2004, Number 2
<< Back Next >>
Rev Mex Patol Clin Med Lab 2004; 51 (2)
Advantages of the culture in an automated equipment and the PCR test for the Mycobacterium tuberculosis diagnosis
Fagundo SR, Cerros SMA, Herrera PE
Language: Spanish
References: 17
Page: 70-74
PDF size: 75.64 Kb.
ABSTRACT
Because of tuberculosis recovered importance, the need to find new faster
and specific diagnostic tools as an impact measure for disease control, has
arisen. Our Laboratory has adopted new technologies as PCR microorganism
identification, automated culture and antimycobacterial susceptibility test
to achieve tuberculosis diagnosis. The present work shows our experience
in evaluating 369 patient’s samples for
Mycobacterium detection by automated
culture means. Samples came from different places of Mexico country in a total
period of eighteen months. By automated culture were isolated 44 positive
samples to Mycobacterium in an average time of 21 days each one. This isolates
then were submitted to PCR characterization and antimycobacterial
susceptibility test against isoniazid, rifampin and ethambutol, the
first three drugs of choice for treatment. PCR was positive in 82% of isolates demonstrating the importance of this test in detecting
false-positive diagnosis of tuberculosis. Forty three per cent of
isolates showed resistance against 2 or 3 of the evaluated drugs
(multi-drug resistance).
REFERENCES
Metchock B, Nolte FS, Wallace RJ Jr. Mycobacterium. In: Murray PR, Baron EJ, Pfaller MA, Tenover FC, Yolken RH editors. Manual of clinical microbiology. 7th ed. Washington, DC: ASM Press. 1999: 399-437.
Montoro E. Micobacterias. En: Llop-Valdéz Dapena-Zuazo. Microbiología y parasitología médicas. Ciudad de La Habana: Edit Ciencias Médicas 2001: 636-385.
Koneman E. Micobacterias. En: Diagnóstico microbiológico. 5a ed. Madrid, España: Edit Médica Panamericana. 2001: 867-926.
Casal M. Tuberculosis: enfermedad reemergente. Invest Cienc 1998; 265: 33-34.
World Health Organization. Fact Sheet No. 104. Revised August 2002.
OPS. OMS. Situación de salud en las Américas. Bol Epidemiol 2000; 21 (4).
Secretaría de Salud. Programa Nacional de Prevención y Control de la Tuberculosis. Manual de Procedimientos. México: 1999: 1-10.
World Health Organization. Anti-tuberculous drug resistance in the world. Report No. 2. Prevalence and trends. The WHO/IUATLD Global project on anti-tuberculous drug resistance surveillance. Geneva: World Health Organization, 2000.
Centers for Disease Control and Prevention. Essential Components of a Tuberculosis Prevention and Control Program. Recommendations of the Advisory Council for the Elimination of Tuberculosis. MMWR Morb Mortal Wkly Rep 1995; 44 (RR-11): 1-6.
OPS. Manual de normas y procedimientos técnicos para la bacteriología de la tuberculosis, Parte I. La Muestra. El Examen Microscópico. OPS Nota Técnica Núm. 26/Rev. I. 1988.
OPS. Manual de normas y procedimientos técnicos para la bacteriología de la tuberculosis, Parte I. El Cultivo. OPS Nota Técnica Núm. 27/Rev. I. 1988a.
NCCLS. Susceptibility testing of mycobacteria, nocardia, and other aerobic actinomyces; tentative standard. 2nd ed. M24-T2. Vol. 20 (26).
Somoskövi C, Ködmön A, Lantos Z, Bartfai L, Tamási J, Füzy PM. 2000. Comparison of recoveries of Mycobacterium tuberculosis using the automated BACTEC MGIT 960 system, the BACTEC 460 TB system and Lowenstein-Jensen medium. J Clin Microbiol 2000; 38: 2395-2397.
Alcaide F, Benítez MA, Escriba JM, Martin R. Evaluation Bactec MGIT 960 and MB/Bact Systems for recovery of mycobacteria from clinical specimens and for species identification by DNA AccuProbe. J Clin Microbiol 2000; 38: 398-400.
Williams-Bouyer N, Yorke R, Lee HI, Woods G. Comparison of BACTEC MGIT and ESP Culture System II for growth and detection of Mycobacteria. J Clin Microbiol 2000; 38 (11): 4167-4170.
Noordhoek GT, van Embden JDA, Kolk AHJ. Reliability of nucleic acid amplification for detection of Mycobacterium tuberculosis: an international collaborative quality control study among 30 laboratories. J Clin Microbiol 1996; (34): 2522-2525.
Telenti A, Marchesi F, Balz M et al. Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis. J Clin Microbiol 1993; (31): 175-178.