Four-year experience of use of the Cobas Amplicor system for rapid detection of Mycobacterium tuberculosis complex in respiratory and nonrespiratory specimens in Greece

被引:25
作者
Levidiotou, S [1 ]
Vrioni, G [1 ]
Galanakis, E [1 ]
Gesouli, E [1 ]
Pappa, C [1 ]
Stefanou, D [1 ]
机构
[1] Univ Ioannina, Sch Med, Dept Microbiol, GR-45110 Ioannina, Greece
关键词
D O I
10.1007/s10096-003-0931-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
To evaluate the experience of a clinical microbiology laboratory with a DNA amplification assay for routine detection of Mycobacterium tuberculosis, the Cobas Amplicor Mycobacterium tuberculosis (MTB) polymerase chain reaction (PCR) assay (Roche Diagnostics Systems, USA) was performed on 7,722 respiratory and 1,451 nonrespiratory specimens collected from 3,321 patients. The results were compared with those of culture in conventional Lowenstein-Jensen medium, culture in the MB/BacT system (Organon Teknika, France), and clinical investigations. A total of 240 of the 254 respiratory specimens culture positive for Mycobacterium tuberculosis were also positive in the PCR assay. Of the 7,300 culture-negative specimens, 45 (0.6%) were positive in the PCR. After detailed interpretation, the overall sensitivity, specificity, and positive and negative predictive values of the PCR assay were 84.5, 99.8, 94.1, and 99.4%, respectively, for respiratory specimens. The PCR assay was more sensitive for smear-positive respiratory specimens (97.1%) than for smear-negative respiratory specimens (48.6%). Of the 18 culture-positive (smear-negative) nonrespiratory specimens, 9 were positive in the PCR. None of the 1,384 culture-negative nonrespiratory specimens were positive in the PCR. The inhibition rates detected by the internal control of the test were 2.2% for respiratory specimens and 3.4% for nonrespiratory specimens. After resolving the discrepancies, the overall sensitivity, specificity, and positive and negative predictive values of the PCR assay were 82.5, 99.8, 94.3, and 99.4%, respectively, when compared to the results of diagnostic culture. In conclusion, the use of the Cobas Amplicor MTB-PCR assay might enable clinical microbiology laboratories with considerable previous experience in molecular biology testing to perform PCR and confirm tuberculosis infection immediately, leading to improved patient management.
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页码:349 / 356
页数:8
相关论文
共 26 条
[1]   Evaluation of the COBAS AMPLICOR MTB system [J].
Bodmer, T ;
Gurtner, A ;
Scholkmann, M ;
Matter, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (06) :1604-1605
[2]   Multicenter study of a commercial, automated polymerase chain reaction system for the rapid detection of Mycobacterium tuberculosis in respiratory specimens in routine clinical practice [J].
Bogard, M ;
Vincelette, J ;
Antinozzi, R ;
Alonso, R ;
Fenner, T ;
Schirm, J ;
Aubert, D ;
Gaudreau, C ;
Sala, E ;
Ruiz-Serrano, MJ ;
Petersen, H ;
Oostendorp, LAB ;
Burkardt, H .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2001, 20 (10) :724-731
[3]  
Centers for Disease Control and Prevention (CDC), 2000, MMWR Morb Mortal Wkly Rep, V49, P593
[4]   LARGE-SCALE USE OF POLYMERASE CHAIN-REACTION FOR DETECTION OF MYCOBACTERIUM-TUBERCULOSIS IN A ROUTINE MYCOBACTERIOLOGY LABORATORY [J].
CLARRIDGE, JE ;
SHAWAR, RM ;
SHINNICK, TM ;
PLIKAYTIS, BB .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (08) :2049-2056
[5]   Evaluation of Amplicor MTB test as adjunct to smears and culture for direct detection of Mycobacterium tuberculosis in the French Caribbean [J].
Devallois, A ;
Legrand, E ;
Rastogi, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (05) :1065-1068
[6]  
EISENACH KD, 1999, MYCOBACTERIA MOL BIO, P161
[7]   Strand displacement amplification and the polymerase chain reaction for monitoring response to treatment in patients with pulmonary tuberculosis [J].
Hellyer, TJ ;
Fletcher, TW ;
Bates, JH ;
Stead, WW ;
Templeton, GL ;
Cave, MD ;
Eisenach, KD .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (04) :934-941
[8]   Comparison of the Roche AMPLICOR MYCOBACTERIUM assay and Digene SHARP Signal System with in-house PCR and culture for detection of Mycobacterium tuberculosis in respiratory specimens [J].
Huang, TS ;
Liu, YC ;
Lin, HH ;
Huang, WK ;
Cheng, DL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (12) :3092-3096
[9]   Evaluation of Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test and Roche PCR-Microwell Plate Hybridization Method (AMPLICOR MYCOBACTERIUM) for direct detection of mycobacteria [J].
Ichiyama, S ;
Iinuma, Y ;
Tawada, Y ;
Yamori, S ;
Hasegawa, Y ;
Shimokata, K ;
Nakashima, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (01) :130-133
[10]  
KENT PT, 1985, US PHS PUBLICATION, P57