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Intrapatient comparison of Mycobacterium leprae by VNTR analysis in nasal secretions and skin biopsy in a Brazilian leprosy endemic region
Author(s) -
Lua. G. C. Lima,
Amanda NB Fontes,
Wei Li,
Philip Noël Suffys,
Varalakshmi Vissa,
Rosa MS Mota,
Rosa LF Almeida,
Maria Araci de Andrade Pontes,
Heitor de Sá Gonçalves,
Cristiane Cunha Frota,
Laura C. Rodrigues,
Carl Kendall,
Lígia Regina Franco Sansigolo Kerr
Publication year - 2016
Publication title -
leprosy review
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 43
eISSN - 2162-8807
pISSN - 0305-7518
DOI - 10.47276/lr.87.4.486
Subject(s) - leprosy , mycobacterium leprae , medicine , skin biopsy , nose , microbiology and biotechnology , lepromatous leprosy , biopsy , dermatology , pathology , surgery , biology
BackgroundThis study compares the strains of genotypes of M. leprae from nasal secretions (NS) and skin biopsy (SB) in the same patient, supplementing conventional epidemiology to gain insight into the infection of leprosy in Fortaleza, Brazil.MethodsThe sample consisted of 38 newly diagnosed leprosy patients attending the National Reference Center of Dermatology Dona Libania (CDERM), in Fortaleza, who tested positive for M. leprae by PCR in DNA extracts of nasal secretions. DNA was also extracted from skin biopsy (SB) scrapings of each patient and used for multiplex PCR amplification of M. leprae VNTR loci. The number of repeats at 15 loci were determined by the fragment length analysis method.ResultsLocus VNTR genotypes were achieved in 38 NS, and in 38 SB specimens.M. leprae strains differed in their genotypes in paired specimens in all but two of38 patients. The genotype similarity in the remainder ranged from 53% to 87%.ConclusionM. leprae 15 VNTR loci genotypes of paired nasal and biopsy skin samples from five patients were identical, while as many as seven loci differed in the 33 other patients. When the NS and biopsy genotypes were pooled and compared, it was found that there was a great variability among different VNTR markers. It is important to investigate other molecular markers suitable for typing genetic variations of the bacilli.

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