-70). The transconjugant of KPN-69 harbored bla KPC-2 and bla TEM-1. The transconjugant of KPN-50 and KPN-70 harbored bla KPC-2, bla TEM-1, bla CTX-M, and rmtB. The transconjugant of KPN-66 and KPN-88 harbored bla SHV-11 (or bla SHV-12), bla CTX-M, and qnrS.
Resistance rates in cluster C (RP-KP, n = 20) were 100% to ampicillin, piperacillin/tazobactam, cefoxitin, cefepime, aztreonam, imipenem, amikacin, gentamycin, tobramycin, ciprofloxacin, levofloxacin, furantoin, sulfamethoxazole, and 40.0% (8/20) to tigecycline. However, resistance rates in cluster A (RN-KP, n = 27) against aforementioned antibiotics were 100% (27/27), 96.3% (26/27), 92.6% (25/27), 22.2% (6/27), 100% (27/27), 100% (27/27), 0 (0/27), 88.9% (24/27), 7.4% (2/27), 100% (27/27), 100% (27/27), 100% (27/27), and 100% (27/27), respectively, as well as 0 (0/27) to tigecycline, which was characterized with significantly lower resistance rates against cefepime (22.2% vs 100%), amikacin (0 vs 100%), tobramycin (7.4% vs 100%), and tigecycline (0 vs 40.0%) when compared with cluster C (p < 0.05).
Medical records revealed that there were no significant differences in gender (male percentage, 81.5% vs 70.0%; median age, 75 vs 77; median Charlson scores, 6.0 vs 6.0; patient distributions (from ICU wards or transferred from ICU wards), 92.6% vs 95%) in patients between cluster A (n = 27) and cluster C (n = 20). As for the crude mortality, it was significantly higher in cluster C than those in cluster A (80.0% vs 51.9%, p < 0.05). The infection-related mortality in cluster C was higher than those in cluster A although the difference was statistically nonsignificant (25.0% vs 14.8%, p > 0.05).
KPC-KP outbreaks have been previously reported in several provinces of China [4, 7–16]. Compared with Western countries, the prevalence of KPC-KP in China is relatively low (2.9%), as described in a 4000-bed tertiary care hospital . However, KPC-KP is an increasing cause for great clinical concern due to its high antibiotic resistance and pathogenicity. In this study, a nosocomial outbreak caused by KPC-KP is described. As shown in Fig. 1, the first clonal replacement of epidemic KPC-KP occurred in ICU wards is confirmed by PFGE of genomic DNA, S1-PFGE of plasmids, replicon typing, and drug resistant characteristics. RP-KP also seems to have a higher dissemination advantage over RN-KP. Although this outbreak was severe in the ICU wards, it was terminated by effective measures, such as hand hygiene intervention, patient isolation, and environmental cleaning. This study suggests that continuous surveillance system and strict infection control measures are necessary and urgent to prevent the spread or outbreak of KPC-KP in health care facilities. It is noteworthy that bacterial culture and susceptibility test require 3–5 days and outbreak might occur during this period of time. Thus, rapid identification of the pathogens is crucial in the active surveillance culture program. On the other hand, considering that colonization frequently precedes infection, early identification of colonized cases might also reduce infections and potential outbreaks.
Although KPC-KP isolates have been identified worldwide, the spread has been proved to be caused by the dominant KP clones (ST258 and ST11). In China, ST11 is the dominant clone of KPC-KP . Some new sequence types of KP have also been frequently described [17, 33]. Here, we reported a new sequence type (ST2040). Compared with the majority of isolates in cluster C (ICU-2), this clone only contains two plasmids (Fig. 1). During the outbreak period, the new ST2040 was only isolated once and didn’t become the epidemic strain. Although resistances are proved to be associated with reduced fitness and virulence of pathogens [34, 35], the clinical resistant KP isolates could survive in those high-density antibiotic environments (health care facilities and day care centers). Thus, as a multi-drug resistant clone, the fitness and pathogenicity of ST2040 might need to be investigated further.
The most frequently encountered ESBLs are TEM-, SHV-, and CTX-M-type β–lactamases. The bla CTX-M, of which prevalence is increased in KP, is carried mainly by IncFII-type plasmids . In this study, the bla CTX-M genes in isolates are also carried by IncFII-type plasmids and could be transferred by conjugation. On the contrary, IncFIIAs plasmids (a new replicon subtype), which harbor bla KPC-2 , bla TEM-1, and bla SHV-11 in isolates of cluster A, seems to be hard to be conjugative.
In this study, 100% (54/54) of isolates are positive for bla SHV, consistent with the hypothesis that chromosomal bla SHV is ubiquitous in KP . The majority of chromosomal SHV, including SHV-1, SHV-11, and its close relatives, are non-ESBLs enzymes. However, most of ESBLs-type SHV enzymes are plasmid-borne. In this study, the prevalence of ESBLs-type SHV enzymes (SHV-2 or SHV-12) and CTX-M enzymes in cluster C is significantly higher than those in cluster A (60% (12/20) vs 0 (0/27, 100% (20/20) vs 11.1% (3/27)). Thus, higher prevalence of cefepime-resistance KP in cluster C might be attributed to the fact that more isolates carry ESBLs enzymes.
PMQR determinants are increasingly reported in KP . In this study, most (86.7%, 13/15) of the acc(6′)-Ib-cr-positive isolates also carry qnrS (Fig. 1). However, two transconjugants from donor isolates (KPN-66 and KPN-88) co-harbored qnrS and acc(6′)-Ib-cr only carry qnrS, but no acc(6′)-Ib-cr. These results suggest that qnrS and acc(6′)-Ib-cr are located in distinct plasmids, which is different from previous studies that qnr alleles are frequently co-expressed with acc(6′)-Ib-cr on the same plasmid [27, 38]. Interestingly, all 19 PQMR-determinants-producers in cluster C are also bla CTX-M -positive and two transconjugants (KPN-66 and KPN-88) co-carry qnrS and bla CTX-M, indicating a significant correlation between the two determinants among these KP isolates.
Isolates producing 16S rRNA methylase frequently exhibit high level of resistance to almost all clinically important aminoglycosides through methylation of the aminoglycoside-binding site . The resistance mechanism caused by 16S rRNA methylase has been reported in KP, and the prevalence of 16S rRNA methylase genes among clinical KP isolates in China is increasing [40, 41]. KPC-KP isolates are multi-drug resistant, but are usually susceptible to aminoglycosides [42–44]. Aminoglycosides also have a significantly higher microbiologic clearance rate than polymyxin B or tigecycline . Here, 37.0% (20/54) of RP-KP showed strong resistance to amikacin (100%) and tobramycin (100%). Co-production of 16S rRNA methylases in KPC-KP could leave limited therapeutic choices for antibacterial treatment and might be associated with higher mortality in this study.
In summary, we reported a nosocomial outbreak of KPC-KP with clonal replacement and a new sequence type (ST2040) of KP in our hospital. ST11 is the dominant clone. The outbreak mainly occurred in ICU wards. The clonal spread was responsible for this outbreak. Our study also suggested that a high degree of awareness and surveillance of KPC-KP should be given to avoid potential outbreaks, especially in ICU wards.
Clinical and laboratory standards institute
Intensive care unit
Klebsiella pneumoniae carbapenemase
KPC-producing Klebsiella pneumoniae
Minimum inhibitory concentration
Multi-locus sequence typing
PCR-based replicon typing
Pulse field gel electrophoresis
Plasmid-mediated quinolone resistance
ribosomal deoxyribonucleic acid
ribosomal ribonucleic acid
The data and materials can be obtained on request from the authors.
SC designed the study and drafted the manuscript. YL and XY performed the experiments and analyzed the data. LZ collected the data. All authors read and approved the final version of this manuscript.
The authors declare that they have no competing interests.
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