Evidence map›Paper›PMID 36476389›Full record

ArticleGut pathogens2022

Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens.

Bilal Djeghout, Samuel J Bloomfield, Steven Rudder, Ngozi Elumogo, Alison E Mather, John Wain, Nicol Janecko

Open access · goldAbstract read
In one paragraph

Article in Gut pathogens, 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
1.8field-weighted citation impact, top 16% 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, 12 citations in OpenAlex.

  1. Article
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  5. HighEpidemiology and infection · 2024
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  6. Capturing clinically relevantMicrobial genomics · 2024
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  7. Article
  8. Evidence of potentialMicrobial genomics · 2023
    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

7 authors at 2 institutions in 1 country.

Bilal Djeghout *Quadram Institute Bioscience, Rosalind Franklin Rd, Norwich Research Park, Norwich, NR4 7UQ, UK.
Samuel J Bloomfield *Quadram Institute Bioscience, Rosalind Franklin Rd, Norwich Research Park, Norwich, NR4 7UQ, UK.
Steven RudderQuadram Institute Bioscience, Rosalind Franklin Rd, Norwich Research Park, Norwich, NR4 7UQ, UK.
Ngozi ElumogoQuadram Institute Bioscience, Rosalind Franklin Rd, Norwich Research Park, Norwich, NR4 7UQ, UK.
Alison E MatherQuadram Institute Bioscience, Rosalind Franklin Rd, Norwich Research Park, Norwich, NR4 7UQ, UK.
John WainQuadram Institute Bioscience, Rosalind Franklin Rd, Norwich Research Park, Norwich, NR4 7UQ, UK.
Nicol JaneckoQuadram Institute Bioscience, Rosalind Franklin Rd, Norwich Research Park, Norwich, NR4 7UQ, UK. nicol.janecko@quadram.ac.uk.
Quadram Institute · GBNorwich Research Park · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R012504/1
6 · The paper itself

Abstract

backgroundCampylobacter jejuni is a pervasive pathogen of major public health concern with a complex ecology requiring accurate and informative approaches to define pathogen diversity during outbreak investigations. Source attribution analysis may be confounded if the genetic diversity of a C. jejuni population is not adequately captured in a single specimen. The aim of this study was to determine the genomic diversity of C. jejuni within individual stool specimens from four campylobacteriosis patients. Direct plating and pre-culture filtration of one stool specimen per patient was used to culture multiple isolates per stool specimen. Whole genome sequencing and pangenome level analysis were used to investigate genomic diversity of C. jejuni within a patient.

resultsA total 92 C. jejuni isolates were recovered from four patients presenting with gastroenteritis. The number of isolates ranged from 13 to 30 per patient stool. Three patients yielded a single C. jejuni multilocus sequence type: ST-21 (n = 26, patient 4), ST-61 (n = 30, patient 1) and ST-2066 (n = 23, patient 2). Patient 3 was infected with two different sequence types [ST-51 (n = 12) and ST-354 (n = 1)]. Isolates belonging to the same sequence type from the same patient specimen shared 12-43 core non-recombinant SNPs and 0-20 frameshifts with each other, and the pangenomes of each sequence type consisted of 1406-1491 core genes and 231-264 accessory genes. However, neither the mutation nor the accessory genes were connected to a specific functional gene category.

conclusionsOur findings show that the C. jejuni population recovered from an individual patient's stool are genetically diverse even within the same ST and may have shared common ancestors before specimens were obtained. The population is unlikely to have evolved from a single isolate at the time point of initial patient infection, leading us to conclude that patients were likely infected with a heterogeneous C. jejuni population. The diversity of the C. jejuni population found within individual stool specimens can inform future methodological approaches to attribution and outbreak investigations.

Indexed as

CampylobacteriosisCampylobacter jejuniGenomic diversityPangenomics

Identifiers

PMID36476389
PMCPMC9727990
OpenAlexW4311284470

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.