Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783255094990471168 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5543126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT narasimhansukanya modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT schuijttimj modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT abrahamnabilm modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT rajeevannallakkandi modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT coumoujeroen modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT grahammorven modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT robsonandrew modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT wumingjie modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT daffresirlei modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT hoviusjoppew modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization AT fikrigerol modulationofthetickgutmilieubyasecretedtickproteinfavorsborreliaburgdorfericolonization |