Cargando…
Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis
Borrelia burgdorferi, the causative agent of Lyme disease, is a vector-borne bacterial infection that is transmitted through the bite of an infected tick. If not treated with antibiotics during the early stages of infection, disseminated infection can spread to the central nervous system (CNS). In n...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933741/ https://www.ncbi.nlm.nih.gov/pubmed/29723263 http://dx.doi.org/10.1371/journal.pone.0196893 |
_version_ | 1783319999768690688 |
---|---|
author | Divan, Ali Casselli, Timothy Narayanan, S. Anand Mukherjee, Sanjib Zawieja, David C. Watt, John A. Brissette, Catherine A. Newell-Rogers, M. Karen |
author_facet | Divan, Ali Casselli, Timothy Narayanan, S. Anand Mukherjee, Sanjib Zawieja, David C. Watt, John A. Brissette, Catherine A. Newell-Rogers, M. Karen |
author_sort | Divan, Ali |
collection | PubMed |
description | Borrelia burgdorferi, the causative agent of Lyme disease, is a vector-borne bacterial infection that is transmitted through the bite of an infected tick. If not treated with antibiotics during the early stages of infection, disseminated infection can spread to the central nervous system (CNS). In non-human primates (NHPs) it has been demonstrated that the leptomeninges are among the tissues colonized by B. burgdorferi spirochetes. Although the NHP model parallels aspects of human borreliosis, a small rodent model would be ideal to study the trafficking of spirochetes and immune cells into the CNS. Here we show that during early and late disseminated infection, B. burgdorferi infects the meninges of intradermally infected mice, and is associated with concurrent increases in meningeal T cells. We found that the dura mater was consistently culture positive for spirochetes in transcardially perfused mice, independent of the strain of B. burgdorferi used. Within the dura mater, spirochetes were preferentially located in vascular regions, but were also present in perivascular, and extravascular regions, as late as 75 days post-infection. At the same end-point, we observed significant increases in the number of CD3+ T cells within the pia and dura mater, as compared to controls. Flow cytometric analysis of leukocytes isolated from the dura mater revealed that CD3+ cell populations were comprised of both CD4 and CD8 T cells. Overall, our data demonstrate that similarly to infection in peripheral tissues, spirochetes adhere to the dura mater during disseminated infection, and are associated with increases in the number of meningeal T cells. Collectively, our results demonstrate that there are aspects of B. burgdorferi meningeal infection that can be modelled in laboratory mice, suggesting that mice may be useful for elucidating mechanisms of meningeal pathogenesis by B. burgdorferi. |
format | Online Article Text |
id | pubmed-5933741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59337412018-05-18 Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis Divan, Ali Casselli, Timothy Narayanan, S. Anand Mukherjee, Sanjib Zawieja, David C. Watt, John A. Brissette, Catherine A. Newell-Rogers, M. Karen PLoS One Research Article Borrelia burgdorferi, the causative agent of Lyme disease, is a vector-borne bacterial infection that is transmitted through the bite of an infected tick. If not treated with antibiotics during the early stages of infection, disseminated infection can spread to the central nervous system (CNS). In non-human primates (NHPs) it has been demonstrated that the leptomeninges are among the tissues colonized by B. burgdorferi spirochetes. Although the NHP model parallels aspects of human borreliosis, a small rodent model would be ideal to study the trafficking of spirochetes and immune cells into the CNS. Here we show that during early and late disseminated infection, B. burgdorferi infects the meninges of intradermally infected mice, and is associated with concurrent increases in meningeal T cells. We found that the dura mater was consistently culture positive for spirochetes in transcardially perfused mice, independent of the strain of B. burgdorferi used. Within the dura mater, spirochetes were preferentially located in vascular regions, but were also present in perivascular, and extravascular regions, as late as 75 days post-infection. At the same end-point, we observed significant increases in the number of CD3+ T cells within the pia and dura mater, as compared to controls. Flow cytometric analysis of leukocytes isolated from the dura mater revealed that CD3+ cell populations were comprised of both CD4 and CD8 T cells. Overall, our data demonstrate that similarly to infection in peripheral tissues, spirochetes adhere to the dura mater during disseminated infection, and are associated with increases in the number of meningeal T cells. Collectively, our results demonstrate that there are aspects of B. burgdorferi meningeal infection that can be modelled in laboratory mice, suggesting that mice may be useful for elucidating mechanisms of meningeal pathogenesis by B. burgdorferi. Public Library of Science 2018-05-03 /pmc/articles/PMC5933741/ /pubmed/29723263 http://dx.doi.org/10.1371/journal.pone.0196893 Text en © 2018 Divan 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Divan, Ali Casselli, Timothy Narayanan, S. Anand Mukherjee, Sanjib Zawieja, David C. Watt, John A. Brissette, Catherine A. Newell-Rogers, M. Karen Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis |
title | Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis |
title_full | Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis |
title_fullStr | Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis |
title_full_unstemmed | Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis |
title_short | Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis |
title_sort | borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal t cells during murine disseminated borreliosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933741/ https://www.ncbi.nlm.nih.gov/pubmed/29723263 http://dx.doi.org/10.1371/journal.pone.0196893 |
work_keys_str_mv | AT divanali borreliaburgdorferiadheretobloodvesselsintheduramaterandareassociatedwithincreasedmeningealtcellsduringmurinedisseminatedborreliosis AT cassellitimothy borreliaburgdorferiadheretobloodvesselsintheduramaterandareassociatedwithincreasedmeningealtcellsduringmurinedisseminatedborreliosis AT narayanansanand borreliaburgdorferiadheretobloodvesselsintheduramaterandareassociatedwithincreasedmeningealtcellsduringmurinedisseminatedborreliosis AT mukherjeesanjib borreliaburgdorferiadheretobloodvesselsintheduramaterandareassociatedwithincreasedmeningealtcellsduringmurinedisseminatedborreliosis AT zawiejadavidc borreliaburgdorferiadheretobloodvesselsintheduramaterandareassociatedwithincreasedmeningealtcellsduringmurinedisseminatedborreliosis AT wattjohna borreliaburgdorferiadheretobloodvesselsintheduramaterandareassociatedwithincreasedmeningealtcellsduringmurinedisseminatedborreliosis AT brissettecatherinea borreliaburgdorferiadheretobloodvesselsintheduramaterandareassociatedwithincreasedmeningealtcellsduringmurinedisseminatedborreliosis AT newellrogersmkaren borreliaburgdorferiadheretobloodvesselsintheduramaterandareassociatedwithincreasedmeningealtcellsduringmurinedisseminatedborreliosis |