Experimental Hamster Infection with a Strain of Leptospira borgpetersenii Ballum Isolated from a Reservoir Mouse in New Caledonia.

Am J Trop Med Hyg

Institut Pasteur International Network, Leptospirosis Research and Expertise Unit, Institut Pasteur de Nouvelle-Calédonie, Noumea, New Caledonia; Anatomic Pathology Laboratory, Territorial Hospital Centre of New Caledonia, Noumea, New Caledonia

Published: May 2015

AI Article Synopsis

  • - Leptospirosis is a disease caused by the bacteria Leptospira, and this study focuses on a strain (B3-13S) from a wild mouse in New Caledonia identified as part of the L. borgpetersenii Ballum serogroup.
  • - When hamsters were infected with the bacteria, they exhibited severe organ damage and tissue lesions similar to those seen with other strains of Leptospira.
  • - The findings suggest that the B3-13S strain can help develop models for studying both severe acute and chronic forms of leptospirosis, which is important as this serogroup is increasingly reported in human cases.

Article Abstract

Leptospirosis is a neglected zoonosis caused by pathogenic Leptospira. In this study, we characterized the virulence of isolate B3-13S obtained from a wild mouse (Mus musculus) captured in New Caledonia, subsequently identified as a bacterium belonging to the L. borgpetersenii serogroup Ballum. Hamsters were infected with an intraperitoneal injection of 2 × 10(8) bacteria, resulting in severe histopathological organ damages consistent with tissue lesions previously observed with other strains. Hamsters were also injected with 1 × 10(8) or 5 × 10(7) bacteria and animals that recovered showed renal carriage of leptospires in concentrations similar to the bacterial load quantified in mouse kidneys, with urinary shedding of bacteria up to 4 weeks postinfection. The serogroup Ballum is increasingly reported in human leptospirosis, and these results highlight the use of the B3-13S isolate for the development of models resulting in either severe acute or chronic forms of the infection, allowing for better characterization of its pathogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426589PMC
http://dx.doi.org/10.4269/ajtmh.14-0462DOI Listing

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