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Review
. 2006 Mar 24:5:7.
doi: 10.1186/1476-069X-5-7.

Cyanobacterial lipopolysaccharides and human health - a review

Affiliations
Review

Cyanobacterial lipopolysaccharides and human health - a review

Ian Stewart et al. Environ Health. .

Abstract

Cyanobacterial lipopolysaccharide/s (LPS) are frequently cited in the cyanobacteria literature as toxins responsible for a variety of heath effects in humans, from skin rashes to gastrointestinal, respiratory and allergic reactions. The attribution of toxic properties to cyanobacterial LPS dates from the 1970s, when it was thought that lipid A, the toxic moiety of LPS, was structurally and functionally conserved across all Gram-negative bacteria. However, more recent research has shown that this is not the case, and lipid A structures are now known to be very different, expressing properties ranging from LPS agonists, through weak endotoxicity to LPS antagonists. Although cyanobacterial LPS is widely cited as a putative toxin, most of the small number of formal research reports describe cyanobacterial LPS as weakly toxic compared to LPS from the Enterobacteriaceae. We systematically reviewed the literature on cyanobacterial LPS, and also examined the much lager body of literature relating to heterotrophic bacterial LPS and the atypical lipid A structures of some photosynthetic bacteria. While the literature on the biological activity of heterotrophic bacterial LPS is overwhelmingly large and therefore difficult to review for the purposes of exclusion, we were unable to find a convincing body of evidence to suggest that heterotrophic bacterial LPS, in the absence of other virulence factors, is responsible for acute gastrointestinal, dermatological or allergic reactions via natural exposure routes in humans. There is a danger that initial speculation about cyanobacterial LPS may evolve into orthodoxy without basis in research findings. No cyanobacterial lipid A structures have been described and published to date, so a recommendation is made that cyanobacteriologists should not continue to attribute such a diverse range of clinical symptoms to cyanobacterial LPS without research confirmation.

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Figures

Figure 1
Figure 1
Schematic of the basic LPS structure. The O-specific polysaccharide is the unit that is most exposed to the external environment and so manifests the greatest structural diversity; lipid A is the most conserved structure.
Figure 2
Figure 2
Primary lipid A structures. E. coli has a bis-phosphorylated diglucosamine backbone with six amide and ester linked fatty acyl chains. The non-endotoxic (and LPS-antagonist) R. sphaeroides lipid A has an identical disaccharide backbone but has five acyl residues, shorter ester-linked primary acyl chains and an unsaturated acyl group. B. fragilis, which expresses low endotoxic potential, has a mono-phosphorylated backbone and five acyl chains with longer chain lengths than those seen in E. coli. Lipid A from Chromobacterium violaceum, like R. sphaeroides, is an LPS antagonist. Figures adapted from: Weintraub et al [91], Rietschel et al [78] and Takayama & Qureshi [84].

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