Experimental Infection of Rattus norvegicus by the Group II Intermediate Pathogen, Leptospira licerasiae

Carla Fernandez Division of Infectious Diseases, Department of Medicine, University of California, San Diego, San Diego, California;

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Aristea A. Lubar Division of Infectious Diseases, Department of Medicine, University of California, San Diego, San Diego, California;

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Joseph M. Vinetz Division of Infectious Diseases, Department of Medicine, University of California, San Diego, San Diego, California;
Laboratorio de Investigación y Desarollo, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Lima, Peru;
Instituto de Medicina Tropical “Alexander von Humboldt”, Universidad Peruana Cayetano Heredia, Lima, Peru

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Michael A. Matthias Division of Infectious Diseases, Department of Medicine, University of California, San Diego, San Diego, California;

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Leptospira licerasiae serovar Varillal, a group II intermediate pathogen species/serovar discovered in the Peruvian Amazon city of Iquitos, is commonly recognized in this region by sera from humans (at least 40% seroprevalence) without a known clinical history of leptospirosis. This high frequency of human seroreactivity remains unexplained. To test the hypothesis that the oral route of infection might explain the high rate of human seroreactivity against L. licerasiae, an experimental infection model using Rattus norvegicus was developed, given that rats were one of the original reservoir hosts identified as being colonized by this leptospire. Sprague–Dawley rats were experimentally exposed via mucosa, direct gastric gavage, or parenteral inoculation with nine different isolates of L. licerasiae originally isolated from Peruvian humans, peridomiciliary rodents, and wildlife. As shown by quantitative polymerase chain reaction of kidney tissue, Leptospira infection via these routes of infection was equally successful. Importantly, the data show that L. licerasiae infects R. norvegicus via the oral route, leading to renal colonization. Not only do these findings confirm the infectiousness of group II Leptospira, but also they underscore the potential importance of oral as well as mucosal and transcutaneous routes of Leptospira infection.

Author Notes

Address Correspondence to Joseph M. Vinetz or Michael A. Matthias, Division of Infectious Diseases, Department of Medicine, University of California, 9500 Gilman Drive, MC 0760, La Jolla, San Diego, CA 92093. E-mails: joseph.vinetz@upch.pe or mmatthias@ucsd.edu

Authors’ addresses: Carla Fernandez, Aristea A. Lubar, and Michael A. Matthias, Division of Infectious Diseases, Department of Medicine, University of California, San Diego, San Diego, CA, E-mails: cfernandezcuadros@ucsd.edu, alubar@ucsd.edu, and mmatthias@ucsd.edu. Joseph M. Vinetz, Center for Tropical Diseases, University of California San Diego School of Medicine, San Diego, CA, E-mail: joseph.vinetz@upch.pe.

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