1992
DOI: 10.1111/j.1651-2227.1992.tb12190.x
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Polymerase chain reaction for detection of Mycobacterium tuberculosis

Abstract: A polymerase chain reaction (PCR) using heat-stable Taq polymerase is described for the specific detection of Mycobacterium leprae, the causative agent of leprosy. A set of primers was selected on the basis of the nucleotide sequence of a gene encoding the 36 kDa antigen of M. leprae. With this set of primers in the PCR, M. leprae could be detected specifically with a detection limit approximating one bacterium. This PCR appears to meet the criteria of specificity and sensitivity required for a useful tool in … Show more

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Cited by 21 publications
(11 citation statements)
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References 16 publications
(1 reference statement)
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“…A PCR na detecção de micobactérias não é à prova de falhas, pois sua sensibilidade na detecção de micobactérias tem sido relatada na faixa de 55-100% [28][29][30][31] . Por outro lado, esta investigação pode ser usada quando a carga bacteriana é muito baixa 15,32 .…”
Section: Discussionunclassified
“…A PCR na detecção de micobactérias não é à prova de falhas, pois sua sensibilidade na detecção de micobactérias tem sido relatada na faixa de 55-100% [28][29][30][31] . Por outro lado, esta investigação pode ser usada quando a carga bacteriana é muito baixa 15,32 .…”
Section: Discussionunclassified
“…The use of fine-needle aspirations in patients without HIV infections is highly variable [8]. A polymerase chain reaction for Mycobacterium tuberculosis of the fine needle aspiration specimen enhances test sensitivity [11]. …”
Section: Discussionmentioning
confidence: 99%
“…We consider 10 fg to be sufficient for practical purposes. This implied that under experimental conditions, at least two tuberculous bacilli being lysed was sufficient for obtaining a positive result and that this was not very different from that of the first step amplification (9).…”
Section: Sensitivitymentioning
confidence: 92%
“…In our previous report, we described the successful detection of Mycobacterium tuberculosis in two patients with tuberculous lymphadenitis using polymerase chain reaction (PCR) (9). However, during the course of the successive study, we found it necessary to devise a more sensitive assay system as well as a standard methodology for sample preparation and for amplification which would be applicable to various forms of clinical samples.…”
mentioning
confidence: 99%