Cargando…
Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens
Macrophages are myeloid-derived phagocytic cells and one of the first immune cell types to respond to microbial infections. However, a number of bacterial pathogens are resistant to the antimicrobial activities of macrophages and can grow within these cells. Macrophages have other immune surveillanc...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786427/ https://www.ncbi.nlm.nih.gov/pubmed/26802627 http://dx.doi.org/10.7554/eLife.10625 |
_version_ | 1782420550194298880 |
---|---|
author | Steele, Shaun Radlinski, Lauren Taft-Benz, Sharon Brunton, Jason Kawula, Thomas H |
author_facet | Steele, Shaun Radlinski, Lauren Taft-Benz, Sharon Brunton, Jason Kawula, Thomas H |
author_sort | Steele, Shaun |
collection | PubMed |
description | Macrophages are myeloid-derived phagocytic cells and one of the first immune cell types to respond to microbial infections. However, a number of bacterial pathogens are resistant to the antimicrobial activities of macrophages and can grow within these cells. Macrophages have other immune surveillance roles including the acquisition of cytosolic components from multiple types of cells. We hypothesized that intracellular pathogens that can replicate within macrophages could also exploit cytosolic transfer to facilitate bacterial spread. We found that viable Francisella tularensis, as well as Salmonella enterica bacteria transferred from infected cells to uninfected macrophages along with other cytosolic material through a transient, contact dependent mechanism. Bacterial transfer occurred when the host cells exchanged plasma membrane proteins and cytosol via a trogocytosis related process leaving both donor and recipient cells intact and viable. Trogocytosis was strongly associated with infection in mice, suggesting that direct bacterial transfer occurs by this process in vivo. DOI: http://dx.doi.org/10.7554/eLife.10625.001 |
format | Online Article Text |
id | pubmed-4786427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47864272016-03-17 Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens Steele, Shaun Radlinski, Lauren Taft-Benz, Sharon Brunton, Jason Kawula, Thomas H eLife Immunology Macrophages are myeloid-derived phagocytic cells and one of the first immune cell types to respond to microbial infections. However, a number of bacterial pathogens are resistant to the antimicrobial activities of macrophages and can grow within these cells. Macrophages have other immune surveillance roles including the acquisition of cytosolic components from multiple types of cells. We hypothesized that intracellular pathogens that can replicate within macrophages could also exploit cytosolic transfer to facilitate bacterial spread. We found that viable Francisella tularensis, as well as Salmonella enterica bacteria transferred from infected cells to uninfected macrophages along with other cytosolic material through a transient, contact dependent mechanism. Bacterial transfer occurred when the host cells exchanged plasma membrane proteins and cytosol via a trogocytosis related process leaving both donor and recipient cells intact and viable. Trogocytosis was strongly associated with infection in mice, suggesting that direct bacterial transfer occurs by this process in vivo. DOI: http://dx.doi.org/10.7554/eLife.10625.001 eLife Sciences Publications, Ltd 2016-01-23 /pmc/articles/PMC4786427/ /pubmed/26802627 http://dx.doi.org/10.7554/eLife.10625 Text en © 2016, Steele et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology Steele, Shaun Radlinski, Lauren Taft-Benz, Sharon Brunton, Jason Kawula, Thomas H Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens |
title | Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens |
title_full | Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens |
title_fullStr | Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens |
title_full_unstemmed | Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens |
title_short | Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens |
title_sort | trogocytosis-associated cell to cell spread of intracellular bacterial pathogens |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786427/ https://www.ncbi.nlm.nih.gov/pubmed/26802627 http://dx.doi.org/10.7554/eLife.10625 |
work_keys_str_mv | AT steeleshaun trogocytosisassociatedcelltocellspreadofintracellularbacterialpathogens AT radlinskilauren trogocytosisassociatedcelltocellspreadofintracellularbacterialpathogens AT taftbenzsharon trogocytosisassociatedcelltocellspreadofintracellularbacterialpathogens AT bruntonjason trogocytosisassociatedcelltocellspreadofintracellularbacterialpathogens AT kawulathomash trogocytosisassociatedcelltocellspreadofintracellularbacterialpathogens |