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Macrophage immunomodulatory activity of extracellular polysaccharide (PEP) of Antarctic bacterium Pseudoaltermonas sp.S-5. | LitMetric

AI Article Synopsis

  • Antarctic bacteria, specifically Pseudoaltermonas sp.S-5, produce a polysaccharide (PEP) that could serve as a biological response modifier (BRM).
  • PEP consists of a mix of Mannose, Glucose, and Galactose in a specific ratio and has a molecular weight of 397 kDa, showing unique gel permeation characteristics.
  • Experimental studies revealed that PEP enhances macrophage activation and increases nitric oxide production while inducing the secretion of key inflammatory cytokines, indicating its potential as a BRM.

Article Abstract

Antarctic bacteria are a novel source of polysaccharides which might have potential applications as biological response modifiers (BRM). A heteropolysaccharide (PEP) was isolated from the liquid culture broth of the Antarctic bacterium Pseudoaltermonas sp.S-5. PEP contained Mannose, Glucose, and Galactose in a ratio of 4.8:50.9:44.3. High performance gel permeation chromatography of this polysaccharide showed a unimodal profile, and the molecular weight was 397 kDa. PEP was studied for its immunological effects on peritoneal macrophage cells. Morphological alterations were observed in macrophages treated with PEP. In vitro exposure to PEP increased the occurrence of activated macrophages and endocytic index in a dose-dependent pattern (2.5-50 μg/ml) after 24h of incubation, since increase of 136% and 133% was detected in the activated macrophage percentage and endocytic index respectively compared to untreated cells. At 200 μg/ml PEP caused a greatest increase (44.5%) in NO production when compared to the control group; however, this polysaccharide did not affect respiratory burst in the absence of PMA. Furthermore, it was demonstrated that PEP induces macrophages to secrete tumor necrosis factor (TNF)-α and interleukin (IL)-1β. These results suggested that PEP from Pseudoaltermonas sp.S-5 can be classified as a BRM.

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Source
http://dx.doi.org/10.1016/j.intimp.2012.02.009DOI Listing

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