Evidence map›Paper›PMID 26892066›Full record

ArticleScientific reports2016

Comparative genomics and functional analysis of the 936 group of lactococcal Siphoviridae phages.

James Murphy, Francesca Bottacini, Jennifer Mahony, Philip Kelleher, Horst Neve, Aldert Zomer, Arjen Nauta, Douwe van Sinderen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
10.8field-weighted citation impact, top 1% 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

41 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Longitudinal Study ofApplied and environmental microbiology · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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 at 3 institutions in 3 countries.

James MurphySchool of Microbiology, University College Cork, Cork, Ireland.
Francesca BottaciniAlimentary Pharmabiotic Centre, University College Cork, Cork, Ireland.
Jennifer MahonySchool of Microbiology, University College Cork, Cork, Ireland.
Philip KelleherSchool of Microbiology, University College Cork, Cork, Ireland.
Horst NeveDepartment of Microbiology and Biotechnology, Max Rubner-Institut, Kiel, Germany.
Aldert ZomerSchool of Microbiology, University College Cork, Cork, Ireland.
Arjen NautaFrieslandCampina, Amersfoort, The Netherlands.
Douwe van SinderenSchool of Microbiology, University College Cork, Cork, Ireland.
University College Cork · IEFrieslandCampina (Netherlands) · NLMax Rubner Institut · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome sequencing and comparative analysis of bacteriophage collections has greatly enhanced our understanding regarding their prevalence, phage-host interactions as well as the overall biodiversity of their genomes. This knowledge is very relevant to phages infecting Lactococcus lactis, since they constitute a significant risk factor for dairy fermentations. Of the eighty four lactococcal phage genomes currently available, fifty five belong to the so-called 936 group, the most prevalent of the ten currently recognized lactococcal phage groups. Here, we report the genetic characteristics of a new collection of 936 group phages. By combining these genomes to those sequenced previously we determined the core and variable elements of the 936 genome. Genomic variation occurs across the 936 phage genome, such as genetic elements that (i) lead to a +1 translational frameshift resulting in the formation of additional structures on the phage tail, (ii) specify a double neck passage structure, and (iii) encode packaging module-associated methylases. Hierarchical clustering of the gene complement of the 936 group phages and nucleotide alignments allowed grouping of the ninety 936 group phages into distinct clusters, which in general appear to correspond with their geographical origin.

Indexed as

Genome, ViralGenomicsAlgorithmsCluster AnalysisDNA, ViralGenetic VariationMarkov ChainsPhylogenySiphoviridaeTranscriptomeViral ProteinsViral TropismDNA, ViralViral Proteins

Identifiers

PMID26892066
PMCPMC4759559
OpenAlexW2343523640

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.