Mary Wilson
Well-known member
Published 22 June 2023
DOI https://doi.org/10.1186/s12985-023-02104-0
Fellows, C.J., Simone-Finstrom, M., Anderson, T.D. et al.
Abstract
Declines in managed honey bee populations are multifactorial but closely associated with reduced virus immunocompetence and thus, mechanisms to enhance immune function are likely to reduce viral infection rates and increase colony viability. However, gaps in knowledge regarding physiological mechanisms or ‘druggable’ target sites to enhance bee immunocompetence has prevented therapeutics development to reduce virus infection. Our data bridge this knowledge gap by identifying ATP-sensitive inward rectifier potassium (K[SUB]ATP[/SUB]) channels as a pharmacologically tractable target for reducing virus-mediated mortality and viral replication in bees, as well as increasing an aspect of colony-level immunity. Bees infected with Israeli acute paralysis virus and provided K[SUB]ATP[/SUB] channel activators had similar mortality rates as uninfected bees. Furthermore, we show that generation of reactive oxygen species (ROS) and regulation of ROS concentrations through pharmacological activation of K[SUB]ATP[/SUB] channels can stimulate antiviral responses, highlighting a functional framework for physiological regulation of the bee immune system. Next, we tested the influence of pharmacological activation of K[SUB]ATP[/SUB] channels on infection of 6 viruses at the colony level in the field. Data strongly support that K[SUB]ATP[/SUB] channels are a field-relevant target site as colonies treated with pinacidil, a K[SUB]ATP[/SUB] channel activator, had reduced titers of seven bee-relevant viruses by up to 75-fold and reduced them to levels comparable to non-inoculated colonies. Together, these data indicate a functional linkage between K[SUB]ATP[/SUB]channels, ROS, and antiviral defense mechanisms in bees and define a toxicologically relevant pathway that can be used for novel therapeutics development to enhance bee health and colony sustainability in the field.
https://virologyj.biomedcentral.com/articles/10.1186/s12985-023-02104-0#citeas
DOI https://doi.org/10.1186/s12985-023-02104-0
Fellows, C.J., Simone-Finstrom, M., Anderson, T.D. et al.
Abstract
Declines in managed honey bee populations are multifactorial but closely associated with reduced virus immunocompetence and thus, mechanisms to enhance immune function are likely to reduce viral infection rates and increase colony viability. However, gaps in knowledge regarding physiological mechanisms or ‘druggable’ target sites to enhance bee immunocompetence has prevented therapeutics development to reduce virus infection. Our data bridge this knowledge gap by identifying ATP-sensitive inward rectifier potassium (K[SUB]ATP[/SUB]) channels as a pharmacologically tractable target for reducing virus-mediated mortality and viral replication in bees, as well as increasing an aspect of colony-level immunity. Bees infected with Israeli acute paralysis virus and provided K[SUB]ATP[/SUB] channel activators had similar mortality rates as uninfected bees. Furthermore, we show that generation of reactive oxygen species (ROS) and regulation of ROS concentrations through pharmacological activation of K[SUB]ATP[/SUB] channels can stimulate antiviral responses, highlighting a functional framework for physiological regulation of the bee immune system. Next, we tested the influence of pharmacological activation of K[SUB]ATP[/SUB] channels on infection of 6 viruses at the colony level in the field. Data strongly support that K[SUB]ATP[/SUB] channels are a field-relevant target site as colonies treated with pinacidil, a K[SUB]ATP[/SUB] channel activator, had reduced titers of seven bee-relevant viruses by up to 75-fold and reduced them to levels comparable to non-inoculated colonies. Together, these data indicate a functional linkage between K[SUB]ATP[/SUB]channels, ROS, and antiviral defense mechanisms in bees and define a toxicologically relevant pathway that can be used for novel therapeutics development to enhance bee health and colony sustainability in the field.
https://virologyj.biomedcentral.com/articles/10.1186/s12985-023-02104-0#citeas