Journal List > Korean J Clin Microbiol > v.14(2) > 1038241

Hwang, Oh, Jang, Uh, Yoon, Kim, and Kim: Evaluation of the Diagnostic Performance of the AdvanSure TB/NTM Real-Time PCR Kit for Detection of Mycobacteria

Abstract

Background

The AdvanSure TB/NTM realtime PCR kit (AdvanSure) was newly developed in Korea to detect Mycobacterium tuberculosis and nontuberculous mycobacteria (NTM) utilizing a specific primer and TaqMan probe targeting the IS6110 and rpoB genes which are unique to these species. The purpose of the present study was to evaluate the clinical utility of AdvanSure by comparing the results of acid-fast staining, mycobacteria culture, COBAS Amplicor MTB PCR (Amplicor), and AdvanSure.

Methods

A total of 182 specimens (105 respiratory and 77 nonrespiratory specimens) were obtained from 165 patients, and acid fast bacilli (AFB) staining, mycobacteria culture, and Amplicor were performed on all specimens. AdvanSure was also performed on the above specimens using the SLAN realtime PCR detection system. The sensitivity and specificity of AdvanSure were analyzed using AFB staining and culture.

Results

Of the 182 specimens, M. tuberculosis was detected in 43 specimens and NTM was detected in 12 specimens according to PCR and/or culture. The sensitivity and specificity of the AdvanSure based on AFB culture were 97.3% (36/37) and 95.5% (127/ 133) in M. tuberculosis and 75.0% (9/12) and 100% (0/133) in NTM, respectively.

Conclusion

AdvanSure could be useful for detecting M. tuberculosis and NTM in the clinical laboratory with high sensitivity and specificity.

REFERENCES

1. Araj GF, Talhouk RS, Itani LY, Jaber W, Jamaleddine GW. Comparative performance of PCR-based assay versus microscopy and culture for the direct detection of Mycobacterium tuberculosis in clinical respiratory specimens in Lebanon. Int J Tuberc Lung Dis. 2000; 4:877–81.
2. Chang HE, Heo SR, Yoo KC, Song SH, Kim SH, Kim HB, et al. Detection of mycobacterium tuberculosis complex using realtime polymerase chain reaction. Korean J Lab Med. 2008; 28:103–8.
crossref
3. Moore DF and Curry JI. Detection and identification of Mycobacterium tuberculosis directly from sputum sediments by Amplicor PCR. J Clin Microbiol. 1995; 33:2686–91.
crossref
4. Johansen IS, Thomsen VØ, Johansen A, Andersen P, Lundgren B. Evaluation of a new commercial assay for diagnosis of pulmonary and nonpulmonary tuberculosis. Eur J Clin Microbiol Infect Dis. 2002; 21:455–60.
5. Bergmann JS and Woods GL. Clinical evaluation of the Roche AMPLICOR PCR Mycobacterium tuberculosis test for detection of M. tuberculosis in respiratory specimens. J Clin Microbiol. 1996; 34:1083–5.
crossref
6. Levidiotou S, Vrioni G, Galanakis E, Gesouli E, Pappa C, Stefanou D. Four-year experience of use of the Cobas Amplicor system for rapid detection of Mycobacterium tuberculosis complex in respiratory and nonrespiratory specimens in Greece. Eur J Clin Microbiol Infect Dis. 2003; 22:349–56.
crossref
7. Kim YJ, Park MY, Kim SY, Cho SA, Hwang SH, Kim HH, et al. Evaluation of the performances of advanSure TB/NTM real time PCR kit for detection of mycobacteria in respiratory specimens. Korean J Lab Med. 2008; 28:34–38.
crossref
8. Diagnostic Standards and Classification of Tuberculosis in Adults and Children. This official statement of the American Thoracic Society and the Centers for Disease Control and Prevention was adopted by the ATS Board of Directors, July 1999. This statement was endorsed by the Council of the Infectious Disease Society of America, September 1999. Am J Respir Crit Care Med. 2000; 161:1376–95.
9. Jung CL, Kim MK, Seo DC, Lee MA. Clinical usefulness of realtime PCR and amplicor MTB PCR assays for diagnosis of tuberculosis. Korean J Clin Microbiol. 2008; 11:29–33.
crossref
10. Reischl U, Lehn N, Wolf H, Naumann L. Clinical evaluation of the automated COBAS AMPLICOR MTB assay for testing respiratory and nonrespiratory specimens. J Clin Microbiol. 1998; 36:2853–60.
crossref
11. Iinuma Y, Senda K, Fujihara N, Saito T, Takakura S, Shimojima M, et al. Comparison of the BDProbeTec ET system with the Cobas Amplicor PCR for direct detection of Mycobacterium tuberculosis in respiratory samples. Eur J Clin Microbiol Infect Dis. 2003; 22:368–71.
crossref

Table 1.
Detection frequency of mycobacteria by based on PCR and culture results
Organisms No. (%)
Mycobacterium tuberculosis 43 (78.2)
Nontuberculous mycobacteria 12 (21.8)
M. intracellulare 6
M. avium 1
M. chelonae 1
M. fortuitum 1
M. gordonae 1
M. kansasii 1
M. terrae 1
Table 2.
Sensitivity and specificity of acid-fast bacilli (AFB) stain and culture, and two PCR methods for detection of mycobacteria based on combination of PCR and culture results
Methods Sensitivity Specificity
AFB stain 47.3% (26/55) 96.1% (122/127)
Culture 89.1% (49/55) 100.0% (127/127)
Amplicor 86.0% (35/43) 96.0% (122/127)
AdvanSure-TB 97.7% (42/43) 92.1% (128/139)
AdvanSure-NTM 75.0% (9/12) 100.0% (170/170)
AdvanSure-TB/NTM 92.7% (51/55) 91.3% (116/127)

Abbreviations: Amplicor, COBAS Amplicor MTB PCR; Advan-sure-TB, Advansure-TB/NTM result for Mycobacterium tuberculosis; Advansure-NTM, Advansure-TB/NTM result for nontuberculous mycobacteria; AdvanSure-TB/NTM, LG AdvanSure TB/NTM realtime PCR.

Table 3.
Comparison of two PCR results according to AFB stain and culture
Final results Results of AFB culture and stain
Culture positive (37/12) Culture negative (133)
Stain-positive (23/1) Stain-negative (14/11) Stain-negative (126) Stain-positive (7)
M. tuberculosis (43)        
 Amplicor-positive (35) 19 14 1 1
 Amplicor-negative (8) 4 0 3 1
 AdvanSure-positive (42) 23 13 4 2
 AdvanSure-negative (1) 0 1 0 0
NTM (12)        
 AdvanSure-positive (9) 1 8 0 0
 AdvanSure-negative (3) 0 3 0 0

Final results were based on the combinations of PCR and AFB culture results

Positive numbers of M. tuberculosis/positive numbers of NTM.

Table 4.
Sensitivity of two PCR methods for M. tuberculosis according to type of specimens based on combination of PCR and culture methods
PCR methods Type of specimens
Respiratory Non-respiratory
Amplicor 83.3% (30/36) 71.4% (5/7)
Advansure-TB/NTM 97.2% (35/36) 100% (7/7)

Abbreviations: See Table 2.

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