Abstract

Background and Aim. Leptospira, the causal agent of leptospirosis, has been isolated from the environment, patients, and wide spectrum of animals in Russia. However, the genetic diversity of Leptospira in natural and anthropurgic foci was not clearly defined. Methods. The recent MLST scheme was used for the analysis of seven pathogenic species. 454 pyrosequencing technology was the base of the whole genome sequencing (WGS). Results. The most wide spread and prevalent Leptospira species in Russia were L. interrogans, L. kirschneri, and L. borgpetersenii. Five STs, common for Russian strains: 37, 17, 199, 110, and 146, were identified as having a longtime and ubiquitous distribution in various geographic areas. Unexpected properties were revealed for the environmental Leptospira strain Bairam-Ali. WGS of this strain genome suggested that it combined the features of the pathogenic and nonpathogenic strains and may be a reservoir of the natural resistance genes. Results of the comparative analysis of rrs and rpoB genes and MLST loci for different Leptospira species strains and phenotypic and serological properties of the strain Bairam-Ali suggested that it represented separate Leptospira species. Conclusions. Thus, the natural and anthropurgic foci supported ubiquitous Leptospira species and the pool of genes important for bacterial adaptivity to various conditions.

Highlights

  • Leptospira is a genus of bacteria that is encountered in all geographical areas, except arctic and arid regions

  • Phylogenetic analysis with 16S rRNA gene sequences showed that L. alstonii and L. kmetyi clustered with the pathogenic Leptospira species [2, 3]

  • The analysis of rpoB gene sequences demonstrated that 29 reference strains belonged to seven pathogenic species, one nonpathogenic species (L. yanagawae), and one intermediate species (L. inadai)

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Summary

Introduction

Leptospira is a genus of bacteria that is encountered in all geographical areas, except arctic and arid regions. Phylogenetic analysis of Leptospira species was performed based on the rrs gene fragment, rpoB gene fragment, and seven concatenated sequences of MLST loci.

Results
Conclusion
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