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Rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses

INTRODUCTION: Blood-feeding arthropods rely on robust cellular and humoral immunity to control pathogen invasion and replication. Tick hemocytes produce factors that can facilitate or suppress microbial infection and pathogenesis. Despite the importance of hemocytes in regulating microbial infection...

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Autores principales: Adegoke, Abdulsalam, Ribeiro, Jose M. C., Brown, Sidney, Smith, Ryan C., Karim, Shahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950277/
https://www.ncbi.nlm.nih.gov/pubmed/36845157
http://dx.doi.org/10.3389/fimmu.2023.1094326
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author Adegoke, Abdulsalam
Ribeiro, Jose M. C.
Brown, Sidney
Smith, Ryan C.
Karim, Shahid
author_facet Adegoke, Abdulsalam
Ribeiro, Jose M. C.
Brown, Sidney
Smith, Ryan C.
Karim, Shahid
author_sort Adegoke, Abdulsalam
collection PubMed
description INTRODUCTION: Blood-feeding arthropods rely on robust cellular and humoral immunity to control pathogen invasion and replication. Tick hemocytes produce factors that can facilitate or suppress microbial infection and pathogenesis. Despite the importance of hemocytes in regulating microbial infection, understanding of their basic biology and molecular mechanisms remains limited. METHODS: Here we combined histomorphology and functional analysis to identify five distinct phagocytic and non-phagocytic hemocyte populations circulating within the Gulf Coast tick Amblyomma maculatum. RESULTS AND DISCUSSION: Depletion of phagocytic hemocytes using clodronate liposomes revealed their function in eliminating bacterial infection. We provide the first direct evidence that an intracellular tick-borne pathogen, Rickettsia parkeri, infects phagocytic hemocytes in Am. maculatum to modify tick cellular immune responses. A hemocyte-specific RNA-seq dataset generated from hemocytes isolated from uninfected and R. parkeri-infected partially blood-fed ticks generated ~40,000 differentially regulated transcripts, >11,000 of which were immune genes. Silencing two differentially regulated phagocytic immune marker genes (nimrod B2 and eater-two Drosophila homologs), significantly reduced hemocyte phagocytosis. CONCLUSION: Together, these findings represent a significant step forward in understanding how hemocytes regulate microbial homeostasis and vector competence.
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spelling pubmed-99502772023-02-25 Rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses Adegoke, Abdulsalam Ribeiro, Jose M. C. Brown, Sidney Smith, Ryan C. Karim, Shahid Front Immunol Immunology INTRODUCTION: Blood-feeding arthropods rely on robust cellular and humoral immunity to control pathogen invasion and replication. Tick hemocytes produce factors that can facilitate or suppress microbial infection and pathogenesis. Despite the importance of hemocytes in regulating microbial infection, understanding of their basic biology and molecular mechanisms remains limited. METHODS: Here we combined histomorphology and functional analysis to identify five distinct phagocytic and non-phagocytic hemocyte populations circulating within the Gulf Coast tick Amblyomma maculatum. RESULTS AND DISCUSSION: Depletion of phagocytic hemocytes using clodronate liposomes revealed their function in eliminating bacterial infection. We provide the first direct evidence that an intracellular tick-borne pathogen, Rickettsia parkeri, infects phagocytic hemocytes in Am. maculatum to modify tick cellular immune responses. A hemocyte-specific RNA-seq dataset generated from hemocytes isolated from uninfected and R. parkeri-infected partially blood-fed ticks generated ~40,000 differentially regulated transcripts, >11,000 of which were immune genes. Silencing two differentially regulated phagocytic immune marker genes (nimrod B2 and eater-two Drosophila homologs), significantly reduced hemocyte phagocytosis. CONCLUSION: Together, these findings represent a significant step forward in understanding how hemocytes regulate microbial homeostasis and vector competence. Frontiers Media S.A. 2023-02-10 /pmc/articles/PMC9950277/ /pubmed/36845157 http://dx.doi.org/10.3389/fimmu.2023.1094326 Text en Copyright © 2023 Adegoke, Ribeiro, Brown, Smith and Karim https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Adegoke, Abdulsalam
Ribeiro, Jose M. C.
Brown, Sidney
Smith, Ryan C.
Karim, Shahid
Rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses
title Rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses
title_full Rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses
title_fullStr Rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses
title_full_unstemmed Rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses
title_short Rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses
title_sort rickettsia parkeri hijacks tick hemocytes to manipulate cellular and humoral transcriptional responses
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950277/
https://www.ncbi.nlm.nih.gov/pubmed/36845157
http://dx.doi.org/10.3389/fimmu.2023.1094326
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