Coxsackievirus B3 Activates Macrophages Independently of CAR-Mediated Viral Entry

Viruses. 2024 Sep 13;16(9):1456. doi: 10.3390/v16091456.

Abstract

Enteroviruses are a genus of small RNA viruses that are responsible for approximately one billion global infections annually. These infections range in severity from the common cold and flu-like symptoms to more severe diseases, such as viral myocarditis, pancreatitis, and neurological disorders, that continue to pose a global health challenge with limited therapeutic strategies currently available. In the current study, we sought to understand the interaction between coxsackievirus B3 (CVB3), which is a model enterovirus, and macrophage cells, as there is limited understanding of how this virus interacts with macrophage innate immune cells. Our study demonstrated that CVB3 can robustly activate macrophages without apparent viral replication in these cells. We also showed that myeloid cells lacked the viral entry receptor coxsackievirus and adenovirus receptor (CAR). However, the expression of exogenous CAR in RAW264.7 macrophages was unable to overcome the viral replication deficit. Interestingly, the CAR expression was associated with altered inflammatory responses during prolonged infection. Additionally, we identified the autophagy protein LC3 as a novel stimulus for macrophage activation. These findings provide new insights into the mechanisms of CVB3-induced macrophage activation and its implications for viral pathogenesis.

Keywords: LC3; coxsackievirus B3 (CVB3); coxsackievirus and adenovirus receptor (CAR); innate immunity; macrophages.

MeSH terms

  • Animals
  • Autophagy
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein* / genetics
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein* / metabolism
  • Coxsackievirus Infections / immunology
  • Coxsackievirus Infections / virology
  • Enterovirus B, Human* / physiology
  • Humans
  • Macrophage Activation*
  • Macrophages* / immunology
  • Macrophages* / virology
  • Mice
  • Mice, Inbred C57BL
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • RAW 264.7 Cells
  • Virus Internalization*
  • Virus Replication

Substances

  • CLMP protein, mouse
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein
  • Microtubule-Associated Proteins

Grants and funding

This work was supported by the Canadian Institutes of Health Research (PJT-173318 and PJT 186101) and Natural Sciences and Engineering Research Council (RGPIN-2022-02979) to H.L. Y.M. was the recipient of the CIHR Research Excellence, Diversity, Independence (REDI) Early Career Transition Award (CIHR AWD-026469) and a Postdoctoral Fellowship from Michael Smith Health Research BC and St. Paul’s Foundation, Centre for Heart Lung Innovation. A.B. was the recipient of a four-year PhD Fellowship from the University of British Columbia and the Laurel L. Watters Research Fellowship.