Evidence map›Paper›PMID 35467402›Full record

ArticleMicrobiology spectrum2022

Within-Host Genetic Variation in Neisseria gonorrhoeae over the Course of Infection.

Jolinda de Korne-Elenbaas, Sylvia M Bruisten, Henry J C de Vries, Alje P van Dam

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  5. Genetic diversity ofGut microbes · 2025
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  6. Local emergence and global evolution ofAntimicrobial agents and chemotherapy · 2024
    Article
  7. Increased clonality amongMicrobial genomics · 2023
    Article
  8. Article
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

4 authors at 2 institutions in 1 country.

Jolinda de Korne-ElenbaasDepartment of Infectious Diseases, Public Health Laboratory, Public Health Service of Amsterdamgrid.413928.5, Amsterdam, the Netherlands.ORCID 0000-0003-2787-6355
Sylvia M BruistenDepartment of Infectious Diseases, Public Health Laboratory, Public Health Service of Amsterdamgrid.413928.5, Amsterdam, the Netherlands.
Henry J C de VriesAmsterdam UMC, University of Amsterdam, Department of Dermatology, Amsterdam Institute for Infection and Immunity (AII), location Academic Medical Center, Amsterdam, the Netherlands.
Alje P van DamDepartment of Infectious Diseases, Public Health Laboratory, Public Health Service of Amsterdamgrid.413928.5, Amsterdam, the Netherlands.
Amsterdam UMC Location University of Amsterdam · NLAmsterdam Institute for Addiction Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Knowledge of within-host genetic variation informs studies on transmission dynamics. We studied within-host genetic variation in Neisseria gonorrhoeae over the course of infection and across different anatomical locations. Isolates were obtained during a clinical trial, and isolates from consecutive time points reflected persistent infections after treatment failure. We compared sequence types (STs) and recombination unfiltered- and filtered core genome single nucleotide polymorphism (SNP) distances in 65 within-host isolate pairs from the same anatomical location over time-obtained with a median interval of 7 days-and 65 isolate pairs across different anatomical locations at one time point. Isolates with different Multi-Locus Sequence Types (MLST), NG-Sequence Types for Antimicrobial Resistance (NG-STAR) and NG-Multi Antigen Sequence Types (NG-MAST) had a median of 1466 recombination filtered SNPs, whereas a median of 1 SNP was found between isolates with identical STs or a different NG-MAST only. The threshold for differentiating between strains was set at 10 recombination filtered SNPs, showing that isolates from persistent infections could have different NG-MASTs. Antibiotic pressure applied through treatment did not lead to an increase in genetic variation in specific genes or in overall extent of variation, compared to variation across anatomical locations. Instead, within-host genetic variation was proposedly driven by the host immune response, as it was concentrated in genomic regions encoding surface exposed proteins involved in host-microbe interaction. Ultimately, 15/228 (6.5%) between-host pairs contained a single strain, suggesting between-host transmission. However, patient reported data are needed to differentiate within-host persistence from between-host transmission.

Indexed as

GonorrheaNeisseria gonorrhoeaeAnti-Bacterial AgentsDrug Resistance, BacterialGenetic VariationHumansMicrobial Sensitivity TestsMultilocus Sequence TypingAnti-Bacterial Agentsbetween-hostgenetic variationNeisseria gonorrhoeaerecombinationSNP distancetransmissionwithin-host

Identifiers

PMID35467402
PMCPMC9241688
OpenAlexW4224441318

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.