%0 Journal Article %1 kugelberg_influence_2010 %A Kugelberg, Elisabeth %A Gollan, Bridget %A Farrance, Christopher %A Bratcher, Holly %A Lucidarme, Jay %A Ibarz-Pavón, Ana Belén %A Maiden, Martin C. J. %A Borrow, Ray %A Tang, Christoph M. %D 2010 %J PLoS ONE %K imported %N 2 %P e9413 %R 10.1371/journal.pone.0009413 %T The Influence of IS1301 in the Capsule Biosynthesis Locus on Meningococcal Carriage and Disease %U http://dx.doi.org/10.1371/journal.pone.0009413 %V 5 %X Previously we have shown that insertion of IS1301 in the sia/ctr intergenic region (IGR) of serogroup C Neisseria meningitidis (MenC) isolates from Spain confers increased resistance against complement-mediated killing. Here we investigate the significance of IS1301 in the same location in N. meningitidis isolates from the UK. PCR and sequencing was used to screen a collection of more than 1500 meningococcal carriage and disease isolates from the UK for the presence of IS1301 in the IGR. IS1301 was not identified in the IGR among vaccine failure strains but was frequently found in serogroup B isolates (MenB) from clonal complex 269 (cc269). Almost all IS1301 insertions in cc269 were associated with novel polymorphisms, and did not change capsule expression or resistance to human complement. After excluding sequence types (STs) distant from the central genotype within cc269, there was no significant difference for the presence of IS1301 in the IGR of carriage isolates compared to disease isolates. Isolates with insertion of IS1301 in the IGR are not responsible for MenC disease in UK vaccine failures. Novel polymorphisms associated with IS1301 in the IGR of UK MenB isolates do not lead to the resistance phenotype seen for IS1301 in the IGR of MenC isolates.

@article{kugelberg_influence_2010, abstract = {Previously we have shown that insertion of {IS1301} in the sia/ctr intergenic region {(IGR)} of serogroup C Neisseria meningitidis {(MenC)} isolates from Spain confers increased resistance against complement-mediated killing. Here we investigate the significance of {IS1301} in the same location in N. meningitidis isolates from the {UK.} {PCR} and sequencing was used to screen a collection of more than 1500 meningococcal carriage and disease isolates from the {UK} for the presence of {IS1301} in the {IGR.} {IS1301} was not identified in the {IGR} among vaccine failure strains but was frequently found in serogroup B isolates {(MenB)} from clonal complex 269 (cc269). Almost all {IS1301} insertions in cc269 were associated with novel polymorphisms, and did not change capsule expression or resistance to human complement. After excluding sequence types {(STs)} distant from the central genotype within cc269, there was no significant difference for the presence of {IS1301} in the {IGR} of carriage isolates compared to disease isolates. Isolates with insertion of {IS1301} in the {IGR} are not responsible for {MenC} disease in {UK} vaccine failures. Novel polymorphisms associated with {IS1301} in the {IGR} of {UK} {MenB} isolates do not lead to the resistance phenotype seen for {IS1301} in the {IGR} of {MenC} isolates.}, added-at = {2011-03-11T10:05:34.000+0100}, author = {Kugelberg, Elisabeth and Gollan, Bridget and Farrance, Christopher and Bratcher, Holly and Lucidarme, Jay and {Ibarz-Pavón}, Ana Belén and Maiden, Martin C. J. and Borrow, Ray and Tang, Christoph M.}, biburl = {https://www.bibsonomy.org/bibtex/2c609939fd4b32423e1f116df6f80e257/jelias}, doi = {10.1371/journal.pone.0009413}, interhash = {0fbfa1e4d99dd139e7489fdfed3e8911}, intrahash = {c609939fd4b32423e1f116df6f80e257}, journal = {{PLoS} {ONE}}, keywords = {imported}, month = feb, number = 2, pages = {e9413}, timestamp = {2011-03-11T10:06:48.000+0100}, title = {The Influence of {IS1301} in the Capsule Biosynthesis Locus on Meningococcal Carriage and Disease}, url = {http://dx.doi.org/10.1371/journal.pone.0009413}, volume = 5, year = 2010 }