Quantitative analysis reveals internalisation of Cryptococcus neoformans by brain endothelial cells in vivo

Cell Microbiol. 2021 Jun;23(6):e13330. doi: 10.1111/cmi.13330. Epub 2021 Apr 7.

Abstract

Migration of Cryptococcus neoformans from the blood to the brain parenchyma is crucial to cause fatal meningoencephalitis. Although mechanisms involved in brain migration of C. neoformans have been widely studied in vitro, less is known about how the fungus crosses the blood-brain barrier (BBB) in vivo. This is in part because of the lack of an approach to quantitatively analyse the dynamics of fungal transmigration into the brain across the BBB in vivo. In this study, we report a novel approach to quantitatively analyse the interactions between C. neoformans and brain endothelial cells in a mouse model using flow cytometry. Using this system, we show that C. neoformans was internalised by brain endothelial cells in vivo and that mice infected with acapsular or heat-killed C. neoformans yeast cells displayed a lower frequency of brain endothelial cells containing the yeast cell compared to mice infected with wild-type or viable yeast cells, respectively. We further demonstrate that brain endothelial cells were invaded by serotype A strain (H99 strain) at a higher rate compared to serotype D strain (52D strain). Our experiments established that internalisation of C. neoformans by brain endothelial cells occurred in vivo and offered a powerful approach to quantitatively analyse fungal migration into the brain.

Keywords: Cryptococcus neoformans; brain migration; central nervous system infections; encephalitis; endothelial cells; flow cytometry; fungal dissemination; fungi; meningitis; opportunistic infections; transcytosis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Biological Transport
  • Blood-Brain Barrier / microbiology*
  • Brain / cytology
  • Brain / microbiology*
  • Cryptococcosis / microbiology
  • Cryptococcus neoformans / pathogenicity*
  • Disease Models, Animal
  • Endothelial Cells / microbiology*
  • Flow Cytometry / methods*
  • Green Fluorescent Proteins
  • Meningoencephalitis / microbiology
  • Mice
  • Mice, Inbred C57BL

Substances

  • Green Fluorescent Proteins