Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Microorganisms (Basel) 2021-02, Vol.9 (2)
Main Authors: 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
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page
container_issue 2
container_start_page
container_title Microorganisms (Basel)
container_volume 9
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
fullrecord <record><control><sourceid>pubmed</sourceid><recordid>TN_cdi_pubmed_primary_33670713</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>33670713</sourcerecordid><originalsourceid>FETCH-pubmed_primary_336707133</originalsourceid><addsrcrecordid>eNqFjsFqwkAQhvegqKivUOYFAolLEz1KsFiwUKj0KmMybqYks8vO5uDb10M997988PEd_olZbPKqzDZlXs3NWvUnf2xX2O1rMTNza8sqrwq7MOHIroPaSyJJsBfs78oK_gYf2EQfOnSUnTE6SiwODh18vl-z2g_Bj9IqoEMWTVCPCYX8-DDSwjdrQxF7OBFrN6AwwleghklXZnrDXmn9x6V5eTuc62MWxutA7SVEHjDeL8-L9t_gFxr6SFM</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>High Content Analysis of Macrophage-Targeting Eh PIb-Compounds against Cutaneous and Visceral Leishmania Species</title><source>PubMed Central database</source><source>ProQuest Publicly Available Content database</source><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</creator><creatorcontrib>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</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 2076-2607
ispartof Microorganisms (Basel), 2021-02, Vol.9 (2)
issn 2076-2607
language eng
recordid cdi_pubmed_primary_33670713
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T10%3A27%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=High%20Content%20Analysis%20of%20Macrophage-Targeting%20Eh%20PIb-Compounds%20against%20Cutaneous%20and%20Visceral%20Leishmania%20Species&rft.jtitle=Microorganisms%20(Basel)&rft.au=Fehling,%20Helena&rft.date=2021-02-18&rft.volume=9&rft.issue=2&rft.issn=2076-2607&rft_id=info:doi/&rft_dat=%3Cpubmed%3E33670713%3C/pubmed%3E%3Cgrp_id%3Ecdi_FETCH-pubmed_primary_336707133%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/33670713&rfr_iscdi=true