A rapid low-cost real-time PCR for the detection of klebsiella pneumonia carbapenemase genes

  • Lijun Wang1,

    Affiliated with

    • Haitong Gu1 and

      Affiliated with

      • Xinxin Lu1Email author

        Affiliated with

        Annals of Clinical Microbiology and Antimicrobials201211:9

        DOI: 10.1186/1476-0711-11-9

        Received: 28 February 2012

        Accepted: 30 April 2012

        Published: 30 April 2012



        Klebsiella pneumonia carbapenemases (KPCs) are able to hydrolyze the carbapenems, which cause many bacteria resistance to multiple classes of antibiotics, so the rapid dissemination of KPCs is worrisome. Laboratory identification of KPCs-harboring clinical isolates would be a key to limit the spread of the bacteria. This study would evaluate a rapid low-cost real-time PCR assay to detect KPCs.


        Real-time PCR assay based on SYBR GreenIwas designed to amplify a 106 bp product of the bla KPC gene from the159 clinical Gram-negative isolates resistant to several classes of β-lactam antibiotics through antimicrobial susceptibility testing. We confirmed the results of real-time PCR assay by the conventional PCR-sequencing. At the same time, KPCs of these clinical isolates were detected by the modified Hodge test (MHT). Then we compared the results of real-time PCR assay with those of MHT from the sensitivity and specificity. Moreover, we evaluated the sensitivity of the real-time PCR assay.


        The sensitivity and specificity of the results of the real-time PCR assay compared with those of MHT was 29/29(100 %) and 130/130(100 %), respectively. The results of the real-time PCR and the MHT were strongly consistent (Exact Sig. (2-tailed) =1. 000; McNemar test). The real-time PCR detection limit was about 0.8 cfu using clinical isolates.


        The real-time PCR assay could rapidly and accurately detect KPCs -harboring strains with high analytical sensitivity and specificity.


        Real-time polymerase chain reaction Klebsiella pneumonia carbapenemase



        Klebsiella pneumonia carbapenemase


        modified Hodge test


        the Clinical Laboratory Standards Institute


        colony forming unit


        Minimum inhibitory concentration.


        Carbapenems are widely used to treat serious infections caused by multi-resistant Gram-negative bacteria. However, beginning with the initial description of a novel KPC from an isolate of K. pneumoniae in 2001 [1], carbapenem resistance in Enterobacteriaceae has been rapidly increasing. KPCs are able to hydrolyze the carbapenems, and cause resistance to multiple classes of antibiotics. Treatment of KPC-producing bacterial infection is thus a considerable challenge for clinicians. KPCs have been reported worldwide, such as North America, South America, Greece, Israel, Puerto Rico, China and so on [26]. The expanding geographic spread of KPCs underscores the importance of clinical recognition of these enzymes. In addition, KPCs have been found in bacteria other than K. pneumoniae, including K. oxytoca[7, 8], P. mirabilis[9], Acinetobacter spp[6], P. aeruginosa , C. freundii[10], S. marcescens and E. coli[11]. This rapid dissemination of KPC is worrisome. Laboratory identification of KPC-harboring clinical isolates will be critical for limiting the spread.

        However, detection of KPC -harboring stains in the clinical laboratory remained a difficult task. The failure of automated susceptibility testing systems to detect KPC-mediated carbapenems resistance was previously reported [1214]. In 2009, the Clinical Laboratory Standards Institute (CLSI) guidelines (M100) recommended MHT to detect carbapenemase production. Wang et al. [15] noted that false positive results could occur when the MHT was used to detect carbapenemase in ESBL-producing isolates. MHT is time-consuming and not routinely tested for E. cloacae, P. aeruginosa in laboratory, so that many molecular detection of bla KPC genes were evaluated [1619]. Rapid and sensitive bla KPC assays are critical to control the spread of bla KPC-harboring bacteria in hospitalized patients.

        In this paper, we would describe the development of a low-cost real-time PCR assay to screen clinical isolates for bla KPC.

        Materials and methods

        Bacterial strains

        The following reference bacterial strains were the negative controls of bla KPC: K. pneumoniaeATCC13883, extended-spectrum-b-lactamase-positive K. pneumoniaeATCC 700603, A. baumaniiATCC 19606, P. aeruginasaATCC 27853, C. albicansATCC 90029, E. coliATCC25922, E. faeciumATCC 35667 and methicillin-resistant S. aureusATCC 43300.

        The 159 clinical isolates including K. pneumoniae, E. coli, E. cloacae, K. oxytoca, S. marcescens, P. mirabilis, MDR A.baumanii and MDR P. aeruginasa. were recovered from multiple infection sites like blood, wound, sputum, catheter, urine and pleural effusion from Beijing Tongren Hospital. These clinical isolates were resistant to several classes of β-lactam antibiotics, which were identified by antimicrobial susceptibility testing.

        Antimicrobial susceptibility testing

        Antimicrobial susceptibility testing was performed with the Vitek 2 susceptibility card AST-GN13 by Vitek 2 automated system (BioMérieux Inc, Durham, NC) according to the manufacturer’s instructions. Minimum inhibitory concentration (MIC) results of imipenem and ertapenem were classified as susceptible, intermediate, or resistant based on the 2010 CLSI breakpoints (susceptible, ≤ 1 μg/ml and ≤ 0.25 μg/ml; intermediate, 2 μg/ml and 0.5 μg/ml; resistant, ≥ 4 μg/ml and ≥ 1 μg/ml, respectively). However, the AST-GN13 card cannot classify organisms as susceptible to ertapenem without the dilutions less than 0.5 μg/ml. All clinical isolates were subsequently tested by MHT. The indicator strains in MHT were E. coli ATCC 25922 for Enterobacteriaceae and K.pneumoniae ATCC 700603 for non- Enterobacteriaceae like P.aeruginosa[20].

        DNA isolation

        Bacterial strains were grown on MacConkey agar and incubated overnight at 35°C. One colony was resuspended in 100 μl of sterile distilled water and the cells were lysed by heating at 100°C for 10 min. Cellular debris was removed by centrifugation at 13000 g for 10 min, and the supernatant was used as a source of template DNA for amplification.

        For analytical sensitivity based on bacterial colony-forming unit (cfu), DNA isolation was performed using the DNeasy Blood&Tissue Kit (Qiagen Sciences, Maryland, USA) according to the protocol suggested by the manufacture. In brief, a bacterial suspension equivalent to that of a 2.0 McFarland standard was prepared in saline, then 200 μl (8.0 × 107 cfu ) suspension were serially diluted 10-fold in saline. Bacterial total nucleic acid was extracted from 200 μl of each dilution and then eluted in 50 μl elution buffer and stored at −20°C.

        bla KPC detection by PCR –sequencing

        The presence of bla KPC was confirmed by conventional PCR and sequencing [1]. The primers included the forward (5’-TGTCACTGTATCGCCGTC-3’) and the reverse (5’- CTCAGTGCTCTACAGAAAACC-3’) , The PCR reaction system contained 0.5 μM each primer, 2 × EasyTaq PCR SuperMix (TransGen Biotech, Beijing, China) and 2 μl DNA template. The reactions were amplified in a My Cycler thermal cycler (BIO-RAD, USA). Cycling parameters were 5 min at 95°C, followed by 35 cycles of 1 min at 95°C, 30s at 58°C, and 1 min 30 s at 72°C. The PCR amplification was ended by a final extension at 72°C for 10 min. sequencing of the PCR products was commercially performed by SinoGenoMax Co. Ltd (Beijing, China). For sequence analysis, the BLAST program from the National Center for Biotechnology Information Web site was used (http: //www. ncbi. nlm. nih.gov/BLAST).

        bla KPC detection by real-time PCR

        The forward primer sequence (5’-TTGTTGATTGGCTAAAGGG-3’) and reverse primer sequence (5’- CCATACACTCCGCAGGTT-3’) were designed in the conservative region of several bla KPC types (bla KPC −2 to bla KPC-13). The bla KPC amplicon was 106 base pairs (GenBank: EU244644).

        The 25 μl real-time PCR mixture contained 12. 5 μl TransStart Green qPCR super MIX (TransGen Biotech, Beijing, China), 0.5 μl PCR enhancer (TransGen Biotech, Beijing, China), 0.2 μM each primer, 9 μl sterile distilled water and 2 μl DNA template. Real-time PCR amplification was performed using the Roche Light cycler 480 Real-time system (Roche Diagnostics, Mannheim, Germany). Cycling parameters were 5 min at 95°C, followed by 40 cycles of 15 s at 95°C, 15 s at 55°C, and 30 s at 72°C. Single fluorescence detection was performed in each cycle at 55°C. Melting curve acquisitions were done immediately after the final amplification step by heating at 96°C for 5 s, cooling to 55°C for 1 min, and heating slowly at 0.11°C per second to 96°C with continuous fluorescence recording. Melting curves were recorded by plotting fluorescence signal intensity versus temperature. Amplicon melting temperatures(Tm) were determined by calculating the derivative of the curve using Roche Light cycler 480 software. The results were visualized by plotting the negative derivative against temperature.

        Specificity and sensitivity

        In order to determine analytical sensitivity of our assay, bla KPC real-time PCR experiments were performed on 10-fold serial dilutions of bacterial cultures (8.0 × 107 cfu). To evaluate the analytical specificity, a panel of reference stains and clinical strains resistant to several classes of β-lactam antibiotics was tested. For statistical analysis, we used the MHT as the reference standard. The differences between sensitivities of the real-time PCR assay and MHT were evaluated with the McNemar test.


        The specificities of the real-time PCR primers for the detection of bla KPC genes were evaluated by the BLAST search program, available at www.ncbi.nlm.nih.gov.

        The bla KPC real-time PCR assay was negative with DNA extracted from the following reference bacterial isolates: K.pneumoniae ATCC 13883, extended-spectrum-b-lactamase-positive K.pneumoniae ATCC 700603, A. baumanii ATCC 19606, P. aeruginasa ATCC 27853, C. albicans ATCC 90029, E. coli. ATCC25922, E. faeciumATCC 35667 and methicillin-resistant S. aureusATCC 43300.

        159 clinical isolates were categorized according to the susceptibility of imipenem or ertapenem (Table 1). 53 isolates were intermediate to resistant to imipenem or ertapenem, and 106 isolates were susceptible to carbapenems. 29 clinical isolates with carbapenem resistance or decreased susceptibility were positive by MHT and by real-time PCR and sequencing, respectively. The 29 clinical isolates included 20 K. pneumoniae (MICs: imipenem ≥ 16 μg/ml, ertapenem ≥ 8 μg/ml), 3 E. coli (one strain MICs: imipenem ≤ 1 μg/ml, ertapenem = 2 μg/ml; two strains MICs: imipenem ≥ 16 μg/ml, ertapenem ≥ 8 μg/ml), 4 E. cloacae (MICs: imipenem ≥ 16 μg/ml, ertapenem ≥ 8 μg/ml), one S. marcescens (MICs: imipenem ≥ 16 μg/ml, ertapenem ≥ 8 μg/ml), and one MDR A. baumanii (MICs: imipenem ≥ 16 μg/ml, ertapenem ≥ 8 μg/ml). One carbapenem-resistant isolate of K. pneumoniae (MICs: imipenem ≥ 16 μg/ml, ertapenem ≥ 8 μg/ml) recovered from sputum was MHT ( − ) / bla KPC ( − ) in our assay. In addition, both isolate of K. pneumonia (MICs: imipenem ≤ 1 μg/ml, ertapenem ≥ 8 μg/ml) and E. coli (MICs: imipenem ≤ 1 μg/ml, ertapenem = 2 μg/ml) were MHT ( − ) / bla KPC ( − ), which were recovered from catheter. All 130 isolates (33 K. pneumoniae, 42 E. coli, 15 E. cloacae, 10 K. oxytoca, one S. marcescens, 8 P. mirabilis, 10 MDR A. baumanii and 11 MDR P. aeruginasa ) were MHT ( − ) / bla KPC ( − ) (Table 2). The sensitivity of the real-time PCR assay as compared to the MHT was 29/29(100 %) with a specificity of 130/130 (100 %). The results of the real-time PCR and the MHT were strongly consistent (Exact Sig. (2-tailed) =1.000; McNemar test).
        Table 1

        Results of Carbapenem susceptibility and MHT of clinical isolates


        No. of isolates

        No. of Carbapenem susceptibility

        No. of MHT*

        Intermediate to resistant




        K. pneumoniae






        E. coli






        E. cloacae






        K. oxytoca






        P. mirabilis






        S. marcescens






        MDR A. baumanii






        MDR P. aeruginasa






        *: MHT modified Hodge test.

        Table 2

        bla KPC Real-time-PCR results compared with the MHT.

        bla KPC Real- time-PCR*










        *: The percent sensitivity was 100 %, and the percent specificity was 100 %.

        Exact Sig. (2-tailed) =1.000; McNemar test.

        All bla KPC genes of KPC-producing isolates in this study were verified as bla KPC-2 by sequencing assay.

        The bla KPC amplicon was distinguished by its specific Tm value. Under our experimental conditions, analysis of the melting curve profile of the PCR products indicated that the products peaked at about 89°C (Figure 1).
        Figure 1

        Plot of the negative derivative of the melting curves vs. temperature: peak indicates the Tm (about 89°C) of isolates. NTC: no template control.

        The analytical sensitivity of the bla KPC real-time PCR assay was determined after serially diluting known concentrations (8.0 × 107 cfu) of clinical isolated carbapenems-resisant K. pneumoniae. The dynamic range of the assay covered nine orders of magnitude from 8.0 × 107 to 0.8 cfu. bla KPC specific fluorescent peaks were detected in the isolates dilutions to about 0.8 cfu (Figure 2).
        Figure 2

        Analytical sensitivity of the bla KPC real-time-PCR assay showing a minimum detection limit of 0.8 CFU.


        Along with the wide use of carbapenem antibiotics, KPCs appeared a major public health concern. Bacterial isolates producing KPCs are able to hydrolyze a broad spectrum of β-lactams including the penicillins, cephalosporins, carbapenems and monobactam. They have the potential to spread rapidly in hospital environments to cause nosocomial infections with high mortality rates [21]. KPC-producing Enterobacteriaceae stains are increasingly spreading throughout China [2, 9, 11, 22]. The dominant clone of KPC-producing K. pneumoniae in China is ST11, which is closely related to ST258 reported worldwide [23]. A rapid method confirming KPCs is significant to control this spread.

        In 2009, the CLSI recommended MHT to screen for the production of carbapenemase in Enterobacteriaceae isolates with elevated MICs for carbapenems or reduced inhibition zones measured by disc diffusion. In 2010, Carbapenem breakpoints have changed in M100-S20U and M100-S21 with 2-fold lower MICs of each category (susceptible, intermediate, and resistant) for the Enterobacteriaceae for imipenem, meropenem, and ertapenem. According to the new criteria, the initial screen test and the confirmatory test by MHT are no longer necessary for routine patient testing. However, one isolate of E. coli with MIC to imipenem as low as 1 μg/ml was confirmed as MHT ( + ) / bla KPC ( + ) in our study. Decreased ertapenem susceptibility has been considered as one of the most sensitive phenotypic indicators of KPC production, but it has been found to be nonspecific [24, 25]. In our laboratory, two clinical isolates MICs to ertapenem as high as 2 μg/ml to 8 μg/ml were MHT ( − ) / bla KPC ( − ). Despite CLSI new recommendations, our laboratory continued to confirm KPC using MHT or PCR.

        The sensitivity and specificity of the MHT have been shown to exceed 90 %; however, several reports have noted false positive results occurred when the MHT was used to detect carbapenemase in ESBL-producing isolates [15, 26]. In addition, it may not be the ideal phenotypic confirmatory test for KPCs since interpretation can be difficult for some isolates such as A. baumanii, P. aeruginasa. In our study, we adjusted the indicator stain to K. pneumoniaeATCC 700603 for non- Enterobacteriaceae in order to eliminate the incidence of indeterminate results of MHT [20]. Thus, an alternative method may prove to be more useful. During the recent few years, molecular methods have been used to rapidly detect bla KPC genes. In particular, real-time PCR assays offered the advantage of shorter turnaround time, which were even developed to detect KPC-containing strains with high analytical specificity and sensitivity in surveillance specimens [27, 28].

        In this study, we validated a rapid, sensitive, and specific real-time-PCR assay for the detection of bla KPC genes. This assay can be performed in less than 4 hours, which will reduce the chance of spreading the organism in the hospital. The real-time PCR assay specifity and sensitivity were 100 % compared to phenotypic KPC activity assessed by MHT and sequencing. Thirteen KPC gene variants have been described, classified in sequential numeric order from bla KPC-1/2 to bla KPC-13. The bla KPC genes are characterized by nonsynonymous single nucleotide substitutions [17]. Our sequencing results showed all 29 KPC-producing isolates harbored bla KPC-2 gene. KPC-2 clinical isolates were widely isolated in most parts of China [23, 29]. Last year, Li et al [30] in China firstly described KPC-3-harboring E. coli and C. freundii. Although KPC-2 and KPC-3 were well described throughout China, we designed the primers in conservative areas to ensure that our assay could almost detect the variants currently described. We identified bla KPC genes by melting curve analysis of the amplification product using SYBR GreenIwith many advantages like low-cost and easy to use. The Tm value of the bla KPC gene was detected at about 89°C. Our assay sensitivity is about one cfu sufficient to detect bla KPC–containing isolates.


        The real-time PCR assay described here provides a useful screening test to detect bla KPC genes rapidly and accurately. Although the real-time PCR assay was unable to identify the specific gene in the bla KPC family in clinical isolates, accurate and rapid identification of this kind of resistance genes is the first step to control their spread.



        The National Science Foundation of China (No. 30970126) and Research Foundation of Beijing Tongue Hospital Affiliated to Capital Medical University (No. 2012-YJJ-010) financially supported this work.

        Authors’ Affiliations

        Department of Laboratory Medicine, Beijing Tongren Hospital, Capital Medical University


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