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High Content Analysis of Macrophage-Targeting Eh PIb-Compounds against Cutaneous and Visceral Leishmania Species
An immunostimulatory glycolipid molecule from the intestinal protozoan parasite ( ) and its synthetic analogs derived from its phosphatidylinositol-b-anchor ( PIb) previously showed considerable immunotherapeutic effects against infection in vitro and in vivo. Here, we describe a high content screen...
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Published in: | Microorganisms (Basel) 2021-02, Vol.9 (2) |
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creator | Fehling, Helena Niss, Hanno Bea, Annika Kottmayr, Nadine Brinker, Christine Hoenow, Stefan Sellau, Julie Gilberger, Tim-Wolf Ting, Frederic Landschulze, Dirk Meier, Chris Clos, Joachim Lotter, Hannelore |
description | An immunostimulatory glycolipid molecule from the intestinal protozoan parasite
(
) and its synthetic analogs derived from its phosphatidylinositol-b-anchor (
PIb) previously showed considerable immunotherapeutic effects against
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
species. We validated the assay using
,
,
and
as well as investigated the anti-leishmanial activity of six immunostimulatory
PIb-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
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
PIb-compounds showing their potential for the treatment of cutaneous and visceral leishmaniasis. |
format | article |
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(
) and its synthetic analogs derived from its phosphatidylinositol-b-anchor (
PIb) previously showed considerable immunotherapeutic effects against
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
species. We validated the assay using
,
,
and
as well as investigated the anti-leishmanial activity of six immunostimulatory
PIb-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
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
PIb-compounds showing their potential for the treatment of cutaneous and visceral leishmaniasis.</description><identifier>ISSN: 2076-2607</identifier><identifier>PMID: 33670713</identifier><language>eng</language><publisher>Switzerland</publisher><ispartof>Microorganisms (Basel), 2021-02, Vol.9 (2)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-1112-7608 ; 0000-0003-4377-8173</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33670713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fehling, Helena</creatorcontrib><creatorcontrib>Niss, Hanno</creatorcontrib><creatorcontrib>Bea, Annika</creatorcontrib><creatorcontrib>Kottmayr, Nadine</creatorcontrib><creatorcontrib>Brinker, Christine</creatorcontrib><creatorcontrib>Hoenow, Stefan</creatorcontrib><creatorcontrib>Sellau, Julie</creatorcontrib><creatorcontrib>Gilberger, Tim-Wolf</creatorcontrib><creatorcontrib>Ting, Frederic</creatorcontrib><creatorcontrib>Landschulze, Dirk</creatorcontrib><creatorcontrib>Meier, Chris</creatorcontrib><creatorcontrib>Clos, Joachim</creatorcontrib><creatorcontrib>Lotter, Hannelore</creatorcontrib><title>High Content Analysis of Macrophage-Targeting Eh PIb-Compounds against Cutaneous and Visceral Leishmania Species</title><title>Microorganisms (Basel)</title><addtitle>Microorganisms</addtitle><description>An immunostimulatory glycolipid molecule from the intestinal protozoan parasite
(
) and its synthetic analogs derived from its phosphatidylinositol-b-anchor (
PIb) previously showed considerable immunotherapeutic effects against
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
species. We validated the assay using
,
,
and
as well as investigated the anti-leishmanial activity of six immunostimulatory
PIb-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
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
PIb-compounds showing their potential for the treatment of cutaneous and visceral leishmaniasis.</description><issn>2076-2607</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFjsFqwkAQhvegqKivUOYFAolLEz1KsFiwUKj0KmMybqYks8vO5uDb10M997988PEd_olZbPKqzDZlXs3NWvUnf2xX2O1rMTNza8sqrwq7MOHIroPaSyJJsBfs78oK_gYf2EQfOnSUnTE6SiwODh18vl-z2g_Bj9IqoEMWTVCPCYX8-DDSwjdrQxF7OBFrN6AwwleghklXZnrDXmn9x6V5eTuc62MWxutA7SVEHjDeL8-L9t_gFxr6SFM</recordid><startdate>20210218</startdate><enddate>20210218</enddate><creator>Fehling, Helena</creator><creator>Niss, Hanno</creator><creator>Bea, Annika</creator><creator>Kottmayr, Nadine</creator><creator>Brinker, Christine</creator><creator>Hoenow, Stefan</creator><creator>Sellau, Julie</creator><creator>Gilberger, Tim-Wolf</creator><creator>Ting, Frederic</creator><creator>Landschulze, Dirk</creator><creator>Meier, Chris</creator><creator>Clos, Joachim</creator><creator>Lotter, Hannelore</creator><scope>NPM</scope><orcidid>https://orcid.org/0000-0003-1112-7608</orcidid><orcidid>https://orcid.org/0000-0003-4377-8173</orcidid></search><sort><creationdate>20210218</creationdate><title>High Content Analysis of Macrophage-Targeting Eh PIb-Compounds against Cutaneous and Visceral Leishmania Species</title><author>Fehling, Helena ; Niss, Hanno ; Bea, Annika ; Kottmayr, Nadine ; Brinker, Christine ; Hoenow, Stefan ; Sellau, Julie ; Gilberger, Tim-Wolf ; Ting, Frederic ; Landschulze, Dirk ; Meier, Chris ; Clos, Joachim ; Lotter, Hannelore</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_336707133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fehling, Helena</creatorcontrib><creatorcontrib>Niss, Hanno</creatorcontrib><creatorcontrib>Bea, Annika</creatorcontrib><creatorcontrib>Kottmayr, Nadine</creatorcontrib><creatorcontrib>Brinker, Christine</creatorcontrib><creatorcontrib>Hoenow, Stefan</creatorcontrib><creatorcontrib>Sellau, Julie</creatorcontrib><creatorcontrib>Gilberger, Tim-Wolf</creatorcontrib><creatorcontrib>Ting, Frederic</creatorcontrib><creatorcontrib>Landschulze, Dirk</creatorcontrib><creatorcontrib>Meier, Chris</creatorcontrib><creatorcontrib>Clos, Joachim</creatorcontrib><creatorcontrib>Lotter, Hannelore</creatorcontrib><collection>PubMed</collection><jtitle>Microorganisms (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fehling, Helena</au><au>Niss, Hanno</au><au>Bea, Annika</au><au>Kottmayr, Nadine</au><au>Brinker, Christine</au><au>Hoenow, Stefan</au><au>Sellau, Julie</au><au>Gilberger, Tim-Wolf</au><au>Ting, Frederic</au><au>Landschulze, Dirk</au><au>Meier, Chris</au><au>Clos, Joachim</au><au>Lotter, Hannelore</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High Content Analysis of Macrophage-Targeting Eh PIb-Compounds against Cutaneous and Visceral Leishmania Species</atitle><jtitle>Microorganisms (Basel)</jtitle><addtitle>Microorganisms</addtitle><date>2021-02-18</date><risdate>2021</risdate><volume>9</volume><issue>2</issue><issn>2076-2607</issn><abstract>An immunostimulatory glycolipid molecule from the intestinal protozoan parasite
(
) and its synthetic analogs derived from its phosphatidylinositol-b-anchor (
PIb) previously showed considerable immunotherapeutic effects against
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
species. We validated the assay using
,
,
and
as well as investigated the anti-leishmanial activity of six immunostimulatory
PIb-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
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
PIb-compounds showing their potential for the treatment of cutaneous and visceral leishmaniasis.</abstract><cop>Switzerland</cop><pmid>33670713</pmid><orcidid>https://orcid.org/0000-0003-1112-7608</orcidid><orcidid>https://orcid.org/0000-0003-4377-8173</orcidid></addata></record> |
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language | eng |
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source | PubMed Central database; ProQuest Publicly Available Content database |
title | High Content Analysis of Macrophage-Targeting Eh PIb-Compounds against Cutaneous and Visceral Leishmania Species |
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