1975
DOI: 10.1128/iai.11.4.609-616.1975
|View full text |Cite
|
Sign up to set email alerts
|

Biological characterization of Fusobacterium necrophorum. Cell fractions in preparation for toxin and immunization studies

Abstract: Fusobacterium necrophorum isolated from bovine liver abscesses was grown in bulk at 37 C for 24 h under a strict anaerobic atmosphere. Harvested washed cells were disrupted ultrasonically and fractionated by differential centrifugation into the intracellular (cytoplasm) and cell wall fractions. Both intact cells and cell fractions induced generalized cytopathic effect on primary pig kidney cultures and caused a variety of signs of illness and/or death of intraperitoneally injected mice. The intact cells, disru… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
6
0

Year Published

1977
1977
2006
2006

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 37 publications
(6 citation statements)
references
References 14 publications
0
6
0
Order By: Relevance
“…Preparation of cell walls and water-soluble and phenol-soluble lipopolysaccharide preparations. Cell walls were prepared according to the procedure of Garcia et al (8), using a sonicated preparation of F. nucleatum as described earlier. Water-soluble and phenol-soluble lipopolysaccharide preparations followed the procedure in Weir (25), using acetonedried whole cells.…”
Section: Methodsmentioning
confidence: 99%
“…Preparation of cell walls and water-soluble and phenol-soluble lipopolysaccharide preparations. Cell walls were prepared according to the procedure of Garcia et al (8), using a sonicated preparation of F. nucleatum as described earlier. Water-soluble and phenol-soluble lipopolysaccharide preparations followed the procedure in Weir (25), using acetonedried whole cells.…”
Section: Methodsmentioning
confidence: 99%
“…Several investigators have attempted to induce protective immunity against F. necrophorum by using a variety of antigenic components. Attempts to induce protective immunity have included the use of whole-cell cultures (Roberts, 1970;Abe et al, 1976a;Cameron and Fuls, 1977;Conlon et al, 1977;Smith et al, 1985Smith et al, , 1989, cytoplasmic fractions (Garcia et al, 1974(Garcia et al, , 1975aGarcia and McKay, 1978), lipopolysaccharides (Garcia et al, 1974(Garcia et al, , 1975aAbe et al, 1976a;Cameron and Fuls, 1977;Conlon et al, 1977;Smith et al, 1985Smith et al, , 1989, outer membrane proteins (Emery and Vaughn, 1986), leukotoxins (Roberts, 1970;Garcia et al, 1975a;Clarke et al, 1986;Emery et al, 1986a,b;Saginala et al, 1996a,b), and culture supernatants (Jensen et al, 1954c;Takeuchi et al, 1984;Saginala et al, 1996aSaginala et al, ,b, 1997. Efficacy has varied from nil to significant protection.…”
Section: Itemmentioning
confidence: 99%
“…F. necrophorum produces a leukotoxin (Beveridge, 1934;Roberts, 1967aRoberts, , 1967bGarcia et al, 1975a;Fales et al, 1977;Coyle-Dennis and Lauerman, 1978;Tan et al, 1994) which is active against a variety of white blood cells, especially polymorphonuclear neutrophiles, which could impede the local immune response at the site of infection. P. intermedia could add to tissue destruction with its ability to degrade lipid materials ) and the production of proteolytic enzymes such as dipeptidyl peptidases and cysteine proteases, the latter also involved in the breakdown of IgG (Slots, 1981;Jansen et al, 1995;Gazi et al, 1997).…”
Section: Pathogenicity Of F Necrophorum As a Trigger Organismmentioning
confidence: 99%