Abstract

BackgroundTrypanosoma brucei, the causative agent of African sleeping sickness, undergoes a complex developmental cycle that takes place in mammalian and insect hosts and is accompanied by changes in metabolism and cellular morphology. While differences in mRNA expression have been described for many genes, genome-wide expression analyses have been largely lacking. Trypanosomatids represent a unique case in eukaryotes in that they transcribe protein-coding genes as large polycistronic units, and rarely regulate gene expression at the level of transcription initiation.ResultsHere we present a comprehensive analysis of mRNA expression in several stages of parasite development. Utilizing microarrays that have multiple copies of multiple probes for each gene, we were able to demonstrate with a high degree of statistical confidence that approximately one-fourth of genes show differences in mRNA expression levels in the stages examined. These include complex patterns of gene expression within gene families, including the large family of variant surface glycoproteins (VSGs) and their relatives, where we have identified a number of constitutively expressed family members. Furthermore, we were able to assess the relative abundance of all transcripts in each stage, identifying the genes that are either weakly or highly expressed. Very few genes show no evidence of expression.ConclusionDespite the lack of gene regulation at the level of transcription initiation, our results reveal extensive regulation of mRNA abundance associated with different life cycle and growth stages. In addition, analysis of variant surface glycoprotein gene expression reveals a more complex picture than previously thought. These data provide a valuable resource to the community of researchers studying this lethal agent.

Highlights

  • Trypanosoma brucei, the causative agent of African sleeping sickness, undergoes a complex developmental cycle that takes place in mammalian and insect hosts and is accompanied by changes in metabolism and cellular morphology

  • This study reports our findings on changes in gene expression between those stages of T. brucei that can be readily studied in the laboratory

  • The slender bloodstream forms (BF) populations showed less than 5% intermediate or stumpy forms and less than 1% expressed procyclin after stimulation

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Summary

Introduction

Trypanosoma brucei, the causative agent of African sleeping sickness, undergoes a complex developmental cycle that takes place in mammalian and insect hosts and is accompanied by changes in metabolism and cellular morphology. BMC Genomics 2009, 10:482 http://www.biomedcentral.com/1471-2164/10/482 pant antigenic variation in which hundreds of variant surface glycoproteins (VSGs) are sequentially displayed on the parasite surface [1] This group of organisms, along with their relatives Trypanosoma congolense and Trypanosoma vivax, have hampered the development of sub-Saharan Africa by their severe effects on cattle and draft animals. In both the mammalian host and the insect vector (tsetse fly), T. brucei undergoes multiple developmental changes that are reflected by changes in morphology, surface proteins, cell division, and metabolism, all stages are extracellular and motile, courtesy of a single flagellum. While T. brucei slender BFs and PFs are routinely cultured in vitro, epimastigotes and metacyclic forms are not readily available

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