Genetic variants linked to the phenotypic outcome of invasive disease and carriage of Neisseria meningitidis Article Swipe
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· 2023
· Open Access
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· DOI: https://doi.org/10.1099/mgen.0.001124
Neisseria meningitidis can be a human commensal in the upper respiratory tract but is also capable of causing invasive diseases such as meningococcal meningitis and septicaemia. No specific genetic markers have been detected to distinguish carriage from disease isolates. The aim here was to find genetic traits that could be linked to phenotypic outcomes associated with carriage versus invasive N. meningitidis disease through a bacterial genome-wide association study (GWAS). In this study, invasive N. meningitidis isolates collected in Sweden ( n =103) and carriage isolates collected at Örebro University, Sweden ( n =213) 2018–2019 were analysed. The GWAS analysis, treeWAS , was applied to single-nucleotide polymorphisms (SNPs), genes and k-mers. One gene and one non-synonymous SNP were associated with invasive disease and seven genes and one non-synonymous SNP were associated with carriage isolates. The gene associated with invasive disease encodes a phage transposase (NEIS1048), and the associated invasive SNP glmU S373C encodes the enzyme N-acetylglucosamine 1-phosphate (GlcNAC 1-P) uridyltransferase. Of the genes associated with carriage isolates, a gene variant of porB encoding PorB class 3, the genes pilE / pilS and tspB have known functions. The SNP associated with carriage was fkbp D33N, encoding a FK506-binding protein (FKBP). K-mers from PilS , tbpB and tspB were found to be associated with carriage, while k-mers from mtrD and tbpA were associated with invasiveness. In the genes fkbp , glmU , PilC and pilE , k-mers were found that were associated with both carriage and invasive isolates, indicating that specific variations within these genes could play a role in invasiveness. The data presented here highlight genetic traits that are significantly associated with invasive or carriage N. meningitidis across the species population. These traits could prove essential to our understanding of the pathogenicity of N. meningitidis and could help to identify future vaccine targets.
Related Topics
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1099/mgen.0.001124
- OA Status
- gold
- Cited By
- 5
- References
- 75
- Related Works
- 10
- OpenAlex ID
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Raw OpenAlex JSON
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https://openalex.org/W4387893260Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.1099/mgen.0.001124Digital Object Identifier
- Title
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Genetic variants linked to the phenotypic outcome of invasive disease and carriage of Neisseria meningitidisWork title
- Type
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articleOpenAlex work type
- Language
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enPrimary language
- Publication year
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2023Year of publication
- Publication date
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2023-10-24Full publication date if available
- Authors
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Lorraine Eriksson, Thor Bech Johannesen, Bianca Stenmark, Susanne Jacobsson, Olof Säll, Sara Thulin Hedberg, Hans Fredlund, Marc Stegger, Paula MöllingList of authors in order
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https://doi.org/10.1099/mgen.0.001124Publisher landing page
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YesWhether a free full text is available
- OA status
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goldOpen access status per OpenAlex
- OA URL
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https://doi.org/10.1099/mgen.0.001124Direct OA link when available
- Concepts
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Neisseria meningitidis, Carriage, Biology, Single-nucleotide polymorphism, Genome-wide association study, SNP, Gene, Genetics, Neisseria, Meningococcal disease, Microbiology, Genotype, Medicine, Bacteria, PathologyTop concepts (fields/topics) attached by OpenAlex
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5Total citation count in OpenAlex
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2025: 3, 2024: 2Per-year citation counts (last 5 years)
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75Number of works referenced by this work
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10Other works algorithmically related by OpenAlex
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