Authors
O A Alfituri2; E Paxton2; J M Brewer1; P Garside1; L J Morrison2; N A Mabbott2;
1 Institute of Infection, Immunity & Inflammation, College of Medicine, Veterinary & Life Sciences, University of Glasgow, Glasgow G12 8TA, Scotland, UK.; 2 The Roslin Institute, The University of Edinburgh, Division of Infection and Immunity, Easter Bush, Midlothian, EH25 9RG, UK.
Discussion
African
trypanosomes are single-celled extracellular protozoan parasites that are
transmitted via the tsetse fly vector across sub-Saharan Africa. Mammalian
infection begins when the tsetse fly injects trypanosomes into the skin. The
parasites invade the circulatory and lymphatic systems, reaching the draining
lymph nodes and disseminate systemically. How this occurs is not known. Chemokines
play important roles in attracting leukocytes towards the lymphatics and lymph
nodes.To investigate
how trypanosomes migrate from the bite site to the draining lymph nodes, we
determined whether chemokines act as chemoattractants for trypanosomes. As
certain chemokines also possess antimicrobial properties, including against the
protozoan parasite Leishmania mexicana ,we tested their potential cytotoxic
effects against T. b. brucei . Our data
showed that these chemokines do not induce chemotaxis of T. b. brucei . The motility characteristics of the parasites were
also not affected. Moreover, these chemokines do not exert any trypanostatic
effects on trypanosomes. This data suggests trypanosomes use alternative cues
to reach the lymphatics post-infection. Identifying
the mechanisms involved in establishing African trypanosome infections in the
skin and their systemic dissemination will aid the development of novel
approaches to block disease transmission.Â