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Differential Distribution of Novel Restriction-Modification Systems in Clonal Lineages of Neisseria meningitidis
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ABSTRACT
Using representational difference analysis, we isolated novel meningococcal restriction-modification (R-M) systems.
Nme
BI, which is a homologue of the R-M system
Hga
I of
Pasteurella volantium
, was present in meningococci of the ET-5 complex and of lineage III.
Nme
AI was found in serogroup A, ET-37 complex, and cluster A4 meningococci.
Nme
DI was harbored by meningococci of the ET-37 complex and of cluster A4, but not by serogroup A meningococci. Two of the R-M systems,
Nme
BI and
Nme
DI, were located at homologous positions between the phenylalanyl-tRNA synthetase genes
pheS
and
pheT
, which appeared to be a preferential target for the insertion of foreign DNA in meningococci. The distribution of the three R-M systems was tested with 103 meningococcal strains comprising 49 sequence types. The vast majority of the strains had either
Nme
BI,
Nme
AI, or both
Nme
AI and
Nme
DI. Using cocultivation experiments, we could demonstrate that
Nme
BI, which was present in ET-5 complex meningococci, was responsible for a partial restriction of DNA transfer from meningococci of the ET-37 complex to meningococci of the ET-5 complex.
American Society for Microbiology
Title: Differential Distribution of Novel Restriction-Modification Systems in Clonal Lineages of
Neisseria meningitidis
Description:
ABSTRACT
Using representational difference analysis, we isolated novel meningococcal restriction-modification (R-M) systems.
Nme
BI, which is a homologue of the R-M system
Hga
I of
Pasteurella volantium
, was present in meningococci of the ET-5 complex and of lineage III.
Nme
AI was found in serogroup A, ET-37 complex, and cluster A4 meningococci.
Nme
DI was harbored by meningococci of the ET-37 complex and of cluster A4, but not by serogroup A meningococci.
Two of the R-M systems,
Nme
BI and
Nme
DI, were located at homologous positions between the phenylalanyl-tRNA synthetase genes
pheS
and
pheT
, which appeared to be a preferential target for the insertion of foreign DNA in meningococci.
The distribution of the three R-M systems was tested with 103 meningococcal strains comprising 49 sequence types.
The vast majority of the strains had either
Nme
BI,
Nme
AI, or both
Nme
AI and
Nme
DI.
Using cocultivation experiments, we could demonstrate that
Nme
BI, which was present in ET-5 complex meningococci, was responsible for a partial restriction of DNA transfer from meningococci of the ET-37 complex to meningococci of the ET-5 complex.
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