4.8 Article

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

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FRONTIERS IN IMMUNOLOGY
卷 14, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2023.1094326

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Hemocytes; clodronate liposome; phagocyte; Rickettsia parkeri; transcriptome; nimrod B2; eater; Amblyomma maculatum

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This study identified five distinct phagocytic and non-phagocytic hemocyte populations in ticks and showed that phagocytic hemocytes play a crucial role in eliminating bacterial infection. The research also revealed that an intracellular tick-borne pathogen modifies tick cellular immune responses by infecting phagocytic hemocytes.
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 similar to 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. ConclusionTogether, these findings represent a significant step forward in understanding how hemocytes regulate microbial homeostasis and vector competence.

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