Evidence map›Paper›PMID 26305157›Full record

ArticleThe ISME journal2016

Rapid host switching in generalist Campylobacter strains erodes the signal for tracing human infections.

Bethany L Dearlove, Alison J Cody, Ben Pascoe, Guillaume Méric, Daniel J Wilson, Samuel K Sheppard

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
19.5field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 145 citations in OpenAlex.

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  18. Review
  19. Article
  20. Article

31 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 1 country.

Bethany L DearloveNuffield Department of Medicine, Experimental Medicine Division, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-3653-4592
Alison J CodyDepartment of Zoology, University of Oxford, Oxford, UK.
Ben PascoeCollege of Medicine, Institute of Life Science, Swansea University, Swansea, UK.ORCID http://orcid.org/0000-0001-6376-5121
Guillaume MéricCollege of Medicine, Institute of Life Science, Swansea University, Swansea, UK.
Daniel J WilsonNuffield Department of Medicine, Experimental Medicine Division, University of Oxford, Oxford, UK.
Samuel K SheppardDepartment of Zoology, University of Oxford, Oxford, UK.
Swansea University · GBUniversity of Oxford · GBCentre for Human Genetics · GB

Funding

Biotechnology and Biological Sciences Research Council MR/L015080/1Department of Health G0800778Medical Research Council G0800778Medical Research Council MR/J013862/1Medical Research Council MR/L015080/1Wellcome Trust 087646Wellcome Trust 087646/Z/08/ZWellcome Trust 101237Wellcome Trust 101237/Z/13/Z
6 · The paper itself

Abstract

Campylobacter jejuni and Campylobacter coli are the biggest causes of bacterial gastroenteritis in the developed world, with human infections typically arising from zoonotic transmission associated with infected meat. Because Campylobacter is not thought to survive well outside the gut, host-associated populations are genetically isolated to varying degrees. Therefore, the likely origin of most strains can be determined by host-associated variation in the genome. This is instructive for characterizing the source of human infection. However, some common strains, notably isolates belonging to the ST-21, ST-45 and ST-828 clonal complexes, appear to have broad host ranges, hindering source attribution. Here whole-genome sequencing has the potential to reveal fine-scale genetic structure associated with host specificity. We found that rates of zoonotic transmission among animal host species in these clonal complexes were so high that the signal of host association is all but obliterated, estimating one zoonotic transmission event every 1.6, 1.8 and 12 years in the ST-21, ST-45 and ST828 complexes, respectively. We attributed 89% of clinical cases to a chicken source, 10% to cattle and 1% to pig. Our results reveal that common strains of C. jejuni and C. coli infectious to humans are adapted to a generalist lifestyle, permitting rapid transmission between different hosts. Furthermore, they show that the weak signal of host association within these complexes presents a challenge for pinpointing the source of clinical infections, underlining the view that whole-genome sequencing, powerful though it is, cannot substitute for intensive sampling of suspected transmission reservoirs.

Indexed as

AnimalsCampylobacterCampylobacter InfectionsCattleCattle DiseasesChickensHost SpecificityHumansPoultry DiseasesSwineSwine Diseases

Identifiers

PMID26305157
PMCPMC4677457
OpenAlexW1837396250

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.