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Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond

Authors :
Christopher D. Huston
Amornrat Naranuntarat Jensen
Louis Maes
Jordi Mestres
Nao Aki Watanabe
Michael Adsetts Edberg Hansen
Roberto Adelfio
Simon Townson
Didier Leroy
Kate Weatherby
Thomas Spangenberg
Manuela Carrasquilla
Kailash P. Patra
Robert E. Sinden
José Brea
Abhai K. Tripathi
W. Armand Guiguemde
Alan Y. Du
Melanie Wree
Katherine T. Andrews
Kirsten K. Hanson
Tyler B. Hughes
Sundari Suresh
Adele M. Lehane
Sangeeta N. Bhatia
Edward J. Wojcik
Andrew Hemphill
Francielly Morais Rodrigues da Costa
Worathad Chindaudomsate
Joseph M. Vinetz
Ben Gold
Sunyoung Kim
Edgar Vigil
Nuha R. Mansour
Mohamed Abdo Rizk
Patrick Valere Tsouh Fokou
Audrey Burton
Laran T. Jensen
David A. Fidock
Aishah Alsibaee
Filipe Silva Villela
Yesmalie Alemán Resto
Rajarshi Guha
Conor R. Caffrey
José A. Fernández Robledo
Thomas J. Ketas
Luke Mercer
Rob Hooft van Huijsduijnen
Maria Jose Lafuente
Wesley C. Van Voorhis
Lauve R. Y. Tchokouaha
Dee A. Carter
Anjo Theron
Benoît Laleu
Kiaran Kirk
Maurice A. Itoe
Robert P. St.Onge
Celia Quevedo
Andrea Ruecker
Paul Henri Amvam Zollo
Francisco-Javier Gamo
Nathan Lee
Alvine Ngoutane Mfopa
Paul Horrocks
Ikuo Igarashi
Nil Gural
Todd R. Golub
Gordana Panic
Jeremy N. Burrows
Phat Voong Vinh
Annette Kaiser
Fabrice Fekam Boyom
Pietro Alano
Anupam Pradhan
Sandra Duffy
Raj N. Misra
Vidya Prasanna Kumar
Aintzane Alday
Timothy N. C. Wells
María Isabel Loza
Sébastien Kicka
William J. Sullivan
Gregory M. Goldgof
Yo Suzuki
Yolanda Corbett
Sally-Ann Poulsen
Vida Ahyong
George Papadatos
Sujeevi Nawaratna
Rafaela Salgado Ferreira
Takaaki Horii
Imran Ullah
Nathalie Narraidoo
Natalie G. Robinett
Simon V. Avery
Grazia Camarda
Iset Medina Vera
Michael T. Ferdig
Fengwu Li
David Plouffe
Joseph L. DeRisi
Jasmeet Samra
Andreas Spitzmüller
Liqiong Liu
Christopher A. Rice
Thierry Soldati
Serge Maximilian Stamm
Suzanne Gokool
Beatrice L. Colon
Shimaa Abd El-Salam El-Sayed
Mark Baker
Kenneth O. Udenze
Na Le Dang
Katrin Ingram-Sieber
Dennis A. Smith
Rays H. Y. Jiang
Marian P. Brennan
Ani Galstian
Paul Willis
Dennis E. Kyle
Ainhoa Alzualde
Sarah Prats
Sheena McGowan
Vicky M. Avery
Jennifer Keiser
John P. Moore
Dalu Mancama
Gregory J. Crowther
Noemi Cowan
Maria B. Cassera
Valentin Trofimov
David Thomas
David J. Sullivan
Diana Ortiz
Nada Abla
S. Joshua Swamidass
Benjamin Blasco
Hoan Vu
Francesco Silvestrini
Anthony J. Chubb
Pamela M. White
Scott M. Landfear
Isabelle Florent
John H. Adams
Ronald J. Quinn
Andrew F. Wilks
Sandra March
Leonardo Lucantoni
Stephen Baker
Tana Bowling
Joachim Müller
Arantza Muriana
Lauren E. Boucher
Ajit Jadhav
Sukjun Lee
Elizabeth A. Winzeler
Choukri Ben Mamoun
Ulrich Schlecht
Daisy D. Colón-López
Marjorie Schmitt
Myles H. Akabas
Isabelle S Lucet
Stephen N. Hewitt
Naoaki Yokoyama
Carl Nathan
Bakela Nare
Cindy Vallières
Lotfi Bounaadja
Kayode K. Ojo
Wesley Wu
Ken Chih-Chien Cheng
Kathryn F. Tonissen
Michael J. Delves
Brian M. Suzuki
Aristea Lubar
Quentin D. Bickle
Stephan Meister
Silvia Parapini
Manuel Llinás
Ngoc Minh Pham
Seunghyun Moon
R. Kiplin Guy
Donatella Taramelli
Lawrence Ayong
Sarah D'Alessandro
Jürgen Bosch
David Little
Istituto Superiore di Sanita [Rome]
Zentrum für Infektiologie [Heidelberg, Germany]
Universität Heidelberg [Heidelberg]-Heidelberg University Hospital [Heidelberg]
University of Nottingham, UK (UON)
Eskitis Institute for Drug Discovery
Griffith University [Brisbane]
Institut Pasteur Korea - Institut Pasteur de Corée
Réseau International des Instituts Pasteur (RIIP)
Oxford University Clinical Research Unit [Ho Chi Minh City] (OUCRU)
Laboratoire de génétique moléculaire et cellulaire
Institut National de la Recherche Agronomique (INRA)
Agence Française de Sécurité Sanitaire des Aliments (AFSSA)
Faculté des Sciences - Yaoundé I
Université de Yaoundé I
Skaggs School of Pharmacy and Pharmaceutical Sciences [San Diego]
University of California [San Diego] (UC San Diego)
University of California-University of California
Dipartimento di Scienze Farmacologiche e Biomolecolari (DiSFeB)
Università degli Studi di Milano [Milano] (UNIMI)
Imperial College London
Eck Institute for Global Health
University of Notre Dame [Indiana] (UND)
Columbia University Medical Center (CUMC)
Columbia University [New York]
Interdisciplinary Nanoscience Centre (iNANO)
Institute of Parasitology
University of Bern
MS Project - Initiation (MSPRI)
Apollo SSC Genève
Keele University
Swiss Tropical and Public Health Institute [Basel]
University of Regina
School of Engineering and Science
University of the West of Scotland (UWS)
Research School of Biology [Canberra, Australie]
Australian National University (ANU)
University of Pennsylvania [Philadelphia]
Laboratory of Microbiology, Parasitology and Hygiene [Antwerpen] (LMPH)
University of Antwerp (UA)
Department of Biochemistry and Molecular Biology
Mayo Clinic
Institute for Wine Biotechnology [University of Stellenbosch - Afrique du Sud]
Stellenbosch University
Oregon Health and Science University [Portland] (OHSU)
Biozentrum
Swiss Institute of Bioinformatics [Lausanne] (SIB)
Université de Lausanne (UNIL)-Université de Lausanne (UNIL)
Laboratoire d'innovation moléculaire et applications (LIMA)
Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Advanced Materials Research Laboratories, Department of Chemistry and Center for Optical ((COMSET)
Clemson University
Université de Genève (UNIGE)
Department of Molecular, Cell, and Developmental Biology, University of California, Santa Cruz
University of California [Santa Cruz] (UCSC)
Department of sanità pubblica-microbiologia-virologia
University of California
Département Réseaux, Information, Multimédia (RIM-ENSMSE)
École des Mines de Saint-Étienne (Mines Saint-Étienne MSE)
Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-Centre G2I
UC San Diego School of Medicine
Medicines for Malaria Venture [Geneva] (MMV)
Princeton University
Institute for Medical Engineering and Science
Harvard University--MIT Division of Health Sciences and Technology
Bhatia, Sangeeta N
Bill & Melinda Gates Foundation
Biochemistry
Center for Drug Discovery
Kicka, Sébastien
Soldati, Thierry
Trofimov, Valentin
Abla, Nada
Source :
PLoS Pathogens, Vol 12, Iss 7, p e1005763 (2016), Van Voorhis, Wesley C; Adams, John H; Adelfio, Roberto; Ahyong, Vida; Akabas, Myles H; Alano, Pietro; Alday, Aintzane; Alemán Resto, Yesmalie; Alsibaee, Aishah; Alzualde, Ainhoa; Andrews, Katherine T; Avery, Simon V; Avery, Vicky M; Ayong, Lawrence; Baker, Mark; Baker, Stephen; Ben Mamoun, Choukri; Bhatia, Sangeeta; Bickle, Quentin; Bounaadja, Lotfi; ... (2016). Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond. PLoS pathogens, 12(7), e1005763. Public Library of Science 10.1371/journal.ppat.1005763 , PLoS Pathogens, PLoS Pathogens, Public Library of Science, 2016, 12 (7), pp.e1005763. ⟨10.1371/journal.ppat.1005763⟩, PLoS pathogens, Recercat. Dipósit de la Recerca de Catalunya, instname, PLOS, PLOS PATHOGENS, e1005763, PLOS Pathogens, PLOS Pathogens, Vol. 12, No 7 (2016) P. e1005763
Publication Year :
2016
Publisher :
Public Library of Science (PLoS), 2016.

Abstract

A major cause of the paucity of new starting points for drug discovery is the lack of interaction between academia and industry. Much of the global resource in biology is present in universities, whereas the focus of medicinal chemistry is still largely within industry. Open source drug discovery, with sharing of information, is clearly a first step towards overcoming this gap. But the interface could especially be bridged through a scale-up of open sharing of physical compounds, which would accelerate the finding of new starting points for drug discovery. The Medicines for Malaria Venture Malaria Box is a collection of over 400 compounds representing families of structures identified in phenotypic screens of pharmaceutical and academic libraries against the Plasmodium falciparum malaria parasite. The set has now been distributed to almost 200 research groups globally in the last two years, with the only stipulation that information from the screens is deposited in the public domain. This paper reports for the first time on 236 screens that have been carried out against the Malaria Box and compares these results with 55 assays that were previously published, in a format that allows a meta-analysis of the combined dataset. The combined biochemical and cellular assays presented here suggest mechanisms of action for 135 (34%) of the compounds active in killing multiple life-cycle stages of the malaria parasite, including asexual blood, liver, gametocyte, gametes and insect ookinete stages. In addition, many compounds demonstrated activity against other pathogens, showing hits in assays with 16 protozoa, 7 helminths, 9 bacterial and mycobacterial species, the dengue fever mosquito vector, and the NCI60 human cancer cell line panel of 60 human tumor cell lines. Toxicological, pharmacokinetic and metabolic properties were collected on all the compounds, assisting in the selection of the most promising candidates for murine proof-of-concept experiments and medicinal chemistry programs. The data for all of these assays are presented and analyzed to show how outstanding leads for many indications can be selected. These results reveal the immense potential for translating the dispersed expertise in biological assays involving human pathogens into drug discovery starting points, by providing open access to new families of molecules, and emphasize how a small additional investment made to help acquire and distribute compounds, and sharing the data, can catalyze drug discovery for dozens of different indications. Another lesson is that when multiple screens from different groups are run on the same library, results can be integrated quickly to select the most valuable starting points for subsequent medicinal chemistry efforts.<br />Author Summary Malaria leads to the loss of over 440,000 lives annually; accelerating research to discover new candidate drugs is a priority. Medicines for Malaria Venture (MMV) has distilled over 25,000 compounds that kill malaria parasites in vitro into a group of 400 representative compounds, called the "Malaria Box". These Malaria Box sets were distributed free-of-charge to research laboratories in 30 different countries that work on a wide variety of pathogens. Fifty-five groups compiled >290 assay results for this paper describing the many activities of the Malaria Box compounds. The collective results suggest a potential mechanism of action for over 130 compounds against malaria and illuminate the most promising compounds for further malaria drug development research. Excitingly some of these compounds also showed outstanding activity against other disease agents including fungi, bacteria, other single-cellular parasites, worms, and even human cancer cells. The results have ignited over 30 drug development programs for a variety of diseases. This open access effort was so successful that MMV has begun to distribute another set of compounds with initial activity against a wider range of infectious agents that are of public health concern, called the Pathogen Box, available now to scientific labs all over the world (www.PathogenBox.org).

Details

Language :
English
ISSN :
15537374 and 15537366
Volume :
12
Issue :
7
Database :
OpenAIRE
Journal :
PLoS Pathogens
Accession number :
edsair.doi.dedup.....ed1aa7e406ea2a739a6d5c26550fa093