Carried Meningococci in the Czech Republic: a Diverse Recombining Population
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Published in: | Journal of Clinical Microbiology Vol. 38; no. 12; pp. 4492 - 4498 |
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Population and evolutionary analyses of pathogenic bacteria are frequently hindered by sampling strategies that concentrate on isolates from patients with invasive disease. This is especially so for the gram-negative diplococcus Neisseria meningitidis, a cause of septicemia and meningitis worldwide. Meningococcal isolate collections almost exclusively comprise organisms originating from patients with invasive meningococcal disease, although this bacterium is a commensal inhabitant of the human nasopharynx and very rarely causes pathological effects. In the present study, molecular biology-based techniques were used to establish the genetic relationships of 156 meningococci isolated from healthy young adults in the Czech Republic during 1993. None of the individuals sampled had known links to patients with invasive disease. Multilocus sequence typing (MLST) showed that the bacterial population was highly diverse, comprising 71 different sequence types (STs) which were assigned to 34 distinct complexes or lineages. Three previously identified hyperinvasive lineages were present: 26 isolates (17%) belonged to the ST-41 complex (lineage 3); 4 (2.6%) belonged to the ST-11 (electrophoretic type [ET-37]) complex, and 1 (0.6%) belonged to the ST-32 (ET-5) complex. The data were consistent with the view that most nucleotide sequence diversity resulted from the reassortment of alleles by horizontal genetic exchange. Population and evolutionary analyses of pathogenic bacteria are frequently hindered by sampling strategies that concentrate on isolates from patients with invasive disease. This is especially so for the gram-negative diplococcus Neisseria meningitidis , a cause of septicemia and meningitis worldwide. Meningococcal isolate collections almost exclusively comprise organisms originating from patients with invasive meningococcal disease, although this bacterium is a commensal inhabitant of the human nasopharynx and very rarely causes pathological effects. In the present study, molecular biology-based techniques were used to establish the genetic relationships of 156 meningococci isolated from healthy young adults in the Czech Republic during 1993. None of the individuals sampled had known links to patients with invasive disease. Multilocus sequence typing (MLST) showed that the bacterial population was highly diverse, comprising 71 different sequence types (STs) which were assigned to 34 distinct complexes or lineages. Three previously identified hyperinvasive lineages were present: 26 isolates (17%) belonged to the ST-41 complex (lineage 3); 4 (2.6%) belonged to the ST-11 (electrophoretic type [ET-37]) complex, and 1 (0.6%) belonged to the ST-32 (ET-5) complex. The data were consistent with the view that most nucleotide sequence diversity resulted from the reassortment of alleles by horizontal genetic exchange. ABSTRACT Population and evolutionary analyses of pathogenic bacteria are frequently hindered by sampling strategies that concentrate on isolates from patients with invasive disease. This is especially so for the gram-negative diplococcus Neisseria meningitidis , a cause of septicemia and meningitis worldwide. Meningococcal isolate collections almost exclusively comprise organisms originating from patients with invasive meningococcal disease, although this bacterium is a commensal inhabitant of the human nasopharynx and very rarely causes pathological effects. In the present study, molecular biology-based techniques were used to establish the genetic relationships of 156 meningococci isolated from healthy young adults in the Czech Republic during 1993. None of the individuals sampled had known links to patients with invasive disease. Multilocus sequence typing (MLST) showed that the bacterial population was highly diverse, comprising 71 different sequence types (STs) which were assigned to 34 distinct complexes or lineages. Three previously identified hyperinvasive lineages were present: 26 isolates (17%) belonged to the ST-41 complex (lineage 3); 4 (2.6%) belonged to the ST-11 (electrophoretic type [ET-37]) complex, and 1 (0.6%) belonged to the ST-32 (ET-5) complex. The data were consistent with the view that most nucleotide sequence diversity resulted from the reassortment of alleles by horizontal genetic exchange. |
Author | M. Musilek S. Gupta P. Kriz E. J. Feil K. A. Jolley M. C. J. Maiden J. Kalmusova |
AuthorAffiliation | Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, Oxford, OX1 3FY, United Kingdom, 1 and National Reference Laboratory for Meningococcal Infections, National Institute of Public Health, Prague, Czech Republic 2 |
AuthorAffiliation_xml | – name: Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, Oxford, OX1 3FY, United Kingdom, 1 and National Reference Laboratory for Meningococcal Infections, National Institute of Public Health, Prague, Czech Republic 2 |
Author_xml | – sequence: 1 givenname: K. A surname: JOLLEY fullname: JOLLEY, K. A organization: Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, Oxford, OX1 3FY, United Kingdom – sequence: 2 givenname: J surname: KALMUSOVA fullname: KALMUSOVA, J organization: National Reference Laboratory for Meningococcal Infections, National Institute of Public Health, Prague, Czech Republic – sequence: 3 givenname: E. J surname: FEIL fullname: FEIL, E. J organization: Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, Oxford, OX1 3FY, United Kingdom – sequence: 4 givenname: S surname: GUPTA fullname: GUPTA, S organization: Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, Oxford, OX1 3FY, United Kingdom – sequence: 5 givenname: M surname: MUSILEK fullname: MUSILEK, M organization: National Reference Laboratory for Meningococcal Infections, National Institute of Public Health, Prague, Czech Republic – sequence: 6 givenname: P surname: KRIZ fullname: KRIZ, P organization: National Reference Laboratory for Meningococcal Infections, National Institute of Public Health, Prague, Czech Republic – sequence: 7 givenname: M. C. J surname: MAIDEN fullname: MAIDEN, M. C. J organization: Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, Oxford, OX1 3FY, United Kingdom |
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Keywords | Human Recombination Genetic variability Healthy subject Neisseriaceae Molecular epidemiology Bacteria Micrococcales Genotype Neisseria meningitidis Phylogeny Genetic transfer |
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Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 Corresponding author. Mailing address: Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, South Parks Road, Oxford, OX1 3FY, United Kingdom. Phone: 44 (1865) 271284. Fax: 44 (1865) 271284. E-mail: martin.maiden@zoo.ox.ac.uk. |
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CiteULike... Population and evolutionary analyses of pathogenic bacteria are frequently hindered by sampling strategies that concentrate on isolates from patients with... ABSTRACT Population and evolutionary analyses of pathogenic bacteria are frequently hindered by sampling strategies that concentrate on isolates from patients... |
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SubjectTerms | Adolescent Adult Bacteriology Biological and medical sciences Carrier State - microbiology Czech Rep Czech Republic Epidemiology Fundamental and applied biological sciences. Psychology Humans Microbiology Neisseria meningitidis Neisseria meningitidis - classification Neisseria meningitidis - genetics Serotyping |
Title | Carried Meningococci in the Czech Republic: a Diverse Recombining Population |
URI | http://jcm.asm.org/content/38/12/4492.abstract https://www.ncbi.nlm.nih.gov/pubmed/11101585 https://search.proquest.com/docview/18022700 https://search.proquest.com/docview/72440565 https://pubmed.ncbi.nlm.nih.gov/PMC87626 |
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