Evidence map›Paper›PMID 28209138›Full record

ArticleBMC genomics2017

Using whole genome sequencing to investigate transmission in a multi-host system: bovine tuberculosis in New Zealand.

Joseph Crispell, Ruth N Zadoks, Simon R Harris, Brent Paterson, Desmond M Collins, Geoffrey W de-Lisle, Paul Livingstone, Mark A Neill, Roman Biek, Samantha J Lycett and 2 more

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Review
  2. Article
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  8. Article
  9. Population structure and history ofMicrobiology spectrum · 2024
    Article
  10. Rescue ofInternational journal of molecular sciences · 2024
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  11. Whole-Genome sequencing in routineMicrobial genomics · 2024
    Article
  12. Genomic comparison betweenFrontiers in veterinary science · 2024
    Article
  13. Article
  14. Whole genome sequencing improves the discrimination betweenOne health (Amsterdam, Netherlands) · 2023
    Article
  15. The Many Hosts of Mycobacteria 9 (MHM9): A conference report.Tuberculosis (Edinburgh, Scotland) · 2023
    Article
  16. Article
  17. Genomic epidemiology ofMicrobial genomics · 2023
    Article
  18. Features ofMicroorganisms · 2023
    Article
  19. Unraveling the epidemiology ofFrontiers in veterinary science · 2023
    Article
  20. Whole genome sequencing ofFrontiers in microbiology · 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

12 authors.

Joseph CrispellInstitute of Biodiversity, Animal Health, and Comparative Medicine, University of Glasgow, Glasgow, Scotland, G61 1QH, UK.
Ruth N ZadoksInstitute of Biodiversity, Animal Health, and Comparative Medicine, University of Glasgow, Glasgow, Scotland, G61 1QH, UK.
Simon R HarrisWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
Brent PatersonTBfree New Zealand, PO Box 3412, Wellington, 6140, New Zealand.
Desmond M CollinsAgResearch, Hopkirk Research Centre, Palmerston North, New Zealand.
Geoffrey W de-LisleAgResearch, Hopkirk Research Centre, Palmerston North, New Zealand.
Paul LivingstoneTBfree New Zealand, PO Box 3412, Wellington, 6140, New Zealand.
Mark A NeillTBfree New Zealand, PO Box 3412, Wellington, 6140, New Zealand.
Roman BiekInstitute of Biodiversity, Animal Health, and Comparative Medicine, University of Glasgow, Glasgow, Scotland, G61 1QH, UK.
Samantha J LycettInfection and Immunity Division, The Roslin Institute, University of Edinburgh, Easter Bush, Midlothian, Scotland, UK.
Rowland R KaoInstitute of Biodiversity, Animal Health, and Comparative Medicine, University of Glasgow, Glasgow, Scotland, G61 1QH, UK. Rowland.Kao@glasgow.ac.uk.
Marian Price-CarterAgResearch, Hopkirk Research Centre, Palmerston North, New Zealand.

Funding

Biotechnology and Biological Sciences Research CouncilWellcome Trust
6 · The paper itself

Abstract

backgroundBovine tuberculosis (bTB), caused by Mycobacterium bovis, is an important livestock disease raising public health and economic concerns around the world. In New Zealand, a number of wildlife species are implicated in the spread and persistence of bTB in cattle populations, most notably the brushtail possum (Trichosurus vulpecula). Whole Genome Sequenced (WGS) M. bovis isolates sourced from infected cattle and wildlife across New Zealand were analysed. Bayesian phylogenetic analyses were conducted to estimate the substitution rate of the sampled population and investigate the role of wildlife. In addition, the utility of WGS was examined with a view to these methods being incorporated into routine bTB surveillance.

resultsA high rate of exchange was evident between the sampled wildlife and cattle populations but directional estimates of inter-species transmission were sensitive to the sampling strategy employed. A relatively high substitution rate was estimated, this, in combination with a strong spatial signature and a good agreement to previous typing methods, acts to endorse WGS as a typing tool.

conclusionsIn agreement with the current knowledge of bTB in New Zealand, transmission of M. bovis between cattle and wildlife was evident. Without direction, these estimates are less informative but taken in conjunction with the low prevalence of bTB in New Zealand's cattle population it is likely that, currently, wildlife populations are acting as the main bTB reservoir. Wildlife should therefore continue to be targeted if bTB is to be eradicated from New Zealand. WGS will be a considerable aid to bTB eradication by greatly improving the discriminatory power of molecular typing data. The substitution rates estimated here will be an important part of epidemiological investigations using WGS data.

Indexed as

Whole Genome SequencingAnimalsBayes TheoremCattleCluster AnalysisMycobacterium bovisNew ZealandPhylogenyTuberculosis, BovineBovine tuberculosisInter-species transmissionNew ZealandSubstitution rateWhole Genome Sequencing

Identifiers

PMID28209138
PMCPMC5314462

What OpenQuestion holds

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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.