Meningococci of the ET-15 clone frequently cause clusters of invasive meningococcal disease (IMD) and are associated with a high case-fatality ratio. Timely typing of strains from outbreaks of IMD caused by this clone is hampered by the low variability of its surface antigens. We present a new Southern blot-based typing method for ET-15 meningococci based on the insertion element IS1301, which was present in all 70 ET-15 strains tested. Fingerprints were stable in vitro over a period of 100 days of cultivation on agar plates. The discriminatory power of IS1301 fingerprinting exceeded that of typing by serogrouping and antigen sequencing of the outer membrane proteins PorA and FetA, as determined by the analysis of 52 epidemiologically unrelated strains. In addition, the method provided conclusive results with regard to the comparison of strains from clusters of IMD. The investigation of insertion sites of IS1301 revealed several new intragenic insertions, among others, into open reading frames homologous to mafB and tspB. A previously described insertion in nadA was present in more than two-thirds of the strains analyzed, suggesting that NadA is probably an unreliable vaccine candidate for the prevention of ET-15 disease.
%0 Journal Article
%1 elias_is1301_2007
%A Elias, Johannes
%A Vogel, Ulrich
%D 2007
%J Journal of Clinical Microbiology
%K Bacterial Bacterial, Chain Data, Elements, Fingerprinting, Fragment Humans, Infections, Length Meningococcal Molecular Neisseria Polymerase Polymorphism, Proteins, Reaction, Restriction Sequence Techniques, Transposable Typing ag_vogel meningitidis, {DNA,} {DNA}
%N 1
%P 159--167
%R 10.1128/JCM.01322-06
%T IS1301 fingerprint analysis of Neisseria meningitidis strains belonging to the ET-15 clone
%U http://www.ncbi.nlm.nih.gov/pubmed/17093016
%V 45
%X Meningococci of the ET-15 clone frequently cause clusters of invasive meningococcal disease (IMD) and are associated with a high case-fatality ratio. Timely typing of strains from outbreaks of IMD caused by this clone is hampered by the low variability of its surface antigens. We present a new Southern blot-based typing method for ET-15 meningococci based on the insertion element IS1301, which was present in all 70 ET-15 strains tested. Fingerprints were stable in vitro over a period of 100 days of cultivation on agar plates. The discriminatory power of IS1301 fingerprinting exceeded that of typing by serogrouping and antigen sequencing of the outer membrane proteins PorA and FetA, as determined by the analysis of 52 epidemiologically unrelated strains. In addition, the method provided conclusive results with regard to the comparison of strains from clusters of IMD. The investigation of insertion sites of IS1301 revealed several new intragenic insertions, among others, into open reading frames homologous to mafB and tspB. A previously described insertion in nadA was present in more than two-thirds of the strains analyzed, suggesting that NadA is probably an unreliable vaccine candidate for the prevention of ET-15 disease.
@article{elias_is1301_2007,
abstract = {Meningococci of the {ET-15} clone frequently cause clusters of invasive meningococcal disease {(IMD)} and are associated with a high case-fatality ratio. Timely typing of strains from outbreaks of {IMD} caused by this clone is hampered by the low variability of its surface antigens. We present a new Southern blot-based typing method for {ET-15} meningococci based on the insertion element {IS1301,} which was present in all 70 {ET-15} strains tested. Fingerprints were stable in vitro over a period of 100 days of cultivation on agar plates. The discriminatory power of {IS1301} fingerprinting exceeded that of typing by serogrouping and antigen sequencing of the outer membrane proteins {PorA} and {FetA,} as determined by the analysis of 52 epidemiologically unrelated strains. In addition, the method provided conclusive results with regard to the comparison of strains from clusters of {IMD.} The investigation of insertion sites of {IS1301} revealed several new intragenic insertions, among others, into open reading frames homologous to {mafB} and {tspB.} A previously described insertion in {nadA} was present in more than two-thirds of the strains analyzed, suggesting that {NadA} is probably an unreliable vaccine candidate for the prevention of {ET-15} disease.},
added-at = {2011-04-07T15:44:20.000+0200},
author = {Elias, Johannes and Vogel, Ulrich},
biburl = {https://www.bibsonomy.org/bibtex/208e2be4485e424797644ba0fa0c2fc1d/hymi},
doi = {10.1128/JCM.01322-06},
interhash = {1bdc56725062e5857d645162c25b45db},
intrahash = {08e2be4485e424797644ba0fa0c2fc1d},
issn = {0095-1137},
journal = {Journal of Clinical Microbiology},
keywords = {Bacterial Bacterial, Chain Data, Elements, Fingerprinting, Fragment Humans, Infections, Length Meningococcal Molecular Neisseria Polymerase Polymorphism, Proteins, Reaction, Restriction Sequence Techniques, Transposable Typing ag_vogel meningitidis, {DNA,} {DNA}},
month = jan,
note = {{PMID:} 17093016},
number = 1,
pages = {159--167},
timestamp = {2011-04-07T16:38:33.000+0200},
title = {{IS1301} fingerprint analysis of Neisseria meningitidis strains belonging to the {ET-15} clone},
url = {http://www.ncbi.nlm.nih.gov/pubmed/17093016},
volume = 45,
year = 2007
}