First Report of Capsule Replacement among Electrophoretic Type 37 Neisseria meningitidis Strains in Italy

MLST.

All 12 strains examined with the C:2a phenotype belonged to the sequence type 11 (ST11)/ET-37 complex, while the 13 C:2b isolates belonged to two different STs, the ST8/A4 cluster and the ST1860/ET-37 complex.

The first C:2b:P1.5/ST1860 strains were isolated in Italy during the year 2000 after a cluster of three cases among young adults, one of whom came from Argentina. These isolates are single-locus mutants of ST11 (gdh), whereas they differ for as many as five loci (aroE, fumC, gdh, pdhC, and pgm) when compared to the ST8 strains found among the majority of the C:2b meningococci isolated before the year 2000 in Italy. This new ST isolated among the Italian C:2b strains has been deposited in the Neisseria MLST database (http://neisseria.org/nm/typing/mlst/ ).

The three B:2a meningococci examined in this study belong to ST11, whereas the B:2b strain, isolated in the year 2002, belongs to ST1860.

PorA VR typing.

For PorA typing, only two regions of the porA gene, which include VR1, VR2, and VR3, were sequenced by following the procedures already described (13). To assign VR sequences to families and variants, the deduced amino acid sequences of VR1 and VR2 were submitted to the N. meningitidis PorA variable region database (http://neisseria.org/nm/typing/pora/ ).

All four serogroup B strains showed the same combination of variants as the serogroup C strain examined, in particular, variants 5, 2, and 36b for VR1, VR2, and VR3, respectively.

PFGE.

The infrequent-cutting restriction enzyme NheI (6) was used in PFGE to demonstrate the direct clonal origin of these four serogroup B strains from the serogroup C meningococci examined as controls.

The fingerprints, together with the dendrogram of similarity (Fig. 1), showed that the four serogroup B strains clustered with the serogroup C strains belonging to the ET-37 complex and were either closely related (differing by one to three bands) or indistinguishable from strain patterns of the A4 cluster. Serotype 2a/ET-37 strains belonged to a single clone, while the 2b strains were divided into two PFGE clones corresponding to the two different STs (ST8 and ST1860). The fingerprints of strains belonging to ST1860, either C:2b or B:2b, were closely related to those of ST11/ET-37, thus emphasizing their genetic similarity.

• Open in new tab
• Download powerpoint

FIG. 1.

PFGE patterns of 29 N. meningitidis strains. On the left is a dendrogram of similarity from cluster analysis generated by unweighted pair group method analysis, obtained by using Diversity Database software version 2 (Bio-Rad). On the right are PFGE-digitized profiles for each phenotype and corresponding ST. The four strains exhibiting capsule switch are indicated in boldface type and circled.

IS1655.

In order to acquire additional information on the relatedness between the ST1860/ET-37 and ST11/ET-37 strains, they were further analyzed for the presence of the insertion sequence (IS) 1655 in the orf2 gene. As recently demonstrated by Claus et al. (3), this IS is present only in ET-37 strains and may differentiate them from those belonging to the A4 cluster. In fact, Fig. 2 shows the presence of an amplicon of the expected size (about 1,460 bp) only between the ST11/ET-37 (lane 1) and ST1860/ET-37 (lane 2) strains.

• Open in new tab
• Download powerpoint

FIG. 2.

PCR results for the presence of IS1655 in the orf2 gene of the N. meningitidis strains examined. Lane M, molecular size markers, 100-bp DNA ladder (New England Biolabs). Lanes 1 and 2 show the presence of the amplicon of about 1,460 bp in one serogroup C strain representative of the ST11/ET-37 complex and in the B:2b:P1.5 switched ST1860/ET-37 strain, respectively. Lane 3 shows a shorter amplicon of about 390 bp in a strain representative of ST8/A4, which lacks the IS1655. Lane 4 shows the absence of the amplicon in a strain representative of ST44/lineage III.

The molecular techniques described in this report confirm the capsule replacement in the four serogroup B meningococci. In particular, switching occurred in three B:2a:P1.5,2 strains, belonging to the ST11/ET-37 complex already described by others (9, 14) as able to switch the capsule, and in one B:2b:P1.5 strain with ST1860, detected for the first time in this study. Alcalá et al. (1) reported that C:2b:P1.5 meningococci isolated in Spain from 1992 to 1999 belong to the ST11/ET-37 complex. In Italy, C:2b:P1.5 meningococci belonging to the ET-37 complex appeared only recently, since the first strain was isolated in the year 2000 and exhibited the new ST1860. All the C:2b:P1.5 strains isolated in previous years belonged instead to the ST8/A4 cluster.

MLST analysis of all C:2b:P1.5 strains isolated between 2000 and 2002 showed that ST1860/ET-37 accounted for about 50% of the total C:2b strains isolated in the country (data not shown). Therefore, it seems that this new ST is gradually displacing the ST8/A4 cluster and that it is responsible for invasive disease mainly in teenagers and young adults. The detection of the switched strains belonging to the ST1860/ET-37 complex deserves special attention to verify if this B variant is also as able to spread as its serogroup C progenitor.

Capsule switching has already been reported in Canada and in Spain after mass vaccination campaigns (2, 8, 14) and in the Czech Republic during an epidemic situation (9). Since in Italy the incidence of invasive meningococcal disease is low and no mass vaccination has been introduced, the presence of capsule-switched strains may be more easily attributable to a selection for competition between meningococcal genotypes in the nasopharynx than to vaccine-induced protective immunity.

However, the emergence of a natural escape mutant for the capsule, within the ET-37 complex known to harbor hypervirulent strains, should be carefully monitored in the future for its impact on the pattern of disease in Italy and elsewhere.