TY - JOUR KW - Bacterial Proteins KW - Dapsone KW - DNA gyrase KW - DNA, Bacterial KW - Drug Resistance, Bacterial KW - Drug Therapy, Combination KW - Ear, External KW - Humans KW - Leprostatic Agents KW - leprosy KW - Mexico KW - Mutation KW - Mycobacterium leprae KW - Ofloxacin KW - polymerase chain reaction KW - Prevalence KW - Rifampin KW - Sequence Analysis, DNA AU - Matsuoka M AU - Suzuki Y AU - Garcia IE AU - Fafutis-Morris M AU - Vargas-González A AU - Carreño-Martinez C AU - Fukushima Y AU - Nakajima C AB -
Mexico is a country with sporadic leprosy cases, and the reemergence of drug resistance is a concern. In this study, molecular analysis of Mycobacterium leprae was employed to clarify the spread of drug-resistant leprosy. Thus, drug resistance-determining regions in the folP1, rpoB, and gyrA genes, which are associated with resistance to dapsone, rifampicin, and ofloxacin, respectively, were analyzed by direct sequencing of the PCR product. No mutations in the folP1 gene were observed in any of the 72 slit skin samples obtained from 38 patients, although two samples carrying a mutation at codon 425 in the rpoB gene, which confers resistance to rifampicin, a key component of multidrug therapy, were identified. In addition, a mutation at codon 91 in the gyrA gene, which correlates with ofloxacin resistance, was found in one sample. These results demonstrate the existence of rifampicin- and ofloxacin-resistant leprosy. Interestingly, wild-type and mutant sequences in the gyrA gene were found to coexist in one clinical sample. In addition, all three drug resistance-related mutations were found in only one of the two earlobes of the patients concerned, suggesting a possible pathway for the spread of drug-resistant M. leprae.
BT - Japanese journal of infectious diseases C1 - http://www.ncbi.nlm.nih.gov/pubmed/21099091?dopt=Abstract C6 - Download full text. DA - 2010 Nov IS - 6 J2 - Jpn. J. Infect. Dis. LA - eng N2 -Mexico is a country with sporadic leprosy cases, and the reemergence of drug resistance is a concern. In this study, molecular analysis of Mycobacterium leprae was employed to clarify the spread of drug-resistant leprosy. Thus, drug resistance-determining regions in the folP1, rpoB, and gyrA genes, which are associated with resistance to dapsone, rifampicin, and ofloxacin, respectively, were analyzed by direct sequencing of the PCR product. No mutations in the folP1 gene were observed in any of the 72 slit skin samples obtained from 38 patients, although two samples carrying a mutation at codon 425 in the rpoB gene, which confers resistance to rifampicin, a key component of multidrug therapy, were identified. In addition, a mutation at codon 91 in the gyrA gene, which correlates with ofloxacin resistance, was found in one sample. These results demonstrate the existence of rifampicin- and ofloxacin-resistant leprosy. Interestingly, wild-type and mutant sequences in the gyrA gene were found to coexist in one clinical sample. In addition, all three drug resistance-related mutations were found in only one of the two earlobes of the patients concerned, suggesting a possible pathway for the spread of drug-resistant M. leprae.
PY - 2010 SP - 412 EP - 6 T2 - Japanese journal of infectious diseases TI - Possible mode of emergence for drug-resistant leprosy is revealed by an analysis of samples from Mexico. UR - http://www.nih.go.jp/JJID/63/412.pdf VL - 63 SN - 1884-2836 ER -