Skip to main content
Download PDF

Evaluation of the clinical value of ELISA based on MPT64 antibody aptamer for serological diagnosis of pulmonary tuberculosis

BMC Infectious Diseases volume 12, Article number: 96 (2012) Cite this article

  • The Erratum to this article has been published in BMC Infectious Diseases 2013 13:430
  • The Erratum to this article has been published in BMC Infectious Diseases 2013 13:410

Abstract

Background

Presently, tuberculosis (TB) poses a global threat to human health. The development of reliable laboratory tools is vital to the diagnosis and treatment of TB. MPT64, a protein secreted by Mycobacterium tuberculosis complex, is highly specific for TB, making antibody to MPT64 a reagent specific for the diagnosis of TB.

Method

Antibody to MPT64 was obtained by a combination of genetic engineering and immunization by the system evolution of ligands by exponential enrichment. A high-affinity aptamer of antibody to MPT64 was selected from a random single-stranded DNA library, and a sandwich ELISA method based on this aptamer was developed. This ELISA method was used to detect TB in 328 serum samples, 160 from patients with pulmonary TB (PTB) and 168 from non-tuberculous controls.

Results

The minimum limit of detection of the ELISA method was 2.5 mg/L, and its linear range varied from 10 mg/L to 800 mg/L. Its sensitivity, specificity, positive likelihood ratio, negative likelihood ratio and area under the curve, with 95 % confidence intervals, were 64.4 % (56.7 %–71.4 %), 99.4 % (96.7 %–99.9 %), 108.2 (15.3–765.9), 0.350 (0.291–0.442) and 0.819 (0.770–0.868), respectively. No significant difference in sensitivity was observed between sputum smear positive (73/112, 65.2 %) and negative (30/48, 62.5 %) individuals.

Conclusions

This sandwich ELISA based on an MPT64 antibody aptamer may be useful for the serological diagnosis of PTB, both in sputum smear positive and negative patients.

Peer Review reports

Background

Being a contagious disease, tuberculosis (TB) poses a global threat to human health. The World Health Organization [1] reported that in 2010, there were 8.8 million (range, 8.5–9.2 million) incident cases of TB, 1.1 million (range, 0.9–1.2 million) deaths from TB among HIV-negative individuals and 0.35 million (range, 0.32–0.39 million) deaths from HIV-associated TB. In China, dramatic reductions in TB cases and deaths have been achieved. Although the Stop TB Partnership target of halving TB prevalence rates by 2015 compared with 1990 was unlikely to be achieved globally, this target had already been reached in the Americas and was close to being reached in the Western Pacific Region [1]. Two important factors have contributed to the resurgence and morbidity of TB: (i) the emergence of multi-drug-resistant and extensively drug-resistant strains of Mycobacterium tuberculosis and (ii) the increasing incidence of HIV globally [2–6]. Most patients with TB have pulmonary TB (PTB), and developing reliable laboratory tools is vital to the diagnosis and treatment of PTB [7].

Antibody to MPT64 has been shown to bind MPT64 protein [8], a highly specific protein secreted by M. tuberculosis (MTB) complex, which includes M. tuberculosis M. bovis and M. africanum[9–11]. Therefore, this antibody may be useful in the detection of TB. We describe here the use of the systematic evolution of ligands by exponential enrichment (SELEX) technique to develop a sandwich ELISA method based on an MPT64 antibody aptamer for the diagnosis of PTB.

Materials and methods

Ethics Statement

All patients were treated in accordance with the Helsinki Declaration on the participation of human subjects in medical research. The study protocol was approved by the Tongji University Ethics Committee (permit number: K08-018), and informed consent was obtained from each participant. Animal studies were approved by the Second Military Medical University Animal Care and Ethics Committee [approval ID: SYXK/2007-0003].

Preparation of antibody to MPT64

Based on the sequence of the H37Rv TB reference strain encoding the MPT64 gene (accession number: NC_000962), we designed forward (5'-CCCATATGCGCATCAAGATCTTCAT-3') and reverse (5'-CCAAGCTTGGCCAGCATCGAGTCG-3') primers, containing Nde I and Hind III restriction sites, respectively. PCR amplification with these primers was performed using H37Rv nucleic acid as template. Subsequently, the purified PCR product was inserted into the T vector using ligase. After digestion with restriction enzyme, pMD18-MPT64 was to pET21a using T4 ligase and the pET21a-MPT64 expression plasmid was used to transform BL21 (DE3) competent cells. Positive recombinant clones were identified by DNA sequencing.

A recombinant clone was inoculated overnight into the Luria Bertani medium at 37°C. The resultant bacteria were lysed with ultrasound and the medium was centrifuged. The sediment was resuspended in 10 % Triton-X 100 buffer, and MPT64 protein was purified on a nickel-agarose column. MPT64 protein was identified by sodium dodecyl sulfate polyacrylamide gel electrophoresis [12] [Figure 1.

Figure 1
figure1

SDS-PAGE analysis of MPT64 protein obtained by genetic recombination. Lanes 1 and 3: markers; Lane 2: purified MPT64 protein (24 kD); Line 4: purified polyclonal antibody to MPT64 (50 kD).

Full size image

Rabbits were immunized with MPT64 protein by subcutaneously injecting a suspension of 0.5 ml phosphate-buffered saline (PBS] containing 0.5 g/L MPT64 protein and 0.5 ml Freund's complete adjuvant into six sites on the back of each rabbit. On days 14, 24, 34, and 44, each rabbit was injected with the same dose of MPT64 protein and Freund's incomplete adjuvant. Rabbit serum was collected, and MPT64 antibody was purified on a CNBr-activated Sepharose 4B column, with the purified antibody identified by western blotting [Figure 2. The details of the method have been described previously [13]. Purified antibody was quantified by the Bradford method [14].

Figure 2
figure2

Western blot for detecting MPT64 purified recombination protein Line 1: control (non-induced recombinant bacteria); Line 2: purified MPT64 recombination protein (24 kD).

Full size image

Construction of a random single-stranded DNA (ssDNA) library

Using the primers 5’-GGGAGCTCAGAATAAACGCTCAA-3’ (forward) and 5’-Biotin-TTCGACATGAGGCCCGGATC-3’ (reverse), a 78-mer ssDNA library was constructed with the sequences, 5’ -GGGAGCTCAGAATAAACGCTCAA-AN35-CGACATGAGGCCCGGATC-3’, with the middle 35 sequences being random. The random ssDNA library and primers were synthesized commercially by Shanghai Sangon Company.

Selection of MPT64 antibody aptamer

The ssDNA library was optimized by PCR amplification to obtain a double-stranded DNA (dsDNA) library. Furthermore, the ssDNA library was constructed by using asymmetric PCR. The amplified product was purified with a phenol-chloroform-isoamyl alcohol mixture (volume ratios, 25:24:1)]. ELISA plates coated with bovine serum were used to remove non-specific nucleotides from the ssDNA library and the purified ssDNA library added to microplates coated with antibody to MPT64. The plates were washed six times with SELEX buffer. SELEX eluate (20.0 mM Tris-HCl, 4.0 mM guanidinium isothiocyanate, 1.0 mM 1,4-dithiothreitol; pH 8.3) was added and allowed to incubate at 80°C for 10 min. The ssDNA was extracted with a phenol-chloroform-ethanol mixture. Using the extracted ssDNA as a template, asymmetric PCR was performed. Then, the next round of screening was performed. The parameters of the SELEX assay are shown in Table 1.

Table 1 Parameters during each round of the SELEX assay
Full size table

After 12 rounds of aptamer selection, the absorbance of the ssDNA reached its maximum value and a single electrophoretic stripe was displayed. This indicated that the purified ssDNA library with high affinity to the anti-MPT64 antibody was saturated. The PCR products were purified using the TIANgen Midi Purification Kit (TIANgen Biotech [Beijing] Co., Ltd.) and subcloned into a pMD 18-T vector with a TA cloning kit (TaKaRa, Dalian, China). The resultant bacteria were used to transform Escherichia coli DH5α strains, and individual bacterial clones were selectively sequenced by a commercial company (Sangon, Shanghai, China).

The affinity of the selected ssDNA aptamers was measured by ELISA. Polystyrene microplates were coated overnight at 4°C with 10 μg/well of anti-MPT64 antibody in 100 μl 0.1 M NaHCO3 (pH 9.4), washed four times with washing buffer (PBS containing 0.05 % Tween 20, pH 7.4) and incubated for 1 hour at room temperature with 200 μl of blocking buffer. The microplates were washed once with washing buffer and 1.0 μg/well of biotin-labeled DNA aptamer in a binding buffer (SHCMK) containing 20.0 mM Hepes, pH 7.35, 1.0 mM CaCl2, 120 mM KCl and 1.0 mM MgCl2 was added. The aptamers and MPT64 antibody were allowed to react at 37°C for 40 min. The plates were washed six times with washing buffer (SHCMK + 0.05 % Tween 20) and incubated at 37°C for 30 min with 100 μl/well of streptavidin-horseradish peroxidase (Sigma, USA) diluted 1:1000 in PBS. Finally, the plate was washed six times with PBST and 100 μl of 1.0 mM tetramethylbenzidine in citrate buffer (0.1 M, pH 4.25), with 2.0 mM H2O2 added as substrate in a ratio of 1:20. The enzymatic reaction was stopped 5 min later by the addition of 50 μl 1.0 M H2SO4 and optical density (OD) of 450 nm was measured spectrophotometrically.

Sandwich ELISA based on the anti-MPT64 antibody aptamer

We assessed the secondary structures of the aptamers using sequencing results and the DNAMAN version 4.0 (Lynnon Corporation, Quebec, Canada). The aptamer with highest affinity to the anti-MPT64 antibody was regarded as the capture and detection aptamer by ELISA. Each microplate well was coated with 0.1 μg of the capture aptamer, and the 5 ' end of the detection aptamer was labeled with biotin. Based on the detection of purified anti-MPT64 antibody at different dilution ratios, the minimum limit of detection and the linear range of this ELISA method were determined.

Serum samples, participant characteristics and validation of the ELISA

We obtained 328 serum samples, 160 from patients with definite PTB and 168 from non-tuberculous controls including 78 healthy volunteers and 90 non-tuberculous patients. All participants were confirmed as being serologically HIV-negative. Of the 90 non-tuberculous patients, 35 had pneumonia, 40 had lung cancer, and 15 had lung abscesses and other conditions. Lowenstein-Jensen (L-J) culture was performed on all of these subjects to rule out TB.

The median ages of the PTB (31 years; range, 12–73 years; IQR [interquartile range], 17–45 years) and non-tuberculous controls (28 years; range, 14–69 years; IQR, 18–42 years) did not differ significantly P > 0.05). Patients were diagnosed with PTB by physicians based on the criteria of the Chinese Anti-tuberculosis Association, mainly including continuous fever and cough for more than 3 weeks, abnormal chest X-ray, weight loss and the demonstration of TB in sputum by L-J culture and standard biochemical identification tests. Sputum smear examinations for PTB and non-tuberculous patients were performed using the Ziehl-Neelsen method at the same time as L-J culture inoculation.

Statistical analysis

The sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR) and area under the curve (AUC), each with 95 % confidence interval (CI), were calculated. All statistical analyses were performed using Stata version 9 (Statacorp, Texas, USA).

Results

Affinity, sequencing and secondary structure of ssDNA aptamers

The OD values of ssDNA aptamers against MPT64 antibody (reflecting affinity) ranged from 0.55 to 1.62 [Table 2]. We elected MPT64-A1, which had a higher affinity (OD value: 1.62) than did the capture aptamer for ELISA. The sequences of aptamer included forward fixed sequences (5’- GGGAGCTCAGAATAAACGCTCAAA-3’), random sequences (5’- AACGCTCAAGAGGCCCGGATC-3’) and reverse fixed sequences (5’-TTCGACATGAGGCCCGGATC-3’). The DNAMAN package predicted that the secondary structure of MPT64-A1 is a stem-loop structure, similar to a large pocket [Figure 3].

Table 2 Affinities of ssDNA aptamers to anti-MPT64 antibody
Full size table
Figure 3
figure3

Secondary structure of the aptamer MPT64-A1 predicted by DNAMAN.

Full size image

Minimum detection limit and linear range of this ELISA

Based on the detection of the purified MPT64 antibody at different dilution ratios, we found that the limit of detection of this method was 2.5 mg/L and the linear range varied from 10 mg/L to 800 mg/L [Figure 4].

Figure 4
figure4

Linear range and minimum detection limit of the ELISA method.

Full size image

Performance of the ELISA for serological diagnosis of PTB

In diagnosing PTB, this method had a sensitivity, specificity, PLR, NLR, and AUC, with 95 % CI, of 64.4 % (56.7 %–71.4 %), 99.4 % (96.7 %–99.9 %), 108.2 (15.3–765.9), 0.35 (0.291–0.442), and 0.819 (0.770–0.868), respectively [Table 3]. Its sensitivity was similar for sputum smear positive (73/112, 65.2 %) and negative (30/48, 62.5 %) individuals [Table 4].

Table 3 Performances of ELISA based on an anti-MPT64 antibody aptamer for serological diagnosis of pulmonary tuberculosis
Full size table
Table 4 ELISA based on an anti-MPT64 antibody aptamer for serological diagnosis of pulmonary tuberculosis with sputum smear positive and negative patients
Full size table

Discussion

MPT64 protein is one of the main filtrate proteins secreted by MTB complex at an early stage. This protein is encoded by the Rv1980c gene, contains 228 amino acids and has a molecular mass of about 24,000 Da. It is a specific protein, being secreted only by the MTB complex [15–18]. In skin tests, this protein has a sensitivity of 87.8 % and a specificity of 100 % for diagnosing active TB [19, 20]. Except for the MTB complex, bioinformatics showed no epitopes similar to MPT64 protein, indicating its uniqueness. Furthermore, few BCG vaccines express MPT64 protein [17], suggesting that anti-MPT64 antibody may be specific for the diagnosis of TB. Therefore, using a combination of immunization and genetic engineering with SELEX, we developed a sandwich ELISA method based on an anti-MPT64 antibody aptamer for the diagnosis of PTB.

SELEX [21, 22] is a combinatorial chemistry technique used in molecular biology to produce single-stranded DNAs or RNAs that specifically bind ligands. SELEX can be used to select high affinity aptamers against target ligands and to obtain specific aptamers from an in vitro pool of random aptamers. SELEX methods have improved drastically in recent years, and several innovative SELEX approaches have been developed, including counter-SELEX, tissue-SELEX, cell SELEX (TECS-SELEX), fluorescent bead SELEX (FluMag-SELEX), capillary electrophoresis SELEX (CE-SELEX), neutral SELEX, and non-SELEX [23–31]. SELEX was recently used to develop a aptamers against counterpart target ligands, such as Campylobacter jejuni[32]; C-reactive protein [33]; heterogeneous nuclear ribonucleoproteins (hnRNPs) A1 [34]; hepatitis C virus envelope glycoprotein E, botulinum neurotoxin [35]; the carboxyl terminus of Kirsten rat sarcoma viral oncogene homolog (K-RAS) protein [36], adenosine [37] and others. Some aptamers against cancer-related proteins, such as platelet-derived growth factor, vascular endothelial growth factor (VEGF), human epidermal growth factor receptor 2, nuclear factor κB, tenascin-C and prostate-specific membrane antigen [24, 38–40], have also been selected. Moreover, aptamers against whole cells, particularly cancer cells, have been selected [38, 41–46]. The aptamers selected by SELEX were demonstrated to have potential clinical value [47–50]. For example, pegaptanib (Macugen), used to treat neovascular age-related macular degeneration, and the anti-VEGF aptamer pegaptanib used to treat human ocular vascular disease, have received approval by the US Food and Drug Administration [51, 52]. In summary, SELEX has attracted widespread attention and the selected aptamers have been used in clinical diagnosis, treatment and drug development.

Functionally, an aptamer is similar to a protein antibody complex obtained following immunization. Among the advantages of aptamers over classical protein antibody complexes are (1) higher specificity and affinity; (2) its binding to a greater variety of target ligands, including biological macromolecules, small molecule organic compounds, inorganic ions, pathogenic microorganisms, and cells; (3) increased convenience and lower cost; and (4) greater stability, including storage at room temperature.

We have utilized the SELEX method to obtain aptamers against anti-MPT64 antibody in order to develop an ELISA method for the diagnosis of TB. Following 12 rounds of screening, we observed a single electrophoretic strip, indicating that the purified ssDNA library with a high affinity for anti-MPT64 antibody was saturated.

However, we observed differences in the affinities of the selected aptamers. Its OD showed that MPT64-A1 had the highest affinity of all aptamers, whereas DNA sequencing showed that absorbances for detecting affinity were relatively constant. We found only small differences among the absorbance values for aptamers with single base differences at the 5', whereas differences in nucleotides at the stem-loop structure at the 3' end had significant effects on affinity to anti-MPT64 antibody. This suggested that the stem-loop structure may be the site at which aptamers bind to the MPT64 antibody. The secondary structure predicted by DNAMAN indicated that MPT64-A1 could form a stem-loop structure like a large pocket.

We found that the limit of detection of our ELISA method was 2.5 mg/L, with a linear range varying from 10 mg/L to 800 mg/L. This suggested that this method was sensitive and could have potential clinical value. ELISA had a high specificity (99.4 %, 95 % CI: 96.7 %–99.9 %) and PLR 108.2 (15.3–765.9) and was appropriate for diagnostic purposes. However, this method had a sensitivity of 64.4 % (95 % CI: 56.7 %–71.4 %) and an NLR of 0.350 (95 % CI: 0.291–0.442), suggesting that this method was not suitable for screening purpose. The AUC (0.819, 95 % CI: 0.770–0.868) showed the reliability of this ELISA method. In addition, the similar sensitivities observed in sputum smear positive and negative patients suggested that this ELISA method may be suitable for the serological diagnosis of sputum smear negative individuals. Since sandwich ELISA is a rapid, simple and very common test used by many laboratories and laboratory staff [53], it should prove feasible and useful in resource-limited settings.

However, we did not include subsets of patients infected with HIV/TB [54], indicating that the clinical value of this ELISA method for a HIV-endemic population remains unknown. Moreover, this study involved only a few specific populations from hospital settings. Therefore, further studies in different and more extensive populations are necessary to evaluate the power of this test for the diagnosis of TB.

Conclusions

Using a combination of genetic engineering with SELEX and rabbit immunization, we developed a novel sandwich ELISA based on an anti-MPT64 antibody aptamer. Clinical validation showed that this ELISA method was a reliable test for the serological diagnosis of PTB and could be used especially for diagnostic purposes. However, this ELISA method could also be suitable for serological diagnosis of sputum smear negative populations.

References

  1. 1.

    World Health Organisation: Global tuberculosis control:WHO Report 2011. 2011, Geneva

    Google Scholar 

  2. 2.

    Aziz MA, Wright A: The World Health Organization/International Union Against Tuberculosis and Lung Disease Global Project on Surveillance for Anti-Tuberculosis Drug Resistance: a model for other infectious diseases. Clin Infect Dis. 2005, 41 (Suppl 4): S258-S262.

    Article  PubMed  Google Scholar 

  3. 3.

    Gandhi NR, Moll A, Sturm AW, Pawinski R, Govender T, Lalloo U, Zeller K, Andrews J, Friedland G: Extensively drug-resistant tuberculosis as a cause of death in patients co-infected with tuberculosis and HIV in a rural area of South Africa. Lancet. 2006, 368 (9547): 1575-1580. 10.1016/S0140-6736(06)69573-1.

    Article  PubMed  Google Scholar 

  4. 4.

    Raviglione MC, Narain JP, Kochi A: HIV-associated tuberculosis in developing countries: clinical features, diagnosis, and treatment. Bull World Health Organ. 1992, 70 (4): 515-526.

    CAS  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Pevzner ES, Vandebriel G, Lowrance DW, Gasana M, Finlay A: Evaluation of the rapid scale-up of collaborative TB/HIV activities in TB facilities in Rwanda. BMC Public Health. 2005-2009, 11: 550-

    Article  Google Scholar 

  6. 6.

    Sandgren A, Strong M, Muthukrishnan P, Weiner BK, Church GM, Murray MB: Tuberculosis drug resistance mutation database. PLoS Med. 2009, 6 (2): e2-10.1371/journal.pmed.1000002.

    Article  PubMed  Google Scholar 

  7. 7.

    Rasanathan K, Sivasankara Kurup A, Jaramillo E, Lonnroth K: The social determinants of health: key to global tuberculosis control. Int J Tuberc Lung Dis. 2011, 15 (Suppl 2): S30-S36.

    Article  PubMed  Google Scholar 

  8. 8.

    Roche PW, Winter N, Triccas JA, Feng CG, Britton WJ: Expression of Mycobacterium tuberculosis MPT64 in recombinant Myco. smegmatis: purification, immunogenicity and application to skin tests for tuberculosis. Clin Exp Immunol. 1996, 103 (2)): 226-232.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Harboe M, Nagai S, Patarroyo ME, Torres ML, Ramirez C, Cruz N: Properties of proteins MPB64, MPB70, and MPB80 of Mycobacterium bovis BCG. Infect Immun. 1986, 52 (1): 293-302.

    CAS  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Goldhofer W, Kreienberg R, Kutzner J, Lemmel EM: Influence of x-rays on the B- and T-cells in the spleen of mice and their reaction on mitogenetic substances (author's transl). Strahlentherapie. 1979, 155 (4): 277-283.

    CAS  PubMed  Google Scholar 

  11. 11.

    Chaudhary M, Gupta S, Khare S, Lal S: Diagnosis of tuberculosis in an era of HIV pandemic: a review of current status and future prospects. Indian J Med Microbiol. 2010, 28 (4): 281-289. 10.4103/0255-0857.71805.

    CAS  Article  PubMed  Google Scholar 

  12. 12.

    Christy KG, LaTart DB: Osterhoudt HW: Modifications for SDS-PAGE of proteins. Biotechniques. 1989, 7 (7)): 692-693.

    CAS  PubMed  Google Scholar 

  13. 13.

    Carroll MW, Moss B: E. coli beta-glucuronidase (GUS) as a marker for recombinant vaccinia viruses. Biotechniques. 1995, 19 (3): 352-354. 356

    CAS  PubMed  Google Scholar 

  14. 14.

    Kruger NJ: The Bradford method for protein quantitation. Methods Mol Biol. 1994, 32: 9-15.

    CAS  PubMed  Google Scholar 

  15. 15.

    Li H, Ulstrup JC, Jonassen TO, Melby K, Nagai S, Harboe M: Evidence for absence of the MPB64 gene in some substrains of Mycobacterium bovis BCG. Infect Immun. 1993, 61 (5): 1730-1734.

    CAS  PubMed  PubMed Central  Google Scholar 

  16. 16.

    Roche PW, Triccas JA, Avery DT, Fifis T, Billman-Jacobe H, Britton WJ: Differential T cell responses to mycobacteria-secreted proteins distinguish vaccination with bacille Calmette-Guerin from infection with Mycobacterium tuberculosis. J Infect Dis. 1994, 170 (5): 1326-1330. 10.1093/infdis/170.5.1326.

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Oettinger T, Andersen AB: Cloning and B-cell-epitope mapping of MPT64 from Mycobacterium tuberculosis H37Rv. Infect Immun. 1994, 62 (5): 2058-2064.

    CAS  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Abe C, Hirano K, Tomiyama T: Simple and rapid identification of the Mycobacterium tuberculosis complex by immunochromatographic assay using anti-MPB64 monoclonal antibodies. J Clin Microbiol. 1999, 37 (11): 3693-3697.

    CAS  PubMed  PubMed Central  Google Scholar 

  19. 19.

    Nakamura RM, Velmonte MA, Kawajiri K, Ang CF, Frias RA, Mendoza MT, Montoya JC, Honda I, Haga S, Toida I: MPB64 mycobacterial antigen: a new skin-test reagent through patch method for rapid diagnosis of active tuberculosis. Int J Tuberc Lung Dis. 1998, 2 (7): 541-546.

    CAS  PubMed  Google Scholar 

  20. 20.

    Nakamura RM, Einck L, Velmonte MA, Kawajiri K, Ang CF, Delasllagas CE, Nacy CA: Detection of active tuberculosis by an MPB-64 transdermal patch: a field study. Scand J Infect Dis. 2001, 33 (6): 405-407. 10.1080/00365540152029846.

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Ellington AD, Szostak JW: In vitro selection of RNA molecules that bind specific ligands. Nature. 1990, 346 (6287): 818-822. 10.1038/346818a0.

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Tuerk C, Gold L: Systematic evolution of ligands by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase. Science. 1990, 249 (4968): 505-510. 10.1126/science.2200121.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Shangguan D, Li Y, Tang Z, Cao ZC, Chen HW, Mallikaratchy P, Sefah K, Yang CJ, Tan W: Aptamers evolved from live cells as effective molecular probes for cancer study. Proc Natl Acad Sci U S A. 2006, 103 (32): 11838-11843. 10.1073/pnas.0602615103.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  24. 24.

    Daniels DA, Chen H, Hicke BJ, Swiderek KM, Gold L: A tenascin-C aptamer identified by tumor cell SELEX: systematic evolution of ligands by exponential enrichment. Proc Natl Acad Sci U S A. 2003, 100 (26): 15416-15421. 10.1073/pnas.2136683100.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Ohuchi SP, Ohtsu T, Nakamura Y: Selection of RNA aptamers against recombinant transforming growth factor-beta type III receptor displayed on cell surface. Biochimie. 2006, 88 (7): 897-904. 10.1016/j.biochi.2006.02.004.

    CAS  Article  PubMed  Google Scholar 

  26. 26.

    Paul A, Avci-Adali M, Ziemer G, Wendel HP: Streptavidin-coated magnetic beads for DNA strand separation implicate a multitude of problems during cell-SELEX. Oligonucleotides. 2009, 19 (3): 243-254. 10.1089/oli.2009.0194.

    CAS  Article  PubMed  Google Scholar 

  27. 27.

    Shi H, Tang Z, Kim Y, Nie H, Huang YF, He X, Deng K, Wang K, Tan W: In vivo fluorescence imaging of tumors using molecular aptamers generated by cell-SELEX. Chem Asian J. 2010, 5 (10): 2209-2213. 10.1002/asia.201000242.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Stoltenburg R, Reinemann C, Strehlitz B: FluMag-SELEX as an advantageous method for DNA aptamer selection. Anal Bioanal Chem. 2005, 383 (1): 83-91. 10.1007/s00216-005-3388-9.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Drabovich AP, Berezovski M, Okhonin V, Krylov SN: Selection of smart aptamers by methods of kinetic capillary electrophoresis. Anal Chem. 2006, 78 (9): 3171-3178. 10.1021/ac060144h.

    CAS  Article  PubMed  Google Scholar 

  30. 30.

    Berezovski MV, Musheev MU, Drabovich AP, Jitkova JV, Krylov SN: Non-SELEX: selection of aptamers without intermediate amplification of candidate oligonucleotides. Nat Protoc. 2006, 1 (3): 1359-1369. 10.1038/nprot.2006.200.

    CAS  Article  PubMed  Google Scholar 

  31. 31.

    Berezovski M, Musheev M, Drabovich A, Krylov SN: Non-SELEX selection of aptamers. J Am Chem Soc. 2006, 128 (5): 1410-1411. 10.1021/ja056943j.

    CAS  Article  PubMed  Google Scholar 

  32. 32.

    Dwivedi HP, Smiley RD, Jaykus LA: Selection and characterization of DNA aptamers with binding selectivity to Campylobacter jejuni using whole-cell SELEX. Appl Microbiol Biotechnol. 2010, 87 (6): 2323-2334. 10.1007/s00253-010-2728-7.

    CAS  Article  PubMed  Google Scholar 

  33. 33.

    Huang CJ, Lin HI, Shiesh SC, Lee GB: Integrated microfluidic system for rapid screening of CRP aptamers utilizing systematic evolution of ligands by exponential enrichment (SELEX). Biosens Bioelectron. 2010, 25 (7): 1761-1766. 10.1016/j.bios.2009.12.029.

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Li S, Xu H, Ding H, Huang Y, Cao X, Yang G, Li J, Xie Z, Meng Y, Li X, et al: Identification of an aptamer targeting hnRNP A1 by tissue slide-based SELEX. J Pathol. 2009, 218 (3): 327-336. 10.1002/path.2543.

    CAS  Article  PubMed  Google Scholar 

  35. 35.

    Tok JB, Fischer NO: Single microbead SELEX for efficient ssDNA aptamer generation against botulinum neurotoxin. Chem Commun (Camb). 2008, 16: 1883-1885.

    Article  Google Scholar 

  36. 36.

    Tanaka Y, Akagi K, Nakamura Y, Kozu T: RNA aptamers targeting the carboxyl terminus of KRAS oncoprotein generated by an improved SELEX with isothermal RNA amplification. Oligonucleotides. 2007, 17 (1): 12-21. 10.1089/oli.2006.0035R1.

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Burke DH, Gold L: RNA aptamers to the adenosine moiety of S-adenosyl methionine: structural inferences from variations on a theme and the reproducibility of SELEX. Nucleic Acids Res. 1997, 25 (10): 2020-2024. 10.1093/nar/25.10.2020.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  38. 38.

    Dastjerdi K, Tabar GH, Dehghani H, Haghparast A: Generation of an enriched pool of DNA aptamers for an HER2-overexpressing cell line selected by Cell SELEX. Biotechnol Appl Biochem. 2011, 58 (4): 226-230. 10.1002/bab.36.

    CAS  Article  PubMed  Google Scholar 

  39. 39.

    Ireson CR, Kelland LR: Discovery and development of anticancer aptamers. Mol Cancer Ther. 2006, 5 (12): 2957-2962. 10.1158/1535-7163.MCT-06-0172.

    CAS  Article  PubMed  Google Scholar 

  40. 40.

    Lupold SE, Hicke BJ, Lin Y, Coffey DS: Identification and characterization of nuclease-stabilized RNA molecules that bind human prostate cancer cells via the prostate-specific membrane antigen. Cancer Res. 2002, 62 (14): 4029-4033.

    CAS  PubMed  Google Scholar 

  41. 41.

    Guo KT, SchAfer R, Paul A, Gerber A, Ziemer G, Wendel HP: A new technique for the isolation and surface immobilization of mesenchymal stem cells from whole bone marrow using high-specific DNA aptamers. Stem Cells. 2006, 24 (10): 2220-2231. 10.1634/stemcells.2006-0015.

    CAS  Article  PubMed  Google Scholar 

  42. 42.

    Kunii T, Ogura S, Mie M, Kobatake E: Selection of DNA aptamers recognizing small cell lung cancer using living cell-SELEX. Analyst. 2011, 136 (7): 1310-1312. 10.1039/c0an00962h.

    CAS  Article  PubMed  Google Scholar 

  43. 43.

    Zueva E, Rubio LI, Duconge F, Tavitian B: Metastasis-focused cell-based SELEX generates aptamers inhibiting cell migration and invasion. Int J Cancer. 2011, 128 (4): 797-804. 10.1002/ijc.25401.

    CAS  Article  PubMed  Google Scholar 

  44. 44.

    Cerchia L, Duconge F, Pestourie C, Boulay J, Aissouni Y, Gombert K, Tavitian B, de Franciscis V, Libri D: Neutralizing aptamers from whole-cell SELEX inhibit the RET receptor tyrosine kinase. PLoS Biol. 2005, 3 (4): e123-10.1371/journal.pbio.0030123.

    Article  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Shamah SM, Healy JM, Cload ST: Complex target SELEX. Acc Chem Res. 2008, 41 (1): 130-138. 10.1021/ar700142z.

    CAS  Article  PubMed  Google Scholar 

  46. 46.

    Berezovski MV, Lechmann M, Musheev MU, Mak TW, Krylov SN: Aptamer-facilitated biomarker discovery (AptaBiD). J Am Chem Soc. 2008, 130 (28): 9137-9143. 10.1021/ja801951p.

    CAS  Article  PubMed  Google Scholar 

  47. 47.

    Cheng C, Dong J, Yao L, Chen A, Jia R, Huan L, Guo J, Shu Y, Zhang Z: Potent inhibition of human influenza H5N1 virus by oligonucleotides derived by SELEX. Biochem Biophys Res Commun. 2008, 366 (3): 670-674. 10.1016/j.bbrc.2007.11.183.

    CAS  Article  PubMed  Google Scholar 

  48. 48.

    Guo KT, Ziemer G, Paul A, Wendel HP: CELL-SELEX: Novel perspectives of aptamer-based therapeutics. Int J Mol Sci. 2008, 9 (4): 668-678. 10.3390/ijms9040668.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  49. 49.

    Dua P, Kim S, Lee DK: Patents on SELEX and therapeutic aptamers. Recent Pat DNA Gene Seq. 2008, 2 (3): 172-186. 10.2174/187221508786241710.

    CAS  Article  PubMed  Google Scholar 

  50. 50.

    Chen F, Zhou J, Luo F, Mohammed AB, Zhang XL: Aptamer from whole-bacterium SELEX as new therapeutic reagent against virulent Mycobacterium tuberculosis. Biochem Biophys Res Commun. 2007, 357 (3): 743-748. 10.1016/j.bbrc.2007.04.007.

    CAS  Article  PubMed  Google Scholar 

  51. 51.

    Vavvas D, D'Amico DJ: Pegaptanib (Macugen): treating neovascular age-related macular degeneration and current role in clinical practice. Ophthalmol Clin North Am. 2006, 19 (3): 353-360.

    PubMed  Google Scholar 

  52. 52.

    Ulrich H, Trujillo CA, Nery AA, Alves JM, Majumder P, Resende RR, Martins AH: DNA and RNA aptamers: from tools for basic research towards therapeutic applications. Comb Chem High Throughput Screen. 2006, 9 (8): 619-632. 10.2174/138620706778249695.

    CAS  Article  PubMed  Google Scholar 

  53. 53.

    Leng SX, McElhaney JE, Walston JD, Xie D, Fedarko NS, Kuchel GA: ELISA and multiplex technologies for cytokine measurement in inflammation and aging research. J Gerontol A Biol Sci Med Sci. 2008, 63 (8): 879-884. 10.1093/gerona/63.8.879.

    Article  PubMed  PubMed Central  Google Scholar 

  54. 54.

    Wanchu A: Advances in serology for diagnosing TB in the HIV infected. Indian J Chest Dis Allied Sci. 2005, 47 (1): 31-37.

    PubMed  Google Scholar 

Pre-publication history

  1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/12/96/prepub

Download references

Acknowledgments

This work was supported by the Ministry of Science and Technology of the People’s Republic of China (No. 2012ZX10003002-008), and the Science and Technology Commission of Shanghai Municipality, Shanghai, P. R. China (No. 10411955100 and No. 11ZR1430200).

Author information

Affiliations

  1. Department of Medical Laboratory, Changzhou Tumor Hospital Soochow University, Changzhou, 213001, China

    Changtai Zhu & Yang Ling

  2. Shanghai Key Laboratory of Tuberculosis, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China

    Changtai Zhu, Hua Yang, Zhonghua Liu, Ruijuan Zheng, Lianhua Qin & Zhongyi Hu

  3. Department of Respiratory Medicine, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China

    Jinming Liu

  4. Shanghai Key Laboratory of Tuberculosis, Shanghai Pulmonary Hospital, Tongji University School of Medicine, No. 507 Zhengmin Rd, Shanghai, 200433, China

    Lianhua Qin & Zhongyi Hu

Authors
  1. Changtai Zhu
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jinming Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Yang Ling
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Hua Yang
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Zhonghua Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Ruijuan Zheng
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Lianhua Qin
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Zhongyi Hu
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding authors

Correspondence to Lianhua Qin or Zhongyi Hu.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

CTZ, ZYH, LHQ and JML designed the study. CTZ, HY, ZHL, RJZ and LHQ performed the experiments. CTZ, JML and YL performed the statistical analysis. CTZ, LHQ and YL wrote the manuscript. JML, HY and ZYH provided valuable insight for revising the manuscript. All authors contributed to the study and have read and approved the final manuscript. ZYH is the guarantor.

An erratum to this article is available at http://dx.doi.org/10.1186/1471-2334-13-430.

Authors’ original submitted files for images

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Zhu, C., Liu, J., Ling, Y. et al. Evaluation of the clinical value of ELISA based on MPT64 antibody aptamer for serological diagnosis of pulmonary tuberculosis. BMC Infect Dis 12, 96 (2012). https://doi.org/10.1186/1471-2334-12-96

Download citation

Keywords

  • MPT64 antibody
  • System evolution of ligands by exponential enrichment (SELEX)
  • ssDNA
  • Aptamer
  • Tuberculosis

BMC Infectious Diseases

ISSN: 1471-2334

Contact us