TY - JOUR KW - Bacterial Proteins KW - Bacterial Typing Techniques KW - Chaperonin 60 KW - Chaperonins KW - Cluster Analysis KW - DNA Fingerprinting KW - DNA-Directed RNA Polymerases KW - genotype KW - Humans KW - Lepromin KW - leprosy KW - Mycobacterium leprae KW - polymerase chain reaction KW - Polymorphism, Restriction Fragment Length AU - Alban SM AU - Sella SR B R AU - Miranda RN AU - Mira M AU - Soccol VT AB -

OBJECTIVES: The aim of the present work was to standardise a PCR-Restriction Fragment Length Polymorphism analysis (PRA) as a tool to detect the mycobacteriologic composition of lepromas from leprosy patients used in the production of lepromin to improve the quality of the Mitsuda test.

DESIGN: PCR-Restriction Fragment Length Polymorphism analysis using hsp65 and rpoB genes were applied to 11 reference strains of mycobacteria, including M. leprae, and the obtained PRA profiles were compared to mycobacteria in clinical specimens.

RESULTS: Out of the biopsies studied, 522% had DNA fragment amplified for both genes (hsp65 and rpoB) for M. leprae. However, other Mycobacterium species were observed in samples of lepromatous leprosy patients. Here we discussed the importance of mycobacteria identification in the antigen of Mitsuda production to be used in the evaluation of leprosy.

CONCLUSIONS: Our results suggest that the use of the molecular approach for sample selection can contribute to an improvement in the quality of produced lepromin.

BT - Leprosy review C1 - http://www.ncbi.nlm.nih.gov/pubmed/19743617?dopt=Abstract CN - ALBAN 2009 DA - 2009 Jun IS - 2 J2 - Lepr Rev LA - eng N2 -

OBJECTIVES: The aim of the present work was to standardise a PCR-Restriction Fragment Length Polymorphism analysis (PRA) as a tool to detect the mycobacteriologic composition of lepromas from leprosy patients used in the production of lepromin to improve the quality of the Mitsuda test.

DESIGN: PCR-Restriction Fragment Length Polymorphism analysis using hsp65 and rpoB genes were applied to 11 reference strains of mycobacteria, including M. leprae, and the obtained PRA profiles were compared to mycobacteria in clinical specimens.

RESULTS: Out of the biopsies studied, 522% had DNA fragment amplified for both genes (hsp65 and rpoB) for M. leprae. However, other Mycobacterium species were observed in samples of lepromatous leprosy patients. Here we discussed the importance of mycobacteria identification in the antigen of Mitsuda production to be used in the evaluation of leprosy.

CONCLUSIONS: Our results suggest that the use of the molecular approach for sample selection can contribute to an improvement in the quality of produced lepromin.

PY - 2009 SP - 129 EP - 42 T2 - Leprosy review TI - PCR-restriction fragment length polymorphism analysis as a tool for Mycobacterium species identification in lepromas for lepromin production. UR - https://leprosyreview.org/article/80/2/12-9142 VL - 80 SN - 0305-7518 ER -