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Whole genome sequence revealed the fine transmission map of carbapenem-resistant Klebsiella pneumonia isolates within a nosocomial outbreak

Antimicrobial Resistance & Infection Control volume 7, Article number: 70 (2018) Cite this article

Abstract

Background

Carbapenem-resistant Klebsiella pneumoniae (CRKP) is a major cause of nosocomial infections worldwide. The transmission route of CRKP isolates within an outbreak is rarely described. This study aimed to reveal the molecular characteristics and transmission route of CRKP isolates within an outbreak of nosocomial infection.

Methods

Collecting case information, active screening and targeted environmental monitoring were carried out. The antibiotic susceptibility, drug-resistant genes, molecular subtype and whole genome sequence of CRKP strains were analyzed.

Results

Between October and December 2011, 26 CRKP isolates were collected from eight patients in a surgical intensive care unit and subsequent transfer wards of Beijing Tongren hospital, China. All 26 isolates harbored blaKPC-2, blaSHV-1, and blaCTX-M-15 genes, had the same or similar pulsed-field gel electrophoresis patterns, and belonged to the sequence type 11 (ST11) clone. By comprehensive consideration of genomic and epidemiological information, a putative transmission map was constructed, including identifying one case as an independent event distinct from the other seven cases, and revealing two transmissions starting from the same case.

Conclusions

This study provided the first report confirming an outbreak caused by K. pneumoniae ST11 clone co-harboring the blaKPC-2, blaCTX-M-15, and blaSHV-1 genes, and suggested that comprehensive consideration of genomic and epidemiological data can yield a fine transmission map of an outbreak and facilitate the control of nosocomial transmission.

Background

Carbapenems remain the first-line therapeutic antimicrobials for severe infections caused by extended-spectrum β-lactamase (ESBL)-producing multidrug-resistant Enterobacteriaceae. However, the emergence of carbapenemase-mediated resistance to all β-lactams, including carbapenems, is a major public health threat [1, 2]. Over the last decade, carbapenem resistance, attributed to the production of carbapenem-hydrolyzing β-lactamases, has been steadily increasing among Enterobacteriaceae isolates, particularly Klebsiella pneumoniae [3]. Carbapenem-resistant K. pneumoniae (CRKP) has emerged in many countries as a result of intra-continental and inter-continental spread [4–6].

Clinically, the K. pneumoniae carbapenemase (KPC) enzyme is one of the most prevalent carbapenemases. The blaKPC genes are predominantly plasmid encoded. In some cases, blaKPC genes exist in particularly clones (such as K. pneumoniae multilocus sequence type (ST) 258 and ST11, which have facilitated their rapid dissemination. Since the first KPC-producing isolate was identified from North Carolina, USA, in 1996 [7], the occurrence of KPC-producing bacteria has been continuously reported in other parts of the USA, Europe, South America, the Middle East, and Asia [5, 8–10]. They have been associated with large nosocomial outbreaks worldwide, including those in China. The CRKP outbreak isolates in China mostly carried blaKPC-2 [11–14] or blaNDM-1 [15–18]. KPC-producing members of the family Enterobacteriaceae have also been associated with high mortality rates, particularly among critically ill patients with a history of prolonged hospitalization [19–21]. These facts strongly suggest a need for the implementation of adequate preventive measures to effectively control the spread of such pathogens.

From October 8th to December 23th, 2011, a total of 12 CRKP strains were isolated from clinical samples of eight patients admitted to the surgical intensive care unit (SICU). Active screening and targeted environmental monitoring were carried out between October 11th and October 27th, and eight CRKP were isolated from nose and throat of inpatient in SICU, as well as environmental samples. Furthermore, six CRKP were retrieved from one case in subsequent transfer wards. In the present study, we carried out a retrospective investigation of the molecular and genomic epidemiology of the outbreak.

Methods

Retrospective analysis of medical records

The medical records of patients from whom CRKP was isolated were reviewed, including time of stay in SICU, bed site, data of the first CRKP isolation, and outcomes. CRKP is defined as resistance to carbapenems according to the Clinical and Laboratory Standards Institute (CLSI) breakpoints [22].

Active screening and targeted environmental monitoring

Targeting KPC-2 K. pneumoniae, active screening and environmental monitoring were carried out as measures of infection control between October 11th and October 27th. The method of active screening and targeted environmental monitoring was described previously [23]. In brief, for active screening, we collected samples from the nose, throat, groin, and axilla of each patient using sterile cotton swabs (the sputum and stool samples were included in our clinical samples), and a real-time PCR assay was used to screen all samples for blaKPC [24]. The first swab of each patient was taken within 48 h upon ICU admission. For targeted environmental monitoring, six environmental sites on the bed sheet were sampled for each KPC-KP positive patient using contact plates (16 cm2; Qingdao Classical Biochemical Equipment, Qingdao, China).

Bacterial identification and antimicrobial susceptibility

Bacterial identification and antibiotic susceptibility testing were initially performed using the VITEK-2 automated system (BioMérieux, France). Escherichia coli ATCC 25922 was used as quality control strain for antibiotic susceptibility testing. Susceptibility category was designated according to the Clinical and Laboratory Standards Institute (CLSI) breakpoints [22]. Susceptibility to tigecycline was defined based on the criteria proposed by the European Committee on Antimicrobial Susceptibility Testing-2011 (susceptible, minimum inhibitory concentration (MIC) ≤ 1 μg/ml).

Phenotypic screening for the presence of carbapenemase was performed using the modified Hodge test (MHT). In addition, ESBL production was tested using the Double-Disk Synergy Test (DDST), as recommended by the CLSI [22].

Determination of carbapenemase genes

We screened carbapenem-resistance genes (blaKPC, blaNMC, blaSME, blaIMI, blaGES, blaNDM, blaIMP, blaVIM, blaSPM, blaGIM, blaSIM, blaOXA-48, blaOXA-51-like, blaOXA-23-like, blaOXA-24-like, blaOXA-58-like, in all strains as described previously [5, 25, 26]. DNA sequencing was performed on both strands of the PCR amplification products. The results were compared and aligned with reference sequences using the online BLAST database.

Pulsed-field gel electrophoresis (PFGE)

We used the 1-day, standardized PFGE protocol for K. pneumoniae [27]. Cell suspensions were placed in polystyrene tubes (Falcon; 12 × 75 mm), and their optical density was adjusted to 3.8–4.0 using a Densimat photometer (BioMérieux, Marcy l’Etoile, France). K. pneumoniae slices were digested using 50 U per slice of XbaI (Takara, Dalian, China) for 4 h at 37 °C, and electrophoresis was performed using a CHEF-DRIII system (Bio-Rad Laboratories, Hercules, CA, USA). Electrophoresis was run with a switch time of 6 s to 36 s for 18.5 h, and images were captured using a Gel Doc 2000 system (Bio-Rad) and converted to TIFF files. The TIFF files were analyzed using the BioNumerics version 5.1 software (Applied Maths, Kortrijk, Belgium).

Multilocus sequence typing (MLST)

MLST with seven genes (gapA, infB, mdh, pgi, phoE, rpoB, and tonB) was performed on isolates according to the protocol described on the K. pneumoniae MLST website (http://bigsdb.pasteur.fr/). Alleles and STs were assigned using the MLST database (http://bigsdb.pasteur.fr/klebsiella/klebsiella.html). Alleles and STs that had not been previously described were submitted to the curator of the database and were assigned new designations.

Whole genome sequencing (WGS), detection of single nucleotide polymorphisms (SNPs), and clustering analysis

The initial strains of each case were selected for WGS. Bacterial strains were sequenced using Illumina sequencing by constructing two paired-end (PE) libraries with average insertion lengths of 500 bp and 2000 bp, respectively. Sequences were generated using an Illumina GA IIx (Illumina Inc., San Diego, CA, USA). Raw data was processed in four steps, including removing reads with 5 bp of ambiguous bases, removing reads with 20 bp of low quality (≤ Q20) bases, removing adapter contamination, and removing duplicated reads. Finally, 100× libraries were obtained with clean PE read data. Assembly was performed using SOAPdenovo v1.05 [28].

The whole-genome sequence of K. pneumoniae HS11286 (GenBank accession: NC_016845.1) was used as the reference sequence, and clean reads of sequenced isolates were mapped to the reference genome by bowtie 2 software under the default parameters [29]. SNPs were then identified using Samtools [30] and combined together according to the reference. SNPs with low quality (read depth < 5) and those located within 5 bps on the same chromosome were removed to avoid the effect of recombination, as described in our previous studies [31, 32]. The isolates were clustered and a heatmap was generated using the heatmap package in R. The transmission route was then reconstructed based on the emergence of different SNPs in each isolate and the case information, including the onset time of infection and the hospitalization time.

Results

Outbreak descriptions

The outbreak occurred in the SICU of Beijing Tongren Hospital, a 1600-bed general tertiary care and university-affiliated teaching hospital in Beijing, China. Beijing Tongren Hospital receives an average of 3500–5000 outpatients and emergency patients per day. SICU has 18 beds.

The index case of this outbreak was identified on October 8th, 2011. Following identification of second CRKP-infection case in the same room on October 10th, and a CRKP carrier on October 11th, an outbreak was declared. Between October 8 and December 23, a total of 50 patients were admitted into the SICU and eight of them were found to have a CRKP infection or colonization though routine clinical culture and active screening (Table 1). The timeline of patient admission and CRKP isolation is showed in Fig. 1.

Table 1 Case descriptions involved in the outbreak of SICU, October to December 2011
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Fig. 1
figure 1

The timeline of patient admission and CRKP isolation. Shadows on the timeline represent the admitting’s duration of the case. Different wards are indicated in different colors. The red arrow indicates the isolation of the strains

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Among the eight patients, four were infected by CRKP and other four were CRKP carrier. Of the four infection cases, one died, one was discharged from the SICU, and two were transferred to other wards and ultimately discharged. It should be noted that cases 1 to 7 overlapped with at least three other cases when in the SICU, but case 8 did not overlap with any other case during SICU stay.

CRKP detected twice from the the bed sheets of case 4 during the outbreak. In addition to active screening and targeted environmental monitoring, other stringent infection prevention and control measures were implemented, including contact precautions, strengthen of hand hygiene, environmental cleaning (including changing the bed linen more frequently for each CRKP-positive patient, and immediately stringent terminal sterilization with hydrogen peroxide after they were discharged from the ward or died), and enhanced antimicrobial stewardship were introduced. For the patients transferred to other wards, contact precautions and follow-up screening were employed until they were discharged from our hospital. Since January 22, 2012 (the discharge date of the last patients with CRKP colonization), over a period of 10 months, no further carbapenem-resistant Enterobacteriaceae (CRE) were isolated in the SICU.

Antibiotic susceptibility and characterization of resistance genes

All 26 CRKP isolates showed same results of antibiotic susceptibility test. The MICs of meropenem, imipenem, and ertapenem were ≥ 16 μg/ml, ≥ 16 μg/ml, and ≥ 8 μg/ml, respectively, for all isolates. All isolates were susceptible to amikacin ((MIC ≤2 μg/ml), gentamicin (MIC ≤1 μg/ml), tobramycin (MIC ≤1 μg/ml), and trimethoprim/sulfamethoxazol (MIC ≤1:19 μg/ml), and were resistant to ampicillin (MIC ≥32 μg/ml), ampicillin/sulbactam (MIC ≥32 μg/ml), piperacillin (MIC ≥128 μg/ml), piperacillin/tazobactam (MIC ≥128 μg/ml), cefazolin (MIC ≥64 μg/ml), cefotetan (MIC ≥64 μg/ml), ceftazidime (MIC ≥64 μg/ml), ceftriaxone (MIC ≥64 μg/ml), cefepime (MIC ≥64 μg/ml), aztreonam (MIC ≥64 μg/ml), ciprofloxacin (MIC ≥4 μg/ml), levofloxacin (MIC ≥8 μg/ml), nitrofurantoin (MIC ≥512 μg/ml), and tigecycline (MIC ≥2 μg/ml). All isolates were positive for carbapenemase and ESBL production by the MHT and DDST assays, respectively. We further confirmed the presence and production of carbapenemases and ESBLs by PCR and sequencing. All 21 isolates harbored the blaKPC-2, blaSHV-1, and blaCTX-M-15 genes and tested negative for other antimicrobial resistance genes (blaNMC, blaSME, blaIMI, blaGES, blaNDM, blaIMP, blaVIM, blaSPM, blaGIM, blaSIM, blaOXA-48, blaOXA-51-like, blaOXA-23-like, blaOXA-24-like, blaOXA-58-like, and blaTEM).

Molecular subtyping analysis by PFGE and MLST

MLST indicated that all 26 isolates belonged to ST11. However, PFGE showed some diversity (Fig. 2). PFGE divided the 26 isolates into seven different PFGE types (PT1–PT7). The dominant PFGE type (PT3) contained 19 isolates. The other six PFGE types showed one to four bands that were different to the dominant PFGE type (PT3). Except for cases 4 and 8, all the first positive cultures from each affected patients belonged to the dominant PFGE type (PT3). The isolates of case 4 (PT4) and case 8 (PT2) showed one and three bands that were different to those of PT3, respectively. Using the interpretation criteria of PFGE patterns proposed by Tenover et al. [33], the first positive culture of cases 1, 2, 3, 5, 6, 7 were the “same strain” and those of cases 4 and 8 were “closely-related strains”.

Fig. 2
figure 2

Clustering of the 26 K. pneumoniae isolates based on PFGE patterns. The first positive cultures of each case are marked by an asterisk. The information of strain ID, PFGE type, patient ID, isolation date, ward, type of specimen, and MLST type is listed to the left of the patterns. ADF, abdominal drainage fluid; BAL, bronchoalveolar lavage

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Excepting for case 8, all six isolates showing different patterns to the dominant PFGE type were isolated from case 4, including three strains from urine, one from sputum, and two from the bed sheet. The two strains isolated from the bed sheet (TRqt-47 and TRqt-48) of case 4 showed one band that was different to the strain isolated from the nose (TRqt-43) on the same day. It was interesting that with increasing time, the PFGE patterns of the strains from case 4 also changed, especially isolates from December 2011. All the strains isolated in October showed dominant patterns or showed only one band different from the dominant pattern; two strains isolated in November (TR221, TR231-m) showed two bands that were different from dominant pattern and another strain isolated in December (TR258) showed four bands that were different from dominant pattern.

Comparison of outbreak isolates based on WGS-based SNPs

We performed WGS and MCG typing of the 26 CRKP isolates, in hope of using the SNPs found in their genomes to determine putative transmission map of this outbreak. Genomic comparisons revealed a total of 32 MCG SNPs among the 26 isolates (Fig. 3). The evolutionary relationships based on MCG typing of the 26 CRKP isolates are outlined and presented in Fig. 4.

Fig. 3
figure 3

Clustering of the 26 K. pneumoniae isolates based on MCG typing. The first positive cultures of each case are marked by an asterisk. The information of strain ID, patient ID, type of specimen, isolation date, and ward are listed to the left of the patterns. ADF, abdominal drainage fluid; BAL, bronchoalveolar lavage

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Fig. 4
figure 4

Evolutionary relationships based on MCG typing of 26 CRKP isolates. Isolates from different patients are indicated in different colors. The first positive cultures of each case are marked by an asterisk

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Five case 2 strains isolated in October showed the same SNP profile as the reference strain K. pneumoniae HS11286. The other case 2 strains isolated in early and late November had one and two SNPs that were different to the reference strain, respectively. All isolates from cases 1 and 3 had only one SNP difference to the reference strain. At the same time, two isolates from case 4, one isolate from case 6, and two isolates from case 7 had the same SNP profile and showed only one SNP difference to the reference strain.

It is worth noting that four case 4 isolates, two from the bed sheet (TRqt-47, TRqt-48) and two from urine (TR221, TR231-m), showed 7–10 SNP differences compared with the initial isolate (TR198) of case 4, and another urine isolate of case 4 (TR258) isolated later had only two SNP differences to TR198, suggesting that the CRKP isolated from case 4 during the study period came from a different source.

The isolate of case 8 (TR262) showed 6–18 SNP differences with other isolates and had five specific SNPs. To determine whether case 8 is related to the other seven cases, the initial isolates of each case were chosen and analyzed. Grouping the eight initial isolates on the basis of the patterns of shared variants partitioned them into two clusters (Fig. 5). Cluster 1 contained seven isolates of cases 1 to 7, and cluster 2 consisted only of case 8. The pairwise distances within cluster 1 were ≤ 3 SNP differences; in contrast, the distances between cluster 2 and cluster 1 isolates were 8 SNP differences. The within-cluster distance of cluster 1 was much smaller than the between-cluster distance, indicating considerable divergence between the two clusters. The epidemiological information of case 8 indicated that they had not overlapped during their hospital stay with any of the other seven patients; therefore, we deduced that cases 1 to 7 probably shared the same transmission route and that case 8 seemed to be an independent event.

Fig. 5
figure 5

Clustering of the eight first positive CRKP cultures of each case based on MCG typing. The matrix of the SNP differences is presented on the left of the cluster tree

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Inference of most likely transmission route

Furthermore, the genomic and epidemiological information were integrated to construct the transmission route. The most likely transmission route is shown in Fig. 6. First, case 2 was suspected of being the source of the outbreak isolates because the CRKP from case 2 showed the same SNP patterns to reference strain K. pneumoniae HS11286. This was also supported by the epidemiological information. Case 1 admitted in the SICU on September 30th, 2011, 9 days before the first CRKP was isolated, which suggested that the CRKP of case 1 was acquired in the hospital. Thus Case 1 is unlikely to be the source. Case 3 checked in the SICU on October 8th, 2011, the same day of first CRKP isolation of case 1; however, case 3 checked in the SICU in the afternoon, and the CRKP-positive sample had already been collected from case 1 in the morning, which suggested that the CRKP of case 1 was not transmitted from case 3. Thus, case 2 was the most likely source of the outbreak isolates.

Fig. 6
figure 6

Putative map of CRKP transmission during the outbreak. The transmission map was constructed with genetic and patient trace data. Nodes represent patients, and arrows indicate a transmission event directly from one patient to another

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Second, the isolates of cases 1 and 3 showed no SNP differences, suggesting direct transmission between them. However, it could not be confirmed that whether case 2 directly transmitted CRKP to case 1 or case 3.

Third, the case 2’s isolate showed one SNP difference to isolates of cases 4 and 7, but two SNP differences to that of cases 5 and 6, suggesting that CRKP from case 2 was genomically closer to cases 4 and 7. However, case 7’s hospital stay did not overlap with that of case 2 and the date of the first isolation of CRKP from case 7 was significantly later than the other cases; therefore, we deduced the case 7’s isolate was transmitted from case 2 through case 4. The isolates of cases 5 and 6 were transmitted from case 4, as there was only one SNP between isolates cases 5 and 6 and that from case 4, but showed more SNPs differences to that of other cases.

Consistent with the genomic and epidemiological information, the integrated map identified two transmissions starting from case 2 (Fig. 6). The first transmission was directly from case 2 to case 1 or case 3, and a transmission was observed between cases 1 and 3. A second transmission from case 2 was predicted to go through case 4 before being transmitted to cases 5, 6, and 7.

Discussion

In this study, we described an outbreak caused by CRKP in a SICU of a large university hospital in China. The CRKP isolates belonged to clone ST11, and coproduced carbapenemase (KPC-2) and ESBLs (CTX-M-15 and SHV-1). ST11 is the dominant clone of KPC-producing K. pneumoniae in China and has also been reported sporadically in the rest of the world, including other regions of Asia [34, 35], America [36], and Europe [37–39]. KPC is the most common carbapenemase in K. pneumoniae and most of the KPC type in China is KPC-2 [40]. Similarly, CTX-M-15 and SHV-1 are the main types of CTX-M-type and SHV-type in China [41]. The coexistence of blaKPC-2 with blaCTX-M-15 type genes in K. pneumoniae was previously reported in Bulgaria [42], Brazil [43], and China [44]. In a recent study, CRKP strains co-harboring the blaKPC-2, blaCTX-M-15, and blaSHV genes were found in several STs including ST11; however, only sporadic strains were reported in that study [44]. As far as we know, this is the first study to report an outbreak caused by CRKP co-harboring the blaKPC-2, blaCTX-M-15, and blaSHV-1 genes, which suggests that attention should be paid to the K. pneumoniae isolates coproducing epidemic carbapenemases and ESBLs, especially the outbreak strains described here belonging to the epidemic ST11 clone.

Given the easy of transfer and acquisition of carbapenemase and ESBLs genes, measures must be implemented to control the outbreak and avoid nosocomial transmission [2, 45]. Agodi et al. reported that cleaning and disinfection of the ICU, segregation of affected patients, barrier nursing, and strict compliance with hand hygiene procedures led to containment of an outbreak of KPC-producing K. pneumoniae [46]. In our study, we applied active screening and targeted environmental monitoring to combat the secondary transmission of imported KPC clones in the SICU. Except for the two index cases, we found that six patients acquired this pathogen during their hospital stay, two of them with urinary tract infections. Some reports stated that the rectum was the most sensitive sampling site for universal screening of CRE [47]. However, during the period of our study, the nose, throat, and sputum were also sensitive sites to detect CRE, which might suggest, indirectly, the important role of the respiratory tract in dissemination during the outbreak. Therefore, it is important to apply active screening with nose, throat, and sputum sampling to detect hospital-acquired cases early during an outbreak.

Additionally, the genetic relatedness between the strains judged by the interpretation criteria proposed by Tenover et al. [33], we drew two additional inferences concerning the strains from case 4. First, with increasing time, the PFGE patterns of strains from case 4 changed, suggesting that genome mutations occurred in the bacteria in vivo for case 4, which was also proved by whole genome sequencing and comparison. Second, the two strains from the bed linen of case 4 were isolated from the same patient at the same time. However the PFGE patterns of the two strains were different. This result may be explained if the two isolates contaminated the bed linen at different times.

Using PFGE, the strain isolated from case 8 was a “closely-related strain” to the other strains. However, case 8 showed weak epidemiological relevance to the other cases, because this case did not overlap with any other case during their SICU stay. So we could not judge the relationship between case 8 and the other cases. We further used WGS-SNP analysis to study the population structure of CRKP isolates from eight cases to reveal the relationships among them. WGS-SNP divided the isolate from case 8 far from the strains of other cases. By combination of the epidemiological information and molecular results, we deduced that (i) cases 1 to 7 were on the same transmission route and that case 8 was an independent event; (ii) case 2, but not case 1 (the index patient), was the source of CRKP in this outbreak; (iii) there were two transmissions starting from case 2.

Conclusions

Though this study is a retrospective study and thus the results of the WGS could not be used to control the nosocomial transmission. However, our data clearly showed that WGS and MCG typing could reveal the details of transmission within a CRKP nosocomial outbreak. In the future, real-time genomic sequencing and analysis of an outbreak should be carried out and the findings could be used to control outbreaks.

Abbreviations

CLSI:

Clinical and Laboratory Standards Institute

CRE:

carbapenem-resistant Enterobacteriaceae

CRKP:

Carbapenem-resistant K. pneumoniae

DDST:

Double-Disk Synergy Test

ESBL:

extended-spectrum β-lactamase

KPC:

K. pneumoniae carbapenemase

MHT:

modified Hodge test

MIC:

minimum inhibitory concentration

MLST:

Multilocus sequence typing

PFGE:

Pulsed-field gel electrophoresis

SICU:

surgical intensive care unit

SNP:

detection of single nucleotide polymorphism

ST:

sequence type

WGS:

Whole genome sequencing

References

  1. Tangden T, Giske CG. Global dissemination of extensively drug-resistant carbapenemase-producing Enterobacteriaceae: clinical perspectives on detection, treatment and infection control. J Intern Med. 2015;277:501–12. https://0-doi-org.brum.beds.ac.uk/10.1111/joim.12342.

    CAS  PubMed  Google Scholar 

  2. Chabah M, Chemsi M, Zerouali K, Alloula O, Lehlimi M, Habzi A, et al. Healthcare-associated infections due to carbapenemase-producing Enterobacteriaceae: bacteriological profile and risk factors. Med Mal Infect. 2016;46:157–62. https://0-doi-org.brum.beds.ac.uk/10.1016/j.medmal.2015.12.015.

    CAS  PubMed  Google Scholar 

  3. Brink A, Coetzee J, Clay C, Corcoran C, van Greune J, Deetlefs JD, et al. The spread of carbapenem-resistant Enterobacteriaceae in South Africa: risk factors for acquisition and prevention. S Afr Med J. 2012;102:599–601.

    PubMed  Google Scholar 

  4. Grundmann H, Livermore DM, Giske CG, Canton R, Rossolini GM, Campos J, et al. Carbapenem-non-susceptible Enterobacteriaceae in Europe: conclusions from a meeting of national experts. Euro Surveill. 2010;15.

  5. Nordmann P, Naas T, Poirel L. Global spread of Carbapenemase-producing Enterobacteriaceae. Emerg Infect Dis. 2011;17:1791–8. https://0-doi-org.brum.beds.ac.uk/10.3201/eid1710.110655.

    CAS  PubMed  PubMed Central  Google Scholar 

  6. Poulou A, et al. Imported Klebsiella pneumoniae carbapenemase-producing K. pneumoniae clones in a Greek hospital: impact of infection control measures for restraining their dissemination. J Clin Microbiol. 2012;50:2618–23. https://0-doi-org.brum.beds.ac.uk/10.1128/JCM.00459-12.

    PubMed  PubMed Central  Google Scholar 

  7. Yigit H, Queenan AM, Anderson GJ, Domenech-Sanchez A, Biddle JW, Steward CD, et al. Novel carbapenem-hydrolyzing-lactamase, KPC-1, from a carbapenem-resistant strain of Klebsiella pneumoniae. Antimicrob Agents Chemother. 2001;45:1151–61.

    CAS  PubMed  PubMed Central  Google Scholar 

  8. Albiger B, Glasner C, Struelens MJ, Grundmann H, Monnet DL. European survey of Carbapenemase-producing Enterobacteriaceae (EuSCAPE) working group. Carbapenemase-producing Enterobacteriaceae in Europe: assessment by national experts from 38 countries, may 2015. Euro Surveill. 2015;20 https://0-doi-org.brum.beds.ac.uk/10.2807/1560-7917.ES.2015.20.45.30062.

  9. Huang SR, Liu MF, Lin CF, Shi ZY. Molecular surveillance and clinical outcomes of carbapenem-resistant Escherichia coli and Klebsiella pneumoniae infections. J Microbiol Immunol Infect. 2014;47:187–96. https://0-doi-org.brum.beds.ac.uk/10.1016/j.jmii.2012.08.029.

    CAS  PubMed  Google Scholar 

  10. Wei ZQ, Du XX, Yu YS, Shen P, Chen YG, Li LJ. Plasmid-mediated KPC-2 in a Klebsiella pneumoniae isolate from China. Antimicrob Agents Chemother. 2007;51:763–5.

    CAS  PubMed  Google Scholar 

  11. Hu L, Liu Y, Deng L, Zhong Q, Hang Y, Wang Z, et al. Outbreak by ventilator-associated ST11 K. pneumoniae with co-production of CTX-M-24 and KPC-2 in a SICU of a tertiary teaching Hospital in Central China. Front Microbiol. 2016;7:1190. https://0-doi-org.brum.beds.ac.uk/10.3389/fmicb.2016.01190.

    PubMed  PubMed Central  Google Scholar 

  12. Li J, Zou MX, Wang HC, Dou QY, Hu YM, Yan Q, et al. An outbreak of infections caused by a Klebsiella pneumoniae ST11 clone coproducing Klebsiella pneumoniae Carbapenemase-2 and RmtB in a Chinese teaching hospital. Chin Med J. 2016;129:2033–9. https://0-doi-org.brum.beds.ac.uk/10.4103/0366-6999.189049.

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Yu J, Tan K, Rong Z, Wang Y, Chen Z, Zhu X, et al. Nosocomial outbreak of KPC-2- and NDM-1-producing Klebsiella pneumoniae in a neonatal ward: a retrospective study. BMC Infect Dis. 2016;16:563.

    PubMed  PubMed Central  Google Scholar 

  14. Zhan L, Wang S, Guo Y, Jin Y, Duan J, Hao Z, et al. Outbreak by Hypermucoviscous Klebsiella pneumoniae ST11 isolates with Carbapenem resistance in a tertiary Hospital in China. Front Cell Infect Microbiol. 2017;7:182. https://0-doi-org.brum.beds.ac.uk/10.3389/fcimb.2017.00182.

    PubMed  PubMed Central  Google Scholar 

  15. Yu J, Wang Y, Chen Z, Zhu X, Tian L, Li L, et al. Outbreak of nosocomial NDM-1-producing Klebsiella pneumoniae ST1419 in a neonatal unit. J Glob Antimicrob Resist. 2016;8:135–9. https://0-doi-org.brum.beds.ac.uk/10.1016/j.jgar.2016.10.014.

    Google Scholar 

  16. Jin Y, Shao C, Li J, Fan H, Bai Y, Wang Y. Outbreak of multidrug resistant NDM-1-producing Klebsiella pneumoniae from a neonatal unit in Shandong Province, China. PLoS One. 2015;10:e0119571. https://0-doi-org.brum.beds.ac.uk/10.1371/journal.pone.0119571.

    PubMed  PubMed Central  Google Scholar 

  17. Zheng R, Zhang Q, Guo Y, Feng Y, Liu L, Zhang A, et al. Outbreak of plasmid-mediated NDM-1-producing Klebsiella pneumoniae ST105 among neonatal patients in Yunnan, China. Ann Clin Microbiol Antimicrob. 2016;15:10. https://0-doi-org.brum.beds.ac.uk/10.1186/s12941-016-0124-6.

    PubMed  PubMed Central  Google Scholar 

  18. Zhu J, Sun L, Ding B, Yang Y, Xu X, Liu W, et al. Outbreak of NDM-1-producing Klebsiella pneumoniae ST76 and ST37 isolates in neonates. Eur J Clin Microbiol Infect Dis. 2016;35:611–8. https://0-doi-org.brum.beds.ac.uk/10.1007/s10096-016-2578-z.

    CAS  PubMed  Google Scholar 

  19. Kontopoulou K, Protonotariou E, Vasilakos K, Kriti M, Koteli A, Antoniadou E, et al. Hospital outbreak caused by Klebsiella pneumoniae producing KPC-2 beta-lactamase resistant to colistin. J Hosp Infect. 2010;76:70–3. https://0-doi-org.brum.beds.ac.uk/10.1016/j.jhin.2010.03.021.

    CAS  PubMed  Google Scholar 

  20. Schwaber MJ, Lev B, Israeli A, Solter E, Smollan G, Rubinovitch B, et al. Containment of a country-wide outbreak of carbapenem-resistant Klebsiella pneumoniae in Israeli hospitals via a nationally implemented intervention. Clin Infect Dis. 2011;52:848–55. https://0-doi-org.brum.beds.ac.uk/10.1093/cid/cir025.

    PubMed  Google Scholar 

  21. Zarkotou O, Pournaras S, Tselioti P, Dragoumanos V, Pitiriga V, Ranellou K, et al. Predictors of mortality in patients with bloodstream infections caused by KPC-producing Klebsiella pneumoniae and impact of appropriate antimicrobial treatment. Clin Microbiol Infect. 2011;17:1798–803. https://0-doi-org.brum.beds.ac.uk/10.1111/j.1469-0691.2011.03514.x.

    CAS  PubMed  Google Scholar 

  22. Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing: Twenty-first Informational Supplement. M100-S25. Wayne: CLSI; 2015.

    Google Scholar 

  23. Sui W, Wang J, Wang H, Wang M, Huang Y, Zhuo J, et al. Comparing the transmission potential of methicillin-resistant Staphylococcus aureus and multidrug-resistant Acinetobacter baumannii among inpatients using target environmental monitoring. Am J Infect Control. 2013;41:411–5. https://0-doi-org.brum.beds.ac.uk/10.1016/j.ajic.2012.08.007.

    PubMed  Google Scholar 

  24. Wang L, Gu H, Lu X. A rapid low-cost real-time PCR for the detection of Klebsiella pneumonia carbapenemase genes. Ann Clin Microbiol Antimicrob. 2012;11:9. https://0-doi-org.brum.beds.ac.uk/10.1186/1476-0711-11-9.

    PubMed  PubMed Central  Google Scholar 

  25. Dallenne C, Da Costa A, Decre D, Favier C, Arlet G. Development of a set of multiplex PCR assays for the detection of genes encoding important beta-lactamases in Enterobacteriaceae. J Antimicrob Chemother. 2010;65:490–5. https://0-doi-org.brum.beds.ac.uk/10.1093/jac/dkp498.

    CAS  PubMed  Google Scholar 

  26. Woodford N. Rapid characterization of beta-lactamases by multiplex PCR. Methods Mol Biol. 2010;642:181–92. https://0-doi-org.brum.beds.ac.uk/10.1007/978-1-60327-279-7_14.

    CAS  PubMed  Google Scholar 

  27. Han H, Zhou H, Li H, Gao Y, Lu Z, Hu K, et al. Optimization of pulse-field gel electrophoresis for subtyping of Klebsiella pneumoniae. Int J Environ Res Public Health. 2013;10:2720–31. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph10072720.

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Li R, Zhu H, Ruan J, Qian W, Fang X, Shi Z, et al. De novo assembly of human genomes with massively parallel short read sequencing. Genome Res. 2010;20:265–72. https://0-doi-org.brum.beds.ac.uk/10.1101/gr.097261.109.

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Langmead B, Salzberg SL. Fast gapped-read alignment with bowtie 2. Nat Methods. 2012;9:357–9. https://0-doi-org.brum.beds.ac.uk/10.1038/nmeth.1923.

    CAS  PubMed  PubMed Central  Google Scholar 

  30. Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, et al. The sequence alignment/map format and SAMtools. Bioinformatics. 2009;25:2078–9. https://0-doi-org.brum.beds.ac.uk/10.1093/bioinformatics/btp352.

    PubMed  PubMed Central  Google Scholar 

  31. Chen C, Zhang W, Zheng H, Lan R, Wang H, Du P, et al. Minimum core genome sequence typing of bacterial pathogens: a unified approach for clinical and public health microbiology. J Clin Microbiol. 2013;51:2582–91. https://0-doi-org.brum.beds.ac.uk/10.1128/JCM.00535-13.

    CAS  PubMed  PubMed Central  Google Scholar 

  32. Du P, Zheng H, Zhou J, Lan R, Ye C, Jing H, et al. Detection of multiple parallel transmission outbreak of Streptococcus suis human infection by use of genome epidemiology, China, 2005. Emerg Infect Dis. 2017;23(2):204–11. https://0-doi-org.brum.beds.ac.uk/10.3201/eid2302.160297.

    PubMed  PubMed Central  Google Scholar 

  33. Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, et al. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol. 1995;33:2233–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  34. Saito R, Takahashi R, Sawabe E, Koyano S, Takahashi Y, Shima M, et al. First report of KPC-2 Carbapenemase-producing Klebsiella pneumoniae in Japan. Antimicrob Agents Chemother. 2014;58:2961–3. https://0-doi-org.brum.beds.ac.uk/10.1128/AAC.02072-13.

    PubMed  PubMed Central  Google Scholar 

  35. Shin SY, Bae IK, Kim J, Jeong SH, Yong D, Kim JM, et al. Resistance to carbapenems in sequence type 11 Klebsiella pneumoniae is related to DHA-1 and loss of OmpK35 and/or OmpK36. J Med Microbiol. 2012;61(Pt 2):239–45. https://0-doi-org.brum.beds.ac.uk/10.1099/jmm.0.037036-0.

    CAS  PubMed  Google Scholar 

  36. Pereira PS, de Araujo CF, Seki LM, Zahner V, Carvalho-Assef AP, Asensi MD. Update of the molecular epidemiology of KPC-2-producing Klebsiella pneumoniae in Brazil: spread of clonal complex 11 (ST11, ST437 and ST340). J Antimicrob Chemother. 2013;68:312–6. https://0-doi-org.brum.beds.ac.uk/10.1093/jac/dks396.

    CAS  PubMed  Google Scholar 

  37. Baraniak A, Grabowska A, Izdebski R, Fiett J, Herda M, Bojarska K, et al. Molecular characteristics of KPC-producing Enterobacteriaceae at the early stage of their dissemination in Poland, 2008–2009. Antimicrob Agents Chemother. 2011;55:5493–9. https://0-doi-org.brum.beds.ac.uk/10.1128/AAC.05118-11.

    CAS  PubMed  PubMed Central  Google Scholar 

  38. Giakkoupi P, Papagiannitsis CC, Miriagou V, Pappa O, Polemis M, Tryfinopoulou K, et al. An update of the evolving epidemic of bla KPC-2-carrying Klebsiella pneumoniae in Greece (2009–10). J Antimicrob Chemother. 2011;66:1510–3. https://0-doi-org.brum.beds.ac.uk/10.1093/jac/dkr166.

    CAS  PubMed  Google Scholar 

  39. Virgincar N, Iyer S, Stacey A, Maharjan S, Pike R, Perry C, et al. Klebsiella pneumoniae producing KPC carbapenemase in a district general hospital in the UK. J Hosp Infect. 2011;78:293–6. https://0-doi-org.brum.beds.ac.uk/10.1016/j.jhin.2011.03.016.

    CAS  PubMed  Google Scholar 

  40. Zhang R, Liu L, Zhou H, Chan EW, Li J, Fang Y, et al. Nationwide surveillance of clinical Carbapenem-resistant Enterobacteriaceae (CRE) strains in China. EBioMedicine. 2017;19:98–106. https://0-doi-org.brum.beds.ac.uk/10.1016/j.ebiom.2017.04.032.

    PubMed  PubMed Central  Google Scholar 

  41. An S, Chen J, Wang Z, Wang X, Yan X, Li J, et al. Predominant characteristics of CTX-M-producing Klebsiella pneumoniae isolates from patients with lower respiratory tract infection in multiple medical centers in China. FEMS Microbiol Lett. 2012;332:137–45. https://0-doi-org.brum.beds.ac.uk/10.1111/j.1574-6968.2012.02586.x.

    CAS  PubMed  Google Scholar 

  42. Markovska R, Stoeva T, Schneider I, Boyanova L, Popova V, Dacheva D, et al. Clonal dissemination of multilocus sequence type ST15 KPC-2-producing Klebsiella pneumoniae in Bulgaria. APMIS. 2015;123:887–94. https://0-doi-org.brum.beds.ac.uk/10.1111/apm.12433.

    CAS  PubMed  Google Scholar 

  43. Seki LM, Pereira PS, de Souza Conceição M, Souza MJ, Marques EA, Carballido JM, et al. Molecular epidemiology of CTX-M producing Enterobacteriaceae isolated from bloodstream infections in Rio de Janeiro, Brazil: emergence of CTX-M-15. Braz J Infect Dis. 2013;17:640–6. https://0-doi-org.brum.beds.ac.uk/10.1016/j.bjid.2013.03.012.

    PubMed  PubMed Central  Google Scholar 

  44. Yan J, Pu S, Jia X, Xu X, Yang S, Shi J, et al. Multidrug resistance mechanisms of Carbapenem resistant Klebsiella pneumoniae strains isolated in Chongqing, China. Ann Lab Med. 2017;37:398–407. https://0-doi-org.brum.beds.ac.uk/10.3343/alm.2017.37.5.398.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. Carmeli Y, Akova M, Cornaglia G, Daikos GL, Garau J, Harbarth S, et al. Controlling the spread of carbapenemase-producing gram-negatives: therapeutic approach and infection control. Clin Microbiol Infect. 2010;16:102–11. https://0-doi-org.brum.beds.ac.uk/10.1111/j.1469-0691.2009.03115.x.

    CAS  PubMed  Google Scholar 

  46. Agodi A, Voulgari E, Barchitta M, Politi L, Koumaki V, Spanakis N, et al. Containment of an outbreak of KPC-3-producing Klebsiella pneumoniae in Italy. J Clin Microbiol. 2011;49:3986–9. https://0-doi-org.brum.beds.ac.uk/10.1128/JCM.01242-11.

    PubMed  PubMed Central  Google Scholar 

  47. Schechner V, Kotlovsky T, Tarabeia J, Kazma M, Schwartz D, Navon-Venezia S, et al. Predictors of rectal carriage of carbapenem-resistant Enterobacteriaceae (CRE) among patients with known CRE carriage at their next hospital encounter. Infect Control Hosp Epidemiol. 2011;32:497–503. https://0-doi-org.brum.beds.ac.uk/10.1086/659762.

    PubMed  Google Scholar 

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Funding

This work was supported by grants from the National Natural Science Foundation of China (NSFC) [grant number 81371861], the Priority Project on Infectious Disease Control and Prevention [grant number 2012ZX10004215] from the Ministry of Science and Technology of the People’s Republic of China and the Capacity-building project for pathogenic bacteria monitoring from Health and Family Planning Commission of the People’s Republic of China [grant number 131031102000150003]. There is no role of the funding body in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

Availability of data and materials

This WGS project has been deposited at GenBank under the Bioproject ID PRJNA313004, accession numbers LUVP00000000-LUGR00000000.

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Author notes

  1. Wenjun Sui, Haijian Zhou and Pengcheng Du contributed equally to this work.

Authors and Affiliations

  1. Department of Clinical Laboratory, Beijing Tongren Hospital, Capital Medical University, Beijing, 100730, China

    Wenjun Sui, Lijun Wang, Mei Wang, Yanfei Huang & Xinxin Lu

  2. State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, 102206, China

    Haijian Zhou, Tian Qin & Hongyu Ren

  3. Collaborative Innovation Centre for Diagnosis and Treatment of Infectious Diseases, Hangzhou, 310003, China

    Haijian Zhou, Tian Qin & Hongyu Ren

  4. Beijing Key Laboratory of Emerging Infectious Diseases, Institute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, 100015, China

    Pengcheng Du & Chen Chen

  5. Surgical Intensive Care Unit, Beijing Tongren Hospital, Capital Medical University, Beijing, 100730, China

    Jing Hou

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  1. Wenjun Sui
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Contributions

XL and HZ designed the study. WS, LW, MW, YH and JH carried out the data collection, active screening and target environmental monitoring. WS, HZ, TQ and HR carried out the experiments. WS, HZ, PD, TQ and CC performed the data analysis. WS, HZ and XL wrote the manuscript. All authors read and approved the final version of the manuscript.

Corresponding authors

Correspondence to Haijian Zhou, Chen Chen or Xinxin Lu.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the scientific and ethics committees of Beijing Tongren Hospital. All clinical specimens from patients were collected for diagnostic testing in hospitals at the request of the attending doctors. The active screening and targeted environmental monitoring was carried out in the case of an emergency investigation and in accordance with the recommendations of “Emergency treatment plan for hospital infection outbreak in Tongren Hospital” and “2007 Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings (https://www.cdc.gov/infectioncontrol/pdf/guidelines/isolation-guidelines.pdf)”. All experiments were performed in accordance with relevant guidelines and regulations. The consent of the patients for the active screening of specimens, including K. pneumoniae detection, was obtained verbally by medical staff in the hospital. The medical records were considered as legal documents. Furthermore, to protect patient privacy, the hospital set up a patient privacy and medical record management system according to the criminal procedure law, civil procedure law, tort liability law, and medical malpractice law in China. Excepting for the patient’s doctor, no one can enter the management system. Although no written informed consent was provided by patients, the above measures are sufficient to protect the patients’ privacy.

Competing interests

The authors declare that they have no competing interests.

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Sui, W., Zhou, H., Du, P. et al. Whole genome sequence revealed the fine transmission map of carbapenem-resistant Klebsiella pneumonia isolates within a nosocomial outbreak. Antimicrob Resist Infect Control 7, 70 (2018). https://0-doi-org.brum.beds.ac.uk/10.1186/s13756-018-0363-8

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Keywords

Antimicrobial Resistance & Infection Control

ISSN: 2047-2994

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