Neisseria meningitidis RTX protein FrpC induces high levels of serum antibodies during invasive disease: polymorphism of frpC alleles and purification of recombinant FrpC
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
11500424
PubMed Central
PMC98664
DOI
10.1128/iai.69.9.5509-5519.2001
Knihovny.cz E-resources
- MeSH
- Alleles MeSH
- Bacterial Proteins genetics immunology isolation & purification metabolism MeSH
- Cytotoxins * MeSH
- Cloning, Molecular MeSH
- Humans MeSH
- Membrane Proteins * MeSH
- Meningococcal Infections immunology microbiology MeSH
- Molecular Sequence Data MeSH
- Neisseria meningitidis immunology metabolism MeSH
- Periplasmic Binding Proteins MeSH
- Polymorphism, Genetic genetics MeSH
- Iron-Binding Proteins MeSH
- Bacterial Outer Membrane Proteins MeSH
- Antibodies, Bacterial blood MeSH
- Recombinant Proteins genetics isolation & purification metabolism MeSH
- Amino Acid Sequence MeSH
- Sequence Analysis, DNA MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bacterial Proteins MeSH
- Cytotoxins * MeSH
- frpC protein, Neisseria meningitidis MeSH Browser
- Membrane Proteins * MeSH
- Periplasmic Binding Proteins MeSH
- Iron-Binding Proteins MeSH
- Bacterial Outer Membrane Proteins MeSH
- Antibodies, Bacterial MeSH
- Recombinant Proteins MeSH
The Neisseria meningitidis FAM20 strain secretes two proteins of unknown function, FrpA and FrpC, which contain typical RTX domains found in cytotoxins from other gram-negative pathogens. To evaluate whether the Frp proteins could be involved in meningococcal virulence, 65 isolates of all serogroups were screened by PCR for the presence of both frp genes. The frpA allele was, however, poorly conserved. A single strain harbored an frpA allele of the previously described size, while large insertions were detected in the frpA loci of 22 isolates (34%), and the 42 remaining isolates (65%) did not contain frpA at all. In contrast, frpC alleles, albeit of variable length, were detected in all invasive and most carrier strains. This suggests that meningococci may produce a family of FrpC proteins of various molecular masses. High levels of both immunoglobulin G (IgG) and IgA class antibodies recognizing recombinant FrpC were indeed detected in convalescent-phase sera of most patients at 2 and 4 to 5 weeks after the first symptoms of meningococcal disease. These results show that FrpC-like proteins are produced and may play a role in invasive meningococcal infections.
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