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Genetic variants linked to the phenotypic outcome of invasive disease and carriage of Neisseria meningitidis

Eriksson, Lorraine, 1990- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Laboratory Medicine, Faculty of Medicine and Health, Örebro University, Örebro, Sweden
Johannesen, Thor Bech (författare)
Department of Bacteria, Parasites and Fungi, Statens Serum Institut, Copenhagen, Denmark
Stenmark, Bianca, 1987- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Region Örebro län,Department of Laboratory Medicine
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Jacobsson, Susanne, 1974- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Region Örebro län,Department of Laboratory Medicine
Säll, Olof, 1980- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Region Örebro län,Department of Infectious Diseases
Hedberg, Sara Thulin (författare)
Department of Laboratory Medicine, Faculty of Medicine and Health, Örebro University, Örebro, Sweden
Fredlund, Hans (författare)
Department of Laboratory Medicine, Faculty of Medicine and Health, Örebro University, Örebro, Sweden
Stegger, Marc (författare)
Department of Laboratory Medicine, Faculty of Medicine and Health, Örebro University, Örebro, Sweden; Department of Bacteria, Parasites and Fungi, Statens Serum Institut, Copenhagen, Denmark
Mölling, Paula, 1971- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Region Örebro län,Department of Laboratory Medicine
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 (creator_code:org_t)
Microbiology Society, 2023
2023
Engelska.
Ingår i: Microbial Genomics. - : Microbiology Society. - 2057-5858. ; 9:10
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • 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.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

Nyckelord

Carriage
Genome-wide association study
Invasive meningococcal disease
Neisseria meningitidis

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