| Literature DB >> 33670713 |
Helena Fehling1, Hanno Niss1, Annika Bea1,2, Nadine Kottmayr1, Christine Brinker2, Stefan Hoenow1, Julie Sellau1, Tim-Wolf Gilberger1,3,4, Frederic Ting5, Dirk Landschulze5, Chris Meier5, Joachim Clos2, Hannelore Lotter1.
Abstract
An immunostimulatory glycolipid molecule from the intestinal protozoan parasite Entamoeba histolytica (Eh) and its synthetic analogs derived from its phosphatidylinositol-b-anchor (EhPIb) previously showed considerable immunotherapeutic effects against Leishmania major infection in vitro and in vivo. Here, we describe a high content screening assay, based on primary murine macrophages. Parasites detection is based on a 90 kDA heat shock protein-specific staining, enabling the detection of several Leishmania species. We validated the assay using L. major, L. braziliensis, L. donovani, and L. infantum as well as investigated the anti-leishmanial activity of six immunostimulatory EhPIb-compounds (Eh-1 to Eh-6). Macrophages infected with dermotropic species were more sensitive towards treatment with the compounds as their viability showed a stronger reduction compared to macrophages infected with viscerotropic species. Most compounds caused a significant reduction of the infection rates and the parasite burdens depending on the infecting species. Only compound Eh-6 was found to have activity against all Leishmania species. Considering the challenges in anti-leishmanial drug discovery, we developed a multi-species screening assay capable of utilizing non-recombinant parasite strains, and demonstrated its usefulness by screening macrophage-targeting EhPIb-compounds showing their potential for the treatment of cutaneous and visceral leishmaniasis.Entities:
Keywords: Leishmania; drug discovery; high content screening; immunotherapy; macrophages
Year: 2021 PMID: 33670713 DOI: 10.3390/microorganisms9020422
Source DB: PubMed Journal: Microorganisms ISSN: 2076-2607