Lipopolysaccharide (LPS) was extracted from six species of Bacteroides
by the phenol/water, petroleum/chloroform/phenol, and Triton/magnesiu
m methods. Yields and chemical analysis demonstrated that the products
were different. Biological activity (endotoxicity) was assessed by th
e limulus amebocyte lysate (LAL) assay, induction of tumor necrosis fa
ctor (TNF) from human mononuclear leukocytes, and a lethality model wi
th galactosamine-sensitized mice. Results showed that endotoxicity var
ied greatly depending on the species and the extraction method. LPS pr
epared by the phenol/water method was most endotoxic and that from Bac
teroides fragilis had the greatest activity, Compared with Escherichia
coli LPS, the phenol/water extract of B. fragilis was sevenfold more
active in the LAL assay and marginally less active (five- to seven-fol
d) in the bioassay for TNF induction. However, when B. fragilis LPS wa
s added to E. coli LPS, the induction of TNF was inhibited. In the mou
se model, B. fragilis LPS was 5,000-fold less toxic. If the gastrointe
stinal tract is the source of the endotoxin in patients with systemic
inflammatory response syndrome, then the obligately anaerobic Bacteroi
des species, which outnumber the facultative species such as E. coli b
y 1,000-fold, should not be overlooked.