Evidence map›Paper›PMID 26497500›Full record

ArticleBMC genomics2015

Novel Moraxella catarrhalis prophages display hyperconserved non-structural genes despite their genomic diversity.

Amir Ariff, Michael J Wise, Charlene M Kahler, Chin Yen Tay, Fanny Peters, Timothy T Perkins, Barbara J Chang

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Viruses · 2025
    Article
  3. Article
  4. Review
  5. Panel 7 - Pathogenesis of otitis media - a review of the literature between 2015 and 2019.International journal of pediatric otorhinolaryngology · 2020
    Review
  6. Review
  7. NovelFrontiers in microbiology · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. 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

7 authors at 1 institution in 1 country.

Amir AriffSchool of Pathology and Laboratory Medicine, The University of Western Australia, Perth, WA, Australia. 20566454@student.uwa.edu.au.
Michael J WiseSchool of Chemistry and Biochemistry, The University of Western Australia, Perth, WA, Australia. michael.wise@uwa.edu.au.
Charlene M KahlerSchool of Pathology and Laboratory Medicine, The University of Western Australia, Perth, WA, Australia. charlene.kahler@uwa.edu.au.
Chin Yen TaySchool of Pathology and Laboratory Medicine, The University of Western Australia, Perth, WA, Australia. alfred.tay@uwa.edu.au.
Fanny PetersSchool of Pathology and Laboratory Medicine, The University of Western Australia, Perth, WA, Australia. fanny.peters@uwa.edu.au.
Timothy T PerkinsSchool of Pathology and Laboratory Medicine, The University of Western Australia, Perth, WA, Australia. tim.perkins@uwa.edu.au.
Barbara J ChangSchool of Pathology and Laboratory Medicine, The University of Western Australia, Perth, WA, Australia. barbara.chang@uwa.edu.au.
The University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMoraxella catarrhalis is an important pathogen that often causes otitis media in children, a disease that is not currently vaccine preventable. Asymptomatic colonisation of the human upper respiratory tract is common and lack of clearance by the immune system is likely due to the emergence of seroresistant genetic lineages. No active bacteriophages or prophages have been described in this species. This study was undertaken to identify and categorise prophages in M. catarrhalis, their genetic diversity and the relationship of such diversity with the host-species phylogeny.

resultsThis study presents a comparative analysis of 32 putative prophages identified in 95 phylogenetically variable, newly sequenced M. catarrhalis genomes. The prophages were genotypically classified into four diverse clades. The genetic synteny of each clade is similar to the group 1 phage family Siphoviridae, however, they form genotypic clusters that are distinct from other members of this family. No core genetic sequences exist across the 32 prophages despite clades 2, 3, and 4 sharing the most sequence identity. The analysis of non-structural prophage genes (coding the integrase, and terminase), and portal gene showed that the respective genes were identical for clades 2, 3, and 4, but unique for clade 1. Empirical analysis calculated that these genes are unexpectedly hyperconserved, under purifying selection, suggesting a tightly regulated functional role. As such, it is improbable that the prophages are decaying remnants but stable components of a fluctuating, flexible and unpredictable system ultimately maintained by functional constraints on non-structural and packaging genes. Additionally, the plate encoding genes were well conserved across all four prophage clades, and the tail fibre genes, commonly responsible for receptor recognition, were clustered into three major groups distributed across the prophage clades. A pan-genome of 283,622 bp was identified, and the prophages were mapped onto the diverse M. catarrhalis multi-locus sequence type (MLST) backbone.

conclusionThis study has provided the first evidence of putatively mobile prophages in M. catarrhalis, identifying a diverse and fluctuating system dependent on the hyperconservation of a few key, non-structural genes. Some prophages harbour virulence-related genes, and potentially influence the physiology and virulence of M. catarrhalis. Importantly our data will provide supporting information on the identification of novel prophages in other species by adding greater weight to the identification of non-structural genes.

Indexed as

Conserved SequenceGenetic VariationGenome, ViralCodonComputational BiologyEvolution, MolecularGenomicsMoraxella catarrhalisMultilocus Sequence TypingPhylogenyProphagesViral Nonstructural ProteinsViral ProteinsVirulenceCodonViral Nonstructural ProteinsViral Proteins

Identifiers

PMID26497500
PMCPMC4619438
OpenAlexW2116604501

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.