Mass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during Salmonella Typhimurium infection

Abstract Salmonella Typhimurium causes a self-limiting gastroenteritis that may lead to systemic disease. Bacteria invade the small intestine, crossing the intestinal epithelium from where they are transported to the mesenteric lymph nodes (MLNs) within migrating immune cells. MLNs are an important...

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Autores principales: Heather E. Hulme, Lynsey M. Meikle, Hannah Wessel, Nicole Strittmatter, John Swales, Carolyn Thomson, Anna Nilsson, Robert J. B. Nibbs, Simon Milling, Per E. Andren, C. Logan Mackay, Alex Dexter, Josephine Bunch, Richard J. A. Goodwin, Richard Burchmore, Daniel M. Wall
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:3a24c8a8c4bd40bd88a9c66a0de21e922021-12-02T15:06:17ZMass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during Salmonella Typhimurium infection10.1038/s41598-017-03100-52045-2322https://doaj.org/article/3a24c8a8c4bd40bd88a9c66a0de21e922017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-03100-5https://doaj.org/toc/2045-2322Abstract Salmonella Typhimurium causes a self-limiting gastroenteritis that may lead to systemic disease. Bacteria invade the small intestine, crossing the intestinal epithelium from where they are transported to the mesenteric lymph nodes (MLNs) within migrating immune cells. MLNs are an important site at which the innate and adaptive immune responses converge but their architecture and function is severely disrupted during S. Typhimurium infection. To further understand host-pathogen interactions at this site, we used mass spectrometry imaging (MSI) to analyse MLN tissue from a murine model of S. Typhimurium infection. A molecule, identified as palmitoylcarnitine (PalC), was of particular interest due to its high abundance at loci of S. Typhimurium infection and MLN disruption. High levels of PalC localised to sites within the MLNs where B and T cells were absent and where the perimeter of CD169+ sub capsular sinus macrophages was disrupted. MLN cells cultured ex vivo and treated with PalC had reduced CD4+CD25+ T cells and an increased number of B220+CD19+ B cells. The reduction in CD4+CD25+ T cells was likely due to apoptosis driven by increased caspase-3/7 activity. These data indicate that PalC significantly alters the host response in the MLNs, acting as a decisive factor in infection outcome.Heather E. HulmeLynsey M. MeikleHannah WesselNicole StrittmatterJohn SwalesCarolyn ThomsonAnna NilssonRobert J. B. NibbsSimon MillingPer E. AndrenC. Logan MackayAlex DexterJosephine BunchRichard J. A. GoodwinRichard BurchmoreDaniel M. WallNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Heather E. Hulme
Lynsey M. Meikle
Hannah Wessel
Nicole Strittmatter
John Swales
Carolyn Thomson
Anna Nilsson
Robert J. B. Nibbs
Simon Milling
Per E. Andren
C. Logan Mackay
Alex Dexter
Josephine Bunch
Richard J. A. Goodwin
Richard Burchmore
Daniel M. Wall
Mass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during Salmonella Typhimurium infection
description Abstract Salmonella Typhimurium causes a self-limiting gastroenteritis that may lead to systemic disease. Bacteria invade the small intestine, crossing the intestinal epithelium from where they are transported to the mesenteric lymph nodes (MLNs) within migrating immune cells. MLNs are an important site at which the innate and adaptive immune responses converge but their architecture and function is severely disrupted during S. Typhimurium infection. To further understand host-pathogen interactions at this site, we used mass spectrometry imaging (MSI) to analyse MLN tissue from a murine model of S. Typhimurium infection. A molecule, identified as palmitoylcarnitine (PalC), was of particular interest due to its high abundance at loci of S. Typhimurium infection and MLN disruption. High levels of PalC localised to sites within the MLNs where B and T cells were absent and where the perimeter of CD169+ sub capsular sinus macrophages was disrupted. MLN cells cultured ex vivo and treated with PalC had reduced CD4+CD25+ T cells and an increased number of B220+CD19+ B cells. The reduction in CD4+CD25+ T cells was likely due to apoptosis driven by increased caspase-3/7 activity. These data indicate that PalC significantly alters the host response in the MLNs, acting as a decisive factor in infection outcome.
format article
author Heather E. Hulme
Lynsey M. Meikle
Hannah Wessel
Nicole Strittmatter
John Swales
Carolyn Thomson
Anna Nilsson
Robert J. B. Nibbs
Simon Milling
Per E. Andren
C. Logan Mackay
Alex Dexter
Josephine Bunch
Richard J. A. Goodwin
Richard Burchmore
Daniel M. Wall
author_facet Heather E. Hulme
Lynsey M. Meikle
Hannah Wessel
Nicole Strittmatter
John Swales
Carolyn Thomson
Anna Nilsson
Robert J. B. Nibbs
Simon Milling
Per E. Andren
C. Logan Mackay
Alex Dexter
Josephine Bunch
Richard J. A. Goodwin
Richard Burchmore
Daniel M. Wall
author_sort Heather E. Hulme
title Mass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during Salmonella Typhimurium infection
title_short Mass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during Salmonella Typhimurium infection
title_full Mass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during Salmonella Typhimurium infection
title_fullStr Mass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during Salmonella Typhimurium infection
title_full_unstemmed Mass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during Salmonella Typhimurium infection
title_sort mass spectrometry imaging identifies palmitoylcarnitine as an immunological mediator during salmonella typhimurium infection
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/3a24c8a8c4bd40bd88a9c66a0de21e92
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