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PLoS Neglected Tropical Diseases Issue Image | Vol. 4(5) May 2010
PLoS Neglected Tropical Diseases Issue Image | Vol. 4(5) May 2010
- Published: May 26, 2010
- https://doi.org/10.1371/image.pntd.v04.i05
Figures
Visceral leishmaniasis: A cellular model for phenotypic drug screening.
This image shows THP-1 human macrophage cells (cytoplasm stained red) infected with Leishmania donovani (yellow), the most deadly Leishmania species and causative agent of visceral leishmaniasis. In this disease cellular model, macrophages are incubated with metacyclic promastigotes, which are phagocytosed by the macrophage and differentiate into replicative amastigotes. There are also promastigotes and intermediate forms of the parasite in the macrophage. Parasite and host cell DNA is stained blue. This study is the first to employ a whole-cell-based model of visceral leishmaniasis to screen for drugs affecting the parasite's viability inside the human macrophage (see Siqueira-Neto et al., doi:10.1371/journal.pntd.0000675).
Image Credit: Jair L. Siqueira-Neto
Citation: (2010) PLoS Neglected Tropical Diseases Issue Image | Vol. 4(5) May 2010. PLoS Negl Trop Dis 4(5): ev04.i05. https://doi.org/10.1371/image.pntd.v04.i05
Published: May 26, 2010
Copyright: © 2010 Lucio H. Freitas-Junior. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This image shows THP-1 human macrophage cells (cytoplasm stained red) infected with Leishmania donovani (yellow), the most deadly Leishmania species and causative agent of visceral leishmaniasis. In this disease cellular model, macrophages are incubated with metacyclic promastigotes, which are phagocytosed by the macrophage and differentiate into replicative amastigotes. There are also promastigotes and intermediate forms of the parasite in the macrophage. Parasite and host cell DNA is stained blue. This study is the first to employ a whole-cell-based model of visceral leishmaniasis to screen for drugs affecting the parasite's viability inside the human macrophage (see Siqueira-Neto et al., doi:10.1371/journal.pntd.0000675).
Image Credit: Jair L. Siqueira-Neto