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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-6904819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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