Ex vivo characterization of the circulating hemocytes of bed bugs and their responses to bacterial exposure

[Display omitted] •At least four types of hemocytes circulate in the hemolymph of bed bugs.•Circulating hemocytes are capable of phagocytosis and degranulation.•Circulating hemocytes increase in size and exhibit DNA replication when stimulated.•Circulating hemocytes express Toll/IMD signaling pathwa...

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Veröffentlicht in:Journal of invertebrate pathology 2020-07, Vol.174, p.107422-107422, Article 107422
Hauptverfasser: Potts, Rashaun, King, Jonas G., Pietri, Jose E.
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Sprache:eng
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Zusammenfassung:[Display omitted] •At least four types of hemocytes circulate in the hemolymph of bed bugs.•Circulating hemocytes are capable of phagocytosis and degranulation.•Circulating hemocytes increase in size and exhibit DNA replication when stimulated.•Circulating hemocytes express Toll/IMD signaling pathway components and known antimicrobial effectors. Bed bugs (Cimex spp.) are urban pests of global importance. Knowledge of the immune system of bed bugs has implications for understanding their susceptibility to biological control agents, their potential to transmit human pathogens, and the basic comparative immunology of insects. Nonetheless, the immunological repertoire of the family Cimicidae remains poorly characterized. Here, we use microscopy, flow cytometry, and RNA sequencing to provide a basal characterization of the circulating hemocytes of the common bed bug, Cimex lectularius. We also examine the responses of these specialized cells to E. coli exposure using the same techniques. Our results show that circulating hemocytes are comprised of at least four morphologically distinct cell types that are capable of phagocytosis, undergo degranulation, and exhibit additional markers of activation following stimulation, including size shift and DNA replication. Furthermore, transcriptomic profiling reveals expression of predicted Toll/IMD signaling pathway components, antimicrobial effectors and other potentially immunoresponsive genes in these cells. Together, our data demonstrate the conservation of several canonical cellular immune responses in the common bed bug and provide a foundation for additional mechanistic immunological studies with specific pathogens of interest.
ISSN:0022-2011
1096-0805
1096-0805
DOI:10.1016/j.jip.2020.107422