Comparison of culture and qPCR for the detection of Pseudomonas aeruginosa in not chronically infected cystic fibrosis patients
- Pieter Deschaght†1Email author,
- Petra Schelstraete†2,
- Guido Lopes dos Santos Santiago1,
- Leen Van Simaey1,
- Filomeen Haerynck2,
- Sabine Van daele2,
- Elke De Wachter3,
- Anne Malfroot3,
- Patrick Lebecque4,
- Christiane Knoop5,
- Georges Casimir5,
- Hedwige Boboli6,
- Frédéric Pierart6,
- Kristine Desager7,
- Mario Vaneechoutte1 and
- Frans De Baets2
© Deschaght et al; licensee BioMed Central Ltd. 2010
Received: 29 April 2010
Accepted: 24 September 2010
Published: 24 September 2010
Pseudomonas aeruginosa is the major respiratory pathogen causing severe lung infections among CF patients, leading to high morbidity and mortality. Once infection is established, early antibiotic treatment is able to postpone the transition to chronic lung infection. In order to optimize the early detection, we compared the sensitivity of microbiological culture and quantitative PCR (qPCR) for the detection of P. aeruginosa in respiratory samples of not chronically infected CF patients.
In this national study, we followed CF patients during periods between 1 to 15 months. For a total of 852 samples, 729 (86%) remained P. aeruginosa negative by both culture and qPCR, whereas 89 samples (10%) were positive by both culture and qPCR.
Twenty-six samples were negative by culture but positive by qPCR, and 10 samples were positive by culture but remained negative by qPCR. Five of the 26 patients with a culture negative, qPCR positive sample became later P. aeruginosa positive both by culture and qPCR.
Based on the results of this study, it can be concluded that qPCR may have a predictive value for impending P. aeruginosa infection for only a limited number of patients.
Cystic fibrosis (CF) is one of the most common genetic disorders, caused by mutations in the CFTR gene, coding for the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein . Mutations in this gene lead to inactivity of the CFTR protein and/or reduced expression of the protein at the cytoplasmic membrane . Improper functioning of the CFTR results in the production of viscous mucus and in a defective innate immunity [2, 3]. The reduced functionality of the mucociliary system and the ongoing inflammation result in an increased sensitivity of the CF airways to infection by bacterial pathogens, of which Pseudomonas aeruginosa and Staphylococcus aureus are the most important. Chronic lung infection with P. aeruginosa is a major cause of morbidity and mortality among the CF patients . It is now well-established that early aggressive antibiotic treatment of new infection with P. aeruginosa is successful in postponing chronic infection. Hence, it is important to detect new infection with P. aeruginosa as early as possible so that eradication treatment can be started as soon as possible [5–7]. Currently, routine detection and identification of P. aeruginosa in respiratory samples is done by conventional methods such as culture and biochemical characteristics. Misidentification can occur due to the variable phenotypic characteristics of this species . Moreover, the sensitivity of culture might be limited, especially when compared to DNA amplification based techniques. Thus far, however, only one group has compared both approaches in a long term study for early detection of P. aeruginosa from CF patients .
In this national study, we followed CF patients during periods between 1 to 15 months and we compared the sensitivity of conventional culture techniques with qPCR for the detection of P. aeruginosa in the respiratory samples from CF patients, not chronically infected by P. aeruginosa.
Patients and sampling
From January 2008 until May 2009, sputum, nasopharyngeal or throat swab samples were routinely collected from 397 CF patients attending all but one of Belgian CF-centres, i.e. Ghent University Hospital (UZG, Ghent), Universitair Ziekenhuis Brussel (UZB, Brussels), St Luc University Hospital (UCL, Brussels), Queen Fabiola Children's University Hospital and Erasme University Hospital (ULB, Brussels), Antwerp University Hospital (UZA, Antwerp), CF Center Liege (CHC - CHR, Liege). Patients were seen every three months and sputum or nasopharyngeal aspirate/throat swab samples were cultured at every visit. Nasopharyngeal aspirates/throat swab samples were collected in case the patients could not expectorate. All 397 included patients, (median age: 14 years, range: 1-53 years), were considered as P. aeruginosa free and not chronically infected according to the criteria used by the different Belgian CF centers, i.e., the European Consensus criteria  or those defined by Lee et al.. For the 252 patients with at least two respiratory samples (median: 3 samples, range: 2-11 samples), the median follow-up time was 6 months (range: 1-15 months). Patients with a P. aeruginosa positive culture were treated according to the standard antibacterial treatment protocols of each center, patients with only a PCR positive result were not treated.
After arrival at the Laboratory Bacteriology Research (LBR), sputum and nasopharyngeal samples were liquefied with Sputasol (Oxoid Ltd., Basingstoke, UK) (1:1, vol/vol, 1 h incubation at 37°C). Throat swabs (ESwab, Copan, Brescia, Italy) were vortexed in the liquid transport medium present in the Eswab tube. For microbiological culture, samples were immediately processed after arrival. For qPCR, at least 200 μl of each sample was stored at -80°C prior to DNA-extraction.
Culture and identification of the bacteria
Fifty μl of the samples were inoculated onto MacConkey Agar plates (Becton Dickinson, Erembodegem, Belgium) and 100 μl into 4 ml Cetrimide Broth (Fluka Biochemika, Buchs, Switzerland) and incubated for at least 24 h at 37°C at ambient atmosphere before examination. Cetrimide Broth was subcultured by inoculating 50 μl onto a Sheep Blood Agar plate (Becton Dickinson), which was also incubated for at least 24 h at 37°C before examination.
After a maximum of 5 days incubation, lactose negative colonies on MacConkey Agar were picked, subcultured onto a 5% Sheep Blood Agar plate (Becton Dickinson) and identified using tDNA-PCR .
Before DNA-extraction, respiratory samples were pre-incubated with proteinase K, i.e. incubation of 200 μl of each sample during 1 h at 55°C in 200 μl proteinase K buffer (1 mg/ml proteinase K, 0.5% SDS, 20 mM Tris-HCl, pH 8.3) with vortexing every 15 min. DNA was extracted using the protocol Generic 2.0.1 on the bioMérieux easyMAG Nuclisens extractor (bioMérieux, Marcy-l'Etoile, France). Final elution volume was 110 μl. This DNA-extraction protocol had been shown previously to be the most sensitive of five different methods .
Quantitative PCR (qPCR), targeting the oprL gene (NP_249664), was performed using primers PAO1 A (5' CAGGTCGGAGCTGTCGTACTC 3') and PAO1 S (5' ACCCGAACGCAGGCTATG 3') and hydrolysis probe oprL TM (5' FAM-AGAAGGTGGTGATCGCACGCAGA-BBQ 3'), manufactured by TIB Molbiol (Berlin, Germany), as described previously . The reaction mixture contained 4 μl of the LightCycler TaqMan Master mix (Roche, Basel, Switzerland), 0.5 μM of each primer, 0.1 μM of the hydrolysis probe, and 5 μl of DNA extract. The final reaction volume was made up to 20 μl by adding water. Cycling was performed on the LightCycler 1.5 (Roche) with an initial hold of 10 min at 95°C, 45 cycles at 95°C for 10 s, at 55°C for 30 s and at 72°C for 1 s.
Using qPCR, the concentration of P. aeruginosa in the respiratory sample is determined as the cycle number whereby the fluorescence signal intensity crosses the detection threshold. This value is expressed as the quantification cycle (Cq). The number of cycles is inversely correlated to the concentration of P. aeruginosa in the sample, e.g. a high cycle number indicates a low the initial concentration of P. aeruginosa in the sputum.
Quality control of culture positive, PCR negative samples
To exclude PCR inhibition as an explanation for the PCR negative, culture positive samples, the PCR mix, containing the DNA extract of the sample, was spiked with an internal amplification control (IAC), as described by Khot et al.. Briefly, 105 Jelly Fish oligonucleotides (105 bp) (IAC-oligo), 0.4 μM forward primer (IAC fw) and 0.4 μM reversed primer (IAC rev) primers were added to the reaction mix, and a separate qPCR experiment, using the SybrGreen kit, was carried out with primers hybridizing to the target DNA. When compared to a set of control samples, i.e. culture and qPCR P. aeruginosa positive samples to which the same amount of IAC had been added, the PCR was considered as inhibited by (the DNA extract of) the sample, when an increase of 3 Cqs could be observed.
To exclude that PCR negativity was due to primer mismatch with the oprL gene of the P. aeruginosa isolates for culture positive, PCR negative samples, oprL PCR was carried out on DNA extracted from the P. aeruginosa isolates, cultured from the same samples.
The study was approved by the ethics committee from Ghent University Hospital (project nr. 2007/503). Written informed consent was obtained from the patients > 18 years, or from the parents for the children.
Differences in Cq values were examined using the Mann-Whitney U test and p values of < 0.05 were considered as significant.
Comparison of the sensitivity of detection by qPCR and culture
Number of samples
qPCR Cq value
26.4 (17-32, 4.3)
29.8 (25-32, 2.7)
27.3 (22-32, 4.3)
31.7 (20-34, 3.2)
Twenty-six samples (3%), obtained from 26 CF patients, were culture negative but qPCR positive (Additional File 1, Table S2). False positivity due to cross reaction with other CF associated bacterial species could be excluded because the specificity of the primer set had been tested and confirmed on a broad set of common CF pathogenic species .
For 23 of these 26 patients, at least one follow-up sample was obtained. Five of these became P. aeruginosa culture positive, of which four after a mean lag time of 3.5 months (range: 2-5 months)(Additional File 1, Table S2, samples nr. 7, 19, 21, 23) and a fifth patient after a lag time of nine months after the first qPCR positive sample (Additional File 1, Table S2, sample nr. 8). The latter patient had in between two culture negative, qPCR negative samples. Three other qPCR positive, culture negative patients (Additional File 1, Table S2, samples nr. 3, 16, 22) had a previous sample that was P. aeruginosa culture and qPCR positive (mean lag time 4.3 months, range 3-5 months). The follow-up samples of these three patients were culture and qPCR negative. The average qPCR Cq value (31.7) for these 26 samples was significantly higher, compared with the Cq value of culture and qPCR positive samples (26.4) (Table 1) (p < 0.001).
Ten samples, obtained from 9 patients, were P. aeruginosa culture positive, but qPCR negative (Additional File 1, Table S3). For five of these ten samples (50%), only one of the culture media yielded a positive result, i.e. three samples remained negative on MacConkey Agar and two sample in Cetrimide Broth. For all these culture positive, PCR negative samples, PCR inhibition could be excluded. Primer mismatch could also be excluded, because the cultured P. aeruginosa isolates were oprL qPCR positive. At least one follow-up sample could be obtained for five of these patients, and for three the follow-up sample(s) was/were culture and qPCR negative, whereas for two patients the follow-up sample(s) was/were culture and qPCR positive.
When taking culture as the gold standard, the PCR had a sensitivity of 90%, a specificity of 85%, a positive predictive value of 77% and a negative predictive value of 99%.
For the samples with a dissimilar culture and qPCR result, there was no relation with the presence of other bacterial species isolated from the respiratory samples (data not presented) and there was no linkage with the sample type (data not presented).
Early detection of Pseudomonas aeruginosa in respiratory samples of CF patients has become of utmost importance, taking into account that it is now possible to postpone chronic infection with the use of early aggressive antibiotic treatment [5–7]. In most routine microbiology laboratories, microbiological culture is still the mainstay for detection of P. aeruginosa. However, other detection methods that might be more sensitive than microbiological culture still need evaluation and validation .
Serological testing for P. aeruginosa antibodies has been proposed as an alternative to culture for the early establishment of new infection episodes. Several groups reported that anti-P. aeruginosa antibodies can be detected prior to P. aeruginosa detection by culture and prior to the onset of chronic infection [16–18]. However, in a cross-sectional study, da Silva Filho and colleagues  found more patients positive with culture or PCR than with serology.
In this prospective study, we evaluated whether qPCR can improve early detection of P. aeruginosa in respiratory samples from CF patients, not yet chronically infected with this organism.
During the last decade, several PCR formats and other molecular methods for the detection of P. aeruginosa have been developed [9, 20–30]. Some groups found a higher sensitivity of PCR in comparison with culture and/or biochemical tests for the detection of P. aeruginosa from respiratory samples of CF patients [9, 19], while others found no difference  or a lower sensitivity for PCR . In this study, we targeted the oprL gene [13, 21], previously shown to be a more sensitive gene locus than the exotoxin A locus, when applied to CF patient airway samples . In a previous study , we compared five DNA-extraction methods, six (q)PCR formats and three culture techniques to optimize and validate the detection of P. aeruginosa in sputum from CF patients. In our hands, using a dilution series of P. aeruginosa in sputum, the three culture methods were equally sensitive to each other but also to the combination of the most sensitive DNA extraction method and the most sensitive amplification assay, i.e. probe based qPCR.
Surprisingly, there is at present only one published study in which P. aeruginosa detection by culture and by qPCR is compared in a long term study . These authors concluded that PCR detected P. aeruginosa on average 4.5 months prior to culture. In our opinion, this conclusion should be interpreted with caution, because also in their study only 5 of the 10 culture negative, PCR positive patients became P. aeruginosa culture positive during the follow-up period. It can also be argued whether the cultured strain was identical as the one causing PCR positivity 4-17 months prior to culture positivity, given the long follow-up period and the fact that the average conversion rate to culture positivity among CF patients can be considered as relatively high. Finally, the authors also found 5 culture positive, PCR negative samples, for which PCR might have become positive later on, however no follow-up data were reported. In our study, we found that out of the 26 qPCR positive, culture negative samples, only 5 follow-up samples became also P. aeruginosa culture positive, of which one became double positive only in the third follow-up episode after initial PCR positivity. The significantly higher Cq values of these 26 samples, compared to the Cq values of double positive samples, suggest a low P. aeruginosa inoculum in the respiratory sample and may explain why the presence of P. aeruginosa was missed by culture. Thus, PCR positivity may have had a predictive value for impending infection in only 5 of the 26 patients, whereas in 21 patients a positive PCR signal became negative again and did not predict a positive culture at the next follow-up sample. For three of the 26 qPCR positive, culture negative patients, the previous sample was P. aeruginosa culture and qPCR positive but the follow-up samples were culture and qPCR negative. This may indicate that qPCR still detected DNA of already killed bacteria. Another 10 samples (1%) were P. aeruginosa qPCR negative but culture positive. False negativity of the qPCR was not the reason for the negative qPCR result, because qPCR inhibition and primer mismatch could be excluded. Interestingly, for 5 of these 10 patients, there was discordance between both culture techniques, suggestive for borderline detection by culture and thus a low inoculum of the pathogen. Such discordance between culture results was observed in only 11 out of 89 qPCR positive samples.
For many samples with discordant qPCR and culture results, a low bacterial inoculum may be the explanation. Based on our results in this study and a previous study , both approaches have comparable sensitivity, and at low inocula both may be at the border of their detection limit. In addition, at low inocula the distribution of the bacteria in the sample may be more uneven and because we used different parts of each sample to perform qPCR respectively culture, randomization may have influenced the qPCR and/or culture result negatively. The presence of a low inoculum can be concluded from the significantly higher Cq values of qPCR positive/culture negative samples, compared to the qPCR positive/culture positive samples and from the fact that cultures were positive for only one of both media used in 5 out of 10 qCPR negative/culture positive samples. Possibly other factors, such as sample type, the presence of other bacterial species or the genotype of the P. aeruginosa isolate might differentially influence the ease with which P. aeruginosa can be detected by culture versus qPCR. Further research is warranted on a larger set of samples with discordant qPCR - bacterial culture results to determine the influence of some of these factors.
The present study indicates that the currently used routine culture techniques perform equally well as DNA amplification techniques for detection of P. aeruginosa in respiratory samples of CF patients, not chronically infected with P. aeruginosa. Looking at it from a different angle, qPCR was both sensitive and specific compared with a gold standard of culture.
These data, gathered on clinical samples, confirm the results of our previous laboratory study in which culture methods were equally sensitive to the combination of the most sensitive DNA extraction method and the most sensitive amplification assay, i.e. probe based qPCR .
Therefore, we may conclude that for this study, based on a large amount of patients and samples, qPCR for P. aeruginosa may have a predictive value for impending P. aeruginosa infection in only a limited number of cases.
Pieter Deschaght is indebted to the IWT for PhD research grant IWT-SB/71184. This study was funded by the Belgian Cystic Fibrosis Association.
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