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Dermal bacterial LPS-stimulation reduces susceptibility to intradermal Trypanosoma brucei infection

Infections with Trypanosoma brucei sp. are established after the injection of metacyclic trypomastigotes into the skin dermis by the tsetse fly vector. The parasites then gain access to the local lymphatic vessels to infect the local draining lymph nodes and disseminate systemically via the bloodstr...

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Autores principales: Alfituri, Omar A., Mararo, Enock M., Steketee, Pieter C., Morrison, Liam J., Mabbott, Neil A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110744/
https://www.ncbi.nlm.nih.gov/pubmed/33972588
http://dx.doi.org/10.1038/s41598-021-89053-2
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author Alfituri, Omar A.
Mararo, Enock M.
Steketee, Pieter C.
Morrison, Liam J.
Mabbott, Neil A.
author_facet Alfituri, Omar A.
Mararo, Enock M.
Steketee, Pieter C.
Morrison, Liam J.
Mabbott, Neil A.
author_sort Alfituri, Omar A.
collection PubMed
description Infections with Trypanosoma brucei sp. are established after the injection of metacyclic trypomastigotes into the skin dermis by the tsetse fly vector. The parasites then gain access to the local lymphatic vessels to infect the local draining lymph nodes and disseminate systemically via the bloodstream. Macrophages are considered to play an important role in host protection during the early stage of systemic trypanosome infections. Macrophages are abundant in the skin dermis, but relatively little is known of their impact on susceptibility to intradermal (ID) trypanosome infections. We show that although dermal injection of colony stimulating factor 1 (CSF1) increased the local abundance of macrophages in the skin, this did not affect susceptibility to ID T. brucei infection. However, bacterial LPS-stimulation in the dermis prior to ID trypanosome infection significantly reduced disease susceptibility. In vitro assays showed that LPS-stimulated macrophage-like RAW264.7 cells had enhanced cytotoxicity towards T. brucei, implying that dermal LPS-treatment may similarly enhance the ability of dermal macrophages to eliminate ID injected T. brucei parasites in the skin. A thorough understanding of the factors that reduce susceptibility to ID injected T. brucei infections may lead to the development of novel strategies to help reduce the transmission of African trypanosomes.
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spelling pubmed-81107442021-05-12 Dermal bacterial LPS-stimulation reduces susceptibility to intradermal Trypanosoma brucei infection Alfituri, Omar A. Mararo, Enock M. Steketee, Pieter C. Morrison, Liam J. Mabbott, Neil A. Sci Rep Article Infections with Trypanosoma brucei sp. are established after the injection of metacyclic trypomastigotes into the skin dermis by the tsetse fly vector. The parasites then gain access to the local lymphatic vessels to infect the local draining lymph nodes and disseminate systemically via the bloodstream. Macrophages are considered to play an important role in host protection during the early stage of systemic trypanosome infections. Macrophages are abundant in the skin dermis, but relatively little is known of their impact on susceptibility to intradermal (ID) trypanosome infections. We show that although dermal injection of colony stimulating factor 1 (CSF1) increased the local abundance of macrophages in the skin, this did not affect susceptibility to ID T. brucei infection. However, bacterial LPS-stimulation in the dermis prior to ID trypanosome infection significantly reduced disease susceptibility. In vitro assays showed that LPS-stimulated macrophage-like RAW264.7 cells had enhanced cytotoxicity towards T. brucei, implying that dermal LPS-treatment may similarly enhance the ability of dermal macrophages to eliminate ID injected T. brucei parasites in the skin. A thorough understanding of the factors that reduce susceptibility to ID injected T. brucei infections may lead to the development of novel strategies to help reduce the transmission of African trypanosomes. Nature Publishing Group UK 2021-05-10 /pmc/articles/PMC8110744/ /pubmed/33972588 http://dx.doi.org/10.1038/s41598-021-89053-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Alfituri, Omar A.
Mararo, Enock M.
Steketee, Pieter C.
Morrison, Liam J.
Mabbott, Neil A.
Dermal bacterial LPS-stimulation reduces susceptibility to intradermal Trypanosoma brucei infection
title Dermal bacterial LPS-stimulation reduces susceptibility to intradermal Trypanosoma brucei infection
title_full Dermal bacterial LPS-stimulation reduces susceptibility to intradermal Trypanosoma brucei infection
title_fullStr Dermal bacterial LPS-stimulation reduces susceptibility to intradermal Trypanosoma brucei infection
title_full_unstemmed Dermal bacterial LPS-stimulation reduces susceptibility to intradermal Trypanosoma brucei infection
title_short Dermal bacterial LPS-stimulation reduces susceptibility to intradermal Trypanosoma brucei infection
title_sort dermal bacterial lps-stimulation reduces susceptibility to intradermal trypanosoma brucei infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110744/
https://www.ncbi.nlm.nih.gov/pubmed/33972588
http://dx.doi.org/10.1038/s41598-021-89053-2
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