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The Dermis as a Delivery Site of Trypanosoma brucei for Tsetse Flies

Tsetse flies are the sole vectors of Trypanosoma brucei parasites that cause sleeping sickness. Our knowledge on the early interface between the infective metacyclic forms and the mammalian host skin is currently highly limited. Glossina morsitans flies infected with fluorescently tagged T. brucei p...

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Autores principales: Caljon, Guy, Van Reet, Nick, De Trez, Carl, Vermeersch, Marjorie, Pérez-Morga, David, Van Den Abbeele, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956260/
https://www.ncbi.nlm.nih.gov/pubmed/27441553
http://dx.doi.org/10.1371/journal.ppat.1005744
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author Caljon, Guy
Van Reet, Nick
De Trez, Carl
Vermeersch, Marjorie
Pérez-Morga, David
Van Den Abbeele, Jan
author_facet Caljon, Guy
Van Reet, Nick
De Trez, Carl
Vermeersch, Marjorie
Pérez-Morga, David
Van Den Abbeele, Jan
author_sort Caljon, Guy
collection PubMed
description Tsetse flies are the sole vectors of Trypanosoma brucei parasites that cause sleeping sickness. Our knowledge on the early interface between the infective metacyclic forms and the mammalian host skin is currently highly limited. Glossina morsitans flies infected with fluorescently tagged T. brucei parasites were used in this study to initiate natural infections in mice. Metacyclic trypanosomes were found to be highly infectious through the intradermal route in sharp contrast with blood stream form trypanosomes. Parasite emigration from the dermal inoculation site resulted in detectable parasite levels in the draining lymph nodes within 18 hours and in the peripheral blood within 42 h. A subset of parasites remained and actively proliferated in the dermis. By initiating mixed infections with differentially labeled parasites, dermal parasites were unequivocally shown to arise from the initial inoculum and not from a re-invasion from the blood circulation. Scanning electron microscopy demonstrated intricate interactions of these skin-residing parasites with adipocytes in the connective tissue, entanglement by reticular fibers of the periadipocytic baskets and embedment between collagen bundles. Experimental transmission experiments combined with molecular parasite detection in blood fed flies provided evidence that dermal trypanosomes can be acquired from the inoculation site immediately after the initial transmission. High resolution thermographic imaging also revealed that intradermal parasite expansion induces elevated skin surface temperatures. Collectively, the dermis represents a delivery site of the highly infective metacyclic trypanosomes from which the host is systemically colonized and where a proliferative subpopulation remains that is physically constrained by intricate interactions with adipocytes and collagen fibrous structures.
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spelling pubmed-49562602016-08-08 The Dermis as a Delivery Site of Trypanosoma brucei for Tsetse Flies Caljon, Guy Van Reet, Nick De Trez, Carl Vermeersch, Marjorie Pérez-Morga, David Van Den Abbeele, Jan PLoS Pathog Research Article Tsetse flies are the sole vectors of Trypanosoma brucei parasites that cause sleeping sickness. Our knowledge on the early interface between the infective metacyclic forms and the mammalian host skin is currently highly limited. Glossina morsitans flies infected with fluorescently tagged T. brucei parasites were used in this study to initiate natural infections in mice. Metacyclic trypanosomes were found to be highly infectious through the intradermal route in sharp contrast with blood stream form trypanosomes. Parasite emigration from the dermal inoculation site resulted in detectable parasite levels in the draining lymph nodes within 18 hours and in the peripheral blood within 42 h. A subset of parasites remained and actively proliferated in the dermis. By initiating mixed infections with differentially labeled parasites, dermal parasites were unequivocally shown to arise from the initial inoculum and not from a re-invasion from the blood circulation. Scanning electron microscopy demonstrated intricate interactions of these skin-residing parasites with adipocytes in the connective tissue, entanglement by reticular fibers of the periadipocytic baskets and embedment between collagen bundles. Experimental transmission experiments combined with molecular parasite detection in blood fed flies provided evidence that dermal trypanosomes can be acquired from the inoculation site immediately after the initial transmission. High resolution thermographic imaging also revealed that intradermal parasite expansion induces elevated skin surface temperatures. Collectively, the dermis represents a delivery site of the highly infective metacyclic trypanosomes from which the host is systemically colonized and where a proliferative subpopulation remains that is physically constrained by intricate interactions with adipocytes and collagen fibrous structures. Public Library of Science 2016-07-21 /pmc/articles/PMC4956260/ /pubmed/27441553 http://dx.doi.org/10.1371/journal.ppat.1005744 Text en © 2016 Caljon et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Caljon, Guy
Van Reet, Nick
De Trez, Carl
Vermeersch, Marjorie
Pérez-Morga, David
Van Den Abbeele, Jan
The Dermis as a Delivery Site of Trypanosoma brucei for Tsetse Flies
title The Dermis as a Delivery Site of Trypanosoma brucei for Tsetse Flies
title_full The Dermis as a Delivery Site of Trypanosoma brucei for Tsetse Flies
title_fullStr The Dermis as a Delivery Site of Trypanosoma brucei for Tsetse Flies
title_full_unstemmed The Dermis as a Delivery Site of Trypanosoma brucei for Tsetse Flies
title_short The Dermis as a Delivery Site of Trypanosoma brucei for Tsetse Flies
title_sort dermis as a delivery site of trypanosoma brucei for tsetse flies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956260/
https://www.ncbi.nlm.nih.gov/pubmed/27441553
http://dx.doi.org/10.1371/journal.ppat.1005744
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