Korean Lepr Bull.  2001 Dec;34(2):13-21.

The application of TD (Touch-Down) PCR in Diagnosis of leprosy and Detection of MDT-resistant M. leprae

Affiliations
  • 1Institute of Hansen's Disease, Korea.
  • 2Department of Pathology College of Medicine, The Catholic University of Korea, Korea.

Abstract

There are several methods for diagnosis of leprosy, including AFB stain, the measurement of PGL-1 (phenolic glycolipid - 1) antigen titer, and DNA-PCR. In this study, we have used the DNA-PCR amplifying the RLEP repetitive sequence. Our result showed that the RLEP primer offered the more sensitive detection and identification of M. leprae DNA in clinical specimens, compared with the other primer, for example, 18-kDa antigen gene. To screen the resistant M. leprae strain of MDT (Multi-Drug Therapy), we have used the TD (Touch-Down) PCR. We arranged and amplified sequences of the genes, folP, rpoB, gyr, 23S rRNA, in M. leprae involved in MDT-resistance, and could obtain the PCR product each gene, simultaneously. This method, based on annealing temperature, was useful to the detection for diagnosis and the screen of MDT-resistant strain of M. leprae, rapidly. Thus, we suggest that the RLEP primer and TD-PCR method are effective in assessing the diagnosis of leprosy and the identification of drug-resistant M. leprae.

Keyword

Leprosy; RLEP repetitive sequence; TD (Touch-Down) PCR

MeSH Terms

Diagnosis*
DNA
Leprosy*
Polymerase Chain Reaction*
Repetitive Sequences, Nucleic Acid
DNA
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