Majority of trypanosomes in freshly drawn blood are tumblers. Blood was freshly drawn from carp and T. carassii swimming behaviour analysed immediately using high-resolution microscopy at 240 frames per second (fps). (A) Relative percentage of tumblers, and intermediate or persistent swimmers (defined in the text) was calculated over a total number of 944 T. carassii, isolated from six different carp infections and imaged over 60 independent acquisitions. (B) Representative tracks of a tumbler (green), intermediate (yellow) and persistent (red) swimmer. The diameter of the circles (23 µm) indicates the average cell-body size of a trypanosome as also shown in (C). The inset table summarizes the straight-line distance covered by the trypanosome (between the first and last track point); the total track length, that is the path covered by the trypanosome in approximately 20 s of acquisition time, indicated in matching colours; and the average speed (μm/s) was calculated on a selection of the acquisitions used in (A). For tumblers, the displacement of the posterior end was used as tracking point. (C) Detailed image of two trypanosomes indicating the total body length including the flagellum (left) and the total cell-body length excluding the flagellum (right). Measurements were acquired on high-resolution images of at least 10 freshly isolated trypanosomes obtained from four independent infections, using more than 20 frames within the same acquisition. Quantification of trypanosome length, swimming speed and directionality was performed with ImageJ-Fijii using the MTrack plug-in. Video 1 displays high-speed videos of the swimming behaviour of tumblers, intermediate and persistent swimmers in carp blood, or of trypanosomes in serum or culture medium.

(A) Blood was freshly drawn from carp and trypanosomes' swimming behaviour immediately imaged using high-resolution microscopy at 240 frames fps. Images are frames (indicated by the numbers) of four different locations within the same field of view, selected from the corresponding Video 2. Note how the posterior end of the parasites is attached to the red blood cell and the flagellum is free to move. (B) Selected frames from Video 2, at the indicated time points, show how T. carassii can also adhere to glass surfaces through the posterior end (white arrow) leaving the body and flagellum free to move.

10.7554/eLife.48388.008Figure 2—source data 1.

(A) Schematic representation of T. carassii swimming in the peritoneal or heart cavity, both environments without hydrodynamic flow and red blood cells; here, most of the trypanosomes are tumblers, only occasionally was a persistent swimmer observed. (B) Selected frame from Video 6, capturing trypanosomes in the peritoneal cavity. More than 100 trypanosomes are present but are not all in focus in the selected frame; the majority are tumblers. The tracks of four representative tumblers (green) and of the only three persistent swimmers (red) are shown. Video 6 contains high-speed videos showing the location and swimming behaviours described above.

(A) Schematic representation of T. carassii swimming in compact tissues such as those in the fins. Most trypanosomes are directional swimmers and both forward and backward swimming were observed. (B) Selected frame from Video 7 showing the tracks of representative persistent swimmers identified in the fins. (C) In less compact tissues and in capillaries without blood flow, trypanosomes could invert their swimming direction in a ‘whip-like’ motion using the available three-dimensional space of the capillary or tissue. The ‘whip-like’ motion combines the swing of the flagellum along one plane (thin arc arrows), accompanied by a 180°C rotation of the flexible cell body along a third axis (rotational arrows). (D) In tissues where trypanosomes reach dead ends such as the interstitial space between vessels, persistent forward swimming translates into a drilling (auger) movement. Video 7 and Video 8 contain high-speed videos showing all locations and swimming behaviours schematically depicted.

Zebrafish larvae (5 dpf) were infected with 200 T. carassii or injected with PVP as non-infected control. Images are selected frames depicting the caudal artery, extracted from high-speed videos where trypanosomes (white open-arrow heads) and red blood cells (RBC, black open-arrow heads) were identified and tracked. (A) Artery of a control, non-infected, fish. Only RBC are present. (B) Artery of an infected fish, 1 dpi, showing a high ratio of RBC:trypanosomes. This frame corresponds to seconds 04:20-04:23 in Video 3, where the same trypanosomes were tracked. (C) Artery of an infected fish, 6 dpi, showing a reduced ratio of RBC:trypanosomes, indicating the onset of anaemia. (D) Artery of an infected fish suffering from severe anaemia, 8dpi, where only trypanosomes are present. The frame is extracted from the corresponding Video 9. Scale bars indicate 25 µm.

Wild type zebrafish larvae (5 dpf) were infected with 200 T. carassii or injected with PVP as non-infected control. Images are selected frames from high-speed videos. (A-C) Representative images of caudal artery and caudal vein (dashed lines) region at various time points after infection. Scale bars indicate 50 µm. (D) Maximum diameter of the caudal vein in non-infected (open symbols) and infected individuals (closed symbols) at 2–3 dpi (squares) and 6–8 dpi (triangles). Each value is the average of at least three measurements taken at different locations within the caudal vein of the same individual. Numbers indicate average and standard deviation.

10.7554/eLife.48388.025Figure 10—source data 1.

(A) Haptomonads stages of Paratrypanosoma confusum: adhesion occurs through an attachment pad forming from the bulge at the base of the flagellum involving extensive remodelling of the flagellum membrane (based on Skalický et al., 2017). The square indicates the location of the flagellar pocket. (B) T. brucei epimastigotes attached through the flagellum to the brush border of the salivary gland epithelium (based on Beattie and Gull, 1997; Schuster et al., 2017; Vickerman and Tetley, 1990). (C) T. congolense adhesion to bovine aorta endothelial cell line via extensive membrane protrusions (filopodia) of the membrane-attached flagellum (based on Beattie and Gull, 1997; Hemphill and Ross, 1995). (D) T. carassii attached through the posterior end, leaving the cell body and flagellum free to move, as also shown in Figure 5.