Cargando…
Bacterial clearance reverses a skewed T-cell repertoire induced by Salmonella infection
Salmonella typhimurium invades the spleen, liver, and peripheral lymph nodes and has recently been detected in the bone marrow and thymus, resulting in a reduced thymic size and a decline in the total number of thymic cells. A specific deletion of the double-positive cell subset has been characteriz...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578521/ https://www.ncbi.nlm.nih.gov/pubmed/26417438 http://dx.doi.org/10.1002/iid3.60 |
_version_ | 1782391129350602752 |
---|---|
author | Leyva-Rangel, Jessica P de los Angeles Hernández-Cueto, Maria Galan-Enriquez, Carlos-Samuel López-Medina, Marcela Ortiz-Navarrete, Vianney |
author_facet | Leyva-Rangel, Jessica P de los Angeles Hernández-Cueto, Maria Galan-Enriquez, Carlos-Samuel López-Medina, Marcela Ortiz-Navarrete, Vianney |
author_sort | Leyva-Rangel, Jessica P |
collection | PubMed |
description | Salmonella typhimurium invades the spleen, liver, and peripheral lymph nodes and has recently been detected in the bone marrow and thymus, resulting in a reduced thymic size and a decline in the total number of thymic cells. A specific deletion of the double-positive cell subset has been characterized, yet the export of mature T cells to the periphery remains normal. We analyzed Salmonella pathogenesis regarding thymic structure and the T-cell maturation process. We demonstrate that, despite alterations in the thymic structure, T-cell development is maintained during Salmonella infection, allowing the selection of single-positive T-cell clones expressing particular T-cell receptor beta chains (TCR-Vβ). Moreover, the treatment of infected mice with an antibiotic restored the normal thymic architecture and thymocyte subset distribution. Additionally, the frequency of TCR-Vβ usage after treatment was comparable to that in non-infected mice. However, bacteria were still recovered from the thymus after 1 month of treatment. Our data reveal that a skewed T-cell developmental process is present in the Salmonella-infected thymus that alters the TCR-Vβ usage frequency. Likewise, the post-treatment persistence of Salmonella reveals a novel function of the thymus as a potential reservoir for this infectious agent. |
format | Online Article Text |
id | pubmed-4578521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45785212015-09-28 Bacterial clearance reverses a skewed T-cell repertoire induced by Salmonella infection Leyva-Rangel, Jessica P de los Angeles Hernández-Cueto, Maria Galan-Enriquez, Carlos-Samuel López-Medina, Marcela Ortiz-Navarrete, Vianney Immun Inflamm Dis Original Research Salmonella typhimurium invades the spleen, liver, and peripheral lymph nodes and has recently been detected in the bone marrow and thymus, resulting in a reduced thymic size and a decline in the total number of thymic cells. A specific deletion of the double-positive cell subset has been characterized, yet the export of mature T cells to the periphery remains normal. We analyzed Salmonella pathogenesis regarding thymic structure and the T-cell maturation process. We demonstrate that, despite alterations in the thymic structure, T-cell development is maintained during Salmonella infection, allowing the selection of single-positive T-cell clones expressing particular T-cell receptor beta chains (TCR-Vβ). Moreover, the treatment of infected mice with an antibiotic restored the normal thymic architecture and thymocyte subset distribution. Additionally, the frequency of TCR-Vβ usage after treatment was comparable to that in non-infected mice. However, bacteria were still recovered from the thymus after 1 month of treatment. Our data reveal that a skewed T-cell developmental process is present in the Salmonella-infected thymus that alters the TCR-Vβ usage frequency. Likewise, the post-treatment persistence of Salmonella reveals a novel function of the thymus as a potential reservoir for this infectious agent. John Wiley & Sons, Ltd 2015-09 2015-05-06 /pmc/articles/PMC4578521/ /pubmed/26417438 http://dx.doi.org/10.1002/iid3.60 Text en © 2015 The Authors. Immunity, Inflammation and Disease Published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Leyva-Rangel, Jessica P de los Angeles Hernández-Cueto, Maria Galan-Enriquez, Carlos-Samuel López-Medina, Marcela Ortiz-Navarrete, Vianney Bacterial clearance reverses a skewed T-cell repertoire induced by Salmonella infection |
title | Bacterial clearance reverses a skewed T-cell repertoire induced by Salmonella infection |
title_full | Bacterial clearance reverses a skewed T-cell repertoire induced by Salmonella infection |
title_fullStr | Bacterial clearance reverses a skewed T-cell repertoire induced by Salmonella infection |
title_full_unstemmed | Bacterial clearance reverses a skewed T-cell repertoire induced by Salmonella infection |
title_short | Bacterial clearance reverses a skewed T-cell repertoire induced by Salmonella infection |
title_sort | bacterial clearance reverses a skewed t-cell repertoire induced by salmonella infection |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578521/ https://www.ncbi.nlm.nih.gov/pubmed/26417438 http://dx.doi.org/10.1002/iid3.60 |
work_keys_str_mv | AT leyvarangeljessicap bacterialclearancereversesaskewedtcellrepertoireinducedbysalmonellainfection AT delosangeleshernandezcuetomaria bacterialclearancereversesaskewedtcellrepertoireinducedbysalmonellainfection AT galanenriquezcarlossamuel bacterialclearancereversesaskewedtcellrepertoireinducedbysalmonellainfection AT lopezmedinamarcela bacterialclearancereversesaskewedtcellrepertoireinducedbysalmonellainfection AT ortiznavarretevianney bacterialclearancereversesaskewedtcellrepertoireinducedbysalmonellainfection |