Iron as a replacement for mucin in the establishment of meningococcal infection in mice
- PMID: 819118
- DOI: 10.1139/m76-120
Iron as a replacement for mucin in the establishment of meningococcal infection in mice
Abstract
Experimental infection of mice with Neisseria meningitidis was established by the injection of the bacteria suspended in solutions of various iron compounds. The progressive and fatal infection caused by otherwise non-lethal doses of organisms was produced in these mice after prior injection with ferrous sulphate or concomitant injection with iron sorbitol citrate or iron dextran. Reduction in LD50 to levels at least comparable to those obtained in the mucin challenge system was achieved; in some serogroups of N. meningitidis the LD50 was decreased more than a million fold. The results suggest that iron, which is a component of hog gastric mucin, is a factor involved in the establishment of meningococcal infection in mice. Use of iron compounds as injection medium offers a more advantageous system than mucin, since controlled administration of chemically defined substances occurs.
Similar articles
-
Iron acquisition and the pathogenesis of meningococcal and gonococcal disease.Med Microbiol Immunol. 1990;179(6):289-95. doi: 10.1007/BF00189607. Med Microbiol Immunol. 1990. PMID: 2128779 Review. No abstract available.
-
Mouse models of infection for Neisseria meningitidis B,2b and Haemophilus influenzae type b diseases.Can J Microbiol. 1986 Jan;32(1):33-7. doi: 10.1139/m86-007. Can J Microbiol. 1986. PMID: 3084050
-
Enhancement of Neisseria meningitidis infection in mice by addition of iron bound to transferrin.Infect Immun. 1981 Oct;34(1):120-5. doi: 10.1128/iai.34.1.120-125.1981. Infect Immun. 1981. PMID: 6795121 Free PMC article.
-
Experimental meningococcal infection in neonatal mice: differences in virulence between strains isolated from human cases and carriers.Can J Microbiol. 1984 Aug;30(8):1042-5. doi: 10.1139/m84-162. Can J Microbiol. 1984. PMID: 6437654
-
[Neisseria meningitidis. The pathophysiological role of lipopolysaccharides in association with meningococcal disease and septic shock].Ugeskr Laeger. 2008 Feb 4;170(6):421-6. Ugeskr Laeger. 2008. PMID: 18252172 Review. Danish.
Cited by
-
Iron acquisition and the pathogenesis of meningococcal and gonococcal disease.Med Microbiol Immunol. 1990;179(6):289-95. doi: 10.1007/BF00189607. Med Microbiol Immunol. 1990. PMID: 2128779 Review. No abstract available.
-
Protection against group B meningococcal disease: evaluation of serotype 2 protein vaccines in a mouse bacteremia model.Infect Immun. 1979 Oct;26(1):110-7. doi: 10.1128/iai.26.1.110-117.1979. Infect Immun. 1979. PMID: 115794 Free PMC article.
-
Protection against infection with Neisseria meningitidis group B serotype 2b by passive immunization with serotype-specific monoclonal antibody.Infect Immun. 1985 Nov;50(2):510-6. doi: 10.1128/iai.50.2.510-516.1985. Infect Immun. 1985. PMID: 3932211 Free PMC article.
-
Potential Mechanisms of Mucin-Enhanced Acinetobacter baumannii Virulence in the Mouse Model of Intraperitoneal Infection.Infect Immun. 2019 Oct 18;87(11):e00591-19. doi: 10.1128/IAI.00591-19. Print 2019 Nov. Infect Immun. 2019. PMID: 31405959 Free PMC article.
-
Iron and infection.Microbiol Rev. 1978 Mar;42(1):45-66. doi: 10.1128/mr.42.1.45-66.1978. Microbiol Rev. 1978. PMID: 379572 Free PMC article. Review. No abstract available.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources