|
|
|
|
¡¡ |
|
¡¡ |
|
|
|
¡¡ |
HOME > ÇÐȸ°£Ç๰ >
¿ë¾î»çÀü |
|
Á¦¸ñ |
Assessment of the susceptibility to antileprotic drugs by RT PCR |
|
|
|
|
ÀúÀÚ |
Min Joo Kim, Se Kon Kim, Ji Chang You, Gue Tae Chae, Soon Ok Kim#, Joo Won Suh#, and Nam Jin Yoo## |
¼Ò¼Ó |
Institute of chronic Diseases, Catholic University Medical College, Dept. of Biological Science, Natural Science Institute, Myong-Ji University#, and Dept. of Pathology, Catholic University Medical College## |
|
|
³âµµ |
1997 |
±Ç |
30 |
|
|
È£ |
2 |
¹øÈ£ |
|
|
|
½ÃÀÛÆäÀÌÁö |
49 |
³¡ÆäÀÌÁö |
55 |
|
|
÷ºÎ |
|
|
|
¿ä¾à |
We investigated whether RT PCR is suitable and relable method for the detection of the viability of Mycobacterium leprae and the assessment of the susceptibility to antileprotic drugs. RT PCR was chosen because it has been demonstrated for rapid, sensitive and specific detection of 18kDa antigen in M. leprae. M. leprae-infected macrophages were exposed to various concentrations of rifampin which has the most bactericidal effect among MDT drugs and whose target site is an bacterial RNA polymerase. After the exposure to rifampin, RNA was isolated, reverse-transcribed, and followed by the detection of cDNA encoding M. leprae-specific 18kDa antigen by PCR. Radiorespirometry, which is the most popular but a time-consuming method, was also compared with the RT PCR method. Both methods whowed a decreasing pattern depending on the concentrations of rifampin. However, RT PCR had more significant effect showing a detection limit of 102 bacilli and the loss of RT PCR signal at low concentrations of rifampin in two days, instead of three weeks. This system for testing viability provides a potential for rapid evaluations of drug susceptibility testing. |
|
|
³»¿ë |
|
| |
¡¡ |
|
|
|
|
|
|
|
|