Volume 11, Number 9—September 2005
Multidrug-resistant Tuberculosis Detection, Latvia
To improve multidrug-resistant tuberculosis (MDR-TB) detection, we successfully introduced the rpoB gene mutation line probe assay into the national laboratory in Latvia, a country with epidemic MDR-TB. The assay detected rifampin resistance with 91% sensitivity and 96% specificity within 1 to 5 days (vs. 12–47 days for BACTEC).
Until recent years, global efforts to reduce the prevalence of multidrug-resistant tuberculosis (MDR-TB), defined as in vitro resistance to at least rifampin and isoniazid, have focused on preventing new cases of acquired MDR-TB. However, countries that already have a high incidence of MDR-TB must implement additional strategies, such as reducing transmission by detecting cases earlier and improving infection control in settings with shared air spaces. As yet undetermined are optimal methods to identify drug-resistant Mycobacterium tuberculosis in a timely and affordable way in resource-limited settings. Standard laboratory methods of detecting drug resistance, such as M. tuberculosis culture and drug susceptibility testing (DST) performed with Löwenstein-Jensen (LJ) medium, are inexpensive but slow; DST results are often not available for 3 to 4 months. Testing methods that use liquid media, such as BACTEC systems (Becton Dickinson, Sparks, MD, USA), can deliver DST results to clinicians within 3 to 4 weeks; however, this technology requires expensive equipment and media.
Several methods that work directly on respiratory specimens and that detect resistance to a limited number of drugs within 1 day to 3 weeks have been reported (1–5). One assay that is commercially available is a line probe assay, a reverse-hybridization assay that detects mutations in the rpoB gene (5–12). Among clinical M. tuberculosis isolates, those with mutations in the rpoB gene are associated with 80% to 90% rifampin resistance (5). Previously published studies using this assay have demonstrated 90%–100% concordance when results are compared to DST results among M. tuberculosis isolates from culture and 78%–98% sensitivity and 84%–100% specificity when applied to respiratory specimens that were positive for acid-fast bacilli (AFB) (5–12). However, these studies involved small numbers of respiratory specimens and were not performed in a national TB laboratory that supports diagnosis, treatment, and care for large numbers of MDR-TB patients.
Latvia is among those countries with the highest prevalence of MDR-TB in the world (13). Rifampin resistance in Latvia is closely associated with resistance to isoniazid; therefore, detecting rifampin resistance should also detect most MDR-TB cases (13). As part of a long-term project to integrate new assays into the Latvian national laboratory protocols to identify MDR-TB patients more quickly, we prospectively compared the results of the line probe assay for rpoB mutations to results with BACTEC DST technology.
We enrolled consecutive patients who were initially seen at or referred to the Latvian State Centre of Tuberculosis and Lung Diseases from January 2003 to March 2004 with AFB-positive respiratory specimens (sputum or bronchoalveolar lavage [BAL] specimens) and identified as being at high risk for MDR-TB. Patients at high risk were defined as those with a history of close contact to a known MDR-TB patient or with a history of previous TB treatment (14).
After sputum specimens were decontaminated (15), we tested for AFB (15) and set up 2 cultures for M. tuberculosis: 1 in LJ medium (15) and 1 in either the BACTEC Mycobacteria Growth Indicator Tube 960 or the BACTEC 460 system per manufacturer's instructions (Becton Dickinson). DNA was extracted from the remaining suspension with the QIAAMP DNA Mini kit (Qiagen, Valencia, CA, USA). Lysate was transferred to the line probe kit INNO-LiPA Rif.TB (Innogenetics, Ghent, Belgium) for amplification, including a second nested reaction with inner primers and the hybridization reaction (manufacturer's instructions). In general, the rpoB gene amplicons were incubated with immobilized, membrane-bound rpoB gene probes, including overlapping wildtype sequences (S1–S5) and 4 of the most frequent mutations (R2:Asp516Val, R4a:His526Tyr, R4b:His526Asp, and R5:Ser531Leu). The kit also includes a probe for M. tuberculosis complex.
DST was performed with the BACTEC 460 system (manufacturer's protocols). We then compared line probe results to M. tuberculosis culture and BACTEC DST results for each patient. We also set up DST on LJ media by using the proportion method (15). All laboratory testing was performed at the Latvian State Centre of Tuberculosis and Lung Diseases, Riga, Latvia. Line probe results were not provided to physicians. Patient identifiers were removed before analysis. The protocol underwent institutional ethical review by the Latvian State Centre of Tuberculosis and Lung Diseases, was determined not to be human subjects research, and was approved as programmatic evaluation by the Centers for Disease Control and Prevention.
In total, 89 (37%) of 243 patients who met the case definition for being at high risk for MDR-TB had AFB-positive respiratory specimens; 77 (87%) were sputum specimens, and 12 (13%) were BAL specimens. M. tuberculosis isolates grew in BACTEC cultures from 86 (97%) of the AFB-positive specimens. Mycobacteria other than M. tuberculosis were identified in 3 of the remaining BACTEC cultures. No dual infections were found. M. tuberculosis complex was also detected by line probe assay in 86 specimens, although for 2 patients M. tuberculosis grew in respiratory specimens in BACTEC cultures but was not detected by the line probe assay, and 2 specimens that were positive for M. tuberculosis complex by line probe assay did not grow in BACTEC but did grow on LJ media. These isolates were injected into the BACTEC 460 system for DST. The line probe assay correctly separated M. tuberculosis complex and nontuberculosis mycobacteria.
The line probe assay had good sensitivity, high specificity, and positive predictive value and negative predictive value for rifampin resistance compared to BACTEC (Table 1). Among the isolates resistant to rifampin by BACTEC DST, the rpoB mutations detected by the line probe included 20 (61%) R5 (Ser531Leu), 8 (24%) R2 (Asp516Val), 1 (3%) R4b (His526Asp), and 1 (3%) ΔS5 (absence of hybridization to 1 wildtype sequence). One rifampin BACTEC DST-susceptible isolate had a line probe result read as ΔS1, ΔS2 (absence of hybridization to 2 wildtype sequences).
Most patients considered high risk for MDR-TB had resistance to at least 1 drug (Table 2). Rifampin resistance was highly correlated with classification as MDR-TB; 32 (97%) of 33 patients with rifampin resistance had MDR-TB. The predictive value of the line probe rpoB mutation result for MDR-TB was 91% (95% confidence interval 92–100).
The line probe assay performed directly on DNA extracted from respiratory specimens gave quicker results for rifampin resistance (median = 4 days, range 1–5) than other methods (BACTEC 460 median = 28 days, range 12–47; LJ median = 58 days, range 47–65). While DST results from the BACTEC liquid culture system were available considerably faster than were results from LJ media, rpoB gene mutation results were available in <1 week.
In Latvia, where nearly 40% of patients had a history of TB treatment and 10% of all new patients without a history of treatment have MDR-TB (13,14), integrating a line probe assay for rpoB gene mutations into regular laboratory services could enhance MDR-TB control efforts. Results from this study demonstrated that in persons considered at high risk for MDR-TB, the line probe assay detected rifampin resistance with 91% sensitivity and 97% specificity on respiratory specimens within 1 to 5 days of specimen collection in a busy clinical laboratory. Additionally, 91% of patients at high risk for MDR-TB, with line probe assay results consistent with rpoB mutations, were ultimately confirmed as having MDR-TB.
In addition, we compared the timeliness of acquiring rifampin DST results between a liquid and solid media system and a line probe assay. Although liquid media were considerably faster than solid media, the line probe assay for rpoB mutations performed directly on respiratory specimens gave results consistent with MDR in <1 week.
Therefore, integrating the use of the line probe assay on AFB-positive respiratory specimens into the Latvian national laboratory could permit much earlier segregation and isolation of infectious patients who have a high likelihood of MDR-TB (thereby reducing MDR-TB transmission) and could facilitate more focused DST practices for first- and second-line TB drugs and more efficient use of resources. The high specificity is reassuring; the use of line probe assay results to inform drug treatment selections would rarely result in missed opportunities to treat with rifampin. Conversely, only 9% of patients infected with a rifampin-resistant isolate would not benefit from early detection of resistance and would, in turn, receive care similar to the current standard.
Several other assays that detect drug resistance within 1 to 3 weeks have been described (1–5). Some of these may perform as well as the line probe assay and be less expensive. We chose the line probe assay for our project because it was commercially available and had been evaluated by several investigators (5–12). Also, the equipment and skills could be applied toward other molecular epidemiologic studies to better understand ongoing transmission of MDR-TB in Latvia. We will evaluate the cost-effectiveness of integrating this assay into the Latvian State Centre of Tuberculosis and Lung Diseases and may also model the cost of new assays as they become available. This study, part of a larger project to reduce the prevalence of MDR-TB in Latvia, is a first step in identifying optimal methods to identify drug-resistant M. tuberculosis in a timely and affordable way in resource-limited settings with high MDR-TB prevalence.
Dr Skenders is the director of the laboratory in the State Centre of Tuberculosis and Lung Diseases, Riga, Latvia.
We thank Kayla Laserson, Tom Shinnick, Jack Crawford, and Sven Hoffner for their insightful comments and discussions and David Temporado and Yvonne Hale for their assistance with laboratory procedures.
Funding for this study was provided by the US Agency for International Development. The agency had no role in determining study design; collecting, analyzing, or interpreting data; writing the report; or deciding to submit the paper for publication.
- Kim BJ, Lee KH, Park BN, Kim SJ, Park EM, Park YG, Detection of rifampin-resistant Mycobacterium tuberculosis in sputa by nested PCR-linked single-strand conformation polymorphism and DNA sequencing. J Clin Microbiol. 2001;39:2610–7.
- Patnaik M, Liegmann K, Peter JB. Rapid detection of smear-negative Mycobacterium tuberculosis by PCR and sequencing for rifampin resistance with DNA extracted directly from slides. J Clin Microbiol. 2001;39:51–2.
- Garcia L, Alonso-Sanz M, Rebollo MJ, Tercero JC, Chaves F. Mutations in the rpoB gene of rifampin-resistant Mycobacterium tuberculosis isolates in Spain and their rapid detection by PCR-enzyme-linked immunosorbent assay. J Clin Microbiol. 2001;39:1813–8.
- Caviedes L, Lee TS, Gilman RH, Sheen P, Spellman E, Lee EH, Rapid, efficient detection and drug susceptibility testing of Mycobacterium tuberculosis in sputum by microscopic observation of broth cultures. The Tuberculosis Working Group in Peru. J Clin Microbiol. 2000;38:1203–8.
- Watterson SA, Wilson SM, Yates MD, Drobniewski FA. Comparison of three molecular assays for rapid detection of rifampin resistance in Mycobacterium tuberculosis. J Clin Microbiol. 1998;36:1969–73.
- De Beenhouwer H, Lhiang Z, Jannes G, Mijs W, Machtelinckx L, Rossau R, Rapid detection of rifampicin resistance in sputum and biopsy specimens from tuberculosis patients by PCR and line probe assay. Tuber Lung Dis. 1995;76:425–30.
- Marttila HJ, Soini H, Vyshnevskaya E, Vyshnevskiy BI, Otten TF, Vasilyef AV, Line probe assay in the rapid detection of rifampin-resistant Mycobacterium tuberculosis directly from clinical specimens. Scand J Infect Dis. 1999;31:269–73.
- Gamboa F, Cardona PJ, Manterola JM, Lonca J, Matas L, Padilla E, Evaluation of a commercial probe assay for detection of rifampin resistance in Mycobacterium tuberculosis directly from respiratory and nonrespiratory clinical samples. Eur J Clin Microbiol Infect Dis. 1998;17:189–92.
- Johansen IS, Lundgren B, Sosnovskaja A, Thomsen Vs VO. Direct detection of multidrug-resistant Mycobacterium tuberculosis in clinical specimens in low- and high-incidence countries by line probe assay. J Clin Microbiol. 2003;41:4454–6.
- Traore H, Fissette K, Bastian I, Devleeschouwer M, Portaels F. 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. 2000;4:481–4.
- Rossau R, Traore H, De Beenhouwer H, Mijs W, Jannes G, De Rijk P, Evaluation of the INNO-LiPA Rif. TB assay, a reverse hybridization assay for the simultaneous detection of Mycobacterium tuberculosis complex and its resistance to rifampin. Antimicrob Agents Chemother. 1997;41:2093–8.
- Drobniewski FA, Watterson SM, Wilson SM, Harris GS. A clinical, microbiological, and economic analysis of a national service for rapid molecular diagnosis of tuberculosis and rifampin resistance in Mycobacterium tuberculosis. J Med Microbiol. 2000;49:271–8.
- World Health Organization. Anti-tuberculosis drug resistance in the world: third global report. Geneva: The Organization; 2004.
- Preidulena I, Laserson K, Leimans J, Mihalovska D, Wells C, Leimane V, Risk factors for primary multidrug resistant tuberculosis in Latvia, 1999-2001. Int J Tuberc Lung Dis. 2001;5:S163.
- Kent PT, Kubica G. Public health mycobacteriology, a guide for the level III laboratory. Atlanta: Centers for Disease Control; 1985.
Suggested citation for this article: Skenders G, Fry AM, Prokopovica I, Greckoseja S, Broka L, Metchock B, et al. Multidrug-resistant tuberculosis detection, Latvia. Emerg Infect Dis [serial on the Internet]. 2005 Sep [date cited]. http://dx.doi.org/10.3201/eid1109.041236
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