Evidence map›Paper›PMID 36322504›Full record

ArticleThe Journal of infectious diseases2022

Genome-Wide Association Studies Identify an Association of Transferrin Binding Protein B Variation and Invasive Serogroup Y Meningococcal Disease in Older Adults.

Laura Maynard-Smith, Jeremy P Derrick, Ray Borrow, Jay Lucidarme, Martin C J Maiden, Robert S Heyderman, Odile B Harrison

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Laura Maynard-SmithDivision of Infection and Immunity, University College London, London, United Kingdom.
Jeremy P DerrickFaculty of Biology, Medicine, and Health, University of Manchester, Manchester, United Kingdom.
Ray BorrowMeningococcal Reference Unit, UK Health Security Agency, Manchester, United Kingdom.
Jay LucidarmeMeningococcal Reference Unit, UK Health Security Agency, Manchester, United Kingdom.
Martin C J MaidenDepartment of Biology, University of Oxford, Oxford, United Kingdom.
Robert S HeydermanDivision of Infection and Immunity, University College London, London, United Kingdom.
Odile B HarrisonDepartment of Biology, University of Oxford, Oxford, United Kingdom.
UK Health Security AgencyUniversity College London · GBUniversity of Oxford · GBUniversity of Manchester · GB

Funding

Department of Health ACF-2015-18-029Department of Health PR-OD-101720007Wellcome Trust 214374/Z/18/ZWellcome Trust 218205/Z/19/Z
6 · The paper itself

Abstract

backgroundNeisseria meningitidis serogroup Y, especially ST-23 clonal complex (Y:cc23), represents a larger proportion of invasive meningococcal disease (IMD) in older adults compared to younger individuals. This study explored the meningococcal genetic variation underlying this association.

methodsMaximum-likelihood phylogenies and the pangenome were analyzed using whole-genome sequence (WGS) data from 200 Y:cc23 isolates in the Neisseria PubMLST database. Genome-wide association studies (GWAS) were performed on WGS data from 250 Y:cc23 isolates from individuals with IMD aged ≥65 years versus < 65 years.

resultsY:cc23 meningococcal variants did not cluster by age group or disease phenotype in phylogenetic analyses. Pangenome comparisons found no differences in presence or absence of genes in IMD isolates from the different age groups. GWAS identified differences in nucleotide polymorphisms within the transferrin-binding protein B (tbpB) gene in isolates from individuals ≥65 years of age. TbpB structure modelling suggests these may impact binding of human transferrin.

conclusionsThese data suggest differential iron scavenging capacity amongst Y:cc23 meningococci isolated from older compared to younger patients. Iron acquisition is essential for many bacterial pathogens including the meningococcus. These polymorphisms may facilitate colonization, thereby increasing the risk of disease in vulnerable older people with altered nasopharyngeal microbiomes and nutritional status.

Indexed as

Meningococcal InfectionsMeningococcal VaccinesNeisseria meningitidisAgedGenome-Wide Association StudyHumansIronNeisseria meningitidis, Serogroup YPhylogenySerogroupTransferrin-Binding Protein BIronMeningococcal VaccinesTransferrin-Binding Protein Binvasive meningococcal diseasemeningococcal serogroup YNeisseria meningitidistransferrin binding protein B

Identifiers

PMID36322504
PMCPMC9748998
OpenAlexW4307935500

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.