4.7 Article

Investigating Virus-Host Interactions in Cultured Primary Honey Bee Cells

期刊

INSECTS
卷 12, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/insects12070653

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资金

  1. National Science Foundation CAREER Program [1651561]
  2. Agriculture and Food Research Initiative (USDA-NIFA-AFRI) program
  3. Montana Department of Agriculture Specialty Crop Block Grant Program [17SC003108]
  4. USDA-NIFA Hatch Multistate [NC-1173]
  5. Project Apis m.-Costco Scholar Fellowship Program for Honey Bee Health
  6. Direct For Biological Sciences
  7. Division Of Integrative Organismal Systems [1651561] Funding Source: National Science Foundation

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The study demonstrated virus-specific responses at the cellular level in honey bees, with potential antiviral mechanisms identified. Further research is needed to fully understand honey bee antiviral defenses. Cultured primary honey bee cells show promise in addressing this knowledge gap in future studies involving multiple viruses.
Honey bee (Apis mellifera) health is impacted by viral infections at the colony, individual bee, and cellular levels. To investigate honey bee antiviral defense mechanisms at the cellular level we further developed the use of cultured primary cells, derived from either larvae or pupae, and demonstrated that these cells could be infected with a panel of viruses, including common honey bee infecting viruses (i.e., sacbrood virus (SBV) and deformed wing virus (DWV)) and an insect model virus, Flock House virus (FHV). Virus abundances were quantified over the course of infection. The production of infectious virions in cultured honey bee pupal cells was demonstrated by determining that naive cells became infected after the transfer of deformed wing virus or Flock House virus from infected cell cultures. Initial characterization of the honey bee antiviral immune responses at the cellular level indicated that there were virus-specific responses, which included increased expression of bee antiviral protein-1 (GenBank: MF116383) in SBV-infected pupal cells and increased expression of argonaute-2 and dicer-like in FHV-infected hemocytes and pupal cells. Additional studies are required to further elucidate virus-specific honey bee antiviral defense mechanisms. The continued use of cultured primary honey bee cells for studies that involve multiple viruses will address this knowledge gap.

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