2019
DOI: 10.1101/513689
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Trypanosoma bruceicolonises the tsetse gut via an immature peritrophic matrix in the proventriculus

Abstract: Projection (MIP) (top) and 3D reconstruction (bottom) of a trapped trypanosome. e, A PM sample from 130 a naïve fly depicting how this tissue looks under DIC and MIP after rendering from multiple z-sections, 131 whilst the orthogonal view shows the XZ/YZ planes of the folded PM section. f, DIC and MIP of an 132 infected PM sample containing trypanosome cysts, whilst the orthogonal XZ-YZ views show 133 trypanosomes trapped within PM layers. A second, smaller cyst-like structure can be seen in the XZ 134 orthogo… Show more

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Cited by 2 publications
(2 citation statements)
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References 55 publications
(38 reference statements)
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“…A key feature of this trap is the corner of the structure, which single parasites preferentially targeted, and into which multiple cells collectively accumulated (leaving other regions of the same trap relatively unoccupied). We found this observation interesting, given that it is similar to T. brucei behaviour previously described in vivo in the peritrophic matrix of its vector host, the tsetse fly [32,38]. While V-shapes are simple shapes, Tryp-Chip sets the basis for further investigations to replicate the geometry of the various environments that T. brucei finds in its insect and mammalian hosts.…”
Section: Discussionsupporting
confidence: 73%
See 1 more Smart Citation
“…A key feature of this trap is the corner of the structure, which single parasites preferentially targeted, and into which multiple cells collectively accumulated (leaving other regions of the same trap relatively unoccupied). We found this observation interesting, given that it is similar to T. brucei behaviour previously described in vivo in the peritrophic matrix of its vector host, the tsetse fly [32,38]. While V-shapes are simple shapes, Tryp-Chip sets the basis for further investigations to replicate the geometry of the various environments that T. brucei finds in its insect and mammalian hosts.…”
Section: Discussionsupporting
confidence: 73%
“…Specifically, our knowledge on mammalian tissue forms and 'intermediate' forms arising during the T. brucei life cycle remains limited [63]. Isolation of parasites from different host reservoirs ( [32,38,[64][65][66][67][68][69][70][71][72][73]), for their longitudinal observation in Tryp-Chip for characterization of multiple features, is an important future step we envisage. Given its potential to visualize single cell motility in free-swimming parasites, Tryp-Chip could be extended for use with other Trypanosoma species, and even other kinetoplastid parasites.…”
Section: Discussionmentioning
confidence: 99%