Neisseria meningitidis RTX protein FrpC induces high levels of serum antibodies during invasive disease: Polymorphism of frpC alleles and purification of recombinant FrpC

Citation
R. Osicka et al., Neisseria meningitidis RTX protein FrpC induces high levels of serum antibodies during invasive disease: Polymorphism of frpC alleles and purification of recombinant FrpC, INFEC IMMUN, 69(9), 2001, pp. 5509-5519
Citations number
23
Categorie Soggetti
Immunology
Journal title
INFECTION AND IMMUNITY
ISSN journal
00199567 → ACNP
Volume
69
Issue
9
Year of publication
2001
Pages
5509 - 5519
Database
ISI
SICI code
0019-9567(200109)69:9<5509:NMRPFI>2.0.ZU;2-5
Abstract
The Neisseria meningitidis FAM20 strain secretes two proteins of unknown fu nction, FrpA and FrpC, which contain typical RTX domains found in cytotoxin s 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 w as, however, poorly conserved. A single strain harbored an frpA allele of t he previously described size, while large insertions were detected in the f rpA 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 mas ses. High levels of both immunoglobulin G (IgG) and IgA class antibodies re cognizing recombinant FrpC were indeed detected in convalescent-phase sera of most patients at 2 and 4 to 5 weeks after the first symptoms of meningoc occal disease. These results show that FrpC-like proteins are produced and may play a role in invasive meningococcal infections.