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...

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Main Authors: Samar Habib, Abdeljabar El Andaloussi, Ahmed Hisham, Nahed Ismail
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4836677?pdf=render
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spelling doaj-087c1ced4426428ea78be804fd5b78fe2020-11-25T00:42:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01114e015322310.1371/journal.pone.0153223NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens.Samar HabibAbdeljabar El AndaloussiAhmed HishamNahed IsmailEhrlichiae 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.http://europepmc.org/articles/PMC4836677?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Samar Habib
Abdeljabar El Andaloussi
Ahmed Hisham
Nahed Ismail
spellingShingle Samar Habib
Abdeljabar El Andaloussi
Ahmed Hisham
Nahed Ismail
NK Cell-Mediated Regulation of Protective Memory Responses against Intracellular Ehrlichial Pathogens.
PLoS ONE
author_facet Samar Habib
Abdeljabar El Andaloussi
Ahmed Hisham
Nahed Ismail
author_sort Samar Habib
title 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_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_sort nk cell-mediated regulation of protective memory responses against intracellular ehrlichial pathogens.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
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.
url http://europepmc.org/articles/PMC4836677?pdf=render
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