Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1975 Feb;11(2):371-9.
doi: 10.1128/iai.11.2.371-379.1975.

Characterization of endotoxin from Fusobacterium necrophorun

Characterization of endotoxin from Fusobacterium necrophorun

M M Garcia et al. Infect Immun. 1975 Feb.

Abstract

Endotoxic lipopolysachharide (LPS) was obtained from phenol-water extraction of cell walls prepared from mass-cultivated Fusobacterium necrophorum. The LPS was relatively free of nucleic acids and low in protein, and constituted about 4% of the cell walls. Upon acid hydrolysis, some of the components detected were hexosamines (7.0%), neutral and reducing sugars (50.5%), heptose (6.4%), 2-keto-3-deoxyoctonate (0.8%), lipid A (21.0%), and phosphorus (1.7%). Under electron microscopy the LPS appeared mainly as ribbon-like trilaminar structures, and upon chemical treatment it displayed a behavior resembling that reported in certain enterobacterial LPS. The LPS was lethal to mice, 11-day-old chicken embryos, and rabbits. Endotoxicity in mice was enhanced at least 1,380-fold by the addition of 12.5 mug of actinomycin D. Induced tolerance to lethal effect of the endotoxin and rapidly acquired resistance to infection by F. necrophrum viable cells were also demonstrated in mice. The endotoxin produced both localized and generalized Shwartzman reactions as well as biphasic pyrogenic responses in rabbits. These results firmly establish the presence of a classical endotoxin in F. necrophorum, thus providing strong support to our recent suggestion that cell wall-associated components may contribute significantly to the pathogenicity of F. necrophorum.

PubMed Disclaimer

References

    1. Infect Immun. 1970 Sep;2(3):229-36 - PubMed
    1. J Infect Dis. 1966 Dec;116(5):529-36 - PubMed
    1. Methods Biochem Anal. 1955;2:279-311 - PubMed
    1. J Biol Chem. 1951 Nov;193(1):265-75 - PubMed
    1. Appl Microbiol. 1971 May;21(5):809-14 - PubMed

MeSH terms

LinkOut - more resources