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