Evidence map›Paper›PMID 31329588›Full record

ArticlePloS one2019

Investigation of the validity of two Bayesian ancestral state reconstruction models for estimating Salmonella transmission during outbreaks.

Samuel Bloomfield, Timothy Vaughan, Jackie Benschop, Jonathan Marshall, David Hayman, Patrick Biggs, Philip Carter, Nigel French

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Quantifying the transmission of antimicrobial resistance at the human and livestock interface with genomics.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2020
    Review
  3. 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

8 authors.

Samuel BloomfieldQuadram Institute, Norwich Research Park, Colney Lane, Norwich, United Kingdom.ORCID 0000-0003-0743-2239
Timothy VaughanDepartment of Biosystems Science and Engineering, ETH Zurich, Zurich, Switzerland.
Jackie BenschopMolecular Epidemiology and Public Health Laboratory, Massey University, Palmerston North, New Zealand.
Jonathan MarshallMolecular Epidemiology and Public Health Laboratory, Massey University, Palmerston North, New Zealand.
David HaymanMolecular Epidemiology and Public Health Laboratory, Massey University, Palmerston North, New Zealand.
Patrick BiggsMolecular Epidemiology and Public Health Laboratory, Massey University, Palmerston North, New Zealand.ORCID 0000-0002-0285-4101
Philip CarterInstitute of Environmental Science and Research, Keneperu, New Zealand.
Nigel FrenchMolecular Epidemiology and Public Health Laboratory, Massey University, Palmerston North, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ancestral state reconstruction models use genetic data to characterize a group of organisms' common ancestor. These models have been applied to salmonellosis outbreaks to estimate the number of transmissions between different animal species that share similar geographical locations, with animal host as the state. However, as far as we are aware, no studies have validated these models for outbreak analysis. In this study, salmonellosis outbreaks were simulated using a stochastic Susceptible-Infected-Recovered model, and the host population and transmission parameters of these simulated outbreaks were estimated using Bayesian ancestral state reconstruction models (discrete trait analysis (DTA) and structured coalescent (SC)). These models were unable to accurately estimate the number of transmissions between the host populations or the amount of time spent in each host population. The DTA model was inaccurate because it assumed the number of isolates sampled from each host population was proportional to the number of individuals infected within each host population. The SC model was inaccurate possibly because it assumed that each host population's effective population size was constant over the course of the simulated outbreaks. This study highlights the need for phylodynamic models that can take into consideration factors that influence the characteristics and behavior of outbreaks, e.g. changing effective population sizes, variation in infectious periods, intra-population transmissions, and disproportionate sampling of infected individuals.

Indexed as

Disease OutbreaksModels, BiologicalSalmonellaSalmonella Infections, AnimalAnimalsBayes Theorem

Identifiers

PMID31329588
PMCPMC6645465

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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.