Evidence map›Paper›PMID 33845877›Full record

ArticleMicrobiome2021

Isolation and characterisation of ΦcrAss002, a crAss-like phage from the human gut that infects Bacteroides xylanisolvens.

Emma Guerin, Andrey N Shkoporov, Stephen R Stockdale, Joan Colom Comas, Ekaterina V Khokhlova, Adam G Clooney, Karen M Daly, Lorraine A Draper, Niamh Stephens, Dimitri Scholz and 2 more

Abstract readVideo-Audio Media
In one paragraph

Article in Microbiome, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

  1. Review
  2. Phase variation inEngineering microbiology · 2026
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  18. Identification and characterization ofMicrobiology spectrum · 2025
    Article
  19. Review
  20. Review
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

12 authors.

Emma Guerin *APC Microbiome Ireland, University College Cork, Cork, Ireland.
Andrey N Shkoporov *APC Microbiome Ireland, University College Cork, Cork, Ireland.
Stephen R StockdaleAPC Microbiome Ireland, University College Cork, Cork, Ireland.
Joan Colom ComasAPC Microbiome Ireland, University College Cork, Cork, Ireland.
Ekaterina V KhokhlovaAPC Microbiome Ireland, University College Cork, Cork, Ireland.
Adam G ClooneyAPC Microbiome Ireland, University College Cork, Cork, Ireland.
Karen M DalyAPC Microbiome Ireland, University College Cork, Cork, Ireland.
Lorraine A DraperAPC Microbiome Ireland, University College Cork, Cork, Ireland.
Niamh StephensConway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4, Ireland.
Dimitri ScholzConway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4, Ireland.
R Paul RossAPC Microbiome Ireland, University College Cork, Cork, Ireland.
Colin HillAPC Microbiome Ireland, University College Cork, Cork, Ireland. c.hill@ucc.ie.ORCID 0000-0002-8527-1445

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe gut phageome comprises a complex phage community of thousands of individual strains, with a few highly abundant bacteriophages. CrAss-like phages, which infect bacteria of the order Bacteroidales, are the most abundant bacteriophage family in the human gut and make an important contribution to an individual's core virome. Based on metagenomic data, crAss-like phages form a family, with four sub-families and ten candidate genera. To date, only three representatives isolated in pure culture have been reported: ΦcrAss001 and two closely related phages DAC15 and DAC17; all are members of the less abundant candidate genus VI. The persistence at high levels of both crAss-like phage and their Bacteroidales hosts in the human gut has not been explained mechanistically, and this phage-host relationship can only be properly studied with isolated phage-host pairs from as many genera as possible.

resultsFaeces from a healthy donor with high levels of crAss-like phage was used to initiate a faecal fermentation in a chemostat, with selected antibiotics chosen to inhibit rapidly growing bacteria and selectively enrich for Gram-negative Bacteroidales. This had the objective of promoting the simultaneous expansion of crAss-like phages on their native hosts. The levels of seven different crAss-like phages expanded during the fermentation, indicating that their hosts were also present in the fermenter. The enriched supernatant was then tested against individual Bacteroidales strains isolated from the same faecal sample. This resulted in the isolation of a previously uncharacterised crAss-like phage of candidate genus IV of the proposed Alphacrassvirinae sub-family, ΦcrAss002, that infects the gut commensal Bacteroides xylanisolvens. ΦcrAss002 does not form plaques or spots on lawns of sensitive cells, nor does it lyse liquid cultures, even at high titres. In keeping with the co-abundance of phage and host in the human gut, ΦcrAss002 and Bacteroides xylanisolvens can also co-exist at high levels when co-cultured in laboratory media.

conclusionsWe report the isolation and characterisation of ΦcrAss002, the first representative of the proposed Alphacrassvirinae sub-family of crAss-like phages. ΦcrAss002 cannot form plaques or spots on bacterial lawns but can co-exist with its host, Bacteroides xylanisolvens, at very high levels in liquid culture without impacting on bacterial numbers. Video abstract.

Indexed as

BacteriophagesGastrointestinal MicrobiomeBacteroidesHumansPhylogenyBacteriophagescrAss-like phagescrAssphageHuman gut phageomeHuman microbiomePhage-host interactions

Identifiers

PMID33845877
PMCPMC8042965

What OpenQuestion holds

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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.