Development of a Multiple-Locus Variable number of tandem repeat Analysis (MLVA) for <it>Leptospira interrogans </it>and its application to <it>Leptospira interrogans </it>serovar Australis isolates from Far North Queensland, Australia
<p>Abstract</p> <p>Background</p> <p>Leptospirosis is a zoonotic disease caused by the genus, Leptospira. <it>Leptospira interrogans </it>is the most common genomospecies implicated in the disease. Epidemiological investigations are needed to distinguish out...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2005-06-01T00:00:00Z.
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| Summary: | <p>Abstract</p> <p>Background</p> <p>Leptospirosis is a zoonotic disease caused by the genus, Leptospira. <it>Leptospira interrogans </it>is the most common genomospecies implicated in the disease. Epidemiological investigations are needed to distinguish outbreak situations or to trace reservoirs of the organisms. Current methodologies used for typing Leptospira have significant drawbacks. The development of an easy to perform yet high resolution method is needed for this organism.</p> <p>Methods</p> <p>In this study we have searched the available genomic sequence of <it>L. interrogans </it>serovar Copenhageni strain Fiocruz L1-130 for the presence of tandem repeats <abbrgrp><abbr bid="B1">1</abbr></abbrgrp>. These repeats were evaluated against reference strains for diversity. Six loci were selected to create a Multiple Locus Variable Number of Tandem Repeats (VNTR) Analysis (MLVA) to explore the genetic diversity within <it>L. interrogans </it>serovar Australis clinical isolates from Far North Queensland.</p> <p>Results</p> <p>The 39 reference strains used for the development of the method displayed 39 distinct patterns. Diversity Indexes for the loci varied between 0.80 and 0.93 and the number of repeat units at each locus varied between less than one to 52 repeats. When the MLVA was applied to serovar Australis isolates three large clusters were distinguishable, each comprising various hosts including <it>Rattus </it>species, human and canines.</p> <p>Conclusion</p> <p>The MLVA described in this report, was easy to perform, analyse and was reproducible. The loci selected had high diversity allowing discrimination between serovars and also between strains within a serovar. This method provides a starting point on which improvements to the method and comparisons to other techniques can be made.</p> |
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| Item Description: | 10.1186/1476-0711-4-10 1476-0711 |