Evidence map›Paper›PMID 40654884›Full record

ArticlebioRxiv : the preprint server for biology2025

Discovering Broader Host Ranges and an IS-bound Prophage Class Through Long-Read Metagenomics.

Jakob Wirbel, Angela S Hickey, Daniel Chang, Nora J Enright, Mai Dvorak, Rachael B Chanin, Danica T Schmidtke, Ami S Bhatt

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jakob WirbelDivision of Hematology, Department of Medicine, Stanford University, Stanford, CA.ORCID 0000-0002-4073-3562
Angela S HickeyDepartment of Genetics, Stanford University, Stanford, CA.ORCID 0000-0003-4407-6894
Daniel ChangDepartment of Genetics, Stanford University, Stanford, CA.ORCID 0000-0003-0076-2833
Nora J EnrightDepartment of Bioengineering, Stanford University, Stanford, CA.ORCID 0000-0003-1557-6638
Mai DvorakDepartment of Biology, Stanford University, Stanford, CA.ORCID 0000-0002-8481-7063
Rachael B ChaninDivision of Hematology, Department of Medicine, Stanford University, Stanford, CA.ORCID 0000-0002-4625-356X
Danica T SchmidtkeDepartment of Microbiology and Immunology, Stanford University, Stanford, CA.ORCID 0000-0001-9509-6188
Ami S BhattDivision of Hematology, Department of Medicine, Stanford University, Stanford, CA.ORCID 0000-0001-8099-2975

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Culture-free pathogen tracking in hospitalized patientsR01AI143757 · NIAID · STANFORD UNIVERSITY · PI BHATT, AMI SIDDHARTH · 2020 to 2023
$3.0M
Emerging novel mechanisms of antibiotic resistance in the prevalent foodborne pathogen, SalmonellaR01AI148623 · NIAID · STANFORD UNIVERSITY · PI BHATT, AMI SIDDHARTH · 2019 to 2023
$2.0M
NIAID NIH HHS R01 AI143757NIAID NIH HHS R01 AI148623NIGMS NIH HHS T32 GM007276
6 · The paper itself

Abstract

Gut bacteriophages profoundly impact microbial ecology and human health, yet they are greatly understudied. Using deep, long-read bulk metagenomic sequencing, a technique that overcomes fundamental limitations of short-read approaches, we tracked prophage integration dynamics in 12 longitudinal stool samples from six healthy individuals, spanning a two-year timescale. While most prophages remain stably integrated into their host over two years, we discover that ~5% of phages are dynamically gained or lost from persistent bacterial hosts. Within the same sample, we find evidence of population heterogeneity in which identical bacterial hosts with and without a given integrated prophage coexist simultaneously. Furthermore, we demonstrate that phage induction, when detected, occurs predominantly at low levels (1-3x coverage compared to the host region). Interestingly, we identify multiple instances of integration of the same phage into bacteria of different taxonomic families, challenging the dogma that phage are specific to a host of a given species or strain. Lastly, we describe a new class of phages, which we name "IScream phages". These phages co-opt bacterial IS30 transposases to mediate their integration, representing a previously unrecognized form of phage domestication of selfish bacterial elements. Taken together, these findings illuminate fundamental aspects of phage-bacterial dynamics in the human gut microbiome and expand our understanding of the evolutionary mechanisms that drive horizontal gene transfer and microbial genome plasticity in this ecosystem.

Indexed as

Insertion sequencesLong-read sequencingMetagenomicsMicrobiomePhages

Identifiers

PMID40654884
PMCPMC12247996

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.