Abstract

Several Mycobacterium leprae gene targets could be used for leprosy diagnostic. PCR sensitivity of some gene targets for specific clinical isolates has not yet been established in Cote d'Ivoire. The present study was conducted to compare the sensitivity of the Pra gene and RLEP targets in the detection of M. leprae from nasal mucus and ear dermal pulp fluid samples from paucibacillary and multibacillary patients. Leprosy patients were classified into Paucibacillary and Multibacillary types. DNA extraction from samples was performed by a guanidine thiocyanate method. PCR technique was performed for M. leprae detection from samples. 84.94 % were positive for RLEP target while 69.94 % were positive for the Pra gene target. For paucibacillary cases with bacteriological index negative, 180 one 258 (69.76 %) were positive for the RLEP target and 193 one 258 (74. 80 %) were positive for Pra gene target. Concerning multibacillary cases with bacteriological index positive samples, 100% of the samples were positive for RLEP target and 65.21 % for Pra gene target. The Pra gene target showed a large difference in detection of M. leprae between paucibacillary and multibacillary forms in leprosy patients. In conclusion, PCR-Pra could be a useful tool for diagnosis of leprosy, mainly in cases of Paucibacillary leprosy or when bacilloscopy is negative. The PCR-RLEP appear to be the best target for early diagnosis of leprosy.

Highlights

  • Leprosy is a chronic infection disease of skin and the peripheral nerves that can entail the inabilities and a social stigmatization [1]

  • Polymerase Chain Reaction (PCR) technique was performed for M. leprae detection from samples. 84.94 % were positive for RLEP target while 69.94 % were positive for the Pra gene target

  • The eradication of a disease being conditioned by the performance of the diagnosis, we evaluated the RLEP and Pra targets in the molecular detection of M. leprae in paucibacillary and multibacillary patients and from the nasal secretions and ear dermal pulp fluid

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Summary

Introduction

Leprosy is a chronic infection disease of skin and the peripheral nerves that can entail the inabilities and a social stigmatization [1] This disease is caused by an environmental mycobacterium, M. leprae, belonging to the same family that bacteria responsible of the tuberculosis and Buruli ulcer. It has been used for the identification of M. leprae from urine and nasal secretions in patients affected by the disease in a recent survey [6]. The eradication of a disease being conditioned by the performance of the diagnosis, we evaluated the RLEP and Pra targets in the molecular detection of M. leprae in paucibacillary and multibacillary patients and from the nasal secretions and ear dermal pulp fluid

Study population
Ethics statement
Biological sample
DNA extraction from nasal secretions and ear dermal pulp fluids samples
PCR for Detecting Pra gene
PCR for detecting Repetitive Element RLEP
PCR products revelation and analysis
Results and discussion
Comparison of PCR positivity for Pra and RLEP according to the clinical forms
Discussion
Conclusion
Disclosure of conflict of interest
Full Text
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