Rapid diagnosis of tuberculosis directly from clinical specimens using a gene chip

被引:13
作者
Chang, H. J. [1 ]
Huang, M. Y. [2 ,3 ,4 ]
Yeh, C. S. [1 ,5 ,6 ]
Chen, C. C. [1 ,5 ,6 ]
Yang, M. J. [2 ]
Sun, C. S. [2 ]
Lee, C. K. [7 ]
Lin, S. R. [1 ,5 ,6 ]
机构
[1] Fooyin Univ, Biomed Technol Dev Ctr, Ta Liao Hsiang 831, Kaohsiung Hsien, Taiwan
[2] Kaohsiung Med Univ, Coll Med, Fac Med, Grad Inst Med, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ, Coll Med, Fac Med, Dept Radiat Oncol, Kaohsiung, Taiwan
[4] Kaohsiung Med Univ Hosp, Dept Radiat Oncol, Kaohsiung, Taiwan
[5] Fooyin Univ, Sch Med & Hlth Sci, Dept Med Technol, Ta Liao Hsiang 831, Kaohsiung Hsien, Taiwan
[6] Dept Med Res, Fooyin, Taiwan
[7] Fooyin Univ Hosp, Dept Internal Med, Div Infect Dis, Pingtung, Taiwan
关键词
Gene chip; membrane array methods; rapid diagnosis; sputum; tuberculosis; MYCOBACTERIUM-TUBERCULOSIS; COLORECTAL-CANCER; EARLY RELAPSE; COMPLEX; BACILLUS; IDENTIFICATION; POLYMORPHISM; PREVALENCE; EVOLUTION;
D O I
10.1111/j.1469-0691.2009.03045.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
P>The aim of this study was to explore a gene chip capable of detecting the presence of Mycobacterium tuberculosis isolates directly in clinical sputum specimens and to compare it with current molecular detection techniques. At first, we selected 13 M. tuberculosis-specific target genes to construct a gene chip for rapid diagnosis. Using the membrane array method, we diagnosed M. tuberculosis by gene chip directly from 246 sputum specimens from patients suspected of having tuberculosis. Among 80 M. tuberculosis complex (MTBC) culture-positive sputum specimens, the MTBC detection rate was 62.5% (50/80) by PCR-restriction fragment length polymorphism (RFLP), 70% (56/80) by acid-fast staining, and 85% (68/80) by the membrane array method. Furthermore, subspecies showed different gene expression patterns in the membrane array. In conclusion, MTBC could be detected directly in sputum by the membrane array method. The rapidity of detection and the capability of differentiating subspecies could make this method useful in the control and prevention of tuberculosis.
引用
收藏
页码:1090 / 1096
页数:7
相关论文
共 28 条
[1]  
[Anonymous], 2007, WHO REP 2007 GLOB TU
[2]   Transmission of Mycobacterium tuberculosis from patients smear-negative for acid-fast bacilli [J].
Behr, MA ;
Warren, SA ;
Salamon, H ;
Hopewell, PC ;
de Leon, AP ;
Daley, CL ;
Small, PM .
LANCET, 1999, 353 (9151) :444-449
[3]   A new evolutionary scenario for the Mycobacterium tuberculosis complex [J].
Brosch, R ;
Gordon, SV ;
Marmiesse, M ;
Brodin, P ;
Buchrieser, C ;
Eiglmeier, K ;
Garnier, T ;
Gutierrez, C ;
Hewinson, G ;
Kremer, K ;
Parsons, LM ;
Pym, AS ;
Samper, S ;
van Soolingen, D ;
Cole, ST .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (06) :3684-3689
[4]   Molecular diagnostics in tuberculosis [J].
Cheng, VCC ;
Yew, WW ;
Yuen, KY .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2005, 24 (11) :711-720
[5]  
Chong IW, 2006, ONCOL REP, V16, P981
[6]   Evolution of tuberculosis control and prospects for reducing tuberculosis incidence, prevalence, and deaths globally [J].
Dye, C ;
Watt, CJ ;
Bleed, DM ;
Hosseini, SM ;
Raviglione, MC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 293 (22) :2767-2775
[7]   Global burden of tuberculosis - Estimated incidence, prevalence, and mortality by country [J].
Dye, C ;
Scheele, S ;
Dolin, P ;
Pathania, V ;
Raviglione, RC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (07) :677-686
[8]   High genetic diversity revealed by variable-number tandem repeat genotyping and analysis of hsp65 gene polymorphism in a large collection of "Mycobacterium canettii" strains indicates that the M-tuberculosis complex is a recently emerged clone of "M-canettii" [J].
Fabre, M ;
Koeck, JL ;
Le Flèche, P ;
Simon, F ;
Hervé, V ;
Vergnaud, G ;
Pourcel, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (07) :3248-3255
[9]   Genome structure in the vole bacillus, Mycobacterium microti, a member of the Mycobacterium tuberculosis complex with a low virulence for humans [J].
Frota, CC ;
Hunt, DM ;
Buxton, RS ;
Rickman, L ;
Hinds, J ;
Kremer, K ;
van Soolingen, D ;
Colston, MJ .
MICROBIOLOGY-SGM, 2004, 150 :1519-1527
[10]   Evaluation of mtp40 genomic fragment amplification for specific detection of Mycobacterium tuberculosis in clinical specimens [J].
Herrera, EA ;
Segovia, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (05) :1108-1113