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Modulation of the tick gut milieu by a secreted tick protein favors Borrelia burgdorferi colonization

The Lyme disease agent, Borrelia burgdorferi, colonizes the gut of the tick Ixodes scapularis, which transmits the pathogen to vertebrate hosts including humans. Here we show that B. burgdorferi colonization increases the expression of several tick gut genes including pixr, encoding a secreted gut p...

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Autores principales: Narasimhan, Sukanya, Schuijt, Tim J., Abraham, Nabil M., Rajeevan, Nallakkandi, Coumou, Jeroen, Graham, Morven, Robson, Andrew, Wu, Ming-Jie, Daffre, Sirlei, Hovius, Joppe W., Fikrig, Erol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543126/
https://www.ncbi.nlm.nih.gov/pubmed/28775250
http://dx.doi.org/10.1038/s41467-017-00208-0
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author Narasimhan, Sukanya
Schuijt, Tim J.
Abraham, Nabil M.
Rajeevan, Nallakkandi
Coumou, Jeroen
Graham, Morven
Robson, Andrew
Wu, Ming-Jie
Daffre, Sirlei
Hovius, Joppe W.
Fikrig, Erol
author_facet Narasimhan, Sukanya
Schuijt, Tim J.
Abraham, Nabil M.
Rajeevan, Nallakkandi
Coumou, Jeroen
Graham, Morven
Robson, Andrew
Wu, Ming-Jie
Daffre, Sirlei
Hovius, Joppe W.
Fikrig, Erol
author_sort Narasimhan, Sukanya
collection PubMed
description The Lyme disease agent, Borrelia burgdorferi, colonizes the gut of the tick Ixodes scapularis, which transmits the pathogen to vertebrate hosts including humans. Here we show that B. burgdorferi colonization increases the expression of several tick gut genes including pixr, encoding a secreted gut protein with a Reeler domain. RNA interference-mediated silencing of pixr, or immunity against PIXR in mice, impairs the ability of B. burgdorferi to colonize the tick gut. PIXR inhibits bacterial biofilm formation in vitro and in vivo. Abrogation of PIXR function in vivo results in alterations in the gut microbiome, metabolome and immune responses. These alterations influence the spirochete entering the tick gut in multiple ways. PIXR abrogation also impairs larval molting, indicative of its role in tick biology. This study highlights the role of the tick gut in actively managing its microbiome, and how this impacts B. burgdorferi colonization of its arthropod vector.
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spelling pubmed-55431262017-08-09 Modulation of the tick gut milieu by a secreted tick protein favors Borrelia burgdorferi colonization Narasimhan, Sukanya Schuijt, Tim J. Abraham, Nabil M. Rajeevan, Nallakkandi Coumou, Jeroen Graham, Morven Robson, Andrew Wu, Ming-Jie Daffre, Sirlei Hovius, Joppe W. Fikrig, Erol Nat Commun Article The Lyme disease agent, Borrelia burgdorferi, colonizes the gut of the tick Ixodes scapularis, which transmits the pathogen to vertebrate hosts including humans. Here we show that B. burgdorferi colonization increases the expression of several tick gut genes including pixr, encoding a secreted gut protein with a Reeler domain. RNA interference-mediated silencing of pixr, or immunity against PIXR in mice, impairs the ability of B. burgdorferi to colonize the tick gut. PIXR inhibits bacterial biofilm formation in vitro and in vivo. Abrogation of PIXR function in vivo results in alterations in the gut microbiome, metabolome and immune responses. These alterations influence the spirochete entering the tick gut in multiple ways. PIXR abrogation also impairs larval molting, indicative of its role in tick biology. This study highlights the role of the tick gut in actively managing its microbiome, and how this impacts B. burgdorferi colonization of its arthropod vector. Nature Publishing Group UK 2017-08-04 /pmc/articles/PMC5543126/ /pubmed/28775250 http://dx.doi.org/10.1038/s41467-017-00208-0 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Narasimhan, Sukanya
Schuijt, Tim J.
Abraham, Nabil M.
Rajeevan, Nallakkandi
Coumou, Jeroen
Graham, Morven
Robson, Andrew
Wu, Ming-Jie
Daffre, Sirlei
Hovius, Joppe W.
Fikrig, Erol
Modulation of the tick gut milieu by a secreted tick protein favors Borrelia burgdorferi colonization
title Modulation of the tick gut milieu by a secreted tick protein favors Borrelia burgdorferi colonization
title_full Modulation of the tick gut milieu by a secreted tick protein favors Borrelia burgdorferi colonization
title_fullStr Modulation of the tick gut milieu by a secreted tick protein favors Borrelia burgdorferi colonization
title_full_unstemmed Modulation of the tick gut milieu by a secreted tick protein favors Borrelia burgdorferi colonization
title_short Modulation of the tick gut milieu by a secreted tick protein favors Borrelia burgdorferi colonization
title_sort modulation of the tick gut milieu by a secreted tick protein favors borrelia burgdorferi colonization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543126/
https://www.ncbi.nlm.nih.gov/pubmed/28775250
http://dx.doi.org/10.1038/s41467-017-00208-0
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