1. Introduction
Tuberculin skin tests by intradermal Purified Protein Derivative (PPD) injection can rapidly detect mycobacterial infection, but it gives a positive result, not only to active TB patients, but also to persons with asymptomatic Mycobacterium tuberculosis infection and M. bovis BCG-vaccinated persons. PPD is composed of >100 proteins and represents all proteins secreted during growth in culture media in vitro, as PPD is prepared through the precipitation of culture filtrates from M. tuberculosis. Different culture batches and precipitation methods result in varied levels of tuberculoprotein (48% to 99%) [1] . Thus, the identification of specific defined antigens that can discriminate between active TB-infected patients and latent or asymptomatic TB-infected/vaccinated persons will lead to more efficient control and better treatment of the disease.
In recent years, several antigens secreted from actively growing M. tuberculosis cultures have been characterized. To achieve a high sensitivity of diagnosis for TB patients, several antigens have been evaluated for their ability to elicit humoral and cell-mediated immune responses. Antigens such as MPT51, 81/88 kDa GlcB protein, and 38 kDa protein elicit antibody responses, whereas the antigens of Ag85, ESAT6, CFP10, and MPT64 elicit T-cell responses [2] . In the search for a new skin test that is specific for the diagnosis of TB infection, ESAT6, MPT64, CFP10, and DPPD (Rv0061) elicit delayed-type hypersensitivity (DTH) in a guinea pig model [2] [3] .
Recent studies reported that M. tuberculosis-specific antigens ESAT6, CFP10, CFP21, and MPT64, alone or in combination, induce a strong DTH response in M. tuberculosis-infected guinea pigs but elicit little response in BCG-vaccinated animals [4] [5] . This observation emphasizes the specificity of these antigens as viable candidates for skin test development. In fact, a TB skin patch test using several TB-specific antigens (including MPT64) has been developed, and a patent has been filed (United State Patent 6979450); however, this test has not been widely used (in Thailand, PPD is still used). Thus, development of an improved skin patch test for TB diagnosis that is suitable for local use is worthwhile.
Calmette and Guerin of the Pasteur Institute passaged a strain of M. bovis 230 times in vitro from 1908 to 1921, thus developing the vaccine strain, M. bovis BCG. Since then, the M. bovis BCG seed lots were distributed to institutions around the world. Serial passage was performed to maintain the BCG strain at different vaccine facilities until lyophilization was introduced in the 1960s. Molecular analysis of genomic DNA by whole-genome DNA microarray revealed that several segments of DNA were missing from M. bovis and M. bovis BCG strains compared to M. tuberculosis H37Rv reference strain. These deletion regions were named RD1 to RD16. Nine regions (RD4, RD5, RD6, RD7, RD9, RD10, RD11, RD12, and RD15) encompassing 61 open reading frames (ORFs) are absent from all M. bovis BCG and M. bovis strains, whereas two regions (RD9 and RD13) with 30 ORFs are absent from M. bovis BCG and some M. bovis strains. Five regions (RD1, RD2, RD8, RD14, and RD16) containing 38 ORFs are present in M. bovis but absent from some or all M. bovis BCG strains. RD1, missing from all M. bovis BCG strains, contains 9 ORFs which include two secretory proteins Rv3874 (CFP10) and Rv3875 (ESAT6). RD2, present in “early strains” such as BCG Russia and BCG Tokyo, contains 11 ORFs which include Rv1980c (MPT64) [6] . Since all M. bovis BCG strains do not secrete CFP10 or ESAT6, these two proteins are appropriate candidates for differentiating between infection with M. tuberculosis and vaccination with M. bovis BCG.
In Thailand, the M. bovis BCG strain used is Tokyo; therefore, in this study, we used the Tokyo strain and compared it to M. tuberculosis H37Rv (laboratory virulent strain). It was previously shown that recombinant MPT64 (rMPT64) was able to elicit a DTH response in guinea pigs sensitized with M. bovis BCG Tokyo similar to that of native MPB64 and native MPT64 isolated from culture filtrates of M. bovis BCG Tokyo (which expresses MPB64) and M. tuberculosis H37Rv (which expresses MPT64), respectively [7] [8] . Thus, in this study, we tested the responses of guinea pigs infected with M. tuberculosis or M. bovis BCG Tokyo by sensitization with PPD or purified recombinant MPT64, CFP10, and ESAT6. The aim of this study was to test whether purified recombinant antigens can induce a DTH reaction comparable to PPD in guinea pigs. This result could lead to the use of specific, purified recombinant antigens to develop an improved skin test for TB diagnosis that could replace the currently used PPD.
2. Materials and Methods
2.1. Molecular Biology Materials and Chemicals
Restriction enzymes, DNA molecular weight markers, and protein molecular weight markers were purchased from New England Biolabs, USA. Takara LA Taq and T4 DNA ligase were obtained from Takara Bio Inc., Japan. The plasmid purification kit was purchased from QIAGEN, USA. Other chemicals and antibiotics were obtained from Sigma-Aldrich Inc., USA. PPD (tuberculin skin test reagent lot# TP0081108/12/201108/06/2012) was acquired from Queen Saovabha Memorial Institute, the Thai Red Cross Society. Protein concentrator MWCO 5000 Da was obtained from Sartorius Stedim Biotech GmbH, Germany (Vivaspin) or Millipore, USA (Amicon ultrafiltration). Talon Superflow Metal Affinity resin was purchased from Clontech Takara Bio Inc., Japan. The HiLoad 16/60 Superdex 75 prep grade gel filtration column was obtained from GE Healthcare, Sweden. The two commercial plasmids used in this study were pGEM-T Easy (PCR cloning vector, AmpR/Ampici- lin resistant, Promega) and pET24b (C-terminal His6-tagged expression vector, KmR/Kanamycin resistant, Novagen).
2.2. Bacterial Strains, Culture Media, and Guinea Pigs
Mycobacterium tuberculosis strain H37Rv (laboratory virulent strain, ATCC 25618) and M. bovis BCG Tokyo (Vaccine strain, Queen Saovabha Memorial Institute, the Thai Red Cross Society) used in this study were grown on Middlebrook 7H11 agar medium or Middlebrook 7H9 liquid medium supplemented with 10% Middlebrook OADC [Oleic acid Albumin Dextrose Catalase] Enrichment (Difco BBL). Escherichia coli DH5α [9] and E. coli BL21 (λDE3) [10] , used as a gene cloning host and protein expression host, respectively, were grown in Luria- Bertani (LB) medium supplemented with 100 μg/mL of ampicillin or 50 μg/mL of kanamycin where appropriate. Guinea pigs (Dunkin Hartley outbred), female, weight 300 - 400 g were acquired from the National Laboratory Animal Center, Mahidol U., Thailand.
2.3. PCR Amplification and Cloning of MPT64 (Rv1980c), CFP10 (Rv3874), and ESAT6 (Rv3875) into pET24b
Genes encoding MPT64 (618 bp, mature peptides Rv1980c), CFP10 (303 bp, Rv3874), and ESAT6 (288 bp, Rv 3875) were PCR amplified from M. tuberculosis H37Rv genomic DNA using three primer pairs (sequences underlined: restriction enzyme recognition sites, sequences in bold: start codon of genes). The primers were designed to clone genes into pET24b to express fusion proteins with His6 at C-termini. For ease of cloning, 5’-primers were designed to include “CATATG” (NdeI recognition site) for which “ATG” is the start codon of Rv3874 and Rv3875. For MPT64 (GenBank: X75361.1), the start codon of mature peptides is “GCG”, thus addition of “CATATG” to 5’-primer resulted in an additional methionine at the N-terminus of rMPT64. The 3’- primers were designed to exclude the stop codon of the genes with addition of restriction enzyme recognition site (NotI or HindIII).
MPT64-S/5’-primer (5’-AAA CAT ATGGCG CCC AAG ACC TAC TGC GAG GAG-3’)
MPT64-ANR/3’-primer (5’-TTT GCG GCC GCG GCC AGC ATC GAG TCG ATC GCG GA-3’)
Rv3874Nde5/5’-primer (5’-TAT ACA TAT GGC AGA GAT GAA GAC C-3’)
Rv3874Hind3/3’-primer (5’-TAT AAA GCT TGA AGC CCA TTT GCG AG-3’)
Rv3875Nde5/5’-primer (5’-TAT ACA TAT GAC AGA GCA GCA GTG G-3’)
Rv3875Hind3/3’-primer (5’-TAT AAA GCT TTG CGA ACA TCC CAG T-3’)
Fifty microliter reaction mixtures containing 100 ng of DNA template (genomic DNA of M. tuberculosis H37Rv or M. bovis BCG Tokyo as control), 2.5 units of Takara LA Taq, 0.4 mM of each dNTP, 0.5 μM of each primer, and 25 μL 2× GC Buffer II were diluted to 50 μL with autoclaved distilled water. The reactions were denatured at 94˚C for 3 min and then cycled through 30 rounds of denaturation at 94˚C for 30 sec, annealing at 60˚C for 30 sec, and extension at 72˚C for 1 min. These cycles were followed by a final cycle at 72˚C for 5 min.
The PCR products Rv1980c, Rv3874, and Rv3875 (amplified from genomic DNA of M. tuberculosis H37Rv) were cloned into the PCR cloning vector pGEM-T Easy and were then sub-cloned into the NdeI-NotI or NdeI-HindIII sites of pET24b to generate pET24Rv1980, pET24Rv3874, and pET24Rv3875. Restriction enzyme digestion and DNA sequencing confirmed that the orientation and sequence of the cloned genes were correct.
2.4. Expression and Purification of Recombinant-His6 Proteins
E. coli BL21 (λDE3) harboring the recombinant plasmid (pET24Rv1980, pET24Rv3874, or pET24Rv3875) was grown in 50 mL of LB medium supplemented with 50 μg/mL kanamycin at 37˚C with shaking (200 rpm) overnight. The next day, the cell cultures were diluted in 500 mL of fresh medium to an OD600 of 0.05 and incubated at 37˚C with shaking at 200 rpm until the cultures reached log phase (OD600 approx. 0.3 - 0.6). Protein induction was initiated by adding IPTG to a final concentration of 0.5 mM and incubating the cultures at 25˚C (for pET24Rv1980 and pET24Rv3874) or 37˚C (for pET24Rv3875) with shaking at 180 rpm for 6 - 12 h. Cells were harvested by centrifugation and washed with PBS.
Cell pellets from 1 L of cell culture were resuspended with 20 mL of equilibration buffer (50 mM sodium phosphate buffer, 300 mM NaCl, 0.1% Triton X-100, and 5% glycerol, pH 7.0). Lysozyme and phenylmethylsulfonyl fluoride (PMSF) were added to the cell suspension to a final concentration of 1 mg/mL and 1 mM, respectively. The cell suspensions were incubated on ice for 30 min, and the cells were disrupted by sonication and centrifuged at 4˚C/16000×g/40 min to separate the cell debris. The supernatants (clear cell lysate) were then subjected to purification by an Immobilized Metal ion Affinity Column (IMAC) using Talon Superflow Metal Affinity resin (Clontech), as recommended by the manufacturer. Purified protein was analyzed in 12% or 15% SDS-PAGE, and the protein bands were visualized by coomassie blue staining.
The elution fractions of purified proteins were pooled and dialyzed against equilibration buffer, pH 7.0 (50 mM sodium phosphate, 300 mM NaCl), until the imidazole concentration was reduced from 150 mM to less than 5 mM. The proteins were concentrated, and the buffer was exchanged using a spin column with a molecular weight cutoff (MWCO) of 5000 Da (5 kDa MWCO).
2.5. Protein Purification by Gel Filtration
Two proteins, rMPT64 and rESAT6, were further purified by gel filtration using an AKTA purification system with the UNICORN 5.1 program (GE Healthcare). The gel filtration column used was a pre-packed HiLoad 16/60 Superdex 75 pg column, the buffer contained 20 mM sodium phosphate and 150 mM NaCl at pH 7.4, and the program parameters were as follows: flow rate = 1 mL/min, injection volume = 1 mL, fraction volume = 3 mL, and elution volume = 1.2 column volume.
All purified proteins were filtered by passing them through an Acrodisc Syringe Filter (0.45 µm) with low protein binding (Pall). The protein concentration was determined using Lowry’s method. The final protein solution was diluted to 1 mg/mL before use in animal tests.
2.6. Cytotoxicity Test
Proteins purified by IMAC (rMPT64, rCFP10, and rESAT6) and proteins purified by IMAC and gel filtration (rMPT64 and rESAT6) were tested for cytotoxicity at a concentration of 50 μg/mL against Vero cells (African green monkey kidney) at Bioassay Laboratory (BIOTEC, Thailand).
2.7. Animal Models of TB and Skin Testing of Antigens
Guinea pigs (Dunkin Hartley outbred, female) were obtained from the Faculty of Veterinary Science, Mahidol University. The in vivo studies were approved by an ethical committee at the Faculty of Veterinary Science, Mahidol University (ethical number MUVS 2009-05), and the experiments were performed in animal BSL3 facilities at the Faculty of Veterinary Science, Mahidol University.
Fifteen guinea pigs weighing 300 - 400 g were divided into 3 groups with 5 animals per group. In groups 1 and 2, animals were infected (intramuscular injection) on day 1 with 105 CFU of M. tuberculosis in 0.1 mL PBS (pH 7.4) and vaccinated (intradermal injection) with 2 × 105 CFU of M. bovis BCG Tokyo in 0.1 mL PBS, respectively. Animals in group 3 served as a naïve control. After 4 weeks, both flanks of the animals were shaved, and skin tests were performed by intradermal injection (as shown in Appendix: Figure S1) with either 10 IU PPD (positive control), the specified amounts of the antigens (1 or 5 μg of single or mixed antigens) diluted in 0.1 mL PBS, or 0.1 mL PBS (negative control). The antigens used were IMAC plus gel filtration-purified rMPT64 and rESAT6 and IMAC-purified rCFP10.
Skin test responses (diameter of erythema/redness) were observed and measured after 24, 48, and 72 h. Erythema diameter greater than 0.5 cm was considered as skin test positive [3] . For ease of interpretation, the erythema formation was determined and scored as follows: 0 = absent, not perceptible; 1 = mild redness, diameter < 0.5 cm; 2 = mild redness, diameter > 0.5 cm; 3 = redness, diameter > 0.5 but < 0.8 cm; 4 = redness, diameter > 0.8 cm; and 5 = redness, diameter > 0.5 cm, papule. Scores of 0 to 1 were considered “negative”, and scores of 2 to 5 were considered a “positive” skin test response.
Skin biopsies were collected at the designated sites (intradermal injection sites) and processed by standard histopathological procedures. The tissue sections were stained with hematoxylin and eosin and observed under a light microscope [11] .
3. Results and Discussion
3.1. PCR Amplification of mpt64 (Rv1980c), cfp10 (Rv3874), and esat6 (Rv3875)
Genes encoding MPT64 (Rv1980c), CFP10 (Rv3874), and ESAT6 (Rv3875) were PCR amplified from M. tuberculosis H37Rv genomic DNA using specific primer pairs as described in Materials and Methods. Control PCR reactions were also performed using genomic DNA of M. bovis BCG Tokyo as template. PCR products were analyzed on 1% agarose gel electrophoresis (Figure 1). The size of PCR fragments of mpt64 (Rv1980c), cfp10 (Rv3874), and esat6 (Rv3875) were 635, 317, and 302 bp, respectively (Figure 1: lane 1, 3, and 5). There was PCR product of mpb64 but not cfp10 and esat6 from M. bovis BCG Tokyo genomic DNA template (Figure 1: lane 2, 4, and 6). These results were consistent with the fact that mpb64 is present but cfp10 and esat6 are absent in M. bovis BCG Tokyo [6] .
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Figure 1. PCR amplification of mpt64 (Rv1980c), cfp10 (Rv3874) and esat6 (Rv3875) from genomic DNA of M. tu- berculosis H37Rv and M. bovis BCG Tokyo. PCR were performed (as described in Materials and Methods) using gene specific primers to amplify mpt64 (Rv1980c), lane 1-2; cfp10 (Rv3874), lane 3-4; and esat6 (Rv3875), lane 5-6. DNA templates used were genomic DNA of M. tuberculosis H37Rv (Mtb: lane 1, 3, and 5) and genomic DNA of M. bovis BCG Tokyo (Mbv: lane 2, 4, and 6). Lane M1 and lane M2, 1 kb DNA Ladder and 100 bp DNA Ladder. Arrows indicate PCR products of mpt64, mpb64, cfp10, and esat6.
3.2. Preparation of Recombinant Antigens rMPT64, rCFP10, and rESAT6
All recombinant antigens (MPT64, CFP10, and ESAT6) were cloned into pET24b and expressed as C-terminal His6-tagged proteins for ease of purification by IMAC. The molecular weights of rMPT64, rCFP10 and rESAT6 were 24.9, 12.5, and 11.5 kDa, respectively. All recombinant proteins prepared by IMAC were >95% pure as shown in Figure 2. The purification profiles of rMPT64 (Figure 2(a)), rCFP10 (Figure 2(b)), and rESAT6
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(b) (c)
Figure 2. SDS-PAGE of rMPT64, rCFP10, and rESAT6 purified by IMAC. Proteins were analyzed on 15% SDS-PAGE and stained with coomassie blue. M, protein MW standard. (a) Purification profile of rMPT64 by IMAC: lane 1, protein MW standard; lane 2, crude protein; lane 3, flow through; lane 4-6, wash; lane 7-13, eluted fraction. The arrow indicates rMPT64 protein; (b) Purified rCFP10; (c) Purified rESAT6.
(Figure 2(c)) are also provided. For rMPT64 and rESAT6, the proteins were further purified by gel filtration after IMAC purification (data not shown). Proteins purified by IMAC or IMAC plus gel filtration were tested for cytotoxicity against Vero cells, and the results showed that at 50 μg/mL, these purified proteins were not toxic (data not shown).
3.3. Skin Test Responses of Guinea Pig
Three groups of guinea pigs (5 animals per group) were sensitized with PPD or recombinant antigens (rMPT64, rCFP10, and rESAT6) after either 28 days of infection with M. tuberculosis H37Rv (group 1), vaccination with M. bovis BCG Tokyo (group 2), or no infection for the naïve control (group 3). Skin test responses were determined and scored after 24, 48, and 72 h (Appendix: Table S1 and Table S2). In the naïve control group (group 3), the animals showed no sign of skin reactions (scoring = 0, data not shown). All animal groups showed no skin reactions when injected with PBS (scoring = 0, data not shown). Most of the DTH reaction subsided after 72 h. M. tuberculosis H37Rv-infected animals responded to rMPT64 weaker than they did to PPD. M. bovis BCG Tokyo-vaccinated animals, on the other hand, exhibited a similar DTH response to rMPT64 and to PPD (Figure 3(a) and Figure 3(b)). Our result is in agreement with previous reports [8] [12] that recombinant MPT64 prepared from E. coli elicited a DTH response in guinea pigs infected with M. bovis BCG Tokyo. Data from the previous reports also suggested that rMPT64 could replace native MPT64/MPB64 in an in vivo study [8] [12] . Although we did not compare the DTH response obtained from rMPT64-His6 with native MPT64, our results (Figure 3(b)) indicate that rMPT64-His6 is active in an in vivo model to the same degree as rMPT64 described in the previous reports.
M. tuberculosis-infected (group 1) animal responses to a single purified antigen were highly variable, and some animals did not respond at all. However, when the three antigens (rMPT64, rCFP10, and rESAT6) were combined, all animals showed positive reactions (Figure 4(a)). On the other hand, one of the M. bovis BCG Tokyo-vaccinated (group 2) animals did not respond to 1 μg of combined antigens. However, at higher dose of 5 μg of combined antigens, all animals showed positive DTH response similar to that observed in M. tuberculosis-infected animals (Figure 4(b)). This outcome emphasizes the requirement for having multiple specific antigens to elicit a clear DTH response.
A previous study showed that all M. tuberculosis-infected guinea pigs responded well to each of the recombinant antigens, CFP10, ESAT6, and MPT64. When the three antigens were combined, the DTH response was greater than that of any single antigen [5] . However, other studies showed that not all animals infected with M. tuberculosis responded to a single antigen [4] [13] [14] . A previous report on the response to rCFP10 was investigated in six M. tuberculosis-infected guinea pigs. During an initial experiment, all six animals responded to rCFP10, but in a second experiment, three animals showed no reactivity to rCFP10 [14] . Another study also showed that in a group of eighteen M. tuberculosis-infected guinea pigs, four animals did not respond to rMPT64, and ten animals did not respond to rESAT6, but when these two antigens were combined, strong DTH
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(a) (b)
Figure 3. Analysis of skin test responses of guinea pigs in group 1 (M. tuberculosis infected) and group 2 (M. bovis BCG Tokyo vaccinated). A group of 5 guinea pigs were infected with M. tuberculosis or vaccinated with M. bovis BCG Tokyo. After 28 days, the animals were sensitized with antigens, and the skin reactions were recorded after 24, 48, and 72 h. The antigens used were 10 IU PPD (a) and 5 μg purified rMPT64 (b).
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(a) (b)
Figure 4. Analysis of DTH scores of guinea pigs from group 1 (M. tuberculosis infected) and group 2 (M. bovis BCG Tokyo vaccinated) in response to antigens after 48 h. A group of 5 guinea pigs were infected with M. tuberculosis (a) or vaccinated with M. bovis BCG Tokyo (b). After 28 days, the animals were sensitized with antigens, and the skin reactions were recorded after 48 h. The antigens used were 10 IU PPD, and 1 and 5 μg of individual purified antigen (rMPT64, rCFP10, and rESAT6) or a combination of these 3 antigens (mixed of 1 μg and mixed of each purified antigen).
reactions were observed in all animals [13] . An investigation of four RD antigens, ESAT6, CFP10, CFP21, and MPT64, showed that these antigens were purified from culture filtrates of M. tuberculosis H37Rv strains and were used to elicit a DTH response in M. tuberculosis H37Rv-infected or M. bovis BCG-vaccinated guinea pigs. As expected, none of these antigens elicited a DTH response in M. bovis BCG-vaccinated guinea pigs, as the RD1 region is absent from the M. bovis BCG genome. In addition, not all of the M. tuberculosis H37Rv-infected animals responded to individual antigens or a combination of the four antigens (two to three out of four animals responded). However, when two antigens were combined in any possible combination, they could detect all four infected animals, and the highest DTH response was induced by a combination of ESAT6 and CFP10. It was suggested from this study that when combining two or more antigens, their immuno-compatibility (recognition by HLA alleles or competition to antigen-presenting cells) should be taken in consideration [4] . It is possible that variations in the DTH response in guinea pigs may be due to genetic restrictions to some specific antigens and not to others. Another study of six recombinant antigens, MPT63, MPT64, MTC28, MPT32, MPT51, and MPT70, demonstrated the use of these antigens individually or in combination to elicit a DTH response in M. bovis BCG Japanese ATCC 35737-immunized guinea pigs. The results showed that the DTH response increased with the number of antigens used [15] . Moreover, a previous study demonstrated that MPT64 alone failed to elicit a DTH response in most human subjects with positive PPD [16] .
Our results showed that all animals in group 2 failed to respond to rCFP10 and rESAT6 due to the absence of genes encoding for cfp10 (Rv3874) and esat6 (Rv3875) in M. bovis BCG Tokyo (Figure 4(b)). This result is in agreement with a previous report that investigated the potential use of four antigens, PE35, PPE68, CFP10, and ESAT6, encoded by M. tuberculosis-specific RD1 region genes, for active TB diagnosis [17] . In the previous report, the four recombinant antigens were tested for a DTH response in guinea pigs injected with M. tuberculosis, M. bovis BCG, M. avium, and M. vaccae. The results confirmed that these antigens elicited positive DTH responses in the M. tuberculosis-injected group but not in BCG-, M. avium-, and M. vaccae-injected guinea pigs. Thus, RD1 antigens elicited an M. tuberculosis-specific DTH response.
New skin test reagents for TB diagnosis in humans should elicit a strong DTH response similar to that obtained from PPD and also be specific to TB infected patients. The three recombinants antigens, rMPT64, rCFP10, and rESAT6, generated in our study have the potential to be used as new skin test reagents. The rMPT64 induces a DTH response comparable to that elicited by PPD in M. bovis BCG Tokyo-sensitized guinea pigs. The rCFP10 and rESAT6 specifically induce a DTH response in guinea pigs infected with M. tuberculosis only. Thus the combined of the three antigens should be further evaluated as skin test reagents in TB diagnosis.
Tissue sections from animals following the intradermal skin test that showed evidence of redness and papule formation were collected at 72 h. Histopathology studies on these lesions showed an infiltration of lymphocytes and macrophages in the dermis, and macrophages were more numerous than lymphocytes. However, the number of infiltrating inflammatory cells was not different between PPD and three other single antigens (rMPT64, rCFP10, and rESAT6) or combined antigens in M. tuberculosis-infected guinea pigs. It was previously reported that examination of the skin tissue of BCG-sensitized guinea pigs with DTH in response to rMPB64 found mononuclear cell infiltration similar to that of skin tissue reacting to PPD [7] . The infiltration of mononuclear cells observed in the histopathology of the skin tissue is considered to be classical DTH.
4. Conclusion
In this report, we produced purified recombinant proteins rMPT64, rCFP10, and rESAT6 and used them as antigens to stimulate DTH responses in guinea pigs. Our results showed that the purified recombinant proteins were pure and non-toxic to Vero cells and could stimulate a DTH response in animals, confirming previous reports [7] [8] [12] -[15] . It was not surprising that the responses observed from purified proteins were less than those obtained from PPD, because PPD is comprised of >100 secreted proteins. Because MPT64 is secreted from actively growing bacteria, our experiment utilized animals that were sensitized with antigens for 4 weeks after vaccination with M. bovis BCG Tokyo, during which time the bacteria were still replicating. Thus, positive results were observed because the situation was similar to that in which the animals were infected with M. tuberculosis. If skin tests had been performed after 8 weeks, skin tests with rMPT64 would have been negative because the bacteria would have already stopped growing. rCFP10 and rESAT6 are specific antigens secreted from M. tuberculosis, and our results showed that in combination with rMPT64, these antigens increased the DTH response and thus helped to differentiate TB infections. More refined experiments on the amount of single and combined antigens used to stimulate DTH should be performed to formulate a diagnostic test for TB infection. Our study has established the foundation for an improved skin test for TB diagnosis in Thailand.
Competing Interests
The authors declare that they have no competing interests.
Acknowledgements
This project was supported by grants from the Cluster Program Management Office (CPMO) and BIOTEC, National Science and Technology Development Agency (NSTDA) (Project P-00-20213 (BT-02-MM-BC-4911) and P-12-01153). The authors thank Duangporn Ungsupravate for technical assistance and thank Dr. Nat Smittipat and Tada Jutayothin for comment and suggestion.
Abbreviations
PPD: Purified Protein Derivative
MPT64: immunogenic protein from M. tuberculosis identical to MPB64 from M. bovis
ESAT6: Early Secreted Antigen Target 6
CFP10: Culture Filtrate Protein 10
PBS: Phosphate Buffer Saline
CFU: Colony Forming Unit
BCG: Bacille Calmette-Guérin
IMAC: Immobilized Metal ion Affinity Chromatography
PCR: Polymerase Chain Reaction
DTH: Delayed-Type Hypersensitivity
RD: Region of Difference
Appendix
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Figure S1. Intradermal injection of antigens on both flanks of a guinea pig. PPD and PBS were used as the positive and negative controls, respectively. Purified antigens were tested individually or in combination. The antigen concentrations used were 1 and 5 μg. Ag1, rMPT64; Ag2, rCFP10; Ag3, rESAT6.
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Table S1. Guinea pig group 1 (M. tuberculosis H37Rv infected): scores of the skin test responses after the guinea pigs were sensitized with antigens for 24, 48, and 72 h.
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Table S2. Guinea pig group 2 (M. bovis BCG Tokyo vaccinated): scores of the skin test responses after the guinea pigs were sensitized with antigens for 24, 48, and 72 h.
NOTES
*Corresponding author.