The dynamic interplay between Trypanosoma brucei and the tsetse fly vector revealed by transcriptome analysis

Datum: 15 juni 2018

Locatie: Stadscampus, Frederik de Tassiszaal - Prinsstraat 13 - 2000 Antwerpen (route: UAntwerpen, Stadscampus)

Tijdstip: 10 uur

Organisatie / co-organisatie: Departement Biologie

Promovendus: Irina Matetovici

Promotor: Jan Van Den Abbeele & Jean-Claude Dujardin

Korte beschrijving: Doctoraatsverdediging Irina Matetovici - Faculteit Wetenschappen, Departement Biologie


A group of devastating vector-borne parasitic diseases, African trypanosomiasis in sub-Saharan Africa, is caused by protozoan parasites of the genus Trypanosoma, including two human-pathogenic species of the T. brucei complex. For their development and transmission, African trypanosomes rely on their blood feeding vector, the tsetse fly (Glossina sp.). Here, the T. brucei parasites must overcome a series of barriers to colonize the midgut and subsequently achieve maturation and infectivity in the salivary glands. Understanding the interactions between trypanosomes and the tsetse fly is of great interest, and could possibly lead to the development of efficient ways to minimize or block the parasite transmission by its vector.

The main goal of this project was to understand the trypanosome-associated changes of immune-related processes in the tsetse fly salivary gland. This was achieved by an extensive comparative transcriptome analysis of T. brucei-infected salivary glands versus non-infected glands. This transcriptome analysis allowed us to gain novel insights into key immune-related genes affected upon infection and on the negative impact the parasite has on the integrity and functioning of the gland epithelium. Through this approach we identified the thioester-containing proteins family as possible immunity-associated molecules involved in controlling the trypanosome parasite. This interesting lead was then further explored more in-depth by revealing detailed information about their structure, evolutionary relationships and expression profiles in response to different trypanosome species – T. brucei and T. congolense.

Additionally, the generated T. brucei “salivary gland population” transcriptome was compared with that of trypanosome population in other infected tsetse tissues (proventriculus and midgut) to identify genes differentially expressed genes that could be related to the parasite sensing of/adaption to these micro-environments. This gene profiling showed evidence of profound differences between T. brucei life stages.

Overall, these findings contribute to a better understanding of the biological impact of the sleeping sickness parasite on the tsetse fly and how the insect vector keeps this impact under control. Moreover, these results offer a foundation for further studies on host-parasite interactions where the simultaneous gene expression analysis of the two organisms is essential