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Use of 3-hydroxy fatty acid concentrations in a murine air pouch infection model as a surrogate marker for LPS activity: a feasibility study using environmental Burkholderia cenocepacia isolates
Authors:Chen Yao-Shen  Lin Hsi-Hsun  Liu Pei-Ju  Tsai Hsin-Ying  Hsueh Pei-Tan  Liu Hung-Yi  Chen Ya-Lei
Affiliation:
  • a Division of Infectious Diseases, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan
  • b Department of Internal Medicine, National Yang-Ming University, Taipei, Taiwan
  • c Graduate Institute of Environmental Education, National Kaohsiung Normal University, Kaohsiung, Taiwan
  • d Department of Infectious Disease, E-DA Hospital/I-Shou University, Kaohsiung, Taiwan
  • e Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan
  • f Department of Biotechnology, National Kaohsiung Normal University, Kaohsiung, Taiwan
  • Abstract:Using a murine hypodermic air pouch infection model designed to mimic the release of bacterial products at physiological levels, 3-hydroxy fatty acid (3-OH FA) and endotoxin unit levels from Burkholderia cenocepacia isolates were assessed. The B. cenocepacia environmental isolates (n = 35) survived in the hypodermic air pouch but did not invade across the peritoneal epithelial layer during a 72-h infection. For all 35 strains, when the molar ratio of C14:0 3-OH FA to C16:0 3-OH FA in the air pouch fluid wash samples was between 1.4 and 2.5, the concentrations of C14:0 3-OH FA were correlated with the endotoxin unit levels. However, both surrogate markers exhibited different correlations to the inflammatory response. The linear regression coefficient was 0.4234 for C14:0 3-OH FA concentrations vs. NO productions, 0.223 for endotoxin unit levels vs. NO productions, 0.5008 for C14:0 3-OH FA concentrations vs. TNF-alpha productions and 0.2869 for endotoxin unit levels vs. TNF-alpha productions. Therefore, C14:0 3-OH FA concentrations, rather than endotoxin unit levels, acted as an immunostimulatory indicator for LPS in the B. cenocepacia isolates.
    Keywords:3-OH FA, 3-hydroxy fatty acid   C16:0 3-OH FA, 3-hydorxyhexadecanoic acid   C14:0 3-OH FA, 3-hydroxytetradecanoic acid   LPS, lipopolysaccharide   GC-MS, gas chromatography-mass spectrometry
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