Locked Nucleic Acid Probe-Based Real-Time PCR Assay for the Rapid Detection of Rifampin-Resistant Mycobacterium tuberculosis.

Drug-resistant Mycobacterium tuberculosis can be rapidly diagnosed through nucleic acid amplification techniques by analyzing the variations in the associated gene sequences. In the present study, a locked nucleic acid (LNA) probe-based real-time PCR assay was developed to identify the mutations in the rpoB gene associated with rifampin (RFP) resistance in M. tuberculosis. Six LNA probes with the discrimination capability of one-base mismatch were designed to monitor the 23 most frequent rpoB mutations. The target mutations were identified using the probes in a "probe dropout" manner (quantification cycle = 0); thus, the proposed technique exhibited superiority in mutation detection. The LNA probe-based real-time PCR assay was developed in a two-tube format with three LNA probes and one internal amplification control probe in each tube. The assay showed excellent specificity to M. tuberculosis with or without RFP resistance by evaluating 12 strains of common non-tuberculosis mycobacteria. The limit of detection of M. tuberculosis was 10 genomic equivalents (GE)/reaction by further introducing a nested PCR method. In a blind validation of 154 clinical mycobacterium isolates, 142/142 (100%) were correctly detected through the assay. Of these isolates, 88/88 (100%) were determined as RFP susceptible and 52/54 (96.3%) were characterized as RFP resistant. Two unrecognized RFP-resistant strains were sequenced and were found to contain mutations outside the range of the 23 mutation targets. In conclusion, this study established a sensitive, accurate, and low-cost LNA probe-based assay suitable for a four-multiplexing real-time PCR instrument. The proposed method can be used to diagnose RFP-resistant tuberculosis in clinical laboratories.

Introduction

The tuberculosis caused by drug-resistant strains of Mycobacterium tuberculosis has been considered as one of the most critical public health issues. The early diagnosis of drug-resistant tuberculosis via a rapid and reliable method can facilitate the administration of effective anti-tuberculosis drugs to patients and prevent the further spread of drug-resistant strains [1]. However, conventional culture-based drug susceptibility test requires several weeks to identify the cases of drug-resistant tuberculosis because of the slow growth of M. tuberculosis [2]. Over the last two decades, studies have considerably focused on the development of new and rapid methods that can be used to diagnose drug-resistant M. tuberculosis in a short period [3-5].

Nucleic acid amplification technique (NAAT) is currently one of the most rapid and sensitive molecular diagnostic tools to detect drug-resistant tuberculosis, which is mechanically developed on the basis of the genetic variations associated with drug resistance in M. tuberculosis [6, 7]. Though the genetic basis of drug resistance is only partially understood, several genes, such as rpoB, inhA, KatG, gyrA, and gyrB, in M. tuberculosis genome have been well documented because they have been highly implicated in drug resistance [8]. In particular, 95% of rifampin (RFP)-resistant strains contains mutations localized in the rpoB gene that encodes the β-subunit of the bacterial RNA polymerase. Reported mutations associated with RFP-resistance in the gene were accumulated in the 81-bp (codon 507 to codon 533) region called the rifampin resistance determination region (RRDR) [8-10]. Moreover, the most high-frequency mutations were localized at codon 516, 526, and 531, as observed worldwide [9, 11, 12]. Consequently, the rpoB genotype of M. tuberculosis has been considered as a genetic target to detect RFP resistance through NAATs.

Among the currently used NAATs, probe-based real-time PCR is one of the most prevalent and reliable approaches to detect drug-resistant M. tuberculosis. This approach can detect gene mutations associated with drug resistance by using the oligonucleotide probe, which is characteristic of mutation discrimination capability. Such probes used in the previously reported assays include the molecular beacon [13, 14], the TaqMan minor groove binder (MGB) probe [15], the sloppy molecular beacon[10], the dual-labeled probe[16, 17], and the padlock probe[18] and others. However, none of these probes exhibit rigid specificity to discriminate single-base mutations in the RRDR of M. tuberculosis in a simple manner. The molecular beacon-based and Taqman MGB-based assays discriminated the wild-type sequences from the mutations based on their differences of quantification cycles (ΔCq) [14, 15]. The sloppy molecular beacon-based and dual-labelled probe-based approaches need additional Tm analyses after the amplification[19]. Padlock probes were used in the rolling circle amplifications, which required complex procedure [18]. In addition to above probes, LNA probe is another kind of probe that has been widely used in real-time PCR to quantitatively detect pathogens [20, 21]. The LNA probe contains oligonucleotide monomers modified with an additional methylene bridge between 2′ oxygen and 4′ carbon of the ribose ring. The modified LNA monomer or monomers in the probe can increase the thermal stability of the probe and help develop short probe designs, which can improve capability of the probe to detect mutations [22]. The reported advantages of the probes include superior sensitivity and specificity to detect mutation, ease of design, and preferable signal-to-noise ratio [23, 24].

In the study, a LNA-probe real-time PCR assay was developed to detect RFP-resistant strains of M. tuberculosis. Six LNA probes that can discriminate one-base mutations have been designed to identify mutations in the RRDR of the rpoB. According to the reports [14], a total of 23 common rpoB mutations associated with RFP-resistant M. tuberculosis, including high-frequency mutations at codon 516, 526, and 531, were collected as the targets to evaluate the LNA probe-based assay. The LNA probe is highly specific; thus, any one-base mismatch can be easily identified through the amplification curves (Cq = 0), without complex determinations or additional Tm analyses. And the proposed assay showed sufficient specificity and sensitivity to detect M. tuberculosis and RFP-resistant M. tuberculosis, validated by a blind test of 154 clinical isolates.

Materials and Methods

Clinical isolates

A reference strain of M. tuberculosis H37Rv (ATCC 27294) and 142 clinical isolates of M. tuberculosis with well-defined information on drug susceptibility and rpoB gene sequence were collected for the present study. The isolates were preserved and cultured at the State Key Laboratory for Infectious Disease Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, and Chinese Center for Disease Control and Prevention (Beijing, P. R. China). The 142 isolates of M. tuberculosis were determined with 88 RFP-susceptible strains and 54 RFP-resistant strains. DNA sequences of the RFP-resistant strains contains 17 types of rpoB mutations (S1 Table), covering the most frequent mutations at codons 516, 526, and 531. The RFP-susceptible strains showed no mutations in the RRDR region of the rpoB gene.

Another set of 12 clinical isolates of non-tuberculosis mycobacterium (NTM) were also collected in the study, including Mycobacterium smegmatis, M. avium, M. terrae, M. shimodii, M. kansasii, M. asiaticum, M. scrofulaceum, M. gordanea, M. chelonea, M. abscessus, M. fortuitum, and M. phlei.

Cloning of the rpoB gene

Corresponding to the rpoB sequences from the M. tuberculosis H37Rv genome (GenBank accession no. L27989) and the 23 common mutations associated with RFP resistance (Table 1), rpoB segments (280 bp) containing the RRDR of wild and mutant types were synthesized and cloned into the pUC 57 vector. The plasmid DNA was used to initially evaluate and optimize probe specificity.

Table 1

Summary of the assay performance for the detection of rpoB mutations.

Mutation codon	Mutation type	Cq values
		LNA-P1	LNA-P2	LNA-P3	LNA-P4	LNA-P5	LNA-P6
507 #	Deletion	N*	27.78	27.84	28.07	29.52	28.43
510	CAG-CAT	24.08	N	24.43	22.96	24.43	25.95
511	CTG-CCG	26.81	N	26.91	28.17	29.46	28.66
511 #	CTG-CGG	26.97	N	27.3	26.15	27.57	28.51
513	CAA-AAA	26.27	N	26.61	27.58	29.32	27.98
513 #	CAA-CCA	27.51	N	27.83	26.61	28.03	29.46
513 #	CAA-CTA	23.69	N	24.00	22.83	24.19	25.60
516	GAC-TAC	24.47	27.62	N	27.70	29.82	26.41
516	GAC-GTC	23.49	27.18	N	27.27	29.53	25.27
516	GAC-GGC	27.91	31.68	N	32.91	33.87	29.06
516–517 #	Deletion	22.15	23.85	N	24.11	25.42	24.15
522	TCG-TTC	23.51	20.82	23.83	N	21.36	25.27
522 #	TCG-CAG	29.03	25.99	29.35	N	26.32	30.73
522 #	TCG-TGG	26.84	24.27	27.14	N	24.60	28.03
526	CAC-TAC	26.74	28.3	27.06	28.38	N	28.43
526	CAC-AAC	25.85	25.32	26.2	25.53	N	27.45
526	CAC-GAC	26.07	27.21	26.58	27.32	N	27.33
526	CAC-TGC	24.84	26.26	25.24	26.38	N	26.35
526 #	CAC-CCC	23.01	22.65	23.40	23.15	N	26.49
526	CAC-CGC	26.98	29.29	27.03	29.95	N	28.71
526	CAC-CTC	25.49	26.91	25.83	26.97	N	27.03
531	TCG-TTG	27.59	28.27	27.59	29.01	29.80	N
531	TCG-TTT	23.95	26.14	24.35	26.20	26.63	N

# Plasmid DNA template;

* Negative result.

DNA extraction

Chromosomal DNA was extracted from fresh bacterial cultures via traditional cetyltrimethylammonium bromide (CTAB) method [25]. In brief, the bacterial cells were digested with lysozyme and proteinase K in the presence of sodium dodecyl sulfate. DNA was released from proteins and other components by using CTAB (final concentration, 40 mM) and then extracted using chloroform-isoamyl alcohol (24:1). The genomic DNA was then isolated through ethanol precipitation and resuspended in Tris-EDTA buffer for storage.

Plasmid DNA was extracted using a QIAamp DNA mini kit (Qiagen, Hilden, Germany) in accordance with the manufacturer’s instructions. The DNA samples were stored at −20°C.

Primers and LNA probes preparation

The real-time PCR primers and probes used in the study are shown in S2 Table. The primers used to amplify rpoB were manually designed to selectively amplify a 206 bp amplicon containing the RRDR. Six LNA probes were designed to identify any mutation in the amplicon and to specifically hybridize with the entire 81 bp RRDR in the wild-type strains by using Beacon Designer software 7.9 (PREMIER Biosoft). Each LNA probe was covalently labeled at the 5′-end with a unique fluorescent reporter dye [6-carboxyfluorescein (FAM), 4,4,7,2′,4′,5′,7′-hexachloro-6-carboxyfluorescein (HEX), or Cy5] and a BHQ at the 3′-end. All of the probes and primers were synthesized by Huirui (Shanghai, China).

The specific primers and probes of Bacillus globigii (ATCC 9372) were also used for the internal amplification control (IAC) and were amplified with M. tuberculosis in one real-time PCR to detect PCR inhibitors. The oligonucleotide sequences of the primers and a Taqman probe were designed using Primer Express 3.0 (Applied Biosystems, Foster City, CA) to target a conserved segment of BgSP in B. globigii (GenBank accession no. L27989). The Taqman probe was labeled with carboxy-X-rhodamine (ROX) to be distinguished from the other dyes.

Evaluation of LNA probes by plasmid DNA through monoplex-probe real-time PCR

Plasmid DNA templates, including the wild-type template and the corresponding mutant templates, were used to determine the specificity of each LNA probes through a monoplex-probe real-time PCR amplification. The monoplex-probe real-time PCR was performed in a final reaction volume of 25 μl containing 2× LightCycler 480-probe master mix (Roche Diagnostics), forward primer of rpoB (rpoB-F2, 400 nM), reverse primer of rpoB (rpoB-R, 400 nM), detecting LNA-probe (240 nM), and 2.5 μl of plasmid DNA template (3.0 × 105 copies/μl). The final volume was adjusted with distilled water. The reaction was run under the following conditions: 95°C for 5 min, followed by 45 cycles of denaturation at 95°C for 15 s, annealing at 65°C for 30 s, and a cooling down step at 37°C for 1 min.

Establishment of the multiplex-probe real-time PCR assay

Multiplex-probe real-time PCR was run in a two-tube formation (Tube A and Tube B), with three differently labeled LNA-probes and an IAC-probe in each tube. A final reaction volume of 30 μl was used in each tube containing 2× LightCycler 480-probe master mix, primers for rpoB (rpoB-F2 and rpoB-R, 800 nM), primers for BgSP (BgSP-F and BgSP-R, 500 nM), a mixture of probes (LNA-P6, LNA-P3, LNA-P1, and IAC-probe in Tube A, 240 nM), or a mixture (LNA-P2, LNA-P5, LNA-P4, and IAC-probe in Tube B, 240 nM), 2.5 μl of the purified DNA of B. globigii (1000 GE/μl), and 2.5 μl of the genomic DNA extracted from mycobacteria.

Real-time PCR was conducted using a LightCycler 480 II instrument. The conditions of PCR amplification were as follows: initial activation at 95°C for 5 min, followed by 45 cycles of denaturation at 95°C for 15 s, annealing at 65°C for 30 s, and a cooling down step at 37°C for 1 min. Four filter combinations (excitation spectrum–emission spectrum) were chosen and set as follows: FAM channel (465 nm–510 nm), HEX channel (498 nm–580 nm), Rox channel (533 nm–610 nm), and Cy5 channel (618 nm–660 nm). The fluorescence in the four channels was determined simultaneously during the annealing step. Before fluorescence was analyzed, color compensation was established in accordance with the manufacturer’s instructions. The quantification cycle (Cq) was obtained by using the LightCycler software program (version 4.0) with the second derivative algorithms.

Result interpretations through the real-time PCR assay

The real-time PCR assay results are described as follows: (1) M. tuberculosis was determined by positive signals from at least four LNA probes; (2) RFP-susceptible M. tuberculosis was determined by positive signals from all of the six LNA probes; (3) RFP-resistant M. tuberculosis was determined by one or two absent probe signals. (4) M. tuberculosis was precluded if signals were absent in three or more probes. (5) Diagnoses were based on a positive signal from the IAC probe (34 < Cq < 40); otherwise, the test was considered invalid.

Determination of the assay sensitivity

The genomic DNA of M. tuberculosis H37Rv was prepared in serial dilutions from 4,000,000 GE/μl to 4 GE/μl to evaluate the assay sensitivity. Then, 2.5 μl of the diluted DNA was used as the template to determine sensitivity for the multiple-probe-based real-time PCR. The templates are tested in triplets at least, as described above. To achieve an improved sensitivity, the nested PCR was introduced into the assay. The first round of the nested PCR was performed in a 20 μl reaction volume containing 2× Light Cycler 480-probe master mix, 250 nM of each primer (rpoB-F1, rpoB-R), 3 μl of DNA, and distilled water. The reaction was run under the following conditions: 95°C for 5 min, followed by 30 cycles of 10 s at 95°C, 15 s at 60°C, and another 15 s at 72°C. The product from the first round of PCR was diluted 100 times with distilled water and used as the template for the second round of real-time PCR as mentioned above.

Determination of the assay specificity to rpoB mutations associated with RFP resistance

DNA samples with 23 different RRDR sequences were prepared to determine the assay capability to discriminate rpoB mutations associated with RFP resistance. Of the templates, 15 were from the genomic DNA of RFP-resistant strains of M. tuberculosis among the sequenced clinical isolates; the other 8 DNA templates were from the plasmid DNA prepared in the study. All the DNA templates were diluted to the concentration ranged from 105 to 106 GE/tube or copies/tube.

Determination of the assay specificity by DNA samples from the NTMs

12 NTM strains were collected and used to confirm the detecting specificity of the proposed assay. Genomic DNA samples were extracted from the NTMs as the templates (approximately 0.1 ng/μl) of the LNA-probe based real-time PCR. DNA sequences from drug-susceptible M. tuberculosis and drug-resistant M. tuberculosis were also prepared and tested as the control.

Validation of the assay by clinical isolates

A total of 154 bacteria samples, including 12 NTM strains and 142 clinical isolates with well-defined information on drug susceptibility and rpoB sequence, were used to evaluate performance of the assay. Each DNA sample was diluted to the concentration of 105 or 106 GE/tube as the template of the real-time PCR. The DNA samples were coded independently and randomly and tested by the assay in a blind test way.

Results

Establishment of the real-time PCR assay

As presented in the design scheme in Fig 1, six fluorescent LNA probes (LNA-P1 to LNA-P6) were designed to identify the genetic variations in the rpoB gene of M. tuberculosis. The probes were assigned to monitor the RRDR region (from codon 507 to codon 533 of rpoB). The LNA probes could identify these single-base mutations in a manner of “probe dropout” (Cq = 0); in this way, the probe could not combine with the mutant target; as a result, negative fluorescence signals were produced during amplification. The six LNA probes were allocated in two tubes to consist of a two-tube form real-time PCR assay. Each tube contained three LNA probes labeled with different dyes. The two reactions were performed simultaneously and shared the same real-time PCR components except the included probes to detect drug-resistant M. tuberculosis. Probe allocation was determined by comparing different probe combinations (S3 Table). Finally, LNA-P1, LNA-P3, and LNA-P6 were placed in tube A, and LNA-P2, LNA-P4, and LNA-P5 were placed in tube B.

Fig 1

Schematic description of the assay and mutation discrimination capability of the six LNA probes.

(a) The assay is performed in a two-tube form with three LNA probes and one IAC probe in each tube to detect M. tuberculosis and RFP-resistant M. tuberculosis. The two tubes share the same real-time PCR components except the included probes. (b) The LNA probes used in the assay could discriminate single-base mutations. The single-base variation in the target sequence prevents the corresponding probe matching and combining with the target; as a result, probe dropout from the sequence occurs (Cq = 0).

An internal amplification control (IAC) based on B. globigii (ATCC 9372) was developed to monitor PCR inhibitors in each tube. The IAC system consists of specific primers and a Taqman probe labeled with Rox, which were targeted at a conserved segment in BgSP of B. globigii. Considering the amplification competition between rpoB and BgSP, we pre-added approximately 2500 GE/tube B. globigii to the reaction mixture to generate a sufficient IAC signal and significantly reduce the interference with rpoB amplification.

Evaluation of the LNA probe by plasmid DNA

Before the assay with multiple probes was established, the capability of each LNA probe to discriminate single-base mutations was initially confirmed in monoplex-probe real-time PCR experiments. Plasmid DNA samples, including the wild-type strains and 23 common types of rpoB sequences with single-base mutations were prepared as template. The results showed that the 23 types of mutant genotypes could be clearly differentiated from the wild targets on the basis of the amplification curves; these mutant genotypes were detected through “probe dropout”. The Cq values of the mutant sequences were determined as negative (Cq = 0) by the second derivative algorithms described in the Materials and methods. The results showed the strong capability of the LNA probe to identify single-base mutations.

All of the LNA probes could combine with the wild-type sequences and generate positive Cq values. In addition, the Cq values of the same concentration of wild DNA (from 7.5 copies/tube to 7.5 × 106 copies/tube) did not significantly vary, although the six probes were aimed at different regions and emitted signals in different fluorescent channels (S1 Fig). The results demonstrated consistent amplification efficiency (determined in accordance with the MIQE Guidelines[26]) and quantifications in the six single-probe PCRs, which facilitate the optimization of the following assay with multiple probes.

Sensitivity of the multiple-probe assay

The real-time PCR assay with multiple LNA probes was developed and optimized after the capacity of each LNA probe was assessed. The genomic DNA was extracted from M. tuberculosis H37Rv and diluted in series (10 GE/tube to 1.0 × 106 GE/tube) to determine the sensitivity of the assay. The results indicated that the limit of detection (LOD) could reach 100 GE/tube with an average Cq value of 37.72 (S4 Table). The LOD was approximately tenfold higher than that of the real-time PCR with single LNA probe (7.5 copies/tube). The decrease in PCR vitality was caused by two factors. One of the factors involved the presence of the inhibitors from the excess by-products because of the multiple-labeled probes, which may inhibit the activity of the DNA polymerase. The other factor included the competition for the IAC amplification in the same reaction cannot be ignored, especially when the primary rpoB target was at a low concentration. The nested PCR amplification was introduced to the real-time PCR assay to overcome these problems; as a result, the LOD was increased to 10 GE/tube (Fig 2a).

Fig 2

Sensitivity of the probe assay for the detection of M. tuberculosis H37Rv.

(a) Amplification curves of M. tuberculosis (10 GE/tube to 1.0 × 106 GE/tube) through the multiple-probe real-time PCR. The LOD could be increased to 10 GE/tube through the combination of nested PCR amplification. (b) Quantification curve for M. tuberculosis. The curve displayed good linearity (R2 = 0.987) for M. tuberculosis at a range of 1.0 × 102 GE/tube to 1.0 × 106 GE/tube.

The quantification curve was also established to quantitatively detect M. tuberculosis (Fig 2b). The x-axis represents the DNA concentration, and the y-axis represents the Cq values (average of the six channels’). The curve displayed good linearity (R2 = 0.987) for M. tuberculosis at a range of 1.0 × 102 GE/tube to 1.0 × 106 GE/tube. The quantification equation was expressed by y = −3.525x + 52.270. The equation revealed an amplification efficiency of 92.2% for the assay; thus, the multiple-probe PCR was strongly reliable.

Detection of the rpoB mutations associated with RFP resistance

The capability of the assay to discriminate rpoB mutations associated with RFP resistance was evaluated to detect RFP-resistant M. tuberculosis. As shown in Table 1, the 23 common rpoB genotypes with single-base mutations could be correctly detected through the assay. The absence of any single-base mutation in the DNA caused the “dropout” of the corresponding LNA probe during amplification (Cq = 0); by contrast, the other LNA probes worked well in the reaction. Our results further indicated that the RFP-resistant M. tuberculosis can be identified on the basis of the “probe dropout” instead of ΔCq values that is used in most other NAAT assays [14, 15]. Previous studies demonstrated the rpoB mutations associated with RFP resistance are mainly single- or double-codon mutations, and triple or more codon mutations have been rarely reported. Therefore, RFP-resistant M. tuberculosis could be determined as positive if one- or two-probe dropout from the target DNA.

Specificity of the assay

The specificity of the assay to M. tuberculosis was confirmed by evaluating the DNA samples extracted from 12 NTM strains (Fig 3). As the results show, M. tuberculosis did not have probe dropouts (RFP-susceptible M. tuberculosis) or did not have more than two dropouts (RFP-resistant M. tuberculosis). However, three or more LNA probe dropouts occurred when the 12 NTM DNA samples were evaluated (S5 Table). Various degrees of homology were observed between NTM and M. tuberculosis H37Rv by analyzing the rpoB gene sequences. As a result, positive LNA probe signals in amplification of the NTM were observed. However, none of the 12 NTMs were identified as M. tuberculosis on the basis of the assay results (details in the Materials and methods). Therefore, the assay was sufficiently specific for M. tuberculosis.

Fig 3

Assay performance with M. tuberculosis and non-tuberculosis mycobacteria (NTM).

M. tuberculosis was diagnosed with no probe dropouts (RFP-susceptible M. tuberculosis) or no more than two dropouts (RFP-resistant M. tuberculosis). The 12 NTM DNA samples were identified with three or more LNA probe dropouts.

Validation of 154 clinical isolates through a blind test

A set of 154 clinical isolates with well-defined information on drug susceptibility and rpoB gene sequence, including NTM strains, RFP-susceptible M. tuberculosis strains and RFP-resistant M. tuberculosis, were used to evaluate the assay performance through a blind test. As the results show (Table 2), 12/12 (100%) of the NTM samples were correctly identified as free of M. tuberculosis. The remaining isolates were all recognized as M. tuberculosis by the assay with a high accuracy of 142/142 (100%). Furthermore, of the 142 strains identified as M. tuberculosis, 88/88 (100%) RFP-susceptible M. tuberculosis strains were accurately detected through the assay. In addition, 52/54 (96.3%) of the RFP-resistant M. tuberculosis strains were correctly determined. Of the total samples, only two RFP-resistant strains were falsely diagnosed as RFP-susceptible M. tuberculosis by the assay. Corresponding DNA Sequences of the RRDR was analyzed in the two discordant samples. An rpoB mutation at codon 510 (CAG-CAC) and a mutation codon 522 (TCG-ATG) were then found in the two RFP-resistant samples. However, both mutations were related to low level of resistance to RFP [27, 28] and were not in the panel of the 23 common mutations. Overall, 152/154 clinical isolates (98.7%) were correctly identified by the assay. The whole results showed a highly specific performance of the assay to detect M. tuberculosis and RFP-resistant M. tuberculosis.

Table 2

Assay performance with 154 clinical isolates.

Sample types	Amount of samples	Amount of samples detected	Amount of samples undetected
not M. tuberculosis	12	12 (100%)	0
RFP-susceptible M. tuberculosis	88	88 (100%)	0
RFP-resistant M. tuberculosis	54	52 (96.3%)	2
Total	154	152 (98.7%)	2

Discussion

In the study, we developed a LNA probe-based assay to determine the genotype of rpoB gene to detect M. tuberculosis and RFP-resistant M. tuberculosis. 23 different mutations in the RRDR, including the high-frequency mutations at codon 516, 526, and 531, were all identified by the LNA probes and the proposed assay. The assay also showed high specificity to M. tuberculosis by testing 12 strains of common NTMs. Sensitivity of the detection could reach 10 GE/reaction by further introducing a nested PCR method. Through the evaluation of clinical isolates, the assay presented a high accuracy of 152/154 (98.7%) to detect M. tuberculosis and RFP-resistant M. tuberculosis.

The proposed assay utilized six well-designed LNA probes as the genotype detector of RRDR. As a result, all the 23 common mutations were highly distinguished by the LNA probes in a manner of “probe dropout”, which could be easily identified through the amplification curves (Cq = 0), without complex determinations or additional Tm analyses. There are several real-time PCR assays developed for the detection of drug-resistance associated mutations by using other kinds of probes, such as the molecular beacon-based Xpert MTB/RFP assay [5], However, the molecular beacon did not identify the mutations at codon 511 (CGG), codon 516 (TAC and GGC), and codon 526 (AAC and CGC) in the way of “probe dropout” [14]. To discriminate these mutations, the assay still needs complex result determinations based on the value of ΔCq between the matched and mismatched hybridization.

The assay contains seven different probes, including six LNA probes and one IAC Taqman probe. Considering the availability of the real-time PCR instrument and easy application of the assay, we developed a real-time PCR assay in a two-tube form instead of one tube. The design requires only a real-time PCR instrument with four fluorescent detecting channels, such as LightCycler 480 II, ABI 7500, SmartCycler, and CFX 96 real-time PCR detecting system. However, the assay could be improved to a single-tube format to exhibit convenience; thus, the assay could be applicable to common instruments. Furthermore, the assay can be transferred to an automatic diagnostic platform with the capability of “sample-in answer out,” similar to the Cepheid GeneXpert system [29], to achieve point-of-care diagnostics of M. tuberculosis.

In summary, six LNA probes were designed to detect drug resistance-associated mutations in rpoB, and these probes have been validated with excellent specificity to detect the common mutations in the RRDR. Moreover, the LNA probe-based real-time assay developed in the study shows sufficient specificity and sensitivity to detect M. tuberculosis and drug-resistant M. tuberculosis, which can become a powerful alternative tool to rapidly diagnose drug-resistant tuberculosis. The assay could also be used to detect the mutations involved in the resistance to other anti-tuberculosis drugs, such as isoniazid, ethambutol, and fluoroquinolone, through designing corresponding specific LNA probes, in future studies.

Amplification efficiency of the six LNA probes.

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rpoB mutations in the RFP-resistant clinical isolates of M. tuberculosis.

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Oligonucleotide primers and probes used in this study.

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Comparison of four different probe combinations by evaluating the wild-type rpoB template at the same concentration.

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Cq values for the detection of M. tuberculosis H37Rv (10 GE/tube to 1.0 × 106 GE/tube) through the real-time PCR.

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Detection results of non-tuberculosis mycobacteria (NTM) and M. tuberculosis.

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