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Mining for natural product antileishmanials in a fungal extract library

Leishmaniasis is a Neglected Tropical Disease caused by the insect-vector borne protozoan parasite, Leishmania species. Infection affects millions of the World's poorest, however vaccines are absent and drug therapy limited. Recently, public-private partnerships have developed to identify new m...

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Autores principales: Mbekeani, A.J., Jones, R.S., Bassas Llorens, M., Elliot, J., Regnault, C., Barrett, M.P., Steele, J., Kebede, B., Wrigley, S.K., Evans, L., Denny, P.W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904819/
https://www.ncbi.nlm.nih.gov/pubmed/31208892
http://dx.doi.org/10.1016/j.ijpddr.2019.05.003
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author Mbekeani, A.J.
Jones, R.S.
Bassas Llorens, M.
Elliot, J.
Regnault, C.
Barrett, M.P.
Steele, J.
Kebede, B.
Wrigley, S.K.
Evans, L.
Denny, P.W.
author_facet Mbekeani, A.J.
Jones, R.S.
Bassas Llorens, M.
Elliot, J.
Regnault, C.
Barrett, M.P.
Steele, J.
Kebede, B.
Wrigley, S.K.
Evans, L.
Denny, P.W.
author_sort Mbekeani, A.J.
collection PubMed
description Leishmaniasis is a Neglected Tropical Disease caused by the insect-vector borne protozoan parasite, Leishmania species. Infection affects millions of the World's poorest, however vaccines are absent and drug therapy limited. Recently, public-private partnerships have developed to identify new modes of controlling leishmaniasis. Most of these collaborative efforts have relied upon the small molecule synthetic compound libraries held by industry, but the number of New Chemical Entities (NCE) identified and entering development as antileishmanials has been very low. In light of this, here we describe a public-private effort to identify natural products with activity against Leishmania mexicana, a causative agent of cutaneous leishmanaisis (CL). Utilising Hypha Discovery's fungal extract library which is rich in small molecule (<500 molecular weight) secondary metabolites, we undertook an iterative phenotypic screening and fractionation approach to identify potent and selective antileishmanial hits. This led to the identification of a novel oxidised bisabolane sesquiterpene which demonstrated activity in an infected cell model and was shown to disrupt multiple processes using a metabolomic approach. In addition, and importantly, this study also sets a precedent for new approaches for CL drug discovery.
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spelling pubmed-69048192019-12-20 Mining for natural product antileishmanials in a fungal extract library Mbekeani, A.J. Jones, R.S. Bassas Llorens, M. Elliot, J. Regnault, C. Barrett, M.P. Steele, J. Kebede, B. Wrigley, S.K. Evans, L. Denny, P.W. Int J Parasitol Drugs Drug Resist Includes articles from the special issue “Novel therapies for cutaneous leishmaniasis”, pp. 106 - 179 Leishmaniasis is a Neglected Tropical Disease caused by the insect-vector borne protozoan parasite, Leishmania species. Infection affects millions of the World's poorest, however vaccines are absent and drug therapy limited. Recently, public-private partnerships have developed to identify new modes of controlling leishmaniasis. Most of these collaborative efforts have relied upon the small molecule synthetic compound libraries held by industry, but the number of New Chemical Entities (NCE) identified and entering development as antileishmanials has been very low. In light of this, here we describe a public-private effort to identify natural products with activity against Leishmania mexicana, a causative agent of cutaneous leishmanaisis (CL). Utilising Hypha Discovery's fungal extract library which is rich in small molecule (<500 molecular weight) secondary metabolites, we undertook an iterative phenotypic screening and fractionation approach to identify potent and selective antileishmanial hits. This led to the identification of a novel oxidised bisabolane sesquiterpene which demonstrated activity in an infected cell model and was shown to disrupt multiple processes using a metabolomic approach. In addition, and importantly, this study also sets a precedent for new approaches for CL drug discovery. Elsevier 2019-06-11 /pmc/articles/PMC6904819/ /pubmed/31208892 http://dx.doi.org/10.1016/j.ijpddr.2019.05.003 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Includes articles from the special issue “Novel therapies for cutaneous leishmaniasis”, pp. 106 - 179
Mbekeani, A.J.
Jones, R.S.
Bassas Llorens, M.
Elliot, J.
Regnault, C.
Barrett, M.P.
Steele, J.
Kebede, B.
Wrigley, S.K.
Evans, L.
Denny, P.W.
Mining for natural product antileishmanials in a fungal extract library
title Mining for natural product antileishmanials in a fungal extract library
title_full Mining for natural product antileishmanials in a fungal extract library
title_fullStr Mining for natural product antileishmanials in a fungal extract library
title_full_unstemmed Mining for natural product antileishmanials in a fungal extract library
title_short Mining for natural product antileishmanials in a fungal extract library
title_sort mining for natural product antileishmanials in a fungal extract library
topic Includes articles from the special issue “Novel therapies for cutaneous leishmaniasis”, pp. 106 - 179
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904819/
https://www.ncbi.nlm.nih.gov/pubmed/31208892
http://dx.doi.org/10.1016/j.ijpddr.2019.05.003
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