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A rapid low-cost real-time PCR for the detection of klebsiella pneumonia carbapenemase genes
Annals of Clinical Microbiology and Antimicrobialsvolume 11, Article number: 9 (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 blaKPC 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.
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 , 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 [2–6]. 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, Acinetobacter spp, P. aeruginosa , C. freundii, S. marcescens and E. coli. 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 [12–14]. In 2009, the Clinical Laboratory Standards Institute (CLSI) guidelines (M100) recommended MHT to detect carbapenemase production. Wang et al.  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 blaKPC genes were evaluated [16–19]. Rapid and sensitive blaKPC assays are critical to control the spread of blaKPC-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 blaKPC.
Materials and methods
The following reference bacterial strains were the negative controls of blaKPC: K. pneumoniae ATCC13883, extended-spectrum-b-lactamase-positive K. pneumoniae ATCC 700603, A. baumanii ATCC 19606, P. aeruginasa ATCC 27853, C. albicansATCC 90029, E. coliATCC25922, E. faecium ATCC 35667 and methicillin-resistant S. aureus ATCC 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.
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.
blaKPC detection by PCR –sequencing
The presence of blaKPC was confirmed by conventional PCR and sequencing . 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).
blaKPC 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 blaKPC types (blaKPC −2 to blaKPC-13). The blaKPC 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, blaKPC 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 blaKPC genes were evaluated by the BLAST search program, available at www.ncbi.nlm.nih.gov.
The blaKPC 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. faecium ATCC 35667 and methicillin-resistant S. aureus ATCC 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 ( − ) / blaKPC ( − ) 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 ( − ) / blaKPC ( − ), 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 ( − ) / blaKPC ( − ) (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).
All blaKPC genes of KPC-producing isolates in this study were verified as blaKPC-2 by sequencing assay.
The blaKPC 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).
The analytical sensitivity of the blaKPC 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. blaKPC specific fluorescent peaks were detected in the isolates dilutions to about 0.8 cfu (Figure 2).
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 . 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 . 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 ( + ) / blaKPC ( + ) 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 ( − ) / blaKPC ( − ). 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. pneumoniae ATCC 700603 for non- Enterobacteriaceae in order to eliminate the incidence of indeterminate results of MHT . Thus, an alternative method may prove to be more useful. During the recent few years, molecular methods have been used to rapidly detect blaKPC 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 blaKPC 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 blaKPC-1/2 to blaKPC-13. The blaKPC genes are characterized by nonsynonymous single nucleotide substitutions . Our sequencing results showed all 29 KPC-producing isolates harbored blaKPC-2 gene. KPC-2 clinical isolates were widely isolated in most parts of China [23, 29]. Last year, Li et al  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 blaKPC 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 blaKPC gene was detected at about 89°C. Our assay sensitivity is about one cfu sufficient to detect blaKPC–containing isolates.
The real-time PCR assay described here provides a useful screening test to detect blaKPC genes rapidly and accurately. Although the real-time PCR assay was unable to identify the specific gene in the blaKPC family in clinical isolates, accurate and rapid identification of this kind of resistance genes is the first step to control their spread.
Klebsiella pneumonia carbapenemase
modified Hodge test
the Clinical Laboratory Standards Institute
colony forming unit
Minimum inhibitory concentration.
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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.
The authors declare that they have no conflict of interest.
LJ Wang carried out the real-time PCR studies, participated in the sequence alignment and drafted the manuscript. HT Gu carried out the bacterium isolation and antibiotic sensitivity test. XX Lu participated in the design of the study and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.