An objective of the 1991 World Health Assembly was the elimination of leprosy as a public health problem by the year 2000. The goal was to achieve a reduction in prevalence of leprosy to less than 1 per 10,000 population. This goal has not been achieved in the most endemic countries, where more than 80% of the global leprosy cases occur, despite the implementation of the Multi Drug Therapy (MDT) program. The number of new cases detected has also not reduced indicating that the transmission of the causative agent Mycobacterium leprae has not been controlled. There are fundamental gaps in the understanding of transmission, and a lack of sensitive methods to track leprosy. Questions remain regarding the nature of the reservoir of M. leprae, the route of infection, and mode of its spread. To address these concerns, a DNA typing method for M. leprae is proposed based on the availability of the genome sequence and the principle of multiple locus variable-number of tandem repeat analysis (MLVA), which has been developed for several other infectious organisms. M. leprae cannot be cultivated in a laboratory and bacteria for research applications is mainly derived from susceptible armadillo or nude mice. This pilot study is therefore designed with two specific aims: 1. Development of a standard molecular typing method using a panel of armadillo derived M. leprae isolates and 2. Application of the optimized methods in a panel of M. leprae DNA derived from biopsies and nasal swabs from patients. The methods involve the PCR amplification of multiple genomic loci containing short tandem repeats for each isolate of M. leprae and the comparison of the fragment length of each locus with that obtained from other isolates. Automated electrophoresis, data collection and analysis will be used. The long-term goal of the study is to provide the tools and techniques suitable for future epidemiological studies such as the role of human, non-human and environmental sources of M. leprae in the transmission of leprosy via nasal or dermal routes of ntry and release of the pathogen and the differentiation of relapse from reinfection in patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Research Grants (R03)
Project #
5R03AI059644-02
Application #
6892828
Study Section
Special Emphasis Panel (ZRG1-BM-1 (02))
Program Officer
Sizemore, Christine F
Project Start
2004-05-15
Project End
2007-04-30
Budget Start
2005-05-01
Budget End
2007-04-30
Support Year
2
Fiscal Year
2005
Total Cost
$72,500
Indirect Cost
Name
Colorado State University-Fort Collins
Department
Microbiology/Immun/Virology
Type
Schools of Veterinary Medicine
DUNS #
785979618
City
Fort Collins
State
CO
Country
United States
Zip Code
80523
Sakamuri, Rama Murthy; Kimura, Miyako; Li, Wei et al. (2009) Population-based molecular epidemiology of leprosy in Cebu, Philippines. J Clin Microbiol 47:2844-54
Kimura, Miyako; Sakamuri, Rama Murthy; Groathouse, Nathan A et al. (2009) Rapid variable-number tandem-repeat genotyping for Mycobacterium leprae clinical specimens. J Clin Microbiol 47:1757-66
Weng, Xiaoman; Wang, Zheng; Liu, Jian et al. (2007) Identification and distribution of Mycobacterium leprae genotypes in a region of high leprosy prevalence in China: a 3-year molecular epidemiological study. J Clin Microbiol 45:1728-34