Lack of intracellular replication of M. tuberculosis and M. bovis BCG caused by delivering bacilli to lysosomes in murine brain microvascular endothelial cells

Oncotarget. 2015 Oct 20;6(32):32456-67. doi: 10.18632/oncotarget.5932.

Abstract

Invasion and traversal of the blood-brain barrier (BBB) by Mycobacterium tuberculosis cause meningeal tuberculosis (TB) in the central nervous system (CNS). Meningeal TB is a serious, often fatal disease that disproportionately affects young children. The mechanisms involved in CNS invasion by M. tuberculosis bacilli are poorly understood. In this study, we microscopically examined endosomal trafficking and measured survival of M. tuberculosis and M. bovis Bacille Calmette-Guérin (BCG) bacilli in murine brain microvascular endothelial cells (BMECs). The results show that both species internalize but do not replicate in BMECs in the absence of a cytotoxic response. Confocal microscopy indicates that bacilli-containing vacuoles are associated with the early endosomal marker, Rab5, late endosomal marker, Rab7, and lysosomal marker, LAMP2, suggesting that bacilli-containing endosomes mature into endolysosomes in BMECs. Our data also show that a subset of intracellular M. tuberculosis, but not BCG bacilli, escape into the cytoplasm to avoid rapid lysosomal killing. However, the intracellular mycobacteria examined cannot spread cell-to-cell in BMECs. Taken together, these data show that with the exception of the small terminal cytoplasmic population of bacilli, M. tuberculosis does not modulate intracellular trafficking in BMECs as occurs in macrophages and lung epithelial and endothelial cells.

Keywords: Immune response; Immunity; Immunology and Microbiology Section; cell-to-cell spread; cytotoxicity; endothelial cells; mycobacterium; trafficking.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / blood supply*
  • Capillary Permeability*
  • Cell Line
  • Endothelial Cells / metabolism
  • Endothelial Cells / microbiology*
  • Endothelial Cells / ultrastructure
  • Lysosomal-Associated Membrane Protein 2 / metabolism
  • Lysosomes / metabolism
  • Lysosomes / microbiology*
  • Lysosomes / ultrastructure
  • Mice
  • Microbial Viability
  • Microscopy, Confocal
  • Microscopy, Electron, Transmission
  • Microvessels / metabolism
  • Microvessels / microbiology*
  • Microvessels / ultrastructure
  • Mycobacterium bovis / growth & development*
  • Mycobacterium bovis / pathogenicity
  • Mycobacterium tuberculosis / growth & development*
  • Mycobacterium tuberculosis / pathogenicity
  • Time Factors
  • Virulence
  • rab GTP-Binding Proteins / metabolism
  • rab5 GTP-Binding Proteins / metabolism
  • rab7 GTP-Binding Proteins

Substances

  • Lysosomal-Associated Membrane Protein 2
  • rab7 GTP-Binding Proteins
  • rab7 GTP-binding proteins, mouse
  • rab GTP-Binding Proteins
  • rab5 GTP-Binding Proteins