Evidence map›Paper›PMID 31208892›Full record

ArticleInternational journal for parasitology. Drugs and drug resistance2019

Mining for natural product antileishmanials in a fungal extract library.

A J Mbekeani, R S Jones, M Bassas Llorens, J Elliot, C Regnault, M P Barrett, J Steele, B Kebede, S K Wrigley, L Evans and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal for parasitology. Drugs and drug resistance, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

A J MbekeaniDepartment of Biosciences and Centre for Global Infectious Diseases, Durham University, Stockton Road, Durham, DH1 3LE, UK.
R S JonesDepartment of Biosciences and Centre for Global Infectious Diseases, Durham University, Stockton Road, Durham, DH1 3LE, UK.
M Bassas LlorensDepartment of Biosciences and Centre for Global Infectious Diseases, Durham University, Stockton Road, Durham, DH1 3LE, UK.
J ElliotDepartment of Biosciences and Centre for Global Infectious Diseases, Durham University, Stockton Road, Durham, DH1 3LE, UK.
C RegnaultGlasgow Polyomics, College of Medical, Veterinary & Life Sciences, University of Glasgow, Garscube Estate, Bearsden, Glasgow, G61 1QH, UK.
M P BarrettGlasgow Polyomics, College of Medical, Veterinary & Life Sciences, University of Glasgow, Garscube Estate, Bearsden, Glasgow, G61 1QH, UK; Wellcome Centre for Integrative Parasitology, Institute of Infection, Immunity and Inflammation, University of Glasgow, University Place, Glasgow, G12 8TA, UK.
J SteeleHypha Discovery Ltd., 957 Buckingham Avenue, Slough, SL1 4NL, UK.
B KebedeHypha Discovery Ltd., 957 Buckingham Avenue, Slough, SL1 4NL, UK.
S K WrigleyHypha Discovery Ltd., 957 Buckingham Avenue, Slough, SL1 4NL, UK.
L EvansHypha Discovery Ltd., 957 Buckingham Avenue, Slough, SL1 4NL, UK.
P W DennyDepartment of Biosciences and Centre for Global Infectious Diseases, Durham University, Stockton Road, Durham, DH1 3LE, UK. Electronic address: p.w.denny@durham.ac.uk.
Durham University · GBHypha Discovery (United Kingdom) · GBUniversity of Glasgow · GBWellcome Centre for Molecular Parasitology · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council MR/P027989/1
6 · The paper itself

Abstract

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.

Indexed as

Small Molecule LibrariesAnimalsAntiprotozoal AgentsBiological ProductsDrug DiscoveryDrug Evaluation, PreclinicalFungiHigh-Throughput Screening AssaysHumansLeishmaniaPublic-Private Sector PartnershipsSecondary MetabolismAntiprotozoal AgentsBiological ProductsSmall Molecule LibrariesCutaneous leishmaniasisFractionationLeishmania mexicanaMetabolomicsNatural productScreening

Identifiers

PMID31208892
PMCPMC6904819
OpenAlexW2949882856

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.