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Evaluation of an FDA approved library against laboratory models of human intestinal nematode infections

BACKGROUND: Treatment options for infections with soil-transmitted helminths (STH) - Ascaris lumbricoides, Trichuris trichiura and the two hookworm species, Ancylostoma duodenale and Necator americanus - are limited despite their considerable global health burden. The aim of the present study was to...

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Autores principales: Keiser, Jennifer, Panic, Gordana, Adelfio, Roberto, Cowan, Noemi, Vargas, Mireille, Scandale, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929775/
https://www.ncbi.nlm.nih.gov/pubmed/27363703
http://dx.doi.org/10.1186/s13071-016-1616-0
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author Keiser, Jennifer
Panic, Gordana
Adelfio, Roberto
Cowan, Noemi
Vargas, Mireille
Scandale, Ivan
author_facet Keiser, Jennifer
Panic, Gordana
Adelfio, Roberto
Cowan, Noemi
Vargas, Mireille
Scandale, Ivan
author_sort Keiser, Jennifer
collection PubMed
description BACKGROUND: Treatment options for infections with soil-transmitted helminths (STH) - Ascaris lumbricoides, Trichuris trichiura and the two hookworm species, Ancylostoma duodenale and Necator americanus - are limited despite their considerable global health burden. The aim of the present study was to test the activity of an openly available FDA library against laboratory models of human intestinal nematode infections. METHODS: All 1,600 drugs were first screened against Ancylostoma ceylanicum third-stage larvae (L3). Active compounds were scrutinized and toxic compounds, drugs indicated solely for topical use, and already well-studied anthelmintics were excluded. The remaining hit compounds were tested in parallel against Trichuris muris first-stage larvae (L1), Heligmosomoides polygyrus third-stage larvae (L3), and adult stages of the three species in vitro. In vivo studies were performed in the H. polygyrus and T. muris mice models. RESULTS: Fifty-four of the 1,600 compounds tested revealed an activity of > 60 % against A. ceylanicum L3 (hit rate of 3.4 %), following incubation at 200 μM for 72 h. Twelve compounds progressed into further screens. Adult A. ceylanicum were the least affected (1/12 compounds active at 50 μM), while eight of the 12 test compounds revealed activity against T. muris L1 (100 μM) and adults (50 μM), and H. polygyrus L3 (200 μM). Trichlorfon was the only compound active against all stages of A. ceylanicum, H. polygyrus and T. muris. In addition, trichlorfon achieved high worm burden reductions of 80.1 and 98.9 %, following a single oral dose of 200 mg/kg in the T. muris and H. polygyrus mouse model, respectively. CONCLUSION: Drug screening on the larval stages of intestinal parasitic nematodes is feasible using small libraries and important given the empty drug discovery and development pipeline for STH infections. Differences and commonalities in drug activities across the different STH species and stages were confirmed. Hits identified might serve as a starting point for drug discovery for STH. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1616-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-49297752016-07-02 Evaluation of an FDA approved library against laboratory models of human intestinal nematode infections Keiser, Jennifer Panic, Gordana Adelfio, Roberto Cowan, Noemi Vargas, Mireille Scandale, Ivan Parasit Vectors Research BACKGROUND: Treatment options for infections with soil-transmitted helminths (STH) - Ascaris lumbricoides, Trichuris trichiura and the two hookworm species, Ancylostoma duodenale and Necator americanus - are limited despite their considerable global health burden. The aim of the present study was to test the activity of an openly available FDA library against laboratory models of human intestinal nematode infections. METHODS: All 1,600 drugs were first screened against Ancylostoma ceylanicum third-stage larvae (L3). Active compounds were scrutinized and toxic compounds, drugs indicated solely for topical use, and already well-studied anthelmintics were excluded. The remaining hit compounds were tested in parallel against Trichuris muris first-stage larvae (L1), Heligmosomoides polygyrus third-stage larvae (L3), and adult stages of the three species in vitro. In vivo studies were performed in the H. polygyrus and T. muris mice models. RESULTS: Fifty-four of the 1,600 compounds tested revealed an activity of > 60 % against A. ceylanicum L3 (hit rate of 3.4 %), following incubation at 200 μM for 72 h. Twelve compounds progressed into further screens. Adult A. ceylanicum were the least affected (1/12 compounds active at 50 μM), while eight of the 12 test compounds revealed activity against T. muris L1 (100 μM) and adults (50 μM), and H. polygyrus L3 (200 μM). Trichlorfon was the only compound active against all stages of A. ceylanicum, H. polygyrus and T. muris. In addition, trichlorfon achieved high worm burden reductions of 80.1 and 98.9 %, following a single oral dose of 200 mg/kg in the T. muris and H. polygyrus mouse model, respectively. CONCLUSION: Drug screening on the larval stages of intestinal parasitic nematodes is feasible using small libraries and important given the empty drug discovery and development pipeline for STH infections. Differences and commonalities in drug activities across the different STH species and stages were confirmed. Hits identified might serve as a starting point for drug discovery for STH. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1616-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-01 /pmc/articles/PMC4929775/ /pubmed/27363703 http://dx.doi.org/10.1186/s13071-016-1616-0 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Keiser, Jennifer
Panic, Gordana
Adelfio, Roberto
Cowan, Noemi
Vargas, Mireille
Scandale, Ivan
Evaluation of an FDA approved library against laboratory models of human intestinal nematode infections
title Evaluation of an FDA approved library against laboratory models of human intestinal nematode infections
title_full Evaluation of an FDA approved library against laboratory models of human intestinal nematode infections
title_fullStr Evaluation of an FDA approved library against laboratory models of human intestinal nematode infections
title_full_unstemmed Evaluation of an FDA approved library against laboratory models of human intestinal nematode infections
title_short Evaluation of an FDA approved library against laboratory models of human intestinal nematode infections
title_sort evaluation of an fda approved library against laboratory models of human intestinal nematode infections
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929775/
https://www.ncbi.nlm.nih.gov/pubmed/27363703
http://dx.doi.org/10.1186/s13071-016-1616-0
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