Evidence map›Paper›PMID 26870613›Full record

ArticlePeerJ2016

Molecular characterisation of the Chlamydia pecorum plasmid from porcine, ovine, bovine, and koala strains indicates plasmid-strain co-evolution.

Martina Jelocnik, Nathan L Bachmann, Helena Seth-Smith, Nicholas R Thomson, Peter Timms, Adam M Polkinghorne

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Current status and future directions ofFrontiers in veterinary science · 2026
    Pooled it
  2. Epidemiology and Genetic Diversity ofPathogens (Basel, Switzerland) · 2025
    Article
  3. Article
  4. Article
  5. Microorganisms · 2023
    Review
  6. Article
  7. Plasmid-mediated virulence inFrontiers in cellular and infection microbiology · 2023
    Review
  8. Article
  9. Completing the Genome Sequence ofPathogens (Basel, Switzerland) · 2021
    Article
  10. Pathogens (Basel, Switzerland) · 2021
    Article
  11. Dissection of Highly PrevalentAntibiotics (Basel, Switzerland) · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

6 authors at 3 institutions in 3 countries.

Martina JelocnikCentre for Animal Health Innovation, University of the Sunshine Coast , Sippy Downs, Queensland , Australia.
Nathan L BachmannCentre for Animal Health Innovation, University of the Sunshine Coast , Sippy Downs, Queensland , Australia.
Helena Seth-SmithFunctional Genomics Center Zurich, University of Zurich , Zurich , Switzerland.
Nicholas R ThomsonInfection Genomics, The Wellcome Trust Sanger Institute , Cambridge , United Kingdom.
Peter TimmsCentre for Animal Health Innovation, University of the Sunshine Coast , Sippy Downs, Queensland , Australia.
Adam M PolkinghorneCentre for Animal Health Innovation, University of the Sunshine Coast , Sippy Downs, Queensland , Australia.
University of the Sunshine Coast · AUUniversity of Zurich · CHWellcome Sanger Institute · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background. Highly stable, evolutionarily conserved, small, non-integrative plasmids are commonly found in members of the Chlamydiaceae and, in some species, these plasmids have been strongly linked to virulence. To date, evidence for such a plasmid in Chlamydia pecorum has been ambiguous. In a recent comparative genomic study of porcine, ovine, bovine, and koala C. pecorum isolates, we identified plasmids (pCpec) in a pig and three koala strains, respectively. Screening of further porcine, ovine, bovine, and koala C. pecorum isolates for pCpec showed that pCpec is common, but not ubiquitous in C. pecorum from all of the infected hosts. Methods. We used a combination of (i) bioinformatic mining of previously sequenced C. pecorum genome data sets and (ii) pCpec PCR-amplicon sequencing to characterise a further 17 novel pCpecs in C. pecorum isolates obtained from livestock, including pigs, sheep, and cattle, as well as those from koala. Results and Discussion. This analysis revealed that pCpec is conserved with all eight coding domain sequences (CDSs) present in isolates from each of the hosts studied. Sequence alignments revealed that the 21 pCpecs show 99% nucleotide sequence identity, with 83 single nucleotide polymorphisms (SNPs) shown to differentiate all of the plasmids analysed in this study. SNPs were found to be mostly synonymous and were distributed evenly across all eight pCpec CDSs as well as in the intergenic regions. Although conserved, analyses of the 21 pCpec sequences resolved plasmids into 12 distinct genotypes, with five shared between pCpecs from different isolates, and the remaining seven genotypes being unique to a single pCpec. Phylogenetic analysis revealed congruency and co-evolution of pCpecs with their cognate chromosome, further supporting polyphyletic origin of the koala C. pecorum. This study provides further understanding of the complex epidemiology of this pathogen in livestock and koala hosts and paves the way for studies to evaluate the function of this putative C. pecorum virulence factor.

Indexed as

Chlamydia pecorumComparative analysesKoalaMolecular characterisationPhylogenyPlasmid

Identifiers

PMID26870613
PMCPMC4748734
OpenAlexW2280688822

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.