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1.
Article in English | IMSEAR | ID: sea-111965

ABSTRACT

A reverse transcription (RT)-PCR assay targeting 16S rRNA of Mycobacterium leprae has been used to detect M.leprae specific nucleic acids. This study has been initiated to gain experience about detection of RNA from seven biopsy specimens by RT-PCR assay using species- specific primers described earlier. These biopsy specimens were from clinically confirmed and untreated leprosy cases belonging to BB and BL types. The earlier reported method was established in our laboratory. 171 bp fragment by RT-PCR was amplified from 4/7 cases. The positives results by RT-PCR were from the biopsies from fresh or short term treated cases whereas negative results were from specimens from long term treated cases showing clinical features of relapse. DNA targeting PCR (36 KDa) showed positivity in both groups. These results suggest that RT-PCR positivity possibly reflect the presence of viable organisms. Thus as earlier predicted RT-PCR assay may be useful for viability determinations for assessing the response to chemotherapy as well as presence of persisters in relapse cases.


Subject(s)
Biopsy , Humans , Leprosy/diagnosis , Mycobacterium leprae/genetics , RNA, Ribosomal, 16S/classification , Reverse Transcriptase Polymerase Chain Reaction , Sensitivity and Specificity , Skin/microbiology
2.
Article in English | IMSEAR | ID: sea-148255

ABSTRACT

Although appendicular involvement in intestinal tuberculosis has been reported in 1.5-3% cases, the prevalence of isolated tuberculosis of appendix is a comparative rarity. We report a patient with provisional clinical diagnosis of appendicitis, who was found to have tuberculosis of appendix on histopathology, after interval appendicectomy. He had no detectable tubercular focus elsewhere in the body. Post-operatively, he was treated with anti-tubercular regimen with uncomplicated clinical recovery.

3.
Indian J Exp Biol ; 2002 Feb; 40(2): 212-5
Article in English | IMSEAR | ID: sea-61665

ABSTRACT

A micropropagation protocol based on axillary bud proliferation has been developed from mature Lagerstromia parviflora adult tree. Nodal segments cultured on woody plant medium supplemented with 5.0 microl. BAP and 0.25 microm IAA gave maximum (86.9%) morphogenetic response. Proliferated shoots (10.7 per explants) were elongated to 3.9 cm within 6 weeks. In vitro produced micro-shoots were subjected to an IBA treatment (500 ppm for 2 min. dip) and placed under misting conditions for rooting. Misting beds were prepared with sand: soil (3:1) for 80.6% rooting and was acclimatized. Shoot length seems to be important to induce adventitious roots. The highest (91.7%) rooting was recorded on shoots ranging a length between 3.1-4.0 cm. Rooted and hardened plants were later transferred to poly bags and maintained in shadenet house. The protocol has the realizes capacity to produce 260 plants from a single explants within 10 months multiplication cycle.


Subject(s)
Botany/methods , Culture Media/pharmacology , Indoleacetic Acids/pharmacology , Plant Physiological Phenomena , Plant Roots/drug effects , Trees/physiology
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