Evidence map›Paper›PMID 30352623›Full record

ArticleMicrobiome2018

A diversity-generating retroelement encoded by a globally ubiquitous Bacteroides phage.

Sean Benler, Ana Georgina Cobián-Güemes, Katelyn McNair, Shr-Hau Hung, Kyle Levi, Rob Edwards, Forest Rohwer

Open access · goldAbstract read
In one paragraph

Article in Microbiome, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
9.0field-weighted citation impact, top 2% 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

44 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2026
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  13. Identification and characterization ofMicrobiology spectrum · 2025
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  19. Knowing and Naming: Phage Annotation and Nomenclature for Phage Therapy.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Review
  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

7 authors at 1 institution in 1 country.

Sean BenlerDepartment of Biology, San Diego State University, 5500 Campanile Drive, San Diego, CA, 92182, USA. sbenler@gmail.com.ORCID 0000-0001-7985-1294
Ana Georgina Cobián-GüemesDepartment of Biology, San Diego State University, 5500 Campanile Drive, San Diego, CA, 92182, USA.
Katelyn McNairDepartment of Computer Science, San Diego State University, 5500 Campanile Drive, San Diego, CA, 92182, USA.
Shr-Hau HungDepartment of Biology, San Diego State University, 5500 Campanile Drive, San Diego, CA, 92182, USA.
Kyle LeviDepartment of Computer Science, San Diego State University, 5500 Campanile Drive, San Diego, CA, 92182, USA.
Rob EdwardsDepartment of Computer Science, San Diego State University, 5500 Campanile Drive, San Diego, CA, 92182, USA.
Forest RohwerDepartment of Biology, San Diego State University, 5500 Campanile Drive, San Diego, CA, 92182, USA.
San Diego State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiversity-generating retroelements (DGRs) are genetic cassettes that selectively mutate target genes to produce hypervariable proteins. First characterized in Bordetella bacteriophage BPP-1, the DGR creates a hypervariable phage tail fiber that enables host tropism switching. Subsequent surveys for DGRs conclude that the majority identified to date are bacterial or archaeal in origin. This work examines bacteriophage and bacterial genomes for novel phage-encoded DGRs.

resultsThis survey discovered 92 DGRs that were only found in phages exhibiting a temperate lifestyle. The majority of phage-encoded DGRs were identified as prophages in bacterial hosts from the phyla Bacteroidetes, Proteobacteria, and Firmicutes. Sequence reads from these previously unidentified prophages were present in viral metagenomes (viromes), indicating these prophages can produce functional viruses. Five phages possessed hypervariable proteins with structural similarity to the tail fiber of BPP-1, whereas the functions of the remaining DGR target proteins were unknown. A novel temperate phage that harbors a DGR cassette targeting a protein of unknown function was induced from Bacteroides dorei. This phage, here named Bacteroides dorei Hankyphage, lysogenizes 13 different Bacteroides species and was present in 34% and 21% of whole-community metagenomes and human-associated viromes, respectively.

conclusionsHere, the number of known DGR-containing phages is increased from four to 92. All of these phages exhibit a temperate lifestyle, including a cosmopolitan human-associated phage. Targeted hypervariation by temperate phages may be a ubiquitous mechanism underlying phage-bacteria interaction in the human microbiome.

Indexed as

BacteroidesGenome, ViralHumansMetagenomeProphagesRetroelementsViral Tail ProteinsRetroelementsViral Tail ProteinsBacteroidesDiversity-generating retroelementsProphageViromes

Identifiers

PMID30352623
PMCPMC6199706
OpenAlexW2895938591

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.