Skip to main content
  • Research article
  • Open access
  • Published:

Molecular characterization of multidrug-resistant tuberculosis against levofloxacin, moxifloxacin, bedaquiline, linezolid, clofazimine, and delamanid in southwest of China



To explore the drug susceptibility of levofloxacin (LFX), moxifloxacin (MFX), bedaquiline (BDQ), linezolid (LZD), clofazimine (CFZ) and delamanid (DLM) against multidrug resistant tuberculosis (MDR-TB) isolates from drug resistance survey of southwest China, and to illustrate the genetic characteristics of MDR-TB isolates with acquired drug resistance.


A total of 339 strains were collected from smear-positive TB patients in the drug resistance survey of southwest China between January 2014 and December 2016. The MICs for the above mentioned drugs were determined for MDR-TB by conventional drug susceptibility testing. Genes related to drug resistance were amplified with their corresponding pairs of primers.


MDR was observed in 88 (26.0%; 88/339) isolates. LFX had the highest resistance rate (50.0%; 44/88), followed by MFX (38.6%; 34/88). The resistance rate to LZD, CFZ, and DLM was 4.5% (4/88), 3.4% (3/88), and 4.5% (4/88), respectively, and the lowest resistance rate was observed in BDQ (2.3%; 2/88). Of the 45 isolates resistant to LFX and MFX, the most prevalent resistance mutation was found in gyrA with the substitution of codon 94 (34/45, 75.6%). Two strains with CFZ - BDQ cross resistance had a mutation in the Rv0678 gene. Of the four LZD resistant isolates, two carried mutations in rplC gene. For the four isolates resistant to DLM, one isolate had mutations in codon 318 of fbiC gene, and two isolates were with mutations in codon 81 of ddn gene.


This study provided evidence of the usefulness of new anti-TB drugs in the treatment of MDR-TB in China.

Peer Review reports


Though effective control programmes have been implemented, TB continues to be a major lethal infectious disease worldwide, with an estimated of 10 million new cases and 1.45 million deaths in 2018 [1]. This situation is complicated further by the emergence of drug-resistant strains, dramatically limiting the treatment options. Hence, improved treatment regimens and new drugs are urgently needed to be developed. Based on the latest evidence about the balance of effectiveness to safety, the new multidrug resistant tuberculosis (MDR-TB) treatment guidelines were released in 2018 by World Health Organization (WHO) with medicines regrouped into three categories [2].

China has the second greatest number of MDR-TB cases in the world1. According to the Fifth National TB Epidemiological Survey, the prevalence of active and smear positive pulmonary TB in western China was greater than that in the middle and eastern regions, which was also higher than the rate of the whole country [3]. Due to the remote mountainous areas and ethnic minorities, it is more difficult to control TB in southwest China. Besides, there is a lack of resistance data on the drugs in the MDR-TB treatment regimen recommended by WHO.

The objective of this study was to explore the drug susceptibility of levofloxacin (LFX), moxifloxacin (MFX), bedaquiline (BDQ), and linezolid (LZD) from group A, clofazimine (CFZ) from group B and delamanid (DLM) from group C against MDR-TB isolates from drug resistance survey of southwest China on the basis of minimum inhibitory concentrations (MIC), and to illustrate the genetic characteristics of MDR-TB isolates with acquired drug resistance.

Materials and methods

Ethics statement

The protocols applied in this study were approved by the Ethics Committee of Chinese center for disease control and prevention, Beijing, China.

Bacterial strains and culture conditions

A total of 339 strains were collected from smear-positive TB patients in the drug resistance survey of southwest of China between January 2014 and December 2016. All isolates were subcultured on the Löwenstein-Jensen (L-J) medium for 4 weeks at 37 °C.

Conventional drug susceptibility testing

Drug susceptibility was determined using the 1% proportion method on L-J medium according to the guidelines of the WHO [4] with rifampin (RIF), 40 μg/ml; isoniazid (INH), 0.2 μg/ml; streptomycin (SM), 10 μg/ml; ethambutol (EMB), 2 μg/ml; capreomycin (CAP), 40 μg/ml; kanamycin (KAN), 30 μg/ml; and ofloxacin (OFX), 2 μg/ml. The MDR-TB was defined as resistance to at least INH and RIF, and XDR-TB was defined as any MDR strain additionally resistant to one fluoroquinolone and one second-line injectable drug.

Minimum inhibitory concentrations

For MDR-TB identified by conventional drug susceptibility testing, the MICs of LFX, MFX, LZD, BDQ, CFZ, and DLM were determined as described previously [5]. The MIC value was defined as the lowest concentration of antibiotic that inhibits visible growth of mycobacteria. By referring to previous literature [6,7,8], susceptibility breakpoints for each antibiotic are shown in Table 1. Mycobacterium tuberculosis H37Rv (ATCC 27249) was used as the control strain.

Table 1 The minimum inhibitory concentrations and susceptibility breakpoints for each antibiotic

DNA extraction and sequencing

Genomic DNA was extracted from freshly cultured bacteria as previously reported [9]. Genes related to drug resistance were amplified with their corresponding pairs of primers (Table 2). The 25 μl PCR mixture was prepared as follows: 12 μl of 2× Taq Master Mix, 1 μl of forward and reverse primers (10 μΜ), 10 μl of distilled H2O and 1 μl of genomic DNA. PCR parameters for amplification were 5 min at 95 °C, followed by 35 cycles at 94 °C for 1 min, 58 °C for 1 min, 72 °C for 1 min, and a final extension at 72 °C for 10 min. PCR products were sent to Tsingke company for sequencing. Sequencing data was aligned with the corresponding sequences of the M. tuberculosis H37Rv reference strain using Bioedit (version software.

Table 2 Primers used in this study for amplification and sequencing

Statistical analysis

SPSS v.17.0 (SPSS Inc., Chicago, IL) was used to carry out χ2 analysis, and differences were considered to be statistically significant if P < 0.05.


Drug susceptibility profiles of MDR-TB strains

MDR was observed in 88 (26.0%; 88/339) isolates with 59 (67.0%; 59/88) resistant to SM, 28 (31.8%; 28/88) resistant to EMB, 6 (6.8%; 6/88) resistant to CAP, 11 (12.5%; 11/88) resistant to KAN, and 35 (39.8%; 35/88) resistant to OFX. In addition, 9 isolates (10.2%; 9/88) were identified as XDR strains.

The results of MICs for MDR-TB isolates against six antibiotics were shown in Table 1. LFX had the highest resistance rate (50.0%; 44/88), followed by MFX (38.6%; 34/88). The resistance rate to LZD, CFZ, and DLM was 4.5% (4/88), 3.4% (3/88), and 4.5% (4/88), respectively, and the lowest resistance rate was observed in BDQ (2.3%; 2/88). In addition, out of the 44 LFX-resistant isolates, 33 (75%) were resistant to MFX, and 2 (66.7%) out of the 3 CFZ-resistant isolates were resistant to BDQ.

Mutations conferring antibiotics resistance

Among the 45 isolates resistant to FQs (44 isolates resistant to LFX, 34 isolates resistant to MFX, and 33 isolates cross resistant to LFX and MFX), the most prevalent resistance mutation of gyrA was the substitution in codon 94 (34/45, 75.6%), resulting in the amino acid substitution of Asp for 13 (13/45, 28.9%) Gly, 11 (11/45, 24.4%) Tyr, 6 (6/45, 13.3%) Ala, and 4 (4/45, 8.9%) Asn. In addition, the second most common substitution occurred in codon 90 with substitution of Ala-Val (8/45, 17.8%). The remaining substitutions were Gly88Cys (1/45, 2.2%), Asp89Asn (1/45, 2.2%), Ser91Pro (1/45, 2.2%). Notably, substitution Ser95Thr in gyrA known to be not associated with FQs resistance was found in all FQs resistance isolates. No nonsynonymous mutations were identified in the gyrB gene (Table 3).

Table 3 Mutations conferring antibiotices resistance

A total of 3 strains were identified as CFZ resistant, sequence analysis revealed that all these strains harbored no nucleotide substitution in the rv1979c gene. And no mutation was observed in atpE gene of BDQ resistant isolates. All two CFZ-BDQ cross resistant strains had a mutation in the Rv0678 gene, one with Gln31Arg substitution and the other with Ser53Pro.

Of the four isolates resistant to LZD, two isolates carried mutations in rplC gene with amino acid substitution of Cys154Arg, while 23S rRNA and rplD gene seemed not to confer LZD resistance among these strains.

In addition, five candidate genes associated with DLM resistance was also analyzed in four DLM-resistant isolates. No mutations were observed in fbiA, fbiB, and fgd1 genes, while one isolate with the mutations in codon 318 of fbiC gene and two isolates in codon 81 of ddn gene.


Since the MDR-TB cases have emerged as a major obstacle to global TB control due to small number of effective drugs and high risk of adverse effects, promising candidates are needed to provide potential solutions to resolve this troublesome dilemma. Following a clinical study of novel regimens recommended for MDR-TB, we investigated drugs resistance from the groups A, B and C, and to analyze the genetic determinants of this resistance in MDR-TB isolates obtained from patients.

For the two newer FQs, our data revealed that 50.0% of MDR-TB strains were resistant to LFX, and 38.6% resistant to MFX in southwest of China. A study from mid-East of China showed that 37% of fluoroquinolone resistance events were in MDR M. tuberculosis isolates [10]. And a total of 76% LFX resistance and 73% MFX resistance MTB isolates were identified in a study from southern China [11]. Another report from Shanghai revealed that among FQ-resistant M. tuberculosis strains, 44% were multidrug-resistant isolates [12]. The higher resistance rate of FQs in China may due to the overuse of FQs in the treatment of undiagnosed bacterial infections, highlights the urgent need to take action to fight FQs misuse in clinical practice. Molecular analysis showed that a total of 75.6% FQr isolates were shown to harbour mutations in gyrA QRDR, with condon 94 being the most predominant mutation site, but no mutation in gyrB gene was observed [12]. The reported frequency in condon 94 is similar to that in Hong Kong (75%) [13] and to that in Rwanda (75%) [14], although it is lower than that in Russia (83%) [15] and higher than that in Taiwan (50%) [16], showing that mutations in gyrA QRDR were the key factor leading to quinolone resistance in M. tuberculosis in China.

As for BDQ and CFZ, more than 95% of MDR-TB strains were susceptible in this study. Though they are now being studied as a component of novel regimens for MDR-TB, mutations in the Rv0678 gene, which causes the overexpression of efflux pump MmpS5-MmpL5, were found to result in cross-resistance between the two drugs [17]. Consistent with previous studies, our data demonstrated that two of three CFZ-resistant isolates had Rv0678 mutations and were cross-resistance to BDQ. However, no mutations in Rv1979c were identified in CFZ-resistant isolates without Rv0678 mutations. Further studies are needed to expand our understanding of mechanisms of resistance to CFZ by identifying additional mutations. Though several target-based resistance mutations in the atpE gene have been described in BDQ-resistant strains, but no atpE mutations were found in this study. Additional mechanisms may be contributed to the resistance of BDQ.

Linezolid was effectively used to treat of MDR strains [6]. According to previous studies, the T460C mutation in rplC gene was the most frequent among the LZD-resistant isolates [18]. In this study, two MDR-TB isolates (2/4, 50%) were identified mutations in the rplC gene, which was in line with previous studies. In addition, polymorphisms in any of five genes (ddn, fgd1, fbiA, fbiB, and fbiC) have been shown to lead to in vitro DLM resistance [8]. Ddn gene, encoding an F420-dependent mycobacterial nitroreductase, was associated with the prodrug activation. Resistance to DLM is caused by the loss of this ability to activate DLM [19]. In a recent study by Liu et al. [20], out of the ten primary resistant isolates, five were MDR-TB isolates with nonsynonymous mutation on ddn. In this study, two MDR isolates with ddn mutation conferring DLM resistance were identified. Besides, previous studies revealed that mutations in the coenzyme F420 biosynthesis pathway result in the loss of M. tuberculosis bacilli’s ability to activate PA-824, another nitroimidazole similar to DLM [21]. So as a member of the coenzyme F420 biosynthesis pathway, FbiC was involved in DLM resistance. In this study, of the three DLM resistant isolates, one isolate with mutation in fbiC gene, suggesting fbiC serves as an important contributor to DLM resistance.


In conclusion, MDR-TB isolates exhibited a high proportion of resistance to FQs, whereas excellent activity against MDR-TB was observed in BDQ, LZD, DLM and CFZ in southwest of China. Strains with mutations in codon 94 of the gyrA gene are more likely to be associated with high-level FQs resistance. In addition, mutations in Rv0678 gene and rplC gene were related to clofazimine-bedaquiline cross resistance and linezolid resistance respectively, and mutations in fbiC and ddn gene may be conferred to delamanid resistance on M. tuberculosis isolates. And this study provides evidence for further application of new anti-TB drugs in the treatment of MDR-TB in China.

Availability of data and materials

Data supporting the results can be found in this paper. The datasets generated during and analyzed during the current study are available from the corresponding author (AD. Shen) on reasonable request.


  1. Global tuberculosis report 2019. Geneva: World Health Organization; 2019.

  2. Rapid communication: key changes to treatment of multidrug- and rifampicin-resistant tuberculosis (MDR/RR-TB).

  3. Wang L, Zhang H, Ruan Y, Chin DP, Xia Y, Cheng S, et al. Tuberculosis prevalence in China, 1990-2010; a longitudinal analysis of national survey data. Lancet. 2014;383(9934):2057–64.

    Article  PubMed  Google Scholar 

  4. World Health Organization. Guidelines for the programmatic management of drug-resistant tuberculosis. Geneva: WHO; 2008.

    Google Scholar 

  5. Zhang D, Wang Y, Lu J, Pang Y. In vitro activity of beta-lactams in combination with beta-lactamase inhibitors against multidrug-resistant mycobacterium tuberculosis isolates. Antimicrob Agents Ch. 2016;60(1):393–9.

    Article  CAS  Google Scholar 

  6. Zhang Z, Pang Y, Wang Y, Liu C, Zhao Y. Beijing genotype of mycobacterium tuberculosis is significantly associated with linezolid resistance in multidrug-resistant and extensively drug-resistant tuberculosis in China. Int Antimicrob Ag. 2014;43(3):231–5.

    Article  CAS  Google Scholar 

  7. Zhang Z, Li T, Qu G, Pang Y, Zhao Y. In vitro synergistic activity of clofazimine and other antituberculous drugs against multidrug-resistant mycobacterium tuberculosis isolates. Int Antimicrob Ag. 2015;45(1):71–5.

    Article  CAS  Google Scholar 

  8. Schena E, Nedialkova L, Borroni E, Battaglia S, Cabibbe AM, Niemann S, et al. Delamanid susceptibility testing of mycobacterium tuberculosis using the resazurin microtitre assay and the BACTEC MGIT 960 system. Int Antimicrob Ag. 2016;71:1532–9.

    CAS  Google Scholar 

  9. Pang Y, Zhou Y, Zhao B, Liu G, Jiang G, Xia H, et al. Spoligotyping and drug resistance analysis of mycobacterium tuberculosis strains from national survey in China. PLoS One. 2012;7(3):e32976.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Che Y, Song Q, Yang T, Ping G, Yu M. Fluoroquinolone resistance in multidrug-resistant mycobacterium tuberculosis independent of fluoroquinolone use. Eur Respir J. 2017;50(6):1701633.

    Article  CAS  PubMed  Google Scholar 

  11. Hameed HMA, Tan Y, Islam MM, Guo L, Chhotaray C, Wang S, et al. Phenotypic and genotypic characterization of levofloxacin- and moxifloxacin-resistant mycobacterium tuberculosis clinical isolates in southern China. J Thorac Dis. 2019;11(11):4613–25.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Zhu C, Zhang Y, Shen Y, Siu GK, Wu W, Qian X, et al. Molecular characterization of fluoroquinolone-resistant mycobacterium tuberculosis clinical isolates from Shanghai, China. Diagn Micr Infec Dis. 2012;73(3):260–3.

    Article  CAS  Google Scholar 

  13. Chan RC, Hui M, Chan EW, Au TK, Chin ML, Yip CK, et al. Genetic and phenotypic characterization of drug-resistant mycobacterium tuberculosis isolates in Hong Kong. J Antimicrob Ch. 2007;59(5):866–73.

    Article  CAS  Google Scholar 

  14. Umubyeyi AN, Rigouts L, Shamputa IC, Fissette K, Elkrim Y, de Rijk PW, et al. Limited fluoroquinolone resistance among mycobacterium tuberculosis isolates from Rwanda: results of a national survey. J Antimicrob Ch. 2007;59(5):1031–3.

    Article  CAS  Google Scholar 

  15. Mokrousov I, Otten T, Manicheva O, Potapova Y, Vishnevsky B, Narvskaya O, et al. Molecular characterization of ofloxacin-resistant mycobacterium tuberculosis strains from Russia. Antimicrob Agents Ch. 2008;52(8):2937–9.

    Article  CAS  Google Scholar 

  16. Huang TS, Kunin CM, Shin-Jung Lee S, Chen YS, Tu HZ, Liu YC. Trends in fluoroquinolone resistance of mycobacterium tuberculosis complex in a Taiwanese medical Centre: 1995-2003. J Antimicrob Ch. 2005;56(6):1058–62.

    Article  CAS  Google Scholar 

  17. Andries K, Villellas C, Coeck N, Thys K, Gevers T, Vranckx L, et al. Acquired resistance of mycobacterium tuberculosis to bedaquiline. PLoS One. 2014;9(7):e102135.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Beckert P, Hillemann D, Kohl TA, Kalinowski J, Richter E, Niemann S, et al. rplC T460C identified as a dominant mutation in linezolid-resistant Mycobacterium tuberculosis strains. Antimicrob Agents Ch. 2012;56:2743–5.

    Article  CAS  Google Scholar 

  19. Haver HL, Chua A, Ghode P, Lakshminarayana SB, Singhal A, Mathema B, et al. Mutations in genes for the F420 biosynthetic pathway and a nitroreductase enzyme are the primary resistance determinants in spontaneous in vitro-selected PA-824-resistant mutants of mycobacterium tuberculosis. Antimicrob Agents Ch. 2015;59(9):5316–23.

    Article  CAS  Google Scholar 

  20. Liu Y, Matsumoto M, Ishida H, Ohguro K, Yoshitake M, Gupta R, et al. Delamanid: from discovery to its use for pulmonary multidrug-resistant tuberculosis (MDR-TB). Tuberculosis. 2018;111:20–30.

    Article  CAS  PubMed  Google Scholar 

  21. Manjunatha UH, Boshoff H, Dowd CS, Zhang L, Albert TJ, Norton JE, et al. Identification of a nitroimidazo-oxazine-specific protein involved in PA-824 resistance in mycobacterium tuberculosis. P Natl Acad Sci USA. 2006;103(2):431–6.

    Article  CAS  Google Scholar 

Download references


All the staff from National Tuberculosis Reference Laboratory in China is also highly acknowledged.


This study was supported by the Beijing Scientific Research Foundation for the Returned Overseas Chinese Scholars, Beijing Health System High-level Health Technology Talents Training Plan (2015–3-081), Beijing Municipal Administration of Hospitals’ Ascent Plan (DFL20181602), and Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support (ZYLX201809).

Author information

Authors and Affiliations



ZHW and HWC equality contributed in study design, data collection, analysis and manuscript writing. XH and SL participated in study design and data collection; WSF and XJ conducted laboratory testing; OXC and SAD revised the manuscript; JWW, ZYL and SAD participated in study design, data analysis and funding support. All the authors have read the manuscript and have approved it.

Corresponding authors

Correspondence to Yanlin Zhao or Adong Shen.

Ethics declarations

Ethics approval and consent to participate

This research has been granted by the Ethics Committee of Chinese center for disease control and prevention, and an informed consent was obtained from each participant/respondent. All methods were carried out in accordance with relevant guidelines and regulations.

Consent for publication

This research including all the paper detail, data, tables and images was consented by all the authors and respondents in this paper for publication. And they will be freely available on the internet.

Competing interests


Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zheng, H., He, W., Jiao, W. et al. Molecular characterization of multidrug-resistant tuberculosis against levofloxacin, moxifloxacin, bedaquiline, linezolid, clofazimine, and delamanid in southwest of China. BMC Infect Dis 21, 330 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: