1977
DOI: 10.1128/iai.15.2.510-517.1977
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Evaluation of experimentally induced Fusobacterium necrophorum infections in mice

Abstract: Two strains of mice, Swiss Webster and DBA/2Cr, were injected intraperitoneally or intravenously with varying dosages of Fusobacterium necrophorum. The ability to eliminate the infection was assessed by quantitative enumeration of the organisms present in the blood, liver, and spleen. Three-to 4-week-old DBA/2Cr mice were highly resistant to both routes of injection. The intraperitoneal injection of older mice failed to demonstrate a dose-effect relationship whereas an intravenous injection of as few as i01 ce… Show more

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Cited by 13 publications
(2 citation statements)
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“…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%
“…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%
“…necrophorum type B strains has been reported to be 5 x 106 CFU per mouse (WENZEL et al 1983)) considerably lower than that obtained with a, human type A strain. I n studies using a bovine strain of Fusobacterium, CONLON et al (1977) found a dose of 4 x lo6 was necessary to produce abscesses in liver, kidney and spleen. Mice were protected from abscess formation when they were pretreated with lipopolysaccharide isolated from the homologous bacterial strain.…”
Section: Discussionmentioning
confidence: 99%