Lysis of tubercle bacilli in fresh and stored sputum specimens: implications for diagnosing tuberculosis in stored and paucibacillary specimens by PCR
© Pathak et al; licensee BioMed Central Ltd. 2007
Received: 21 November 2006
Accepted: 04 September 2007
Published: 04 September 2007
Nucleic acid amplification techniques are being used increasingly in diagnosing tuberculosis. In developing countries clinical samples are often stored for subsequent analysis since molecular tests are conducted at only a limited number of laboratories. This study was conducted to assess the speed at which mycobacteria undergo autolysis and free DNA is detected in the supernatant during low-temperature storage.
Eighty-seven smear positive sputa from tuberculosis patients were analysed immediately and after storage at -20°C. Timelines of 1 and 2 months were selected to assess the maximum extent of DNA loss that occurred during storage. All samples remained PCR- and smear-positive at 1 month and only 1 sample turned negative after 2 months. Bacterial lysis in the specimens was demonstrated by PCR analysis of supernatant fractions; 53% of the freshly analysed samples contained mycobacterial DNA in supernatants. PCR positivity increased significantly during storage (to 69% and 77% after 1 and 2 months of storage, respectively, P < 0.0001). Storage-associated bacterial lysis was accompanied by a decrease in smear grade status in 28 of 87 samples (P < 0.0001 after 2 months of storage) and a significant storage-associated reduction in bacterial numbers in the remaining samples.
We conclude that (i) freshly isolated sputum contains both intact and lysed mycobacteria, (ii) lysis increased during storage and (iii) supernatant fractions routinely discarded during sample processing contain mycobacterial DNA. We propose that supernatant is a valuable sample for PCR for both fresh and stored specimens, particularly those with a low bacterial load in addition to conventional sediment.
TB is an enormous public health challenge worldwide, with an estimated global incidence of 0.136% in 2005  which is likely to be aggravated by the HIV/AIDS pandemic. Therefore there is great pressure on clinical laboratories to rapidly and accurately detect and identify clinically important mycobacteria. TB is routinely diagnosed worldwide by smear microscopy and culture. In spite of its lack of sensitivity and inability to distinguish between tubercle bacilli and other mycobacteria, the former technique is widely used in TB control programmes on account of its speed, simplicity and low cost. Apart from lungs, TB also occurs in other body sites wherein the paucibacillary load often poses a significant diagnostic challenge [2, 3]. Nucleic acid amplification technologies are being intensively assessed in diagnosing extrapulmonary TB owing to their speed, specificity and sensitivity . However their application is limited to sophisticated laboratories in developing countries including India and samples are often stored prior to analysis. Studies that have evaluated the effect of sample shipment and storage on the performance of conventional and nucleic acids-based tests concluded that accurate diagnosis rests on minimal transport time and lowest possible storage and shipping temperatures [4–6]. Furthermore, in case of paucibacillary specimens, diagnostic methods are no different from those employed for high load or fresh samples. The inherent delay in obtaining culture results is a serious limitation of the gold standard; therefore it was proposed that when smear microscopy and DNA amplification were both positive, the diagnosis of active TB could be considered established . For these various reasons PCR is being increasingly considered as an adjunct test for diagnosing TB in resource-poor settings also.
We developed a sample processing procedure, USP methodology, that is compatible with microbiology and inhibition-free PCR in both pulmonary and extrapulmonary samples [8–10]. In the present study, we assessed the effect of low temperature storage on the efficacy of M. tuberculosis detection in fresh and stored USP-processed sputum. The key finding was that a significant number of fresh specimens contained lysed mycobacteria and lysis increased during storage. As a consequence supernatant PCR positivity increased with sample storage. Thus supernatant is a novel and useful sample for enhancing PCR performance in clinical samples.
In a preliminary study conducted to assess the impact of sputum storage on PCR, maximum bacterial autolysis in untreated samples was noted during room temperature vs. 4°C or -20°C storage (Dudeja M, unpublished observations). The present study was designed to assess the effect of storage at -20°C of NALC-treated sputum on bacterial lysis. We chose 1 and 2 months of storage as it exceeded the likely interval between sample collection and PCR analysis. PCR and smear microscopy were employed to assess the speed of storage-associated changes in bacterial load. Bacterial lysis was confirmed by simultaneous analysis of sputum supernatants that are conventionally discarded
Effect of sample storage on PCR
Effect of sample storage on USP smear status
Effect of sample storage on bacterial load
We made several noteworthy conclusions in this study that evaluated the impact of sputum storage on the speed at which bacteria underwent autolysis and released DNA in the supernatant. Firstly, our results indicate that delays of upto a month do not adversely affect PCR and smear microscopy results. Secondly, although a statistically significant decline in smear grades was observed on storage only 1 sample changed from smear-positive to -negative upon storage. The apparent negligible effect of storage on the sensitivity of smear microscopy was attributed to (i) the use of highly sensitive USP smear microscopy (detection limit ≈ 300–400 bacilli/ml of sputum ) and (ii) a high initial bacterial load. Thirdly, the PCR status of sediments was not altered with storage perhaps due to a high initial bacterial load, use of the multicopy IS6110 target assay and the addition of more template DNA in PCR (enabled by efficient inhibitor removal using USP processing, ref. ). The final and most significant finding was that DNA was recovered from supernatants from the majority of freshly processed samples. Additional lysis occurred during storage and was reflected by an increase in the number of PCR positive supernatants. Since the sputum was stored after NALC processing, DNA retrieved from the supernatant fraction thereafter (S1 and S2) was derived solely from bacteria lysed during storage and/or subsequent thawing. For the sample that turned smear-negative and sediment PCR-negative after storage; supernatant PCR that was initially negative turned positive after storage. Thus, the DNA lost from pellet was retrieved in the supernatant. This observation assumes significance in paucibacillary specimens that are generally subjected to a concentration step before analysis. Thus, supernatants that are conventionally discarded during sample processing would be a valuable specimen for PCR testing and offset the disadvantage associated with analyzing stored or low-load samples.
We conclude that performing supernatant PCR in addition to sediment PCR and highly sensitive USP smear microscopy would increase the efficiency of TB diagnosis in case of fresh and stored paucibacillary specimens.
Eighty-seven direct smear positive sputum specimens were collected from patients attending the Microbiology and DOTS centre at New Delhi Tuberculosis Centre, New Delhi before they were placed on antitubercular therapy. The left-over sputa were stored at 4°C within 5–6 hours of collection and processed within the next 6–36 hours.
Specimen processing and storage
The sputa were processed as outlined in Fig. 1. Briefly, they were digested with 0.2 volumes of 2.5% N-acetyl L-cysteine (NALC) for 5 min and homogenized by vortexing in the presence of 5–6 sterile 3 mm glass beads for 5–10 min . The liquefied sputum was distributed into three approximately equal portions. One portion (portion 1) was processed immediately by centrifugation at room temperature for 15 min at 8000 rpm (~10,000 g, GSA rotor, Sorvall RC5B Plus centrifuge, USA) to yield fresh supernatant and fresh pellet fractions (FS and FP, respectively in Fig. 1). The sediment fractions (FP) were processed by the USP method (see below) and used for smear microscopy and PCR. The remaining portions (Portion 2 and Portion 3) of NALC-treated sputum were centrifuged, the supernatants were discarded and the pellets were resuspended in sterile phosphate-buffered saline (PBS) equivalent to the original volume of the NALC homogenate and stored for 1 and 2 months at -20°C (Fig. 1).
Universal sample processing (USP)
The sputum sediments (FP, P1 and P2) were processed by the USP method as described . Briefly, to FP or P1 or P2, 1.5 to 2 volumes of USP solution (5 M guanidinium hydrochloride (GuHCl), 50 mM Tris-HCl, pH 7.5, 25 mM EDTA, 0.5% Sarcosyl, 0.15 M β-mercaptoethanol) was added. After incubation for 5–10 min the contents were centrifuged at room temperature at 8000 rpm for 15 min as above. The supernatant was discarded; the sediment was washed with water and then resuspended in 600 μl of 0.05% Tween 80. Smears were prepared on clean microscopic glass slides using 10% of the USP-processed specimen, subjected to Ziehl-Neelsen staining, examined under oil-immersion lens and graded as described .
DNA was isolated from the remainder of the USP-processed sediment as described . Briefly 60–80 μl of resuspension solution containing 10% Chelex-100 0.3% Tween 20 and 0.03% Triton X-100 was added to the processed sediments FP, P1 and P2 (Fig. 1), mixed well and incubated at 90°C for 40 min. The extracted DNA was used for PCR.
DNA was isolated from the supernatant samples, FS, S1 and S2, (Fig. 1), using the DNA bind method  with minor modifications. Briefly, per volume of supernatant, 2 volumes of DNA bind solution [6 M GuHCl, 20 mM EDTA, 50 mM Tris-HCl pH 7.0, and 1% diatomaceous earth were added to FS, S1 and S2 fractions. After incubating for 5 min at room temperature, the mixture was centrifuged as described above. The supernatant was discarded and the pellet was washed four times with wash buffer (50 mM Tris-HCl pH 7.4, 200 mM NaCl, 10 mM EDTA and 50% ethanol). The pellet was rinsed with acetone and dried briefly at 65°C. DNA was eluted by resuspending diatoms in water (10% of original supernatant volume) and heating at 65°C for 10 min.
Sample processing and PCR were carried out in dedicated areas using dedicated pipettes and filter guard tips to prevent cross contamination. M. tuberculosis DNA was detected by PCR using primers targeting IS6110 . Briefly a 40-μl reaction was set up containing 0.5 μM each of primers T4 (5' CCTGCGAGCGTAGG CGTCGG 3') and T5 (5' CTCGTCCAGCGCCGCTTCGG 3'), 1.5 mM MgCl2, 0.2 mM dNTPs, 1 U of Taq DNA polymerase (GeneTaq, MBI Fermentas, Vilnius, Lithuania) and 10 μl of template DNA in case of sediment fractions or 4 μl of template DNA in case of supernatant fractions. In case of supernatants, neat, 1:5 and 1:10 dilutions were subjected to amplification. DNA negative and positive control reactions without DNA and containing 10 to 20 ng of M. tuberculosis H37Rv DNA, respectively were routinely set up. The thermal cycling parameters were initial denaturation at 94°C for 10 minutes followed by 45 cycles each of 1 minute at 94°C and 1 minute and 30 seconds at 60°C with a final extension of 5 minutes at 72°C. The 123-bp PCR product was detected by electrophoresis on 2.3% agarose gel followed by ethidium bromide staining and visualization under UV light. For the experiment described in Fig. 2, only 35 cycles of amplification were used. The devR PCR assay yielded a 164-bp amplification product .
The significance of the decrease in smear grade status and of the increase in supernatant PCR positivity was determined by McNemar's chi square test using Stata 9.0 software (StataCorp LP, College Station, Texas, USA). The significance of the decrease in bacterial load observed during storage was determined using the nonparametric Friedman Anova test followed by multiple comparison. P values of < 0.05 were considered significant (SPSS 10.0.1 software, Chicago, USA). The median, interquartile values and box plots (Fig. 6) were calculated and generated using Stata 9.0 software.
The authors thank Ms. Kalaivani, Department of Biostatistics, AIIMS for help with statistical analysis of the data and for assistance in preparation of the figures. Dr. Nirmaljit Kaur and Dr. Mona are gratefully acknowledged for providing help during the course of this study. Technical assistance provided by Mr Sanjay Kumar is also acknowledged. DP is thankful to DBT for Master's Scholarship and SC is thankful to I.C.M.R. for Senior Research Fellowship. This study was supported by funding to JST by AIIMS, New Delhi and the Department of Biotechnology, Govt. of India.
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