Unknown

Dataset Information

0

Identification and characterization of a novel anti-inflammatory lipid isolated from Mycobacterium vaccae, a soil-derived bacterium with immunoregulatory and stress resilience properties.


ABSTRACT: RATIONALE:Mycobacterium vaccae (NCTC 11659) is an environmental saprophytic bacterium with anti-inflammatory, immunoregulatory, and stress resilience properties. Previous studies have shown that whole, heat-killed preparations of M. vaccae prevent allergic airway inflammation in a murine model of allergic asthma. Recent studies also demonstrate that immunization with M. vaccae prevents stress-induced exaggeration of proinflammatory cytokine secretion from mesenteric lymph node cells stimulated ex vivo, prevents stress-induced exaggeration of chemically induced colitis in a model of inflammatory bowel disease, and prevents stress-induced anxiety-like defensive behavioral responses. Furthermore, immunization with M. vaccae induces anti-inflammatory responses in the brain and prevents stress-induced exaggeration of microglial priming. However, the molecular mechanisms underlying anti-inflammatory effects of M. vaccae are not known. OBJECTIVES:Our objective was to identify and characterize novel anti-inflammatory molecules from M. vaccae NCTC 11659. METHODS:We have purified and identified a unique anti-inflammatory triglyceride, 1,2,3-tri [Z-10-hexadecenoyl] glycerol, from M. vaccae and evaluated its effects in freshly isolated murine peritoneal macrophages. RESULTS:The free fatty acid form of 1,2,3-tri [Z-10-hexadecenoyl] glycerol, 10(Z)-hexadecenoic acid, decreased lipopolysaccharide-stimulated secretion of the proinflammatory cytokine IL-6 ex vivo. Meanwhile, next-generation RNA sequencing revealed that pretreatment with 10(Z)-hexadecenoic acid upregulated genes associated with peroxisome proliferator-activated receptor alpha (PPAR?) signaling in lipopolysaccharide-stimulated macrophages, in association with a broad transcriptional repression of inflammatory markers. We confirmed using luciferase-based transfection assays that 10(Z)-hexadecenoic acid activated PPAR? signaling, but not PPAR?, PPAR?, or retinoic acid receptor (RAR) ? signaling. The effects of 10(Z)-hexadecenoic acid on lipopolysaccharide-stimulated secretion of IL-6 were prevented by PPAR? antagonists and absent in PPAR?-deficient mice. CONCLUSION:Future studies should evaluate the effects of 10(Z)-hexadecenoic acid on stress-induced exaggeration of peripheral inflammatory signaling, central neuroinflammatory signaling, and anxiety- and fear-related defensive behavioral responses.

SUBMITTER: Smith DG 

PROVIDER: S-EPMC6626661 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Identification and characterization of a novel anti-inflammatory lipid isolated from Mycobacterium vaccae, a soil-derived bacterium with immunoregulatory and stress resilience properties.

Smith David G DG   Martinelli Roberta R   Besra Gurdyal S GS   Illarionov Petr A PA   Szatmari Istvan I   Brazda Peter P   Allen Mary A MA   Xu Wenqing W   Wang Xiang X   Nagy László L   Dowell Robin D RD   Rook Graham A W GAW   Rosa Brunet Laura L   Lowry Christopher A CA  

Psychopharmacology 20190522 5


<h4>Rationale</h4>Mycobacterium vaccae (NCTC 11659) is an environmental saprophytic bacterium with anti-inflammatory, immunoregulatory, and stress resilience properties. Previous studies have shown that whole, heat-killed preparations of M. vaccae prevent allergic airway inflammation in a murine model of allergic asthma. Recent studies also demonstrate that immunization with M. vaccae prevents stress-induced exaggeration of proinflammatory cytokine secretion from mesenteric lymph node cells stim  ...[more]

Similar Datasets

| S-EPMC10049321 | biostudies-literature
| S-EPMC4896712 | biostudies-literature
| S-EPMC7813891 | biostudies-literature
| S-EPMC7749860 | biostudies-literature
| S-EPMC5587859 | biostudies-literature
| PRJEB282 | ENA
| S-EPMC8448689 | biostudies-literature
| S-EPMC5796941 | biostudies-literature
| S-EPMC91628 | biostudies-literature
| S-EPMC6129419 | biostudies-literature