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NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens
Ehrlichiae are gram-negative obligate intracellular bacteria that cause potentially fatal human monocytic ehrlichiosis. We previously showed that natural killer (NK) cells play a critical role in host defense against Ehrlichia during primary infection. However, the contribution of NK cells to the me...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836677/ https://www.ncbi.nlm.nih.gov/pubmed/27092553 http://dx.doi.org/10.1371/journal.pone.0153223 |
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author | Habib, Samar El Andaloussi, Abdeljabar Hisham, Ahmed Ismail, Nahed |
author_facet | Habib, Samar El Andaloussi, Abdeljabar Hisham, Ahmed Ismail, Nahed |
author_sort | Habib, Samar |
collection | PubMed |
description | Ehrlichiae are gram-negative obligate intracellular bacteria that cause potentially fatal human monocytic ehrlichiosis. We previously showed that natural killer (NK) cells play a critical role in host defense against Ehrlichia during primary infection. However, the contribution of NK cells to the memory response against Ehrlichia remains elusive. Primary infection of C57BL/6 mice with Ehrlichia muris provides long-term protection against a second challenge with the highly virulent Ixodes ovatus Ehrlichia (IOE), which ordinarily causes fatal disease in naïve mice. Here, we show that the depletion of NK cells in E. muris-primed mice abrogates the protective memory response against IOE. Approximately, 80% of NK cell-depleted E. muris-primed mice succumbed to lethal IOE infection on days 8–10 after IOE infection, similar to naïve mice infected with the same dose of IOE. The lack of a recall response in NK cell-depleted mice correlated with an increased bacterial burden, extensive liver injury, decreased frequency of Ehrlichia-specific IFN-γ-producing memory CD4(+) and CD8(+) T-cells, and a low titer of Ehrlichia-specific antibodies. Intraperitoneal infection of mice with E. muris resulted in the production of IL-15, IL-12, and IFN-γ as well as an expansion of activated NKG2D(+) NK cells. The adoptive transfer of purified E. muris-primed hepatic and splenic NK cells into Rag2(-/-)Il2rg(-/-) recipient mice provided protective immunity against challenge with E. muris. Together, these data suggest that E. muris-induced memory-like NK cells, which contribute to the protective, recall response against Ehrlichia. |
format | Online Article Text |
id | pubmed-4836677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48366772016-04-29 NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens Habib, Samar El Andaloussi, Abdeljabar Hisham, Ahmed Ismail, Nahed PLoS One Research Article Ehrlichiae are gram-negative obligate intracellular bacteria that cause potentially fatal human monocytic ehrlichiosis. We previously showed that natural killer (NK) cells play a critical role in host defense against Ehrlichia during primary infection. However, the contribution of NK cells to the memory response against Ehrlichia remains elusive. Primary infection of C57BL/6 mice with Ehrlichia muris provides long-term protection against a second challenge with the highly virulent Ixodes ovatus Ehrlichia (IOE), which ordinarily causes fatal disease in naïve mice. Here, we show that the depletion of NK cells in E. muris-primed mice abrogates the protective memory response against IOE. Approximately, 80% of NK cell-depleted E. muris-primed mice succumbed to lethal IOE infection on days 8–10 after IOE infection, similar to naïve mice infected with the same dose of IOE. The lack of a recall response in NK cell-depleted mice correlated with an increased bacterial burden, extensive liver injury, decreased frequency of Ehrlichia-specific IFN-γ-producing memory CD4(+) and CD8(+) T-cells, and a low titer of Ehrlichia-specific antibodies. Intraperitoneal infection of mice with E. muris resulted in the production of IL-15, IL-12, and IFN-γ as well as an expansion of activated NKG2D(+) NK cells. The adoptive transfer of purified E. muris-primed hepatic and splenic NK cells into Rag2(-/-)Il2rg(-/-) recipient mice provided protective immunity against challenge with E. muris. Together, these data suggest that E. muris-induced memory-like NK cells, which contribute to the protective, recall response against Ehrlichia. Public Library of Science 2016-04-19 /pmc/articles/PMC4836677/ /pubmed/27092553 http://dx.doi.org/10.1371/journal.pone.0153223 Text en © 2016 Habib 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 Habib, Samar El Andaloussi, Abdeljabar Hisham, Ahmed Ismail, Nahed NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens |
title | NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens |
title_full | NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens |
title_fullStr | NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens |
title_full_unstemmed | NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens |
title_short | NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens |
title_sort | nk cell-mediated regulation of protective memory responses against intracellular ehrlichial pathogens |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836677/ https://www.ncbi.nlm.nih.gov/pubmed/27092553 http://dx.doi.org/10.1371/journal.pone.0153223 |
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