A Brucella virulence factor targets macrophages to trigger B-cell proliferation

J Biol Chem. 2013 Jul 12;288(28):20208-16. doi: 10.1074/jbc.M113.453282. Epub 2013 May 29.

Abstract

Brucella spp. and Trypanosoma cruzi are two intracellular pathogens that have no evolutionary common origins but share a similar lifestyle as they establish chronic infections for which they have to circumvent the host immune response. Both pathogens have a virulence factor (prpA in Brucella and tcPrac in T. cruzi) that induces B-cell proliferation and promotes the establishment of the chronic phase of the infectious process. We show here that, even though PrpA promotes B-cell proliferation, it targets macrophages in vitro and is translocated to the cytoplasm during the intracellular replication phase. We observed that PrpA-treated macrophages induce the secretion of a soluble factor responsible for B-cell proliferation and identified nonmuscular myosin IIA (NMM-IIA) as a receptor required for binding and function of this virulence factor. Finally, we show that the Trypanosoma cruzi homologue of PrpA also targets macrophages to induce B-cell proliferation through the same receptor, indicating that this virulence strategy is conserved between a bacterial and a protozoan pathogen.

Keywords: Bacteria; Brucella; Lymphocyte; Macrophages; Myosin; Virulence Factors.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Isomerases / genetics
  • Amino Acid Isomerases / immunology
  • Amino Acid Isomerases / metabolism
  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / immunology*
  • Bacterial Proteins / metabolism
  • Blotting, Western
  • Brucella abortus / immunology
  • Brucella abortus / metabolism
  • Brucella abortus / pathogenicity
  • Cell Line
  • Cell Proliferation*
  • Cells, Cultured
  • Female
  • Macrophages / immunology*
  • Macrophages / parasitology
  • Macrophages / virology
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Fluorescence
  • Nonmuscle Myosin Type IIA / immunology
  • Nonmuscle Myosin Type IIA / metabolism
  • Protein Binding
  • Protozoan Proteins / genetics
  • Protozoan Proteins / immunology
  • Protozoan Proteins / metabolism
  • Spleen / cytology
  • Spleen / immunology
  • Spleen / metabolism
  • Trypanosoma cruzi / immunology
  • Trypanosoma cruzi / metabolism
  • Trypanosoma cruzi / pathogenicity
  • Virulence / immunology
  • Virulence Factors / genetics
  • Virulence Factors / immunology*
  • Virulence Factors / metabolism

Substances

  • Bacterial Proteins
  • Protozoan Proteins
  • Virulence Factors
  • Nonmuscle Myosin Type IIA
  • Amino Acid Isomerases