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Infection and Immunity, August 1999, p. 3842-3846, Vol. 67, No. 8
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Antigenic Variation of the Class I Outer Membrane Protein in
Hyperendemic Neisseria meningitidis Strains in The
Netherlands
Aldert
Bart,1,*
Jacob
Dankert,1,2 and
Arie
van der
Ende1
Department of Medical Microbiology, Academic
Medical Center, University of Amsterdam, 1105 AZ
Amsterdam,1 and Reference Laboratory
for Bacterial Meningitis, University of Amsterdam/RIVM, 1100 DE
Amsterdam,2 The Netherlands
Received 17 December 1998/Returned for modification 9 February
1999/Accepted 10 May 1999
Since 1980, the number of cases of meningococcal disease caused by
serogroup B isolates with the P1.4 serosubtype has greatly increased in
The Netherlands. Screening for this serosubtype in the strain
collection of The Netherlands Reference Laboratory for Bacterial
Meningitis revealed that a low number of P1.4 strains had been present
in the Dutch meningococcal population since 1965. Genotyping of P1.4
strains showed that one cluster of strains, the hyperendemic lineage
III (D. A. Caugant et al., J. Infect. Dis. 162:867-874,
1990), is responsible for the increase since 1980. The diversity of the
porA genes, which encode the P1 protein on which
serosubtyping is based, was studied for genotypically different P1.4
strains and for lineage III strains expressing antigenically different
P1 proteins. Sequence analysis showed that porA genes of
genotypically distinct strains that express antigenically
indistinguishable P1 proteins are identical only in the
epitope-encoding region, suggesting that this region has spread through
the meningococcal population via horizontal gene transfer. Analysis of
porA genes of lineage III strains showed that both
horizontal gene transfer and partial deletion of the epitope-encoding
region may contribute to the different antigenic properties for P1 of
these strains. Phase variation of expression of the porA
gene seems to account for most nonreacting strains. These results show
that serosubtyping may underestimate the rise of a hyperendemic clone.
*
Corresponding author. Present address: Department of
Medical Microbiology, Vrije Universiteit, 1081 BT Amsterdam, The
Netherlands. Phone: (31-20) 4448308. Fax: (31-20) 4448318. E-mail:
a.bart.mm{at}med.vu.nl.
Infection and Immunity, August 1999, p. 3842-3846, Vol. 67, No. 8
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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