Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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High throughput screening for chemical inducers of stumpy formation in Trypanosoma brucei


ABSTRACT: During the bloodstream stage of the Trypanosoma brucei lifecycle, the parasite exists as the proliferative slender-form or the non-proliferative, transmissible, stumpy-form. The transition from the slender to stumpy-form is stimulated by a density-dependent mechanism and is important in infection dynamics, ordered antigenic variation and disease transmissibility. Here, we use a monomorphic reporter cell line in a whole-cell fluorescence-based assay to screen over 6000 small molecules from a kinase-focussed compound library for their ability to induce stumpy-like formation in a high-throughput screening programme. This identified one compound able to induce modest, yet specific, changes in gene expression indicative of a partial differentiation to stumpy forms. This not only provides a potential tool for the further understanding of stumpy formation, but also demonstrates the use of high throughput screening in the identification of compounds able to induce specific phenotypes, such as differentiation, in African trypanosomes. Examination of gene expression in response to treatment with DDD00015314.

ORGANISM(S): Trypanosoma brucei brucei

SUBMITTER: Alasdair Ivens 

PROVIDER: E-GEOD-46483 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

High-throughput chemical screening for antivirulence developmental phenotypes in Trypanosoma brucei.

MacGregor Paula P   Ivens Alasdair A   Shave Steven S   Collie Iain I   Gray David D   Auer Manfred M   Matthews Keith R KR  

Eukaryotic cell 20140117 3


In the bloodstream of mammalian hosts, the sleeping sickness parasite, Trypanosoma brucei, exists as a proliferative slender form or a nonproliferative, transmissible, stumpy form. The transition between these developmental forms is controlled by a density-dependent mechanism that is important for the parasite's infection dynamics, immune evasion via ordered antigenic variation, and disease transmissibility. However, stumpy formation has been lost in most laboratory-adapted trypanosome lines, ge  ...[more]

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