Evidence map›Paper›PMID 31163033›Full record

ArticlePLoS neglected tropical diseases2019

The diversity, evolution and ecology of Salmonella in venomous snakes.

Caisey V Pulford, Nicolas Wenner, Martha L Redway, Ella V Rodwell, Hermione J Webster, Roberta Escudero, Carsten Kröger, Rocío Canals, Will Rowe, Javier Lopez and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Prevalence and Antimicrobial Resistance Patterns ofAnimals : an open access journal from MDPI · 2025
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  4. One health (Amsterdam, Netherlands) · 2024
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  5. Detection ofMicroorganisms · 2024
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  6. Article
  7. Review
  8. Surveys on Pet-Reptile-Associated Multi-Drug-ResistantAntibiotics (Basel, Switzerland) · 2023
    Article
  9. One Health Approach: Invasive California Kingsnake (Animals : an open access journal from MDPI · 2023
    Article
  10. Article
  11. Article
  12. Zoonotic potential and prevalence ofInfection ecology & epidemiology · 2021
    Review
  13. Article
  14. Genomic characterization ofMicrobial genomics · 2020
    Article
  15. Article
  16. Antimicrobial Drug Resistance inFrontiers in veterinary science · 2020
    Article
  17. Genomic diversity ofWellcome open research · 2020
    Article
  18. Infection and immunity · 2019
    Review
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

16 authors at 4 institutions in 1 country.

Caisey V PulfordDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0003-2500-9119
Nicolas WennerDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Martha L RedwayDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Ella V RodwellDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Hermione J WebsterDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Roberta EscuderoDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Carsten KrögerDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0003-0461-1530
Rocío CanalsDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Will RoweDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Javier LopezAnimal Health Department, Chester Zoo, Cheshire, United Kingdom.
Neil HallEarlham Institute, Norwich Research Park, Norwich, United Kingdom.
Paul D RowleyCentre for Snakebite Research and Interventions, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Dorina TimofteInstitute of Veterinary Science, University of Liverpool, Leahurst Campus, Cheshire, United Kingdom.
Robert A HarrisonCentre for Snakebite Research and Interventions, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Kate S BakerDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Jay C D HintonDepartment of Functional and Comparative Genomics, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
University of Liverpool · GBLiverpool School of Tropical Medicine · GBChester Zoo · GBUniversity of East Anglia · GB

Funding

Biotechnology and Biological Sciences Research Council BB/CSP17270/1Biotechnology and Biological Sciences Research Council BB/L024209/1Medical Research Council MR/L01839X/1Wellcome TrustWellcome Trust 106690/A/14/ZWellcome Trust 106914/Z/15/Z
6 · The paper itself

Abstract

backgroundReptile-associated Salmonella bacteria are a major, but often neglected cause of both gastrointestinal and bloodstream infection in humans globally. The diversity of Salmonella enterica has not yet been determined in venomous snakes, however other ectothermic animals have been reported to carry a broad range of Salmonella bacteria. We investigated the prevalence and diversity of Salmonella in a collection of venomous snakes and non-venomous reptiles. METHODOLOGY/PRINCIPLE

findingsWe used a combination of selective enrichment techniques to establish a unique dataset of reptilian isolates to study Salmonella enterica species-level evolution and ecology and used whole-genome sequencing to investigate the relatedness of phylogenetic groups. We observed that 91% of venomous snakes carried Salmonella, and found that a diverse range of serovars (n = 58) were carried by reptiles. The Salmonella serovars belonged to four of the six Salmonella enterica subspecies: diarizonae, enterica, houtanae and salamae. Subspecies enterica isolates were distributed among two distinct phylogenetic clusters, previously described as clade A (52%) and clade B (48%). We identified metabolic differences between S. diarizonae, S. enterica clade A and clade B involving growth on lactose, tartaric acid, dulcitol, myo-inositol and allantoin. SIGNIFICANCE: We present the first whole genome-based comparative study of the Salmonella bacteria that colonise venomous and non-venomous reptiles and shed new light on Salmonella evolution. Venomous snakes examined in this study carried a broad range of Salmonella, including serovars which have been associated with disease in humans such as S. Enteritidis. The findings raise the possibility that venomous snakes could be a reservoir for Salmonella serovars associated with human salmonellosis.

Indexed as

Genetic VariationAnimalsPrevalenceSalmonella entericaSalmonella Infections, AnimalSerogroupSnakesWhole Genome Sequencing

Identifiers

PMID31163033
PMCPMC6548357
OpenAlexW2949253850

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.