Long-term evolution of antigen repertoires among carried meningococci
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
087622
Wellcome Trust - United Kingdom
PubMed
20129981
PubMed Central
PMC2871849
DOI
10.1098/rspb.2009.2033
PII: rspb.2009.2033
Knihovny.cz E-zdroje
- MeSH
- alely MeSH
- antigeny bakteriální genetika imunologie MeSH
- bakteriální proteiny genetika MeSH
- biologické modely MeSH
- genetická variace MeSH
- lidé MeSH
- meningokoková meningitida mikrobiologie MeSH
- molekulární evoluce * MeSH
- Neisseria meningitidis genetika imunologie MeSH
- poriny genetika imunologie MeSH
- přenašečství mikrobiologie MeSH
- proteiny vnější bakteriální membrány genetika imunologie MeSH
- rekombinace genetická MeSH
- selekce (genetika) MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- antigeny bakteriální MeSH
- bakteriální proteiny MeSH
- FrpB protein, bacteria MeSH Prohlížeč
- porin protein, Neisseria MeSH Prohlížeč
- poriny MeSH
- proteiny vnější bakteriální membrány MeSH
Most studies of bacterial pathogen populations have been based on isolates collected from individuals with disease, or their contacts, over short time periods. For commensal organisms that occasionally cause disease, such as Neisseria meningitidis, however, the analysis of isolates from long-term asymptomatic carriage is necessary to elucidate their evolution and population structure. Here, we use mathematical models to analyse the structuring and dynamics of three vaccine-candidate antigens among carried meningococcal isolates collected over nearly 30 years in the Czech Republic. The data indicate that stable combinations of antigenic alleles were maintained over this time period despite evidence for high rates of recombination, consistent with theoretical models in which strong immune selection can maintain non-overlapping combinations of antigenic determinants in the presence of recombination. We contrast this antigenic structure with the overlapping but relatively stable combinations of the housekeeping genes observed among the same isolates, and use a novel network approach to visualize these relationships.
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