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Ribeiro, J. M.

Publications and source records attributed to Ribeiro, J. M..

2 recordsLinked to original sources

Tick Innate Immune Responses to Hematophagy and Ehrlichia Infection at Single-Cell Resolution

Ticks rely on robust cellular and humoral immune responses to control microbial infection. However, several aspects of the ticks innate immune system remain uncharacterized, most notably that of the immune cells (called hemocytes), which are known to play a significant role in cellular and humoral responses toward microbes. Despite the importance of hemocytes in regulating microbial infection, our understanding of their basic biology and molecular mechanisms remains limited. Therefore, we believe that a more detailed understanding of the role of hemocytes in the interactions between ticks and tick-borne microbes is crucial to illuminate their function in vector competence and to help identify novel targets for developing new strategies to block tick-borne pathogen transmission. This study examined hemocytes from the lone star tick (Amblyomma americanum) at the transcriptomic level using the 10X genomics single-cell RNA sequencing platform to analyze hemocyte populations from unfed, partially blood-fed, and Ehrlichia chaffeensis-infected ticks. Our data exhibit the identification of twelve and nineteen distinct hemocyte populations, respectively, from uninfected and Ehrlichia-infected ticks. Our results show a significant increase of clusters representing granulocyte and oenocytoids populations with Ehrlichia infection. This work opens a new field of tick innate immunobiology to understand the role of hemocytes, particularly in response to prolonged blood-feeding (hematophagy) and tick-microbial interactions. SignificanceThe immune response of ticks plays a crucial role in their ability to survive and transmit pathogens. Hemocytes, the primary immune cells in arthropods, are key mediators of ticks immune defense and provide deep insights into immune responses to microbial infection. However, tick hemocytes cellular complexity and heterogeneity have posed challenges for comprehensive characterization. This study employed single-cell RNA sequencing (scRNA-seq) to profile tick hemocytes and elucidate their transcriptional diversity. We identified distinct subpopulations of hemocytes and characterized their unique gene expression profiles. We observed significant variation in immune-related gene expression between hemocyte subpopulations during hematophagy and in response to Ehrlichia infection, suggesting specialized functional roles. Our analysis revealed potential marker genes associated with specific hemocyte functions. Our study provides the first comprehensive single-cell atlas of tick hemocytes, shedding light on these cells molecular diversity and immune functions. The findings enhance our understanding of tick-host interactions and offer a step toward understanding arthropod immunobiology.

immunology↗

Integrative assessment of the transcriptome and virome of the poultry red mite Dermanyssus gallinae.

Dermanyssus gallinae is a blood-feeding mite that parasitises on wild birds and farmed poultry. The D. gallinae mite has a short life cycle of fewer than two weeks from the egg to an egg-laying female. The remarkably swift processing of blood, together with the capacity to blood-feed in most developmental stages, makes this mite a highly debilitating pest. We have constructed developmental stage-specific transcriptomes, through Illumina RNA-seq, to mine the repertoire of protein-encoding mRNA transcripts, products of which participate in key processes that ensure the success of blood digestion, rapid ontogeny, and immunity. As a result of high reproductive capacity, the prevalence of D. gallinae in egg-producing poultry farms globally causes significant economic losses. Acaricides that are used to limit the reproduction of D. gallinae mites target cys-loop ion channels, which are widely shared across the phylogeny of invertebrates. To catalogue a comprehensive list of potential invertebrate-specific ion channels, we have constructed and analysed an additional RNA-seq library of D. gallinae micro-dissected midguts, a tissue with direct exposure to host blood and potential anti-parasitics. We phylogenetically defined groups of cys-loop proteins and probed their sensitivity to selected acaricides. Ultimately, we have catalogued all assembled transcripts and their expression values in a hyper-linked excel sheet with available sequences of individual contigs. The transcriptomic data were complemented by mass-spectrometry (MS)-based metabolite identification and by viability assays using selected inhibitors applied either by microinjection or through artificial membrane feeding. Additionally, we have described the RNA-virome of D. gallinae and identified a novel virus dubbed Red Mite Quaranjavirus 1.

microbiology↗