Abstract
BackgroundDetection of Mycobacterium leprae in slit skin smear (SSS) is a gold standard technique for the leprosy diagnosis. Over recent years, molecular diagnosis by using PCR has been increasingly used as an alternative for its diagnosis due to its higher sensitivity. This study was carried out for comparative evaluation of PCR and SSS microscopy in a cohort of new leprosy cases diagnosed in B. P. Koirala Institute of health Sciences, Dharan, Nepal.Methodology/Principal FindingsIn this prospective crossectional study, 50 new clinically diagnosed cases of leprosy were included. DNA was extracted from SSS and PCR was carried out to amplify 129 bp sequence of M. leprae repetitive element. Sensitivity of SSS and PCR was 18% and 72% respectively. Improvement of 54% case detection by PCR clearly showed its advantage over SSS. Furthermore, PCR could confirm the leprosy diagnosis in 66% of AFB negative cases indicating its superiority over SSS. In the paucibacillary (PB) patients, whose BI was zero; sensitivity of PCR was 44%, whereas it was 78% in the multibacillary patients.Conclusions/SignificanceOur study showed PCR to be more sensitive than SSS microscopy in diagnosing leprosy. Moreover, it explored the characteristic feature of PCR which detected higher level of early stage(PB) cases tested negative by SSS. Being an expensive technique, PCR may not be feasible in all the cases, however, it would be useful in diagnosis of early cases of leprosy as opposed to SSS.
Highlights
Leprosy is a chronic infectious disease which mainly affects the skin, nasal mucosa, and peripheral nerve
Leprosy has been eliminated at the national level, but region wise eastern Nepal has still the higher number of leprosy cases
Slit-skin smear (SSS), the routine diagnostic method was compared with the molecular method polymerase chain reaction (PCR) for the detection of new clinically diagnosed cases at BPKIHS
Summary
Leprosy is a chronic infectious disease which mainly affects the skin, nasal mucosa, and peripheral nerve. It is caused by Mycobacterium leprae, an acid-fast bacillus which is transmitted via droplets from the nose and mouth during close contacts with untreated cases [1]. DNA based PCR have shown superior performance to detect bacilli in clinical samples [4,5,6,7,8]. Their application is not wide in resources poor countries.
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