Modification of the structure and activity of lipid A in Yersinia pestis lipopolysaccharide by growth temperature

Infect Immun. 2002 Aug;70(8):4092-8. doi: 10.1128/IAI.70.8.4092-4098.2002.

Abstract

Yersinia pestis strain Yreka was grown at 27 or 37 degrees C, and the lipid A structures (lipid A-27 degrees C and lipid A-37 degrees C) of the respective lipopolysaccharides (LPS) were investigated by matrix-assisted laser desorption ionization-time-of-flight (MALDI-TOF) mass spectrometry. Lipid A-27 degrees C consisted of a mixture of tri-acyl, tetra-acyl, penta-acyl, and hexa-acyl lipid A's, of which tetra-acyl lipid A was most abundant. Lipid A-37 degrees C consisted predominantly of tri- and tetra-acylated molecules, with only small amounts of penta-acyl lipid A; no hexa-acyl lipid A was detected. Furthermore, the amount of 4-amino-arabinose was substantially higher in lipid A-27 degrees C than in lipid A-37 degrees C. By use of mouse and human macrophage cell lines, the biological activities of the LPS and lipid A preparations were measured via their abilities to induce production of tumor necrosis factor alpha (TNF-alpha). In both cell lines the LPS and the lipid A from bacteria grown at 27 degrees C were stronger inducers of TNF-alpha than those from bacteria grown at 37 degrees C. However, the difference in activity was more prominent in human macrophage cells. These results suggest that in order to reduce the activation of human macrophages, it may be more advantageous for Y. pestis to produce less-acylated lipid A at 37 degrees C.

MeSH terms

  • Animals
  • Carbohydrate Conformation
  • Cell Line
  • Humans
  • Lipid A / chemistry
  • Lipid A / immunology*
  • Lipopolysaccharides / chemistry
  • Lipopolysaccharides / immunology
  • Macrophages / immunology
  • Mice
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Structure-Activity Relationship
  • Temperature
  • Tumor Necrosis Factor-alpha / biosynthesis
  • U937 Cells
  • Yersinia pestis / growth & development
  • Yersinia pestis / immunology*

Substances

  • Lipid A
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha