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J Clin Microbiol. Nov 2009; 47(11): 3501–3506.
Published online Sep 16, 2009. doi:  10.1128/JCM.01209-09
PMCID: PMC2772627

Mycobacterium tuberculosis Strains with Highly Discordant Rifampin Susceptibility Test Results[down-pointing small open triangle]

Abstract

The objectives of this study were to investigate the origin of highly discordant rifampin (rifampicin) (RMP) drug susceptibility test results obtained for Mycobacterium tuberculosis strains during proficiency testing. Nine Supra-National Tuberculosis Reference Laboratories tested the RMP susceptibilities of 19 selected M. tuberculosis strains, using standard culture-based methods. The strains were classified as definitely resistant (R) (n = 6) or susceptible (S) (n = 2) or probably resistant (PR) (n = 8) or susceptible (PS) (n = 3) based on rpoB mutations and treatment outcome. All methods yielded a susceptible result for the two S and three PS strains lacking an rpoB mutation and a resistant result for one R strain with a Ser531Leu mutation and one PR strain with a double mutation. Although the remaining 12 R and PR strains had rpoB mutations (four Asp516Tyr, three Leu511Pro, two Leu533Pro, one each His526Leu/Ser, and one Ile572Phe), they were all susceptible by the radiometric Bactec 460TB or Bactec 960 MGIT methods. In contrast, only one was susceptible by the proportion method on Löwenstein-Jensen medium and two on Middlebrook 7H10 agar. Low-level but probably clinically relevant RMP resistance linked to specific rpoB mutations is easily missed by standard growth-based methods, particularly the automated broth-based systems. Further studies are required to confirm these findings, to determine the frequency of these low-level-resistant isolates, and to identify technical improvements that may identify such strains.

The prevalence of multidrug-resistant (MDR) tuberculosis (TB) is rising globally, posing a serious threat to TB control. (25) MDR TB does not respond to treatment with first-line drugs, (3), and its management using second-line drugs has not yet been properly organized by most control programs (25). Although MDR TB is defined as resistance to at least isoniazid and rifampin (rifampicin) (RMP), the key determinant for treatment failure is RMP resistance. Detection of RMP resistance has thus been proposed as a proxy for MDR TB diagnosis, as well as for epidemiological monitoring (14, 20, 24). RMP drug susceptibility testing (DST), by conventional methods based on growth as well as by newer genetic techniques, is generally considered the most reliable (1, 8). Highly consistent results were obtained during the early proficiency testing (PT) rounds among the Supra-National TB Reference Laboratories (SRLS) of the World Health Organization (WHO)/International Union against Tuberculosis and Lung Disease network. Consequently, Laszlo et al. proposed a 99% efficiency target for RMP DST by the SRLs (8). However, 15 of 240 quality control strains (6.2%) distributed from 1999 to 2007 yielded less than 80% agreement for RMP resistance among the SRLs, insufficient for a judicial result. The panels were designed to contain approximately 50% resistance to all first-line TB drugs in various combinations. This precondition resulted in overrepresentation of rare profiles. The SRLs employed one of the four recognized standard culture-based DST methods, and the discordant results were not clearly correlated with a particular method or systematic technical errors. DNA sequencing of the PT rounds’ problem strains invariably showed some rpoB gene mutation. All of the mutations encountered had been described previously and were generally considered to confer RMP resistance, though sometimes at a low level (11), and available clinical data were usually suggestive of RMP resistance.

We report here the results of an SRL investigation into the cause of this RMP resistance-testing problem.

MATERIALS AND METHODS

The coordinating SRL in Antwerp, Belgium, constituted a panel of 19 M. tuberculosis strains isolated from retreatment cases (Table (Table1),1), selected either on the basis of discordant results in earlier PT or because of an RMP MIC close to the breakpoint at pretesting on Löwenstein-Jensen (LJ) medium. The strains were further characterized by rpoB sequencing covering all regions of the gene with known resistance-conferring mutations, including those outside cluster I of the core region (15), supplemented with information on the final outcome of standard treatment with first-line drugs, when available. Strains were classified as resistant (R), probably resistant (PR), susceptible (S), or probably susceptible (PS) to RMP by applying the following criteria: R, mutation present and clinical failure on an RMP-containing treatment; PR, mutation present and treatment outcome either unknown or “cure” (usually with subsequent bacteriologically proven relapse) on the standard retreatment regimen, WHO category 2 (23); PS, no mutation but subsequent failure or relapse after category 2 treatment; and S, no mutation and cured without registered relapse.

TABLE 1.
Panel strain classification and characteristics

The presence of a mutation described as conferring resistance to RMP thus took precedence over the treatment outcome, since it is known that patients may fail or relapse from treatment due to other reasons than (RMP) drug resistance, while conversely, a low proportion of TB patients seem to be cured spontaneously, independent of drug resistance (3, 6). Table Table11 shows details of the panel strains. Of the 14 strains with rpoB mutations, 6 (R1 to R6) were classified as resistant to RMP (mutation plus treatment failure) and 8 (PR1 to PR8) as probably resistant, 5 of which were isolated from relapse cases after category 2 treatment. The mutations identified from the panel strains were Asp516Tyr (n = 4), Leu511Pro (n = 3), Leu533Pro (n = 2), His526Leu, His526Ser, Ser531Leu, and Ile572Phe (n = 1 each), by the Escherichia coli codon numbering system. One strain had the double mutation Met515Ile and Asp516Tyr. Ten clones of this strain were tested and showed identical nucleotide changes, thus ruling out a possible mixture of strains. None of the rpoB sequencing patterns showed simultaneously a wild type and a mutation peak, also suggesting the absence of strain mixtures. Three strains (PS1 to PS3) were considered probably susceptible to RMP (no mutation but category 2 treatment failure or relapse). The two strains called susceptible (S1 and S2) showed a wild-type rpoB sequence without any clinical suspicion of RMP resistance. Most R, PR, and PS strains were resistant to one or more of the other first-line TB drugs. All strains except two originated from long-term monitoring of drug resistance among retreatment cases in Bangladesh.

This panel was sent to nine volunteer SRLs for blinded RMP DST. Each SRL used its standard RMP susceptibility-testing method(s), based on the original publication of the proportion method (performed on LJ medium or Middlebrook 7H10 agar) or on the manufacturer's instructions (Bactec 460 TB radiometric and Bactec 960 MGIT) (2). Six of the participating SRLs performed DST using the LJ proportion method, two reported results by the Middlebrook 7H10 agar proportion method, and two by Bactec 460 radiometric and two by Bactec 960 MGIT DST. Three SRLs reported results with the proportion method, as well as one of the Bactec methods, and some reported incomplete sets of results. To provide more detailed information, the MIC was determined by each method, using RMP at 10, 20, 30, 40, and 80 μg/ml in LJ medium or at 0.25, 0.5, 1, 2, and 4 μg/ml in agar and Bactec medium, but maintaining the interpretation criteria recommended for each method. The ratio of the MICs to the standard critical concentration for the medium used (40 μg/ml for LJ medium, 2 μg/ml for radiometric Bactec medium, and 1 μg/ml for agar and MGIT) was calculated to allow comparison of MICs obtained with the different methods used. MICs out of the range of RMP concentrations tested were arbitrarily assigned a value corresponding to the next higher or lower dilution. A MIC/critical concentration ratio of >1 was interpreted as resistant.

RESULTS

Figure Figure11 shows summary DST results by strain as the average MIC/critical concentration ratio for each method. All methods were able to detect resistance for strains R1 (Ser531Leu) and PR7 (Met515Ile Asp516Tyr double mutation), both yielding the highest ratios, but they all indicated strain PR6 (Leu511Pro) as susceptible, with ratios ranging from 0.13 (agar proportion and Bactec) to 0.38 (LJ proportion method). All S and PS strains tested susceptible by all methods on liquid or solid media. All other R and PR strains were considered susceptible with liquid but resistant with solid media, except strain R4 (Asp516Tyr), which tested susceptible by the agar proportion method.

FIG. 1.
Average results of RMP susceptibility tests by method and strain. The ratio of the MIC to the critical concentration is shown, with resistance defined as a ratio of >1. LJ, LJ medium; Radiometric, Bactec 460 radiometric method; MGIT, Bactec 960 ...

Individual results on LJ medium are shown in Fig. Fig.22 for five SRLs. The ratio of the MIC to the critical concentration never exceeded 4, since the highest concentration used (80 μg/ml) was only twice the critical concentration. Most results confirmed the presumptive resistance classification, but 8/14 R and PR strains resulted in an occasional discordant result and 1 strain (PR6) was consistently declared susceptible. Overall, 21/67 (31%) MICs for these strains remained below the resistance breakpoint.

FIG. 2.
RMP MIC ratios by the proportion method on LJ medium, read after 6 weeks of incubation, by SRL and strain. The ratio of the MIC to the critical concentration is shown, with resistance defined as a ratio of >1. LJ 6W, LJ medium, read after 6 weeks ...

Figure Figure33 shows individual results with the agar proportion, Bactec radiometric, and MGIT methods (each from two SRLs). On agar, only the R4 and PR6 strains were consistently susceptible, but 9/14 R and PR strains showed discordant results due to a large difference in MICs between the two SRLs, and 12/27 (44%) MICs for these strains remained below the resistance breakpoint. With both radiometric Bactec 460TB and Bactec 960 MGIT, and at all four SRLs, only the R1 and PR7 strains were found to be resistant, while all others were consistently declared susceptible. Overall, 40/47 (85%) of the R and PR Bactec test results were susceptible.

FIG. 3.
RMP MIC ratios with the agar proportion and Bactec radiometric or Bactec MGIT method, by SRL and strain. The ratio of the MIC to the critical concentration is shown, with resistance defined as a ratio of >1. Radiometric, Bactec 460 radiometric ...

DISCUSSION

Our study shows that RMP DST can yield highly discordant results, even among proficient laboratories, due to the existence of M. tuberculosis strains with borderline susceptibility. Alternative explanations, such as mixtures consisting of susceptible and resistant strains, (22) or heteroresistance with simultaneous presence of susceptible and resistant clones of the same strain (16), are unlikely. First, none of the DNA-sequencing patterns showed an overlapping mutation and wild-type nucleotide. Second, for nine strains with highly discordant results in the PT rounds, IS6110 fingerprinting had systematically shown identical patterns for all 10 clones tested per strain (data not shown).

It was obvious that particular DST methods are more prone to missing low-level RMP resistance. Four SRLs using the Bactec radiometric or MGIT 960 method declared all borderline strains susceptible, yielding a resistant result only when the average ratio of the MIC to the critical concentration was at least 4. The Centers for Disease Control and Prevention (CDC) DST performance evaluation program found in their 2008 round that only 19% of laboratories using the MGIT and 42% of those using the Bactec radiometric method reported such an RMP borderline strain as resistant versus 70% of agar proportion method users (CDC Atlanta, GA, unpublished data). Susceptible Bactec results from genotypically RMP-resistant strains have been reported occasionally in the literature. Traore and coworkers found that 4/39 (10%) RMP-resistant isolates from Uganda, with mutations in codon 511, 516, or 533 and resistant by phage and colorimetric DST, were missed by the Bactec radiometric method (21).

The bacteriologically unfavorable treatment outcomes for most of the borderline resistant strains from our panel suggest that these specific mutations may have clinical significance. Another question is how frequently they are encountered in clinical practice. Their reported rarity may be misleading, since virtually all publications describe the frequency of rpoB mutations starting from phenotypically RMP-resistant isolates, while our study shows that they are easily missed by routine phenotypic DST. In a systematic sample of Hong Kong strains investigated independently of phenotypic DST results, Leu511Pro, Leu533Pro, and His526Leu represented 22% (19/85) of all the mutations compared to less than 10% among all phenotypically RMP-resistant strains of previous years. (27) The distribution of rpoB mutations may differ with geographic origin and treatment history. However, among strains recovered from Bangladesh retreatment cases, these three mutations also represented 18% (40/221) (data not shown). Population studies based on molecular screening without culture-based DST preselection are thus required, particularly among early MDR TB suspects (late converters, failures of WHO category 1 treatment, and first-line treatment relapses).

Acquisition of RMP resistance may reduce the fitness of TB bacilli, depending on the type of mutation. The most prevalent Ser531Leu mutation has been shown to be the least impairing, while very rare mutations or those known only from in vitro experiments show severe growth inhibition with some assays (9, 12). The fitness deficit may diminish or disappear due to compensation mechanisms with prolonged patient treatment (4, 5). Moreover, the Ser531Leu mutation and some mutations in codons 513 and 526 have generally been reported as conferring high-level resistance, and they comprise 90% or more of those found among phenotypically RMP-resistant isolates. A large variety of other mutations have been occasionally or consistently associated with low-level RMP resistance (7, 13, 17, 19). Those resulting in the lowest MICs and most frequently missed in this study, i.e., Leu511Pro and Leu533Pro, have been considered susceptible by some authors (11), although a very high MIC has occasionally been reported, as well (10). The strain with the highest MIC, diagnosed as resistant by all methods and SRLs, had the Ser531Leu mutation. The only other (probably) resistant strain consistently detected, albeit with lower MICs, had the double mutation Met515Ile Asp516Tyr. Both are known to confer low-level resistance (11), but together they resulted in a MIC higher than those of the four single Asp516Tyr-mutated isolates in our panel. Of the double mutations reported in the literature, usually at least one confers low-level resistance, and mutations such as Leu511Pro occurred exclusively in combination in some series (17). Acquisition and selection of additional mutations under treatment pressure might be another bacillus survival mechanism, an argument for considering these low-resistance mutations clinically relevant. The Ile572Phe mutant from our panel, for which we could find only one report, has not been associated with borderline resistance (28). However, four of our five strains with this mutation showed a low MIC at pretesting by the coordinating SRL (our unpublished data).

In our study using selected difficult strains, low-level resistance was easily missed with the current standard DST methods and systematically with the rapid, automated Bactec systems. Considering all strains yielding discordant results in the WHO/ International Union against Tuberculosis and Lung Disease PT rounds 6 to 14, only 27% of 106 Bactec results from seven SRLs indicated RMP resistance, although all of these strains had an rpoB mutation. In order to avoid calling such strains RMP susceptible, our methods may thus need modification. Prolonged incubation and a larger inoculum size may be necessary to disclose the resistance of poorly growing strains, and the RMP critical concentration used with the proportion and Bactec methods may be too high.

One of the reasons for the Bactec failures may be too early endpoint readings. Traore et al. reported a growth index below the resistance criterion for his strains, which might eventually have been reached after extended incubation. Extending the incubation of borderline strains is usual in many laboratories using solid media, but this is not possible with the standard Bactec MGIT automated system. That a sufficiently long incubation time is important to disclose drug resistance is common knowledge for the LJ proportion method. With only about 30% susceptible results for R and PR strains, in our study, LJ proportion was the most sensitive method of reading tests at the standard 6 weeks, but this proportion doubled for interim readings at 4 weeks, reported additionally by four of the SRLs (details not shown).

Suo et al. recommended lowering the RMP breakpoint to 0.5 μg/ml with the radiometric method (18). Screening at two concentrations (40 and 20 μg/ml in LJ medium, applying a 10% criterion for the lower concentration) was originally suggested by Canetti et al. as a more accurate variant of the proportion method (2).

Under TB control program conditions, a very high sensitivity is more important than a few days less turnover time for RMP DST, which may represent only a minor fraction of the total delay before the start of MDR TB treatment (26). Missing early RMP resistance has serious consequences because of the highly standardized care in high-prevalence, low-income countries, resulting in death or default from treatment and continued transmission of RMP-resistant TB. Moreover, human immunodeficiency virus-related immune deficiency and drug malabsorption might compensate for the fitness loss of these strains, with high rates of successful transmission.

Conclusions.

Low-level but clinically probable M. tuberculosis RMP resistance, linked to specific rpoB mutations, is easily missed by standard growth-based methods, particularly the rapid, automated broth-based systems (Bactec 460 and MGIT 960). Its true frequency remains unknown and should be investigated, but it might be considerable among patients with clinical suspicion of drug resistance. If this hypothesis is confirmed, adaptation of the standard DST methods will be needed.

Acknowledgments

We gratefully acknowledge the participation of the Barcelona, Brisbane, and Lisbon SRLs in this study.

Footnotes

[down-pointing small open triangle]Published ahead of print on 16 September 2009.

REFERENCES

1. Barnard, M., H. Albert, G. Coetzee, R. O'Brien, and M. E. Bosman. 2008. Rapid molecular screening for multidrug-resistant tuberculosis in a high-volume public health laboratory in South Africa. Am. J. Respir. Crit. Care Med. 177:787-792. [PubMed]
2. Canetti, G., W. Fox, A. Khomenko, D. A. Mitchison, N. Rist, and N. A. Smelev. 1969. Advances in techniques of testing mycobacterial drug sensitivity, and the use of sensitivity tests in tuberculosis control programmes. Bull. W. H. O. 41:21-43. [PMC free article] [PubMed]
3. Espinal, M. A., S. J. Kim, P. G. Suarez, K. M. Kam, A. G. Khomenko, G. B. Migliori, J. Baéz, A. Kochi, C. Dye, and M. C. Raviglione. 2000. Standard short-course chemotherapy for drug-resistant tuberculosis. Treatment outcomes in 6 countries. JAMA 283:2537-2545. [PubMed]
4. Gagneux, S., C. Davis Long, P. M. Small, T. Van, G. K. Schoolnik, and B. J. M. Bohannan. 2006. The competitive cost of antibiotic resistance in Mycobacterium tuberculosis. Science 312:1944-1946. [PubMed]
5. Gillespie, S. H., O. J. Billington, A. Breathnach, and T. D. McHugh. 2002. Multiple drug-resistant Mycobacterium tuberculosis: evidence for changing fitness following passage through human hosts. Microb. Drug Resist. 8:273-279. [PubMed]
6. Grzybowski, S. 1991. Natural history of tuberculosis. Epidemiology. Bull. Int. Union Tuberc. Lung Dis. 66:193-194. [PubMed]
7. Hwang, H.-Y., C.-Y. Chang, L.-L. Chang, S.-F. Chang, Y.-H. Chang, and Y.-J. Chen. 2003. Characterization of rifampicin-resistant Mycobacterium tuberculosis in Taiwan. J. Med. Microbiol. 52:239-245. [PubMed]
8. Laszlo, A., M. Rahman, M. Espinal, and M. Raviglione. 2002. Quality assurance programme for drug susceptibility testing of Mycobacterium tuberculosis in the WHO/IUATLD Supranational Reference Laboratory Network: five rounds of proficiency testing, 1994-1998. Int. J. Tuberc. Lung Dis. 6:748-756. [PubMed]
9. Mariam, D. H., Y. Mengistu, S. E. Hoffner, and D. I. Andersson. 2004. Effect of rpoB mutations conferring rifampin resistance on fitness of Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 48:1289-1294. [PMC free article] [PubMed]
10. Moghazeh, S. L., X. Pan, T. Arain, C. K. Stover, J. M. Musser, and B. N. Kreiswirth. 1996. Comparative antimycobacterial activities of rifampin, rifapentine, and KRM-1648 against a collection of rifampin-resistant Mycobacterium tuberculosis isolates with known rpoB mutations. Antimicrob. Agents Chemother. 40:2655-2657. [PMC free article] [PubMed]
11. Ohno, H., H. Koga, S. Kohno, T. Tashiro, and K. Hara. 1996. Relationship between rifampin MICs and rpoB mutations of Mycobacterium tuberculosis strains isolated in Japan. Antimicrob. Agents Chemother. 40:1053-1056. [PMC free article] [PubMed]
12. O'Sullivan, D. M., T. D. McHugh, and S. H. Gillespie. 2005. Analysis of rpoB and pncA mutations in the published lterature: an insight into the role of oxidative stress in Mycobacterium tuberculosis evolution? J. Antimicrob. Chemother. 55:674-679. [PubMed]
13. Ramaswami, S., and J. M. Musser. 1998. Molecular genetic basis of antimicrobial agent resistance in Mycobacterium tuberculosis: 1998 update. Tuberc. Lung Dis. 79:3-29. [PubMed]
14. Rieder, H. L., A. Van Deun, K. M. Kam, S. J. Kim, T. M. Chonde, A. Trébucq, and R. Urbanczik. 2007. Priorities for tuberculosis bacteriology services in low-income countries, 2nd ed., p. 1-120. International Union against Tuberculosis and Lung Disease, Paris, France.
15. Rigouts, L., O. Nolasco, P. de Rijk, E. Nduwamahoro, A. Van Deun, A. Ramsay, J. Arevalo, and F. Portaels. 2007. Newly developed primers for comprehensive amplification of the rpoB gene and detection of rifampin resistance in Mycobacterium tuberculosis. J. Clin. Microbiol. 45:252-254. [PMC free article] [PubMed]
16. Rinder, H., K. T. Mieskes, and T. Löscher. 2001. Heteroresistance in Mycobacterium tuberculosis. Int. J. Tuberc. Lung Dis. 5:339-345. [PubMed]
17. Siddiqi, N., M. Shamim, S. Hussain, R. K. Choudhary, N. Ahmed, Prachee, S. Banerjee, G. R. Savithri, M. Alam, N. Pathak, A. Amin, M. Hanief, V. M. Katoch, S. K. Sharma, and S. E. Hasnain. 2002. Molecular characterization of multidrug-resistant isolates of Mycobacterium tuberculosis from patients in North India. Antimicrob. Agents Chemother. 46:443-450. [PMC free article] [PubMed]
18. Suo, J., C. R. Chang, T. P. Lin, and L. B. Heifets. 1988. Minimal inhibitory concentrations of isoniazid, rifampin, ethambutol, and streptomycin against Mycobacterium tuberculosis strains isolated before treatment of patients in Taiwan. Am. Rev. Respir. Dis. 138:999-1001. [PubMed]
19. Taniguchi, H., H. Aramaki, Y. Nikaido, Y. Mizuguchi, M. Nakamura, T. Koga, and S. I. Yoshida. 1996. Rifampicin resistance and mutation of the rpoB gene in Mycobacterium tuberculosis. FEMS Microbiol. Lett. 144:103-108. [PubMed]
20. Traore, H., K. Fissette, I. Bastian, M. Devleeschouwer, and F. Portaels. 2000. Detection of rifampicin resistance in Mycobacterium tuberculosis isolates from diverse countries by a commercial line probe assay as an initial indicator of multidrug resistance. Int. J. Tuberc. Lung Dis. 4:481-484. [PubMed]
21. Traore, H., S. Ogwang, K. Mallard, M. L. Joloba, F. Mumbowa, K. Narayan, S. Kayes, E. C. Jones-Lopez, P. G. Smith, J. J. Ellner, R. D. Mugerwa, K. D. Eisenach, and R. McNerney. 2007. Low-cost rapid detection of rifampicin resistant tuberculosis using bacteriophage in Kampala, Uganda. Ann. Clin. Microbiol. Antimcrob. 6:1-6. [PMC free article] [PubMed]
22. van Rie, A., T. C. Victor, M. Richardson, R. Johnson, G. D. van der Spuy, E. J. Murray, N. Beyers, N. C. Gey van Pittius, P. D. van Helden, and R. M. Warren. 2005. Reinfection and mixed infection cause changing Mycobacterium tuberculosis drug-resistance patterns. Am. J. Respir. Crit. Care Med. 172:636-642. [PMC free article] [PubMed]
23. World Health Organization. 2003. Treatment of tuberculosis: guidelines for national programmes, 3rd ed. World Health Organization document WHO/CDS/TB/2003.313. World Health Organization, Geneva, Switzerland.
24. World Health Organization. 2004. The WHO/IUATLD Global Project on Anti-Tuberculosis Drug Resistance Surveillance. Anti-tuberculosis drug resistance in the world. Report no. 3. World Health Organization document WHO/CDS/TB/2004.343. World Health Organization, Geneva, Switzerland.
25. World Health Organization. 2008. The WHO/IUATLD Global Project on Anti-Tuberculosis Drug Resistance Surveillance. Anti-tuberculosis drug resistance in the world. Report No. 4. World Health Organization document WHO/HTM/TB/2008.394. World Health Organization, Geneva, Switzerland.
26. Yagui, M., M. T. Perales, L. Asencios, L. Vergara, C. Suarez, G. Yale, C. Salazar, M. Saavedra, S. Shin, O. Ferroussier, and P. Cegielski. 2006. Timely diagnosis of MDR-TB under program conditions: is rapid drug susceptibility testing sufficient? Int. J. Tuberc. Lung Dis. 10:838-843. [PubMed]
27. Yip, C. W., K. L. Leung, D. Wong, D. T. L. Cheung, M. Y. Chu, H. S. Tang, and K. M. Kam. 2006. Denaturing HPLC for high-throughput screening of rifampicin-resistant Mycobacterium tuberculosis isolates. Int. J. Tuberc. Lung Dis. 10:625-630. [PubMed]
28. Yuen, L. K. W., D. Leslie, and P. J. Coloe. 1999. Bacteriological and molecular analysis of rifampin-resistant Mycobacterium tuberculosis strains isolated in Australia. J. Clin. Microbiol. 37:3844-3850. [PMC free article] [PubMed]

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