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 |
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Authors: | Chen Yao-Shen Lin Hsi-Hsun Liu Pei-Ju Tsai Hsin-Ying Hsueh Pei-Tan Liu Hung-Yi Chen Ya-Lei |
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Affiliation: | a Division of Infectious Diseases, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwanb Department of Internal Medicine, National Yang-Ming University, Taipei, Taiwanc Graduate Institute of Environmental Education, National Kaohsiung Normal University, Kaohsiung, Taiwand Department of Infectious Disease, E-DA Hospital/I-Shou University, Kaohsiung, Taiwane Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwanf Department of Biotechnology, National Kaohsiung Normal University, Kaohsiung, Taiwan |
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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. |
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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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