TY - JOUR KW - Animals KW - Antigens, Bacterial KW - Base Sequence KW - DNA, Bacterial KW - Gene Amplification KW - Humans KW - leprosy KW - Molecular Sequence Data KW - Mycobacterium KW - Mycobacterium leprae KW - polymerase chain reaction KW - Predictive Value of Tests KW - Species Specificity AU - Hackel C AU - Houard S AU - Portaels F AU - Elsen A AU - Herzog A AU - Bollen A AB -

Oligonucleotide primers have been used to amplify DNA regions of the M. leprae genome by the polymerase chain reaction. A first set of primers, PLp1 and PLp2, identifies a specific 386 bp DNA fragment located in the gene coding for the 65 kDa antigen of M. leprae. A second pair of primers, targetted to the same gene, leads to the amplification of a 154 bp DNA piece conserved in mycobacteria. Primers PLp1 and PLp2 discriminate the pathogenic species from other mycobacteria, detect down to 40 bacilli, and constitute potentially useful tools for the identification of M. leprae in clinical specimens.

BT - Molecular and cellular probes C1 - http://www.ncbi.nlm.nih.gov/pubmed/2199822?dopt=Abstract DA - 1990 Jun DO - 10.1016/0890-8508(90)90054-4 IS - 3 J2 - Mol. Cell. Probes LA - eng N2 -

Oligonucleotide primers have been used to amplify DNA regions of the M. leprae genome by the polymerase chain reaction. A first set of primers, PLp1 and PLp2, identifies a specific 386 bp DNA fragment located in the gene coding for the 65 kDa antigen of M. leprae. A second pair of primers, targetted to the same gene, leads to the amplification of a 154 bp DNA piece conserved in mycobacteria. Primers PLp1 and PLp2 discriminate the pathogenic species from other mycobacteria, detect down to 40 bacilli, and constitute potentially useful tools for the identification of M. leprae in clinical specimens.

PY - 1990 SP - 205 EP - 10 T2 - Molecular and cellular probes TI - Specific identification of Mycobacterium leprae by the polymerase chain reaction. VL - 4 SN - 0890-8508 ER -