Evidence map›Paper›PMID 31463770›Full record

ArticleVirus genes2019

Assessing circovirus gene flow in multiple spill-over events.

Shubhagata Das, Kate Smith, Subir Sarker, Andrew Peters, Katherine Adriaanse, Paul Eden, Seyed A Ghorashi, Jade K Forwood, Shane R Raidal

Abstract read
PubMed Publisher
In one paragraph

Article in Virus genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. High Prevalence of a Novel Circovirus in the European Hedgehog (Transboundary and emerging diseases · 2024
    Article
  6. Article
  7. Article
  8. The Oryx Antelope (Pathogens (Basel, Switzerland) · 2021
    Article
  9. 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

9 authors.

Shubhagata DasSchool of Animal and Veterinary Sciences, Charles Sturt University, Boorooma Street, Wagga Wagga, NSW, 2650, Australia.
Kate SmithSchool of Biomedical Sciences, Charles Sturt University, Boorooma Street, Wagga Wagga, NSW, 2650, Australia.
Subir SarkerDepartment of Physiology, Anatomy and Microbiology, School of Life Sciences, La Trobe University, Melbourne, 3086, Australia.
Andrew PetersSchool of Animal and Veterinary Sciences, Charles Sturt University, Boorooma Street, Wagga Wagga, NSW, 2650, Australia.ORCID http://orcid.org/0000-0003-4938-2823
Katherine AdriaanseHealesville Sanctuary, Zoos Victoria, Badger Creek Road, Healesville, VIC, 3777, Australia.
Paul EdenHealesville Sanctuary, Zoos Victoria, Badger Creek Road, Healesville, VIC, 3777, Australia.
Seyed A GhorashiSchool of Animal and Veterinary Sciences, Charles Sturt University, Boorooma Street, Wagga Wagga, NSW, 2650, Australia.ORCID http://orcid.org/0000-0002-9820-5308
Jade K ForwoodSchool of Biomedical Sciences, Charles Sturt University, Boorooma Street, Wagga Wagga, NSW, 2650, Australia.ORCID http://orcid.org/0000-0003-3267-9997
Shane R RaidalSchool of Animal and Veterinary Sciences, Charles Sturt University, Boorooma Street, Wagga Wagga, NSW, 2650, Australia. shraidal@csu.edu.au.ORCID http://orcid.org/0000-0001-7917-8976

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The establishment of viral pathogens in new host environments following spillover events probably requires adaptive changes within both the new host and pathogen. After many generations, signals for ancient cross-species transmission may become lost and a strictly host-adapted phylogeny may mimic true co-divergence while the virus may retain an inherent ability to jump host species. The mechanistic basis for such processes remains poorly understood. To study the dynamics of virus-host co-divergence and the arbitrary chances of spillover in various reservoir hosts with equal ecological opportunity, we examined structural constraints of capsid protein in extant populations of Beak and feather disease virus (BFDV) during known spillover events. By assessing reservoir-based genotype stratification, we identified co-divergence defying signatures in the evolution BFDV which highlighted primordial processes of cryptic host adaptation and competing forces of host co-divergence and cross-species transmission. We demonstrate that, despite extensive surface plasticity gathered over a longer span of evolution, structural constraints of the capsid protein allow opportunistic host switching in host-adapted populations. This study provides new insights into how small populations of endangered psittacine species may face multidirectional forces of infection from reservoirs with apparently co-diverging genotypes.

Indexed as

Evolution, MolecularAnimalsBird DiseasesCapsid ProteinsCircoviridae InfectionsCircovirusGene FlowGenotypeHost SpecificityParrotsPhylogenyPsittaciformesCapsid ProteinsCircovirusMicrobiomePBFDPsittacine beak and feather diseaseViral ecology

Identifiers

What OpenQuestion holds

Textmetadata
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.