Document Type
Article
Publication Date
11-2007
Abstract
New therapeutic alternatives against leishmaniasis remain a priority. The activity of azithromycin against Leishmania (Leishmania) major has been previously demonstrated. Different responses among species of Leishmania make species-specific drug screening necessary. The activity of azithromycin against Leishmania (Viannia) braziliensis and Leishmania (Leishmania) amazonensis was evaluated in golden hamsters infected through footpad injections of metacyclic promastigotes, and compared with untreated controls and animals treated with meglumine antimoniate. Footpad thickness, lesion cultures and dissemination sites were analyzed. Treatment of golden hamsters with oral azithromycin at 450mg/kg had no activity against infections with Leishmania (Leishmania) amazonensis. For infections due to Leishmania (Viannia) braziliensis, azithromycin demonstrated significant activity relative to untreated controls, but inferior to meglumine antimoniate, for controlling lesion size. Neither drug was able to totally eliminate parasites from the lesions. It was concluded that azithromycin has activity against Leishmania (Viannia) braziliensis but not against Leishmania (Leishmania) amazonensis in this model.
Recommended Citation
Sinagra, Angel; Luna, Concepción; Abraham, David; Iannella, Maria del Carmen; Riarte, Adelina; and Krolewiecki, Alejandro J., "The activity of azithromycin against Leishmania (Viannia) braziliensis and Leishmania (Leishmania) amazonensis in the golden hamster model." (2007). Department of Microbiology and Immunology Faculty Papers. Paper 141.
https://jdc.jefferson.edu/mifp/141
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License
PubMed ID
18200413
Language
English
Comments
This article is the authors’ final published version in Revista da Sociedade Brasileira de Medicina Tropical, Volume 40, Issue 6, November-December 2007, Pages 627-630.
The published version is available at https://doi.org/10.1590/s0037-86822007000600005. Copyright © Sinagra et al.